2012 h2 Chemistry PDF

JC-2 Examination Papers
2012
Chemistry
College
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ANDERSON JUNIOR COLLEGE

Preliminary Examinations 2012
CHEMISTRY
9647/01
Higher 2
19 September 2012
Paper 1 Multiple Choice
Additional Materials:
1 hour
Multiple Choice Answer Sheet

Data Booklet
READ THESE INSTRUCTIONS FIRST

Write in soft pencil.
Do not use staples, paper clips, highlighters, glue or correction fluid.
There are forty questions on this paper. Answer all questions. For each question there are four
possible answers A, B, C and D.
Choose the one you consider correct and record your choice in soft pencil on the Multiple
Choice Answer Sheet.
Each correct answer will score one mark. A mark will not be deducted for a wrong answer.
Any rough working should be done in this booklet.

Write your name, PDG and NRIC/FIN number, including the reference letter.
Shade the NRIC / FIN number.
Exam Title:
JC 2 Prelim
Exam Details: H2 Chem / Paper 1

Date:
19/09/2012
This document consists of 17 printed pages.

AJC Prelim 2012
9647/01/H2
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2
Section A
For each question there are four possible answers, A, B, C and D. Choose the one you
consider to be correct.
The first stage in the manufacture of nitric acid is the oxidation of ammonia by oxygen.
aNH3(g) + bO2(g)
cNO(g) + dH2O(g)
What are the values for a, b, c and d?
a
4
b
5
c
4
d
6
The nickelcadmium rechargeable battery is based on the following overall reaction.

Cd + 2NiOOH + 4H2O
Cd(OH)2 + 2Ni(OH)2.H2O
What is the oxidation number of nickel at the beginning and at the end of the reaction?
Beginning
+1.5
End
+2
+2
+3
+3
+2
+3
+4
Which element has an equal number of paired and unpaired electrons in its orbitals with
principal quantum number 2?
A
Beryllium
Carbon
Nitrogen
Oxygen
AJC Prelim 2012
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3
4
Americium241 is commonly used in smoke detectors. It works by emitting a constant

stream of alpha particles which are similar to the nucleus of 4He.
Strontium90 is another radioactive substance which can be used as a tracer for
medicinal or agriculture uses. On decaying, it emits beta particles which can be
considered as electrons.
A small amount of Americium241 and Strontium90 are separately placed in an
ionisation chamber to emit a constant stream of radiation and the emitted particles are
passed through an electric field.
+
1
2
What would be the path of the emitted particles in an electric field?
Americium241
(aparticles)
1
Strontium90
(bparticles)
2
Which of the following is not a feature in the corresponding ion?
Ion
HF2
Feature
Hydrogen bond
NO2
Unpaired electron
CO32
Delocalised electrons
C6H5O
All bond angles are 120
AJC Prelim 2012
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4
6
Two gas bulbs, E and F, are connected by a stopcock. Bulb E contains argon and bulb F
contains oxygen gas. The pressure and volume of gas in each bulb at 25 C is shown
below.
Bulb E
Bulb F
Volume / dm3
7v
Pressure / kPa
5p
The stopcock is then opened and the gases were allowed to mix at 25 C. Subsequently,
the temperature of the mixture is raised and the final pressure is found to be 9p.
What is the temperature of the gases in the mixture that gives a pressure of 9p?
50 C
596 C
50 K
596 K
Solutions of hydrogencarbonates can react with acids as follows.

HCO3(aq) + H+(aq)
H2O(l) + CO2(g)
DHo = +12.7 kJ mol1
Given the following enthalpy changes:

species
H2O(l)
CO2(g)
HCO3(aq)
DH qf / kJ mol1
285.8
393.5
692.0
What is the standard enthalpy change of formation of H+(aq)?

25.4 kJ mol1
0.0 kJ mol1
+25.4 kJ mol1
+1384 kJ mol1
The Gibbs free energy change of a system determines whether a reaction is spontaneous,
while the equilibrium constant indicates the extent of reaction.
What does the following pair of values for a reaction system indicate?
DG f
values
50.8
Kc
5.80 x 108
No reaction
Position of equilibrium lies to the left
Some extent of reaction
Reaction goes to completion
AJC Prelim 2012
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5
9
The electrolysis of a highly concentrated aqueous solution of potassium hydroxide was

carried out using an iron anode and a platinum cathode. After a current was passed
through the cell for some time, 360 cm3 of gas was collected at the cathode (measured at
r.t.p.) while there was a loss of mass of 0.279 g at the anode.
Which of the following ions is a likely product at the anode?
A
10
Fe2+
Fe3+
FeO44
FeO42
The percentage of ammonia obtainable, if equilibrium was established during the Haber
process, is plotted against the operating pressure for two temperatures, 400 C and
500 C.
Which diagram correctly represents the two graphs?
A
% NH3 at
equilibrium
% NH3 at
equilibrium
pressure/ 103 kPa
pressure/ 103 kPa
% NH3 at
equilibrium
% NH3 at
equilibrium
3
pressure/ 10 kPa
3
pressure/ 10 kPa
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11
Water dissociates into H+ and OH as shown.

H+ + OH
H2O
At 25 C, the equilibrium [H+] is 107 mol dm3; [H2O] = 55.6 mol dm3.
What is the order of increasing numerical value of pH, pKa and pKw for this equilibrium at
this temperature?
12
smallest
pH
pKw
largest
pKa
pH
pKa
pKw
pKw
pKa
pH
pKa
pKw
pH
Bromocresol green is an acidbase indicator with a pH range of 3.8 to 5.4. The acidic
colour of the indicator is yellow and the alkaline colour is blue.
Two drops of the indicator are added to each of the four aqueous solutions listed below.
Which solution has its colour not correctly stated?
13
Aqueous solution of MgCl2
blue
Equal proportions of sodium ethanoate and ethanoic acid

[pKa of ethanoic acid = 4.7]
green
Dilute HCl of concentration 3.0 x 105 mol dm3
yellow
Aluminium oxide in aqueous solution
blue
Lead is the final product formed by a series of changes in which the ratedetermining
step is the radioactive decay of uranium238. The radioactive decay is a first order
reaction with a halflife of 4.5 x 109 years.
What would be the age of a rock sample, originally leadfree, in which the molar
proportion of uranium to lead is now 1:3?
A
2.25 x 109 years
4.5 x 109 years
9.0 x 109 years
13.5 x 109 years
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14
Na2S2O3 reacts with dilute HCl to give a pale yellow precipitate. If 1 cm3 of 0.1 mol dm3
HCl is added to 10 cm3 of 0.02 mol dm3 Na2S2O3 the precipitate forms slowly. If the
experiment is repeated with 1 cm3 of 0.1 mol dm3 HCl and 10 cm3 of 0.05 mol dm3
Na2S2O3 the precipitate forms more quickly.
Which of the following helps to explain this observation?
15
The activation energy of the reaction is lower when 0.05 mol dm3 Na2S2O3 is used.
The reaction proceeds by a different pathway when 0.05 mol dm3 Na2S2O3 is used.
The collisions between reactant particles are more violent when 0.05 mol dm3
Na2S2O3 is used.
The reactant particles collide more frequently when 0.05 mol dm3 Na2S2O3 is used.
Consecutive elements G, H and I are in the third period of the Periodic Table. Element H
has the highest first ionisation energy and the lowest melting point.
What could be the identities of G, H and I?
16
Aluminium, silicon, phosphorus
Magnesium, aluminium, silicon
Silicon, phosphorus, sulfur
Sodium, magnesium, aluminium
Use of the Data Booklet is relevant to this question.

A 5.00 g sample of an anhydrous Group II metal nitrate loses 3.29 g in mass when heated
strongly.
Which metal is present?
17
Magnesium
Calcium
Strontium
Barium
Which suggestion concerning the element astatine (proton number 85) is consistent with
its position in Group VII?
A
The element is a solid at room temperature and pressure.
Hydrogen astatide is more stable to heat than hydrogen iodide.
Silver astatide is soluble in aqueous ammonia.
Hydrogen astatide is a weak acid.
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18
The structures of two complexes are as shown.

O
O
O
O
N
Co
CO
N Ni CO
CO
O
[Co(edta)] -
[Ni(CO)3(py)]
where py =
Which of the following statements is correct?
19
Both complexes contain two different ligands.
Co in the complex has four unpaired delectrons.
The oxidation number of Co in the complex is +2.
The electronic configuration of nickel in the complex is [Ar] 3d7.
Platinum(IV) chloride combines with ammonia to form compounds in which the

coordination number of platinum is 6. A formula unit of one of the compounds contains a
cation and only one chloride ion.
What is the formula of this compound?
20
Pt(NH3)6Cl4
Pt(NH3)5Cl4
Pt(NH3)4Cl4
Pt(NH3)3Cl4
Limonene occurs in oil of lemons and is used to flavour some citrus drinks. The structure
of limonene is shown below.
limonene
How many optical isomers will be formed when limonene is reacted with cold acidified
potassium manganate(VII)?
A
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32
9
21
When heated with chlorine, 2,2dimethylbutane undergoes free radical substitution.

In a propagation step, the free radical X is formed.
CH3
CH3CH2
CH3
Cl
+ HCl
CH3
How many different forms of X are possible?

A
22
A compound has the following structure.
OH
CH2Br
CH2CH2Cl
Cl
Which of the following is obtained when alcoholic sodium ethoxide is added to this
compound?
A
OH
OH
CH2OCH2CH3
CH2CH2OCH2CH3
CH3CH2O
CH2Br
CH3CH2O
D
OCH2CH3
OH
CH2Br
CH2OCH2CH3
Cl
AJC Prelim 2012
OCH2CH3
Cl
CH CH2
9647/01/H2
CH CH2
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10
23

2.76 g of ethanol were mixed with an excess of aqueous acidified potassium
dichromate(VI). The reaction mixture was then boiled under reflux for one hour. The
organic product was then collected by distillation.
The yield of product was 75.0 %.
What mass of product was collected?
A
24
1.98 g
2.07 g
2.70 g
4.80 g
The Grignard Reaction is the addition of an organomagnesium halide, RMgX (Grignard

reagent) to a carbonyl compound to form an alcohol. For example, the reaction with
methanal leads to the formation of a primary alcohol as shown.
O
H
1. CH3MgBr
2.
OH
H 2O
OH
Which of the following pairs of reagents could be used to produce

A
O
MgBr
and
O
MgBr
and
O
and
MgBr
O
and
25
MgBr
Which of the following, in aqueous solutions of equal concentration, is arranged in order of

decreasing pH value?
A
CH3CH2OH, C6H5OH, CH3CO2H, ClCH2CO2H, CH3COCl
CH3CH2OH, C6H5OH, ClCH2CO2H, CH3CO2H, CH3COCl
CH3COCl, ClCH2CO2H, CH3CO2H, C6H5OH, CH3CH2OH
CH3COCl, CH3CH2OH, C6H5OH, CH3CO2H, ClCH2CO2H
AJC Prelim 2012
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26
Two isomers, L and M, C6H12O, react with alkaline aqueous iodine to form a yellow
precipitate. However, unlike L, M can also react with both PCl5 and ethanoyl chloride. M
undergoes oxidation to form two compounds, both of which also form a yellow precipitate
with alkaline aqueous iodine.
Which combination could L and M be?
27
(CH3)2CHCOCH2CH3
CH3CH=CHC(OH)(CH3)2
CH3COCH(CH3)CH2CH3
CH3CH=C(CH3)CH(OH)CH3
CH3COCH2CH(CH3)2
(CH3)2C=CHCH(OH)CH3
(CH3)2CHCOCH2CH3
(CH3)2C=C(CH3)CH2OH
The reaction scheme below outlines the production of 3amino2methylbutylamine from

compound J.
J
alcoholic NaCN
H2(g)
H2N
NH2
Ni catalyst
3-amino-2-methylbutylamine
Which compound could J be?

A
(CH3)2C(Br)CHBrCH3
CH3CH(Br)CHBrCH3
CH3CH(NH2)C(CH3)2Br
CH3CH(NH2)CHBrCH3
28 The reaction conditions for four different transformations are given below.
Which transformation has a set of conditions that is not correct?
A
CF3CH2Cl + Br2
CH2
uv light
CF3CHBrCl + HBr
KMnO4, H+
CH2 + 11[O]
CHCH
CH3 + HNO3
4CO2 + 3H2O
heat
heat
CH3 + H2O
C
NO2
CHO
CHCl2
+ 2OH-
Cl
heat
Cl
Cl
AJC Prelim 2012
+ 2Cl- + H2O
Cl
9647/01/H2
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12
29
Cannabinoids are active chemicals in the Cannabis plant that cause druglike effects
throughout the body including the central nervous system and the immune system.
Nabilone, a synthetic cannabinoid, has therapeutic use as adjunct analgesic for
neuropathic pain while Cannabidiol, a naturally occurring cannabinoid in the plant, is
effective as a typical antipsychotics in treating schizophrenia.
O
OH
OH
OH
HO
Cannabidiol
Nabilone
Which reagent would not react with either of these two cannabinoids?
A
An aqueous solution of ammoniacal silver nitrate
Alkaline potassium manganate(VII) solution
2,4-dinitrophenylhydrazine
Aqueous bromine
AJC Prelim 2012
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13
30
Penicillin is widely used to kill bacteria. The general structure of a penicillin molecule is
given below.
O
O
CO2H
C
N
R = an aryl group
N
H
What is produced when penicillin is boiled with excess aqueous sodium hydroxide?
A
CO2- Na+
O
O
R
B
+-
Na
O
O-Na+
O2C
CO2- Na+
HN
and
H2N
C
+-
Na
O
O-Na+
O2C
CO2- Na+
H2N
and
H3N
O
O
R
AJC Prelim 2012
CO2- Na+
C
O-Na+
and
H2N
9647/01/H2
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14
Section B
For each of the question in this section, one or more of the three numbered statements 1 to 3
may be correct.
Decide whether each of the statements is or is not correct (you may find it helpful to put a tick
against the statements that you consider to be correct.)
The responses A to D should be selected on the basis of
A
1, 2 and 3
are correct
1 and 2
only are correct
2 and 3
only are correct
1 only
is correct
No other combination of statements is used as a correct response.
31
Sodium hydrogensulfide, NaSH, is used to remove hair from animal hides.

Which statements about the SH ion are correct?
32
33
It contains 18 electrons.
3 lone pairs of electrons surround the sulfur atom.
Sulfur has an oxidation state of +2.
Which physical properties are due to hydrogen bonding between molecules?

1
Water has a higher boiling point than H2S.
Ice floats on water.
The HOH bond angle in water is approximately 104o.

An electrochemical cell is set
VO2+(aq),VO2+(aq)|Pt(s) halfcell.
up
using
Fe2+(aq)|Fe(s)
halfcell
and
Which of the following gives a correct effect on the Eocell and a correct explanation for the
effect when each of the changes is made to the cell separately?
Change
Add KCN(aq) to the
Fe2+(aq)|Fe(s) halfcell
Effect on Eocell
Increases
Explanation
Concentration of Fe2+(aq)
decreases
Add water to the

VO2+(aq),VO2+(aq)|Pt(s) halfcell
Decreases
Concentration of water
increases
Increase temperature of the

Fe2+(aq)|Fe(s) halfcell
No change
Temperature change does

not affect Eo
AJC Prelim 2012
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15
34
35
Which of the following processes will result in an increase in entropy?

1
The sublimation of solid carbon dioxide.
The decomposition of dinitrogen tetraoxide.
The formation of calcium carbonate from calcium oxide and carbon dioxide.
X, Y and Z are elements in the same period of the Periodic Table. The oxide of X is
amphoteric, the oxide of Y is basic and the oxide of Z is acidic.
What is the correct order of trend for these elements?
36
Proton number: Y < X < Z
Atomic radius: Z < X < Y
Melting point:
X<Z<Y
A student observed the reactions when sodium chloride and sodium iodide were each
reacted separately with concentrated sulfuric acid and concentrated phosphoric acid. The
observations were recorded in the table.
conc. H2SO4
conc. H3PO4
Sodium chloride
steamy fumes formed
steamy fumes formed
Sodium iodide
purple fumes formed
steamy fumes formed
Which of the following deductions can be made from these observations?
37
Concentrated sulfuric acid is a stronger oxidising agent than iodine.
Concentrated sulfuric acid is a weaker oxidising agent than chlorine.
Concentrated phosphoric acid is a stronger oxidising agent than concentrated sulfuric

acid.
Which of the following reactions will form a product that rotates planepolarised light?
CH3
CH
CH3
CH2Br
CH3
CH3
CH3
heated under reflux with aqueous KOH
with cold alkaline KMnO4(aq)
CH3COCH3 with HCN in trace amounts of a base at 10 oC.
AJC Prelim 2012
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38
The following route shows the acidcatalysed reaction of an alkene with hydrogen azide,
HN3, to form an imine.
R
H+
R H
R H
HN3
R
N
R
N2
R H
H+
R
R H
imine
Which of the following types of reaction occur in the synthesis of imine?
39
Elimination
Electrophilic addition
Nucleophilic substitution
Milk, red meat, liver and egg white are sources of Vitamin B2.
OH
OH
OH
CH2
CH
CH
CH
H3C
H3C
CH2OH
O
NH
Vitamin B2
Which of the following statements about Vitamin B2 are incorrect?
1
It is soluble in water.
1 mol of Vitamin B2 reacts with excess metallic sodium to produce 4 mol of hydrogen
gas.
A yellow precipitate is formed when acidified 2,4DNPH is added to Vitamin B2.
AJC Prelim 2012
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17
40
The diagram below shows two segments of a protein molecule.
NH
O
CH2
CH
CH
CH2
CO
NH
NH3
CH2
CH
CH
CH2
CO
SH
SH
Which of the following, when added to the protein, will cause the interactions which exist
between the two segments to be broken?
1
hot water
0.100 mol dm3 sodium hydroxide
0.100 mol dm3 lead(II) nitrate
AJC Prelim 2012
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18
H2 Chemistry 9647
Question
Number
1
2
3
4
5
AJC 2012 Prelim
Paper 1 40 marks
A
C
B
D
B
Question
Number
21
22
23
24
25
6
7
8
9
10
D
B
D
D
A
26
27
28
29
30
C
D
C
A
B
11
12
13
14
15
A
C
C
D
C
31
32
33
34
35
B
B
D
B
B
16
17
18
19
20
B
A
B
D
C
36
37
38
39
40
B
D
B
A
A
AJC Prelim 2012
Key
9647/01/H2
Key
C
C
C
D
A
NAME:______________________________ PDG:__________ Register No: _____

CHEMISTRY
9647/02
Higher 2
13 September 2012
Paper 2 Structured Questions
2 hours
Candidates answer on the Question Paper.

Data Booklet

Write your name, PDG and register number on all the work you hand in.
Write in dark blue or black pen.
You may use a pencil for any diagrams, graphs or rough working.
Answer ALL questions.
A Data Booklet is provided.
At the end of the examination, fasten all your work securely together.
The number of marks is given in brackets [ ] at the end of each question or part question.
For Examiners Use
1
2
3
4
5
Total
AJC Prelim 2012
9647/02/H2
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2
1
Planning (P)
Suppose you are given a solution containing Zn2+, Al3+, Cl and I ions.
You are also provided with the following:
reagents
apparatus
NaOH(aq),
test tubes,
NH3(aq),
filter funnel and
HNO3(aq),
filter paper
HCl(aq),
AgNO3(aq) and
distilled water
(a)
(i)
Name the reagent, from the list provided, that can be used to convert both the Cl and I
ions to precipitates.
...
(ii)
Name another reagent, from the list provided, that can be used to dissolve one of the
precipitates formed in (a)(i).
...
[2]
(b)
Using the reagents you have identified in (a), you are to devise a sequence of steps, by which
the halides in the mixture could be separated such that each halide is present in a separate
precipitate.
In your plan, you need to include details on the reagents you will use, expected observations
and state the location of each anion (i.e. in a solution or precipitate) after each step. You may
present your answer in the form of a table or flow chart.
[2]
AJC Prelim 2012
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3
A small amount of dilute nitric acid is usually added before the addition of the reagent you
have chosen in (a)(i).
(c)
Suggest a reason why this is done.

.
.
[1]
One of the cations present in the above mixture, Zn2+ or Al3+, can be removed as a precipitate,
on reaction with excess of either NaOH(aq) or NH3(aq).
(d)
Identify the reagent to be added in excess and which cation, Zn2+ or Al3+, can be removed as
a precipitate. Explain your answer using relevant equations.
Reagent to be added in excess .
Cation precipitated ...
Explanation.
.
.
[2]
You are provided with 3 unlabeled bottles each containing one of the following organic halogen
derivatives.
bromobenzene, C6H5Br
(bromomethyl)benzene, C6H5CH2Br
ethanoyl bromide, CH3COBr
You are also provided with the following:

reagents
apparatus
NaOH(aq),
test tubes,
NH3(aq),
filter funnel,
HNO3(aq),
filter paper and
HCl(aq),
Bunsen burner
AgNO3(aq) and
distilled water
(e)
Outline a logical sequence of chemical tests that would enable you to identify each of the
compounds.
You need to describe in a clear, stepwise manner, the tests used to identify each compound.
For each test, you need to include
details on the reagents and conditions you will use,
their quantities and
the expected observations for each compound tested
in that particular step.
You may present your answer in the form of a table or flow chart.
AJC Prelim 2012
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[5]
[Total: 12]
5
2
(a)
(i)
The value of pV is plotted against p for the following three gases, where p is the
pressure and V is the volume of the gas.
1 mol CO2 at 298 K
1 mol CO2 at 473 K
1 mol SO2 at 298 K
pV
Graph C
Graph A: 1 mol of CO2 at 298 K
Graph B
p
Given that graph A represents the graph for 1 mol of CO2 at 298 K, identify and explain
what graphs B and C represent.
Graph B: ..
Graph C: ..
...
...
...
...
...
AJC Prelim 2012
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6
The van der Waals equation as shown below is often used to account for the discrepancies
between experimental and theoretical behaviour of real gases.
(p +
n 2a
)(V nb) = nRT
V2
p is the pressure, V the volume, T the temperature, n the amount of substance (in mol), and
R the gas constant. The van der Waals constants a and b are characteristic of the substance
and are independent of temperature.
(ii)
Given that the van der Waals constants a and b for SO2 is 0.687 Pa m6 mol2 and
5.68 x 105 m3 mol1 respectively, calculate the actual pressure exerted by 1 mol of SO2
in a 0.5 dm3 container at 25 oC.
(iii) Calculate the pressure exerted by SO2 as described in (a)(ii) if it obeys the ideal gas
law.
(iv) Suggest a reason for the discrepancy in the pressures obtained in (a)(ii) and (a)(iii).
...
...
...
...
[6]
7
(b)
A wide range of sulfur oxoanions exist and many of them are widely used in laboratory
synthesis. Four of such oxoanions have two sulfur (S) atoms. The average oxidation number
of S and number of oxygen in the anions are shown in the table below.
oxoanion
average
oxidation
number of S
number of
oxygen atoms
+2
+3
+6
All four sulfur oxoanions have a negative charge of 2.

Only D has one central atom.
In D, E and F only,
the sulfur atoms are bonded directly to each other and
no oxygen atom is attached to another oxygen atom.
(i)
Suggest a value for x and y in the table.

Value of x:
(ii)
........
Value of y: ....
Suggest the structural formulae of D and E.
Structural formula of D
Structural formula of E
(iii) Using VSEPR theory, suggest the shape of oxoanion E with respect to each S atom.
...
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(iv) Oxoanion G is a powerful oxidising agent.
G + 2e
2SO42
Eo = +2.01 V
Using the above data and information given in the question, draw the dotandcross
diagram of oxoanion G.
[5]
(c)
Thionyl halides such as SOCl2 are commonly used in the halogenation of organic
compounds. The reaction also results in the production of hydrogen halide vapour.
The following sketch shows the trend of vapour pressure exerted by the different thionyl
halides at a given temperature.
vapour pressure
SOF2
X
HF
SOCl2
SOBr2
F
(i)
Cl
Br
Explain the above trend in terms of structure of, and bonding in, each of these thionyl
halides.
...
...
...
9
(ii)
The mark X indicates the vapour pressure exerted by hydrogen fluoride at a given
temperature.
On the same axes, indicate the expected vapour pressure exerted by each of the other
two hydrogen halides at the same temperature.
(iii) Explain why the vapour pressure exerted by hydrogen fluoride is lower than that
exerted by thionyl fluoride at the given temperature.
...
...
...
[5]
[Total: 16]
AJC Prelim 2012
9647/02/H2
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10
3
In a typical laboratory, gas phase reactions are difficult to control and hence not common.
Industrial production utilising gas phase reactions are similarly difficult to control and typically only
used for manufacture of organic chemicals, sulfuric acid (Contact process) or ammonia (Haber
process).
The Contact process used to produce sulfuric acid involves a threestage process. Using V2O5 as
a catalyst, reaction II achieves 99.5% conversion of sulfur dioxide to sulfur trioxide. The essential
reactions are as follows:
I:
II:
III:
(a)
S(g) + O2(g)
2SO2(g) + O2(g)
SO3(g) + H2O(l)
(i)
AJC Prelim 2012
SO2(g)
2SO3(g)
H2SO4(l)
DH = 308 kJ mol1
DH = 192 kJ mol1
DH = 130 kJ mol1
Write an expression each for Kc and Kp of reaction II.

1
Hence show that Kp = Kc (
).
RT
9647/02/H2
11
The following graph shows how the concentration of SO3 varies with time in reaction II.
t2
t1
(ii)
A change in condition was introduced to the reaction mixture at t1 such that the
concentration of SO3 increases at a different rate after t1.
The dotted line in the graph above illustrates how the concentration of SO3 would vary
with time if no change in condition was introduced at t1.
Suggest what this change could be and explain your answer.
...
...
...
(iii) The equilibrium mixture at t2 was suddenly heated to a higher temperature.

Sketch on the graph above to show how the concentration of SO3 would change from t2
till equilibrium is reached.
(iv) Suggest and explain whether reaction II should be conducted at high or low pressure.
[6]
AJC Prelim 2012
9647/02/H2
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12
(b) Using the Data Booklet, calculate the average bond energy of the S=O bond in reaction II.
[2]
[Total: 8]
13
4
(a)
Aspartic acid is a nonessential amino acid that can be synthesised by the human body. It
plays a vital role in the construction of other amino acids and biochemicals in the citric acid
cycle. It is also needed for stamina and assists the liver by removing excess ammonia and
other toxins from the bloodstream.
HO2C
CO2H
NH2
aspartic acid
The three pKa values associated with aspartic acid are given in the following table.
acarboxyl
R group
aamino
(i)
pKa
1.88
3.65
9.60
Using the protonated form of aspartic acid, suggest a reason why the pKa value of the R
group of aspartic acid is higher than that of the acarboxyl group.
.....
.....
........
(ii)
Sketch the pHvolume added curve you would expect to obtain when 30 cm3 of NaOH is
added to 10 cm3 of the protonated form of aspartic acid of the same concentration.
Show clearly on your curve where the three pKa values occur.
pH
Volume of
NaOH / cm3
AJC Prelim 2012
9647/02/H2
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14
(iii)
Explain what is meant by the term isoelectric point of an amino acid. Hence suggest the
structure of aspartic acid at its isoelectric point.
Indicate clearly the isoelectric point of aspartic acid on your curve obtained in (a)(ii) with
an X.
......
......
......
Structure of aspartic acid

at isoelectric point
(iv)
With the aid of an equation, explain how aspartic acid can maintain the pH of a solution at
pH 3.65 on the addition of a small amount of H+(aq). Show clearly the structure of
aspartic acid in your equation.
Equation:
......
......
15
(v)
Using your answers to (ii) and (iv), calculate the change in pH when 50.0 cm3 of
0.0200 mol dm3 HCl(aq) is added to 100.0 cm3 solution of 0.100 mol dm3 aspartic acid
at pH 3.65.
You may represent the acid as HA and the conjugate base as A in your working.
[12]
AJC Prelim 2012
9647/02/H2
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16
(b)
(i)
Describe the reagents and conditions needed to hydrolyse a protein in the laboratory to
form a mixture of its constituent amino acids.
.....
.....
(ii)
A polypeptide H was analysed and found to contain the following amino acids.
amino acid
abbreviation
number of
residues
aspartic acid
Asp
glycine
Gly
serine
Ser
tyrosine
Tyr
valine
Val
Analysis gave the following results:

The Nterminal was shown to be ser.
On reaction with the enzyme chymotrypsin, which hydrolyses at the carboxylic
acid end of tyr, H gave two tripeptides.
On reaction with a special reagent which digests at the carboxylic acid end of val,
H gave two peptides. One of these two was a dipeptide of sequence glyser.
Use the above information to determine the amino acid sequence of polypeptide H.
Justify your answer.
[You should use the same 3letter abbreviations as shown above to write out the amino
acid sequence.]
[4]
[Total: 16]
17
5 (a)
Compound J, is a nonnarcotic analgesic commonly sold in pharmacy. Refluxing J in the

presence of dilute sulfuric acid produces K and ethanoic acid.
Table 1 and Table 2 below show results of the analysis of compound K.
Table 1
Elemental Analysis (%)
C
60.8
4.4
34.8
Melting point / oC
159
Table 2
Reaction
Reagent
1
Excess aqueous Br2
(i)
Result
White solid, L formed which has Mr = 295.8.
Aqueous Na2CO3
Effervescence of gas.
Excess Na metal
About 174 cm3 of a colourless gas is evolved when

1 g of K is used at room temperature.
When vaporised in a suitable apparatus, 0.12 g of K occupies a volume of 37.5 cm3 at

250 oC and a pressure of 101 kPa. Calculate the molar mass of K.
Molar mass of K:..

(ii)
Hence using your answer in (a)(i) and Table 1, deduce the molecular formula of K.
Molecular formula of K:..

(iii)
Name the functional group that reaction 1 shows to be present in K.

.
(iv)
Name the functional group present in K that is confirmed by reaction 2.

.
AJC Prelim 2012
9647/02/H2
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18
(v)
Use your answers to (a)(ii) (a)(iv) to account for the result in reaction 3.
(vi)
State the molecular formula of L in reaction 1.

Molecular formula of L:..
(vi)
Hence suggest two possible structural formulae of K. Draw the displayed formulae of your
compounds in the boxes below.
Compound 1
(vii)
Compound 2
Given that one of the compounds in (a)(vi) has a melting point of 214 oC, state the identity
of K and explain your choice.
K is compound
Explanation: .
.
(viii) Hence deduce the structure of compound J.
Structure of J
[12]
19
(b) Glycolic acid, HOCH2CO2H, is a colourless, odourless and hygroscopic crystalline solid that is
highly soluble in water. It is commonly used in various skincare products. It can be prepared
from ethanedial by the Cannizzaro reaction, discovered in 1853.
When ethanedial, CHOCHO is reacted with aqueous NaOH and the product treated with dilute
sulfuric acid, the following reaction sequence in the Cannizzaro reaction takes place.
Stage I
CHOCHO + NaOH
HOCH2CO2Na
Stage II
HOCH2CO2Na + H+
HOCH2CO2H + Na+
(i)
What is unusual about the overall reaction?

....
(ii)
The following shows part of the mechanism in stage I where hydroxide ion attacks
ethanedial in an aqueous medium.
O O
O O
HO
H C C H
HO C C H
H
O O
HO C C H + H
Intermediates
Using the intermediates given above, propose a further 3step mechanism to form
HOCH2CO2Na.
In your answer, show relevant charges, lone pairs of electrons and movement of electrons.
(iii)
What is the role of the H produced in (b)(ii)?

....
AJC Prelim 2012
9647/02/H2
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20
(iv)
When a similar experiment is carried out using benzaldehyde as the starting material, two
organic products are obtained.
CHO
benzaldehyde
Write the structural formulae of the two products and state the ratio in which they might be
produced.
Structure of product
Ratio of products
[8]
[Total: 20]
(a)
(b)
(i)
AgNO3(aq)
(ii)
NH3(aq)
2012 H2 Chemistry Prelim Examinations Paper
Solutions
2
Step
Expected
Observations
Yellow ppt
Location of each
anion
Cl and I exists as
AgX in the ppt
2. Add excess NH3(aq) to

the residue.
Filter the mixture.
Yellow residue
Colourless filtrate
I exists as AgI in
residue
Cl remains in filtrate
3. Add HNO3(aq) to the

filtrate.
White ppt
Cl exists as AgCl in
the ppt
1. Add excess AgNO3(aq).

Filter the mixture.
Filter the mixture after adding excess AgNO3(aq) and after adding excess NH3 to the residue
correct identification of ions
Yellow ppt with AgNO3 in step 1. White ppt negates the mark.
(Note: white ppt is obscured by the yellow ppt.)
Yellow residue and colourless filtrate in step 2.
White ppt with acid in step 3.
FYI
The mixture has to be filtered after adding AgNO3 to separate AgCl and AgI from the cations
so that insoluble metal hydroxides would not be formed when NH3(aq) is added.
(c)
To remove other anions (e.g. CO32- and SO32-) that form insoluble compound with Ag+(aq).
(All nitrates are soluble).
(d)
Reagent: NH3(aq)
and
cation: Al3+
Al(OH)3 is insoluble while Zn(OH)2 is soluble in excess NH3(aq) due to complex formation.
Al3+ + 3OH
Zn(OH)2 + 4NH3
Al(OH)3(s)
[Zn(NH3)4]2+(aq) + 2OH
[allow 2 separate equations showing dissolving of Zn(OH)2]

Zn(OH)2
Zn2+ + 2OH
2+
[Zn(H2O)6] + 4NH3
[Zn(NH3)4]2+ + 6H2O
2
(e)
Step 1: To 2 cm depth of each of the unknown in a test tube, add a few drops of AgNO3(aq).
(allow distilled water gives white fumes)
C6H5Br
No ppt
C6H5CH2Br
No ppt
CH3COBr
Cream ppt
Step 2: To fresh samples of 2 cm depth each of the other 2 compounds in a test tube, add
NaOH(aq) and heat gently for 5 minutes.
Step 3: To the cooled samples of each of the remaining 2 compounds in a test tube, add
excess HNO3(aq), followed by AgNO3(aq).
C6H5Br
No ppt
C6H5CH2Br
Cream ppt
Appropriate reagents: AgNO3(aq), NaOH(aq), HNO3(aq)

Appropriate conditions : heat (not reflux, warm), (cool), excess
Quantities mentioned in all 3 steps: 2 cm depth / 1 5 cm3, (a few drops)
Correct observations in steps 1 and 3
Alternatives:
Add distilled water or dil HCl. Only ethanoyl bromide gives white fumes.
Add aqueous silver nitrate and heat. Only ethanoyl bromide and (bromomethyl)benzene give
cream ppt.
3
2
(a)
(i)
Graph B is CO2 at 473 K whilst graph C is SO2 at 298 K.

SO2 deviates more than CO2 at 298 K. SO2 molecules are held by stronger permanent
dipolepermanent dipole attractions (or van der Waals forces of attraction) as compared
to weaker instantaneous dipoleinduced dipole attractions (or van der Waals forces of
attraction) between CO2 molecules.
CO2 at 473 K deviates less than CO2 at 298 K. At higher temperature, CO2 molecules
possess higher average kinetic energy and are more able to overcome forces of
attraction between the molecules.
(ii)
p=
nRT
n 2a
- 2
(V - nb ) V
(1)(8.31)(298 )
(1) 2 (0.687 )
(0.5 x10 -3 - 5.68 x10 -5 ) (0.5 x10 -3 ) 2
= 5.588 x 106 2.748 x 106
= 2.84 x 106 Pa
=
(iii) Using the ideal gas equation,

p = nRT/V
(1)(8.31)(298 )
=
(0.5 x10 -3 )
= 4.95 x 106 Pa
(iv) The actual pressure exerted is much lower than the pressure calculated from the ideal
gas equation as forces of attraction between SO2 molecules are not negligible.
(b)
(i)
x: +5; y: 8
(ii)
2-
2-
S
S
O
O
E
D
(iii) Trigonal pyramidal w.r.t. to each S atom.
(iv)
2-
O
O
O
S O O S
O
O
4
(c)
(i)
Thionyl halides exist as simple covalent molecules held together by van der Waals
forces of attractions.
Across the series from SOF2 to SOBr2, as the no. of electrons / size of the electron
cloud increases, the strength of van der Waals forces of attractions (idid) between the
molecules also increases.
As the boiling point increases, the vapour pressure decreases.
(ii)
vapour pressure
SOF2
X
HCl
X
HBr
X
HF
SOCl2
SOBr2
Cl
2 points must be above SOCl2 and SOBr2

2 points must be above HF
(iii)
HF molecules are held together by stronger hydrogen bonds.

Thus, the vapour pressure of HF is lower than that of SOF2.
Br
5
3
(a)
(i)
Kc =
Kp =
[SO3 ] 2
[SO2 ] 2 [O2 ]
( pSO3 )2
( pSO2 )2 ( pO2 )
Using pV = nRT
p = (n/V)RT
= cRT
Kp =
([SO 3 ]RT) 2
([SO 2 ]RT) 2 ([O 2 ]RT)
[SO 3 ] 2
[SO 2 ] 2 [O 2 ]RT
[SO 3 ] 2
1
(
)
2
[SO 2 ] [O 2 ] RT
= Kc (
(ii)
1
) (shown)
RT
The equilibrium [SO3] does not change but equilibrium is reached faster. Hence the effect
is due to the addition of a catalyst at t1.
(iii) A higher temperature will favour the reverse endothermic reaction. Hence the position of
equilibrium will shift to the left. The equilibrium concentration of SO3 will thus be lower.
t1
t2
6
(iv) The reaction should be conducted at a high pressure.
The forward reaction results in a decrease in the number of moles of gaseous molecules.
Hence the position of equilibrium will shift to the right to decrease pressure by producing
fewer gas molecules. Thus, increasing the yield of SO3 produced.
(b)
SO2 has 2 S=O bonds and SO3 has 3 S=O bonds.

From reaction II:
4S=O + O=O
6S=O
Let x be the bond energy of S=O

(4x + (+496)) 6x = 192
2x = 192 496
x = 344 kJ mol1
(a)
(i)
HO2C
a CO2
NH3+
aNH3+ group is electronwithdrawing.

aCO2 group being closer/nearer to the aNH3+ group is more stablised as the negative
charge is dispersed to a greater extent.
(ii)
pH
9.60
3.65
X
1.88
(iii)
10
15
20
25
30
correct shape
correctly labeled 3 pH values (that correspond to the 3 pKa values)
correctly labeled equivalence volumes & volumes at MBC
Isoelectric point is the pH at which the amino acid carries no net charge.
Accept pH at which the amino acid exists as zwitterionic form.
Volume of
NaOH added /
cm3
7
CO2-
HO2C
NH3
Isoelectric point correctly indicated (with an X) on curve.

(iv)
CO2-
O2C
NH3
H+
CO2-
HO2C
NH3
The (conjugate) base reacts with the added H+ thus maintaining the pH of the solution.
(v)
n(aspartic acid) present = 0.100 x 100/1000 = 0.01 mol

At pH = 3.65 (= pKa of Rgroup)
[HA] = [A]
nHA = nA = 0.01/2 = 0.005 mol
nH+ added = 0.0200 x 50/1000 = 0.001 mol
A + H+
HA
nHA present after HCl is added = 0.005 + 0.001 = 0.006 mol
nA present after HCl is added = 0.005 0.001 = 0.004 mol
+
Ka = [H ][A ]
[HA]
103.65
0.004
)
0.150
0.006
(
)
0.150
[H + ](
[H+] = 3.358 x 104 mol dm3

pH = 3.474
Change in pH = 3.474 3.65 = 0.176
(b)
(i)
aq NaOH or dilute HCl / H2SO4

heat under reflux for a prolonged period / several hours
8
(ii)
serasptyrvalglyser
-
correct sequence with 6 a.a. residues
Justification of answer:
serasptyrvalglyser
enzyme 2 tripeptides obtained:
serasptyr & valglyser
Nterminal
serasptyrvalglyser
special reagent 2 peptides obtained; one

of these is a dipeptide glyser
-
Any 2 points
For students:
1. special reagent digests at carboxylic end of val giving glyser valglyser
2. enzyme hydrolyses at carboxylic end of tyr tyrvalglyser
3. ser at Nterminal serasptyrvalglyser
9
5
(a)
(i)
(101 000) (37.5 x 106) = (0.12/M) (8.31) (250+273)

Molar mass = 137.7 g mol1
Mr = 138
(ii)
Elemental Analysis (%)

C
H
O
60.8
4.4
34.8
5.06
4.4
2.18
2.32
2.0
1
n(12 x 2.32 + 2 + 16) = 137.7 => n = 3

C7H6O3
(iii)
Phenol
(iv)
Carboxylic acid
(v)
1 mol of K contains 2 mol of OH group, hence produces 1 mol H2 gas.

Volume of gas expected to produce from 1 g of K:
1/138 x 24000 = 174 cm3
(vi)
L: C7H4O3Br2
Possible K:
O
C O H
H
O
C O H
O H
(vii)
COOH
OH
K can form intramolecular hydrogen bonding leading to less extensive intermolecular

hydrogen bonding resulting in lower melting point.
(viii)
COOH
OCOCH3
(b)
(i)
Disproportionation has taken place.
10
(ii)
O O
O O dH
HO C C H
d+
H OH
O OH
HO C C H + OH
HO C C H
H
Curly arrows, charges and intermediate
O OH
HO C C H + NaOH
H
(iii)
O OH
NaO C C H + H2O
H
Nucleophile or reducing agent
(iv)
COOH
Ratio: 1:1
CH2OH

CHEMISTRY
9647/03
Higher 2
17 September 2012
Paper 3 Free Response Questions
2 hours
Candidates answer on separate paper.

Data Booklet
Writing paper
Graph paper

Write your name, PDG and register number on all the work you hand in.
Write in dark blue or black pen on both sides of the paper.
You may use a pencil for any diagrams, graphs or rough working.
Answer any four questions.
Start each question on a fresh sheet of paper.
You are reminded of the need for good English and clear presentation in your answers.
AJC Prelim 2012
9647/03/H2
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2
1
(a)
Sodium dichromate(VI), Na2Cr2O7, is used widely in organic synthesis as well as in the

process of leather tanning. The principal ore of chromium called chromite, FeCr2O4, is used
in the manufacture of sodium dichromate(VI) via a 2stage process.
In the first stage of the process, the ore is fused with soda ash (sodium carbonate) and air at
a temperature of 1000 C. The following equation represents this stage.
4FeCr2O4 + aNa2CO3 + bO2
(i)
cFe2O3 + dNa2CrO4 + eCO2
Complete the balancing of the above equation by deducing the values for a, b, c, d and
e.
In the second stage, the products are extracted with hot water. Orange crystals of sodium
dichromate(VI) separate out during the evaporation stage of the process.
(ii)
Suggest a reagent that can be added to the hot water extract to produce the
dichromate(VI) solution in the second stage of the process.
[2]
(b)
Draw a fully labeled diagram to show how the standard electrode potential of the
Cr2O72(aq)/Cr3+(aq) system could be measured by a standard hydrogen electrode. Show the
direction of electron flow in the circuit.
[3]
(c)
When zinc metal is added to an acidified solution of aqueous chromium(III) solution, the
solution turns from green to blue. When the excess zinc is filtered off and the blue solution is
left to stand for several hours in the absence of air, it slowly turned back to green and a
colourless gas is evolved.
Explain these observations, quoting appropriate Eo values from the Data Booklet.
[3]
(d)
A chromiumcontaining ion, CrOxn, disproportionates in acid solution to produce a mixture of

chromium(III) ions and dichromate(VI) ions.
A solution containing 7.5 x 103 mol of CrOxn ions was acidified and the disproportionation
occurred. The resulting solution contained 2.5 x 103 mol of dichromate(VI) ions.
Using the information given, calculate the oxidation number of chromium in the ion CrOxn.
[2]
AJC Prelim 2012
9647/03/H2
3
(e)
Transition metals such as chromium, iron and zinc and their compounds have found wide
applications in electrical energystorage technology. New technologies involving the
inventions of redox flow batteries and metalair batteries have emerged in recent years.
Electrolytes containing chromium ions and iron ions are used in a redox flow battery called
ironchrome battery (ICB). Electricity is generated from the battery by the halfcell reactions
of these electrolytes that flow into a cell. The two electrolytes in the cell are separated by an
ion selective membrane. Inert electrodes with optimum power acceptance are used in this
battery.
ion selective membrane
flow of electrolyte
flow of electrolyte
electrode
electrode
electrolyte
tank
electrolyte
tank
electrolyte
pump
(i)
electrolyte
electrical load
pump
Using the Data Booklet, select appropriate halfcell reactions of chromium ions and iron
ions that would produce the largest standard cell potential in the ICB.
Write a balanced equation for the overall reaction that takes place when the battery
discharges.
(ii)
Explain the role of the ion selective membrane in the operation of the ICB.
An example of a metalair battery is the zincair battery, commonly used as small button
cells in watches and hearing aids. When a gaspermeable, liquidtight membrane sealing
tab in the button cell is removed, oxygen in the air is absorbed into an alkaline electrolyte.
The positive electrode is made of porous carbon and the negative electrode consists of zinc.
The electrolyte used is a paste containing potassium hydroxide.
(iii) A zincair button cell has a cell potential of 1.59 V.
Using relevant data from the Data Booklet, calculate the electrode potential for the
reaction at the anode. Suggest an equation for the reaction that takes place at this
electrode.
(iv) The zinc electrode of a new zincair button cell weighs 1.9 g. The cell can run until
80 % of the zinc is consumed.
Calculate the maximum amount of current that can be drawn from the cell if it is
expected to last for 30 days.
AJC Prelim 2012
9647/03/H2
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4
(v)
Considering the cell reactions in the two batteries described above, suggest the battery
that would be expected to discharge electricity at a faster rate. Give a reason for your
answer.
(vi) Common alkaline batteries contain zinc and manganese(IV) oxide in a paste of
potassium hydroxide. The overall cell reaction is shown below.
Zn(s) + MnO2(s) + H2O(l)
ZnO(s) + Mn(OH)2(s)
Based on this information, suggest an advantage, other than lower cost, that the
zincair battery has over the common alkaline battery of similar weight. Explain your
answer.
[10]
[Total: 20]
AJC Prelim 2012
9647/03/H2
5
2
(a)
Data concerning some Group II sulfates and hydroxides, at 298 K, are given in the table
below. Further data may be found in the Data Booklet.
lattice energy /
kJ mol1
2959
2704
2572
DHhydration of
M2+ / kJ mol1
1890
1562
1414
DHhydration of
SO42 / kJ mol1
1160
1160
1160
Mg(OH)2
Ca(OH)2
Sr(OH)2
solubility /
mol dm3
1.6 x 104
2.5 x 102
3.4 x 102
lattice energy /
kJ mol1
2993
2644
2467
DHhydration of
M2+ / kJ mol1
1890
1562
1414
2 x DHhydration of
OH / kJ mol1
1100
1100
1100
(i)
Define the term lattice energy.
(ii)
Explain the following:
(iii)
(b)
MgSO4
CaSO4
SrSO4
solubility /
mol dm3
2.2
1.5 x 102
7.1 x 103
The magnitude of the lattice energy of Group II sulfates decreases from MgSO4
to SrSO4.
II
The DHhydration of M2+ becomes less exothermic from Mg2+ to Sr2+.
Hence, suggest qualitatively why the solubility of Group II sulfates decreases from
MgSO4 to SrSO4, while the solubility of Group II hydroxides increases from Mg(OH)2 to
Sr(OH)2.
[7]
Many metal sulfates have very different industrial uses. For example, the mercury(I) sulfate
reference electrode (MSRE) is the second most commonly used reference electrode while
calcium sulfate products are used as an economical and FDAapproved source of
supplemental calcium.
The numerical values of the solubility product, Ksp, for these two sulfates at 298 K are:
Ksp of mercury(I) sulfate, Hg2SO4 = 7.4 x 107
Ksp of calcium sulfate, CaSO4 = 2.4 x 105
During a Chemistry experiment, a student mixed 25.0 cm3 of 0.1 mol dm3 Hg+ with 25.0 cm3
of 0.1 mol dm3 Ca2+ ions and labeled it as solution J.
(i)
The student was then instructed to add solid potassium sulfate to solution J slowly.
Calculate the minimum concentrations of sulfate ions required to precipitate the first
trace of mercury(I) sulfate and first trace of calcium sulfate, respectively.
(ii)
Using your answers to (b)(i), state and explain which metal sulfate will be precipitated
first when solid potassium sulfate was added slowly to solution J.
Hence, calculate the maximum mass of this metal sulfate precipitated, without
precipitating the other.
[6]
AJC Prelim 2012
9647/03/H2
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6
(c)
Calcium oxide is commonly known as quicklime. Since it reacts readily with water, it does not
occur naturally and has to be produced by heating limestone.
(i)
By using relevant data from the Data Booklet and the following data, construct a
labeled energy level diagram, showing clearly all the enthalpy changes involved and
the chemical species at each stage.
Hence, use it to calculate the lattice energy of calcium oxide.
first electron affinity of oxygen

second electron affinity of oxygen
enthalpy change of atomisation of calcium
enthalpy change of formation of calcium oxide
(ii)
AJC Prelim 2012
kJ mol1
147
+753
+178
635
Suggest and explain how the magnitude of the lattice energy of Ca3N2 might compare
with that of CaO.
[7]
[Total: 20]
9647/03/H2
7
3
(a)
Aromatic sulfonic acids are useful intermediates in the preparation of dyes and
pharmaceuticals. The sulfonic acid group has the same structure as part of the sulfuric acid
molecule. 4methylbenzenesulfonic acid can be prepared by treating methylbenzene with
sulfur trioxide and concentrated sulfuric acid.
SO3H
c. H2SO4 + SO3
heat
CH3
CH3
4-methylbenzenesulfonic acid
(i)
Identify and sketch the shapes of the hybrid orbitals around one carbon atom in the
benzene molecule.
(ii)
In the first step of this reaction, sulfur trioxide behaves as a Brnsted base.
Write an equation to illustrate the reaction between concentrated sulfuric acid and
sulfur trioxide.
(iii)
Hence, name and describe the mechanism for the reaction involved in the preparation
of 4methylbenzenesulfonic acid, including curly arrows to show the movement of
electrons, and all charges.
Another sulfonic acid derivative, 4aminobenzenesulfonic acid, is used in the manufacture of

sulfonamide drugs, which are used to treat pneumonia and related diseases. Its structure is
given below.
SO3H
NH2
(iv)
Explain why 4aminobenzenesulfonic acid is a weaker acid than sulfuric acid.
(v)
Describe a simple chemical test to distinguish between 4aminobenzenesulfonic acid

and 4methylbenzenesulfonic acid.
[You may ignore the reactivity of SO3H group in both molecules.]
[8]
AJC Prelim 2012
9647/03/H2
[Turn over
8
(b)
Compound K has a molecular formula C8H9NO3. Treating compound K with hot acidified
potassium manganate(VII) gives compound L, C7H5NO4, which produces effervescence with
sodium hydrogencarbonate.
Heating compound K under reflux with acidified potassium dichromate(VI) gives compound
M, C8H7NO4. When compound M is treated with tin and concentrated hydrochloric acid,
followed by careful neutralisation using an aqueous alkali, compound N, C8H9NO2, is
obtained.
1 mol of compound N reacts with 2 mol of aqueous bromine. Treatment of compound N with
anhydrous phosphorus pentachloride produces compound O, C8H7NO.
(i)
Deduce the structures of compounds K O and explain the chemistry of the reactions
involved.
(ii)
Compound O can be separated from any unreacted compound N that is left in the
product mixture. This can be done by shaking the product mixture with cold dilute
hydrochloric acid. The two layers (organic and aqueous layers) formed are then
allowed to stand.
In which layer will compounds N and O be present, respectively?
Hence, explain why compounds N and O can be separated in this process.
[12]
[Total: 20]
AJC Prelim 2012
9647/03/H2
9
4
(a)
Four different chromium(III) complexes with the formula Cr(H2O)6Cl3 can be prepared under
various conditions. Each complex contains a cation in which the coordination number of
chromium is 6. The complexes may be distinguished by their colours and by the amount of
lead(II) chloride precipitated when aqueous lead(II) nitrate is added to aqueous solutions
containing each of the complexes.
complex
colour
T
U
V
W
violet
pale green
dark green
dark green
does the complex have a

dipole moment?
no
yes
yes
no
no. of moles of PbCl2

precipitated per mole of complex
1.5
1.0
0.5
0.5
(i)
What do you understand by the term complex ion?
(ii)
Explain why an aqueous solution of T is coloured.
(iii) Using the results of the reaction with lead(II) nitrate, suggest, with reasons, the
structural formulae for the cation present in T, U and V.
(iv) Describe the shape of and bonding in the cation in W. Illustrate your answer with a full
structure of this cation in W, showing the disposition of the atoms.
(v)
(b)
Explain the presence or absence of a dipole moment for complexes V and W

respectively.
[9]
The arrangement of electrons in the dorbitals depends on the spin states of complexes.
The following diagram shows how the dorbitals are split in an octahedral environment.
energy gap E
dorbitals of an
isolated Fe2+ ion
dorbitals of Fe2+ ion

in presence of ligands
In a high spin state, the electrons occupy all the dorbitals singly, before starting to pair up
in the lower energy dorbitals.
In a low spin state, the lower energy dorbitals are filled first, by pairing up if necessary,
before the higher energy dorbitals are used.
(i)
AJC Prelim 2012
Use diagrams like the one above to show the electronic distribution of a Fe2+ ion in a
high spin state, and in a low spin state.
Show in your diagram, the relative size of the energy gap E for each spin state.
9647/03/H2
[Turn over
10
Many transition elements and their compounds are paramagnetic, which means that they
are attracted to a magnetic field. This property is due to the presence of unpaired
electron(s) in the dorbitals.
The table below shows the relative paramagnetisms of some iron complexes.
formula of complex
[Fe(H2O)6]2+
[Fe(H2O)6]3+
[Fe(CN)6]4
[Fe(CN)6]3
(ii)
relative paramagnetism
4
5
0
1
Using your answer to (b)(i) and the information given above concerning
paramagnetisms of the different complexes, state and explain which ligand, H2O or
CN, will cause a larger energy gap E between its dorbitals.
(iii) Hence, suggest explanation for the relative paramagnetisms of the hydrated Fe2+ and
Fe3+ complexes.
[5]
(c)
When water ligands in a hydrated metal ion are substituted by other ligands, the equilibrium
constant for the reaction is referred to as the stability constant, Kstab of the new complex.
The following table lists two stability constants for the following reaction.
[Fe(H2O)6]3+ + nL
(where n is a whole number)
L
SCN
CN
(d)
n
1
6
[Fe(H2O)6nLn](3n)+ + nH2O
Kstab
9 x 102
1 x 1034
(i)
Write the expression for the stability constant, Kstab, for L = SCN and state its units.
(ii)
Use the data given in the table to predict the predominant complex formed when a
solution containing equal concentrations of both SCN and CN ions was added to a
solution containing Fe3+(aq) ions.
[3]
Iron(III) ions catalyse the reaction between iodide ions and peroxodisulfate ions (S2O82) in
aqueous solution.
By considering relevant Eo values from the Data Booklet, explain how iron(III) ions function
as a catalyst for the reaction between I- and S2O82-, writing equations where appropriate.
[3]
[Total: 20]
AJC Prelim 2012
9647/03/H2
11
5
(a)
The oxidation of acidified iodide ions by hydrogen peroxide is represented by

2I(aq) + H2O2(aq) + 2H+(aq)
I2(aq) + 2H2O(l)
To determine the order of reaction, n, with respect to iodide ions, the rate can be followed by
adding a small but fixed volume of sodium thiosulfate solution to the constant volume system
of reaction mixture together with 1 cm3 of starch solution and measuring the time taken for the
blue black colour to appear. The results are given below.
[I(aq)] / mol dm3
0.0040
0.0060
0.0080
0.010
0.012
Experiment
1
2
3
4
5
Time (t) / s
74.0
49.4
37.0
30.0
25.0
(i)
Explain the relationship between the time taken for the formation of the blue black
colour and the initial rate of reaction.
(ii)
In the experiments, the concentrations of hydrogen peroxide and hydrogen ions used
are very much higher than that of the iodide solution.
Explain why this is necessary.
(iii)
Evaluate 1/t for each experiment and hence plot a suitable graph to determine the
order of reaction, n, with respect to iodide ions.
State clearly your reasoning.
(iv)
Further studies show that the rate equation for the reaction is
Rate = k [I]n [H2O2]
Based on this information and your answer to (a)(iii), state two conclusions you can
make about the mechanism of this reaction.
[9]
(b)
(i)
0.1 mol each of the four chlorides below is separately added to 1 dm3 of water.
Copy the diagram below and sketch a graph showing the variation in pH of these
resulting solutions.
pH
NaCl AlCl3 CCl4

(ii)
AJC Prelim 2012
PCl5
Account for the pH of the aqueous solutions of carbon tetrachloride and phosphorus
pentachloride. Write balanced equations for the reactions, if applicable.
[4]
9647/03/H2
[Turn over
12
(c)
Potassium chloride and potassium iodide can be distinguished by treating the compounds
separately with concentrated sulfuric acid.
Describe what you would observe if concentrated sulfuric acid is added to separate samples
of the solids KCl and KI. Suggest an explanation for the differences in reaction, and write
equations illustrating the types of reaction undergone.
[4]
(d)
There are three bottles labeled X, Y and Z in the laboratory. Each bottle contains one of the
following reagents: Cl2(aq), KI(aq) and KBr(aq).
The following tests were carried out and the results were summarised in the table below.
Experiment
1
2
3
Procedure
mixing reagent in bottle X
with reagent in bottle Y
mixing reagent in bottle X
with reagent in bottle Z
mixing reagent in bottle Y
with reagent in bottle Z
Observations
mixture remains colourless
mixture turns brown
mixture turns brown
(i)
Which bottle contains Cl2(aq)? Write a balanced equation to support your answer.
(ii)
If hexane is also provided, how would you use it to identify the contents of the other two
bottles? Include the observations in your answer.
[3]
[Total: 20]
AJC Prelim 2012
9647/03/H2
1
2012 H2 Chemistry Preliminary Examination Paper 3 Solutions
1
(a)
(i)
4FeCr2O4 + 8Na2CO3 + 7O2
2Fe2O3 + 8Na2CrO4 + 8CO2
a = 8, b = 7, c = 2, d = 8, e = 8
(ii)
Any dilute acid e.g. dilute H2SO4 or dilute HCl
(b)
voltmeter
electron flow
V
H2 at 25 C & 1 atm
salt
bridge
Pt electrode
platinised Pt electrode
1.00 mol dm3 Cr2O72 (aq),

1.00 mol dm3 Cr3+ (aq),
1.00 mol dm3 H+ (aq)
correct components of each halfcell
direction of electron flow
(c)
Zn2+ + 2e
Cr3+ + e
1.00 mol dm3 H+ (aq)
Zn
Cr2+
0.76 V
0.41 V
Zn reduces Cr3+ to blue Cr2+(aq);
Eocell = +0.35 V > 0,
2H+ + 2e
H2
0.00 V
The acid present in the solution oxidises blue Cr2+ back to green Cr3+; Eocell = + 0.41 V,
producing H2 gas.
(d)
Mole ratio of CrOxn : Cr2O72 = 7.5 x 103 : 2.5 x 103 = 3 : 1

Thus, 3 mol of CrOxn disproportionate to 1 mol of Cr2O72 and 1 mol of Cr3+
Let O.N. of Cr be y.
y 3 = 2(6) 2y
y=5
O.N. of Cr in the ion CrOxn = +5
(e)
(i)
Fe3+ + e
Cr3++ e
Fe2+
Cr2+
+0.77 V
0.41 V
Eocell = +1.18 V
Fe3+ + Cr2+
Fe2+ + Cr3+
2
(ii)
When cell discharges, iron halfcell becomes less positive and the chromium halfcell
becomes more positive. Passage of current would stop. Membrane allows anions to
pass through to maintain electrical neutrality in the two halfcells. (not allowing the
positive ions to pass through, otherwise selfdischarge or short circuit occurs) [2]
(iii) Eocell = Eored Eoox

1.59 = +0.40 Eoanode
Eoanode = 1.19 V
Anode: Zn + 4OH
(or Zn + 2OH
Zn(OH)42 + 2e
Zn(OH)2 + 2e)
(iv) Q = 0.8 x 1.9/65.4 x 2 x 96500 = 4486 C

Current = 4486 / (30 x 24 x 60 x 60) = 1.73 x 103 A
(v)
ICB is expected to discharge faster as it involves simple electron transfer reactions,

while energy is needed to break covalent bonds in O2 (and H2O) in the zincair battery.
(vi) Znair battery has higher energy density as it uses air as the oxidising agent, unlike the
heavier oxidising agent, MnO2, used in the alkaline battery. Thus, more zinc can be
packed within a cell of similar weight.
(a)
(i)
It is the amount of energy evolved when 1 mole of solid ionic compound is formed from
its constituent gaseous ions at 298 K and 1 atm.
(ii)
I: As the cationic radius increases down the group, interionic distance increases
OR state that L.E. a
and cationic radius (r+) increases down the group.
Thus, the strength of electrostatic forces of attraction between the M2+ and SO42 ions
decreases. Hence, the magnitude of L.E. decreases.
+
II: DHhydration of the cation a q
r+
As the cationic radius increases down the group,

OR the charge density of the cation decreases.
Thus, the strength of iondipole interactions formed between M2+ and water molecules
decreases and hence DHhydration becomes less exothermic.
(iii) DHsolution = L.E. + DHhydration of M2+ + DHhydration of anion
For Group II sulfates, the decrease in |L.E| is less than that of |DHhydration of M2+|. Thus,
DHsolution becomes more positive down the group and solubility decreases
For Group II hydroxides, size of the OH anion is much smaller than that of the SO42
anion. The decrease in |L.E| is more than that of |DHhyd of M2+|. Thus, DHsolution becomes
more negative down the group and solubility increases.
OR
The size of the cation is much smaller than that of the anion (SO42), thus the decrease
in |L.E| is less significant than the decrease in the |DHhydration|.
3
Conversely, the size of the OH anion is much smaller than that of the SO42 anion, thus
the decrease in |L.E| is more significant than the decrease in the |DHhydration|.
(b)
(i)
For Hg2SO4, min. [SO42] = 7.4 x 107 / (0.1/2)2 = 2.96 x 104 mol dm3
For CaSO4, min. [SO42] = 2.4 x 105 / (0.1/2) = 4.80 x 104 mol dm3
(ii)
Since min. [SO42] required to precipitate first trace of Hg2SO4 is lower, Hg2SO4 will be
precipitated first.
When max. Hg2SO4 is precipitated, i.e. when first trace of CaSO4 appears,
[SO42]in solution = 4.80 x 104 mol dm3
\ [Hg+]in solution = [7.4 x 107 / (4.80 x 104)]1/2 = 0.0393 mol dm3
n(Hg+) in 50 cm3 solution = 0.0393 x 50/1000 = 1.97 x 103 mol
n(Hg+) precipitated = 0.1 x 25.0/1000 1.97 x 103 = 5.30 x 104 mol
2Hg+ + SO42
Hg2SO4
n(Hg2SO4) precipitated = x n(Hg+) precipitated = x 5.30 x 104 = 2.65 x 10 4 mol

Max. mass of Hg2SO4 precipitated = 2.65 x 10 4 x (2 x 201 + 32.1 + 4 x 16.0) = 0.132 g
(c)
(i)
Energy / kJ mol1
Ca2+(g) + O2(g)
147 + 753
Ca2+(g) + 2 e + O(g)
+590 + 1150
Ca(g) + O(g)
(+496)
Ca(g) + O2(g)
0
L.E
+178 Ca(s) + O2(g)
635
CaO(s)
L.E of CaO = ( 147 + 753 + 590 + 1150 + (496) + 178) + (635)

= 3410 kJ mol1 (3 s.f.)
4
(ii)
(a)
magnitude of the L.E. of Ca3N2 should be larger than that of CaO due to a larger charge
on N3
OR due to more ionic attractions between 5 mol of ions in 1 mol of Ca3N2 than between
2 mol of ions in 1 mol of CaO.
(i)
sp2 hybrid orbitals
HSO4 + HSO3+
(ii)
H2SO4 + SO3
(iii)
Electrophilic substitution [1]
H
SO3H+
slow
CH3
CH3
SO3H
SO3H
+ HSO4-
CH3
SO3H
fast
+ H2SO4
CH3
correct arrow movement

correct carbocation intermediate and regeneration of catalyst
(iv)
The lone pair of electrons on N atom is delocalised into the benzene ring. This further
intensifies the negative charge on the sulfonate anion, making it less stable.
(v)
Add aqueous bromine to each compound.

Observation: orange solution of bromine turns colourless and a white precipitate is
formed for 4aminobenzenesulfonic acid. Bromine solution remains orange and no
precipitate formed for 4methylbenzenesulfonic acid
OR
Heat each compound with KMnO4 in dilute H2SO4.
Observation: purple KMnO4 turns colourless for 4methylbenzenesulfonic acid. KMnO4
remains purple for 4aminobenzenesulfonic acid.
OR
Add cold HCl / H2SO4
Observation:
4aminobenzenesulfonic
acid
dissolves
methylbenzenesulfonic gives two immiscible layers.
in
HCl
but
(c)
(i)
OH
COOH
NO2
NO2
L
OH
NO2
OH
NH2
O
NH
O
Reaction
Treating compound K,
C8H9NO3, with hot acidified
potassium manganate(VII)
gives compound L, C7H5NO4.
Type of reaction
oxidation
Deduction
loss of 1 C
sidechain oxidation
occurred.
L produces effervescence with

sodium hydrogen carbonate.
acidbase reaction
Carboxylic acid group in L

reacted with sodium
hydrogen carbonate.
L contains carboxylic acid
group, COOH.
Heating compound K under

reflux with acidified potassium
dichromate(VI) gives
compound M, C8H7NO4.
oxidation
gain in 1 O, loss of 2 H
1o alcohol in K is
oxidised to COOH in M.
Compound M is treated with tin

and concentrated hydrochloric
acid, followed careful
neutralisation, compound N,
C8H9NO2 is obtained.
reduction
NO2 group in M is
reduced to NH2 group in
N.
6
1 mole of compound N reacts
with 2 moles of aqueous
bromine.
electrophilic
substitution
N is a phenylamine.
-Br is substituted at
positions 2, 4 or 2, 6 w.r.t
the NH2 group
Treatment of compound N with

anhydrous phosphorus
pentachloride produces
compound O, C8H7NO.
N is first converted to
acyl chloride, by PCl5
via nucleophilic
substitution.
The CH2COOH group

must be adjacent to the
NH2 group in N to enable
ring formation/formation of
a cyclic amide
The acyl chloride

formed then
undergoes intra
molecular
condensation with the
NH2 group to form a
cyclic amide O.
(ii)
Compound N will dissolve in the aqueous layer while compound O will remain in the organic
layer. The basic NH2 group in compound N will react with cold dilute HCl to give an ionic
product which can form strong iondipole interactions with water molecules.
Compound O is neutral and does not react with cold dilute HCl, hence remains in the organic
layer.
(a)
(i)
Complex ion consists of a central metal ion or atom surrounded by ligands via dative
bonds.
(ii)
In the presence of ligands,

the partiallyfilled 3d orbitals are split into two levels (nondegenerate) with a small
energy gap
energy is absorbed from the visible light region when an electron promotes from a
lower level d orbital to a vacant higher energy d orbital, i.e. dd transition,
colour of the complex T is the complement of the colour absorbed.
(iii)
Number of moles of free Cl per mole of complex = 2 x number of moles of PbCl2

precipitated per mole of complex
T: 1.5 mol of PbCl2 precipitated
=> 3 moles of free Cl per mole of complex
=> cation is [Cr(H2O)6]3+
U: 1 mol of PbCl2 precipitated
=> 2 moles of free Cl per mole of complex and 1 mole of Cl as ligand per mole of
complex
=> cation is [Cr(H2O)5Cl]2+
V: 0.5 mol of PbCl2 precipitated
=> 1 mole of free Cl per mole of complex and 2 moles of Cl as ligand per mole of
complex
=> cation is [Cr(H2O)4Cl2]+
7
(iv)
Error! Objects cannot be created from editing field codes.

OH2
Octahedral with respect to Cr3+. H2O and Cl ligands are dative bonded to the Cr(III) atom
in the complex.
OH
Cl
2
(v)
The dipole moment ofIII the 2 CrCl bonds which are on the same side in V do not cancel
each other so it hasCr
an overall dipole moment.
The
dipole moment of the 2 Cl
CrCl bonds which are on opposite sides in W cancel out
H2O
each other so net dipole moment is zero.
(b)
(i)
OH
Fe2+ ion: 1s2 2s2 2p6 3s22 3p6 3d6
energy gap
low spin state

(ii)
energy gap
high spin state
CN will cause a larger energy gap E between its dorbitals

In the presence of CN ligands, the relative paramagnetism is lower. This means that
electrons are paired up and arranged in a low spin state. Hence, the energy gap is larger.
(iii)
In the presence of water ligands, the electrons of Fe2+(aq) and Fe3+(aq) are arranged in a
high spin state
where there are 4 unpaired electrons in the dorbitals of Fe2+(aq)
and 5 unpaired electrons in the dorbitals of Fe3+(aq).
Hence the relative paramagnetism of the Fe2+(aq) and Fe3+(aq) ions is 4 : 5.
(c)
(i)
Kstab =
[Fe(SCN)(H 2 O) 52+ ]
[Fe(H 2 O) 36+ ][SCN - ]
units: mol1 dm3
(ii)
(d)
Since Kstab for the complex formed by CN and Fe3+ ions (1 x 1034) is much larger than that
by SCN and Fe3+ ions (9 x 102). [Fe(CN)6]3 is more stable than [Fe(SCN)(H2O)5]2+, hence
the predominant complex formed is [Fe(CN)6]3.
S2O82(aq) + 2e Error! Objects cannot be created from editing field codes. 2SO42 (aq)
E = +2.01V
Fe3+(aq) + e Error! Objects cannot be created from editing field codes. Fe2+(aq)
E = +0.77V
I2(aq) + 2e Error! Objects cannot be created from editing field codes. 2I (aq)
E = +0.54V
8
Step 1: Formation of intermediate
2Fe3+(aq) + 2I(aq)
2Fe2+(aq) + I2(aq)
Ecell = +0.23V
Step 2: Regeneration of the catalyst

2Fe2+(aq) + S2O82(aq)
2Fe3+(aq) + 2SO42(aq) Ecell = +1.24V
(a)
(i)
Since a fixed volume of thiosulfate is used in each experiment, rate can be measured by
the time taken for fixed amount of iodine liberated, i.e. rate 1/t.
(ii)
So that [H2O2] and [H+] are kept effectively constant and will not affect the rate of
reaction / rate is only affected by the concentration of [I].
(iii) evaluate (1/t)

labelled axes: yaxis (1/t); xaxis [I]
bestfit straight line drawn through the origin
correctly plotted points
Rate [I]n [H2O2]y [H+]z
Since rate 1/t and [H2O2] and [H+] are effectively constant, 1/t [I]n.
Since a straight line which passes through the origin is obtained when (1/t) is plotted
against [I], n = 1.
(iv) 1. It is a multistep mechanism.
2. H+ is not involved in the ratedetermining step.
3. 1 (mol) of I and 1 (mol) of H2O2 are involved in the ratedetermining step.
(b)
(i)
pH
NaCl AlCl3 CCl4
(ii)
PCl5
PCl5 undergoes hydrolysis in water but not CCl4.

CCl4 has no vacant lowlying (energetically accessible) dorbitals to accept the lone pair
of electrons from the water molecules. Therefore, it will not undergo hydrolysis.
OR
PCl5 has vacant lowlying 3dorbitals to accept the lone pair of electrons from the water
9
molecules. Hence, it will undergo hydrolysis to give H3PO4 and HCl, resulting in an
acidic solution.
PCl5 + 4H2O
(c)
H3PO4 + 5HCl
Steamy / white fumes of HCl observed for KCl, violet / purple fumes of I2 observed for KI.
KCl + H2SO4
KI + H2SO4
8HI + H2SO4
KHSO4 + HCl
HI + KHSO4
4I2 + H2S + 4H2O
I being a stronger reducing agent (than Cl) will reduce H2SO4 to H2S / itself oxidised to I2.
(d)
(i)
(ii)
Bottle Z
Cl2 + X
2Cl + X2 where X = Br or I
Knowing that bottle X and Y is either KBr or KI, add hexane to the two brown mixtures
obtained, separately.
If the organic layer is purple, bottle contains KI.
If the organic layer is redbrown, bottle contains KBr.
CATHOLIC JUNIOR COLLEGE

JC2 PRELIMINARY EXAMINATIONS
Higher 2
CHEMISTRY
9647/01
Wednesday 29 August 2012
1 hour
Additional Materials: Multiple Choice Answer Sheet

Data Booklet
Write and/or shade your name, NRIC / FIN number and HT group on the Multiple Choice Answer Sheet in
the spaces provided.
There are forty questions in this paper. Answer all questions. For each question, there are four possible
answers, A, B, C and D.
Choose the one you consider correct and record your choice in soft pencil on the separate Answer
Sheet.
Read the instructions on the Multiple Choice Answer Sheet very carefully.
Calculators may be used.
This document consists of 18 printed pages and 0 blank page.
2
Section A
Gallium (Ar = 69.7) occurs naturally as two isotopes,

percentage of
A
33 %
71
31 Ga
69
31 Ga
and
71
31 Ga.
What is the
atoms in a sample of naturally occurring gallium?

B
35 %
60 %
65 %
The mineral tellurite, TeO2 (Mr = 160.0) is often used in the manufacture of optic fibres. It
was found that 1.01 g of TeO2 in an ore sample required exactly 60 cm3 of
0.035 mol dm3 acidified K2Cr2O7 for complete reaction. In this reaction, Cr2O72 is
converted into Cr3+.
What is the oxidation state of Te in the final product?
A
+2
+3
+5
+6

What do the ions 35Cl and 40Ca2+ have in common?
A
B
C
D
Both ions have 18 neutrons.

Both ions have more protons than neutrons.
Both ions contain the same number of nucleons.
Both ions have an outer electronic configuration 3s2 3p6.
Carbodiimides are often used in organic synthesis as dehydrating agent to activate

carboxylic acids towards amide or ester formation. Carbodiimides consist of the general
structure, RN=C=NR where R is an alkyl group.
What is the most likely bond angle at each nitrogen atom in carbodiimides?
A
107
118
120
180
Myoglobin, Mb, is an oxygen-carrier protein that exists in the muscle fibres of most
mammals. Each Mb molecule will bind to one O2 molecule, according to the following
equation.
Mb(aq) + O2(aq)
Kc = 1106 mol1 dm3
MbO2(aq)
Given that the concentration of O2 is 6.5 106 mol dm3, what is the percentage of
MbO2 in a Mb-MbO2 mixture?
A
50.5 %
65.0 %
86.7 %
9647/01/CJC JC2 Preliminary Exam 2012
88.4 %
3
6
The enthalpy changes involving some oxides of nitrogen are given below:
N2(g) + O2(g) 2NO(g)
H = +180 kJ mol1
2NO2(g) + O2(g) N2O5(g)
H = 55 kJ mol1
N2(g) + O2(g) N2O5(g)
H = +11 kJ mol1
What is the enthalpy change, in kJ mol1, of the following reaction?

2NO(g) + O2(g) 2NO2(g)
A
235
125
114
57
The Thermit Reaction involves mixing iron(III) oxide with aluminium powder in a crucible,
with a suitable fuse to start the reaction. The reaction is as follows:
Fe2O3(s) + 2Al(s) Al2O3(s) + 2Fe(l)
The fuse is first ignited, where it will burn in oxygen, forming the oxide with a large
release of heat required for the Thermit reaction to take place. The commonly used
material for the fuse is a clean magnesium strip.
Which of the following does not help to explain why a strip of magnesium is suitable to
be used as a fuse?
A
B
C
D
The large amount of heat energy released on igniting the fuse enables the
reactants to overcome the high activation energy involved.
Magnesium removes the thin layer of oxide on aluminium, thus allowing aluminium
to react with the iron(III) oxide.
The numerical value of the enthalpy change of formation of magnesium oxide is
very large.
The strip increases the surface area for magnesium to react with the oxygen at a
faster rate.
When a precipitate is formed, Gppto, in J mol1, is given by the following expression

Gppto = 2.303RTlog Ksp
Data about AgBr is as follows: Ksp(AgBr) = 5.01013 mol2 dm6, Hppto = 84.4 kJ mol1
What is the Sppto, in J mol1 K1, for the formation of AgBr(s) at 298 K?
A
47.8
0.0478
+0.0478
+47.8
[Turn over
4
9
The secondary structure of DNA is the double helix. The formation of the double helix
involves two DNA chains, where one has the bases Adenine (A) and Guanine (G),
interacting with the bases Thymine (T) and Cytosine (C) on the other chain as shown
below:
T
A
NH2
Base pairs
Adenine
Thymine
HN
sugar
N
Guanine
CH3
N
sugar
Cytosine
Sugar phosphate
backbone
N
H2N
NH
sugar
N
N
NH2
sugar
The two chains coil together in a helical fashion, and this process is an example of
self-assembly.
What are the correct signs of H and S for the formation of the double helix?
5
10
The cell below is set up under standard conditions:

Pt(s) / Sn2+(aq), Sn4+(aq) // HNO2(aq), H+(aq) / NO(g) / Pt(s)
Ecello = +0.84 V
Which of the following changes will cause the cell e.m.f. to be less than +0.84 V
immediately after the cell is being set up?
A
B
C
D
11
adding NaOH(aq) to the HNO2(aq) / NO(g) half-cell

adjusting the partial pressure of NO(g) to be 0.5 atm
adding water to the Sn4+(aq)/Sn2+(aq) half-cell
adding SnCl2 to the Sn4+(aq)/Sn2+(aq) half-cell

The cell shown in the diagram is set up under standard conditions where X and Y are
platinum electrodes.
Cl2(g)
Cl(aq)
Fe2+(aq) and Fe3+(aq)

X
Y
Half-cell A
Half-cell B

A
B
C
D
12
Changing X to Fe in half-cell A will not affect Ecello.

The voltmeter will show a reading of about 1.80 V.
The electrons will flow from Y to X through the voltmeter.
Y will be the positive electrode.
Ethyl ethanoate is a common ester formed during production of wines. It gives the aroma
found in younger wines and contributes towards the fruitiness perception in wine. The
formation of ester in wine can be illustrated by the following equation.
CH3CH2OH + CH3CO2H
CH3CO2CH2CH3 + H2O
Kc = 4.0, H = 20 kJ mol1
Which of the following statement is correct about the above equilibrium?

A
B
C
D
As water is removed from wine, [CH3CO2CH2CH3] and Kc increases.

As temperature of the wine decreases, [CH3CO2CH2CH3] and Kc increases.
As water is added to the wine, [CH3CO2CH2CH3] increases.
As CH3CO2H is removed from the wine, [CH3CO2CH2CH3] increases.
[Turn over
6
13
HA is a weak acid and can have different degree of acidity in aqueous solution and in
liquid ammonia. The respective equations that represent their dissociations are as follow.
HA + H2O
HA + NH3
A + H3O+
A + NH4+
Which of the following statement is correct?

A
B
C
D
14
Ammonia is more polar than water, resulting in greater dissociation of HA.

Degree of dissociation of HA is identical in aqueous solution and liquid ammonia.
pKa of NH3 is larger than that of H2O, hence HA is a stronger acid in liquid
ammonia.
Kb of NH3 is larger than that of H2O, hence HA is a stronger acid in liquid ammonia.
Amylase is the first enzyme discovered and isolated. It acts as a catalyst in the
hydrolysis of starch.
In a single experiment, the rate of hydrolysis of starch was monitored as the reaction
proceeded and the following graph was obtained.
rate
0
x
[starch]
Which of the following statement about the reaction is not correct?

A
B
C
D
15
When [starch] is smaller than x, the rate changes as [starch] changes.

When [starch] is larger than x, the active sites of amylase are fully occupied.
The order of reaction with respect to starch is constant at all concentrations.
Throughout the experiment, [amylase] remains constant as it is not used up.
Oxides of two unknown elements of the third period have the following properties. Both
can be dissolved in an alkali and when added separately to water, the resultant pH was
approximately 7 and 3 respectively.
Which of the following pairs could have been the oxides?
A
B
C
D
Al2O3 and P4O10

Al2O3 and Na2O
Na2O and SiO2
SO3 and P4O10
7
16
Two students were tasked to prepare pure hydrogen iodide from solid potassium iodide.
The first student used concentrated H2SO4 as the reagent, while the second student
used concentrated H3PO4 instead. Only one student was successful in preparing pure
hydrogen iodide.
Which of the following is the most likely explanation and/or observation?
A
B
C
D
17
First student was unsuccessful, as hydrogen iodide formed further react to give
purple fumes of iodine and hydrogen sulfide which contaminates the product.
First student was successful, as hydrogen iodide can be quickly isolated due to its
low boiling point.
Second student was unsuccessful, as H3PO4 is a weaker acid than H2SO4, thus
hydrogen iodide cannot be formed.
Second student was successful, as H3PO4 is a weaker reducing agent than H2SO4.
Transition metals have many interesting properties.

Which statement correctly describes a property unique to transition metals?
A
B
C
D
18
They form metal ions which form dative covalent bonds with ligands.
They form compounds which can exhibit colours due to partially filled d-orbitals.
They are the only metals which have high melting and boiling points.
They are the only metals which have variable oxidation states.
The bond lengths in buta-1,3-diyne differs from those which might be expected.
The carbon-carbon bond length in ethane (C2H6) is 0.154 nm and in ethyne (C2H2) is
0.120 nm. The single C2-C3 bond in buta-1,3-diyne, however is shorter than the single
bond in ethane: it is 0.137 nm.
1
HC
2
C
4
CH
3
C
0.137 nm
1,3-buta-diyne
What helps to explain this C2-C3 bond length in buta-1,3-diyne?

A
B
C
D
19
It is an sp-sp overlap.
It is an sp2-sp overlap.
The sp3-sp3 overlap is pulled shorter by a p-p (-bond) overlap.
The electrons in the filled p-orbitals on C2 and C3 repel each other.
Which of the following gases is not removed by catalytic converters from the exhaust
fumes of cars?
A
CO
H2O
NO2
CH4
[Turn over
8
20
Potassium sodium tartrate, also known as Rochelle salt, is used medicinally as a laxative
and has the following structure.
OH
Na O
O K+
O
OH
Which of the following could be part of the reaction sequence to synthesise Rochelle
salt?
HCN(aq)
+ NaCN
(CHO)2
10 oC - 20 oC
KCN(alc)
CH2BrCH2Br
intermediate
KOH(aq)
+ NaOH(aq)
intermediate
KOH(aq)
+ NaOH(aq)
reflux
21
HCN(aq),
NaOH(aq)
CH3COCH3
10 C- 20 oC
CH3(CH2)3Cl
KOH(aq)
Rochelle salt
reflux
intermediate
KMnO4,
OH-(aq)
Rochelle salt
reflux
intermediate
reflux
KMnO4,
OH-(aq)
reflux
Phenylamine can be synthesised via a one-step reaction as shown below.

NaNH2, NH3(l)
Cl
What type of reaction has occurred?

A
B
C
D
Rochelle salt
reflux
Electrophilic substitution
Nucleophilic addition
NH2
+ NaCl
Rochelle salt
9
22
A halogen derivative, X, was first warmed with aqueous sodium hydroxide, followed by
adding excess of dilute nitric acid and aqueous silver nitrate. A precipitate was produced.
Dilute aqueous ammonia was then added and a colourless solution is obtained. Which of
the following could be the identity of compound X?
Br
Cl
CH2I
CH2CH2Cl
23
Estrone, one of several natural estrogens, can be converted from cholesterol via
steriodogenesis. The structures of both compounds are shown below.
O
HO
HO
estrone
cholesterol
Which of the following cannot be used to distinguish estrone from cholesterol?

A
B
C
D
2,4-dinitrophenylhydrazine, warm
neutral FeCl3(aq)
PCl5
Br2(aq)
[Turn over
10
24
Compound R was warmed with aqueous iodine in the presence of aqueous sodium
hydroxide. After filtration and removal of unreacted iodine, the resultant organic product
was heated with ethanol in the presence of concentrated sulfuric acid to give ethyl
butanoate.
Which of the following could compound R be?
OH
HO
25
Which procedure gives the highest yield of ethyl benzoate?

A
B
C
D
26
refluxing CH3CO2H with SOCl2, then adding phenol

refluxing CH3CH2OH with concentrated HCl, then adding C6H5CO2H
refluxing C6H5CO2H with SOCl2, then adding CH3CH2OH
refluxing CH3CH2OH with concentrated H2SO4, then adding C6H5CO2H
Antipyrine is a drug used in reducing fever. The synthesis of antipyrine involves the
reaction between compound P and phenylhydrazine.
Compound P +
NHN
NHNH2
+ H2O
phenylhydrazine
CH3
CH2CO2CH2CH3
antipyrine
Which of the following statements regarding compound P is true?

A
B
C
D
P reacts with warm aqueous alkaline iodine to form one organic product.
P gives a silver mirror when heated with Tollens reagent.
P turns hot acidified potassium dichromate(VI) from orange to green.
P contains two carbonyl groups which can both react with cold alkaline HCN.
11
27
Cocaine is medicinally valued as a local anaesthetic. The structure of cocaine is shown

below.
CO2CH3
N
CH3
O
C
O
Which pair of compounds would produce cocaine when reacted together?

CO2CH3
H
+
N
CH3
OH
O
CO2H
N
CH3
O
C
+ CH3OH
CH2OH
N
CH3
O
C
+ HCO2H
COCl
N
CH3
O
C
+ HCO2H
28
2-bromopropane, (CH3)2CHBr, W, may be used as the starting material for synthesising

(CH3)2C(OH)CO2H.
Which of the following sequences would result in the highest yield of (CH3)2C(OH)CO2H?
A
W (CH3)2C(OH)CN (CH3)2C(OH)CO2H
W (CH3)2CH(CN) (CH3)2CH(CO2H) (CH3)2C(OH)CO2H
W (CH3)2CH(OH) CH3COCH3 (CH3)2C(OH)CN (CH3)2C(OH)CO2H
W (CH3)2CBr2 (CH3)2C(Br)CN (CH3)2C(OH)CO2 (CH3)2C(OH)CO2H
[Turn over
12
29
What is the correct order of increasing pKb for the following four compounds?
O
CH3
N
CH3
30
III
II
A
B
C
D
NH2
NH2
Cl
CH3
IV
I, IV, III, II
II, III, IV, I
III, I, II, IV
IV, III, II, I
Tyrosine, a building block for several neurotransmitters, has the structure as shown
below. Tyrosine has three pKa values of 2.20, 9.11 and 10.07, which correspond to the
CO2H, NH3+ and phenol groups respectively.
H
HO
CH2
CO2H
NH3+
In an aqueous solution at pH 9.5, how much charge will be carried on different parts of
each molecule of Tyrosine?
total number of
positive charges
A
B
C
D
0
0
1
1
total number of
negative charges
1
2
0
2
13
Section B
For each of the questions in this section, one or more of the three numbered statements 1 to 3
may be correct. Decide whether each of the statements is or is not correct (you may find it
helpful to put a tick against the statements that you consider to be correct). The responses A to
D should be selected on the basis of:
A
1, 2 and 3 1 and 2 only 2 and 3 only 1 only

are correct
are correct
are correct
correct
is
31
The titration curve of the protonated form of alanine, NH2CH(CH3)CO2H, is as shown.

14
12
10
pH 8
6
4
2
1.0
2.0
Moles of OH per mole of protonated amino acid
The two stages of this titration are associated with two different dissociation constants,
pK1 and pK2.
H3N + CH(CH3)CO2H + OH -
H3N + CH(CH3)CO2 - + H2O
pK1 = 2.4
H3N + CH(CH3)CO2 - + OH -
H2NCH(CH3)CO2 - + H2O
pK2 = 9.7
Which statements are correct for alanine?

1
2
3
Equal concentrations of H3N + CH(CH3)CO2H and H3N + CH(CH3)CO2 - are present

at pH = 2.4
There is no net charge on alanine at the point when the slope of the curve is at
maximum at its centre.
The form H2NCH(CH3)CO2 - is the major species present at pH 9.7.
[Turn over
14

are correct
are correct
are correct
correct
is
32
Ketones react with HCN solution in the presence of NaCN catalyst to form cyanohydrins,
which are useful intermediates in organic syntheses. In investigations of the reaction
between propanone and HCN, the following results were obtained.
Initial concentrations of reactants / mol dm3
[(CH3)2CO]
[HCN]
[NaCN]
0.020
0.025
0.020
0.040
0.020
0.020
0.020
0.025
Relative initial rate / mol dm3 s1
0.004
0.004
0.003
0.002
1.00
1.25
0.75
1.00
Which conclusions can be drawn about the kinetics of this reaction under these
conditions?
1
2
3
33
The reaction is zero order with respect to HCN.

The rate-determining step involves only propanone and NaCN.
When the concentration of propanone used in the reaction is in large excess, the
reaction appears to be first order with respect to NaCN.

Which of the following are chemically stable when left to stand in the atmosphere?
1
2
3
a solution of K3Fe(CN)6
a solution of CrCl2
a mixture of NaOH(aq) and FeSO4(aq)
15
34
In which of the following pairs are the members, I and II,
stereoisomers of each other and
the overall dipole moment of I is larger than that of II?

I
II
H3C
H3C
Cl
Br
C
Cl
O2N
C
Br
C
Br
O2N
Br
Br
Br
Br
H
Br
H
Cl
35
C
C
C
Br
C
C
H
Cl
Br
Solid magnesium hydroxide is typically added to paint coatings as fire retardant to

prevent spread of fire. This is possible as solid magnesium hydroxide decomposes in a
similar manner to Group II nitrates.
Mg(OH)2 MgO + H2O
Magnesium hydroxide decomposes at about 300 oC to give water vapour which prevents
oxygen from reaching the burning material. At the same time, it is an endothermic
reaction that absorbs heat energy.
However, barium hydroxide is less suitable as flame retardants. Which of the following
statements explain this?
1
2
3
Barium hydroxide when fully decomposed produces less amount of water vapour
per mole of hydroxide, thus it is less effective.
Barium hydroxide decomposes at a much higher temperature, therefore it may not
release enough water vapour at the start of a fire.
Barium hydroxides are much more soluble and may not remain on the painted
material for a long period of time.
[Turn over
16

are correct
are correct
are correct
correct
is
36
Citronella oil is a well-known plant-based insect repellent and one of the key chemical
compounds found in the oil is citronellal.
C1
C3
C2
Citronellal
Which of the following statements about citronellal are correct?
1
2
3
37
The bond length of C1-C2 is expected to be shorter than that of C2-C3 bond due to
sp3-sp2 overlap.
Optical and geometrical isomerism are both possible in citronellal.
Reaction of citronellal with hydrogen and a suitable catalyst will produce a
compound with three chiral centres.
1-phenylethanol, C6H5CH(OH)CH3, was reacted in a three-step reaction using the

following reagents.
Step 1: Br2, catalyst
Step 2: K2Cr2O7, H+, reflux
Step 3: HCN, NaCN, 15 C
Which of the following is true?
1
2
3
The final product has no effect on plane-polarised light.

Iron(III) bromide can be used as a catalyst for step 1.
Nucleophilic substitution has occurred in step 3.
17
38
Lovastatin is a naturally occurring drug found in food such as oyster mushrooms and red
yeast rice. It can lower cholesterol levels and thus prevent cardiovascular disease.
HO
O
O
O
O
Lovastatin
Which of the following is true when lovastatin is refluxed with excess aqueous sodium
hydroxide?
1
2
3
39
One of the organic products contains three hydroxyl groups.

1 mol of lovastatin reacts with 3 mol of aqueous NaOH.
Three organic products are formed.
Which of the following statements regarding compound X is true?

CH3
CONHCH2CH2CO2H
HN
CH3
C
H
compound X
1
2
3
1 mol of compound X reacts with 3 mol of cold dilute hydrochloric acid.

1 mol of compound X reacts with 2 mol of ethanoyl chloride.
1 mol of compound X reacts with aqueous bromine to give an acidic solution.
[Turn over
18

are correct
are correct
are correct
correct
is
40
The structure of the herbicide Karbutilate is shown below.

O
H
C
N
N(CH3)2
O
O
C(CH3)3
C
N
H
Karbutilate
What would be the products formed when Karbutilate is subjected to prolonged boiling
with aqueous dilute hydrochloric acid?
1
CO2
+NH3
2
OH
(CH3)2NH
SOLUTIONS
1
B
11
C
21
C
31
B
2
D
12
B
22
D
32
A
3
D
13
D
23
D
33
D
4
B
14
C
24
B
34
C
5
C
15
A
25
C
35
C
6
C
16
A
26
C
36
D
7
B
17
B
27
B
37
B
8
A
18
A
28
C
38
D
9
A
19
B
29
B
39
C
10
A
20
A
30
A
40
B

Higher 2
CANDIDATE
NAME
CLASS
2T
CHEMISTRY
9647/02
Tuesday 21 August 2012
2 hours

Additional Materials: Data Booklet
Write your name and class in the boxes provided above.
Write in dark blue or black pen on both sides of the paper. [PILOT FRIXION ERASABLE PENS ARE NOT
ALLOWED]
You may use a soft pencil for any diagrams, graphs or rough working.
Answer all questions. Write your answers in the space provided.
The number of marks is given in brackets [ ] at the end of each question or part of the question.
For Examiners Use

Paper 1
Paper 2
Paper 3
/ 40
Q1
/ 12
Q2
/13
Q3
/21
Q4
/12
Q5
/14
Q1
/20
Q2
/20
Q3
/20
Q4
/20
Q5
/20
Total
/ 72
/ 80
/ 192
[Turn over
1
Planning (P)
Eggshells are rich in calcium carbonate and make good plant fertilisers to replenish
calcium, an essential nutrient in plant growth. The eggshells are normally crushed and
sprinkled around the plants. The shells will slowly decompose and enrich the soil. The
decomposition of CaCO3(s) may be represented as:
CaCO3(s) CaO(s) + CO2(g)
In the laboratory, all Group II carbonates, MCO3, can be decomposed by heating to give
the corresponding oxide, MO, and carbon dioxide, CO2.
You are to design an experiment to investigate how the rate of decomposition of Group II
carbonates varies down the group.
In addition to the standard apparatus available in a school laboratory for gas collection, you
are provided with the following materials,
samples of carbonates of magnesium, calcium, strontium and barium,
a stopwatch
(a) Briefly describe how you would measure the rate of decomposition of the different
carbonates in order to enable comparison.
.
.
. [1]
(b) Draw a diagram of the apparatus and experimental set up that you would use to carry
out the experiment. Show clearly the following:
the apparatus used to heat the carbonate, and
how the carbon dioxide will be collected.
Label each piece of apparatus used, indicating its size or capacity.
[2]
3
(c)
The temperature of the Bunsen flame varies depending on the ratio of the fuel to
oxygen burnt. Besides keeping to the same fuel to oxygen ratio, suggest how you
would control another factor in the heating to ensure a fair comparison of the rate of
decomposition of different carbonates.
.
. [1]
(d) Other than the use of safety goggles, state one hazard that must be considered when
planning the experiment and suggest how you would keep this risk to a minimum.
.
.
.
.
. [2]
(e)
With reference to the apparatus in (b), show how you would calculate the mass of
each carbonate used in the experiment.
[Mr: MgCO3 = 84.3; CaCO3 = 100.1; SrCO3 = 147.6; BaCO3 = 197.0]
[2]
[Turn over
4
(f)
Draw a table with appropriate headings (and units) to show the data you would record
and the values you would calculate in order to plot a suitable graph to show the
variation in the rates of decomposition of the carbonates.
Sketch, and explain, the shape of the graph you would expect from your results. Label
clearly the axes.
Explanation:
.
.
.
.
.
.
.[4]
[Total: 12]
5
2 (a)
Carbon dioxide is used in beverage carbonation. Cylinders of pressurised carbon

dioxide are used to produce carbonated drinks. One such cylinder has an internal
volume of 3.0 dm3 and contains 4.6 kg of carbon dioxide.
(i) Calculate the pressure (in Pascals) the carbon dioxide gas would exert inside the
cylinder at 28 C.
(ii) To find the pressure of a fixed amount of carbon dioxide gas under certain
conditions, the van der Waals equation given below should be used.
an
p +
(V - n b) = n R T
V
Without further calculation, explain how the pressure obtained using the van der
Waals equation would differ from that in (a)(i).
...
...
[3]
(b)
Real gases like carbon dioxide can be liquefied at low temperatures just by applying
pressure. Gases can be liquefied by pressure alone if the temperature is below their
critical temperature, Tc. At temperatures above Tc, the gas cannot be liquefied,
regardless of the pressure applied. The critical temperature of carbon dioxide is
31.1 C.
(i)
Explain why real gases like carbon dioxide can be liquefied just by applying
pressure.
..
..
(ii) By considering structure and bonding, suggest a value for the critical temperature
of methane and give a reason for your choice.
..
..
..
[2]
[Turn over
6
(c)
Beyond the critical temperature and pressure, carbon dioxide exists as a supercritical
fluid, a state that resembles a gas but has density closer to that in the liquid phase.
Carbon dioxide is now well established as a solvent for use in extraction.
(i) Suggest a reason why supercritical carbon dioxide is preferred as a solvent to
extract caffeine from solid coffee over organic solvents like benzene.
..
..
......
(ii) Suggest why small amounts of ethanol need to be added to supercritical carbon
dioxide to increase the solubility of polyphenols for extraction. An example of a
polyphenol is shown below.
H3CO
OH
HO
....
.
....
[2]
(d)
Ethanedioate ions, C2O42, can be oxidised by hot acidified aqueous potassium

manganate(VII) to form carbon dioxide.
(i) Draw the structure of ethanedioate ions, C2O42-, and give the bond angle around
the central carbon atom.
7
(ii) Construct a balanced equation for the reaction between ethanedioate ions and hot
acidified potassium manganate(VII).
(iii) 1.63 g of a salt, KHC2O4H2C2O4, was dissolved in distilled water and made up to
250 cm3 solution. Calculate the volume of 0.020 mol dm3 KMnO4 required to react
with 20.0 cm3 of the KHC2O4H2C2O4 solution.
[Mr of KHC2O4H2C2O4 = 218.1]
[4]
(e) (i) The reaction between acidified potassium manganate(VII) and ethanedioate ions is
usually carried out at a higher temperature of 60 C. Suggest why the rate of this
reaction is slow at room temperature.
.
....
[Turn over
8
The graph of rate against time for the reaction between acidified potassium
manganate(VII) and ethanedioate ions is shown below.
rate
A
x
time
(ii) Suggest the species responsible for the increase in rate of reaction before point A,
and identify the property which enables it to act as a catalyst in this reaction.
.
....
[2]
[Total: 13]
9
3 Iron is the fourth most common element in the Earths crust, and has many applications
throughout the history of mankind. In nature, iron exists in many different mineral ores,
consisting of iron in either +2 or +3 oxidation state. In prehistoric era, iron compounds were
more commonly used as pigment without further purification. Limonite, which has the
general formula of FeO(OH)nH2O, was used as a yellow pigment as early as 10 000 B.C.
(a) (i) Complete the electronic configuration of Fe3+.
1s2 ...
(ii) Briefly explain why iron in mineral ores is found in variable oxidation states, but
for s-block elements, for example calcium, there is usually only one oxidation
state.
.......
.......
.......
.......
[3]
(b) A mineralogist dissolved 100 g of a certain pure limonite in concentrated HCl to form a
yellow solution. It was found that 3.2 mol of HCl had reacted based on the equation,
FeO(OH).nH2O + 4HCl FeCl4 + (n+2)H2O + H+
(i) State the formula of this limonite (with n as an integer):
(ii) Suggest the shape of FeCl4 : ....
(iii) Explain, with reference to FeCl4, why transition element complexes are coloured.
..
..
..
..
..
..
[5]
[Turn over
10
(c) In recent times, with much better understanding of chemistry, iron and its compounds
are widely used as catalysts and reagents in synthesis of chemicals. In particular, the
ferrate(VI) ion, FeO42-, is a strong oxidising agent that is used in green chemistry and
water purification due to its non-toxic by-products.
Ferrate(VI) ions are not stable in acidic conditions and easily oxidise water to give
oxygen. Hence, they are often produced in an alkaline medium.
Some Eo data of chlorate(I) and ferrate(VI) ions are given below.
Fe3+ + 4H2O
FeO42- + 4H2O + 3e Fe(OH)3 + 5OH
2ClO + 4H+ + 2e Cl2 + 2H2O
ClO + H2O + 2e Cl + 2OH
FeO42- + 8H+ + 3e
Eo = +2.20 V
Eo = +0.80 V
Eo = +1.63 V
Eo = +0.89 V
(i) By selecting relevant Eo data from the Data Booklet and using the information
above, explain with suitable calculation,
I
why ferrate(VI) ions are not stable in acidic conditions,
II
why it is feasible to form potassium ferrate(VI), K2FeO4, by reacting KClO with

Fe(OH)3 in the presence of KOH.
(ii) Hence write a balanced overall equation for the formation of K2FeO4.
..
(iii) Would you expect an acidified solution of K2FeO4 to be a stronger or weaker
oxidising agent compared to an acidified solution of KMnO4? Support your answer
with relevant Eo values from the Data Booklet.
..
.....
....
11
(iv)
Hence draw the structure of the possible organic product formed when hot
acidified purple K2FeO4 reacts with the following compound and suggest the
expected observations.
CH2CH2OH
CH3
Observations: ..
....
....
[8]
(d) White light contains all the colours in the visible spectrum. Each of these colours is
associated with a certain wavelength, l. The formula relating energy and wavelength is,
E=
hc
where h = 6.626 x 1034 J s,

c = 3.00 x 108 m s1
l has the unit of m.
(i)
Wavelength, l (109 m)
Colour of light
400
Violet
450
Blue
500
Green
550
Yellow
600
Orange
650
Red
By considering the appearance of green iron(II) compounds and yellow iron(III)

compounds, state the colour of light absorbed for these compounds.
Iron(II) .
Iron(III) .
[Turn over
12
(ii) Hence, calculate the energy associated with the respective colours absorbed.
Energy of colour absorbed by

Iron(II) compounds: .
Iron(III) compounds:
(iii) Using your answer in (d)(ii), complete the diagram below to show the relative
energies of the d-orbitals, and the electronic distribution of the metal ion in each
compound. In each case, label clearly the energy required for the promotion of an
electron from the lower energy d-orbitals to the higher energy d-orbitals.
Assume that all electrons occupy the lower energy orbitals before the higher energy
orbitals.
Energy
_ _
_ _ _
Iron(II) compound
Iron(III) compound
[5]
[Total: 21]
13
4
Cymobarbatol is an antimutagenic agent isolated from the marine algae Cymopolia barbata.
The structure of cymobarbatol is shown below.
Br
Br
HO
Cymobarbatol
(a) Name two functional groups, other than phenyl and ether, which are present in the
cymobarbatol molecule.
[2]
(b) Identify the chiral carbons in cymobarbatol molecule by placing an asterix (*) against
each chiral carbon on the structure above.
[1]
(c) Draw the structural formula of each organic product formed when cymobarbatol is
treated with the following reagents.
O
In each reaction, assume that the
ring remains unaltered.
(i) ethanolic NaOH, heated under reflux
(ii) concentrated ethanolic NH3, heated in a sealed tube
[2]
[Turn over
14
(d) Cymobarbatol will also react with aqueous NaOH under reflux condition.
(i) Given that one mole of cymobarbatol reacts with two moles of aqueous NaOH, write
a balanced equation for this reaction.
(ii) When the bromine atoms in cymobarbatol are replaced by iodine atoms, how would
you expect the rate of its hydrolysis reaction to compare to that of cymobarbatol?
Explain your answer.
....
....
....
.......
(iii) Describe the expected observations when aqueous AgNO3, followed by

concentrated aqueous ammonia, is subsequently added to the resultant mixture in
(d)(i). Explain your answer with relevant equations.
....
.....
.....
....
.....
....
....
....
....
....
....
[7]
[Total: 12]
15
5
There are a number of structural isomers of molecular formula CnHnO2. In particular, one of
the isomers, B, is used as a tincture in perfumes and as a food additive.
(a)
To find the value of n, a 1.00 g sample of B was burned in an excess of oxygen, and
the gases produced were first passed through a U-tube containing P4O10 (to absorb the
water vapour) and then bubbled through concentrated NaOH(aq). The P4O10 in the
U-tube increased in mass by 0.529 g.
(i) Write an equation for the reaction of P4O10 with water vapour and state the pH of
the resultant solution.
..
(ii) Suggest why anhydrous CaCl2 cannot be used in place of P4O10 in the U-tube.
.....
.....
(iii) Calculate the number of moles of water produced.
(iv) Use the above data to show that the value of n = 8.
[5]
[Turn over
16
(b)
A reaction scheme involving compound B is shown below.
LiAlH4 in dry ether

B, C8H8O2
C, C8H10O2
heating
with
acidified K2Cr2O7(aq)
neutral
FeCl3(aq)
violet
colouration
heating
with
conc. H2SO4
D, C8H8O
orange
solution
HBr(g)
E, C8H9OBr
(i) Based on the above information, draw three possible structural isomers of B,
which are labelled as B1, B2 and B3 in the boxes below.
B1
B2
B3
(ii) Based on the structural isomer B1, draw the structural formulae of C, D and E.
E
[6]
17
(c)
A structural isomer of D, C8H8O, which is labelled as F, contains a C-O-C bond.

F does not react with HBr(g).
(i) Suggest a structural formula of F.
(ii) Although F does not react with HBr(g), it can react with concentrated HBr(aq). The
reaction of F with concentrated HBr(aq) is similar to the reaction of primary
alcohols with concentrated HBr(aq). The process involves the following two
stages:
H
Stage I
RCH2-OH
+ H+
RCH2
O
H
Stage II
H
RCH2
+ Br
H
RCH2
Br
+ H-OH
Suggest a mechanism for the Stage II process in the reaction of F with

concentrated HBr(aq), including curly arrows to denote movement of electrons,
and all charges. You do not need to draw the 3-dimensional representation of the
molecules involved.
[3]
[Total: 14]
[Turn over
PAPER 2
Planning (P)
Eggshells are rich in calcium carbonate and make good plant fertilisers to replenish calcium,
an essential nutrient in plant growth. The eggshells are normally crushed and sprinkled
around the plants. The shells will slowly decompose and enrich the soil. The decomposition
of CaCO3(s) may be represented as:
In the laboratory, all Group II carbonates, MCO3, can be decomposed by heating to give the
corresponding oxide, MO, and carbon dioxide, CO2.
You are to design an experiment to investigate how the rate of decomposition of Group II
carbonates varies down the group.
In addition to the standard apparatus available in a school laboratory for gas collection, you
are provided with the following materials,
samples of carbonates of magnesium, calcium, strontium and barium,
a stopwatch
(a)
Briefly describe how you would measure the rate of decomposition of the different
carbonates in order to enable comparison.
.
measure time taken to produce (collect) the same volume of CO2(g) from
each carbonate
.
.
rate 1
[1]
time
(b) Draw a diagram of the apparatus and experimental set up that you would use to carry
out the experiment. Show clearly the following:
the apparatus used to heat the carbonate, and
how the carbon dioxide will be collected.
Label each piece of apparatus used, indicating its size or capacity.
or (inverted measuring
cylinder over water)
[2]
3
(c) The temperature of the Bunsen flame varies depending on the ratio of the fuel to
oxygen burnt. Besides keeping to the same fuel to oxygen ratio, suggest how you
would control another factor in the heating to ensure a fair comparison of the rate of
decomposition of different carbonates.
Bunsen burner at same distance from the reaction vessel.
.
. [1]
(d) Other than the use of safety goggles, state one hazard that must be considered when
planning the experiment and suggest how you would keep this risk to a minimum.
1. hot apparatus use heat-proof gloves or let apparatus cool before
.
handling
.
2. potential suck back (if water allowed to suck back, hot boiling tube
.
would crack and shatter) remove delivery tube from water when
heating is stopped.
.
. [2]
(e)
With reference to the apparatus in (b), show how you would calculate the mass of
each carbonate used in the experiment.
[Mr: MgCO3 = 84.3; CaCO3 = 100.1; SrCO3 = 147.6; BaCO3 = 197.0]
Note: 1. Vol of CO2(g) collected must not exceed capacity of

collection device.
2. Mass of each carbonate used must contain the same
number of moles.
Let volume of CO2(g) collected = 40 cm3
[vol and mol of CO2(g)]
Since molar gas volume at r.t.p. = 24 dm3,

= 1.67 103 mol
mol of CO2 =
MCO3 MO + CO2
\ minimum mol of MCO3 = mol of CO2 = 1.67 103 mol
Mr of MCO3 = (Ar of M ) + [12.0 + 3(16.0)] = (Ar of M ) + 60.0
Let mol of carbonate = 2.00 103 mol
[same mol of
each
carbonate]
mass of MCO3 = nMr = 2.00 103 [(Ar of M ) + 60.0]

\ mass of MgCO3 = (2.00 103) 84.3 = 0.169 g
mass of CaCO3 = (2.00 103) 100.1 = 0.200 g
mass of SrCO3
= (2.00 103) 147.6 = 0.295 g
mass of BaCO3 = (2.00 103) 197.0 = 0.394 g

[2]
4
(f)
Draw a table with appropriate headings (and units) to show the data you would record
and the values you would calculate in order to plot a suitable graph to show the
variation in the rates of decomposition of the carbonates.
Mr
MgCO3
84.3
CaCO3
100.0
SrCO3
147.6
BaCO3
197.0
time / s
1
time
/ s1
Sketch, and explain, the shape of the graph you would expect from your results. Label
clearly the axes.
/ s1
0
Mr of MCO3
Explanation:
Down the group, as the cation increases in size (while the charge
.
remains unchanged), the charge density decreases and the polarising
.
power of the cation also decreases.
.
Hence, the larger cations polarise (distort ) the carbonate anion less and
.
the compound is thus relatively stable to heat.]
[decrease in charge density of

.
cation; less polarisation of anion]
.
.
[4]
[Total: 12]
2 (a) Carbon dioxide is useful in beverage carbonation. Cylinders of pressurised carbon dioxide
are used to produce carbonated drinks. One such cylinder has an internal volume of 3.0
dm3 and contains 4.6 kg of carbon dioxide.
(i) Calculate the pressure (in Pascals) the carbon dioxide gas would exert inside the
cylinder at 28 C.
pV = nRT
-3
p (3 x 10 ) =
4.6103
44
(8.31)(28+273)
p = 8.72 x 107 Pa
(ii) To find the pressure of a fixed amount of carbon dioxide gas under certain conditions,
the van der Waals equation should be used.
an
p +
(V - n b) = n R T
V
Without further calculation, explain how the pressure obtained using the above
equation would differ from that in (a)(i).
The
pressure obtained would be lower since intermolecular forces of attraction
...
exist between CO2 molecules.
...
[3]
(b) Real gases like carbon dioxide can be liquefied at low temperatures just by applying
pressure. Gases can be liquefied by pressure alone if their temperature is below their
critical temperature, Tc. The critical temperature of carbon dioxide is 31.1 C.
(i)
Explain why real gases like carbon dioxide can be liquefied just by applying
pressure.
At high pressure, the molecules are very close together, and the
...
intermolecular forces of attraction become significant.
...
(ii)
By considering structure and bonding, suggest a value for the critical temperature of
methane and give a reason for your choice.
Any value less than that of carbon dioxide will be accepted as the answer. The
...
van der Waals forces of attraction between methane molecules is weaker
...
compared to that between carbon dioxide molecules because CH4 has a
...
smaller electron cloud.
[2]
6
(c)
Beyond the critical temperature and pressure, carbon dioxide exists as a supercritical
fluid, a state that resembles a gas but has density closer to that in the liquid phase.
Carbon dioxide is now well established as a solvent for use in extraction.
(ii) Suggest why supercritical carbon dioxide is preferred as a solvent to extract caffeine
from solid coffee over organic solvents like benzene.
Carbon
dioxide is non-toxic while benzene is toxic and should be kept away
....
from food and beverages. OR
...
The carbon dioxide can be easily removed as a gas by depressurizing.
..
(iii) Suggest why small amounts of ethanol need to be added to supercritical carbon
dioxide in the extraction of polyphenols. An example of a polyphenol is shown
below.
OCH3
OH
HO
The ethanol molecules added can form hydrogen bonds with the phenol
...
groups present and this increase the solubility of polyphenols.
...
...
[2]
(d)
Ethanedioate ions, C2O42, can be oxidised by hot acidified aqueous potassium

manganate(VII) to form carbon dioxide.
(i) Draw the structure of ethanedioate ions, C2O42, and give the bond angle around the
central carbon atom.
O
C
120
O-
7
(ii) Construct a balanced equation for the reaction between ethanedioate ions and hot
acidified potassium manganate(VII).
C2O42- 2CO2 + 2eMnO4- + 8H+ + 5e- Mn2+ + 4H2O
Overall equation: 5C2O42- + 2MnO4- + 16H+ 2Mn2+ + 10CO2 + 8H2O
(iii) 1.63 g of a salt, KHC2O4H2C2O4, was dissolved in distilled water and made up to
250 cm3 solution. Calculate the volume of 0.020 mol dm3 of KMnO4 required to
react with 20.0 cm3 of the KHC2O4H2C2O4 solution.
[Mr of KHC2O4H2C2O4 = 218.1]
Amount of C2O42- ions present = 2 x
Amount of MnO4- required =
Volume of MnO4- required =
2
5
1.63
218.1
20
= 0.0011958 mol
x 0.0011958 = 0.0004783 mol
0.0004783
0.020
= 0.0239 dm3 = 23.9 cm3

[4]
The graph of rate against time for the reaction between acidified potassium
manganate(VII) and ethanedioate ions is shown below.
rate
time
(e)
(i) The reaction between acidified potassium manganate(VII) and ethanedioate ions is
usually carried out at a higher temperature of 60 C. Suggest why the rate of this
reaction is slow at room temperature.
Both
C2O42- and MnO4- are negatively charged and the activation energy for
.
the..
reaction is high due to repulsion between the ions.
(ii)
Suggest the species responsible for the increase in rate of reaction before point A,
and identify the property which enables it to act as a catalyst in this reaction.
Mn2+. It can exist in variable oxidation states.
.
..
[2]
[Total: 13]
3
Iron is the fourth most common element in the Earths crust, and has many applications
throughout the history of mankind. In nature, iron exists in many different mineral ores,
consisting of iron in either +2 or +3 oxidation state. In prehistoric era, iron compounds were
more commonly used as pigment without further purification. Limonite, which has the
general formula of FeO(OH)nH2O, was used as a yellow pigment as early as 10 000 B.C.
(a) (i) Complete the electronic configuration of Fe3+.
2s2 2p6 3s2 3p6 3d5
1s2 ...
(ii)Briefly explain why iron in mineral ores are found in variable oxidation states, but for
s-block elements, for example calcium, there is usually only one oxidation state.
Iron has valence electrons of similar energy in both the 3d and 4s orbitals,
...
thus it can lose electrons from both the 4s and 3d orbitals, giving rise to
...
variable oxidation states. However s-block elements can only lose valence
...
electrons in the s orbitals, resulting in only 1 oxidation state.
...
[3]
(b) A mineralogist dissolved 100 g of a certain pure limonite in concentrated HCl to form a
yellow solution. It was found that 3.2 mol of HCl had reacted based on the equation,
FeO(OH).nH2O + 4HCl FeC4 + (n+2)H2O + H+
FeO(OH).2H2O
(i) State the formula of this limonite (with n as an integer):
Tetrahedral [or square planar]

Suggest the shape of FeC4 : ....
9
(ii) Explain, with reference to FeC4 , why transition element complexes are coloured.
When Cl- ligands are bonded to the Fe3+ they will cause the originally
...
partially-filled degenerate d-orbitals to split into 2 energy levels with small
...
energy gap.
...
When electron from the lower d-orbitals absorbs energy in the visible light
...
region, it will be excited to the higher d* orbital. Such transition is d-d* electronic
...
transition.
...
[5]
Complementary colours, yellow, which is not absorbed will be observed as the
colour of FeC
.
(c) In recent times, with much better understanding of chemistry, iron and its compounds are
widely used as catalysts and reagents in synthesis of chemicals. In particular, the
2
ferrate(VI) ion, FeO4 , is a strong oxidising agent that is used in green chemistry and
water purification due to its non-toxic by-products.
Ferrate(VI) ions are not stable in acidic conditions and easily oxidise water to give
oxygen. Hence they are often produced in an alkaline medium.
Some Eo data of chlorate(I) and ferrate(VI) are given below.
2
FeO4 + 8H+ + 3e- Fe3+ + 4H2O

2
FeO4 + 4H2O + 3e- Fe(OH)3 + 5OH

2ClO + 4H+ + + 2e- Cl2 + 2H2O
ClO + H2O + 2e- Cl + 2OH
Eo = +2.20 V
Eo = +0.80 V
Eo = +1.63 V
Eo = +0.89 V
(i) By selecting relevant Eo data from the Data Booklet and using the information above,
explain with suitable calculation,
I
why ferrate(VI) ions are not stable in acidic conditions.
O2 + 4H+ + 4e 2H2O Eo = +1.23V
Eorxn = +2.20 -1.23 = +0.99 V
As Eorxn is positive, the reaction is feasible, and ferrate will oxidise water to
give oxygen.
10
II
why it is feasible to form potassium ferrate(VI), K2FeO4, by reacting KClO with

Fe(OH)3 in the presence of KOH.
3e- + 4H2O + FeO
Fe(OH)3 + 5OH-
ClO + H2O + 2e- Cl + 2OH
Eo = +0.80 V
Eo = +0.89 V
Eorxn = +0.89 - 0.80 = +0.09 V > 0, hence the reaction is feasible.
(ii) Hence write a balanced overall equation for the formation of K2FeO4.
4KOH + 2Fe(OH)3 + 3KClO 3KCl + 5H2O + 2K2FeO4
..
(iii) Would you expect an acidified solution of K2FeO4 to be a stronger or weaker

oxidising agent compared to an acidified solution of KMnO4? Support your answer
with relevant Eo values from the Data Booklet.
MnO + 8H+ + 5e- Mn2+ + 4H2O Eo = +1.52 V
..
Comparing the Eo values of +1.52 V and + 2.20V, FeO undergoes reduction more
....
readily, thus it is a stronger oxidising agent compared to MnO

....
(iv) Hence draw the structure of the possible organic product formed when hot acidified
purple K2FeO4 reacts with the following compound and suggest the expected
observations.
CH2CH2OH
CO2H
CH3
CO2H
Observations :..
Efferversence of carbon dioxide is observed, and the solution changes from
....
purple FeO to yellow Fe3.
....
[8]
11
(d) White light contains all the colours in the visible spectrum. Each of these colours is
associated with a certain wavelength, l. The formula relating energy and wavelength is,
E = hc/l ,
where h = 6.626 x 1034 J s,

c = 3.00 x 108 m s-1
l has the units of m.
(i)
Wavelength, l (109 m)
Colour of light
400
Violet
450
Blue
500
Green
550
Yellow
600
Orange
650
Red
By considering the appearance of green iron(II) compounds and yellow iron(III)

compounds, state the colour of light absorbed for these compounds.
Violet
Red
Iron(II):
Iron(III).
(ii) Hence, with the information above, calculate the energy associated with the
respective colours absorbed.
For Red absorbed by iron (II), E = (6.626 x 10-34) (3.00 x 108)/(650 x 10-9)
= 3.06 x 10-19 J
For Violet absorbed by iron (III), E = (6.626 x 10-34) (3.00 x 108)/(400 x 10-9)
= 4.97 x 10-19 J
Energy of colour absorbed by
3.06 x 10-19 J
Iron(II) compounds:
4.97 x 10-19 J
Iron(III) compounds:
12
(iii) Using your answer in (d)(ii), complete the diagram below to show the relative
energies of the d orbitals, and the electronic distribution of the respective
compounds. In each case, label clearly the energy difference required for the
promotion of an electron upon absorption of light.
Assume all electrons occupy the lower energy orbitals before the higher energy
orbitals.
Energy
_ _
_ _ _
_ _
3.06 x 10-19 J
_ _ _
Iron(II) compounds
4.97 x 10-19 J
Iron(III) compounds
[5]
[Total: 21]
4
Cymobarbatol is an antimutagenic agent isolated from the marine algae Cymopolia barbata.
The structure of cymobarbatol is shown below.
Br
Br
*
*
HO
HO
*
Br
Br
Cymobarbatol
(a) Name two functional groups, other than phenyl and ether, that are present in the
cymobarbatol molecule.
phenol, secondary bromoalkane, bromoarene
[2]
(b) Identify the chiral carbons in cymobarbatol molecule by placing an asterix (*) against
each chiral carbon on the structure above.
[1]
(c) Draw the structural formula of each organic product formed when cymobarbatol is
O
In the following reactions, the
ring remains unaltered.
13
(i) ethanolic NaOH, heated under reflux
Br
Na-O
(ii) concentrated ethanolic NH3, heated in a sealed tube

Br
NH2
HO
[2]
(d) Cymobarbatol will also react with aqueous NaOH under reflux condition.
(i) Given that one mole of cymobarbatol reacts with two moles of aqueous NaOH, write a
balanced equation for this reaction.
Br
Br
+ 2OHHO
Br
+ H2O + Br-
OH
(ii) When bromine in cymobarbatol is replaced by iodine, how would you expect the rate
of its hydrolysis reaction to compare to that of cymobarbatol? Explain your answer.
...
When bromine in cymobarbatol is replaced by iodine, the rate of reaction is
faster than cymobarbatol.
...
This is because the C-I bond is longer and hence weaker than the C-Br bond
(since I atom is larger than Br atom).
...
...
14
(iii) Describe the expected observations when aqueous AgNO3, followed by
concentrated aqueous ammonia, is subsequently added to the resultant mixture in
(d)(i). Explain your answer with relevant equations.
A cream ppt. of AgBr will be observed to form when aq. AgNO3 is added.
....
It will then dissolve in the concentrated aq. NH3 solution to form a
colourless solution.
.....
Ag+(aq) + 2 NH3(aq) [Ag(NH3)2]+(aq)
equation I
.....
Ag+ (aq) reacts with NH3(aq) to form a soluble complex, [Ag(NH3)2]+ from
equation I.
....
equilibrium II
AgBr(s) Ag+(aq) + Br-(aq)
.....
As [Ag+] decreases, the position of equilibrium II shifts to the right and
....
hence more AgBr dissolves
[OR]
....
When excess NH3(aq) is added such that ionic product of AgBr < Ksp of
AgBr, all the AgBr will dissolve completely.
....
....
....
....
[7]
[Total: 12]
5
There are a number of structural isomers of molecular formula CnHnO2. In particular, one of
the isomers, B, is used as a tincture in perfumes and as a food additive.
(a) To find the value of n, a 1.00 g sample of B was burned in an excess of oxygen, and the
gases that were produced were first passed through a U-tube containing P4O10 (to
absorb the water vapour) and then bubbled through concentrated NaOH(aq). The P4O10
in the U-tube increased in mass by 0.529 g.
(i) Write an equation for the reaction of P4O10 with water vapour and state the pH of the
resultant solution.
P4O10 + 6H2O 4H3PO4. pH = 1 to 2
.
(ii) Suggest why anhydrous CaCl2 cannot be used in place of P4O10 in the U-tube.
Calcium chloride will absorb water vapour to form a neutral solution, and
..
would absorb some of the CO2 formed.
..
(iii) Calculate the number of moles of water produced.
Amount of H2O = 0.529 = 0.0294 mol
18
15
(iv) Use the above data to show that the value of n = 8.

Amount of B =
1.00
1.00
=
12n + n + 32 13n + 32
mol
CnHnO2 n H2O
2
Thus
1.00
n
13n + 32 2
= 0.0294
Therefore n = 8
[5]
(b) A reaction scheme involving compound B and its related compounds, C to E, undergo
the following reactions:
LiAlH4 in dry ether
B, C8H8O2
C, C8H10O2
heating
with
conc. H2SO4
heating
with
acidified K2Cr2O7(aq)
neutral
FeCl3(aq)
D, C8H8O
orange
solution
violet
colouration
HBr(g)
E, C8H9OBr
(i) Based on the above information, draw three possible structural isomers of B, which
are labeled as B1, B2 and B3 in the boxes below.
OH
OH
OH
O
C
CH3
CH3
B1
B2
CH3
B3
16
(ii) Based on your structure of B1, draw the structures of C, D and E.
Br
OH
OH
OH
OH
H
C
C
CH3
C
CH3
CH2
[6]
(c) A structural isomer of D, C8H8O, which is labelled as F, contains a C-O-C bond.
F does not react with HBr(g).
(i) Suggest a structural formula of F.
F is
O
or
(ii)Although F does not react with HBr(g), it can react with concentrated HBr(aq). The
reaction of F with concentrated HBr(aq) is similar to the reaction of primary alcohols
with concentrated HBr(aq). The process involves two stages:
H
Stage I
RCH2-OH
+ H+
RCH2
O
H
Stage II
RCH2
H
+ Br
Br
RCH2
+ H-OH
Suggest a mechanism for the Stage II process in the reaction of F with concentrated
HBr(aq), including curly arrows to denote movement of electrons, and all charges.
You do not need to draw the 3-dimensional representation of the molecules involved.
OH+
OH
Br
Br OR
OH+
OH
Br
Br
[arrows, lone pair on Br- indicated, SN2 mechanism]
[3]
[Total: 14]

Higher 2
CHEMISTRY
Paper 3 Free Response
9647/03
Friday 24 August 2012
2 hours

Additional Materials: Answer Paper
Data Booklet
Write your name and class on all the work you hand in.
ALLOWED]
A Data Booklet is provided
[Turn over
2
1
This question relates to the chemistry of Be, Mg, Al and their compounds.
(a) Beryllium compounds are toxic air pollutants. Inhalation of high levels of beryllium can
cause inflammation of the lungs in humans and long-term exposure may cause chronic
beryllium disease (berylliosis), in which granulomatous lesions develop in the lung.
(i) Given that charge density
Be2+,
Mg2+
and
Al3+,
ionic charge
ionic radius
, calculate the relative charge densities of
using relevant data from the Data Booklet.
(ii) Hence, predict what is observed when aqueous sodium hydroxide is gradually
added to aqueous beryllium sulfate until the sodium hydroxide is in an excess.
Write equations for all reactions that have taken place.
(iii) Suggest the pH of the solution formed when beryllium chloride is dissolved in
water. Give your reasoning.
(iv) Magnesium ions are essential for the action of some enzymes (e.g. alkaline
phosphatase found in the liver) by receiving electron pairs from oxygen and
nitrogen atoms in the protein. It is thought that beryllium compounds are poisonous
because they displace magnesium ions from these enzymes.
Suggest a reason why beryllium ions should behave in this way.
(v) Beryllium chloride may be used as a catalyst in the chlorination of benzene.
Suggest a reason why this is possible. Outline the mechanism to show how
beryllium chloride is involved in this reaction.
[10]
3
(b) A student carried out a kinetics experiment using a roll of magnesium ribbon that had
been exposed to air for some time. He placed a piece of magnesium ribbon of mass
0.12 g into a flask containing 15.0 cm3 of 1.0 mol dm3 hydrochloric acid. The progress
of the reaction was followed by measuring the pressure of the system at different times.
The graph below shows the results of the experiment.
pressure of
the system
A
0
B
time
(i) Determine, by calculation, the limiting reagent for the experiment.

(ii) Account for the change in pressure of the system as shown in the graph at points
A, B, and from C onwards.
[4]
(c) An alloy of aluminium and magnesium is used in boat-building.
A 1.75 g sample of the alloy was dissolved in the minimum volume of 4 mol dm3
hydrochloric acid and the solution was then made alkaline by the addition of aqueous
sodium hydroxide until no further reaction occurred. The resultant mixture was filtered
and the residue, X, rinsed with distilled water, all washings being added to the filtrate,
Y. After air drying, 0.18 g of X was obtained. Carbon dioxide was passed into Y and a
white solid, Z, which contained aluminium, was collected. Heating Z to constant mass
gave a residue of mass 3.16 g.
Suggest the identities of X, Y and Z, and determine the percentage composition by
mass of the alloy.
[6]
[Total: 20]
[Turn over
4
2
2-chlorobutane undergoes hydrolysis with NaOH(aq) via two different reaction pathways, in
the same reaction, to form a mixture of two enantiomeric products.
CH3CHClCH2CH3 + NaOH CH3CH(OH)CH2CH3 + NaCl
In one of the hydrolysis reaction pathways, only one product is formed and inversion of
configuration occurs in the product. In the other reaction pathway, a racemic mixture is
formed.
(a) In an experiment, one optical isomer of 2-chlorobutane undergoes hydrolysis and two
enantiomeric products in a ratio of 95%:5% are formed.
(i) Draw the structures of the two enantiomeric products.
(ii) One enantiomer is formed in a much higher percentage compared to the other.
Explain clearly how this disparity arises by examining the mechanisms of both
reaction pathways. You should name both mechanisms involved but an outline of
the mechanism is not required.
(iii) Write a rate equation for the reaction pathway that results in the inversion of the
configuration and draw its energy profile diagram, given that the enthalpy change
of the hydrolysis is exothermic.
(iv) Suggest the percentage of 2-chlorobutane that undergoes hydrolysis via the
reaction pathway in (a)(iii).
(v) Hence deduce how much faster the rate of this reaction pathway in (b)(ii)
compares to that of the other reaction pathway.
[9]
(b) 2-chlorobutane is commonly produced from but-1-ene via reaction with hydrogen
chloride.
CH2=CHCH2CH3(g) + HCl(g) CH3CHClCH2CH3(l)
(i) Name the other possible product in the above reaction.
(ii) Predict the sign of S for this reaction, showing your reasoning.
(iii) Using relevant bond energy values from the Data Booklet, calculate the
approximate value of H for the reaction in (b).
(iv) Bond energies quoted from the Data Booklet are average values. Other than this,
explain why the method in (b)(iii) is not the most accurate for determining H of
the reaction.
(v) Deduce how the rate of reaction of but-1-ene with hydrogen halides will vary from
H-F to H-I, and give your reasoning.
5
(vi) While HCl react readily with alkenes under room conditions, HCN does not. Based
on concepts of chemical bonding, suggest possible reasons for this.
[10]
(c) HCl can be prepared by adding concentrated sulfuric acid to solid sodium chloride.
However when concentrated sulfuric acid is added to sodium iodide, the yield of HI is
very low. Explain.
[1]
[Total: 20]
[Turn over
6
3
This question explores the chemistry of zinc in biochemistry, organic chemistry and
electrochemistry.
(a) Angiotensin I, a simple protein, undergoes hydrolysis with the aid of an enzyme, known
as angiotensin-converting enzyme (ACE) to form angiotensin II. Angiotensin II is an
important hormone that causes blood vessels to constrict, resulting in a rise in blood
pressure.
(i) State how proteins can be hydrolysed to form a mixture of their constituent amino
acids.
Some of the amino acids found in angiotensin II are shown below.
H
H
H2N C CO2H
H2N C CO2H
CH
CH3 CH3
CH2
H2N C CO2H
H2N
CH2CH2CH2
C NH
OH
valine
(val)
tyrosine
(tyr)
arginine
(arg)
The side chains (R-groups) of angiotensin II could bind to targeted proteins through
suitable R-group interactions. The R-group interactions are also used to maintain two
specific protein structures.
(ii) Briefly describe one protein structure that involves R-group interactions.
(iii) Suggest three different types of R-group interactions in which the side chains of
angiotensin II could bind to targeted proteins. Your answer should clearly indicate
the side chains that might be involved.
(iv) Another enzyme that functions similarly as ACE is carboxypeptidase. The active
site of carboxypeptidase contains NH3+ group and a Zn2+ ion, which are both
crucial in binding to suitable proteins.
Below shows the hydrolysis of a protein (represented by RCONHCH(R)CO2)
catalysed by this enzyme, where ------ represents interactions between the enzyme
and the protein.
active
Zn2+
site of
O
R
R'
enzyme
N
H
O-
protein
(substrate, S)
Enzymes, E
active
Zn2+
site of
O
R
enzyme
O+
H3N
H3N
ES Complex
site of
O-
R'
N
H
active
Zn2+
hydrolysis
R'
O
H2N
O
O+
H3N
enzyme
7
If there is a mutation such that carboxypeptidase does not contain Zn2+, the
enzyme will fail to function effectively as a catalyst. By using the above information,
suggest why.
[6]
(b) Lucas reagent is used to distinguish primary, secondary and tertiary alcohols. It
consists of a solution of anhydrous ZnCl2 in concentrated HCl. Upon addition of Lucas
reagent at 28 C, tertiary alcohols give immediate cloudiness, secondary alcohols give
cloudiness within 5 minutes and primary alcohols have no cloudiness. The overall
reaction that has occurred can be represented as
ROH + HCl RCl + H2O
(i) Draw three structural isomers with molecular formula C4H10O that can be
distinguished using Lucas reagent and state the observation for each isomer.
(ii) Hence from your observation in (b)(i), suggest a possible product that is
responsible for the cloudiness of the mixture.
(iii) Four structural isomers of molecular formula C3H6O2 are as follows:
E: CH3CH(OH)CHO
F: CH3COCH2OH
G: HOCH2CH2CHO
H: HCO2CH2CH3
Show how isomers E to H can be adequately distinguished from one another by

the use of simple chemical tests. You should also give brief descriptions of the
chemical tests and expected observations for each isomer.
[7]
[Turn over
8
(c) About 12 million tonnes of zinc are produced every year, of which 70 % are obtained
through mining. The ore is first roasted to produce zinc oxide, which is then further
processed to obtain pure zinc through a series of steps.
(i) In the first step, ZnO is reacted with dilute sulfuric acid. Write a balanced equation
for this reaction.
The next step involves electrolysis of the resulting solution obtained in (c)(i). A current
of 10 000 A is passed through the solution in a series of electrolytic cells and zinc is
deposited on the cathode of each cell. After 24 hours, each cell is shut down, the zinc
coated cathodes are rinsed and pure zinc is mechanically stripped from the cathode.
(ii) Write the half-equations for each electrode reaction and hence, construct the
overall balanced equation.
(iii) Assuming that only one cell is involved in the production in a 24-hour period
I
Calculate the mass of zinc produced in 24 hours.
II Hence, calculate the thickness, in cm, of the zinc sheet produced.
Given: current density = 500 A m2 of zinc deposited
density of zinc = 7.14 g cm3.
[Current density is defined as the current flowing per unit area.]
[7]
[Total: 20]
9
4
Piperidines are widely-used building blocks in the synthesis of organic compounds in the
pharmaceutical industry. A possible synthetic route to prepare of 2-methylpiperidine is
shown below.
H
N
I
CN
HO
II
CN
Cl
III
2-methylpiperidine
(a) (i) State the type of reaction that has occurred in stage I and identify a suitable
reagent used.
(ii) Explain why stage I has to be carried out in an anhydrous condition. Include in
your answer any relevant equation.
(iii) Draw the dot-and-cross diagram of the reagent used in stage I.
(iv) Suggest the structure of compound L and state the reagent and conditions
required in stage II.
[8]
(b) Benzoic acid and 2-methylpiperidine can be used to synthesise piperocaine, a local
anaesthesia used for infiltration and nerve block, via a two-step reaction. Benzoic acid
is first converted into an intermediate, R, which is then converted to piperocaine.
O
O
C
OH
piperocaine
Suggest the reagents and conditions required for each step and draw the structure of
intermediate R produced.
[4]
[Turn over
10
(c) Benzoic acid is used as an antiseptic due to its ability to inhibit the growth of bacteria.
Salicylic acid, a monohydroxybenzoic acid, has a similar function. The structure and
solubility of both compounds in water are given in the table below.
Name
Solubility / mol dm3
Structure
HO
Benzoic
acid
0.0238
HO
Salicylic
acid
OH
0.0145
(i) By considering structure and bonding, explain the difference in solubility of

benzoic acid and salicylic acid.
(ii) Suggest a simple chemical test that can be used to distinguish benzoic acid from
salicylic acid. State the reagents and conditions used and describe clearly the
observations for each of the compound. Write a balanced equation for any
reaction that occurs.
[5]
(d) Salicylic acid is also an important active metabolite of aspirin, a drug to relieve minor
aches and pains, to reduce fever, and as an anti-inflammatory medication.
O
OH
O
O
aspirin
The synthesis of aspirin involves treating salicylic acid with ethanoic anhydride, an acid
derivative, in the presence of concentrated phosphoric acid. This esterification process
(shown below) yields aspirin and ethanoic acid, which is considered a by-product of this
reaction.
O
OH
O
OH
OH
conc. H3PO4
ethanoic anhydride
heat
OH
O
aspirin
11
(i)
(ii)
(iii)
Suggest why salicylic acid will not react with itself to produce an ester given the
conditions stated above.
Suggest another reagent that can be used in place of ethanoic anhydride in the
synthesis of aspirin from salicylic acid.
The synthesis of aspirin from salicylic acid with ethanoic anhydride may occur as
follows.
conc. H3PO4
OH+
O
OH
protonated f orm of ethanoic anhydride
OH+
OH
OH
H
O+
II
HO
III
O
OH
O
O
HO
H+
Suggest the types of reactions occurring in stages I and II.

[3]
[Total: 20]
[Turn over
12
5
(a) The Gabriel synthesis is a chemical reaction that transforms primary alkyl halides
into primary amines using potassium phthalimide. It gives a high yield of primary
amines and an example of the Gabriel synthesis is shown below.
Step I
O
O
KOH
N K+
NH
O
O
potassium phthalimide
Step II
O
N K+
CH3CH2X
NCH2CH3 + KX
X = Cl or Br
O
Step III
O
NCH2CH3
H2O / OH-
CH3CH2NH2
(i) Step I is unusual as the amide hydrogen is quite acidic, hence it can react with
KOH to produce potassium phthalimide. Suggest why the amide hydrogen is
acidic in this case.
(ii) What type of reaction is step III?
(iii) Suggest a structure for M.
[3]
13
(b) 1-phenylmethanamine (C6H5CH2NH2) is a versatile organic compound which is used
as a raw material for the production of Vitamin H. It is also an active ingredient in
the production of nylon fibres.
1-phenylmethanamine can be produced via a similar two-step Gabriel amine
synthesis.
O
CH2NH2
H2O / OH-
N
N K+
1-phenylmethanamine
Suggest the structures of compounds N and P.
[2]
(c) Phenylamine, along with its chlorine-substituted derivatives, is widely used in biology,
medicine, as well as the paint and varnish industry.
(i)
Suggest a synthetic route to form 2-methylphenylamine from methylbenzene.

H2N
-met
CH3
m ne
hylphe yla i
2
2-methylphenylamine
(ii) The reaction below can proceed in the absence of a catalyst. Explain why milder
conditions are required for this reaction compared to chlorination of benzene.
Cl
NH2
NH2
Cl2(aq)
CH3
CH3
Cl
[3]
[Turn over
14
(d) The Hofmann rearrangement is another organic reaction used to synthesis primary
amines. It involves the reaction of a primary amide with aqueous alkaline bromine to
form a primary amine with one less carbon atom than the starting material.
H
CH3
H
NH2
Br2 + OH-(aq)
CH3
CH3
NH2
CH3
1-phenylmethanamine (C6H5CH2NH2) can also be produced in a three-step sequence

given below where the last step is a Hofmann reaction.
I
CH2CO2H
II
Q
Br2, OH-(aq)
CH2NH2
(i) Draw the structures of compounds Q and S.

(ii) Suggest reagents and conditions required for stages I and II.
[4]
(e) (i) Arrange the following compounds in order of decreasing basicity. Explain your
answer.
CH3
NH2
CH2NH2
and NH3.
(ii) Calculate the pH of the resulting solution when 25 cm3 of 0.0200 mol dm3 HCl is
added to 25 cm3 of 0.0300 mol dm3 1-phenylmethanamine (C6H5CH2NH2).
(The Kb value of 1-phenylmethanamine is 2.19 x 105 mol dm3.)
(iii) A 0.0200 mol dm3 solution of 1-phenylmethanamine was mixed with an equal
volume of 0.00100 mol dm3 of aqueous magnesium sulfate. Determine whether a
precipitate would be formed in this experiment.
(The numerical Ksp value of magnesium hydroxide is 1.8 x 1012).
[8]
[Total: 20]
~ END OF PAPER ~
SOLUTIONS

Higher 2
CHEMISTRY
9647/03
Friday 24 AUGUST 2012
2 Hours

Additional Materials: Answer Paper
Data Booklet
ALLOWED]
A Data Booklet is provided
[Turn over
2
1
This question relates to the chemistry of Be, Mg, Al and their compounds.
(a) Beryllium compounds are toxic air pollutants. Inhalation of high levels of beryllium can
cause inflammation of the lungs in humans and long-term exposure may cause chronic
beryllium disease (berylliosis), in which granulomatous lesions develop in the lung.
(i) Given that charge density
ionic charge
ionic radius
, calculate the relative charge densities of
Be2+, Mg2+ and Al3+, using relevant data from the Data Booklet.
Be2+: 64.5, Mg2+: 30.8, Al3+: 60.0
(ii) Hence, predict what is observed when aqueous sodium hydroxide is gradually
added to aqueous beryllium sulfate until the sodium hydroxide is in an excess.
Write equations for all reactions that have taken place.
- white ppt, which dissolves in excess NaOH to give a colourless solution
Be2+(aq) + 2OH-(aq) Be(OH)2(s)
Be(OH)2(s) + 2OH-(aq) Be(OH)42-(aq)
(iii) Suggest the pH of the solution formed when beryllium chloride is dissolved in
water. Give your reasoning.
pH 3
Be2+ ions have high charge density, which polarises neighbouring H2O
molecules; hence, weakening OH and H+ lost
(iv) Magnesium ions are essential for the action of some enzymes (e.g. alkaline
phosphatase found in the liver) by receiving electron pairs from oxygen and
nitrogen atoms in the protein. It is thought that beryllium compounds are poisonous
because they displace magnesium ions from these enzymes.
Suggest a reason why beryllium ions should behave in this way.
Be2+ ions have higher charge density (or greater polarising power) than Mg2+;
hence has greater tendency to receive electron pairs to form dative covalent
bonds.
(v) Beryllium chloride may be used as a catalyst in the chlorination of benzene.
Suggest a reason why this is possible. Outline the mechanism to show how
beryllium chloride is involved in this reaction.
[10]
In BeCl2, Be atom has only 4 outer electrons and so, is able to act as lone
pair acceptor (to generate Cl+ electrophile)
BeCl2 + Cl2 BeCl3- + Cl+
3
H
Cl
Cl+
Cl
Cl
BeCl3-
+ BeCl2
+ HCl
(b) A student carried out a kinetics experiment using a roll of magnesium ribbon that had
been exposed to air for some time. He placed a piece of magnesium ribbon of mass
0.12 g into a flask containing 15.0 cm3 of 1.0 mol dm3 hydrochloric acid. The progress
of the reaction was followed by measuring the pressure of the system at different times.
The graph below shows the results of the experiment.
pressure of
the system
time
(i) Determine, by calculation, the limiting reagent for the experiment.

Mg + 2HCl MgCl2 + H2
amt of Mg =
0.12
= 0.00494 mol
24.3
amt of HCl = 1.0 x
15.0
= 0.015 mol
1000
since Mg 2 HCl,
hence, amt of HCl required for reaction = 2 x 0.00494 = 0.00988 mol < 0.015
mol (initial amount of HCl used )
Hence, Mg is the limiting reagent.
(ii) Account for the change in pressure of the system as shown in the graph at points
A, B, and from C onwards.
4
At A initially rate is slow; due to layer of oxide/MgO formed on the surface
of Mg ribbon due to oxidation in air
At B rapid increase in rate; reaction is exothermic, heat evolved increases
rate of reaction
C onwards decrease in rate; as Mg (limiting reagent) is used up
[4]
(c)
An alloy of aluminium and magnesium is used in boat-building.

A 1.75 g sample of the alloy was dissolved in the minimum volume of 4 mol dm3
hydrochloric acid and the solution was then made alkaline by the addition of aqueous
sodium hydroxide until no further reaction occurred. The resultant mixture was filtered
and the residue, X, rinsed with distilled water, all washings being added to the filtrate,
Y. After air drying, 0.18 g of X was obtained. Carbon dioxide was passed into Y and a
white solid, Z, which contained aluminium, was collected. Heating Z to constant mass
gave a residue of mass 3.16 g.
Suggest the identities of X, Y and Z, and determine the percentage composition by
mass of the alloy.
On dissolution in HCl (aq):
Mg(s) + 2HCl (aq) MgCl2 (aq) + H2(g) (and)
Al + 3HCl AlCl3 (aq) + 3/2 H2 (g)
On addition of excess NaOH (aq) till no further reaction occurs:

Mg2+ + 2OH- Mg(OH)2(s) Residue X: Mg(OH)2
Al3+ + 3OH- Al(OH)3 (s)
Al(OH)3 (s) + OH- (aq) Al(OH)4- (aq) Filtrate Y: NaAl(OH)4 [not Al(OH)4-]
On addition of CO2 into Y:

2NaAl(OH)4 (aq) + CO2 2Al(OH)3(s) + Na2CO3 (aq) White solid Z: Al(OH)3
Heating Z to constant mass:
2Al(OH)3(s) Al2O3 (s) + 3H2O (aq) residue of mass 3.16g = Al2O3 (s)
X Mg(OH)2
Y NaAl(OH)4
Z Al(OH)3
mass of Mg in Mg(OH)2 =
mass of Al in Al2O3 =
% of Mg in alloy =
24.3
24.3
x 0.18 =
x 0.18 = 0.0750 g
24.3 + 2(16.0 + 1.0)
58.3
2(27.0)
54.0
x 3.16 =
x 3.16 = 1.67 g
2(27.0) + 3(16.0)
102.0
0.0750
x 100 = 4.29 %
1.75
5
% of Al in alloy =
1.67
x 100 = 94.4 %
1.75
[6]
[Total: 20]
2-chlorobutane undergoes hydrolysis with NaOH(aq) via two different reaction pathways in
the same reaction to form a mixture of two enantiomeric products.
CH3CHClCH2CH3 + NaOH CH3CH(OH)CH2CH3 + NaCl
In one of the hydrolysis reaction pathways, only one product is formed and inversion of
configuration occurs in the product. For the other reaction pathway, a racemic mixture is
formed.
(a) In an experiment, one optical isomer of 2-chlorobutane undergoes hydrolysis and two
enantiomeric products in a ratio of 95%:5% are formed.
(i) Draw the structures of the two enantiomeric products.
CH2CH3
H
H3C
CH2CH3
*
OH
HO
H
CH3
Few students scored full marks for this part. Many students could not represent the
enantiomers appropriately.
Common errors:
1. No mirror line drawn (or) mirror line drawn as solid line.
2. Enantiomers are not represented as mirror images of each other.
3. Enantiomers are not represented in terms of tetrahedral geometry / 3D
configuration.
4. Wedge and dotted line of 3D configuration not drawn in correct direction.
5. -CH2CH3 often wrongly represented as H3CHC- in enantiomer structures.
(ii) One enantiomer is formed in a much higher percentage compared to the other.
Explain clearly how this disparity arises by examining the mechanisms of both
reaction pathways. You should name both mechanisms involved but an outline of
the mechanism is not required.
SN2 mechanism
H3C
CH3CH2
OHH3C
CH2CH3
HO
Cl
CH2CH3
Cl
HO
CH3
H
+ Cl-
Only 1 product formed;

inversion of configuration
compared to reactant
SN1 mechanism
CH3CH2
H
H3C
H
d+
CH2CH3CH3CH2
CH2CH3
HO
Cl
d-
OH
CH3
OH
OH
H
CH3
H
H3C
racemic product f ormed
carbocation intermediate
Hydrolysis of 2-chlorobutane occurs via both SN2 and SN1 mechanisms. A

racemic product is formed via the SN1 mechanism whereas only 1 chiral
product is formed during the SN2 mechanism. As such, one of the enantiomers
is formed in a greater proportion compared to the other.
One of the enantiomers is formed in a much greater percentage as the reaction
proceeds largely via the SN2 mechanism that results in the formation of 1 chiral
product.
(iii) Write a rate equation for the reaction pathway that results in the inversion of the
configuration and draw its energy profile diagram, given that the enthalpy change
of the hydrolysis is exothermic.
rate = k[CH3CHClCH2CH3][OH-]
Energy
transition state
Ea
H < 0
Reactants (or)
CH3CHClCH2CH3
Products (or) CH3CH(OH)CH2CH3
Reaction Pathway
(iv) Suggest the percentage of 2-chlorobutane that undergoes hydrolysis via the
reaction pathway in (a)(iii).
90%
(v) Hence deduce how much faster the rate of this reaction pathway in (b)(ii)
compares to that of the other reaction pathway.
9 times faster
[9]
(b) 2-chlorobutane is commonly produced from but-1-ene via reaction with hydrogen
chloride.
CH2=CHCH2CH3(g) + HCl(g) CH3CHClCH2CH3(l)
(i) Name the other possible product in the above reaction.
1-chlorobutane
(ii) Predict the sign of S for this reaction, showing your reasoning.
CH2=CHCH2CH3 (g) + HCl (g) CH3CHClCH2CH3 (l)
S < 0
Since 1 mol of CH3CHClCH2CH3 (l) is formed from 1 mol of CH2=CHCH2CH3 (g)
and 1 mol of HCl (g), number of gas molecules in the system decreases as
reaction proceeds. As molecules in the gaseous state have more ordered
arrangement, hence entropy of system decreases.
(iii) Using relevant bond energy values from the Data Booklet, calculate the
approximate value of H for the reaction in (b).
CH2=CHCH2CH3 (g) + HCl (g) CH3CHClCH2CH3 (l)
Bond broken Bond Energy / kJ mol-1
Bond formed Bond energy / kJ mol-1
C=C
+610
C-C
-350
H-Cl
+431
C-H
-410
C-Cl
-340
H = +610 + 431 -350 -410 340 = -59 kJ mol-1
(iv) Bond energies quoted from the Data Booklet are average values. Other than this,
explain why the method in (b)(iii) is not the most accurate for determining H of
the reaction.
8
CH3CHClCH2CH3 formed in the reaction is a liquid, whereas the bond energy
method is only applicable for a gaseous system / bond energy refers to the
energy required to break 1 mole of a covalent bond between two atoms in the
gaseous state whereas CH3CHClCH2CH3 formed is in the liquid state.
(v) Deduce how the rate of reaction of but-1-ene with hydrogen halides will vary from
H-F to H-I, and give your reasoning.
The rate of reaction will increase from H-F to H-I as the bond energy of H-X
decreases from H-F to H-I.
As the rate determining step of the mechanism involves the breaking of the
H-X bond, the weaker the H-X bond, the more readily it will break, thus
increasing the rate of reaction with but-1-ene.
This question was generally well-answered.
(vi) While HCl react readily with alkenes under room conditions, HCN does not. Based
on concepts of chemical bonding, suggest possible reasons for this.
HCN is a weaker electrophile than HCl.
C-H bond in HCN is non-polar in nature, hence C-H bond does not break
readily to release H+.
[10]
(c) HCl can be prepared by adding concentrated sulphuric acid to solid sodium chloride.
However when concentrated sulphuric acid is added to sodium iodide, the yield of HI is
very low. Explain.
[1]
I- is a stronger reducing agent compared to Cl- hence it is able to further react
with H2SO4 by reducing it to H2S while itself is oxidised to I2. As such, small
amount of HI remains.
[Total: 20]
3
This question explores the chemistry of zinc in biochemistry, organic chemistry and
electrochemistry.
(a) Angiotensin I, a simple protein, undergoes hydrolysis with the aid of an enzyme, known
as angiotensin-converting enzyme (ACE) to form angiotensin II. Angiotensin II is an
important hormone that causes blood vessels to constrict, resulting in a rise in blood
pressure.
(i) State how proteins can be hydrolysed to form a mixture of their constituent amino
acids.
6 mol dm-3 HCl or H2SO4 or NaOH, and heat for several hours (eg 6 hours)
Some of the amino acids found in angiotensin II are shown below.

H
H
H
H2N C CO2H
H2N C CO2H
CH
CH2
CH3
H2N C CO2H
NH2
N
CH2CH2CH2
CH3
NH
OH
valine
(val)
tyrosine
(tyr)
arginine
(arg)
The side chains (R-groups) of angiotensin II could bind to targeted proteins through
suitable R-group interactions. The R-group interactions are also used to maintain two
specific protein structures.
(ii) Briefly describe one protein structure that involves R-group interactions.
Tertiary structure and its description (also accept quaternary structure)
(iii) Suggest three different types of R-group interactions in which the side chains of
angiotensin II could bind to targeted proteins. Your answer should clearly indicate
the side chains that might be involved.
van der waals forces of attraction with CH(CH3)2 from valine or CH2-C6H5
from tyrosine or CH2CH2CH2- from arginine (or non-polar alkyl side chain)
hydrogen bonding with phenol from tyrosine or C=NH or NH2 from arginine
ionic bonding with NH3+ group from arginine
(iv) Another enzyme that functions similarly as ACE is carboxypeptidase. The active
site of carboxypeptidase contains NH3+ group and a Zn2+ ion, which are both
crucial in binding to suitable proteins. Below shows the hydrolysis of a protein
(represented by RCONHCH(R)CO2) catalysed by this enzyme.
active
Zn2+
site of
O
R
enzyme
N
H
O-
H3N
O+
H3N
site of
R'
N
H
active
Zn2+
site of

enz me
R'
protein
active
Zn2+
hydrolysis
R'
O
H2N
O
O+
H3N
enzyme
10
If there is a mutation such that carboxypeptidase does not contain Zn2+, it will fail to
function effectively as a catalyst. By using the above information, suggest why.
Protein cannot effectively bind to active site of enzyme due to absence of
ion-dipole attractions between Zn2+ ions and C=O group
[6]
(b) Lucas reagent is used to distinguish primary, secondary and tertiary alcohols. It
consists of a solution of anhydrous ZnCl2 in concentrated HCl. Upon addition of Lucas
reagent at 28 C, tertiary alcohols give immediate cloudiness, secondary alcohols give
cloudiness within 5 minutes and primary alcohols have no cloudiness. The overall
reaction that has occurred can be represented as
ROH + HCl RCl + H2O
(i) Draw three structural isomers with molecular formula C4H10O that can be
distinguished using Lucas reagent and state the observation for each isomer.
CH3CH2CH2CH2OH or (CH3)2CHCH2OH : no cloudiness
CH3CH(OH)CH2CH3 : cloudiness within 5 minutes
(CH3)3COH : immediate cloudiness
(ii) Hence from your observation in part (i), suggest a possible product that is
responsible for the cloudiness of the mixture.
CH3CH(Cl)CH2CH3 or (CH3)3CCl
(iii) Four structural isomers of molecular formula C3H6O2 are:
E: CH3CH(OH)CHO
F: CH3COCH2OH
G: HOCH2CH2CHO
H: HCO2CH2CH3
Show how isomers E to H can be adequately distinguished from one another by

the use of simple chemical tests. You should also give brief descriptions of the
chemical tests and expected observations for each isomer.
11
1 Add Lucas
reagent.
2 Add Na
metal.
3 Add SOCl2
or PCl5.
4 Add
alkaline
I2(aq) and
heat.
5 Add 2,4dinitrophen
yl-hydrazine
and heat.
6 Add
Tollens
reagent and
heat.
7 Add
Fehlings
solution
and heat.
8 Add
acidified
KMnO4 and
heat.
E:
CH3CH(OH)CHO
F:
CH3COCH2OH
G:
HOCH2CH2CHO
H: HCO2CH2CH3
Cloudiness
within 5
minutes
Effervescence
(of H2)
observed
Steamy fumes
(of HCl)
observed
Yellow ppt (of
CHI3) formed.
No
cloudiness
No cloudiness
No cloudiness
Effervescence
(of H2)
observed
Steamy fumes
(of HCl)
observed
Yellow ppt (of
CHI3) formed.
Effervescence
(of H2)
observed
Steamy fumes
(of HCl)
observed
No ppt
No
Effervescence
Orange ppt
formed
Orange ppt
formed
Orange ppt
formed
Silver mirror
formed
No silver
mirror
Silver mirror
formed
No silver
mirror
Red ppt (of

Cu2O) formed
No ppt
Red ppt (of

Cu2O) formed
No ppt
Purple KMnO4
decolourised.
Purple KMnO4
decolourised.
Purple KMnO4
decolourised.
Purple KMnO4
decolourised
and
effervescence
(of CO2)
observed. [due
to formation of
HCO2H on
acidic
hydrolysis,
which gets
oxidised to
CO2 and H2O.
No fumes
Yellow ppt (of

CHI3) formed.
(due to
CH3CH2OH
formed on
hydrolysis.)
No ppt
[7]
(c) About 12 million tonnes of zinc are produced every year, of which 70 % are obtained
through mining. The ore is first roasted to produce zinc oxide, which is then further
processed to obtain pure zinc through a series of steps.
12
(i) In the first step, ZnO is reacted with dilute sulfuric acid. Write a balanced equation
for this reaction.
ZnO + H2SO4 ZnSO4 + H2O or ZnO + 2H+ Zn2+ + H2O
The next step involves electrolysis of the resulting solution obtained in (i). A current of
10 000 A is passed through the solution in a series of electrolytic cells and zinc is
deposited on the cathode of each cell. After 24 hours, each cell is shut down, the zinc
coated cathodes are rinsed and pure zinc is mechanically stripped from the cathode.
(ii) Write the half-equations for each electrode reaction and hence, construct the
overall balanced equation.
At cathode: Zn2+ + 2e Zn
At anode: 2H2O O2 + 4H+ + 4e
Overall: 2Zn2+ + 2H2O 2Zn + O2 + 4H+
(iii) Assuming that only one cell is involved in the production in a 24-hour period
I
Calculate the mass of zinc produced in 24 hours.
Zn2+ 2e Zn
Total charge passed through in 24 hours = 10 000 x 24 x 60 x 60
= 8.64 x 108 C
Amount of electrons =
1
2
Amount of Zn =
8.64 10 8
9.65 10 4
= 8.953 x 103 mol
x 8.953 x 103 = 4.477 x 103 mol
Mass of Zn = 4.477 x 103 x 65.4 = 2.93 x 105 g ( = 293 kg)

II Hence, calculate the thickness, in cm, of the zinc sheet produced.
Given: current density = 500 A m2 of zinc deposited
density of zinc = 7.14 g cm3.
[Current density is defined as the current flowing per unit area]
5
Total volume of Zn deposited = 2.93 10 = 4.1036 x 104 cm3
7.14
Total surface area =
Thickness =
10 000
500
4.1036 10 4
2.00 10 5
= 20 m2 = 2 x 105 cm2
= 0.205 cm
[7]
13
[Total: 20]
4
Piperidines are widely used building blocks in the synthesis of organic compounds in the
pharmaceutical industry. A possible synthetic route of 2-methylpiperidine is shown
below.
H
N
I
CN
HO
II
CN
Cl
III
2-methylpiperidine
(a) (i) State the type of reaction that has occurred in stage I and identify a suitable
reagent used.
PCl5 / PCl3 / SOCl2
(ii) Explain why stage I has to be carried out in an anhydrous condition. Include in
your answer any relevant equation.
PCl5 / PCl3 / SOCl2 undergoes hydrolysis when reacted with water.
PCl5 + H2O POCl3 + 2 HCl
OR PCl3 + 3H2O H3PO3 + 3HCl
OR SOCl2 + H2O SO2 + 3HCl
(iii) Draw the dot-and-cross diagram of the reagent used in stage I.
(iv) Suggest the structure of compound L and state the reagent and conditions
required in stage II.
14
Cl
NH2
L
LiAlH4 in dry ether, r.t.p.
OR heat with H2 over Ni catalyst at 140oC
[8]
(b) Benzoic acid and 2-methylpiperidine can be used to synthesise piperocaine (shown
below), a local anaesthesia used for infiltration and nerve block, via a two-step
reaction. Benzoic acid is first converted into an intermediate, R, which is then
converted to piperocaine.
O
O
C
OH
piperocaine
Suggest a synthetic route for piperocaine. State clearly the reagents and conditions
required for each step and draw the structure of intermediate R produced.
[4]
HO
HN
O
HO
2-methylpiperidine
Cl
O
Cl
H2SO4, reflux
reflux
piperocaine
R
benzoic acid
(c) Benzoic acid is used as an antiseptic due to its ability to inhibit the growth of bacteria.
Salicylic acid, a monohydroxybenzoic acid, has a similar function. The structure and
solubility of both compounds in water are shown in the table below.
Name
Structure
HO
Benzoic
acid
0.0238
HO
Salicylic
acid
Solubility / mol dm3
O
OH
0.0145
(i) By considering structure and bonding, explain the difference in solubility of

benzoic acid and salicylic acid.
Both compounds are simple covalent molecules and can form hydrogen
bonding with water molecules.
15
However, intramolecular hydrogen bonding is present in salicylic acid due to
the close proximity of the carboxyl group and hydroxyl group.
Thus, the hydrogen bonding between salicylic acid and water is less
extensive than the hydrogen bonding between benzoic acid and water.
This results in the lower solubility of salicylic acid in water.
(ii) Suggest a simple chemical test that can be used to distinguish benzoic acid from
salicylic acid. State the reagents and conditions used and describe clearly the
observations for each of the compound. Write a balanced equation for any
reaction that occurs.
Add Br2(aq) to each compound separately at room temperature.
Br2(aq) turned from brown to colourless when reacted with salicylic acid due to
the presence of phenol.
Br2(aq) remained brown when reacted with benzoic acid
O
OH
OH
OH
OH
+ 2Br2
Br
+ 2HBr
Br
OR
Add Neutral FeCl3(aq) to each compound separately
Purple Coloration when reacted with salicylic acid due to the presence of phenol.
No such coloration with benzoic acid
[5]
(d) Salicylic acid is also an important active metabolite of aspirin(shown below), a drug to
relieve minor aches and pains, to reduce fever, and as an anti-inflammatory
medication.
O
OH
O
O
aspirin
16
The synthesis of aspirin involves treating salicylic acid with ethanoic anhydride, an acid
derivative, in the presence of concentrated phosphoric acid. This esterification process
(shown below) yields aspirin and ethanoic acid, which is considered a by-product of this
reaction.
O
OH
O
OH
OH
conc. H3PO4
heat
OH
O
ethanoic anhydride
aspirin
(i) Suggest why salicylic acid will not react with itself to produce an ester given the
conditions stated above.
Phenol is too weak a nucleophile (as the lone pair of electrons on the oxygen
can delocalised into the benzene ring, thus less available for donation) for
esterification with benzoic acid to occur.
(ii) Suggest another reagent that can be used in place of ethanoic anhydride in the
synthesis of aspirin from salicyclic acid.
Ethanoyl Chloride
(iii) The synthesis of aspirin from salicyclic acid with ethanoic anhydride may oocur as
follows.
O
conc. H3PO4
OH+
O
OH
protonated f orm of ethanoic anhydride
OH+
OH
OH
H
O+
II
HO
III
O
OH
O
O
HO
O
H+
17
Suggest the types of reactions occurring in stage I and II.
I.
II.
Acid-base reaction
[3]
[Total: 20]
(a) The Gabriel synthesis is a chemical reaction that transforms primary alkyl halides
into primary amines using potassium phthalimide. It gives a high yield of primary
amines and an example of the Gabriel synthesis is shown below.
Step I
O
O
KOH
N K+
NH
O
O
o
ass
um
t
i
p
phthalimide
Step II
O
O
N K+
CH3CH2X
NCH2CH3 + KX
X = Cl or Br
O
O
Step III
O
NCH2CH3
H2O / OH-
CH3CH2NH2
(i) Step I is unusual as the amide hydrogen is quite acidic, hence it can react with
KOH to produce potassium phthalimide. Suggest why the amide hydrogen is
acidic in this case.
Presence of two electron-withdrawing C=O groups increases polarisation of
N-H bond and weakens the N-H bond, hence amide hydrogen is acidic.
(ii) What type of reaction is step III?
Step II: hydrolysis
(iii) Suggest a structure for M.
18
O
OOO
[3]
(b) 1-phenylmethanamine (C6H5CH2NH2) is a versatile organic compound which is used
as a raw material for the production of Vitamin H and is also an active ingredient in
the production of nylon fibres.
1-phenylmethanamine can be produced via a similar two-step Gabriel amine
synthesis.
O
CH2NH2
OH- / H2O
N
K+
1-phenylmethanamine
Suggest the structures of compounds N and P.

N:
CH2Br
[2]
CH2Cl
or
P:
CH2
(c) Phenylamine, along with its chlorine-substituted derivatives, is widely used in biology,
medicine as well as the paint and varnish industry.
(i)
Suggest a synthetic route to form 2-methylphenylamine from methylbenzene.

H2N
CH3
2-methylphenylamine
19
CH3
CH3
CH3
conc. HNO3, conc H2SO4,

30C
NO2
1. conc HCl, Sn, reflux

2. NaOH
NH2
(ii) The reaction below can proceed in the absence of a catalyst. Explain why milder
conditions are required for this reaction compared to chlorination of benzene.
Cl
NH2
NH2
Cl2(aq)
CH3
CH3
Cl
Presence of electron-donating NH2 group increases electron-density on the

benzene ring or activates the ring towards electrophilic substitution and thus
milder conditions are required for the reaction to occur. Aqueous chlorine is
used to allow polysubstitution to occur.
Comments
(1) Many students lose this mark due to poor phrasing, using words like charge density of
the benzene or the negativity of the benzene ring is increased. These are not
accepted since it is not an ion to begin with!
[3]
(d) The Hofmann rearrangement is another organic reaction used to synthesis primary
amines. It involves the reaction of a primary amide with aqueous alkaline bromine to
form a primary amine with one less carbon atom than the starting material.
H
Br2 + OH-(aq)
CH3
NH2
CH3
CH3
NH2
CH3
1-phenylmethanamine (C6H5CH2NH2) can also be produced in a three-step sequence

given below where the last step is a Hofmann reaction.
20
I
CH2CO2H
Br2, OH-(aq)
II
S
CH2NH2
(i) Draw the structures of compounds Q and S.

Q:
CH2COCl
S:
CH2CONH2
(ii) Suggest reagents and conditions required for stages I and II.
Stage I:PCl5, rt / SOCl2, reflux / PCl3 reflux
Stage II: NH3, rt
[4]
(e) (i) Arrange the following compounds in order of decreasing basicity. Explain your
answer.
CH3
and NH3.
CH2NH2
NH2
H2N
CH3
CH2NH2
> NH3 >
CH2NH2
is the strongest base as the presence of electron-donating

alkyl group increases availability of lone pairs of electrons on N and thus
make it more available to accept a proton.
CH3
NH2
is the weakest base as the lone pair of electrons on N can be

delocalised into the benzene ring and thus lone pair of electrons is less
available to accept proton.
(ii) Calculate the pH of the resulting solution when 25 cm3 of 0.0200 mol dm3 HCl is
added to 25 cm3 of 0.0300 mol dm3 1-phenylmethanamine (C6H5CH2NH2).
(The Kb value of 1-phenylmethanamine is 2.19 x 105 mol dm3.)
21
CH2NH2
25
= 0.00075 mol
CH2NH3+ Cl-
HCl
25
= 0.0005 mol
= 0.0005 mol
A weak base and the conjugate acid is present in the final solution (i.e.
alkaline buffer present)
pOH = pKb + lg
[]
[]
= - lg (2.19 x 10-5) + lg
pH = 14 - 4.961 = 9.04
= 4.961
(iii) A 0.0200 mol dm3 solution of 1-phenylmethanamine was mixed with an equal
volume of 0.00100 mol dm3 of aqueous magnesium sulfate. Determine whether a
precipitate would be formed in this experiment.
(The numerical Ksp value of magnesium hydroxide is 1.8 x 1012).
[OH] = . . = 0.0004680 mol dm-3

Ionic product of Mg(OH)2 = [Mg2+][OH]2 =
x ( . )2
= 1.10 x 10 -10 > Ksp of Mg(OH)2

Yes, a precipitate would be formed.
[8]
[Total: 20]
Name:
Index Number:
Class:
DUNMAN HIGH SCHOOL

Preliminary Examination
Year 6
H2 CHEMISTRY
9647/01
20 September 2012
1 hour
Optical Answer Sheet

Data Booklet
INSTRUCTIONS TO CANDIDATES
1. Write your name, index number and class on this question paper.
2. There are forty questions on this paper. Answer all questions. For each question there
are four possible answers A, B, C and D.
Choose the one you consider correct and record your choice in soft pencil on the
separate Optical Mark Sheet.
3. Each correct answer will score one mark. A mark will not be deducted for a wrong
answer.
4. Any rough working should be done in this booklet.
5. You may use a calculator.
This question paper consists of 21 printed pages and 1 blank page.

DHS 2012
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2
Section A
To determine the mass of arsenic present in a sample of pesticide, all the arsenic was
first converted to arsenate ion, AsO43-. 1.25 x 10-3 mol of AgNO3 was then added to
precipitate AsO43- as Ag3AsO4. The excess Ag+ ions needed 3.64 cm3 of
0.054 mol dm-3 KSCN to form silver thiocynate, AgSCN.
Calculate the mass of arsenic (Ar = 74.9) present in the sample of pesticide.
0.015 g
0.026 g
0.079 g
0.488 g
In an experiment, a sample was vapourised, ionised and passed through an electric

field. Analysis of the deflection occurring at the electric region revealed the following
data for the sample. It was observed that a beam of Na+ gives an angle of deflection of
4.3.
4.4a
+
What are the possible identities of unknown particles, q and r, and the value of a?
q
Be2+
Br-
22.0
Be2+
S2-
6.2
Ba2+
Br-
1.2
Ba2+
S2-
1.4
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3
How many moles of electrons must be removed from each mole of methylbenzene,
C6H5CH3, when it is oxidised to benzoic acid, C6H5COOH?
A
Which graph correctly describes the behaviour of fixed masses of the ideal gases I and
J, where I has a higher Mr than J?
A
Constant T
Constant T
PV
C
PV
Constant P
J
PV
Constant P
I
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PV
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5
A student used the setup below to heat a can containing 300 g of water.
The following data were recorded:

mass of propan1ol burnt
= mg
change in temperature of water = DT C
Given that:
relative molecular mass of propan1ol
= 60.0
enthalpy change of combustion of propan1ol = 2021 kJ mol1
specific heat capacity of water
= c J g1 K1
What is the efficiency of this heating process?
m 2021 1000
100%
300 c DT 60.0
m c DT 60.0
100%
300 2021 1000
300 c DT 60.0
100%
m 2021
300 c DT 60.0
100%
m 2021 1000
Which of the following statements best explains why calcium and chlorine form CaCl2
rather than CaCl?
A
Less energy is required to remove one electron from the calcium atom than to
remove two electrons.
More energy is released in forming chloride ions from chlorine molecules in the
formation of CaCl2(s) than in the formation of CaCl(s).
The lattice energy of CaCl(s) is less exothermic than that of CaCl2(s).
When CaCl(s) is formed from its elements, more energy is released than when
CaCl2(s) is formed from its elements.
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7
An exothermic chemical reaction proceeds by two stages.

stage 1
reactants
stage 2
intermediate
products
The activation energy of stage 1 is 50 kJ mol1. The overall enthalpy change of reaction
is 100 kJ mol1.
Which diagram could represent the energy level diagram for the reaction?
A
B
100
75
50
25
0
-25
100
75
50
25
0
-25
reactants
-50
-75
-100
-50
-75
-100
products
progress of reaction
products
D
100
75
50
25
0
-25
-50
-75
-100
100
75
50
25
0
-25
reactants
-50
-75
-100
products
reactants
products
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reactants
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8
A student set up the hydrogen electrode shown in the diagram below.
What would have to be changed to make this a standard hydrogen electrode?
the acid solution used
the temperature of the gas and of the acid solution
the pressure of the gas
the metal comprising the electrode
The graph below shows how the fraction of a substance, X, represented by one of the
following compounds in the equilibrium mixture shown below varies with temperature at
pressures of y Pa and z Pa.
4NH3(g) + 3O2(g)
2N2(g) + 6H2O(g)
DH = 1267 kJ mol1
Identify X and the correct magnitudes of y and z.

X
Pressure
NH3
z>y
N2
z>y
O2
y>z
H2O
y>z
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10
The value of the ionic product of water, Kw, varies with temperature.
temperature / oC Kw / mol2 dm6
0
0.1 1014
10
0.3 1014
25
1.0 1014
What can be deduced from this information?
11
Molar concentration of H+ ions decreases with temperature.
The ionic dissociation of water decreases by a factor of 10 between 0 C and

25 C.
The association of water molecules by hydrogen bonding increases as

temperature increases.
Water is no longer a neutral liquid at temperatures below 25 C.
Ozone in the earths atmosphere decomposes according to the equation:

2O3(g) 3O2(g)
This reaction is thought occur via a twostep mechanism:
Step 1
Step 2
O3(g)
O2(g) + O(g)
O3(g) + O(g) 2O2(g)
fast, reversible
slow
What rate law is consistent with this mechanism?
12
Rate = k[O3]2 / [O2]
Rate = k[O3]2 / [O2]3
Rate = k[O3]
Rate = k[O3]2
S is a transition element. The 3d subshell of S in the compound K[S(C2O4)2(NH3)2]

contains 3 electrons. How many unpaired electrons does S contain when it is in the
elemental state?
A
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13
A reaction scheme starting from aqueous copper(II) sulphate solution is shown below.
Both G and H are coppercontaining species.
CuSO4(aq)
NH3(aq)
excess
NH3(aq)
II
Na4edta(aq)
2[Cu(edta)] (aq)
III
14
NH3 is a ligand in reaction I.
Reaction II is a redox reaction.
H is a deep blue solution containing [Cu(NH3)3(H2O)3]SO4.
The entropy of the system increases when reaction III occurs.
W, X, Y and Z are elements in Period 3.

W has greater electrical conductivity than Y but lower first ionisation energy than X. Y
has higher melting point than W, and Z has a greater atomic radius than W.
Based on this information, which of the following is a possible arrangement of these
elements in increasing proton number?
15
W, X, Y, Z
X, Y, W, Z
Y, X, Z, W
Z, W, Y, X
An aqueous solution of sodium carbonate is added very slowly, till excess, to a solution
containing 0.2 mol dm3 of zinc nitrate and 0.1 mol dm3 of silver nitrate at 25 C.
The numerical value of the solubility product of zinc carbonate at 25 C is 1.4 1011
and that of silver carbonate is 8.1 1012.
Which statement describes what happens in the solution?
A
Both zinc carbonate and silver carbonate are precipitated at the same time.
Zinc carbonate is precipitated first, followed by silver carbonate.
Silver carbonate is precipitated first, followed by zinc carbonate.
Only silver carbonate is precipitated.
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16
17
Which of the following statements about the Group VII compounds is correct?
A
The halogens increase in oxidising power down the group.
The Ksp values of the silver halides decrease down the group.
The lattice energy of the silver halides becomes more exothermic down the
group.
The hydration energy of the gaseous halide ions becomes more negative down
the group.
What is the total number of different chloroethanes, of formula C2H6nCln, where n can
be any integer from 1 to 6?
A
18
19
10
In which sequence is it correctly stated that the value of pKa decreases continuously?
A
C2H5OH > C6H5OH > CH3CO2H > CCl3CO2H
CH3CO2H > CCl3CO2H > C2H5OH > C6H5OH
CCl3CO2H > CH3CO2H > C2H5OH > C6H5OH
Oxidation of an alkene X gives a diol; further oxidation gives a diketone. Which one of
the following could be X?
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20
Compound Z, which has an aromatic ring structure, is subjected to oxidative

degradation under suitable conditions.
Z
What are the most likely organic products from this reaction?
CO 2H
and
A
CO 2H
CO 2H
B
CO 2H
O
C
CO 2H
CO 2H
D
CO 2H
21
CO 2H
An account in a students notebook read:

An excess of aqueous bromine was added to aqueous phenol in a testtube.
2,4,6Tribromophenol was produced as a creamywhite precipitate suspended in a
yellow alkaline solution.
Which statement in this account must have been wrong?
A
The precipitate is 2,4,6tribromophenol
The precipitate obtained is creamywhite.
The resultant solution is alkaline.
The resultant solution is yellow.
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22
Citric acid, which causes the sharp taste of lemon juice, has the following formula.
CH2CO 2H
HO
CO 2H
CH2CO 2H
Which of the following reacts completely with 1 mol of citric acid?
23
3 mol of PCl5(s)
3 mol of Na2CO3(aq)
4 mol of NaOH(aq)
4 mol of Na(s)
CS has the structure shown below, is an active component of tear gas and is readily
hydrolysed.
H
C
CN
C
CN
Which of the following is a possible hydrolysis product of CS?

H
NH2
CO 2-
C
CO 2-
NH2
H
CONH2
CO 2H
CONH2
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24
Members of an ethyl ester homologous series have the general formula

O
R
O
where R = CnH2n+1, and n = 0, 1, 2
CH2CH3
Each member undergoes Claisen condensation with either itself or another member of
the series to form a bketo ester. For example, the first member of the series, ethyl
ethanoate, combines with itself in the presence of sodium ethanoate, followed by
acidification, to form ethyl 3oxobutanoate. Ethanol is eliminated in the process.
O
2
H3C
1. CH3CH2ONa
O
CH2CH3
2. H3O+
O
O
H3C
CH2CH3
CH3CH2OH
ethyl 3-oxobutanoate
(b-keto ester)
ethyl ethanoate
Which one of the following is a possible product of the Claisen condensation between
ethyl ethanoate and the fourth member of the series?
CH3
O
CH3
H3C
CH(CH3)2
O
H3C
CH(CH3)2
CH2CH3
H3C
O
O
CH3
CH2CH2CH2CH3
O
H3C
O
O
CH3
CH2CH3
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25
At alkaline pH, Sangers reagent, also known as FDNB, reacts with the amine group in
terminal amino acid residues of polypeptide chains. Upon hydrolysis, coloured
dinitrophenyl compounds are produced. An example of such a reaction is as follows:
O 2N
1.
O
H2N
CH3
H3C
FDNB
N
CH3
NO 2
C
+
NH2 OH
2. H3O+
O 2N
NO 2
Which of the following terms or phrases best describes the type of reaction illustrated
above?
26
Elimination
Which of the following mechanistic steps is least likely to occur?

O-
H3C
+ CN H C
3
CN
+ Br
+ HBr
Br
CH3
Br
+ Br
CH3
Br
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CH32I
CH2
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+ I
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14
Questions 27 and 28 refer to amino acid, arginine, which has the structure below.
pKa = 12.48
NH+
2
H2N
NH
OH pKa = 2.01
NH3+
pKa = 9.04
arginine
27
Which of the following is the zwitterion form of arginine?

NH
O-
NH
H2N
NH+
2
H2N
H2N
NH2
NH+
2
O
O-
NH
NH+
3
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NH
NH2
NH
H2N
O
O-
NH
NH+
3
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28
An aqueous alkali is gradually added to a certain volume of an acidic solution of

arginine. The concentration of each solution is similar. Which of the following graphs
best represents the change of pH during the reaction?
(pI represents the isoelectric point of arginine, and equivalents of OH represent the
number of moles of OH that reacts with one mole of H+ in an acidbase reaction.)
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29
Partial hydrolysis of insulin, the hormone essential for carbohydrate metabolism, gives
the following tripeptide.
Which compound could be obtained by further hydrolysis of this tripeptide?

A
CH3CH(CO2H)2
(CH3)2CHCH(NH2)CONH2
C
D
30
CH2(CO2H)CH2CH(NH2)CONHCH(CH3)CO2H
A hexapeptide, P, is hydrolysed to the following dipeptides:

IleuVal
AlaPro
LysLeu
Carboxypeptidase, an enzyme which hydrolyses the peptide bond of an amino acid
residue at the Cterminus, acts on P to liberate valine. 2,4dinitrofluorobenzene, which
reacts with an amino acid residue at the Nterminus to form dinitrophenylamino acid,
reacts with P to yield, after hydrolysis, 2,4dinitrophenylalanine. Which of the following
is the amino acid sequence of polypeptide P?
A
AlaProLysLeuIleuVal
ValIleuLysLeuProAla
IleuValAlaProLysLeu
LysLeuAlaProIleuVal
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Section B
For each of the questions in this section, one or more of the three numbered statements 1 to
3 may be correct.
Decide whether each of the statements is or is not correct (you may find it helpful to put a
tick against the statements that you consider to be correct).
A
1, 2 and 3
are
correct
1 and 2
only are
correct
2 and 3
only are
correct
1 only
is
correct

31
An amalgam is formed when mercury is used to dissolve another metal. The amalgam
used in dental filling is a mixture of mercury and tin, Sn8Hg. The diagram below shows
an electrochemical cell formed between an amalgam filling and a gold inlay.
O2 + 4H+ + 4e
Some standard electrode potentials are given below.

Sn2+/Sn8Hg 0.13 V
Au3+/Au
+1.50 V
3+
1.66
Al /Al
O2/H2O
+1.23
Which of the following statement(s) about the amalgam is/are true?
1
Regular consumption of acidic beverages promotes the corrosion of the amalgam

filling.
When a piece of aluminium foil is in contact with the amalgam filling, the
amalgam filling becomes the cathode.
Sn2+ ions are momentarily discharged when the amalgam filling is in contact with
the gold inlay.
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A
1, 2 and 3
are
correct
1 and 2
only are
correct
2 and 3
only are
correct
1 only
is
correct

32
Ammonia is manufactured industrially by the Haber Process as shown.

N2(g) + 3H2(g)
2NH3(g)
DH < 0
The operating conditions are:

400 to 450 C; a pressure of 200 atm; an iron catalyst
Which of the following statement(s) is/are true about the Haber process for the
manufacture of ammonia?
33
At higher temperatures, the production of ammonia becomes thermodynamically

less feasible.
At higher pressures, the yield goes down but the rate of production of ammonia is
faster.
The presence of a catalyst shifts the equilibrium position to the right and
increases the yield.
Three unsaturated compounds undergo hydrogenation to form cyclohexane as follows.

DH / kJ mol1
Predicted Experimental
cyclohexene
+ H2
cyclohexa1,3diene
+ 2H2
240
232
benzene
+ 3H2
360
208
120
Which of the following deduction(s) can be made from the data above?
1
The delocalisation of p electrons in benzene lowers the predicted energy content

of benzene by 152 kJ mol1.
Cyclohexane is the most stable amongst all four substances.
Cyclohexa1,3diene has a higher energy content than cyclohexene.
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A
1, 2 and 3
are
correct
1 and 2
only are
correct
2 and 3
only are
correct
1 only
is
correct
34
35
Sodium hydrogensulfide, NaSH, is used to remove hair from animal hides. Which
statement(s) about the SH ion is/are correct?
1
Three lone pairs of electrons surround the sulfur atom.
Its conjugate acid contains a total of 18 electrons.
Sulfur has an oxidation state of +2.
Zinc protoporphyrin (ZPP) is a compound found in red blood cells when heme
production is inhibited by the presence of lead or by a lack of iron in blood.
A structure of a molecule of ZPP is shown as follows.
Zinc is situated in the centre of a planar arrangement of four nitrogen atoms.

What does this structure suggest about the bonding around zinc?
1
dative covalency
s bonding
oxidation state of zinc is zero
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A
1, 2 and 3
are
correct
1 and 2
only are
correct
2 and 3
only are
correct
1 only
is
correct

36
In an experiment, r mol of chlorine gas was bubbled into excess hot aqueous
potassium hydroxide. Which of the following statement(s) is/are incorrect regarding
this reaction?
1
Oxidation number of chlorine changes from 0 to 1 and 0 to +5
3r mol of potassium hydroxide was required and
5
r mol of potassium chloride
3
was produced.
3
37
38
A disproportionation reaction occurred and the final products obtained included

potassium chlorate(I) and potassium chlorate(V).
Which of the following statement(s) about Group II elements from Mg to Ba is/are

correct?
1
The pH of the solution from the reaction of the metal oxides with water decreases
down the group.
The reactivity of the elements with water increases down the group.
The decomposition temperature of the carbonates increases down the group.
Longchain alkanes are converted on an industrial scale into alkylsulfates for use as
detergents, e.g. sodium dodecyl benzene sulfonate (SDBS).
ONa
CH3(CH2)10CH2
SDBS
What deduction(s) about the properties of SDBS can be made from this structure?
1
Part of the structure is polar and is waterattracting.
The alkyl chain is soluble in oil droplets.
The shape of the molecule is tetrahedral about the sulfur atom.
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A
1, 2 and 3
are
correct
1 and 2
only are
correct
2 and 3
only are
correct
1 only
is
correct

39
A sun protection cream contains the following ester as its active ingredient.
O
O
O
What are the products of its partial or total hydrolysis by aqueous sodium hydroxide?
40
CH=CHCO 2 - Na
H3CO
CH3CH2CH2CH2CH(CH2CH3)CH2ONa+
CH3CH2CH2CH2CH(CH2CH3)CO2Na+
The following diagram shows some laboratory apparatus.
icewater
mixture
Which preparation(s) could this apparatus be used for?

1
bromoethane, from ethanol, sodium bromide and concentrated sulfuric acid.
propanal, from propanol, sodium dichromate(VI) and sulfuric acid.
1,2dibromopropane, from bromine and propene.
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BLANK PAGE
DHS 2012
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2012 DHS Preliminary Examination

H2 Chemistry 9647/01 Answer Key
Question
Number
1
Question
Number
21
22
23
24
25
26
27
28
29
10
30
11
31
12
32
13
33
14
34
15
35
16
36
17
37
18
38
19
39
20
40
Key
Key
C
2012 DHS Preliminary Examination

H2 Chemistry 9647/01 Solutions
3
Section A
1
B
Ag+unreacted + SCN AgSCN
D
Construct a half-equation for the oxidation of
methylbenzene:
C6H5CH3 + 2H2O C6H5COOH + 6H+ + 6e
Alternatively,
Moles of Ag+unreacted
= No. of moles of SCN
3.64
=
0.054 = 1.9656 x 104 mol
1000
*C
H
Moles of As = Moles of AsO43

= 1/3 x 1.053 x 103
Mass of As = 1/3 x 1.053 x 103 x 74.9
= 0.026g
2
q
Extent of deflection
m
(charge is denoted by q; mass is denoted by m)
*C
OH
O.S. of *C before oxidation = 4 7 = 3

O.S. of *C after oxidation = 4 1 = +3
Change in O.S. = +3 (3) = +6
\ 6 electrons are removed during oxidation of
methylbenzene to benzoic acid.
3Ag+reacted + AsO43 Ag3AsO4

Moles of Ag+reacted
= (1.25 x 103) 1.9656 x 104
= 1.053 x 103 mol
[O]
C
For options A and B,
pV = nRT
pV = (m/M)RT = constant
Graph of P against pV should be a vertical
line at a particular value of pV.
D
Heat absorbed by water
300 c DT
=
kJ mol1
1000
m
mol
60.0
Heat released by burning m g of propan-1-ol =
m 2021
kJ mol1
60.0
\ Efficiency of heating process
300 c DT
1000
=
100
m 2021
60.0
300 c DT 60.0
=
100%
m 2021 1000
Moles of propan-1-ol burnt =
For options C and D,

pV = nRT = (mR/M)T pV T
Since the Mr of I is higher, the gradient of
the line is gentler.
Cations will be deflected towards the negative

plate and anions towards the positive plate.
Na+
Be2+
Ba2+
S2
Br
1/23.0 x (23 x 4.3)

2/9.0 x (23 x 4.3)
2/137 x (23 x 4.3)
2/32.1 x (23 x 4.3)
1/79.9 x (23 x 4.3)
4.3
22.0
1.4
6.2
1.2
2012 DHS Preliminary Examination (H2 Chemistry 9647/01 Solutions)
Calcium and chlorine form CaCl2 rather than

CaCl because DHf(CaCl2) is more exothermic
than DHf(CaCl).
DHf is the sum of enthalpy changes involved in
a series of processes leading from the
elements to the compounds:
1. Forming separate atoms from elements
(DHat)
2. Forming positive (from the metal atom) or
negative (from the non-metal atom) ions.
(Sum of I.E. or sum of E.A.)
3. Combining the ions together in an ionic
lattice held together by the attraction
between oppositely charged ions (LE).
For CaCl,
w less energy is required to ionise the Ca
atom only once, to Ca+
w only one Cl atom needs to be formed from
Cl2 and converted into a Cl- ion
w lattice energy released by forming a 1:1
lattice of singly charged ions is less
exothermic than that for CaCl2, which
involves Ca2+ ions.
Option C is the best answer.
100
75
50
25
0
-25
-50
-75
-100
10
Ea = +50 kJ mol-1
formation of
intermediate
reactants
[H+] =
A
products
A
In 1.0 mol dm3 sulfuric acid, [H+] = 2.0 mol
dm3. To make the electrode a standard
hydrogen electrode, either change the acid to a
1.0 mol dm3 monoprotic acid (option A), or
halve the concentration of sulfuric acid used.
H2O(l) H+(aq) + OH(aq)

Kw = [H+][OH]
DH = -100 kJ mol-1
8
Kw
At 25 oC, [H+] = 1.0 107 mol dm3

At 10 oC, [H+] = 0.5 107 mol dm3
At 0 oC, [H+] = 0.3 107 mol dm3
Ionic dissociation of water increases
by a factor of 3.3 between 0 oC and
25 oC.
Extent of hydrogen bonding cannot
be deduced from the given
information.
[H+] = [OH] at 0 oC, 10 oC and
25 oC. Thus water remains a neutral
liquid at these temperatures.
However pH of neutral water is no
longer 7.0, but increases with
decreasing temperature.
B
Since forward reaction is exothermic, higher
temperatures will favour the backward reaction.
This increases [NH3] and [O2] and decreases
[N2] and [H2O] at higher temperatures. Thus
the two downwardsloping graphs apply to
either N2 or H2O.
At a higher pressure, backward reaction is
favoured, and [N2] and [H2O] decreases. Thus,
z > y.
11
13
Rate law is determined by slow step in

proposed mechanism, i.e. Rate = k[O3][O].
This rate law cannot be compared directly with
the experimental rate equation because it
contains the concentration of an intermediate,
O. Thus we need to express rate law in a way
that removes the intermediate O.
A
B
K [O 3 ]
[O 2 ][O]
[O] =
[O 2 ]
[O 3 ]
Assuming that Step 1 equilibrium is established
quickly before O is reacted with O3 in Step 2,
From Step 1, K =
Rate = k[O3][O] =
k ' K [O 3 ] 2
k [O 3 ] 2
=
[O 2 ]
[O 2 ]
where k = kK
12
[S(C2O4)2(NH3)2]
Let the oxidation number of S be x.
x + 2(2) + 2(0) = 1
x = +3
:
S0
14
15
ZnCO3(s) Zn2+(aq) + CO32(aq)

Ksp = [Zn2+][CO32] = 1.4 1011
\ [CO32] at which first trace of ZnCO3 appears
=
1.4 10 -11
= 7 1011 mol dm3
0.2
Ag2CO3(s) 2Ag2(aq) + CO32(aq)

Ksp = [Ag+]2[CO32] = 8.1 1012
\ [CO32] at which first trace of Ag2CO3
appears =
= 8 1010 mol dm3
Thus ZnCO3 will precipitate first when [CO32]

reaches 7 1011 mol dm3. When [CO32]
reaches 8 1010 mol dm3, Ag2CO3 will
precipitate next.
B
A
B
8.1 10 -12
0.1
16
(d3)
B
First trace of precipitate appears when ionic
product = Ksp.
(Wrong) NH3 acts as a weak base and

a ligand in Reaction I.
(Wrong) G is Cu(OH)2 and H is
[Cu(NH3)4]2+
Oxidation state of Cu remains at +2.
\ It is not a redox reaction.
(Wrong) H is a deep blue solution
containing [Cu(NH3)4(H2O)2]SO4.
(Correct) When edta4 binds to the
Cu2+during ligand exchange, 4 moles of
NH3 and 2 moles of H2O is released.
\ The entropy of the system increases
when reaction III occurs.
Z has a greater atomic radius than W

Z is earlier on in the period (Z..W..)
W has greater electrical conductivity than Y
and Y has higher boiling point than W
Y is in Group IV and hence W is a metal
(not Si)
S3+
-
C
(Wrong) Down the group, oxidising

power decreases.
(Correct) Down the group, Ksp value
decreases.
(Wrong) Down the group, lattice energy
of AgX becomes less exothermic due to
the increasing anionic radius of halides.
(Wrong) Down the group, the hydration
energy decreases due to the increasing
anionic radius of halides.
17
19
formula
C2H5Cl
C2H4Cl2
C2H3Cl3
C2H2Cl4
5
6
C2HCl5
C2Cl6
distribution
of Cl atoms
C1
C2
1
0
2
0
1
1
3
0
2
1
3
1
2
2
3
2
3
3
20
OH
O
OH
benzylic hydrogen
1
1
Thus, side-chains on Z which can be oxidised

are:
O
C
H
C
2
2
B
Alkyl side-chains on a benzene ring are
susceptible to oxidative degradation if they
possess at least one benzylic hydrogen atom.
product(s) of oxidation
HO
no. of
chloroethanes
Total no. of different chloroethanes = 9

18
+ CO2
A
The stronger an acid, the lower the pKa value.
The following lists the four acids used in the
options:
w CH3CO2H
w CCl3CO2H
w C2H5OH
w C6H5OH
II
O
I
II
Increasing acid strength:

C2H5OH < C6H5OH < CH3CO2H < CCl3CO2H
Decreasing pKa value:
It is only possible to oxidise the

carbon atom in CH2 to a lower
oxidation state of +2 in C=O, rather
than +3 in COOH.
There is only 1 C atom connecting
both benzene rings. If I is oxidised to
COOH, one of the benzene rings has
to be reduced by replacing the
oxidised carbon with a hydrogen
atom.
II may be regarded as 2 separate alkyl
groups, with each being oxidised to
COOH.
21
C
A
B
C
22
23
(Account
is
correct)
Electrophilic
substitution of phenol by bromine in
aqueous medium yields a tri-substituted
product, rather than a mono-substituted
one.
(Account is correct) Ppt is 2,4,6tribromophenol, which is white.
(Account is wrong) Resultant solution
contains 2,4,6-tribromophenol, which is
acidic.
(Account is correct) Resultant solution is
yellow, due to the presence of excess
dissolved bromine.
Nitrile groups on CS are hydrolysed to either

salts of carboxylic acids (alkaline hydrolysis) or
carboxylic acids (acid hydrolysis).
24
1 mol COOH reacts with 1 mol

PCl5, and 1 mol OH group reacts
with 1 mol PCl5.
\ 1 mol citric acid reacts with 4 mol
PCl5.
3 mol tribasic acid reacts with 1 mol
Na2CO3. (Alcohols are neutral, and
do not react with Na2CO3.)
\ 1 mol citric acid reacts with 13
mol Na2CO3.
1 mol COOH reacts with 1 mol
NaOH. (Alcohols are neutral, and
do not react with NaOH.)
\ 1 mol citric reacts with 3 mol
NaOH.
1 mol COOH reacts with 1 mol Na,
and 1 mol OH group reacts with 1
mol Na.
\ 1 mol citric acid reacts with 4 mol
Na.
R
Product of Claisen condensation of ethyl esters
must be an ethyl b-keto ester:
O
O
L
CH3
R
R
A
O
CH3
Options B and D are not possible.
source
segment L
segment R
ethyl ethanoate ethyl ethanoate
ethyl ethanoate
II
II
II
ethyl ethanoate
II
4th member of series has 2 isomers:
D
A
Explanation for option A:

Option A is one of four possible products
resulting from the condensation of two different
esters, i.e. ethyl ethanoate and isomer II:
O
I
H3C
O
CH3
II
CH3
H3C
CH3
Option C is not possible, since it is derived

from an isomer of the 5th member:
O
H3C
CH3
25
A
A substituent group (fluorine atom), and not a
hydrogen, is substituted without disruption to
the aromaticity of the benzene ring. This is
therefore not an electrophilic substitution
reaction.
F is highly electronegative. The C atom to
which F atom is attached is d+, and can attract
a nucleophile.
This reaction is therefore a nucleophilic
substitution reaction, with
O
CH3
H2N
CH3
H
O
being the nucleophile, and F atom being the
leaving group.
5
26
C
Mechanism C involves the electrophilic addition
of Br2 to methylbenzene. This destroys the
aromaticity of the benzene ring and is
energetically not favourable.
27
B
In arginine, pKa of side-chain =NH2+ group is
higher than pKa of aNH3+ group. Thus aNH3+
group will be de-protonated first before
zwitterion is formed.
28
29
Since an acidic solution of arginine is used,

there are three groups, i.e. a-COOH, a-NH2,
and protonated basic side group, to be
neutralised.
\ This reaction may be regarded as a triprotic
acid whose neutralisation takes place in three
stages. This eliminates pH titration graphs for
diprotic acids (options A and B).
a-COOH is neutralised first, followed by aNH3+, and finally the protonated basic side
group.
At half-equivalence point for each neutralisation
stage, pH = pKa of each respective acidic
group.
CH3
OH
OH
NH
H3C
NH
O
O
NH2
X
CH3
Y
Hydrolysis of this tripeptide will break the amide

linkage at X and / or Y.
30
A
Amino acid residue at N terminus: alanine (Ala)
Amino acid residue at C terminus: valine (Val)
Thus P is (N) Ala-Pro-Lys-Leu-Ileu-Val (C).
Section B
32
31
33
34
A
1
2N2(g) + 3H2(g) 2NH3(g)

Over time, the amalgam filling is
oxidised by dissolved oxygen in the
saliva.
o
(E )cell = E (O2/H2O) E
2+
(Sn8Hg/Sn ) = +1.23 (0.13) =
+1.36 V > 0
An acidic medium results in
o
E (O2/H2O)
and
(E )cell
becoming more positive. Corrosion
becomes thermodynamically more
feasible.
Contact between aluminum foil and
amalgam filling short-circuits the
cell in Statement 1. Al reduces Sn2+
to Sn, and amalgam becomes the
cathode.
o
E (Sn8Hg/Sn2+) is more negative
o
than E (Au3+/Au). When Au is in
contact with the amalgam, a
galvanic cell is set up with the
amalgam filling as the anode and
gold inlay as the cathode.
Tin in the amalgam is oxidised to
Sn2+ and releases electrons to the
gold cathode where oxygen is
reduced preferentially.
o
[E (O2/H2O) is less positive than
o
E (Au3+/Au). Thus O2 is reduced.]
DH = ve
DG = DH TDS
DS < 0 TDS is always positive.
DG < 0 only if |DH| > |TDS|
At high temperatures, |DH| < |TDS|
and DG > 0.
\ Reaction becomes less feasible
as temperature increases.
At higher pressures, by LCP,
equilibrium position lies more to the
right to favour the side of the
reaction with fewer gas molecules,
i.e. formation of NH3.
\ Yield of NH3 increases.
Higher pressures increase rate of
reaction
between
gaseous
reactants.
Presence of a catalyst does not
affect yield.
However a catalyst increases both
the forward and backward reaction.
S xH
1
2
P
P
No. of lone pairs around S atom = 3

SH accepts an H+ ion to become
its conjugate acid, H2S.
Hx S
xH
No. of electrons from S atom = 16

No. of electrons from H atoms = 2
Charge = 0
\ Total no. of electrons on H2S
= 16 + 2 = 18
O.S. of S = 6 8 = 2
35
37
2
3
P
O
Protoporphyrin molecule is a chelate.

Each N atom / ion shares a lone pair
with central Zn2+ ion to form a dative
bond.
Each ZnN bond is a s-bond.
Structure of ligand before bonding:
38
39
D
The ester is hydrolysed by NaOH(aq) to form
the following products:
The pH of the solution from the

reaction of the metal oxides with
water increases down the group.
The reactivity of the elements with
water increases down the group.
The decomposition temperature of
the carbonates increases down the
group due to the decrease in the
polarising effect on the carbonate
ion.
O
O- Na+
and
HO
hydrocarbon
(hydrophobic part
of molecule)
polar
(hydrophilic part
of molecule)
ONa
Thus Zn has an oxidation state of +2.

36
CH3(CH2)10CH2
O
P
Oxidation
number
of
chlorine
changes from 0 in Cl2 to 1 in Cl
and to +5 in ClO3.
6OH(aq) + 3X2(aq) 5 X(aq) +
XO3(aq) + 3 H2O(l)
5
r
3
2r mol of KOH was required and

3
B
1
2
P
P
C
1
40
Ionic portion of SDBS is attracted to

polar solvents like water
hydrophilic
Hydrocarbon portion of SDBS is
soluble in organic solvents
hydrophobic
There are 4 bond pairs and 0 lone
pair around S atom.
Bromoethane is more volatile than

ethanol, and propanal is more
volatile than propanol. Thus both
products will distil over as they are
being produced while the other
substances remain in the flask.
Propene is a gas at r.t.p.
mol of KCl was produced.

A
disproportionation
reaction
occurred.
However,
the
final
products obtained included chloride
and potassium chlorate (V).
Name:
Index Number:
Class:
DUNMAN HIGH SCHOOL

Year 6
H2 CHEMISTRY
9647/02
Paper 2 Structured
14 September 2012
2 hours
1
Write your name, index number and class on this cover page.
Answer all questions.
Write your answers in the spaces provided on the question paper.
You may use a calculator.
FOR EXAMINERS USE

Question
No.
Marks
12
14
18
10
Total
10
[72]
_______________________________________________________________________________________________

DHS 2012
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Answer all questions in the space provided.

1
Planning
This question is about the kinetics of ureasecatalysed hydrolysis of urea in phosphate and
citrate buffer solutions.
Urease is an enzyme that breaks down urea, CO(NH2)2, into carbon dioxide and ammonia.
The production of ammonia raises the pH of the buffered solution mixture and can be
detected using a suitable acidbase indicator.
CO(NH2)2 + H2O CO2 + NH3
Urease is active over a wide range of pH so a few indicators can be used provided that the
original solution mixture is buffered at the right pH to start with.
The colour change of bromomothymol blue and phenolphthalein in acidbase medium is
shown in the table:
Indicator
bromothymol blue
phenolphthalein
pKind
7.0
9.3
pH range
5.97.6
8.310.0
Colour change
Yellow(in acid) blue (in alkali)
Colourless(in acid)pink (in alkali)
Phosphate and citrate present in the buffer solutions do not react with urea or urease.
In order to study the effect of the enzyme concentration on the rate of hydrolysis of urea, you
are provided with
Choice of two indicators, bromothymol blue and phenolphthalein
Choice of two buffered solutions, phosphate buffer at pH 7 and citrate buffer at pH 5
2% of urea solution
3% urease solution
distilled water
In a preliminary experiment, a solution mixture containing 20 cm3 of urea solution, 8 cm3 of
buffer solution, 6 cm3 of urease solution, 6 cm3 of water took 40 seconds for the indicator to
show a colour change.
It is found that the time taken for the indicator in the reaction mixture to change colour
doubled when urease used is diluted with an equal amount of water.
(a)
(i)
Suggest the appropriate choice of indicator and the buffer solution used in the
preliminary experiment.
Choice of buffer solution:

Choice of indicator:
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(ii)
Using the results of the preliminary experiment predict the relationship between
the rate of hydrolysis of urea and concentration of urease.
[2]
(b) (i)
A student designed a series of experiments to investigate the prediction in the

preliminary experiment by initial rate method.
Complete the table below to show
all volumes to be used such that a simple comparison of the time taken for
endpoint of the indicator can be made with the preliminary experiment.
how the measurements would be processed(that is, complete the heading

for the last column) to enable the student to confirm or reject the preliminary
prediction.
Expt
Volume
of urea/
cm3
Volume of
urease/
cm3
Volume
of buffer/
cm3
Volume
of water/
cm3
20
Time
taken,
t/ s
40
P: Preliminary experiment
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(ii)
Outline the procedural steps that the student would take to carry out the
designed experiments in (b)(i),stating any assumption(s) made.
Your plan should include:
o the apparatus used to measure the various volumes;
o the sequence that the various solutions are mixed;
o how the time for the colour change of indicator is measured; and
o other experimental details to ensure the consistency of the experiment.
You may also assume that standard laboratory apparatus are available.
(iii)
Explain how the results of the experiments will confirm or reject the preliminary
prediction.
[8]
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(c)
The rate of this reaction is also studied when the temperature is varied. Give a sketch
of a graph to show how the rate will vary with temperature. Explain the shape of your
sketch.
rate
T/ C
20
[2]
[Total: 12]
Ethanoic acid, also commonly known as acetic acid, is an important chemical due to its
varied uses in the industry.
(a)
The preferred industrial method for its manufacture is by carbonylation of methanol, an

exothermic reaction, accounting for 65% of the total world ethanoic acid manufacturing
capacity.
CH3OH(aq) + CO(g)
CH3CO2H(aq)
The conditions employed are:
150 200 C
30 60 atm
rhodiumbased catalyst
Using Le Chateliers Principle, explain why the above moderate pressure is chosen as
the process condition.
[2]
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(b)
The graph below shows the changes in pH when a 25.0 cm3 sample of vinegar, with
ethanoic acid as its main component, is titrated against 0.45 mol dm3 aqueous sodium
hydroxide.
Region A
(i)
Using the information provided, show by calculations that the acid dissociation
constant, Ka of ethanoic acid has an approximate numerical value of 1.85 x 105.
(ii)
State a suitable indicator for this titration. Explain your choice.

Indicator:
Reason for choice:
[5]
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(c)
The buffer produced at region A in (b) consists of a weak acid and its conjugate base.
(i)
Draw a diagram to illustrate the shape of the anion present. State the shape
about each carbon atom and its respective bond angles.
(ii)
With clear reference to your drawing in c(i), state the type of hybridisation
present for each carbon atom in the anion.
(iii)
The boiling points of both components of the buffer are given below.
weak acid
conjugate base
118 C
881 C
With reference to the structures and interactions present, account for the large
difference in the boiling points shown.
[7]
[Total: 14]
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(a)
Sodium chlorate(I), NaClO, found in household bleach produces chlorine upon

addition of acidified dilute hydrochloric acid according to the equation below.
ClO(aq) + 2H+(aq) + Cl(aq) Cl2(aq) + H2O(l)
A 10.0 cm3 sample of a household bleach is diluted to 100 cm3. 25.0 cm3 of this
solution is then pipetted out into a conical flask containing dilute hydrochloric acid.
Excess potassium iodide solution is added and the resultant solution turns brown.
This resultant solution is then titrated against 0.100 mol dm3 sodium thiosulfate
solution and required 15.20 cm3 for complete reaction.
(i)
Identify the specie that is responsible for the brown colouration and state the
reaction that has taken place.
(ii)
Calculate the concentration of the sodium chlorate(I) in the household bleach in

g dm3.
concentration= ..........................g dm3

[4]
DHS 2012
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(b)
A small portion of three unlabelled samples of KCl, KBr and KI are reacted with
concentrated phosphoric acid separately and each of the hydrogen halide gases
produced are immediately passed through identical setups as shown.
(i)
Suggest a hydrogen halide that can be identified using this setup, clearly
stating the equation of the reaction taking place and the expected observations
for the organic layer.
Hydrogen halide:
Equation:
Expected observations:
(ii)
Describe a chemical test that can be carried out to distinguish between the two
remaining potassium halide solutions and explain the expected observations.
Chemical Test:
Observations:
[4]
[Total: 8]
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10
(a)
Magnesium oxide is one of the products formed when magnesium carbonate

decomposes.
MgCO3(s) MgO(s) + CO2(g)
(i)
DH = +100 kJ mol1
The decomposition of magnesium carbonate was studied at two different

temperatures, to determine the ideal temperature for the industrial production of
magnesium oxide. The products were bubbled into limewater and the
observations are as follows:
Temperature / K
1050
400
Effect on limewater
White precipitate
No white precipitate
At a certain temperature, it was found that the reaction ceases to be feasible.

Given the following entropy values, determine this temperature.
Compound
MgCO3(s)
MgO(s)
CO2(g)
Entropy / J mol1 K1
65.7
26.9
213.6
T=...............................
(ii)
DHS 2012
Hence, suggest why it is necessary to determine the unknown temperature

instead of carrying out the industrial production of magnesium oxide at 1050K.
9647/02
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11
(iii)
Using the data provided and relevant data from the Data Booklet, construct an
appropriate fully-labelled energy cycle to calculate the lattice energy of
magnesium carbonate.
Enthalpy Term
Enthalpy change of atomisation of magnesium
Sum of 1st and 2nd electron affinities of oxygen
Enthalpy change of formation of magnesium carbonate
Enthalpy change of formation of CO2(g)
O2(g) + CO2(g) CO32(g)
DH / kJ mol1
+148
+657
1096
393
778
[7]
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12
(b)
The plots of pV/RT against p for one mole of an ideal gas and one mole of carbon
dioxide gas from the decomposition of magnesium carbonate at 300K are given below.
(i)
Show, on the same axes, how one mole of sulfur dioxide, SO2 will behave at the
same temperature of 300K. Label your graph clearly.
pV/RT
p
(ii)
Explain the difference in behavior between carbon dioxide and sulfur dioxide at
300K.
(iii)
Explain what happens when sulfur dioxide gas is cooled to 100K. Illustrate your
answer clearly on the same axes in b(i).
[4]
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13
(c)
The temperatures for the thermal decomposition of carbonates of Group II elements

magnesium to radium are as shown.
Compound
Decomposition Temperature / C
MgCO3
CaCO3
SrCO3
BaCO3
RaCO3
540
900
1290
1350
720
It was suggested that the decomposition temperature for radium carbonate to be

720 C. Comment on the accuracy of this suggestion.
[3]
(d)
Write approrpiate equations to illustrate the reactions of PCl3 and AlCl3 with water.
Hence, state the observations when they are separately added to test tubes containing
aqueous magnesium carbonate.
PCl3
AlCl3
[4]
[Total: 18]
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14
The diagram below shows the synthetic pathway by which compound F may be prepared.
The inorganic side product, which is produced together with compound F, is constantly
removed from the reaction mixture.
CH3
Cl
CH3
O 2N
Step 1
CH3
Cl
C6H9OCl
CH3
H2N
Step 3
Step 2
CH3
OH
C6H9O 2Cl
CH3
H2N
CH3
Cl
F
CH3
H2N
(a)
Give the structural formulae for compounds D and E.
[2]
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15
(b)
Suggest the reagents and conditions for steps 2 and 3.

Step 2:
Step 3:
[2]
(c)
Draw the structures of the organic products formed when compound F is reacted with
each of the following:
(i)
Cl2 in AlCl3, room temperature
(ii)
KOH(aq), reflux
(iii)
cold dilute nitric acid
[4]
DHS 2012
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16
(d)
Describe a chemical test that can be used to distinguish between compounds A and B.
Reagent(s) & conditions:
Observations:
[2]
[Total: 10]
The reaction scheme below shows the final stages in the synthesis of compound S.
Cl
CH2CH2OH
Cl
COOH
Cl
O
NH
OH
Cl
S
(a)
Draw the displayed formulae of compounds R and Q.
[2]
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17
(b) Give the synthetic route, involving not more than three steps, from P to Q. In your
answer, suggest the reagent(s) and conditions involved in each step and draw the
structural formulae of the intermediate organic products. Name the type of reaction
occurring at each step.
[6]
(c)
In the reaction of R and Q, another organic compound can also possibly be formed.
Draw the structural formula of the organic compound and explain how its formation
may arise.
[2]
[Total: 10]
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18
BLANK PAGE
DHS 2012
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Name:
Index Number:
Class:
DUNMAN HIGH SCHOOL

Year 6
H2 CHEMISTRY
9647/03
18 September 2012
2 hours

Graph Paper
Write your name, register number and class on this question paper and on the Cover Sheet provided.

At the end of the examination:
Fasten all work securely together with the Cover Sheet on top.
Hand in the question paper separately.
The total marks for this paper is 80 marks.

@DHS 2012
[Turn over
2
1
The study of organic compounds includes the collection of kinetic data and thermodynamic
data of the compounds.
(a)
The kinetics of the hydrolysis of the ester, CH3CH2CO2CH3, may be investigated by the
following method.
CH3CH2CO2CH3 + H2O CH3CH2CO2H + CH3OH
In a 1 dm3 mixture, 0.350 mol of the ester was hydrolysed by heating with water and using
hydrochloric acid as catalyst. The following results were obtained.
Time/s
0
340
680
1080
1440
(b)
Concentration of CH3CH2CO2H/mol dm3

0
0.105
0.185
0.243
0.278
(i)
Suggest how the progress of this reaction may be followed in order to obtain the
results as stated.
(ii)
By drawing a suitable graph using the data given above, show that the reaction is
first order with respect to the ester. It has been found that the hydrolysis reaction is
first order with respect to the hydrochloric acid.
(iii)
Deduce the units of the rate constant.
(iv)
State and explain the effect of a catalyst on the rate constant.
(v)
Using suitable bond energy values from the Data Booklet, calculate the H for the
hydrolysis of the ester.
(vi)
Given that the standard enthalpy change of reaction for the hydrolysis is
+7.6 kJ mol1, suggest a reason for the difference between this given value and
the value that you have calculated in (a)(v).
[11]
Hydrolysis of ester can be achieved in the biological system by enzymes known as

esterase. Enzymes are proteins that catalysed a specific chemical transformation in the
biological system. Such enzymes are generally quaternary proteins.
(i)
Sketch and explain the graph showing how the rate of hydrolysis changes with
increasing concentration of the ester.
(ii)
Explain the meaning of quaternary structure of proteins.
(iii)
List 2 other major functions of proteins in the body.
(iv)
Suggest and explain a chemical method for distinguishing the following pair of
esters. You should state the expected observations.
HCO2CH2CH3 and CH3CH2CO2CH3
[9]
[Total: 20]
DHS 2012
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3
2
This question is about the chemistry of the transition metal, nickel and its compound.
(a)
Explain why the colour of [Ni(NH3)6]2+(aq) is blue.
(b)
Ni(CO)4 is a compound formed by the reaction between nickel and carbon monoxide. The
Mond process was developed by Ludwig Mond to extract and purify nickel from its ores.
One of the stages of this process involves the decomposition of Ni(CO)4 at 227 C to give
nickel as shown in this equation below:
Ni(CO)4(g)
[3]
Ni(s) + 4CO(g)
The equilibrium constant, Kp, for the equilibrium at 227 C is 1.01 atm3. A sample of
gaseous Ni(CO)4 was placed in a 2 dm3 evacuated container at 227 C. At equilibrium, the
partial pressure of CO was 2.00 atm.
[1 atm = 1.01 x 105 Pa]
(i)
Sketch the shapes of the hybrid orbitals around the C atom in carbon monoxide.
(ii)
Write an expression for Kp.
(iii)
Calculate the total pressure of the system at equilibrium.
(iv)
Calculate the mass of Ni(CO)4 placed in the container initially.

[8]
(c)
Ni is commonly used in catalytic hydrogenation reactions. One such example is given

below.
Compound A, C10H12NOCl, has a chiral centre and dissolves in dilute sulfuric acid. It
reacts with 2,4dinitrophenylhydrazine to form an orange precipitate, but does not react
with Tollens reagent. A reacts with H2 in the presence of Ni catalyst followed by addition
of aqueous bromine to form B, C10H11NOClBr3. When 1 mol of compound B is heated
under reflux with aqueous iodine and excess alkali, followed by careful acidification,
compound C, C8H4NO4Br3 is formed together with 2 mol of yellow solid CHI3.
Deduce the structures of compounds A, B and C, giving reasons for your answer.
[9]
[Total: 20]
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4
3
This question is about the varied chemical uses of HCl.
(a)
(i)
In the electrolysis of a solution of hydrochloric acid with inert platinum electrodes, an

ammeter showed a reading of 0.450 A in the external circuit of the cell. 110 cm3 of
gas was evolved at the cathode after 30 minutes under room temperature and
pressure. Determine the actual current used in the electrolysis process. Hence,
determine the percentage error (if any) of the ammeter reading.
(ii)
A student carried out a reaction involving acidified potassium dichromate(VI),

together with an unknown halfcell which consists of transition metal ions. The
Gibbs Free Energy of the reaction was known to be 324 kJ mol1 and the
procedure involved transferring 6 mol of electrons from the unknown solution to
potassium dichromate(VI).
Using the expression of DGq = nFEqcell, where n is the number of moles of electrons
transferred, F is the Faraday constant and Eqcell is the overall cell potential,
determine the Eqcell value and hence deduce the identity of the unknown half cell.
[4]
(b)
A sample of sodium hypochlorite, NaOCl, was dissolved in 100 cm3 of 0.123 mol dm3
HOCl (pKa = 7.50) solution forming a buffer of pH 6.20. The buffer is then used to absorb
HCl gas. Calculate the concentration of gaseous HCl (in mol dm3) that is required to be
added to the buffer solution until it reaches pH 6.
[5]
(c)
The decomposition temperature of hydrogen chloride is close to 3000 K. Predict, with

reasoning, if the decomposition temperature of hydrogen astatide would be higher or lower
than 3000 K.
[3]
(d)
Concentrated hydrochloric acid is commonly used in the reduction of trinitrobenzene

(2,4,6trinitrobenzene).
(i)
Suggest the complete set of reagents, together with concentrated HCl, to be used in
this reduction process.
(ii)
Suggest the structural formula of the product formed.
(iii)
Explain the relative basicity between the product formed in (d)(ii) and the melamine
molecule as shown below in terms of their structures. The melamine molecule
contains a triazine ring with 3 nitrogen atoms present in the ring.
NH2
N
H2N
N
N
NH2
Melamine
[5]
DHS 2012
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5
(e)
2,4,6trinitrobenzene can also undergo FriedelCrafts alkylation with CH3Cl to form

2,4,6trinitromethylbezene. The alkyl side chain can then be further reacted to form useful
halogen derivatives. However, some side products like hydrogen chloride gas and
compound D can also be formed in the process.
NO 2
O 2N
CH2
O 2N
NO 2
CH2
NO 2
O 2N
Compound D
Using 2,4,6trinitromethylbezene as the starting material, describe an appropriate
mechanism that would result in the production of compound D.
[3]
[Total: 20]
DHS 2012
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6
4
Chlorine and its compounds are used to manufacture many products such as pesticides,
medicines, plastics, bleaches and solvents.
(a)
1 mol of the following compounds is added to 1 dm3 of water.

CH3COCl, ClCH2COOH and SiCl4
Arrange the compounds in order of increasing pH of the resultant mixture formed. Briefly
explain your answers, giving equations where appropriate.
[4]
(b)
(c)
Both chloric(I) acid, HOCl and hydrogen chloride react with propene. In the reaction
between chloric(I) acid and propene, chlorine is added to carbon-1 of propene in the
major product. However, in the reaction between hydrogen chloride and propene, chlorine
is added to carbon-2 of propene in the major product.
(i)
Draw the displayed formula of the major product formed between propene and
chloric(I) acid.
(ii)
Explain briefly why chlorine from chloric(I) acid and from hydrogen chloride add to
different carbon atoms in their reactions with propene.
[4]
Despite health and environmental concerns, the chlorinated compound MCPA, is widely
used as a weed killer.
OCH2COOH
CH3
Cl
MCPA
Using not more than 3 steps, draw a reaction scheme to show how MCPA can be
synthesised from 2methylphenol.
[3]
(d)
Compound E is a derivative of MCPA which may be a potential insecticide. The synthesis

of Compound E is given below.
OH
OC(CH3)3
CH3
CH3
NaOH
(CH3)3CCl
Cl
Cl
Compound E
Describe the mechanism for the synthesis of Compound E.
DHS 2012
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[3]
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7
(e)
Describe the variation in melting points of the chlorides of the elements from sodium to
phosphorus and explain the variation in terms of structure and bonding.
[4]
(f)
Describe a reaction, without the use of bromide solution, which shows that chlorine is a
stronger oxidising agent than iodine.
[2]
[Total: 20]
DHS 2012
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8
5
Phosphorus is an element in Period 3 of the Periodic Table with wide ranging application
in inorganic and organic synthesis.
(a)
Explain why the first ionisation energy of phosphorus is higher than that of sulfur, S, and
arsenic, As, respectively.
[2]
(b)
Define the second ionisation energy of phosphorus with an appropriate equation.
(c)
When heated in air, phosphorus and sodium forms oxides which can react with acids,
bases or water.
(d)
(e)
[2]
(i)
Write balanced equations for the reaction between oxides for the two elements and
an appropriate acid or base.
(ii)
Describe the reactions, if any, of the two oxides with water containing universal
indicator. Chemical equations are not required.
[5]
Phosphoric acid is used as a catalyst in the industrial preparation of CH3CH2CH(OH)CH3

from compound F, CH3CH2CH=CH2.
(i)
State the reagent and any other conditions required in this industrial preparation.
(ii)
Compound G, which is an isomer of F, exists as a pair of geometric isomers.

Deduce the structure of G.
(iii)
Predict the carboncontaining products obtained when F and G are separately

heated with acidified potassium manganate(VII).
[3]
PCl5 is used for substitution reactions in organic chemistry.

An optically active compound P, with molecular formula C3H7O2N, reacts with PCl5 to give
white fumes. When a solution containing P is warmed with aqueous sodium hydroxide, a
pungent gas is evolved. Upon acidification of the resulting mixture, compound Q, C3H6O3,
can be isolated. When Q is warmed with concentrated sulphuric acid, a cyclic compound
R, C6H8O4, is formed. Compound S is a structural isomer of Q and is not optically active.
When S is warmed with concentrated sulphuric acid, a noncyclic compound T, C3H4O2, is
produced.
Deduce the structures of compounds P, Q, R, S and T. Explain the chemistry of the
reactions described.
[8]
[Total: 20]
DHS 2012
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[Turn over
Name:
Index Number:
Class:
DUNMAN HIGH SCHOOL

Year 6
H2 CHEMISTRY
Paper 3 Free Response (Suggested Solutions)
9647/03
18 September 2012
2 hours
Write your name, register number and class on this question paper and on the Cover Sheet provided.

At the end of the examination:
Fasten all work securely together with the Cover Sheet on top.
Hand in the question paper separately.
The total marks for this paper is 80 marks.

@DHS 2012
[Turn over
2
The study of organic compounds includes the collection of kinetic data and thermodynamic
data of the compounds.
(a)
The kinetics of the hydrolysis of the ester, CH3CH2CO2CH3, may be investigated by the
following method.
CH3CH2CO2CH3 + H2O CH3CH2CO2H + CH3OH
In a 1 dm3 mixture, 0.350 mol of the ester was hydrolysed by heating with water and using
hydrochloric acid as catalyst. The following results were obtained.
Time/s
0
340
680
1080
1440
(i)
Concentration of CH3CH2CO2H/mol dm3

0
0.105
0.185
0.243
0.278
Suggest how the progress of this reaction may be followed in order to obtain the
results as stated.
Taking samples of reaction at the stated intervals (i.e. at 340 s, 680 s, 1080 s
and 1440 s) and quenching it with large amount of cold water. Titrate sample
with dilute NaOH and suitable indicator.
(ii)
By drawing a suitable graph using the data given above, show that the reaction is
first order with respect to the ester. It has been found that the hydrolysis reaction is
first order with respect to the hydrochloric acid.
y = -1E-07x2 + 0.0003x + 0.001
[RCOOH]/mo ldm
0.3
0.25
0.2
0.15
0.1
0.05
0
0
200
400
600
800
1000
1200
1400
1600
Time/s
The half life of the ester is approximately 640 seconds based on the data. Hence,
the order of reaction with respect to the ester is 1 since a constant half life is
established.
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(iii)
Deduce the units of the rate constant.

Rate = k[ester][HCl]
Units for k is mol1 dm3 s1
(iv)
State and explain the effect of a catalyst on the rate constant.

The catalyst increases the rate constant by decreasing the activation energy
of the reaction and offers an alternative pathway for reaction.
(v)
Using suitable bond energy values from the Data Booklet, calculate the H for the
hydrolysis of the ester.
H = [ 8 410 + 2 350 + 2 360 + 740 + 2 460] [8 410 + 2 350 + 2 360
+ 740 + 2 460]
= 0 kJ mol1
(vi)
Given that the standard enthalpy change of reaction for the hydrolysis is
+7.6 kJ mol1, suggest a reason for the difference between this given value and
the value that you have calculated in (a)(v).
The ester is not in gaseous phase which would make the calculation by bond
energy inaccurate.
[11]
(b)
Hydrolysis of ester can be achieved in the biological system by enzymes known as

esterase. Enzymes are proteins that catalysed a specific chemical transformation in the
biological system. Such enzymes are generally quaternary proteins.
(i)
Sketch and explain the graph showing how the rate of hydrolysis changes with
increasing concentration of the ester.
Rate
[ester] / mol dm-3
At low concentration of ester, the rate of hydrolysis is roughly proportional to the

concentration of ester and therefore the order of reaction with respect to ester is
about 1.
At moderate concentration of ester, the rate of hydrolysis is no longer proportional
to the concentration of ester and therefore the order of reaction with respect to
ester is mixed order.
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At high concentration of ester, the rate of hydrolysis is independent to the
concentration of ester and therefore the order of reaction with respect to ester is
about 0.
(ii)
Explain the meaning of quaternary structure of proteins.

The quaternary structure of a protein refers to the spatial arrangement of two or
more polypeptide chains, held together into a specific geometry by bonding
interactions like van der Waals forces, hydrogen bonding, ionic bonds and disulfide
bridges.
(iii)
List 2 other major functions of proteins in the body.

w
w
w
w
w
w
w
w
(iv)
As enzymatic catalysts (e.g. amylase breaks down starch in the digestive

system)
As transport molecules (e.g. haemoglobin transports oxygen)
As storage molecules (e.g. iron is stored in the liver as a complex with protein
ferritin)
In movement (e.g. proteins are the major component of muscles)
For mechanical support (e.g. skin and bone contain collagen a fibrous protein)
Mediate cell responses (e.g. rhodopsin is a protein in the eye used for vision)
For immunity / protection against diseases (antibody proteins)
For control of growth and cell differentiation (hormones)
Suggest and explain a chemical method for distinguishing the following pair of
esters. You should state the expected observations.
HCO2CH2CH3 and CH3CH2CO2CH3
Method 1:
Add aqueous NaOH separately to the 2 compounds and heat. Then, add aqueous
iodine to both compounds.
Observations:
Yellow ppt. observed for HCO2CH2CH3.
No yellow ppt. observed for CH3CH2CO2CH3.
OR
Method 2:
Add acidified KMnO4 separately to the 2 compounds and heat.
Observations:
For HCO2CH2CH3, purple colour is decolourised. Effervescence observed. Gas
evolved gives white precipitate with limewater. (Gas is CO2.)
For CH3CH2CO2CH3, purple colour is decolourised. No effervescence observed.
[9]
[Total: 20]
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This question is about the chemistry of the transition metal, nickel and its compound.
(a)
Explain why the colour of [Ni(NH3)6]2+(aq) is blue.

The d orbitals of Ni2+ are split into two groups of different energy levels by NH3 ligands.
When white light shines on the complex, a d electron undergoes dd transition and is
promoted to a higher energy d orbital. During the transition, the d electron absorbs in
the orange region of the visible spectrum. The blue colour observed is the colour of
transmitted light, which is a mixture of remaining wavelengths that are not absorbed.
[3]
(b)
Ni(CO)4 is a compound formed by the reaction between nickel and carbon monoxide. The
Mond process was developed by Ludwig Mond to extract and purify nickel from its ores.
One of the stages of this process involves the decomposition of Ni(CO)4 at 227 C to give
nickel as shown in this equation below:
Ni(CO)4(g)
Ni(s) + 4CO(g)
The equilibrium constant, Kp, for the equilibrium at 227 C is 1.01 atm3. A sample of
gaseous Ni(CO)4 was placed in a 2 dm3 evacuated container at 227 C. At equilibrium, the
partial pressure of CO was 2.00 atm.
[1 atm = 1.01 x 105 Pa]
(i)
Sketch the shapes of the hybrid orbitals around the C atom in carbon monoxide.
Show 2 sp hybrid orbitals
(ii)
Write an expression for Kp.

Kp =
(iii)
Calculate the total pressure of the system at equilibrium.

(2.00)4 / pNi(CO)4 = 1.01
pNi(CO)4 = 15.842 = 15.8 atm
total pressure of system = 15.842 + 2.00 = 17.8 atm
(iv)
Calculate the mass of Ni(CO)4 placed in the container initially.
Initial p/atm
Eqm p/atm
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= 16.3
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Ni(s) + 4CO(g)
2.00
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Let mass of Ni(CO)4 be m.
pV = nRT = (m/M)RT
16.3 x 1.01 x 105 x 2 x 103
= {m / [58.7 + 4 x (12.0 + 16.0)]} x 8.31 x (227 + 273)
m = 135.27 = 135 g
[8]
(c)
Ni is commonly used in catalytic hydrogenation reactions. One such example is given

below.
Compound A, C10H12NOCl, has a chiral centre and dissolves in dilute sulfuric acid. It
reacts with 2,4dinitrophenylhydrazine to form an orange precipitate, but does not react
with Tollens reagent. A reacts with H2 in the presence of Ni catalyst followed by addition
of aqueous bromine to form B, C10H11NOClBr3. When 1 mol of compound B is heated
under reflux with aqueous iodine and excess alkali, followed by careful acidification,
compound C, C8H4NO4Br3 is formed together with 2 mol of yellow solid CHI3.
Deduce the structures of compounds A, B and C, giving reasons for your answer.
A has comparable number of carbon and hydrogen atoms and more than 6 carbon
atoms
A contains a benzene ring
A dissolves in dilute acid

A undergoes neutralisation and is likely to contain an amine group
A undergoes condensation with 2,4DNPH to form a orange precipitate, but does not
undergo oxidation with Tollens reagent
A contains a ketone
A undergoes reduction with H2/Ni to give B

Ketone in A is reduced to a secondary alcohol
A undergoes electrophilic substitution with aqueous Br2 to give B, which contains 3

bromine atoms.
A contains phenylamine group
B undergoes oxidation with aq alkaline I2

B likely to contain CH3CH(OH)
C contains carboxylic acid groups
B also undergoes nucleophilic substitution with excess alkali due to loss of Cl in the
molecular formula of compound C
B is a chloroalkane
2 moles of CHI3 is formed per mole of compound B

3rd and 5th position of the benzene ring must be substituted
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NH2
Br
Cl
H
Br
Cl
CH3
CH3
NH2
NH2
Br
CH3
CH3 Br
OH
Br
OH
OH
Br
[9]
[Total: 20]
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3
This question is about the varied chemical uses of HCl.
(a)
(i)
In the electrolysis of a solution of hydrochloric acid with inert platinum electrodes, an

ammeter showed a reading of 0.450 A in the external circuit of the cell. 110 cm3 of
gas was evolved at the cathode after 30 minutes under room temperature and
pressure. Determine the actual current used in the electrolysis process. Hence,
determine the percentage error (if any) of the ammeter reading.
At the cathode, 2H+ + 2e H2
Amount of hydrogen gas evolved = 110 / 24000 = 0.004583 mol
Amount of hydrogen gas evolved =
Error! Objects cannot be created from editing
field codes.
Q = 0.004583 x 2 x 96500 = 884.583 C
Q 884.583
I=
=
= 0.4914 A
t
30 60
0.450 - 0.4914
% error =
100% = 8.42%
0.4914
(ii)
A student carried out a reaction involving acidified potassium dichromate(VI),

together with an unknown halfcell which consists of transition metal ions. The
Gibbs Free Energy of the reaction was known to be 324 kJ mol1 and the
procedure involved transferring 6 mol of electrons from the unknown solution to
potassium dichromate(VI).
Using the expression of DGq = nFEqcell, where n is the number of moles of electrons
transferred, F is the Faraday constant and Eqcell is the overall cell potential,
determine the Eqcell value and hence deduce the identity of the unknown half cell.
Using G = nFEqcell
324 x 103 = 6 (96500) Eqcell
Eqcell = + 0.560 V
Since procedure involved transfer of 6 mol of electrons from potassium dichromate
(VI) to the unknown solution,
Reduction: Cr2O72 + 14H+ + 6e 2Cr3+ + 7H2O
Ered = +1.33 V
(+1.33)
Using Eqcell = Eqred Eqoxd

0.560 = +1.33 Eqoxd
Eqoxd = (0.560 1.33) = +0.77 V
The Eqoxd tally with the Fe3+/Fe2+ half cell
[4]
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(b)
A sample of sodium hypochlorite, NaOCl, was dissolved in 100 cm3 of 0.123 mol dm3
HOCl (pKa = 7.50) solution forming a buffer of pH 6.20. The buffer is then used to absorb
HCl gas. Calculate the concentration of gaseous HCl (in mol dm3) that is required to be
added to the buffer solution until it reaches pH 6.
[5]
pH = pKa + lg Error! Objects cannot be created from editing field codes.
6.20= 7.50 + lg Error! Objects cannot be created from editing field codes.
lgError! Objects cannot be created from editing field codes. = 1.30
Error! Objects cannot be created from editing field codes. = 0.0501
Error! Objects cannot be created from editing field codes.= 0.0501 x 0.123
= 0.006162 mol dm3
On addition of HCl, let x be the concentration of H+
[HOCl]new
= 0.123 + x
[OCl ]new
= 0.006162 x
6.00 = 7.50 + lg Error! Objects cannot be created from editing field codes.
6.00 = 7.50 + lg Error! Objects cannot be created from editing field codes.
1.50 = lg Error! Objects cannot be created from editing field codes.
0.03162 = Error! Objects cannot be created from editing field codes.
0.03162(0.123) + 0.03162x = 0.006162 x
1.03162x = 0.00227
x = 0.00220 mol dm3
(c)
The decomposition temperature of hydrogen chloride is close to 3000 K. Predict, with

reasoning, if the decomposition temperature of hydrogen astatide would be higher or lower
than 3000 K.
The decomposition temperature of
3000 K because down the group,
covalent bond length of HX increases.
covalent bond strength decreases.
bond dissociation energy decreases.
\ thermal stability decreases.
hydrogen
astatide
would
be
lower
than
[3]
(d)
Concentrated hydrochloric acid is commonly used in the reduction of trinitrobenzene

(2,4,6trinitrobenzene).
(i)
Suggest the complete set of reagents, together with concentrated HCl, to be used in
this reduction process.
Tin with (excess) concentrated HCl, followed by aqueous NaOH
(ii)
Suggest the structural formula of the product formed.

NH2
H2N
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(iii)
Explain the relative basicity between the product formed in (d)(ii) and the melamine
molecule as shown below in terms of their structures. The melamine molecule
contains a triazine ring with 3 nitrogen atoms present in the ring.
NH2
N
H2N
N
N
NH2
Melamine
Melamine is less basic. The lone pair of electrons on the N atom from the amine
group in melamine is more delocalised into the p electron cloud in triazine ring
because of the electronegative N atoms present in the ring. The availability of the
lone pair of electrons to accept a proton for dative bonding is reduced.
[5]
(e)
2,4,6trinitrobenzene can also undergo FriedelCrafts alkylation with CH3Cl to form

2,4,6trinitromethylbezene. The alkyl side chain can then be further reacted to form useful
halogen derivatives. However, some side products like hydrogen chloride gas and
compound D can also be formed in the process.
NO 2
O 2N
CH2
O 2N
NO 2
NO 2
CH2
O 2N
Compound D
Using 2,4,6trinitromethylbezene as the starting material, describe an appropriate
mechanism that would result in the production of compound D.
[3]
Initiation
Cl Cl
uv
2 Cl
(Note: must use chlorine radicals so that hydrogen chloride will be produced as the side
product in the propagation step)
Propagation
NO 2
NO 2
CH3 + Cl
O 2N
O 2N
NO 2
CH2 + HCl
NO 2
Termination
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NO 2
O 2N
O 2N
CH2
NO 2
CH2
O 2N
NO 2
NO 2
O 2N
O 2N
CH2
NO 2
NO 2
CH2
O 2N
[Total: 20]
Chlorine and its compounds are used to manufacture many products such as pesticides,
medicines, plastics, bleaches and solvents.
(a)
1 mol of the following compounds is added to 1 dm3 of water.

CH3COCl, ClCH2COOH and SiCl4
Arrange the compounds in order of increasing pH of the resultant mixture formed. Briefly
explain your answers, giving equations where appropriate.
[4]
Resultant mixture formed when 1 mole of ClCH2COOH is added to 1 dm3 of water is the
least acidic as ClCH2COOH ionises only partially in water:
ClCH2COOH + H2O
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ClCH2COO- + H3O+
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Resultant mixture formed when 1 mole of CH3COCl is added to 1 dm3 of water is fairly
acidic as CH3COCl hydrolyses, forming HCl which is a strong acid:
CH3COCl (l) + H2O (l) CH3COOH (aq) + H+ (aq) + Cl- (aq)
Resultant mixture formed when 1 mole of SiCl4 is added to 1 dm3 of water is the most
acidic as 1 mole of SiCl4 hydrolyses to form 4 mole of HCl:
SiCl4 (aq) + 2H2O (l) SiO2 (s) + 4H+ (aq) + 4Cl- (aq)
Hence, in order of increasing pH of the resultant mixture formed on reaction with water:
SiCl4, CH3COCl, ClCH2COOH
(b)
Both chloric(I) acid, HOCl and hydrogen chloride react with propene. In the reaction
between chloric(I) acid and propene, chlorine is added to carbon-1 of propene in the
major product. However, in the reaction between hydrogen chloride and propene, chlorine
is added to carbon-2 of propene in the major product.
(i)
Draw the displayed formula of the major product formed between propene and
chloric(I) acid.
Cl
(ii)
Explain briefly why chlorine from chloric(I) acid and from hydrogen chloride add to
different carbon atoms in their reactions with propene.
[4]
In HOCl, Cl is partially positive so that Cl+ is the electrophile and Cl+ adds to
carbon-1 to form the more stable carbocation.
Subsequent addition of OH- results in the formation of the major product with
chlorine added to carbon-1.
In HCl, chlorine is partially negative so that the electrophile is H+ rather than Cl+.
Hence H+ adds to carbon-1 to form the more stable carbocation.
(c)
Despite health and environmental concerns, the chlorinated compound MCPA, is widely
used as a weed killer.
OCH2COOH
CH3
Cl
MCPA
Using not more than 3 steps, draw a reaction scheme to show how MCPA can be
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synthesised from 2methylphenol.
[3]
OH
OH
O
CH3
CH3 Cl in CCl
2
4
OCH2COOH
CH3
CH3 ClCH COO- reflux

2
NaOH
H+
Cl
(d)
Cl
Cl
Compound E is a derivative of MCPA which may be a potential insecticide. The synthesis

of Compound E is given below.
OH
OC(CH3)3
CH3
CH3
NaOH
(CH3)3CCl
+
Cl
Cl
Compound E
Describe the mechanism for the synthesis of Compound E.
H3C
CH3
d+ dCl
C
slow
(CH3)3C
Cl
CH3
(CH3)3C
CH3
fast
CH3
Cl
Cl
(e)
OC(CH3)3
Describe the variation in melting points of the chlorides of the elements from sodium to
phosphorus and explain the variation in terms of structure and bonding.
[4]
Melting points of sodium chloride and magnesium chloride are higher than that of
aluminium chloride, silicon tetrachloride and phospohorus pentachloride.
This is because NaCl and MgCl2 have giant ionic lattice structures and a large amount
of energy is required to overcome strong electrostatic forces of attrations between
the ions so that their melting points are high.
Al2Cl6, SiCl4 and PCl5 have simple molecular structure with weak van der Waals
forces between the molecules so their melting points are lower than the ionic NaCl and
MgCl2.
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The order of increasing melting point is SiCl4, PCl5 and Al2Cl6 since van der Waals forces
increases also in that order due to greater ease of distortion of electron cloud as the
number of electrons increases from SiCl4 to PCl5 to Al2Cl6.
(f)
Describe a reaction, without the use of bromide solution, which shows that chlorine is a
stronger oxidising agent than iodine.
[2]
React aqueous sodium thiosulfate separately with chlorine and iodine.
Chlorine is strong enough an oxidising agent to oxidise S2O32- to SO42- but iodine is too
weak an oxidising agent to oxidise S2O32- to SO42-. Instead, iodine oxidises S2O32- only to
S4O62-.
OR
React aqueous iron(II) sulphate separately with chlorine and iodine.
Chlorine is strong enough an oxidising agent to oxidise Fe2+ to Fe3+ but iodine is too weak
an oxidising agent to oxidise Fe2+ to Fe3+.
[Total: 20]
Phosphorus is an element in Period 3 of the Periodic Table with wide ranging application
in inorganic and organic synthesis.
(a)
Explain why the first ionisation energy of phosphorus is higher than that of sulfur, S, and
arsenic, As, respectively.
[2]
Interelectronic repulsion between paired 3p electrons in S makes it easier to remove
one of the paired 3p electron compared to the unpaired 3p electron of P. Therefore the
first ionisation energy of P is higher than that of S.
As has a larger atomic radius and outermost electron of As experiences larger shielding
effect by inner shell of electrons. Therefore the first ionisation energy of P is higher than
that of As.
(b)
Define the second ionisation energy of phosphorus with an appropriate equation.
[2]
The second I.E is the energy required to remove one mole of electron from one mole of
singly positively charged gaseous phosphorus ions to form one mole of doubly
positively charged gaseous phosphorus ions.
P+ (g) P2+ (g)
(c)
When heated in air, phosphorus and sodium forms oxides which can react with acids,
bases or water.
(i)
Write balanced equations for the reaction between oxides for the two elements and
an appropriate acid or base.
Na2O (s) + 2HCl (aq) 2NaCl (aq) + H2O (l)
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P4O6 (s) + 12NaOH (aq) 4Na3PO3(aq) +6H2O (l)
P4O10 (s) + 12NaOH(aq) 4Na3PO4(aq) +6H2O (l)
(ii)
Describe the reactions, if any, of the two oxides with water containing universal
indicator. Chemical equations are not required.
[5]
Na2O reacts vigorously with water to form basic solution
UI colour in solution: blue/purple
P4O6 or P4O10 reacts readily with water to form acidic solution.
UI colour in solution: red
(d)
Phosphoric acid is used as a catalyst in the industrial preparation of CH3CH2CH(OH)CH3

from compound F, CH3CH2CH=CH2.
(i)
State the reagent and any other conditions required in this industrial preparation.
Steam, 65 atm, 300C
(ii)
Compound G, which is an isomer of F, exists as a pair of geometric isomers.

Deduce the structure of G.
CH3CH=CHCH3
(iii)
Predict the carboncontaining products obtained when F and G are separately

heated with acidified potassium manganate(VII).
[3]
F: CH3CH2COOH and CO2
G: CH3COOH
(e)
PCl5 is used for substitution reactions in organic chemistry.

An optically active compound P, with molecular formula C3H7O2N, reacts with PCl5 to give
white fumes. When a solution containing P is warmed with aqueous sodium hydroxide, a
pungent gas is evolved. Upon acidification of the resulting mixture, compound Q, C3H6O3,
can be isolated. When Q is warmed with concentrated sulphuric acid, a cyclic compound
R, C6H8O4, is formed. Compound S is a structural isomer of Q and is not optically active.
When S is warmed with concentrated sulphuric acid, a noncyclic compound T, C3H4O2, is
produced.
Deduce the structures of compounds P, Q, R, S and T. Explain the chemistry of the
reactions described.
[8]
P is optically active
P is chiral
P undergoes substitution reaction with PCl5
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alcohol present in P
P undergoes alkaline hydrolysis to form NH3 when heated with NaOH
primary amide is present in P
Q undergoes esterification/condensation/nucleophilic acyl substitution
R contains ester group
S is not optically active
S is not chiral
S undergoes elimination with conc. H2SO4 to from T
alkene present in T
Structure of P:
Structure of Q:
CH3
H
CH3
CONH2
OH
OH
Structure of R:
Structure of S:
H3C
H
COOH
H
H
CH3
CH2COOH
OH
Structure of T:
H
H
C
C
COOH
[Total: 20]
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INNOVA JUNIOR COLLEGE

JC 2 PRELIMINARY EXAMINATION 2
in preparation for General Certificate of Education Advanced Level
Higher 2
CANDIDATE
NAME
CLASS
INDEX NUMBER
CHEMISTRY
9647/01
11 September 2012
1 hour

Data Booklet

Choose the one you consider correct and record your choice in soft pencil on the separate
Answer Sheet.
Read the instructions on the Answer Sheet very carefully.

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2
Section A
For each question there are four possible answers, A, B, C, and D. Choose the one you
1
Methane was burned in an incorrectly adjusted burner. The methane was converted into a
mixture of carbon dioxide and carbon monoxide in the ratio of 98:2, together with water
vapour.
What will be the volume of oxygen consumed when y dm3 of methane is burned?
A
1.99y dm3
0.995y dm3
1.995y dm3
0.99y dm3
To identify an oxide of nitrogen, 0.10 mol of the oxide was mixed with 10 dm3 of hydrogen
gas and passed over a heated catalyst. At the end of the reaction, 0.4 dm3 of hydrogen gas
remained. The ammonia produced required 125 cm3 of 1.6 mol dm-3 HCl for neutralisation.
All gasoues volumes were measured at room temperature and pressure.
What is the formula of the oxide of nitrogen?
NO
NO2
N2O
N2O4
A 2 g sample of hydrogen at temperature T and of volume V exerts a pressure of p.

Deuterium, 21 H is an isotope of hydrogen.
Which of the following would also exert a pressure p at the same temperature?
2 g of deuterium of volume V
4 g of deuterium of volume V
a mixture of 1 g of hydrogen and 2 g of deuterium of total volume V
a mixture of 2 g of hydrogen and 1 g of deuterium of total volume 2V
Which atom has the highest ratio of unpaired electrons to paired electrons in its ground
state?
A
boron
nitrogen
carbon
oxygen
Which one of the following pairs consist of a planar molecule and a polar molecule?
A
C6H5CH3 and CO2
CH2=CHCHO and CH3OCH3
C6H12 and H3PO4
C6H6 and CCl4
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3
6
Which of the following statements describe a phenomenon which can be explained by

intermolecular hydrogen bonding?
A
The melting points of the Group I hydroxides increase with increasing relative
molecular mass.
CH3OCH3 (Mr = 46) as a higher boiling point than CH3CH2CH3 (Mr = 44)
Ice has a lower density than water at 0oC.
Glycine, NH2CH2COOH has a higher solubility in water than butane.
The kinetics of the reaction between H+ (aq) and S2O32 can be invesitgated experimentally
by varying the volumes of HCl(aq) and Na2S2O3(aq) used and determining the time taken, t,
for the formation of sulfur to completely obscure the cross as shown in the diagram.
S2O32(aq) + 2H+(aq)
S(s) + SO2(g) + H2O(l)
HCl(aq) + Na2S2O3(aq)
cross
The table below shows the experimental results obtained.
Experiment
1
2
3
4
1.0 mol dm
HCl(aq)
10.0
15.0
15.0
20.0
-3
Volume used / cm3

0.040 mol dm-3
Na2S2O3(aq)
5.0
5.0
10.0
20.0
t/s
H2O(l)
25.0
20.0
15.0
0.0
170
170
85
x
What is the value of x in Experiment 4?

A
21
85
43
170
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4
8
A simple decomposition reaction is shown below.

AB(g)
A(g) + B(g)
The rate equation was found to be as follows.

Rate = k[AB] where rate constant, k = 0.2 s-1
Estimate the time taken for AB(g) to reach one eighth of its initial concentration of
1.5 mol dm-3.
3.0 s
10.4 s
7.5 s
13.9 s
Hydrogen iodide dissociates into its elements according to the following equation.
2HI(g)
H2(g) + I2(g)
H = +9 kJ mol1
A mixture of H2(g), I2(g) and HI (g) rapidly comes to equilibrium in a 2.0 L container. After
the reaction has been at equilibrium for 10 minutes, the volume of the container is suddenly
reduced to 1.3 L at constant temperature.
Which one of the following graphs best represents the effect of this decrease in volume on
the concentration of the gases in the mixture?
A
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5
10
Phosphorus(V) chloride, PCl5, decomposes to form phosphorus(III) chloride, PCl3, and

chlorine, Cl2 according to the equation
PCl5(g)
PCl3(g) + Cl2(g)
Four different flasks, 1, 2, 3 and 4, at the same temperature, contain a mixture of PCl5, PCl3
and Cl2. The concentration, in mol dm-3, of these components in each of the flasks is shown
below. In three of the four flasks, the mixture of gases is at equilibrium.
In which one is the mixture of gases not at equilibrium?
11
Flask
[PCl5(g)]
[PCl3(g)]
[Cl2(g)]
0.15
0.20
0.30
0.20
0.15
0.15
0.10
0.10
0.40
0.30
0.80
0.15
Two titrations were performed as shown below
Which of the following statements is true?

A
The weak acid will require a greater volume of NaOH solution than the strong acid to
reach the equivalence point.
The weak acid will require a smaller volume of NaOH solution than the strong acid to
reach the equivalence point.
The weak acid will require the same amount of NaOH as the strong acid to reach the
equivalence point.
The equivalence point in a titration of a weak monoprotic acid with NaOH solution
cannot be determined.
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6
12
Strontium hydride is an ionic compound. The standard enthalpy changes, H1 and H2 are
known.
Sr(s) Sr2+(g) + 2e
H1
H2(g) + 2e 2H(g)
H2
What additional data is needed to determine the lattice energy of strontium hydride?
13
The first ionisation energy of hydrogen.
The standard enthalpy change of atomisation of hydrogen.
The standard enthalpy change of atomisation of strontium.
The standard enthalpy change of formation of strontium hydride.
Four half cells are constructed as follows.

Half cell I: an electrode of metal P in a 1.0 M solution of P+(aq) ions
Half cell II: an electrode of metal Q in a 1.0 M solution of Q+(aq) ions
Half cell III: an electrode of metal R in a 1.0 M solution of R+(aq) ions
Half cell IV: an electrode of Cu(s) metal in a 1.0 M solution of Cu2+(aq) ions
The half cells are connected in pairs, as shown below, to form a series of galvanic cells.
For each cell, the polarity of the electrodes and the voltage generated are recorded.
Half cells
used
I and IV
II and IV
III and IV
II and III
Positive
electrode
P
Cu
Cu
Q
Negative
electrode
Cu
Q
R
R
Voltage (V)
0.46
0.57
1.10
0.53
Which one of the following alternatives lists the metals in order of increasing strength as
reducing agents?
14
R, Q, Cu, P
P, Cu, R, Q
Cu, P, Q, R
P, Cu, Q, R
Aqueous sodium chloride (brine) is electrolysed by using inert electrodes in a cell which is
stirred so that the products of electrolysis are able to react. The cell is kept cold.
Which one of the following pairs of substances is among the major products?
A
Hydrogen and sodium chlorate(I)
Hydrogen and sodium chlorate(V)
Hydrogen and chlorine only
Sodium hydroxide and chlorine only
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15
The structure of compound X is given below.
Compound X
How many chiral centres are there in the product when compound X is hydrogenated with
sodium boron hydride?
16

Based on bond energies listed in the Data Booklet, what are the possible products of the
following reaction?
CH3 + CH3CH2Cl
17
CH4 + CH3CHCl
CH3CH2CH3 + Cl
CH3CH2CH2 + HCl
CH3CH2CH2Cl + H
An organic compound Y undergoes the following reactions:

(i)
(ii)
(iii)
It decolourises a solution of bromine in tetrachloromethane.

It reacts with sodium bromide in concentrated sulfuric acid.
It reacts with hot alkali to produce a compound with two alcohol functional groups.
Which compound could be Y?

A
HOH2CCH=CHCH=CHCH2Cl
Cl2CHCH=CHCH2COOH
BrCH2CH2CHClCH2COCl
ClCH2CH2CH=CHCH(Cl)CH2OH
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18
Ibuprofen is an anti-inflammatory agent.
ibuprofen
Which of the following could be part of a sequence for synthesizing ibuprofen?
[In the sequence below, R =
.]
RCHCH2OH
CH3
KMnO4, OH-(aq)
H+(aq)
cold
19
In which of the following sequences does the value of pKa decrease continuously?
A
CH3CO2H > CCl3CO2H > C2H5OH
> C6H5OH
CCl3CO2H > CH3CO2H > C6H5OH
> C2H5OH
C2H5OH
> C6H5OH
> CH3CO2H > CCl3CO2H
C6H5OH
> C2H5OH
> CH3CO2H > CCl3CO2H
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20
The production of 4-chloro-3-nitrobenzoic acid from methylbenzene is as follows:
Which of the following shows the correct intermediates for 1 and 2 with the highest yield of
the final product?
1
CH3
COOH
Cl
Cl
CH3
CH3
B
NO2
Cl
COOH
Cl
COOH
NO2
CH3
CH3
D
NO2
NO2
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21
An account in a students notebook read:

An excess of aqueous bromine was added to aqueous phenol in a test tube,
2,4,6-tribromophenol was produced as a creamy-white precipitate suspended in a yellow
alkaline solution.
Which statement in this account must have been incorrect?
22
The precipitate is not 2,4,6-tribromophenol, but a mixture of 2- and 4-bromophenol.
The precipitate obtained is not creamy-white, but yellow.
The resultant solution is not alkaline, but acidic.
The resultant solution is not yellow, but purple.
Ethanoic acid can be made by direct carbonylation of methanol, in presence of a rhodium

catalyst.
rhodium
CH3OH + CO
CH3COOH
catalyst
Using a similar method, which of the following could be expected to produce compound W?
COOH
H
CH2COOH
CH2COOH
Compound W
OH
OH
COOH
CH2COOH
CH2OH
COOH
CH2OH
OH
CH2COOH
CH2COOH
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CH2COOH
CH2OH
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23
The amino acids glutamine and glutamic acid can react with each other to form amide
linkages.
NH2
HO
OH
OH
NH2
NH2
glutamine
glutamic acid
What is the maximum number of different compounds, each containing one amide linkage,
that can be formed from one molecule of glutamine and one molecule of glutamic acid?
24
B is synthetic nonapeptide that is resynthesised from the amino acids found in honey bee
venom. To investigate the sequence of amino acids in B, the nonapeptide was first
hydrolysed by two enzymes. The protein fragments were then separated and their
sequence determined.
The following protein fragments were obtained from the first enzyme which hydrolysed the
peptide chain at the carboxylic end of the amino acid isoleucine, Ile.
Arg-Ile
Ser-Lys-Trp-Ile
Lys-Leu-Arg
The second enzyme, which hydrolysed the peptide chain at the carboxylic end of the amino
acid lysine, Lys, yielded the following fragments
Arg-Ile-Ser-Lys
Trp-Ile-Lys
Leu-Arg
Which of the following is the correct primary structure of the nonapeptide B?
25
Lys-Leu-Arg-Ile-Ser-Lys-Trp-Ile-Lys
Trp-Ile-Lys-Leu-Arg-Ile-Ser-Lys-Trp
Arg-Ile-Ser-Lys-Trp-Ile-Lys-Leu-Arg
Ser-Lys-Trp-Ile-Lys-Leu-Arg-Ile-Ser
Haemoglobin is the oxygen carrying pigment in red blood cells. It contains two -sub-units
and two -sub-units. What are the main forces responsible for holding the four subunits
together?
A
van der Waals forces
peptide bonds
electrostatic forces
hydrogen bonds
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26
Two properties of non-metallic elements and their atoms are as follows.

property 1
property 2
has an oxide that can form a strong acid in water

has no paired 3p electrons
Which properties do phosphorus and sulfur have?
27
phosphorus
sulfur
1 and 2
1 only
1 only
1 and 2
1 and 2
1 and 2
2 only
1 only
At 900 C, CaCO3 decomposes producing CO2 and the metal oxide.

At 1100 C, CaSO4 decomposes producing SO3 and the metal oxide.
Which statement explains the greater stability of CaSO4?
28
CaCO3 has a higher lattice energy than CaSO4.
The CO2 molecule is smaller than SO3.
The charge density of CO32- is greater than that of SO42-.
CO32- ions are more easily polarised than SO42-.
X is a salt of one of the halogens chlorine, bromine, iodine, or astatine (proton number 85).
The reaction scheme shows a series of reactions using a solution of X as the starting
reagent.
What could X be?

A
sodium chloride
potassium iodide
sodium bromide
potassium astatide
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29
30
How does concentrated sulfuric acid behave when it reacts with sodium chloride?
A
as an acid only
as an acid and oxidising agent
as an oxidising agent only
as a reducing agent only
The diagram shows some reactions of salt Q.
What is the identity of Q?

A
Al2(SO4)3
ZnSO3
PbSO4
ZnSO4
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14
Section B
may be correct.
Decide whether each of the statements is or is not correct (you may find it helpful to put a tick
against the statements that you consider to be correct).
A
1, 2 and 3 are correct
1 and 2 are correct
2 and 3 are correct
1 only is correct.

31
32
33
Which of the following quantities is equal to the Avogadro constant?

1
The number of oxygen atoms in 49.9 g of allactite, Mn7(AsO4)2(OH)8, of molar mass

798 g mol-1
The number of aqueous chloride ions in a solution containing 0.5 mol of the complex,
[Cr(H2O)5Cl]Cl2
The number of ions in 168 g of Reineckes salt, NH4[Cr(NH3)2(SCN)4], of molar mass

336 g mol-1
Which of the following is hydrogen bonded in the liquid state?

1
CH3NH2
CH3CHO
CH2F2
Which suggested mechanisms are consistent with the experimentally obtained rate
equations?
1
Rate = k[NO]2[H2]
Rate = k[A]2[B]
2NO + H2
N2O + H2O (slow)
N2O + H2
N2 + H2O
2A
A2
A2 + B
A2B + A
3
Rate = k[HBr][O2]
2HBr + O2
HBrO + HBr
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(fast)
(fast)
A2B
(slow)
A3B (fast)
2HBrO
H2O + Br2
(slow)
(fast)
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34
The use of the Data Booklet is relevant to this question.

An example of a reaction catalysed by transition metal ions is given below:
S2O82(aq) + 2I(aq) 2SO42(aq) + I2(aq)
The Eo, values for the half-reactions are:
Eo, (I2 / I ) = +0.54 V
Eo, (S2O82 / SO42) = +2.01 V
Which of the following transition metal ions can be used to catalyse this reaction?
35
Fe3+
Co3+
V3+
Which compounds could undergo elimination reaction when treated with hot ethanolic
potassium hydroxide?
H
H3C
CH3
Br
Br
Br
Br
CH3
Br
Br
CH3
H3C
CH2Br
CH3
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A
1, 2 and 3 are correct
1 and 2 are correct
2 and 3 are correct
1 only is correct.

36
37
Which of the following statements is true for the compound below?
It is a non-planar compound.
When boiled with aqueous sodium hydroxide, it is converted to
It will react with 2,4-dinitrophenylhydrazine at room temperature.
Esters can be synthesized by reaction of a carboxylate anion with an alkyl halide.

RCO2 + RX RCO2R + X
where X = Cl, Br or I
Which of the following esters can be prepared using this method?

1
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38
39
40
Which of the following mixture produce ND3 gas upon heating?

[D = 21 H, an isotope of hydrogen]
1
CaO (s) and ND4Cl (s)
CH3CN and NaOD in D2O
CH3CONH2 and NaOD in D2O
Which properties in the sequence hydrogen chloride, hydrogen bromide and hydrogen
iodide steadily increase?
1
thermal stability
bond length
ease of oxidation
The rock dolomite is a double carbonate of magnesium and calcium, CaCO3.MgCO3.

When heated strongly, a product called calcined dolomite is formed which is used to line
some furnaces for the production of metals.
Why is calcined dolomite used for this purpose?
1
It is a refractory material.
It will absorb acidic impurities in metallurgical processes.
It will reduce metallic oxides to metals.
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INNOVA JUNIOR COLLEGE

JC2 PRELIMINARY EXAMINATION 2
in preparation for General Certificate of Education Advanced Level
Higher 2
CANDIDATE
NAME
CLASS
INDEX NUMBER
9647/02
CHEMISTRY
11 September 2012
2 hours
Candidates answer on the Question Paper

Write your index number, name and civics group.
You may use pencil for any diagrams, graphs or rough working.
ForExaminersUse
SectionA
1
12
12
3
You are advised to show all working in calculations.
You are reminded of the need for good English and
clear presentation in your answers.
You are reminded of the need for good handwriting.
Your final answers should be in 3 significant figures.
15
12
11
10
Significant
figures
You may use a calculator.

The number of marks is given in brackets [ ] at the end of each
question or part question.
At the end of the examination, fasten all your work
securely together.
Handwriting
Total
72
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2
For
Examiners
Use
Answer ALL questions on the spaces provided.

1
Planning (P)
A student was given 50 cm3 of three acidic solutions labelled X, Y and Z. She was asked
to provide the identities of them by conducting a simple experiment.
The identities of the three solutions are
1 mol dm-3 ethanoic acid, CH3COOH
1 mol dm-3 hydrochloric acid, HCl
Her teacher advised her to measure the temperature change of the reactions and
calculate the enthalpy change of neutralisation of an acid and base reaction. The student
is also provided with 200 cm3 of 1 mol dm-3 sodium hydroxide, NaOH.
The student let the volume ratio of each of the three solutions to sodium hydroxide be 1:1.
She tested the experiment and realised that with this volume ratio, she is unable to
differentiate the different concentrations of hydrochloric acid.
(a)
Construct balanced equations for the reactions between the given acids and base.
[1]
(b)
The following table shows the volumes used by the student.

Explain, with the aid of calculation, why the students experiments will not aid the
differentiation of the different concentrations of hydrochloric acid.
Experiment
1
2
Volume of 1 mol
dm-3 NaOH / cm3
50
50
Volume of 1 mol
dm-3 HCl / cm3
50
Volume of 2 mol
dm-3 HCl / cm3
50
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
.[2]
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3
(c)
Write a plan which will allow an identification of the three solutions to be made. You
may use the reagents and apparatus normally found in a school or college
laboratory. However, you are not provided with an indicator.
In your plan you should give essential details, including quantities, of the
identification procedure.
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
[6]
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For
Examiners
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4
(d)
Explain how you can make use of your experimental data to identify the three
solutions.
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
.[2]
(e)
Discuss one possible source of error in conducting your experiment and suggest
improvement to produce a more reliable result.
...........................................................................................................................
...........................................................................................................................
.....[1]
[Total: 12]
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Examiners
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5
2
(a)
Iodine is not very soluble in water but in the presence of iodide ions, it can dissolve
to form a tri-iodide complex as follows:
I2 + I I3
(i)
Draw a dot and cross diagram for the tri-iodide ion and hence state its shape
and bond angle.
Shape.
Bond angle
(ii)
Explain why fluorine does not form the corresponding F3 ion.

.
.....
[3]
(b)
IF7 is a colourless gas prepared by the direct combination of iodine and fluorine.
The IF bond energy can be obtained from thermochemical data.
Standard enthalpy change of formation of IF7(g) = 944 kJ mol1
Standard enthalpy change of atomisation of iodine = +107 kJ mol1
(i)
Define what is meant by the standard enthalpy change of formation of IF7.

.
.
(ii)
Draw an energy cycle diagram to determine the IF bond energy.

Incorporate values from the data above and any other relevant data from the
Data Booklet into the diagram.
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Examiners
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6
(iii)
Explain why the IF bond energy is not the mean of the II and FF bond
values.
.
.
[6]
(c)
The typical daily food requirement of a person can be considered to be 1.2 kg of

carbohydrate. The person obtains energy by oxidation of the carbohydrate, which
can be represented by the formula (CH2O)n.
(i)
Construct an equation for the complete oxidation(combustion) of the

carbohydrate (CH2O)n.
.
(ii)
The empirical relative formula mass of the carbohydrate is 30. Use your
equation in (i) to calculate the number of moles of oxygen required by the
person each day.
(iii)
Calculate the volume of oxygen at room temperature and pressure for a

human with a lifetime of 70 years.
[3]
[Total:12]
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For
Examiners
Use
(a)
Panadol is the trade name for paracetamol or acetaminophen which is an over the
counter analgesic (pain reliever) and antipyretic (fever reducer).
It can be synthesised in the lab from phenol via a series of steps.
OH
OH
dil HNO3
II
I
B
N
H
CH3
C
O
paracetamol
(i)
State the reagents and conditions for step I and step II.
Step I:
Reagent(s): .....
Condition(s): ...
Step II:
Reagent(s): .....
Condition(s): ...
(ii)
Draw the structures of compound A and B in the boxes below.

A:
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B:
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For
Examiners
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8
Paracetamol can be easily hydrolysed by aqueous NaOH to produce
compound C and D. In the spaces below, write the formulae of the two
products.
(iii)
D:
C:
[6]
(b)
One of the causes of fever is bacterial infection. Alcohol solutions are used as
disinfectants on the skin as it can penetrate the bacterial cell wall and denature
the proteins inside the cell.
(i)
What do you understand by the term denaturation of proteins?
(ii)
The part of the protein molecule which is affected by the ethanol added is as
follows:
O
CH2
H
O
CH2
H
represents R group interaction
Suggest what R group interaction was disrupted by ethanol.
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9
(iii)
Another application of denaturation is found in the making of cheese. Casein

is the predominant protein found in milk. When Lactobacillus bacterium is
added to milk, lactic acid (2-hydroxypropanoic acid) is produced.
CH3
H
C
OH
OH
2-hydroxypropanoic acid
Besides hydrogen bonding, suggest and write an equation to explain what R
group interaction is disrupted when lactic acid is produced.
Explanation............................................
.........
Equation
[4]
(c)
The following table compares the pKa values of ethanol, 2-hydroxypropanoic acid
with that of ethanoic acid.
(i)
compound
formula
pKa
Ethanol
CH3CH2OH
15.9
Ethanoic acid
CH3COOH
4.76
CH3CH(OH)COOH
3.86
Suggest a reason why pKa value of ethanoic acid is so much less than ethanol.
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10
(ii)
Suggest a reason why 2-hydroxypropanoic acid is more acidic that ethanoic

acid.
[3]
(d)
The degree of dissociation (ionisation) of ethylamine, CH3CH2NH2, in 0.010 mol dm-3

aqueous solution is 0.17.
(i)
Calculate the hydroxide ion concentration of this solution.
(ii)
Calculate a value for the base dissociation constant, Kb, for ethylamine, stating
the units.
[2]
[Total: 15]
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For
Examiners
Use
11
For
Examiners
Use
4 (a)
Nucleophiles are electron-rich species that can donate electrons and attack regions of low
electron density. Reactions 1 and 2 show how the nucleophile, Nu, reacts with two
different carbonyl groups.
O
R
OH
R1
+ Nu
R1
Reaction 1
Nu
O
O
R
+ Nu
R
Nu
Reaction 2
where X: Cl, Br, I

The intermediates, X and Y, shown below are formed by nucleophilic attack on two
different compounds containing a carbonyl group of low electron density.
X
(i)
State the nucleophile required to form intermediate X and Y respectively.

Nucleophile for intermediate X: .
Nucleophile for intermediate Y: ..
(ii)
Identify the organic starting material to form intermediate X.
(iii)
State the type of reaction that gives intermediate Y.

..
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12
(iv)
For
Examiners
Use
Suggest a mechanism for the complete reaction in which Y is an intermediate.
[7]
(b) In a reaction discovered just over 100 years ago by the German chemist Karl Fries,
compound G is converted into compound K when it is heated with AlCl3.
Compound K is a structural isomer of G.
H3C
AlCl3
K (C8H8O2)
Compound G
Compound K is a 1,4-disubstituted benzene derivative. It is insoluble in water, but

dissolves in NaOH(aq). It gives a white precipitate with Br2(aq), and a yellow precipitate
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(i)
For
Examiners
Use
Use the information given, name the functional groups in compound K.
(ii)
Deduce the structural formula of K.
(iii)
Draw the structural formulae for the aromatic products when compound K
undergoes the following reactions.
[5]
[Total: 12]
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14
5
(a)
An element M forms an oxide which is a powerful oxidising agent.

An acidified solution of the oxide of M, MOx (x = 1, 2 or 3) will oxidise Mn2+(aq) to
MnO4(aq), itself reduced to the element M.
When 10.0 cm3 of 0.5 mol dm-3 of MOx was reacted with 0.40 moldm-3 Mn2+(aq) in the
presence of H+(aq), 15.0 cm3 of Mn2+(aq) was needed for complete reaction.
(i)
Calculate the number of moles of electrons donated by Mn2+.
(ii)
Calculate the mole ratio of MOx and electrons accepted by MOx.
(iii) Determine the original oxidation number of M and the value of x.
(iv) Construct an equation for the reaction between MOx(aq) and acidified Mn2+(aq).
[4]
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For
Examiners
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15
For
Examiners
Use
(b)
Water, H2O, covers 70.9% of the Earths surface and is vital for all known forms of life.
About 0.005% of water molecules consist of an oxygen atom bonded to two atoms of
the hydrogen isotope, deuterium, 21 D.
Deuterium oxide, D2O, is known as heavy water and is used for research in chemical
reactions because deuterium atoms react less quickly than normal hydrogen atoms,
1
1 H.
Like H2O, pure D2O is weakly ionised.
2D2O
D3O+ + OD
For D2O, we can use the term KD instead of KW and pD instead of pH.
(i)
Explain what is meant by dynamic equilibrium.
(ii)
For pure D2O, KD = 1.35 x 10-15. Calculate the values of the following.
I. [D3O+]
II. pD
(iii) For this system, KD increases when temperature increases. Suggest and explain
whether the ionic dissociation of heavy water is an exothermic or endothermic
process.
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(iv) When pure H2O and pure D2O are mixed, exchange of H and D atoms takes
place and the following equilibrium is established.
D2O(l) + H2O(l)
2HDO(l)
A mixture of 30 g of D2O and 27 g of H2O was placed in a vessel at 298 K. At

equilibrium, it was found that the degree of dissociation of D2O is 0.49. Calculate
the Kc for this system.
[7]
[Total: 11]
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Examiners
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17
6
Many copper minerals are found in hydrothermal deposits where they were formed by
crystallization from very hot solutions which were trapped underground at high pressures.
One such copper mineral is chalcopyrite, CuFeS2.
Copper is extracted from the ore chalcopyrite, CuFeS2, in a three-stage process.
In the first stage of this extraction, the chalcopyrite is heated with silicon dioxide and
oxygen.
(a)
Balance the following equation for this first stage in which copper sulfide is formed.
...CuFeS2 + ..SiO2 + ..O2
Cu2S + .FeSiO3 + SO2

[1]
(b)
Write the electronic configuration for Cu+ in Cu2S:

Cu+
[1]
(c)
When water is added to white anhydrous CuSO4, the solid dissolves to give a blue
solution. On addition of concentrated NH4Cl (aq), the solution changes to a yellowgreen due to formation of copper containing species D. Concentrating the solution
produces green crystals E of an ammonium salt with empirical formula CuN2H8Cl4.
(i)
Suggest the formulae of cation present in E.

Cation present in E ........................................
(ii)
Suggest the formulae of anion D.

Anion D
(iii)
Suggest a balanced equation for the formation of anion D from aqueous

CuSO4.
When excess of NH3 (aq) is added to species D, the yellow green solution turns to a
deep blue solution.
(iv)
Use this information and the information above to suggest the strength of NH3,
H2O and Cl ligands in decreasing order.
> >
[4]
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18
(d)
When a dilute aqueous solution containing a bidendate ligand, ethanedioate ion,

C2O42-, is added to a solution containing aqueous copper(II) ions, a ligand exchange
reaction occurs. In this reaction, four water molecules in the hydrated copper ion are
replaced and a new complex F is formed.
(i)
Explain what is meant by a bidendate ligand.
(ii)
Suggest the formulae of complex F formed.

Identity of F .
(iii)
In the complex F formed, the two water molecules are opposite each other.
Draw a diagram to show how the ethanedioate ions are bonded to a copper ion
and give a value for one of the O-Cu-O bond angles. You are not required to
show the water molecules.
O-Cu-O bond angle:

[4]
[Total: 10]
PRELIM 2 INNOVA
9647/02/2012
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1
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Answer ALL questions on the spaces provided.

1
Planning (P)
A student was given 50 cm3 of three acidic solutions labelled X, Y and Z. She was asked
to provide the identities of them by conducting a simple experiment.
The identities of the three solutions are
1 mol dm-3 ethanoic acid, CH3COOH
Her teacher advised her to measure the temperature change of the reactions and
calculate the enthalpy change of neutralisation of an acid and base reaction. The student
is also provided with 200 cm3 of 1 mol dm-3 sodium hydroxide, NaOH.
The student let the volume ratio of each of the three solutions to sodium hydroxide be 1:1.
She tested the experiment and realised that with this volume ratio, she is unable to
differentiate the different concentrations of hydrochloric acid.
(a)
Construct balanced equations for the reactions between the given acids and base.[1]
HCl + NaOH NaCl + H2O [ m]
CH3COOH + NaOH CH3COONa + H2O [ m]
(b)
The following table shows the volumes used by the student.

Explain, with the aid of calculation, why the students experiments will not aid the
differentiation of the different concentrations of hydrochloric acid.
Experiment
1
2
Volume of 1 mol
dm-3 NaOH / cm3
50
50
Volume of 1 mol
dm-3 HCl / cm3
50
Volume of 2 mol
dm-3 HCl / cm3
50
50
= 0.05 moles
1000
50
= 0.05 moles
No. of moles of 1 mol dm-3 HCl = 1 x
1000
50
No. of moles of 2 mol dm-3 HCl = 2 x
= 0.10 moles
1000
NaOH is the limiting reagent [ m]
No. of moles of 1 mol dm-3 NaOH = 1 x
No. of moles of water formed (for the acids) = 0.05 moles

Thus, the amount of water produced is the same throughout Thus, the heat evolved /
temperature change measured will be the same for the different concentrations of
HCl, unable to differentiate the different concentration of HCl.
Note: The enthalpy change of neutralisation of different [HCl] will be the same.
[2]
PRELIM 2 INNOVA
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2
(c)
Write a plan which will allow an identification of the three solutions to be made. You
may use the reagents and apparatus normally found in a school or college
laboratory. However, you are not provided with an indicator.
In your plan you should give essential details, including quantities, of the
identification procedure.
To insert lines[6]
Procedure
1.By using a 50cm3/100cm3 measuring cylinder, place 50cm3 of NaOH, into the dry
polystyrene cup provided supported with a glass beaker.
2. Measure and note the initial temperature of NaOH solution using a 1.0 oC interval
thermometer.
3.By using a second 50cm3/100cm3 measuring cylinder (otherwise must mention
washing & drying of the previous m.cyliner), measure 25 cm3 of acidic solution X.
4.Note the initial temperature of solution X.
(both initial temp taken to find the average initial temp)
5.Add solution X to the cup in step 1.
6.Stir gently with a thermometer and note the highest temperature reached
7. Repeat the experiment (steps 1 to 6) with solutions Y and Z, using different
measuring cylinders or mentioned in procedure measuring cylinder must be dry.
Record all your readings (temperature) in an appropriate table. or a sample table is
drawn.
(d)
Explain how you can make use of your experimental data to identify the three
solutions.
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
...........................................................................................................................
[2]
Feasibility of the identification depends on volume used in the experiment.

Must use results obtained (either Hneu calculated or T) .
When VNaOH should be greater than VHCl:
PRELIM 2 INNOVA
9647/02/2012
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-using enthalpy change of neutralisation calculated:

Due to partial dissociation of CH3COOH, some heat is absorbed to dissociate the
weak acid. Thus, the Hneu is less exothermic/smaller T than HCl of same
concentration.
In this experiment, more no. of moles of water produced with 2.0 mol dm-3 HCl used
is than when 1.0 mol dm-3 HCl used. Thus, the one with a larger/twice the T is the
one using solution 2.0 mol dm-3 HCl.
(Although different concentration of HCl used in the experiment, they will have same
Hneu calculated. )
(e)
Discuss one possible source of error in conducting your experiment and suggest
improvement to produce a more reliable result.
...........................................................................................................................
...........................................................................................................................
[1]
-
Heat loss to the surrounding is not taken into account, the enthalpy change
of neutralisation is less exothermic than expected. Use a lid to cover the cup
to reduce heat loss.
(dependent on thermometer used) There is a percentage error in the
enthalpy change calculated as the 1oC interval thermometer is used. Use a
thermometer with higher precision (0.2oC interval) to reduce the percentage
error.
Slow response of thermometer. Use a data logger with temperature sensor
instead.
[Total: 12]
(a)
Iodine is not very soluble in water but in the presence of iodide ions, it can dissolve
to form a tri-iodide complex as follows:
I2 + I- I3(i)
Draw a dot and cross diagram for the tri-iodide ion and hence state its shape
and bond angle.
Bond angle of 180.
Thus the complex is linear in shape.
PRELIM 2 INNOVA
9647/02/2012
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4
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(ii)
Explain why fluorine does not form the corresponding F3- ion.
Fluorine, being in Period 2, is not able to expand it outermost
shell to accommodate 10 electrons.
[3]
(b)
IF7 is a colourless gas prepared by the direct combination of iodine and fluorine.
The IF bond energy can be obtained from thermochemical data.
Standard enthalpy change of formation of IF7(g) = 944 kJ mol1
Standard enthalpy change of atomisation of iodine = +107 kJ mol1
(i)
Define what is meant by the standard enthalpy change of formation of IF7.

It is the enthalpy change when 1 mole of IF7 is formed from its constituent
elements, iodine and fluorine in their standard states under standard
conditions of 1 atm and 298 K.
(ii)
Draw an energy cycle diagram to determine the I-F bond energy.

Incorporate values from the data above and any other relevant data from the
Data Booklet into the diagram.
7BE(I-F) -944.0 = +107+
7
(+158)
2
BE(I-F) = +229 kJ mol-1
(iii)
(c)
Explain why the IF bond energy is not the mean of the II and FF bond
values.
Fluorine is more electronegative than iodine. The covalent bond between the
atoms is polarised, giving rise to a stronger bond.
[6]
The typical daily food requirement of a person can be considered to be 1.2 kg of
carbohydrate. The person obtains energy by oxidation of the carbohydrate, which
can be represented by the formula (CH2O)n.
PRELIM 2 INNOVA
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(i)
Construct an equation for the complete oxidation(combustion) of the

carbohydrate (CH2O)n.
(CH2O)n + nO2 nCO2 + nH2O
(ii)
The empirical relative formula mass of the carbohydrate is 30. Use your
equation in c(i) to calculate the number of moles of oxygen required by the
person each day.
Moles of carbohydrate = 1200/30n = 40/n mol
Moles of oxygen = n x 40/n = 40 mol
(iii)
Calculate the volume of oxygen at room temperature and pressure for a

human with a lifetime of 70 years.
Moles of oxygen in 70 years = 40 x 70 x 365 = 1.02 x 106 mol
Volume at rtp = 1.02 x106 x 24 = 2.45 x 107 dm3
[3]
[Total:12]
(a)
Panadol is the trade name for paracetamol or acetaminophen which is an over the
counter analgesic (pain reliever) and antipyretic (fever reducer).
It can be synthesised in the lab from phenol via a series of steps.
OH
OH
dil HNO3
II
I
B
N
H
CH3
C
O
paracetamol
(i)
State the reagents and conditions for step I and step II.
Step I:
Reagent(s): .....
Condition(s): ...
Step II:
PRELIM 2 INNOVA
9647/02/2012
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Reagent(s): .....
Condition(s): ...
Step 1 : Sn, concentrated HCl; heat with reflux
Then NaOH (aq); room temperature
Step 2: CH3COCl, r.t.
(ii)
Draw the structures of compound A and B in the boxes below.

A:
B:
B:
A:
OH
OH
NO2 [1]
NH2 [1]
Paracetamol can be easily hydrolysed by aqueous NaOH. In the spaces

below, write the formulae of the two products.
(iii)
C:
D:
C:
D:
Ans
CH3COO-Na+
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7
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O-Na+
N
H
[6]
(b)
One of the causes of fever is bacterial infection. Alcohol (ethanol) solutions are
used as disinfectants on the skin as it can penetrate the bacterial cell wall and
denature the proteins inside the cell.
(i)
What do you understand by the term denaturation of proteins?
Denaturation of proteins refer to the disruption of the shape of the

protein molecule without altering its primary structure but resulting in the
loss of biological activity.
(ii)
The part of the protein molecule which is affected by the ethanol added is as
follows:
O
CH2
H
O
CH2
H
represents R group interaction
Suggest what R group interaction was disrupted by ethanol.
(iii)
Ethanol disrupts the intermolecular hydrogen bonds

Another application of denaturation is found in the making of cheese. Casein
is the predominant protein found in milk. When Lactobacillus bacterium is
added to milk, lactic acid (2-hydroxypropanoic acid) is produced.
CH3
O
CH
HO
PRELIM 2 INNOVA
9647/02/2012
C
OH
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Besides hydrogen bonding, suggest and write an equation to explain
what R group interaction is disrupted in this case.
Explanation ............................................
.........
Equation
Lactic acid produced disrupts the ionic bonds in the protein
-COO - + H + -COOH
[4]
(c)
The following table compares the pKa values of ethanol, 2-hydroxypropanoic acid
with that of ethanoic acid.
(i)
compound
formula
pKa
Ethanol
CH3CH2OH
15.9
CH3CHOHCOOOH
3.86
Ethanoic acid
CH3COOH
4.76
Suggest a reason why pKa value of ethanoic acid is so much less than ethanol.
Comparing the pKa values, ethanoic acid is more acidic] than alcohol
because
CH3CH2O- + H3O+
CH3CH2OH + H2O
For the ethoxide ion, CH3CH2O-, the electron donating ethyl group
intensifies the negative charge on the oxygen atom of the anion (ethoxide
PRELIM 2 INNOVA
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ion).Thus, the anion is not stable, hence less acidic than ethanoic acid.
CH3COOH + H2O
CH3COO- + H3O+
For the ethanoate ion, there is a delocalisation of the negative charge

over the two oxygen atoms. . This disperses the negative charge and
stabilises the anion. Thus CH3COO- is more stable than CH3CH2O-.
(ii)
Suggest a reason why 2-hydroxypropanoic acid is more acidic that ethanoic

acid.
[3]
The higher acidity is due to the stabilisation of the carboxylate ion by
intramolecular hydrogen bonding with the hydroxy group.
(d)
The degree of dissociation (ionisation) of ethylamine (CH3CH2NH2) in 0.010 moldm-3

aqueous solution is 0.17.
(i)
Calculate the hydroxide ion concentration of this solution.

Ans:
[OH-] = concentration x degree of dissociation = c
= 0.010 x 0.17 = 0.0017 = 1.7 x 10-3
(ii)
Calculate a value for the base dissociation constant, Kb, for ethylamine
(CH3CH2NH2), stating the units.
Kb =
[OH ][CH 3CH 2 NH 3 ] (1.7 x10 3 ) 2

=
= 2.89 x 10-4 mol dm-3
[CH 3CH 2 NH 2 ]
0.01
[2]
[Total: 15]
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(a)
Nucleophiles are electron-rich species that can donate electrons and attack regions of low
electron density.
O
R
OH
R1
+ Nu
R1
Reaction 1
Nu
O
O
R
+ Nu
Nu
Reaction 2
where X: Cl, Br, I
The intermediates, X and Y, shown below are formed by nucleophilic attack on the
above two different compounds containing a carbonyl group of low electron density.
(i)
State the nucleophile to form intermediate X and Y respectively.

Nucleophile for intermediate X: .
Nucleophile for intermediate Y: ..
[2]
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Nucleophile for intermediate X:: CN

Nucleophile for intermediate Y:: NH3
(ii)
Identify the organic starting material to form intermediate X.

[1]
Butan-2-one or CH3CH2COCH3
(iii)
State the type of reaction that gives intermediate Y.

..[1]
(iv)
Describe a mechanism for the complete reaction in which Y is an intermediate.

[3]
(b)
In a reaction discovered just over 100 years ago by the German chemist Karl Fries,
compound G is converted into compound K when it is heated with AlCl3.
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Compound K is a structural isomer of G.
H3C
AlCl 3
K (C8H8O2)
Compound G
Compound K is a 1,4-disubstituted benzene derivative. It is insoluble in water, but

dissolves in NaOH(aq). It gives a white precipitate with Br2(aq), and a yellow precipitate
(i)
Use the information given above to name the functional groups in compound K.
..
..
Phenol & ketone
(ii)
Suggest the structural formula of K.

OH
COCH3
(iii)
Suggest structures for the aromatic products of the following reactions.
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[5]
With I2 + NaOH:
With Br2(aq)
O-
With NaOH(aq)
OH
Br
COO-
Br
COCH3
[Total: 12]
(a)
An element M forms an oxide which is a powerful oxidising agent.

An acidified solution of the oxide of M, MOx (x = 1, 2 or 3) will oxidise Mn2+(aq) to
MnO4(aq), itself reduced to the element M.
When 10.0 cm3 of 0.5 mol dm-3 of MOx was reacted with 0.40 moldm-3 Mn2+(aq) in
PRELIM 2 INNOVA
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14
the presence of H+(aq), 15.0cm3 of Mn2+(aq) was needed for complete reaction.
(i)
Calculate the number of moles of electrons donated by Mn2+.
Mn2+ + 4H2O MnO4 + 8H+ + 5e

Mol of Mn2+ =
15
x 0.40 = 6.00 x 10-3 mol
1000
Mol of e donated by Mn2+ = 5 x 6.00 10-3 = 0.03 mol = mol of e accepted by MOx
(ii)
Calculate the mole ratio of MOx and electrons accepted by MOx.

Mol of MOx =
10
x 0.5 = 5.00 x 10-3 mol
1000
MOx : mol of e accepted by MOx

5 x 10-3: 0.03
1: 6
(iii)
Determine the original oxidation number of M and the value of x.

MOx + 6e M
Original oxidation number of M = + 6
(iv)
x=3
Construct an equation for the reaction between MOx(aq) and acidified
Mn2+(aq).
[O]: Mn2+ + 4H2O MnO4 + 8H+ + 5e

[R]: MO3 + 6e + 6H+ M + 3H2O
Overall: 6Mn2+ + 9H2O + 5MO3 6MnO4 + 18H+ + 5M
(b)
Water, H2O, covers 70.9% of the Earths surface and is vital for all known forms of
life. About 0.005% of water molecules consist of an oxygen atom bonded to two
atoms of the hydrogen isotope, deuterium, 21 D.
Deuterium oxide, D2O, is known as heavy water and is used for research in
chemical reactions because deuterium atoms react less quickly than normal
hydrogen atoms, 11 H.
Like H2O, pure D2O is weakly ionised.
2D2O
D3O+ + OD
For D2O, we can use the term KD instead of KW and pD instead of pH.
(i)
Explain what is meant by dynamic equilibrium.

Dynamic equilibrium is a system in which the forward and the backward
reactions are taking place at the same rate and thus the concentrations of
reactants and products remain constant.
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15
(ii)
For
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For pure D2O, KD = 1.35 x 10-15. Calculate the values of the following.
I. [D3O+]
II. pD
(I) [D3O+] = (1.35 x 10-15)1/2 = 3.67 x 10-8 mol dm-3
(II) pD = lg(3.67 x 10-8) = 7.43
(iii)
For this system, KD increases when temperature increases. Suggest and

explain whether the ionic dissociation of heavy water is an exothermic or
endothermic process.
As temperature increases, position of equilibrium shifts to the right since KD
increases. By LCP, increase in temperature favours endothermic reaction by
absorbing additional heat. Thus ionic dissociation of heavy water is
endothermic.
[5]
(iv)
When pure H2O and pure D2O are mixed, exchange of H and D atoms takes
place and the following equilibrium is established.
D2O(l) + H2O(l)
2HDO(l)
A mixture of 30 g of D2O and 27g of H2O was placed in a vessel at 298 K. At

equilibrium, it was found that the degree of dissociation of D2O is 0.49.
Calculate the Kc for this system.
[2]
30
= 1.5 mol
20
27
Mol of H2O =
= 1.5 mol
18
Mol of D2O =
ninitial / mol
D2O(l)
1.5
+ H2O(l)
1.5
2HDO(l)
0
change / mol 1.5 x 0.49

= 0.735 0.735
+1.47
nfinal / mol
1.47
0.765
0.765
1.47 2
(
)
[ HDO] 2
V
Kc =
3.69
0.765 2
[ H 2 O][ D2 O]
(
)
V
[Total: 11]
6
Many copper minerals are found in hydrothermal deposits where they were formed by
crystallization from very hot solutions which were trapped underground at high pressures.
One such copper mineral is chalcopyrite, CuFeS2.
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16
Copper is extracted from the ore chalcopyrite (CuFeS2) in a three-stage process.
In the first stage of this extraction, the chalcopyrite is heated with silicon dioxide and
oxygen.
(a)
Balance the following equation for this first stage in which copper sulfide is formed.
...CuFeS2 + ..SiO2 + ..O2
Cu2S + .FeSiO3 + SO2

[1]
2CuFeS2 + 2SiO2 + 4O2

(b)
Cu2S + 2FeSiO3 + 3SO2
Write the electronic configuration for Cu+ in Cu2S:

Cu+
1s2 2s2 2p6 3s2 3p6 3d10
[1]
(c)
When water is added to white anhydrous CuSO4, the solid dissolves to give a blue
solution. On addition of concentrated NH4Cl (aq), the solution changes to a yellowgreen due to formation of copper containing species D. Concentrating the solution
produces green crystals E of an ammonium salt with empirical formula CuN2H8Cl4.
(i)
Suggest the formulae of cation present in E.

Cation present in E ........................................
NH4+
(ii)
Suggest the formulae of anion present in D

Identify of D
CuCl42-
(iii)
Suggest a balanced equation for the formation of D from aqueous CuSO4.
Cu(H2O)62+ (aq) + 4Cl- (aq) CuCl42- + 6H2O
When excess of NH3 (aq) is added to species D, the yellow green solution turns to a
deep blue solution.
(iii) Use this information and the information above to suggest the strength of NH3,
H2O and Cl ligands in decreasing order.
> >
NH3>Cl->H2O
[4]
(d)
When a dilute aqueous solution containing a bidendate ligand, ethanedioate ion

(C2O42-) is added to a solution containing aqueous copper(II) ions, a ligand exchange
reaction occurs. In this reaction, four water molecules in the hydrated copper ion are
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17
For
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replaced and a new complex F is formed.
(i)
Explain what is meant by a bidendate ligand.

Ligands which contains two groups that have a lone pair of electrons each
which can be donated to the central metal ion, forming two dative bonds.
(ii)
Identity of F .
[Cu(C2O4)2(H2O)2]2-
In the complex F formed, the two water molecules are opposite each other. Draw a
diagram to show how the ethanedioate ions are bonded to a copper ion and give a
value for one of the O-Cu-O bond angles. You are not required to show the water
molecules.
(iii)
Diagram of Complex F
(iv)
O-Cu-O bond angle:

90o
[4]
PRELIM 2 INNOVA
9647/02/2012
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INNO
OVA JUNIOR COL
LLEGE
JC 2 PRELIMINARY E
EXAMINA
ATION 2
in prep
paration for General Ce
ertificate of Education Advanced
A
LLevel
Higher 2
CANDIDAT
TE
NAME
DEX NUMB
BER
IND
CLASS
CHEMIISTRY
Paper 3 Frree Respon
nse
9647/03
14 Septem
mber 2012
2 hours

Additional Materials: Writing Pa
apers
Data book
klet
Cover Pag
ge
READ THE
ESE INSTR
RUCTIONS FIRST
Write yourr name and class on all the work yyou hand in.
Write in da
ark blue or black
b
pen on both side
es of the pap
per.
You may u
use a soft pencil for any
y diagrams , graphs or rough work
king.
Do not use
e staples, paper clips, highlighters
h
s, glue or co
orrection fluid.
Answer 4 o
out of 5 questions.
Begin each
h answer on
n a fresh sh
heet of pape
er.
You are ad
dvised to sh
how all work
king in calcu
ulations.
You are re
eminded of the
t need for good Eng lish and cle
ear presenta
ation in you r answers.
You are re
eminded of the
t need for good hand
dwriting.
Your final a
answers sh
hould be in 3 significantt figures.
At the end of the exam
mination, fa
asten all you
ur work securely togeth
her.
The numbe
er of markss is given in the bracketts [ ] at the end of eac
ch question or part que
estion.
This document consists o

of 13 printed
d pages and
d 1 blank paage.
Innova Junio
or College
[T
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2
Answer 4 out of 5 questions.
1
(a)
(b)
N,N-dimethyltryptamine is a psychoactive drug whose primary action is to alter

cognition and perception. Depending on the dose and method of administration, its
subjective effects can range from short-lived milder psychedelic states to powerful
immersive experiences.
(i)
Suggest a reason why N,N-dimethyltryptamine is soluble in acidic solutions.
(ii)
Would you expect N,N-dimethyltryptamine to have a high or low melting point?

Explain your answer in terms of structure and bonding.
[4]
para-Methoxyamphetamine first came into circulation in the early 1970s and went by
the street names of "Chicken Powder" and "Chicken Yellow" and was found to be
the cause of a number of drug overdose deaths in the United States and Canada at
that time. It can be synthesised by the following route.
(i)
Suggest reagents and conditions for steps II and III.
(ii)
What type of reaction is step II?
(iii) Suggest why compound J is converted into K before step II is carried out.
(iv)
What type of stereoisomerism does para-methoxyamphetamine exhibits? Draw

the structures of the stereoisomers of para-methoxyamphetamine.
[6]
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9647/03/2012
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3
(c)
(d)
Propene is an important starting product in the petrochemical industry and is often

used as the raw material for a wide variety of products.
(i)
Name and describe the mechanism of the reaction between propene and
hydrogen bromide.
(ii)
The bromine atom in the product from (i) is very reactive towards nucleophilic
reagents. The bromine atom in 1bromopropene is unreactive towards
nucleophilic reagents. Suggest an explanation for the unreactivity of the
bromine atom in 1bromopropene.
[5]
Compound P is a neutral, sweet-smelling liquid with molecular formula C5H8O2. It

reacts with hot sulfuric acid to give a single compound Q, C5H10O3. Q has two
stereoisomers and gives a pale yellow precipitate with alkaline iodine and
compound R. Deduce the structures of P, Q and R.
[5]
[Total:20]
PRELIM 2 INNOVA
9647/03/2012
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4
2
(a)
(b)
(c)
When a precipitate is formed, Gppt, in kJ mol-1, is given by the following

expression.
2.303RT log K sp
Gppt =
1000
(i)
Given that the Ksp value of BaF2 is 1.70 x 10-6 at 298 K, calculate Gppt, in
kJ mol-1, for BaF2.
(ii)
The standard enthalpy change of formation of BaF2 is 858 kJ mol-1. Use your
answer in (a)(i) to calculate Sppt, in J mol-1 K-1 for the formation of the
precipitate at 298 K.
(iii)
Explain the significance of the sign of your answer in (ii).
(iv)
Predict and explain whether the precipitation will be feasible at high or low
temperature.
(v)
Suggest how the magnitude of the lattice energy of BaF2 might compare to that
of BaCl2. Explain your answer.
[7]
In the past, chemical analysis was carried out by chemists using traditional
laboratory apparatus. Many qualitative tests used depended on an application of the
principles of solubility product.
(i)
Write an expression for the Ksp of barium fluoride.
(ii)
Predict whether precipitation occurs if 50.0 cm3 of 0.150 mol dm3 of Ba(OH)2
solution is mixed with 50.0 cm3 of 0.100 mol dm3 of KF solution in the
laboratory.
The Ksp of BaF2 is 1.70 x 10-6 mol3 dm-9.
[3]
Myrcene is a naturally occurring compound found in the leaves of bay trees. It is

known to be a polyunsaturated hydrocarbon. It can react with hydrogen to produce a
saturated hydrocarbon.
In a laboratory investigation, a 1.00 g sample of pure myrcene fully reacted with
exactly 510 cm3 of hydrogen gas measured at 20.0C and 105.0 kPa. In this
reaction, myrcene was converted to a saturated alkane with a molecular formula
C10H22.
(i)
What type of reaction has occurred between the myrcene and hydrogen?
(ii)
Calculate the amount, in moles, of hydrogen reacting.
(iii)
Calculate the mass of C10H22 produced in the reaction.
(iv)
Determine the number of double bonds in each molecule of myrcene.

[6]
PRELIM 2 INNOVA
9647/03/2012
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5
(d)
In September 2009, the wholesale of weedkiller containing chlorate(V) ions was

banned in various European countries.
Chlorate(V) ions can act as a strong oxidising agent in acid solution according to the
following half equation:
ClO3(aq) +6H+(aq) + 6e Cl(aq) + 3H2O(l)
In an experiment, 25.0 cm3 of a sample of sodium chlorate(V) solution reacted with
an excess of sodium iodide, NaI. The iodine produced required 25.00 cm3 of
1 mol dm-3 of sodium thiosulfate, Na2S2O3, for complete reaction.
(i)
Write a balanced equation between chlorate(V) ions and iodide ions in acidic
medium.
(ii)
Calculate the number of moles of iodine liberated by the chlorate(V) solution.
(iii)
Calculate the concentration of sodium chlorate(V) in the solution.

[4]
[Total: 20]
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6
3
(a)
A sample of aspirin was prepared by reacting 2.20 g of salicylic acid with 4.20 cm3 of
ethanoic anhydride in a conical flask. After heating for 20 minutes the reaction
mixture was cooled and white crystals precipitated. The crystals were then collected,
dried to constant mass and weighed.
The equation for the reaction is:
The following results were obtained.

mass of salicylic acid
volume ethanoic anhydride
mass of product
2.20 g
4.20 cm3
2.25 g
Use the following data to answer the questions below.
aspirin
ethanoic anhydride
salicyclic acid
molar mass (g mol-1)

180
102
138
density (g cm-3)
1.08
(i)
Calculate the initial amount, in moles, of salicylic acid used in this

preparation.
(ii)
What initial amount, in moles, of ethanoic anhydride was used?
(iii)
What is the maximum mass of aspirin that can theoretically be produced from
these reagents?
(iv)
Determine the percentage yield in this preparation.
(v)
To check whether the aspirin obtained is contaminated with salicyclic acid, a

simple chemical test can be carried out. Suggest what reagent can be used
and state the observation.
(vi)
In carrying out the above preparation, the acid anhydride used must not
contain moisture. Write an equation for the reaction between ethanoic
anhydride with water.
(vii)
Acid chlorides closely resemble the acid anhydrides in chemical reactions.

They also react with nucleophilic reagents but at a faster rate and therefore
more difficult to handle.
Suggest another reason why ethanoyl chloride is not used in the above
preparation of aspirin.
[7]
PRELIM 2 INNOVA
9647/03/2012
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7
(b)
A compan
ny wish to manufacture
m
e solid oxide
e fuel cell fo
or use in thee home. Th
hese fuel
cells usess natural ga
as to prod uce electric
city through
h an electrrochemical process
summarise
ed in the dia
agram belo w.
(i)
Wrrite an equa
ation for the
e reaction at
a the cathode where aatmospheric
c oxygen
is converted
c
to
o oxide ionss.
(ii)
A complex se
eries of rea
kes place at
a the anodde. These may be
actions tak
sum
mmarised by
b the half-e
equation:
4O2-(g) + C
CH4(g)
CO2(g) + 2H2O(g)) + 8e
Wrrite an equa
ation that re
epresents th
he overall re
eaction thatt takes plac
ce in this
fue
el cell.
(iii)
Suggest one way

w in whicch a fuel cell differs from
m other galvvanic cells.
[3]
(c)
cation of co
opper can be
e carried ou
ut in an appparatus similar to
The electrrolytic purific
the one sh
hown below
w.
impurre copper anode
pure copper cathode
anode slludge
CuSO
C
4(aq)
Most of th
he current passed
p
thro
ough the cell is used to dissolvee the coppe
er at the
anode and
d precipitate
e pure copp
per onto the
e cathode. However,
H
a small prop
portion of
it is waste
ed in dissolv
ving the imp
purities at the anode which
w
then re
remain in so
olution.
When a current of 20
0.0 A was p
passed thro
ough the ce
ell for 10.0 hours, it wa
as found
that 225 g of pure cop
pper was de
eposited on
n the cathod
de.
Calculate the followin
ng, using ap
ppropriate data from the
e Data Boooklet,
(i)
num
mber of mo
oles of copp
per produced
d at the cathode
(ii)
num
mber of mo
oles of elect rons neede
ed to produc
ce this coppper
PRELIM 2 INNOVA
9647/03/20
012
[T
Turn over
(d)
(iii)
number of moles of electrons that passed through the cell
(iv)
Hence calculate the percentage of the current through the cell that has been
wasted in dissolving the impurities at the anode.
[4]
(i)
State what is meant by an acidic buffer solution.
(ii)
Explain, using relevant equations, how a mixture of HClO and NaClO can
regulate pH when relatively small amount of acid or base is added to the
solution.
(iii)
Explain why NaClO exists as a solid whereas HClO exists as a liquid under
standard condition.
[6]
[Total: 20]
PRELIM 2 INNOVA
9647/03/2012
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9
4
(a)
By considering the likely mechanism of each reaction, suggest reasons why

reaction I below must be heated for some time for it to occur, whereas reaction II
takes place almost instantaneously at room temperature.
CH3CH2CH2Br(l) + NaOH(aq) CH3CH2CH2OH(aq) + NaBr(aq)
reaction I
HBr(aq) + NaOH(aq) H2O + NaBr(aq)
reaction II
[2]
(b)
How would the rate of reaction between CH3CH2CH2Cl(l) and NaOH(aq) compare to
that of reaction I? Use appropriate data from the Data Booklet to explain your
answer.
[2]
(c)
In the presence of ethanolic potassium hydroxide, there is a competition between

substitution and elimination of the bromoalkane. The data below shows some
examples.
n
o
i
t
a
n
i
m
i
l
e
Type of
bromoalkane
Conditions
(CH3)2CHBr
Secondary
(CH3)2CHBr
Secondary
(CH3)3CBr
Tertiary
2 mol dm-3 OH- in 60 %

ethanol*
2 mol dm-3 OH- in 80 %
ethanol*
2 mol dm-3 OH- in
100 % ethanol
n
o
i
t
u
t
i
t
s
b
u
s
Formula of
bromoalkane
ratio
1.5
2.2
13.0
* the remainder is water

Using the data given above, draw the structural formula of the major product of each
of the following reactions:
(i)
Heating (CH3)2CHCH2Br with NaOH(aq)
(ii)
Heating CH3CH2CHBrCH2CH3 with NaOH in 100 % ethanol
(iii)
Heating (CH3)3CBr with NaOH in 100 % ethanol

[3]
(d)
The rate constant for the reaction of CH3CH2CHBrCH3 and KCN was measured at
various temperatures and the results are shown below.
T/ K
k/ s-1
300
3.7 x 10-5
310
9.4 x 10-5
320
5.5 x 10-4
330
2.0 x 10-3
(i)
Deduce the overall order of this reaction.
(ii)
From the plotted graph given and by using the modified Arrhenius equation,
T
E aR
ln k = constant
determine the activation energy, Ea, of the reaction.
PRELIM 2 INNOVA
9647/03/2012
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10
P lot of ln k ag
gainst
(ii)
Estim
mate the ra
ate constan
nt of the reaction at 340 K and hhence calculate the
half--life of the re
eaction at th
he same tem
mperature.
[5]
Caffe
eine is a sttimulant fou
und in coffee and tea. It is also addded to colla drinks.
The structure off caffeine iss given belo
ow.
(e)
(i)
Copyy the above

e structure and label (with
(
a *) all
a the carboon atoms with
w bond
angles of 109 ..
(ii)
On the structure
e that you h
have drawn,, draw a circ
cle round ann amide gro
oup.
PRELIM 2 INNOVA
9647/03/20
012
[T
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11
(iii)
Deca
affeinated coffee
c
and tea are ma
ade by extracting the caffeine frrom solid
coffe
ee or tea us
sing a solve nt.
Sugg
gest, with tw
wo reasonss, which of the followin
ng industriaal solvents would
w
be
the most
m
suitable.
Benzene
e
A hydroc
carbon, succh as cycloh
hexane
Liquid ca
arbon dioxid
de
[5]
(f)
Iron is an
n extremely
y importantt metal used in haem
moglobin too transportt oxygen
moleculess from the lu
ungs to mu
uscle cells and
a to carry
y carbon diooxide in the
e reverse
direction.
One haem
moglobin mo
olecule con
ntains four haem
h
group
ps, each of which conttains one
iron atom.. In the hae
em group fo
our nitrogen
n atoms are
e in the sam
me plane as
s the iron
atom. The
e oxygen mo
olecule is a
attached abo
ove this pla
ane, and thee iron atom is joined
to a protein chain below this plan
ne.
(i)
How
w many oxyg
gen atoms could one haemoglobi
h
n molecule transport?
(ii)
By what
w
type of
o bonding is the oxyg
gen molecule likely to be held to the iron
atom
m in haem?
(iii)
Wha
at is the geo
ometry of bo
onding arou
und the iron atom?
[3]
[Total:20]
[
PRELIM 2 INNOVA
9647/03/20
012
[T
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12
5
(a)
Bromine containing products, such as sodium bromate is frequently used in hair

straightener and conditioning products.
(i)
Write a balanced equation for the reaction that can make a solution that
contains sodium bromate(I) under suitable condition in the laboratory.
(ii)
Bromine can be obtained from the sodium bromide dissolved in sea water by
the following step:
Blowing out the bromine with air and absorbing it in aqueous sodium
carbonate.
This step produces a mixture of solution Z and sodium bromide in the molar
ratio of 1:5. Z has the following composition by mass:
Na, 15.2%; Br, 52.9%; O, 31.8%
(iii)
(iv)
I.
Calculate the empirical formula of Z.
II.
Construct an equation for the formation of Z in the above step

mentioned.
An acidified aqueous solution of Z reacts with hydrogen sulfide, H2S, to give a

precipitate of sulfur and an orange red solution. On shaking with
trichloroethane, the colour is transferred to the organic layer.
I.
State the role of H2S and suggest an identity for the orange red
solution.
II.
Construct a balanced equation for the reaction.
When solid calcium fluoride reacts with concentrated sulfuric acid, gaseous
hydrogen fluoride is produced. A similar reaction occurs with solid calcium
chloride but with solid calcium bromide, bromine is formed.
I.
Write an equation for the reaction of solid calcium fluoride with

concentrated sulfuric acid.
II.
Explain why when reacted with concentrated sulfuric acid, solid calcium
bromide form bromine whereas solid calcium chloride forms hydrogen
chloride? Suggest a possible reaction product of the concentrated
sulfuric acid in the reaction.
[9]
PRELIM 2 INNOVA
9647/03/2012
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13
(b)
Acyl chlorides are useful intermediates for making various acid derivatives. The
following reaction shows two reactions of acyl chlorides.
Reaction scheme 1
Reaction scheme 2
(i)
Suggest the structures of acyl chlorides B and C used in reaction scheme 1

and 2.
(ii)
Suggest the type of polymer E.
(iii)
Both compound B and compound D are soluble in water.
(iv)
I.
Write a balanced equation when compound B dissolves in water and

describe the effect of the resulting solution on Universal Indicator
solution.
II.
Explain why compound D is soluble in water.
Suggest an observation for reaction scheme 2.

[7]
(c)
Ca2+ and Cl are isoelectronic but the radii of the ions are different.
(i)
Explain the term isoelectronic.
(ii)
With the aid of the Data Booklet, explain the above observation as fully as you can.
(iii)
State two ways in which the behaviour of Ca2+ ions in an electric field differs from
that of Cl ions.
[4]
[Total:20]
PRELIM 2 INNOVA
9647/03/2012
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14
BLANK PAGE
PRELIM 2 INNOVA
9647/03/2012
[Turn over
2012H2Prelim2Essaysolutions_13aug
(a)
N,N-dimethyltryptamine is a psychoactive drug whose primary action is to alter

cognition and perception. Depending on the dose and method of administration, its
subjective effects can range from short-lived milder psychedelic states to powerful
immersive experiences.
N
N
H
(i)
N,N-dimethyltryptamine
Suggest a reason why N,N-dimethyltryptamine is soluble in acidic solutions.

It will react with acid to form a salt / cation which is able to form ion-dipole
interactions with water molecules.
(ii)
Would you expect N,N-dimethyltryptamine to have a high or low melting point?

Explain your answer in terms of structure and bonding.
It is expected to have a low melting point. It has a simple molecular structure
with weak van der Waals forces between molecules. Thus less energy is
required to break the weak forces.
[4]
(b)
Propene is an important starting product in the petrochemical industry and is often

used as the raw material for a wide variety of products.
(i)
Name and describe the mechanism of the reaction between propene and
hydrogen bromide.
[3]
Electrophilic Addition
Step 1
Step 2
(ii)
The bromine atom in the product from b(i) is very reactive towards nucleophilic
reagents. The bromine atom in 1bromopropene is unreactive towards
nucleophilic reagents. Suggest an explanation for the unreactivity of the
bromine atom in 1bromopropene.
[2]
In 1-bromopropene, the p orbital of Br overlaps with the orbital of adjacent C
atom, strengthening the C Br bond. Thus, the C Br bond is too strong to be
broken and hence unreactive towards nucleophilic reagents.
OR
In 1-bromopropene, the C atom is adjacent to the double bond and hence less
electron deficient and thus less susceptible to nucleophilic attacks.
(c)
para-Methoxyamphetamine first came into circulation in the early 1970s and went by
the street names of "Chicken Powder" and "Chicken Yellow" and was found to be
the cause of a number of drug overdose deaths in the United States and Canada at
that time. It can be synthesised by the following route.
(i)
Suggest reagents and conditions for steps II and III.

II: CH3Br / CH3I/ CH3Cl, heat with reflux
2
III: NH3 in ethanol, heat in a sealed tube
(ii)
What type of reaction is step II?

(iii) Suggest why compound J is converted into K before step II is carried out.
To generate a stronger nucleophile, phenoxide ion.
(iv)
What type of stereoisomerism does para-methoxyamphetamine exhibits? Draw

the structures of the stereoisomers of para-methoxyamphetamine.
Optical isomerism
O
CH2
CH2
C
H
H2N
NH2
CH3
mirror
C
H
CH3
[6]
(d)
Compound P is a neutral, sweet-smelling liquid with molecular formula C5H8O2. It

reacts with hot sulfuric acid to give a single compound Q, C5H10O3. Q has two
stereoisomers and gives a pale yellow precipitate with alkaline iodine and
compound R. Deduce the structures of P, Q and R.
P undergoes acidic hydrolysis with hot sulfuric acid to give Q. P is an ester.
Q contains CH3CH(OH) since it undergoes mild oxidation with alkaline iodine.
Q only contains 1 chiral carbon since it has two stereoisomers.
[5]
[Total:20]
(a)
When a precipitate is formed, Gppt, in kJ mol-1, is given by the following

expression.
Gppt =
(i)
2.303RT log K sp
1000
Given that the Ksp value of BaF2 is 1.70x10-6 at 298K, calculate Gppt, in
kJ mol-1, for BaF2.
Gppt = [2.303 x 8.31 x 298 x log (1.70x 10-6)] 1000 = -32.9 kJ mol-1
(ii)
The standard enthalpy change of formation of BaF2 is 858 kJ mol-1. Use your
answer in (a)(i) to calculate Sppt, in J mol-1 K-1 for the formation of the
precipitate at 298K.
G = H TS
-32.9 = -858 (298) S
S = -2.77 kJ mol-1K-1
= -2770 J mol-1K-1
(iii) Explain the significance of the sign of your answer in (ii).

The sign is negative which means that entropy decreases as the system is
more ordered/less disordered when there is a phase change from aqueous
to solid state.
(iv)
Predict and explain whether the precipitation will be feasible at high or low
temperature.
Since S is negative, (-T S) is always positive. At high temperature, the
magnitude of (-T S) would be greater than H. Hence G would be positive
and the reaction would not be feasible. Therefore the reaction is feasible at
low temperature.
(v)
Suggest how the magnitude of the lattice energy of BaF2 might compare to that
of BaCl2. Explain your answer.
Although fluoride ion and chloride ion have the same charge,
fluoride ion is smaller than chloride ion.
|L.E| |
q q
| or Since lattice energy is inversely proportional to the
r r
5
ionic radius
Therefore the magnitude of the lattice energy of BaF2 would be greater
than that of BaCl2.
[7]
(b)
In the past, chemical analysis was carried out by chemists using traditional
laboratory apparatus. Many qualitative tests used depended on an application of the
principles of solubility product.
(i)
Write an expression for the Ksp of barium fluoride.

Ksp = [Ba2+][F- ]2
(ii)
Predict whether precipitation occurs if 50.0 cm3 of 0.150 mol dm3 of Ba(OH)2
solution is mixed with 50.0 cm3 of 0.100 mol dm3 of KF solution in the laboratory.
The Ksp of BaF2 is 1.70 x 10-6 mol3 dm-9.
[Ba2+]new =
[F- ]new =
0.150
= 0.075 mol dm-3
2
0.100
= 0.05 mol dm-3
2
IP = [Ba2+][F- ]2 = 0.075 x (0.05)2 = 1.875 x 10-4 mol3 dm-9
1.875 x 10-4 mol3 dm-9 > Ksp
Precipitation occurs.
[3]
(c)
Myrcene is a naturally occurring compound found in the leaves of bay trees. It is

known to be a polyunsaturated hydrocarbon. It can react with hydrogen to produce a
saturated hydrocarbon.
In a laboratory investigation, a 1.00 g sample of pure myrcene fully reacted with
exactly 510 cm3 of hydrogen gas measured at 20.0C and 105.0 kPa. In this
reaction, myrcene was converted to a saturated alkane with a molecular formula
C10H22.
What type of reaction has occurred between the myrcene and hydrogen?
(i)
Addition of hydrogen /hydrogenation/redox/ reduction
(ii)
Calculate the amount, in moles, of hydrogen reacting.

no of moles of H2 = pV / RT
= 105 x 103 x 510 x 10-6 / (8.31 x [20.0 +273])
= 0.0220 mol
(iii) Calculate the mass of C10H22 produced in the reaction.

mass of C10H22 = mass of myrcene + mass of H2
6
mass of H2 = 0.0220 x 2.0 = 0.044 g
mass of C10H22 = 1.00 + 0.0440 = 1.04 g
(iv)
Determine the number of double bonds in each molecule of myrcene.

no of moles of C10H22 = 1.044 / 142 = 7.35x10-3 mol = n(myrcene)
equation for reaction is myrcene + xH2 C10H22
n(H2) / n(myrcene) = x / 1
0.0220 / 7.35x10-3 = x
3=x
3 molecules of H2 added to each myrcene molecule. Hence there are 3 C=C
double bonds.
The following is an alternate approach.
no of moles of C10H22 = 7.35x10-3 mol
no of moles of myrcene = 7.35x10-3
Molar mass of myrcene = 1.0 / 7.35x10-3= 136 g mol-1
molar mass of myrcene is 6 less than molar mass C10H22.
3 H2 molecules added to each myrcene molecule
3 C=C double bonds.
One mark was awarded if 3 double bonds was stated, but to obtain the second
mark a logical explanation of how the number of double bonds was determined
was required.
[6]
(d)
In September 2009, the wholesale of weedkiller containing chlorate(V) ions was

banned in various European countries.
Chlorate(V) ions can act as a strong oxidising agent in acid solution according to the
following half equation:
ClO3 (aq) +6H+ (aq) + 6e Cl (aq) + 3H2O(l)
In an experiment, 25.0 cm3 of a sample of sodium chlorate(V) solution reacted with
an excess of sodium iodide, NaI. The iodine produced required 25.00 cm3 of
1 mol dm-3 of sodium thiosulfate, Na2S2O3, for complete reaction.
(i)
Write a balanced equation between chlorate(V) ions and iodide ions in acidic
medium.
[R] ClO3- +6H+ + 6e Cl- + 3H2O
[O] 2I- I2 + 2e
Overall: ClO3- +6H+ + 6I- Cl- + 3H2O + 3I2
(ii)
Calculate the number of moles of iodine liberated by the chlorate(V) solution.

[R] :
I2 + 2e
2I
[O] :
2S2O32
S4O62 + 2e
I2 + 2S2O32
2I + S4O62
No of moles of thiosulfate =
25
x 1 = 0.025 mol
1000
No of moles of iodine = 0.025 2 = 0.0125 mol

(iii) Calculate the concentration of sodium chlorate(V) in the solution.
Mole Ratio
ClO- : I2
1:3
No of moles of chlorate = 0.0125 3 = 4.167 x 10-3 mol

Concentration of sodium chlorate(V) =
4.167 x10 3
= 0.167 mol dm-3
25
1000
[4]
[Total: 20]
(a)
A sample of aspirin was prepared by reacting 2.20 g of salicylic acid with 4.20 cm3 of
ethanoic anhydride in a conical flask. After heating for 20 minutes the reaction
mixture was cooled and white crystals precipitated. The crystals were then collected,
dried to constant mass and weighed.
O
O
O
C
OH
H
O
OH
C
CH3
O
C
O
CH3
CH3
+ CH3
C
OH
salicyclic acid(s)
ethanoic anhydride(l)
aspirin(s)
The following results were obtained.

mass of salicylic acid
volume ethanoic anhydride
mass of product
2.20 g
4.20 cm3
2.25 g
Use the following data to answer the questions below.
aspirin
ethanoic anhydride
salicyclic acid
(i)
molar mass (g mol-1)

180
102
138
Calculate the initial amount, in moles, of salicylic acid used in this preparation.
no of moles of salicylic acid =
(ii)
density (gcm-3)
1.08
2.20
= 0.0159 mol
138
What initial amount, in moles, of ethanoic anhydride was used?

mass of ethanoic anhydride = Volume x Density
= 4.20 x 1.08 g
no of moles of ethanoic anhydride = 4.20 x
1.08
= 0.0445 mol
102
(iii) What is the maximum mass of aspirin that can theoretically be produced from
these reagents?
Salicylic acid is the limiting reagent
no of moles of aspirin = no of moles of salicylic acid = 0.0159 mol
mass of aspirin = 0.0159 x 180 = 2.86 g
(iv)
Determine the percentage yield in this preparation.

9
% yield = [mass of aspirin collected/mass of aspirin theoretical] x 100

=
2.25
x 100
2.86
= 78.4 %
To check whether the aspirin obtained is contaminated with salicyclic acid, a
simple chemical test can be carried out. Suggest what reagent can be used
and state the observation.
(v)
Neutral FeCl3 (aq)(reacts with phenol), forming purple coloration

OR
Br2(aq), orange decolourise & white ppt formed.
In carrying out the above preparation, the acid anhydride used must not
contain moisture. Write an equation for the reaction between ethanoic
anhydride with water.
(vi)
O
H
C
O
CH3
O
CH3
CH3
+ CH3
O
H2O
C
CH3
(vii)
C
OH
C
O
CH3
2CH3COOH
Acid chlorides closely resemble the acid anhydrides in chemical reactions.

They also react with nucleophilic reagents but at a faster rate and therefore
more difficult to handle.
Suggest another reason why ethanoyl chloride is not used in the above
preparation of aspirin.
HCl fumes will be produced which is a toxic gas
(b)
[7]
A company wish to manufacture solid oxide fuel cell for use in the home. These fuel
cells uses natural gas to produce electricity through an electrochemical process
summarised in the diagram below.
(i)
Write an equation for the reaction at the cathode where atmospheric oxygen is
10
converted to oxide ions.
O2(g) + 4e
Or
(ii)
1
O2(g) + 2e
2
2O2-(g)
O2-(g)
A complex series of reactions takes place at the anode. These may be

summarised by the half-equation
4O2-(g) + CH4(g)
CO2(g) + 2H2O(g) + 8e
Write an equation that represents the overall reaction that takes place in this
fuel cell.
CH4(g) +2O2(g)
CO2(g) + 2H2O(g)
(iii) Suggest one way in which a fuel cell differs from other galvanic cells.
fuel cells require a continuous supply of reactants, whereas in a galvanic cell
they are stored in the cell
or
some products are removed from fuel cells
or
fuel cell electrodes are porous.
[3]
(c)
The electrolytic purification of copper can be carried out in an apparatus similar to

the one shown below.
Most of the current passed through the cell is used to dissolve the copper at the
anode and precipitate pure copper onto the cathode. However, a small proportion of
it is wasted in dissolving the impurities at the anode which then remain in solution.
When a current of 20.0 A was passed through the cell for 10.0 hours, it was found
that 225 g of pure copper was deposited on the cathode.
Calculate the following, using appropriate data from the Data Booklet.
(i)
number of moles of copper produced at the cathode

amount of copper =
(ii)
225
= 3.54 mol
63.5
number of moles of electrons needed to produce this copper

amount of electrons needed = 2 3.54 = 7.08/9 (7.087) mol
11
(iii) number of moles of electrons that passed through the cell

no. of coulombs = 20 10 60 60 = 7.2 105 C
no. of moles of electrons =
(iv)
7.2 10 5
= 7.46 mol
96500
Hence calculate the percentage of the current through the cell that has been
wasted in dissolving the impurities at the anode.
[4]
percentage wasted = 100
(7.461 7.087)
= 5.01 (5.0)%
7.461
[4]
(d)
(i)
State what is meant by an acidic buffer solution.

Acidic buffer solution is a mixture of a weak acid and its soluble salt
and resist pH changes when little amount of acid or alkali is added.
(ii)
Explain, using relevant equations, how a mixture of HClO and NaClO can
regulate pH when relatively small amount of acid or base is added to the
solution.
Small additional H+ ions are removed by the large reservoir of NaClO
NaClO + H+ HClO + Na+
Small additional OH ions are removed by large reservoir of HClO

HClO + OH- ClO + H2O
(iii) Explain why NaClO exists as a solid whereas HClO exists as a liquid under
standard condition.
NaClO has giant ionic structure which consists of strong electrostatic forces of
attraction between oppositely charged ionswhereas HClO has simple
molecular structure which consists of weak van der Waals forces between
molecules.
Less energy is needed to break the weak VDW. Hence NaClO exists as a
solid whereas HClO exists as a liquid.
2 correct structures stated[6]
[Total: 20]
12
(a)
By considering the likely mechanism of each reaction, suggest reasons why

reaction I below must be heated for some time for it to occur, whereas reaction II
takes place almost instantaneously at room temperature.
CH3CH2CH2Br(l) + NaOH(aq) CH3CH2CH2OH(aq) + NaBr(aq)
HBr(aq) + NaOH(aq) H2O + NaBr(aq)
II
[2]
Reaction I involves breaking of strong covalent bonds, thus heat is required.

Reaction II involves reaction of opposite charge ions attracting one another,
thus the reaction occurs instantaneously.
(b)
How would the rate of reaction between CH3CH2CH2Cl(l) and NaOH(aq) compare
to that of reaction I? Use appropriate data from the Data Booklet to explain your
answer.
[2]
This hydrolysis reaction involves breaking of C-X bond. Since C-Cl bond (BE of
340 kJ mol-1) is stronger] than that of C-Br bond (BE of 280 kJ mol-1), the rate
of hydrolysis to break C-Cl bond in CH3CH2CH2Cl(l) is slower.
(c)
In the presence of ethanolic potassium hydroxide, there is a competition between

substitution and elimination of the bromoalkane. The data below shows some
examples.
n
o
i
t
a
n
i
m
i
l
e
Type of
bromoalkane
Conditions
(CH3)2CHBr
Secondary
2 mol dm-3 OH- in

60 % ethanol*
1.5
(CH3)2CHBr
Secondary
2 mol dm-3 OH- in

80 % ethanol*
2.2
(CH3)3CBr
Tertiary
2 mol dm-3 OH- in

100 % ethanol
13.0
n
o
i
t
u
t
i
t
s
b
u
s
Formula of
bromoalkane
ratio
* the remainder is water
Using the data given above, draw the structural formula of the major product of
each of the following reactions:
13
[3]
(i)
Heating (CH3)2CHCH2Br with NaOH(aq)

(CH3)2CHCH2OH
(ii)
Heating CH3CH2CHBrCH2CH3 with NaOH in 100 % ethanol

CH3CH2CH=CHCH3
(iii)
Heating (CH3)3CBr with NaOH in 100 % ethanol

(CH3)2C=CH2
The rate constant for the reaction of CH3CH2CHBrCH3 and KCN was
measured at various temperatures and the results are shown below.
(d)
(i)
T/K
300
310
320
330
k/s-1
3.7 x 10-5
9.4 x 10-5
5.5 x 10-4
2.0 x 10-3
Deduce the overall order of this reaction.

[1]
1st order because the unit of rate constant is s-1.
(ii)
From the plotted graph given and by using the modified Arrhenius equation,
ln k = constant Ea/ RT
14
determine the activation energy, Ea, of the reaction.
[2]
The slope of the line is found to be Ea /R

Thus, slope =
10 4.6
= -13500 = Ea /R
3.3 2.9 103
Ea = 112.2 kJ mol-1
(ii)
Estimate the rate constant of the reaction at 340 K and hence calculate the
half-life of the reaction at the same temperature.
[2]
From the graph at 340 K,
ln k = 5.10
15
thus, k = 6.10 x 10-3 s-1
since t1/2 = ln 2 /k = 114 s
Caffeine is a stimulant found in coffee and tea. It is also added to cola drinks.
The structure of caffeine is given below.
(e)
O
H3C
CH3
N
CH3
(i)
Copy the above structure and label (with a *) all the carbon atoms with bond
angles of 109 .
(ii)
On the structure that you have drawn, draw a circle round an amide group.
16
(iii) Decaffeinated coffee and tea are made by extracting the caffeine from solid
coffee or tea using a solvent.
Suggest, with two reasons, which of the following industrial solvents would be
the most suitable.
Benzene
A hydrocarbon, such as cyclohexane
Liquid carbon dioxide

[5]
Liquid carbon dioxide is the most suitable solvent

Reason 1: Liquid carbon dioxide is not toxic.
Reason 2: Liquid carbon dioxide has low boiling point & can be easily
evaporated off without leaving any odour.
(f)
Iron is an extremely important metal used in haemoglobin to transport oxygen

molecules from the lungs to muscle cells and to carry carbon dioxide in the reverse
direciton.
One haemoglobin molecule contains four haem groups, each of which contains one
iron atom. In the haem group four nitrogen atoms are in the same plane as the iron
atom. The oxygen molecule is attached above this plane, and the iron atom is
joined to a protein chain below this plane.
17
(i)
How many oxygen atoms could one haemoglobin molecule transport?

[1]
8 atoms (also allow 4 oxygen molecules)
(ii)
By what type of bonding is the oxygen molecule likely to be held to the iron
atom in haem?
[1]
Dative bond / co-ordinate bond
(iii) What is the geometry of bonding around the iron atom?

[1]
Octahedral / 6 co-ordinate
[Total:20]
18
5.
(a)
Bromine containing products, such as sodium bromate is frequently used in hair

straightener and conditioning products.
(i)
Write a balanced equation for the reaction that can make a solution that
contains sodium bromate(I) under suitable condition in laboratory.
Br2 + 2 NaOH NaBr + NaBrO + H2O
(ii)
Bromine can be obtained from the sodium bromide dissolved in sea water by
the following step:
Blowing out the bromine with air and absorbing it in aqueous sodium
carbonate.
This step produces a mixture of solution Z and sodium bromide in the molar
ratio of 1:5. Z has the following composition by mass:
Na, 15.2%; Br,52.9%; O,31.8%
I.
Calculate the empirical formula of Z.
II.
Construct an equation for the formation of Z in the above step

mentioned.
Na
Br
Mass in 100g
15.2
52.9
31.9
Mr
23.0
79.9
16.0
No. of moles
0.66
0.66
1.99
Simplest ratio
Empirical formula of Z : NaBrO3

II:
3 Br2 + 6 OH- BrO3- + 5 Br- + 3 H2O
(iii) An acidified aqueous solution of Z reacts with hydrogen sulphide, H2S, to give
a precipitate of sulphur and an orange red solution. On shaking with
trichloroethane, the colour is transferred to the organic layer.
19
State the role of H2S and suggest an identity for the orange red
solution.
II
Construct a balanced equation for the reaction.
I)
II
It is acting as a reducing agent.

Orange red solution is bromine.
Half equation:
H2S
S + 2e + 2H+
2BrO3- + 12H++ 10e
Br2 + 6H2O
Overall equation: 5H2S + 2H+ + 2BrO3- 5S + Br2 + 6H2O
(iv)
When solid calcium fluoride reacts with concentrated sulfuric acid, gaseous
hydrogen fluoride is produced. A similar reaction occurs with solid calcium
chloride but with solid calcium bromide, bromine is formed.
I
Write an equation for the reaction of solid calcium fluoride with

concentrated sulfuric acid.
II
Explain why when reacted with concentrated sulfuric acid, solid

calcium bromide form bromine whereas solid calcium chloride forms
hydrogen chloride? Suggest a possible reaction product of the
concentrated sulfuric acid in the reaction.
I. CaF2 + 2H2SO4 2HF + Ca(HS04)2
II. With conc. H2SO4, CaBr2 produces HBr which is readily oxidised by conc.
H2SO4 to Br2.
CaCI2, however, produces HCI which is not further oxidised by conc. H2SO4 .
A possible reaction product is SO2.
[2HBr + H2SO4 Br2 + SO2 + 2H2O]
20
[9]
(b)
Acyl chlorides are useful intermediates for making various acid derivatives. The
following reaction shows two reactions of acyl chlorides.
Reaction scheme 1
Reaction scheme 2
(i)
Suggest the structures of acyl chlorides used in reaction scheme 1 and 2. [2]
B:
(ii)
C:
Suggest the type of polymer E. [1]

Ester
21
(iii) Both compound B and compound D are soluble in water.
I.
II.
Write a balanced equation when compound B dissolves in water and

describe the effect of the resulting solution on Universal Indicator
solution.
Explain why compound D is soluble in water.
I.
1m for equation
The solution turns red.
II. Compound D is an amide, it is able to form compatible interactions

with water which is hydrogen bonding between the compound D
and water molecules
Thus, compound D is soluble in water.
Suggest an observation for reaction scheme 2.
(iv)
Steamy white fumes of HCl

[7]
(c)
Ca2+ and Cl are isoelectronic but the radii of the ions are different.
(i)
Explain the term isoelectronic.

Ions that contain the same number of electrons.
(i)
With the aid of the Data Booklet, explain the above observation as fully as you can.
-
Both Ca2+ and Cl- are isoelectronic, hence same shielding effect.
However, Ca2+ (20 protons) has higher nuclear charge than Cl- (17 protons)
hence higher effective nuclear charge.
Hence there is stronger electrostatic attraction between nucleus and valence
electrons of Ca2+.
Thus, valence electrons of Ca2+ are pulled closer to the nucleus and Ca2+ is
smaller.
Ca2+ has smaller ionic radiuWs than CI-.
22
(iii)
State two ways in which the behaviour of Ca2+ ions in an electric field differs from
that of Cl ions.
Ca2+ are deflected towards the negative potential. Cl- ionsare deflected
towards the positive potential.
Ca2+ will be deflected to a greater extend as it has higher charge/mass ratio
compared to Cl-.
[4]
[Total:20]
23
Formatted: Font: (Default) Arial, 11 pt, Bold
Formatted: Centered
Formatted Table
JURONG JUNIOR COLLEGE

JC 2 PRELIMINARY EXAMINATION
Higher 2
CHEMISTRY
9647/01
20 13 September 2012
Formatted: Not Highlight
1 hour

Data Booklet

Write your name, class and shade your exam index number on the Answer Sheet in the spaces
provided.
Formatted: Justified
Sheet.
A Data Booklet is provided. Do not write anything on the Data Booklet.
This document consists of 13 16 printed pages and 1 blank page.

9647/01/Prelim 2012
[Turn Over
2
[Turn over
Formatted: Left
SECTION A
For each question there are four possible answers, A, B, C and D. Choose the one you consider
to be correct.
1.

When x mol of cobalt is added to a solution containing y mol of cobalt(III) ions, cobalt(II)
ions are formed in the resultant solution.
In the resultant solution, the number of moles of cobalt(II) ions are three times that of
cobalt(III) ions. Hence, which of the following are possible values of x and y?
2.
In an experiment, a sample of gadolinium element was vaporised, ionised and passed

through an electric field. Analysis of the deflection occurring at the electric field region
revealed the following data for a beam of 157Gd+.
X
2
157
Formatted: Font: (Default) Arial, 11 pt
Gd+1
Formatted: Font: 11 pt
Formatted: Superscript
Source
3.
+
X
What would be the angle of deflection for a sample of doubly charged strontium ions?
Formatted: Font: Not Bold
0.6
3.6
7.2
16.5
Formatted: Left
In which pair of molecules is the strength of intermolecular forces of I greater than that of
II?
I
II
CH3CH2CH2F
CH3CH2CHF2
trans CH3CCl=CClCH3
cis CH3CCl=CClCH3
CH4
H2O
CH3CH2COOH
CH3CH2CH2OH
9647/01/Prelim 2012
[Turn Over
3
4.
The equation below represents the reaction of gaseous atoms of non-metal Y and of
hydrogen to form gaseous Y2H6 molecules.
DH = 2775 kJ mol-1
2Y(g) + 6H(g) Y2H6(g)

The bond energy of an H-Y bond is 395 kJ mol-1.
What is the bond energy of a Y-Y bond?
405.0 kJ mol-1
202.5 kJ mol
-1
+202.5 kJ mol-1
+405.0 kJ mol-1
Formatted: Font: Bold

5.
Hydrogen peroxide slowly decomposes into water and oxygen.
Formatted: Font: (Asian) Chinese (PRC)
2H2O2(l) 2H2O(l) + O2(g)
Given that the standard enthalpy change of formation of H2O2(l) is 188 kJ mol1 and
standard enthalpy change of formation of H2O(l) is 286 kJ mol1, calculate the enthalpy
change of this decomposition.
A
B
6.
98 kJ mol1
196 kJ

Formatted: Font: (Default) Arial, Font color: Black, English
(United States)
mol1
mol1
+98 kJ
+300 kJ mol1

(United States), Not Highlight
(United States)
Nitrosyl chloride, NOCl, decomposes on heating according to the equation below:

Formatted: Font: (Default) Arial
NOCl(g) NO(g) + Cl2(g)
When 100 cm3 of nitrosyl chloride was placed in a closed container at constant pressure
and heated to a constant temperature, it was found that nitrogen monoxide constitutes
40% of the equilibrium mixture.
What is the total volume of gases in the equilibrium mixture at the temperature of the
reaction?
A
100 cm3
125 cm3
9647/01/Prelim 2012
150 cm3
167 cm3
[Turn Over
4
7.
The equilibrium constant for the reaction represented by the following equation is smaller
than 1.0. Which of the following gives the correct relative strengths of the acids and bases
in the reaction?
HPO42(aq) + H2BO3(aq) H2PO4 (aq) + HBO32 (aq)
Acids
A
B
C
D
Bases
H2PO4 > H2BO3
H2BO3 > H2PO4
H2PO4 > HPO4
Formatted: Centered
and
H2BO3 > HPO4
HBO32 > HPO42
and
and
HBO3
HBO3
> HPO4
> H2BO3
Formatted: Font: Bold, Not Highlight

H2PO4 > HBO32
and

8.
Formatted: Space Before: 6 pt
A sparingly soluble barium salt dissociates in solution according to the equation:

BaL2(s)
Ba2+(aq)
Formatted: Left, Space Before: 6 pt
+ 2L (aq)
If the solubility product of BaL2 is q mol3 dm9, what is the concentration of L at
equilibrium in a saturated solution of BaL2?

1
q 3

4
q3
Field Code Changed
(2q) 3
Field Code Changed

Field Code Changed
Field Code Changed
9.
A commercial pharmaceutical drug X has a constant halflife of 2.0 hours. The drug will lose
its effectiveness in the human body once its mass falls below 40 mg.
Given that a patient was prescribed with 320 mg tablet form of drug X, how often should he
take his prescription in order to maintain the effectiveness of drug in his body?
1.
every 2.0 hours
every 6.0 hours
every 4.0 hours
every 8.0 hours
Formatted: Highlight
When x mol of cobalt is added to a solution containing y mol of cobalt(III) ions, and
coblatcobalt(II) ions are formed in the resultant solution.
Formatted: Font: (Default) Times New Roman, Highlight
In the resultant solution, the number of moles of cobalt(II) ions are three times that of
cobalt(III) ions. Hence, which of the following are possible values of x and y?
9647/01/Prelim 2012
[Turn Over
5
2.
A plasma is a gaseous mixture in which the atoms have been completely stripped of their
electrons, leaving bare nuclei. Because of its possible use in controlled nuclear fusion
reactions, plasma behavior has been intensively studied.
Formatted Table
When 1H and 4He nuclei, each carrying a certain electric charge, are passed between two
plates, carrying a certain electric charge, 1H and 4He nuclei they are deflected differently.
The deflection path of 1H is shown in the diagram below.
Formatted: Font: (Default) Arial, 11 pt, Font color: Black,

Highlight
1H
R
Which of the following is correct?
3.
In which pair of molecules is the intermolecular forces of molecule I greater than that in
molecule II?
II
CH3CH2CH2F
CH3CH2CHF2
Trans CH3CH=CHCH3
Cis CH3CH=CHCH3
CH4
H2O
CH3CH2COOH
CH3CH2CH2OH
4.
The equation below represents the combustion of gaseous atoms of non-metal X and of
hydrogen to form gaseous X2H6 molecules.
DH = 2775 kJ mol-1
2X(g) + 6H(g) X2H6(g)
-1
The bond energy of an H-X bond is 395 kJ mol .
What is the bond energy of an X-X bond?
405.0 kJ mol-1
202.5 kJ mol
-1
+202.5 kJ mol-1
+405.0 kJ mol-1
5.
The following energy cycle represents the enthalpy changes in the formation of carbon
dioxide from its constituent elements in their standard states.
Formatted Table
9647/01/Prelim 2012
[Turn Over
6
Which substances are present at level Y in this diagram?
Formatted: Space After: 0 pt
C(g) + 2O(g)
C(g) + O2(g)
C(s) + O2(g)
CO2(g)
6.
In an experiment, 7.75 x 10-3 mol sample of AlCl3 was allowed to dimerise in a 1.8 dm3
container at 200C. At the end of the reaction, the gases exerted a total pressure of
3.745 x 103 Pa. Assuming AlCl3 behaves as an ideal gas, calculate the mole fraction of
AlCl3 that has dimerised.
2AlCl3 (g)
Al2Cl6 (g)
0.053
0.106
0.894
0.947
Formatted: Font: (Default) Arial, 11 pt, Highlight

7.
HPO42(aq) + H2BO3(aq)
H2PO4 (aq) + HBO32 (aq)
The equilibrium constant for the reaction represented by the equation above is smaller
than 1.0. which of the following gives the correct relative strengths of the acids and bases
in the reaction?
Acids
Formatted: Space After: 0 pt, Don't adjust space between
Latin and Asian text, Don't adjust space between Asian text
and numbers
Bases
H2PO4 > H2BO3
and
HBO32 > HPO42
HBO32 > HPO42
and
HBO32 > HPO42
H2PO4 > H2BO3
and
HPO42 > HBO32
H2BO3 > H2PO4
and
H2PO4 > HBO32

8.
A sparingly soluble barium salt dissociates in solution according to the equation:

BaL2(s)
Ba2+(aq) + 2L(aq)
If the solubility product of BaL2 is q mol3 dm9, what is the concentration of L at
q

4

equilibrium in a saturated solution of BaL2(aq)?

1
3
1
3
(2q)
1
3
9647/01/Prelim 2012
[Turn Over
7
Formatted: Justified, Indent: Left: 0", Hanging: 0.5", Space
Before: 0 pt, Line spacing: 1.5 lines
9.
A commercial pharmaceutical drug X has a halflife of 2.0 hour. The drug will lose its
effectiveness in the human body once theits mass of drug falls below 40 mg.
Given that a patient was prescribed with 320 mg tablet form of drug X, how often should he
take his prescription in order to maintain the effectiveness of drug in his body?
A
every 2.0 hours
every 6.0 hours
every 4.0 hours
every 8.0 hours
9647/01/Prelim 2012
[Turn Over
10.
Pepsin is a digestive enzyme found in gastric juice that aids in the digestion of proteins. The
graph below shows how the rate of a reaction varies with the concentration of protein (react
(reactant) concentration for pepsin enzyme.
rate of
rate of
reaction
reaction
Formatted: Centered
Formatted: Font: (Default) Arial, 11 pt, Font color: Text 2
[protein]
[protein]
Which of the following can be deduced from the graph above?
Formatted Table
The rate is first order at low protein concentration of protein and zero order at high
protein concentration of protein.
B
B
The rate is second order at low concentration of protein and zero order at high
concentration of protein.Increasing the protein concentration will increase the rate of
reaction.
Increasing the protein concentration will increase the rate of reaction.
Formatted: Justified, Line spacing: single
The rate is second order at low protein concentration and zero order at high protein
concentration.
The enzyme is unable to function at high protein concentrations of protein.
10.
The reaction of hydrogen peroxide with iodide ions in an acidic solution is first order with
respect to hydrogen peroxide as well as iodide ions, and zero order with respect to
hydrogen ions.
Formatted Table
H2O2(aq) + 2H+(aq) + 2I -(aq) 2H2O(l) + I2(aq)

Two experiments were carried out. Which of the following pairs of diagrams represents
the variation of [H2O2] and [H+] with time?
Experiment 1: In the presence of
excess [I -]
Formatted Table
Experiment 2: In the presence of

excess [I -] and [H2O2]
9647/01/Prelim 2012
[Turn Over
9
[H+]
[H2O2]
time
[H2O2]
time
[H+]
time
time
[H+]
[H2O2]
time
time
[H+]
[H2O2]
11.
time
time
The standard electrode potentials of Ag+l|Ag(s), Zn2+|(aq)lZn(s) and Cu2+(aq)|lCu(s) are

+0.80 V, -0.76 V and +0.34 V, respectively.
Which of the following conclusions can be drawn from these data?
Silver is less electropositive than copper.
Silver displaces zinc from a solution containing zinc ions.Silver displaces zinc from
a solution containing zinc ions.
Zinc ion has a greater tendency to be reduced than copper ion.Silver is an oxidising
agent.
Zinc has a lower tendency than silver to form positively charged ions.
Formatted: Font: 11 pt, Not Highlight

Formatted: Font: 11 pt, (Asian) Chinese (PRC)
(United States), Not Highlight
Formatted: Font: Not Highlight
9647/01/Prelim 2012
[Turn Over
10
12
Four metals Pb, x, y and z, were connected in pairs as shown in the diagram below and the
1 voltage was recorded.
.
V

Formatted Table
salt bridge
1 mol dm3 Fe2+(aq),
1 mol dm3 Fe3+(aq),
25oCMetal electrode
1 mol dm3 Cl(aq),

25oCMetal electrode
The results obtained are set outrecorded in the table below.

Negative terminal
Pb
y
z
Positive terminal
x
Pb
Pb
Formatted: Centered
Voltage (V)
0.35
1.10
2.60
Formatted Table
Formatted: Centered
Formatted: Font: Italic
Formatted: Centered
Formatted: Centered
Whaich set shows an increase in the reducing power of the metals?t is the order of
increasing ease of oxidation of the metals?
Formatted: Right: -0.03", Space Before: 0 pt, Don't adjust

space between Latin and Asian text, Don't adjust space
between Asian text and numbers
Formatted: Right: -0.03", Space Before: 0 pt, Don't adjust
space between Latin and Asian text, Don't adjust space
between Asian text and numbers
13.
weakest
strongestz, y, Pb, x
Pb
Formatted: Font: 11 pt, Not Italic
Pb, x, y, z

x,
y,
Pb
Pb
Pb
,z
x, Pb, y, z
Which property of Group II elements (beryllium to barium) decreases with increasing

atomic number?

Formatted Table
reactivity with water
solubility of hydroxides second ionisation energy

Formatted: Font: (Asian) Chinese (PRC), Not Highlight
9647/01/Prelim 2012
[Turn Over
11
C
second ionisation energy solubility of hydroxides
thermal stability of the carbonates

(United States)
Formatted: Indent: Left: 0", First line: 0", Space Before: 6
pt
145.
The element astatine lies below iodine in Group VII of the Periodic Table.
Which one of the following properties is correct for astatine?
A
It forms diatomic molecules which dissociates less readily than chlorine molecules.
It reacts explosively with hydrogen.
It can oxidise iodide to iodine.
It exists as a crystalline solid.

(United States)
pt
Formatted: Font color: Red


pt
153 The following graph shows the first ionisation energies of eight consecutive elements J to
. R, which have atomic numbers between 3 to 20 in the Periodic Table.
9647/01/Prelim 2012
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Formatted: Space Before: 6 pt, After: 0 pt
12
1st Ionisation Energy/ kJ mol-1
L
J
P
N
Atomic Number
Which one of the following statements about the elements is false?
Commented [HZY1]: False questioning 1
R has the highest melting point.
The ionic radius of J is larger than the ionic radius of K.
Q forms a insoluble hydroxide which dissolves in excess dilute NaOH(aq).
OxideChloride of P gives a higher pH than oxidechloride of N when reacteds with

water.

14.
Which property of Group II elements (beryllium to barium) decreases with increasing

atomic number?

Formatted: Font: Times New Roman
15.
reactivity with water
second ionisation energy
solubility of hydroxides
stability of the carbonates
The element astatine lies below iodine in Group VII of the Periodic Table.
Which one of the following properties is correct for astatine?

It forms diatomic molecules which dissociates less readily than chlorine molecules.
It reacts explosively with hydrogen.
It can oxidise iodide to iodine.
It exists as a crystalline solid.
9647/01/Prelim 2012

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13.
13
The following graph shows the first ionisation energies of eight consecutive elements J
to R, which have atomic numbers between 3 to 20 in the Periodic Table.
Formatted Table
1st Ionisation Energy/ kJ mol-1
L
J
P
Q
Atomic Number
Which one of the following statements about the elements is false?
14.
15.
Q forms a hydroxide which reacts with dilute NaOH(aq).
R has the highest melting point.
The ionic radius of J is larger than the ionic radius of K.
Chloride of P gives a higher pH than chloride of N when reacts with water.
Which one of the following is not true for radium, the last member of Group II in the
Periodic Table?
Radium compounds tend to be covalent rather than ionic.
Radium compounds conduct electricity when molten.
Radium is the most reactive Group II element.
Radium reacts with water to release hydrogen gas.
Which one of the following statements about Group VII chemistry is false?
The colour intensity of the elements increases down the group.
Formatted Table
The volatility of hydrogen iodide is smaller than that of hydrogen chloride.
The reaction between chlorine and sodium thiosulfate results in the oxidation state of
sulfur increasing from +2 to +2.5.
Formatted: Justified, Tab stops: 0.5", Left
116
A chromium compound dissolves in water to give a green solution E which undergoes the
9647/01/Prelim 2012
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14
. following reactions.
NH3(aq)
E
green solution
F
purple solution
H2O2(aq)
G
yellow solution
H+(aq)
H
orange solution
Which of the following statements isabove observations is incorrect?

The reaction of E to form F is a ligand displacement reaction.
The complex ion in F is a more stable than that incomplex than E.
The chromium-containing ion inThe yellow solution G containsis
The reaction of G to H is an acid-base reaction.
Cr2O72- ions Cr2O72 - .
Formatted: Subscript, Not Highlight

Formatted: Superscript, Not Highlight
Formatted: Superscript, Not Highlight
Field Code Changed
17.

Which of the following is not true about the first row transition metals or its compounds?
A
Fe(CN)63- does not can oxidises Br- to Br2..
CrCl2(aq) is chemically unstable when left to stand in the atmosphere.
On addition of H2O2(aq) to acidified KMnO4(aq), the purple solution remains.
DC
On addition of CoF3 to water, a gas that relights gives a pop sound with the
glowinglighted splint is produced.A mixture of excess NaOH(aq) and FeCl3(aq)
produces a gas that relights a glowing splint.
18.
Commented [HZY6]: False questioning 5. Quite tedious to do 5

consecutive questions of reverse psychology.
Formatted: Subscript
Formatted: Left, None, Don't keep with next
On addition of H2O2(aq) to hot acidified KMnO4(aq), the purple solution remainsis

decolourised.
In black and white photographic film, light converts silver chloride into metallic silver. After
the film has been developed, the unreacted silver chloride is removed by reaction with
sodium thiosulfate to produce a fixed negative.
Formatted: Font: (Default) Times New Roman, Not Highlight

Formatted: Left, None, Don't keep with next
Formatted: Font: (Default) Times New Roman, Italic

AgCl + 2Na2S2O3 4Na+ + Cl + [Ag(S2O3)2]3

What is the function of the thiosulfate ion?
Formatted: Normal (Web), Space Before: 6 pt
to make the silver ions soluble
to oxidise the silver ions
to oxidise the silver metal

9647/01/Prelim 2012
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15
D
19.
to reduce the silver ions
Species with the molecular formula CH3 can act as an electrophile, a free radical or a
nucleophile depending on the number of outer shell electrons on the central carbon
atom.
How many outer shell electrons must be present on carbon atom offor CH3 to act as an
electrophile, a free radical or a nucleophilein these different ways?
Formatted: Normal (Web), Space Before: 6 pt, After: 6 pt

Formatted: Normal (Web), Space Before: 6 pt, After: 6 pt
A
B
C
D
CH3 as an electrophile
6
6
7
8
CH3 as a free radical

7
8
6
7
CH3 as a nucleophile
8
7
8
6
Formatted: Indent: Left: 0", First line: 0"
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20.
The diagram shows the structure of the naturally-occurring molecule cholesterol.
Formatted Table
H3C
CH3
H
H
CH3
HO
Cholesterol is separately treated with

cold, dilute acidified KMnO4,
hot, concentrated acidified KMnO4.
What is the change in the number of chiral carbon atoms in the molecule during each
reaction?
cold, dilute acidified KMnO4
hot, concentrated acidified KMnO4
+1
+1
+2
+2
H3C

Field Code Changed
CH3
H
H
CH3
HO
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17
21.
When heated with chlorine, 2,2-dimethylbutane undergoes free radical substitution.

The alkyl free radical R is formed in the propagation step as shown. the hydrocarbon 2,2dimethylbutane undergoes free radical substitution.
In a propagation step the free radical R is formed.
Formatted: Left
CH3
CH3CH2C
CH3
Cl
HCl
CH3
How many different forms of R are possible?

A
22.
Compound W was used in the following synthesis route.

HCN,
trace KCN
COCH
CH2
Compound X
Br2(aq)
Compound Y
Compound W
How many sp, sp2 and sp3 hybridised carbon atoms are there in compound Y?
sp
sp2
sp3
67
67
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18.
Platinum(IV) chloride forms a compound with ammonia in which the co-ordination number of
Pt is 6. The formula unit of one such compounds is found to contain a cation and only two
chloride ions.
Which of the following correctly shows the formula of this compound?
19.
Pt(NH3)6Cl4
Pt(NH3)4Cl4
Pt(NH3)5Cl4
Pt(NH3)3Cl4
Which of the following cannot behave as a nucleophile?

A
N(CH2CH3)3
CH3CH2OH
P(C6H5)3
CH3CH2Li
Commented [HZY7]: A and B are the same actually.

Commented [HZY8]: I think D is not in syllabus. Dont think
the students will know about this.
20.
Cholecalciferol,( Vitamin D3) has the structure shown below. It is generated in the skin
when light energy is absorbed. How many stereoisomers does the molecule have?
Commented [HZY9]: Tried setting a question like this last time,
was rejected by the senior teachers as this is not required in syllabus.
May consider changing to find chiral centres instead
21.
25
26
27
28
Formatted Table
Each of the following compounds is effective as a refrigerant.

The release of wWhich one of these, when released into the atmosphere, will causes the
greatest depletion of the ozone layer?
A
22.
CCl2F2
CH3OCH3
CH3CHF2
CH3CH2CH3
Compound W was used in the following synthesis route.
What are the numbers ofHow many sp, sp2 and sp3- hybridised carbon atroms are there in
compound Y?
Formatted: Centered
0, 6, 4
Formatted: Centered
0, 7, 3
Commented [HZY10]: Can be clearer by putting a header row

that says which number belongs to which hybridised C.
1, 6, 3
Formatted: Centered
1, 7, 2

Formatted: Underline, Not Highlight
23.
In which reaction does the underlined carbon -containing organicin the reactant haveve a
bond angle that is larger than the carbon-containingits corresponding carbon in the

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Commented [HZY11]: Have a feeling the senior teachers will
not like this question, cos there are many bond angles in the organic
pdt/cpd and can cause ambiguity.
product?
reducing ethanoic acidCH3CO2H with lithium aluminium hydrideLiAlH4
heating ethanal CH3CHO with acidified potassium dichromate (VI)K2Cr2O7
complete combustion of ethene CH2=CH2 in air
heating bromoethane CH3CH2Br under reflux with alcoholic potassium hydroxideKOH

Formatted: Underline, Not Highlight
Formatted: Font: (Default) Times New Roman, Italic
Formatted: Underline
24.
A mixture of one mole of CH2ClCOCl and one mole of C6H5Cl is heated under reflux with
dilute aqueous NaOH.
What are the organic compounds in the final reaction mixture?
24.
CH2ClCO2 and C6H5OH
CH2OHCOCl and C6H5Cl
CH2OHCO2 and C6H5O
CH2OHCO2 and C6H5Cl
Under identical conditions, even though it proceeds by the same mechanism, reaction 1
is faster than reaction 2.
Formatted Table
reaction 1: CH3CHBrCH3 + NaCN CH3CH(CN)CH3 + NaBr

reaction 2: CH3CHBrCH3 + NaI CH3CHICH3 + NaBr
What factor will explain this result?
25.
The CI bond is a stronger bond than the CBr bond.
The CNN bond is a stronger bond than the CI bond.
The cyanide ion is a stronger nucleophile than the iodide ion.
The bromidcyanide ion is a weaker stronger nucleophile than the iodideiodide ion.

The following compound is a flavoring agent in food.
9647/01/Prelim 2012
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20
O
O
CCH3
CHO
Which of the following reagents will give a positive chemical test result with the above
compound?
phosphorus pentachloride
aqueous alkaline iodine
acidified potassium dichromate(VI)
Commented [HZY12]: Not to sure about this, but I think the

ester can be hydrolysed under this test. Cos need heat for this as
well.
neutral aqueous iron(III) chloride
FfFehlings solution

well.
Formatted Table
26.
Which reaction will give 2-chloropropane in the best yield?
Formatted: Font color: Red, Highlight

Formatted Table
25.
propane gas with chlorine gas in the presence of ultraviolet light
propan-2-ol with dilute NaCl(aq)
propan-2-ol with SOCl2
propene with dilute HCl(aq)

The following compound is a flavoring agent in food.

Formatted Table
Which of the following reagents will react with the above compound?
A
propanoic acid in the presence of concentrated sulfuric acid
neutral aqueous iron(III) chloride
Fehlings solution

well.
26. When equimolar amounts of organic compounds R, S, T and U are added separately to
water, solutions of increasing pH values are obtained.
Which set of identities of compounds R to U is correct?
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21
27.
CH3CH2CO2H
CH3CHBrCO2H
CH3CH2CONH2
CH3CHClCH2NH2
CH3CH2CO2H
CH3CHBrCO2H
CH3CHClCH2NH2
CH3CH2CONH2
CH3CHBrCO2H
CH3CH2CO2H
CH3CH2CONH2
CH3CHClCH2NH2
CH3CHBrCO2H
CH3CH2CO2H
CH3CHClCH2NH2
CH3CH2CONH2
The reddish brown colour of aqueous bromine is discharged when a solution of

phenylamine is added to it. Which statement explains this observation?
A
Bromine displaces hydrogen in the benzene ring.
The NH2 group of phenylamine is substituted by bromine.
Bromine forms a colourless complex with phenylamine.
Phenylamine reduces Br2 to Br .

Formatted: Font color: Red
26.
Which of the following reagents and conditions to form 2-chloropropane are correct?The
reaction conditions for four different reactions are given. Which reaction has the correct
conditions?
[(alc) indicates an alcoholic solution.]
Formatted: Font: Arial, 11 pt

butaneCH3CH3(g)
CH3CH2Cl + HCl
(l) + Cl2(aq)
uv light
with+
Cl2(aq),
presence
of
ultraviolet
light
Formatted: Centered
Formatted
AlCl3(s)
Cl + HCl
...

butan-2-ol with Cl2(aq)
butan-2-ol with SOCl2(s)CH2=CH2(g) + HBr(g)
CH3CH2I(l) + NaOH(alc)
heat
CH3CH2Br

Field Code Changed
CH3CH2OH + NaI but-1-ene with HCl(aq)
Formatted
...
Formatted: Centered
27.
Which halogenoalkane will undergo an SN1 reaction and produce a yellow precipitate
when AgNO3(aq) is added to it?
Formatted
...
Formatted: Centered
Formatted
...
Formatted: Centered
Formatted
...
1-chlorobutane
Formatted: Indent: Left: 0", Hanging: 0.25", Space Before:

30 pt
1-iodobutane
2-chloro-2-methylpropane
Formatted
2-iodo-2-methylpropane
...
Formatted: Font:
Formatted: Centered
Formatted
9647/01/Prelim 2012
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22
28.
Consider the following reaction scheme.

AlCl3
Cl
Step II
Step I
OH
N
Step III
Step IV
Cl
Cl
Which of the type of reactions is incorrect?

Formatted
Step
Type of reaction
Electrophilic substitutionCondensation
II
Reduction
9647/01/Prelim 2012
Formatted: Font:
Formatted: Font:
Formatted: Font:
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23
Formatted Table
III
Elimination
IV
Nucleophilic additionElectrophilic addition

29.
30.
Which mixtures, on heating, will not produce a basica nbasic alkaline product containing
deuterium, D?
A
C6H5CH2CN in D2 with Ni catalyst
(ND2H2)2SO4 and NaOD in D2O CH3CH=CH2 with D2O(g) in the presence of H3PO4
catalyst
CH3CH=CH2 with D2O(g) in the presence of H3PO4 catalyst (ND2H2)2SO4 and NaOD in
D2O
CH3CH2CONH2 and NaOD in D2O

Which of the following about the amino acid, methionine, is true?

NH2
COOH
S
Methionine
30.
It migrates towards the cathode in a solution of Na2CO3(aq).
It exists predominantly as a zwitterion in a solution of pH 2.
It exists as a crystalline solid with high melting point.
It forms covalent disulfide linkage with another methionine molecule.
Which of the following statements about the amino acid, methionine, is true?
Formatted: Font:
Formatted: Font:
NH2
Formatted Table
COOH
S
methionine
It migrates towards the cathode under an applied electric current in a solution of

Na2CO3(aq).
It exists predominantly as a zwitterion in a solution of pH 12.
It exists as a crystalline solid with high melting point.
It forms covalent disulfide linkage with another methionine molecule.
Formatted Table
SECTION B
9647/01/Prelim 2012
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24
may be correct.
Decide whether each of the statements is or is not correct.
A
1, 2 and 3 are
correct
1 and 2 only are

correct
2 and 3 only are

correct
1 only is
correct

31.
Gaseous particle Y has a proton number of n+1 and a charge of +2. Gaseous particle X
has proton number n and is isoelectronic with Y.
Which of the following statements are true?

31.
X has a larger radius than Y.
X requires less energy than Y when an electron is removed from each particle.
X releases less energy than Y when an electron is added to each particle.
Formatted: English (Singapore)

Which of the following statements about 20.3 g of Co2(SO4)3 is correct?

[Molar mass of Co2(SO4)3 = 406 g
Formatted: Body Text Indent 2, Space After: 0 pt, Tab

stops: 0.38", Left + 0.88", Left
Formatted: Font: Bold, Subscript, Not Highlight
mol1]
It contains 9.6 g of oxygen.
It contains 0.15 mol of SO42 ions
It contains 1.5 x 1023 ions.

32. In Wwhich reactionof the following have ais negative the standard entropy change, DS,
negative?

Formatted Table
Pb(NO3)2(aq) + CaSO4(aq)
PbSO4(s) + Ca(NO3)2(aq)
Changing The change in temperaturethe temperature of of nitrogen gas from -50 oC

to -20 oC.
2Na(s) + 2H2O(l)
2NaOH(aq) + H2(g)

Field Code Changed
32. Which of the following has a negative standard entropy change, DSo?
1
Pb(NO3)2(aq) + CaSO4(aq)
The change in temperature of nitrogen gas from -50 oC to -20oC.
2Na(s) + 2H2O(l)
Field Code Changed

PbSO4(s) + Ca(NO3)2(aq)

Field Code Changed
2NaOH(aq) + H2(g)

Field Code Changed
33.
Why does a mixture of nitrogen gas and hydrogen gas react together faster with the
addition of a catalyst?
1
The activation energy of the reaction is lowered.
There is an increase in frequency of effective collision between the molecules.
9647/01/Prelim 2012
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3
34.
Commented [HZY15]: Thought options 2 & 3 are the same

thing.
Nitrogen molecules and hydrogen molecules collide more frequently.
The numerical values of the solubility product of strontium carbonate and strontium
fluoride are 8.7 109 and 4.0 1011 respectively at 25 oC.
1
Strontium carbonate has a lower solubility than strontium fluoride.
Addition of sodium fluoride to a solution containing strontium fluoride does not affect
the solubility product of strontium fluoride.
33.
Addition of sodium fluoride to a saturated solution of strontium fluoride decreases the

solubility of stontium fluoride.

Formatted Table
1, 2 and 3 are
correct
1 and 2 only are

correct
2 and 3 only are

correct
1 only is
correct
Catalysts are used in many reversible reactions. Finely divided iron is used in the Haber
process.

Formatted Table
N2(g) + 3H2(g) 2NH3(g)
What effect does iron have on this equilibrium?
34.
It lowers the value of activation energy for the forward reaction.
It increases the rate of the reverse reaction.
It increases the average kinetic energy of the reacting particles.
Formatted Table
1, 2 and 3 are
correct
1 and 2 only are

correct
2 and 3 only are

correct
1 only is
correct
The numerical values of the solubility product of strontium carbonate and strontium
fluoride are 8.7 109 and 4.0 1011 respectively at 25 oC.

Formatted Table
Formatted: Space Before: 6 pt, After: 0 pt, Tab stops:
2.51", Left
Formatted: Space Before: 6 pt, After: 0 pt, Tab stops:
2.51", Left

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Addition of potassium fluoride to a solution containing strontium fluoride does not

affect the solubility product of strontium fluoride.
Addition of potassium fluoride to a saturated solution of strontium fluoride decreases

the solubility of strontium fluoride.
Strontium fluoride has a higher solubility than strontium carbonate. fluoride will not be
precipitated when potassium fluoride is added to a solution mixture containing
strontium carbonate precipitate.
35. Which of the following statements are correct for the sequence hydrogen chloride, hydrogen
bromide and hydrogen iodide?
1 The thermal stability of hydrogen halides decreases.The enthalpy change of formation
becomes more exothermic.
2 The polarity of the hydrogen halide molecule decreases. The thermal stability of
hydrogen halides decreases.
3 The enthalpy change of formation becomes more exothermic.The polarity of the

hydrogen halide molecule decreases.

36.
When the yellow liquid NCl3 is stirred into aqueous sodium hydroxide, the reaction that
occurs can be represented by the following equation.
2NCl3(l) + 6NaOH(aq) N2(g) + 3NaCl (aq) + 3NaOCl (aq) + 3H2O(l)
Which of the following statements are true at will be the result for this reaction?

Formatted: Indent: Left: 0", Space Before: 6 pt, After: 0 pt
Formatted: Font: Times New Roman, Italic
Formatted: Normal (Web), Space Before: 6 pt
The oxidation state of nitrogen atom changes from -3 to 0.undergoes a redox

reaction.
A bleaching solution remainsis produced after the reaction.
The final solution gives a precipitate with acidified silver nitrate.

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27
A
1, 2 and 3 are
correct
1 and 2 only are

correct
2 and 3 only are

correct
1 only is
correct
37.
The diagram shows some laboratory apparatus.

cold water
Formatted: Font color: Text 1

Formatted: Centered
heat

Formatted: Centered
Which preparations could this apparatus be used for?

bromoethane, from ethanol, sodium bromide and concentrated sulfuric acid
ethanal, from ethanol, sodium dichromate(VI) and sulfuric acid
1,2--dibromoethane, from bromine and ethene
9647/01/Prelim 2012
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Formatted: Centered
Formatted: Footer distance from edge: 0.22"
38.
With vigorous oxidation using hot concentrated nitric acid, ketones can be oxidised to
acids. The chemical equation showing the oxidation of propanone is as follows.
Formatted: Centered, Space After: 0 pt
H3C
O + 3 [O]
hot HNO3
CH3COOH + CO2
H3C
What are the products formed when butanone undergoes the same type of oxidation?
36.
CO2
CH3CO2H
CH3CH2CO2H
1, 2 and 3 are
correct
1 and 2 only are

correct
2 and 3 only are

correct
1 only is
correct
Disaccharides, C12H22O11, are important in the human diet. For example, sucrose is found
in pastries and lactose occurs in milk products.
Both of these compounds can be hydrolysed.
sucrose + H2O CH2OH(CHOH)4CHO + CH2OH(CHOH)3COCH2OH
glucose
fructose
lactose + H2O CH2OH(CHOH)4CHO + CH2OH(CHOH)4CHO

glucose
galactose
Which statements about these hydrolysis products are correct?

1
Glucose and fructose have structural isomers.
9647/01/Prelim 2012
29
37.
38.
Glucose and galactose are optical isomers.
Glucose and galactose are ketones.
Commented [HZY16]: Sorry but I cant see why, from the

lactose equation.
Which of the following are the environmental consequences arising from unburnt
hydrocarbons produced from the internal combustion engine?
1
Production of photochemical smog.
Respiration and breathing difficulties.
Formation of acid rain.
Ketones are generally resistant to oxidation. With vigorious oxidation using hot nitric acid,
ketones can be oxidised to acids.
The chemical equation showing the oxidation of penta-3-one is as follows.
H3C
C
O + 3 [O]
hot HNO3
CH3COOH + CO2
H3C
What are the products formed when propanone undergoes the same type of oxidation?
39.
CO2
CH3CO2H
HCO2H
Formatted Table
1, 2 and 3 are
correct
1 and 2 only are

correct
2 and 3 only are

correct
1 only is
correct
Formatted Table
The cholesterol-lowering agents called statins, such as Ppravastatin, are among the most
widely prescribed drugs in the world.
O
HO
OH
OH
O
C
OH
CH3
Pravastatin
Which of the following statements about Pravastatin are correct?

1
1 mole of Pravastatin reacts with 2 moles of hot NaOH(aq).
When 1 mole of Pravastatin is treated with an excess of Na, 2 moles of H2 are

produced.
In the presence of a suitable catalyst, 1 mole of Pravastatin reacts with 4 moles of

HCl(g).
9647/01/Prelim 2012
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30
40.
Formatted Table
Which of the following statements about compound Z are correct?
NH2
OH
H2N
NH2
O
compound Z
40.
Z can be hydrolysed to produce amino acids.
Z gives an orange precipitate with Bradys reagent.Z forms an ester with ethanoyl
chloride.
Z forms amide and ester functional groups with ethanoyl chloride. Z gives an orange
precipitate with Bradys reagent.
NH2
N
NH2

OH
H2N
Formatted: Left, Indent: Left: 0", First line: 0", Space After:
0 pt
Which of the following statements about compound Z are correct?

O
Formatted: Left, Space After: 0 pt
O
compound Z
Which of the following statements about this compound are correct?
1
Z gives an orange precipitate with 2,4-dinitrophenylhydrazine reagent.
1 mole of Z reacts with 4 moles of ethanoyl chloride.
One mole of Z can be hydrolyzed to produce 2 moles of amino acids.
Formatted: Indent: Left: 0", First line: 0", Space After: 0

pt
0 pt
0 pt
39.
1, 2 and 3 are
correct
1 and 2 only are

correct
2 and 3 only are

correct
1 only is
correct

pt
The cholesterol-lowering agents called statins, such as pravastatin, are among the most
widely prescribed drugs in the world.
0 pt
pt
Formatted: Left, Indent: Left: 0", First line: 0"
O
HO
Formatted Table
OH
OH
C
CH3
Formatted: Left
OH
Pravastatin
Formatted: Left
Formatted: Left, Tab stops: Not at 2.51"
Which of the following statements about pravastatin are correct?
9647/01/Prelim 2012
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31
40
1 mole of pravastatin reacts with 2 moles of hot NaOH(aq).
When 1 mole of pravastatin is treated with an excess of Na, 2 moles of H2 is

produced.
Formatted: Left
When 1 mole of pravastatin is treated with hot SOCl2, 3 moles of HCl(g) is evolved.
Formatted: Left
The following compound, Z, is a by-product formed in the body that counteracts the effect of
the drug administered to patients to treat herpesfor treatment of herpes.
Commented [HZY17]: Imine present. Dun think the team will

be comfortable about it.
OH
H2N
N
H
N
NH2
0 pt
NH2
Formatted: Left

Which of the following statements about this compound are correct?
Z gives an orange precipitate with Bradys reagent.
1 mole of Z reacts with 4 moles of ethanoyl chloride.
0 pt
One mole of Z can be hydrolyzed to produce 2 moles of amino acids.

pt
0 pt
pt
0 pt
pt
Formatted: Centered, Tab stops: 0.51", Left
Formatted: Font: Arial, 11 pt, Bold
Formatted: Centered
Formatted: Centered, Space Before: 6 pt
pt, Tab stops: Not at 0.5"
Formatted: Centered
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edge: 0.22"
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9647/01/Prelim 2012
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Suggested Worked Solutions for 2012 JC2 Prelim Paper 1 (9647/01)
1.
1.
11.
21.
31.
2.
12.
22.
32.
3.
13.
23.
33.
4.
14.
24.
34.
5.
15.
25.
35.
6.
16.
26.
36.
7.
17.
27.
37.
8.
18.
28.
38.
9.
19.
29.
39.
10.
20.
30.
40.
Co3+ + e Co2+
2.
charge/mass angle of deflection
Co Co2+ + 2e
Particle
Overall eqn: Co + 2Co3+ 3Co2+
157Gd+
1
= 0.00637
157
87.6Sr2+
2
= 0.0228
87.6
Co3+,
charge/mass
Co3+
For the resulting mixture to contain

must be in excess (more than double the
amount of Co). When x=1, y=3,
Co + 2Co3+ 3Co2+
Initial amt/mol
Final amt/mol
Angle of deflection for
87.6Sr2+
=(
0.0228
x 2)
0.00637
= 7.2o.
Ans: B
3.
II
CH3CH2CH2F
CH3CH2CHF2
Polar molecule. Permanent dipolepermanent dipole forces of attraction

between molecules.
Polar molecule with larger dipole moment than

CH3CH2CH2F. Stronger permanent dipole-permanent
dipole forces of attraction than that of I.
trans CH3CCl=CClCH3
cis CH3CCl=CClCH3
Non-polar molecule. van der Waals

forces of attraction between
molecules.
Polar molecule. Stronger permanent dipolepermanent dipole forces of attraction than weaker
VDW forces of attraction between I molecules.
CH4
H2O
van der Waals forces of attraction

between molecules
Stronger hydrogen bonding between molecules than

the weaker VDW forces of attraction between I
molecules.
CH3CH2COOH
CH3CH2CH2OH
More extensive hydrogen bonds

between molecules as they exist as
dimers (formation of more extensive
hydrogen bonding between 2 RCO2H
molecules) than that of II.
hydrogen bond between molecules.
Ans: C
Ans: D
2012 JJ Prelim H2 Chemistry (9647)
Paper 1 (9647/01) Suggested Worked Solutions
Page 1 of 11
4.
Given,
5.
Using the formula,
2Y(g) + 6H(g) Y2H6(g) DH = 2775 kJ mol-1
DH,rxn=SDH,f(products) - SDH,f (reactants)
Y2H6(g) 2Y(g) + 6H(g) DH = +2775 kJ mol-1
DH,r = 2DH,f(H2O) - 2DH,f(H2O2)
DHr = E(Y-Y )+6E(Y-H)
= 2(286) 2(188) = 196 kJ mol 1

Note: DH,f(O2) = 0 kJ mol 1as O2 is an element.
E(Y-Y) = +2775 - 6(395) = + 405 kJ mol 1
Ans: B
Ans: D
6.
Let x be the volume of NOCl(g) that reacted.

NOCl (g) NO(g) + Cl2(g)
Eqm volume/cm3 100-x
Total volume of gases at eqm = (100+x) cm3

% of NO at eqm =
x
x 100 % = 40 %
100 + 1/ 2x
Solving, x=50 cm3

Hence, total volume of gases at eqm
=100 + (50) = 125 cm3
Ans: B
7.
HPO42(aq) + H2BO3(aq) H2PO4(aq) + HBO32(aq)

conjugate
conjugate
base
acid
acid of
base of
HPO42
H2BO3
H2PO4 and H2BO3 are acids and HBO32 and HPO42 are bases. Hence option C and D are wrong.
Since the equilibrium constant < 1.0, there will be a higher [HPO42(aq)] and [H2BO3(aq)] and a lower
[H2PO4(aq)] and [HBO32(aq)] at equilibrium.
Since [H2PO4(aq)] < [H2BO3(aq)] H2PO4 ionises to a greater extent than H2BO3 to give H+.
Hence H2PO4 is a stronger acid than H2BO3
Since [HBO32(aq)] < [HPO42(aq)] HBO32 ionises to a greater extent than to give OH-. Hence
HBO32 is a stronger base than HPO42.
Strength of acids: H2PO4 > H2BO3

Strength of bases: HBO32 > HPO42
Ans: A
8.
BaL2(s) Ba2+(aq) + 2L(aq)
9.
Given Ksp = [Ba2+(aq)][L (aq)]2 = q
mol3 dm9
Let [L] at equilibrium be x mol dm3

\ Ksp =
Given t1/2 = 2.0 hour

After first half-life,
mass of X = (320) = 160 mg
After the second half-life,
x 2
(x) = q
2
mass of X = (160) = 80 mg
x3
=q
2
After the third half-life,

mass of X = (80) = 40 mg
x = (2q)Error! Objects cannot be created
from editing field codes. = [L ] at equilibrium
Hence, drug X will still be effective after 3 halflives (3 x 2.0 = 6.0 hour).
Ans: D
Ans: C
Page 2 of 11
10.
Rate = k[H2O2][I-],
For expt 1: Rate = k[H2O2] where k = k[I-]
The graph of [H2O2] against time is a downward sloping curve with decreasing gradient.
For expt 2: Rate = k where k = k[I-][H2O2]
The graph of [H+] against time is a decreasing straight line with a constant gradient.
Ans: B
11.
E,Ag+|Ag = +0.80 V, E,Zn2+|Zn = -0.76 V, E,Cu2+|Cu = +0.34 V

A : () E,(Ag+/Ag) is more positive than E,(Cu2+/Cu) Cu has the greater tendency to be oxidised than
Ag. Hence, silver is less electropositive (tendency to lose e- undergoes oxidation) than copper.
B : () E,(Ag+/Ag) is more positive than E,(Zn2+/Zn) Zn has the greater tendency to be oxidised than
Ag. Hence, zinc displaces silver from a solution containing silver ions.
C : () E,(Zn2+/Zn) is more negative than E,(Cu2+/Cu) Zn2+ has the lower tendency to be reduced than
Cu2+.
D : () E,(Ag+/Ag) is more positive than E,(Zn2+/Zn) Zn has the greater tendency to be oxidised than
Ag. Hence, zinc has a higher tendency than silver to form positively charged ions.
Ans: A
12.
Result
Negative terminal
Positive terminal
(anode)
(cathode)
(1)
Pb
0.35
(2)
Pb
1.10
(3)
Pb
2.60
Voltage (V)
Using (1), Pb undergoes oxidation and x undergoes reduction. The reducing power of Pb is higher
than that of x.
Using (2) and (3), both y and z undergo oxidation and Pb undergoes reduction. The reducing power
of y and z is higher than that of Pb.
Since the voltage recorded in (3) is higher than that in (2), the reducing power of z is higher than that of
y. \ from weakest to strongest reducing power: x, Pb, y, z
Ans: D
13.
A : () Reactivity of Group II elements with cold water increases down the group. {Mg reacts slowly; Ca
reacts readily; Ba & Sr react vigorously.}
M(s) + 2H2O(l) M(OH)2(aq) + H2(g) , where M = Ca, Sr and Ba
B : () Solubility of Group II hydroxides and oxides increases down the group. As a result, the pH of
the resulting hydroxide solutions increases {from pH 9 in Mg(OH)2 to pH 12 in Ca(OH)2 to pH 14 in
Ba(OH)2}.
MO(s) + H2O(l) M(OH)2(aq), where M = Ca, Sr and Ba
MgO(s) + H2O(l) = Mg(OH)2(aq)
C : () Second ionisation energy of elements decreases from Be to Ba. This is due to an increase in
ionic radii of M+(g) and the increase in shielding effect which outweighs the effect of increasing nuclear
charge.
D : () Down the group, thermal stability of Group II carbonates increases.
MCO3(s) MO(s) + CO2(g)
As the ionic radius of the M2+ increases down the Group, the charge density of the M2+ decreases. The
ability of M2+ to polarise the large CO32 anion decreases down the group.
Ans: C
Page 3 of 11
14.
A : () Atomic radius of At is larger than Cl and 15.

At-At bond is longer and weaker than Cl-Cl
bond and so At2 dissociates more readily than
Cl2.
From the large drop in 1st ionisation energy from

M to N, we can deduce that M is the last
element in the 2nd Period (Ne) and N is the first
element in the 3rd Period (Na).
B : () It reacts explosively with hydrogen.
A : () R is Si. It has the highest melting point.

(Giant covalent structure, with strong Si-Si
covalent bonds)
X2(g)+H2(g) 2HX(g), DHr

(where X = Cl, Br and I )
DHr = E(X-X) + E(H-H) 2E(H-X)
As H-X bond energy decreases, DHr becomes
less exothermic(less energetically feasible).
Error! Objects cannot be created from
editing field codes.Reactivity of X2 with H2
decreases down the group from Cl2 to I2.
C : () Down the group, E,(X2/X) becomes
less positive, indicating that the oxidising
power decreases down the group. Thus At2 will
not be able to oxidise I- to I2.
D : () Volatility of halogens (X2) decreases
down group VII from Cl2 to I2. There is an
increase in strength of van der Waals' forces
between X2 molecules as the no. of electrons
per X2 molecules increases from Cl2 to At2.
Thus At2 exists as crystalline solid.
Ans: D
B : () J is nitrogen and K is oxygen. Both N3and O2- are isoelectronic, thus as nuclear charge
increases from N3- and O2-, while the shielding
effect by inner shell electrons remains relatively
constant, the ionic radius of N3- (J) is larger than
that of O2- (K).
C : () Q is aluminium. Al forms an insoluble
hydroxide, which dissolves in excess dilute
NaOH(aq).
Al(OH)3(s) + OH-(aq) [Al(OH)4]-(aq)
[Note: Being amphoteric, Al(OH)3 reacts with
both aqueous acids and alkalis.
Al(OH)3(s) + 3H+ (aq) Al3+(aq) + 3H2O(l)]
D : () Oxide of P (Mg) gives a lower pH than
oxide of N (Na) when reacted with water.
Na2O(s) reacts vigorously with water to form a
strongly alkaline NaOH(aq) solution with pH =
13-14.
Na2O(s) + H2O(l) 2NaOH(aq)
MgO(s) is sparingly soluble in water and hence
dissolves with water to a small extent to form
limited quantity of Mg(OH)2(aq), a weakly
alkaline solution with pH = 9.
MgO(s) + H2O(l) = Mg(OH)2(aq)
Mg(OH)2(aq) Mg2+(aq) + 2OH(aq)
Ans: D
16.
A : () A change in colour indicates either the possibility of a redox reaction or a ligand exchange
reaction.
[Cr(H2O)6]3+ + 6NH3
green
[Cr(NH3)6]3+ + 6H2O
purple
B : () Since NH3 replaces the H2O ligand, as it forms a stronger dative covalent bond with Cr3+ and
thus a more stable complex ion than [Cr(H2O)6]3+.
C : () The yellow solution is CrO42- (Cr2O72- is orange in colour).
D : () 2CrO42- + H2O = Cr2O72- + 2OHCrO42- ionises in water, giving Cr2O72- + 2OH-. Thus it reacts with H+ to give Cr2O72- and H2O.
2CrO42- + 2H+
G
base
Cr2O72- + H2O
H
conjugate acid
Ans: C
Page 4 of 11
17.
A : () Fe(CN)63- + e Fe(CN)64-
+0.36V
2Br-
Br2 + 2e
+1.07V
Eocell = 0.36 (+1.07) = -0.71 V < 0 (energetically not feasible). Hence Fe(CN)63- is not able to oxidise
Br- to Br2.
B : () in atmosphere indicates reaction in presence of O2.
O2 + 4H++ 4e 2H2O +1.23V
-0.41V
Cr2+
Cr3+ + e
Eocell = 1.23 (- 0.41) = +1.64V >0 (energetically feasible). Hence CrCl2 is chemically unstable as it will
be oxidised to CrCl3.
C : () MnO4- + 8H+ + 5e Mn2+ + 2H2O +1.52V
O2 + 2H+ + 2e H2O2
+0.68V
Eocell = 1.52 0.68 = +0.84V >0 (energetically feasible). On addition of H2O2 to acidified KMnO4, the
purple solution decolourises.
D : () When NaOH(aq) and FeCl3(aq) is mixed, Fe(OH)3(s) is formed.
Fe(OH)2 + OH- -0.56V
Fe(OH)3 + e
O2 + 2H2O + 4e 4OH-
+0.40V
Eocell = 0.56 (+0.40) = 0.96V <0(energetically not feasible). \Fe(OH)3 does not react with OH- to
give O2.
Ans: B
18.
AgCl + 2Na2S2O3 4Na+ + Cl- + [Ag(S2O3)2]3-
19.
Error! Objects cannot be created from

H
A : () The reaction causes silver ions to

dissolve through the formation of a silver
complex, [Ag(S2O3)2]3- which is soluble.
B, C and D: () Silver is neither oxidised or
reduced as the oxidation state of Ag remains at
+1 in both AgCl and [Ag(S2O3)2]3-.
Ans: A
editing field codes.
C
H
H
electrophile
free radical
nucleophile
No.of outershell e- on C atom of CH3+ = 2(3)= 6

No.of outershell e- on C atom of CH3 =2(3)+1=7
No.of outershell e- on C atom of CH3- =2(3)+2=8
Ans: A
20.
With cold, dilute acidified KMnO4:

H3C
CH3
H
H
CH3
H
HO
*
OH
OH
After mild oxidation, there is an increase

in two new chiral carbon atoms.
Page 5 of 11
(continue on next page

20.
With hot, concentrated acidified KMnO4:

H3C
H3C
CH3
CH3
oxidation
CH3
CH3
HO
HO
This carbon is not chiral after oxidation

After strong oxidation, there is a
decrease in one chiral carbon atom.
Answer : D
21.
Note: the three CH3 groups bonded to C3 are equivalent.

Cl can abstract H atoms from CH3 of C1, CH2 of C2 or any of the three CH3 groups bonded to
C3 to form 3 different forms of X.
CH3
CH3CH2C
1 2
3
CH3
Cl
CH3
CH3
CH2CH2C
CH3
CH3
CH3
+ CH3CHC
CH3
CH3 +
CH2CH2C
CH2
CH3
CH3
Answer : B
22.
X:
Y:
OH H
C
CN
OH H
CH2
Ce
OH
Br
6 sp2 hybridised
carbon atoms in
the benzene ring.
Ca, Cb and Cd are sp3

hybridised (ie. 4 electron
pair).
Ce is sp hybridized (ie. 2
electron pairs).
Answer : C
Page 6 of 11
23.
Error! Objects cannot be created

from editing field Reduction
codes.
A: ()
120o
109.5o
O
OH
120o
H
C: ()
120o
D : () The nucleophiles in reaction 1 and 2 are

cyanide ion and iodide ion respectively. The
bromide ion is not acting as a nucleophile.
H
C
Combustion
Ans: C
120o
180o
H
H3C
D: ()
C : () The cyanide ion is a stronger nucleophile

than the iodide ion, hence the substitution
proceeds faster.
CH3C
H
A : () The CI bond is a weaker bond than the

CBr bond.
B : () The CN bond is not broken in the
mechanism.
Oxidation
CH3C
B: ()
24.
Br
Elimination
H
C
109.5o
120o
Ans: A
25.
A : () Absence of carboxylic acid and alcohol functional groups which could react with PCl5.
B : () No pale yellow ppt will be formed due to the absence of -COCH3 (in aldehydes or ketones)
or -CH(OH)CH3 group (in alcohols) in reactant or product.
O
O
alkaline
hydrolysis
CCH3
CH3CO2
CHO
CHO
oxidation
C : ()
CCH3
CCH3
CO2H
CHO
Potassium dichromate (VI) turns from orange to green.
26.
D : () Fehlings solution only gives a positive chemical test for aliphatic aldehyde, not for aromatic
aldehyde.
Answer : C
uv light
A : () CH3CH3(g) + Cl2(g)
CH3CH2Cl + HCl
B: ()
AlCl3(s)
(l) + Cl2(g)
D : () CH3CH2I(l) + NaOH(aq)
Note if its CH3CH2I(l) + NaOH(alc)
Cl + HCl
CH3CH2OH + NaI
CH2=CH2 + H2O, elimination occurs.
Page 7 of 11
Answer : C
27.
Primary halogenoalkane generally undergoes 28.

reaction.
Tertiary
halogenoalkane
SN2
generally undergoes SN1 reaction. The yellow
ppt is AgI, hence the halogenoalkane must be
iodoalkane (eliminate option A & C).
AlCl3
Cl
B: ()
1 alkyl
group
+ AlCl4
+ AlCl3
primary
CH3CH2CH2C
Step I
Cl
H halogenoalkane
acts as an electrophile
This electrophile
This acts as an
and
and undergoes electrohpilic
undergoes electrophilic
substitution
substitution with benzene
with benzene ring
.
rin totoform
form MM.
Ans: A
D: ()
CH3
CH3C
CH3
tertiary
halogenoalkane
I
3 alkyl groups
Ans: D
29.
A: () C6H5CH2CN + D2
Ni
C6H5CH2CD2ND2
reduction
(resembles C6H5CH2CH2NH2, primary amine, which is basic)

B : () (ND2H2)+ + OD
ND2H (or NDH2) + HDO (or D2O)
acid-base reaction
(resembles NH3, which is basic)

C : ()CH3CH=CH2 + D2O(g)
CH3CH(OD)CH2D
electrophilic addition
(resembles CH3CH(OH)CH3,an alcohol, which is not basic)

NaOD
D : () CH3CH2CONH2
CH3CH2CO2-Na+ + NH2D
(resembles NH3, which is basic)
Answer : C
30.
NH2
A : () In Na2CO3(aq), it migrates towards the positively charged anode.

S
B : () It exists as a cation in a solution of pH 1.
COO
NH3
S
COOH
C : () It exists as a solid with high melting point due to the presence of strong ionic bonds between
groups of oppositely charged zwitterions.
NH3
S
COO
(zwitterion)
Page 8 of 11
.
30.
D : () To form covalent disulfide linkage with another molecule, it has to be -SH, and not -SCH3.
-SCH3 cannot form
disulfide linkage
NH2
COOH
S
methionine
Answer : C
31.
Gas particle Y has (n+1) protons and a charge 32.

of 2+. Error! Objects cannot be created from
editing field codes.no. of electrons = (n+1
2) = n 1
Gas particle X has n protons and (n-1)
electrons. Error! Objects cannot be created
from editing field codes.charge of X is 1+.
(1): () X has a smaller nuclear charge than Y,
hence X has a larger radius than Y.
(2): () The electron removed is less tightly
bound to the singly charged X than the doubly
charged Y. Hence less energy is required to
remove the electron.
(1): () D S<0. Decrease in disorder due to

precipitation of PbSO4(s).
(2): ()DS>0. Increase in disorder since kinetic
energy of particles increases causing a
broadening
of
the
Boltzmann
energy
distribution. Error! Objects cannot be created
from editing field codes.more ways of
arrangement of energy quanta.
(3): ()DS>0. Increase in disorder as reaction
proceeds with an increase in number of gas
particles from 0 to 1 mole.
Answer : D
(3): () The electron added is less tightly

bound to the singly charged X than the doubly
charged Y. Hence less energy is released
when the electron is added to X.
Answer : A
33.
(1) and (2) : () The iron catalyst provides an 34.

alternative reaction path of lower Ea than
that of the uncatalysed reaction. Thus, the
number of molecules with energy greater than
the lowered activation energy increases.
Frequency of effective collisions between
molecules increases and hence rate of
reaction increases by the same extend for the
forward and backward reaction.
(3) : () Catalyst does not increase the kinetic
energy of the reacting particles.
Answer : B
(1) : () Solubility product, Ksp is only affected

by temperature.
(2) : () The presence of the common ion F,
Equilibrium
position
of
increases
[F-].
2+
SrF2(s) Sr (aq) 2F-(aq) will shift to left, hence
decreasing the solubility of strontium fluoride.
(3) : () Let solubility of SrCO3 be x.
x2 = 8.7 x 109
x = (8.7 x 109)1/2 = 9.33 x 105 mol dm3
Let solubility of SrF2 be y.
4.0 x 1011 = (y)(2y)2 = 4y3
1
4.0 10 -11 3
y =
= 2.15 x 104 mol dm3

\SrF2 is more soluble than SrCO3.
Answer : A
Page 9 of 11
35.
(1) : () Atomic radius increases from Cl, Br to 36.

I. HX bonds become longer and weaker.
Thus, HX bond energy decreases from HCl,
to HBr and HI, and is more easily broken
under heating.
(1) : () Since N is more electronegative than

Cl, o.s of Cl in NCl3 = +1. Hence the oxidation
state of N in NCl3 is -3 and it changes to 0 (in
N2).
(2) : () As electronegativity decreases from

Cl, Br, I, polarity of hydrogen halide decreases
from HCl, HBr, HI.
(3) :() Cl- from NaCl forms AgCl precipitate

with AgNO3(aq).
(3) : () The enthalpy change of formation of

HX becomes less exothermic. HF is most
energetically stable with respect to F2 and
H2, and hence it is most readily formed.
Whereas HI is least energetically stable with 37.
respect to I2 and H2, and hence it is not
readily formed. (HI bond formed is very
weak.)
(Note: The acid added is to remove any NaOH

left, so as to prevent precipiation of Ag2O.)
Answer : B
38.
(2) : () NaClO(aq) is the bleaching solution.
Answer : A
(1) and (2) : () To prepare the gaseous
products, bromoethane and ethanal, heating is
required with their respective reagents and
conditions. The products can then be
condensed and collected as the distillate.
(3) :() To prepare 1,2dibromoethane, heating
is not required.
Answer : B
Pattern observation:
oxidised to HCO2H, which
is further oxidised to CO2
H3C
When this C C
bond is broken
+ 3 [O]
hot HNO3
CH3COOH + CO2
H3C
oxidised to
For butanone,
oxidised to
H3C
C
When this C C
bond is broken
+ 3[O]
hot HNO3
CH3CH2COOH + CO2
CH2CH3
oxidised to
oxidised to
Page 10 of 11
H3C
When this C C
bond is broken
O + 3[O]
hot HNO3
2CH3COOH
oxidised to
CH2CH3
(1), (2) and (3) : ()
Answer : A
39.
(1) : () Alkaline
hydrolysis O
HO
OH
OH
O
C
Acid-base reaction
OH
Alcohol do
not react
with NaOH!
CH3
2 moles of NaOH(aq) are required to react with the ester via alkaline hydrolysis and carboxylic acid via
acid-base reaction.
(2) : ()
O
HO
OH
OH
4 OH groups 2H2(g)
Redox reaction
O
C
OH
CH3
Na reacts with 3OH groups and 1 RCOOH group to produce 2 moles of H2.
(3) : ()
O
HO
OH
OH
Electrophilic addition with alkenes and

substitution reaction with alcohol
O
C
OH
CH3
1 mole of Pravastatin reacts with 5 moles of HCl(g).

Answer : B
40.
(1) : ()
Page 11 of 11
NH2
OH
H2N
N
H
N
NH2
O
hydrolysis
NH2
O
+
H2N
N
H
OH
OH
NH2
NH2
Note: Amino acids contain at least one amino group (-NH2) and one carboxyl group (-COOH).
(2): () There is no aldehyde or ketone functional groups in compound Z.
(3): () Ethanoyl chloride forms only amides with the -NH2 groups in Z. Esters will not be formed.
Answer : D
Page 12 of 11

Higher 2
CANDIDATE
NAME
EXAM INDEX
NUMBER
CLASS
CHEMISTRY
9647/02
12 September 2012
2 hours
Candidates answer on Question Paper.

Data Booklet

For Examiners Use
1
2
3
4
5
6
Total
[Turn over
2
1.
Planning (P)
You are to plan an investigation into the thermal decomposition of caesium nitrate,
CsNO3.
You may make use the following data when planning your investigation.
Data:
Group I element
cation
Ionic radius / nm
lithium
Li+
0.060
sodium
Na+
0.095
potassium
K+
0.133
rubidium
Rb+
0.148
caesium
Cs+
0.176
Equation for the thermal decomposition of lithium nitrate and sodium nitrate are given
below:
2Li2O(s) + 4NO2(g) + O2(g)
1.
4LiNO3(s)
2.
2NaNO3(s) 2NaNO2(s) + O2(g)

Nitrogen dioxide gas
Oxygen gas
NO2
O2
brown in colour
colourless
soluble in water
almost insoluble in water
poisonous
powerful oxidant
1 mol of any gas occupies a volume of approximately 24 dm3 at room temperature

and atmospheric pressure.
Ar: Cs, 133;
(a)
N, 14.0;
O, 16.0
Predict which of the equations below will represent the thermal decomposition
of caesium nitrate. Place a tick against the equation of your choice.
4CsNO3(s) 2Cs2O(s) + 4NO2(g) + O2(g)
2CsNO3(s) 2CsNO2(s) + O2(g)
Use the data provided to explain your prediction.
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9647/02/Prelim 2012
[2]
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1.
(b)
You are to plan an experiment in which
(i)
caesium nitrate is heated

gas is collected
the volume of gas collected is measured
the experimental results are used to confirm or reject your prediction
Draw a diagram of the apparatus you would use in this experiment.
Your apparatus should use only standard items found in college
laboratory.
Label each piece of apparatus used, indicating its size or capacity and
state the gas or gases collected on your diagram.
[3]
(ii)
Calculate the volume of gas you would expect to collect at room

temperature and atmospheric pressure if 1 mol of caesium nitrate
completely decomposed according to your predicted equation in (a).
[1]
9647/02/Prelim 2012
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4
1.
(c)
Use your answer to (b)(ii) and the capacity of the apparatus selected in (b)(i) to
calculate the maximum mass of CsNO3 that can be used in your experiment.
[1]
(d)
Outline, in a series of numbered steps, the method to be used in the

experiment.
Make certain that the steps you describe are in the correct order.
You need not explain how the apparatus is assembled.
Indicate clearly how you will know when decomposition is complete.
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9647/02/Prelim 2012
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1.
(e)
What should be done when decomposition is complete to ensure that the

volume of the gas measured in the apparatus is the correct volume?
.............................................................................................................................
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.............................................................................................................................
(f)
[1]
Identify a risk present in the method you have described and suggest how you
would minimise this risk.
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[1]
[Total: 12]
9647/02/Prelim 2012
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2.
(a)
(i)
Write an equation for the reaction between chlorine and cold aqueous
sodium hydroxide and state the type of reaction that occurs.
Type of reaction:
(ii)
The resultant solution obtained in (a)(i) is heated and a further reaction

occurs. Write an equation for the overall reaction between chlorine and
sodium hydroxide.
[3]
(b)
Chlorine forms a variety of oxides and oxoanions. A series of standard

reduction potentials involving the chlorine oxoanions, in alkaline medium, are
given below.
ClO
ClO2
ClO3
ClO4
+
+
+
+
H2O
H2O
H2O
H2O
half-equation
+ 2e = Cl
+ 2e = ClO
+ 2e = ClO2
+ 2e = ClO3
+
+
+
+
2OH
2OH
2OH
2OH
E,/V
0.89
0.67
0.33
0.35
Using the above data and information in the Data Booklet, predict the final
product formed when excess zinc metal is added to an alkaline solution of
chlorate(V), ClO3. Support your answer with E,cell calculations.
[4]
9647/02/Prelim 2012
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7
2.
(c)
Chlorine dioxide, ClO2, is a highly reactive gas that is used as a disinfectant to

kill water-borne bacteria, viruses and fungi.
Draw a dot-and-cross diagram to show the arrangement of valence electrons
in the ClO2 molecule. Hence suggest why chlorine dioxide is highly reactive.
.............................................................................................................................
.............................................................................................................................
(d)
[2]
Despite having similar relative molecular mass, the boiling point of chlorine is
34 oC and that of chlorine dioxide is 11 oC.
Give an explanation to account for this large difference in boiling points.
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[2]
[Total: 11]
3.
(a)
Aluminium is obtained by electrolysis of molten Al2O3 using inert electrodes.

(i)
Give ion-electron equations, with state symbols, for the electrode

processes:
at the cathode:
at the anode: ......
(ii)
Calculate the mass of aluminium produced when a current of 8 A is

passed for 100 minutes through the molten Al2O3.
[5]
9647/02/Prelim 2012
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8
3.
(b)
The enthalpy change of formation of Al2O3 can be calculated from a Born-Haber

cycle.
Construct the Born-Haber cycle for the formation of Al2O3, using the following
data and relevant data from the Data Booklet. Hence, calculate the enthalpy
change of formation of Al2O3.
DH / kJ mol-1
Enthalpy change of atomisation of aluminium
+644
+702
Lattice energy of Al2O3
13311
[5]
9647/02/Prelim 2012
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9
3.
(c)
Aluminium chloride exists in two different forms in the vapour state. When some
Al2Cl6 was added into a reaction vessel, the following equilibrium is slowly set
up.
Al2Cl6(g) = 2AlCl3(g)
At different times during the experiment, changes were made to the conditions
in the reaction vessel. At each time, there was only one change made to the
condition in the reaction vessel.
The change in the concentrations in the equilibrium mixture with time is shown
in the graph below.
Concentration
Al2Cl6
AlCl3
T1
(i)
T2
T3
time
Suggest the changes that caused the equilibrium shifts at time:

T1: .
T2: .
(ii)
Explain whether the conversion of Al2Cl6 to AlCl3 is expected to be

exothermic or endothermic.
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9647/02/Prelim 2012
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3.
(c)
(iii)
Sketch on the same axes of the given graph on page 9, the changes in
the concentration of Al2Cl6 and AlCl3 when the mixture was cooled at
time T3.
Explain your answer with reference to your conclusion made in (c)(ii).
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(iv)
At a total pressure of 1 atm and 673 K, Al2Cl6 was 30% dissociated into
AlCl3.
Calculate the equilibrium constant, Kp, including its units, at 673 K.
[9]
[Total: 19]
9647/02/Prelim 2012
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4.
(a)
Copper is a transition element that forms a rich variety of compounds with

varying oxidation states.
Cu(NO3)2(aq) is a blue solution which can undergo the following reactions.
Cu(NO3)2(aq)
SO2
conc HCl
D
white solid
Cu2O(s)
NH3(aq)
excess
conc HCl
A
pale blue ppt
conc NH3(aq)
excess
NH3(aq)
E
colourless solution
oxidises in air
B
deep blue solution
C
colourless solution
B, C and E contain complex ions of copper.

Both compound D and complex ion E contain copper and chlorine only.
The oxidation number of copper in C, D and E are the same.
(i)
What are the formulae of the compound A and of the cation present in B?
A: .
(ii)
B:
Suggest a balanced equation for the formation of B from A.

...
(iii)
State the role of SO2 in the conversion of Cu(NO3)2 to Cu2O.

.....................
(iv)
The composition of complex ion C by mass is Cu, 65.1%, N, 28.7%,

H, 6.2%.
Use the data to determine the empirical formula and identity of complex
ion C.
9647/02/Prelim 2012
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4.
(a)
(v)
Suggest the formulae of compound D and complex ion E, given that the
coordination number of Cu in complex ion E is the same as that in C.
D: .
(b)
E:
[8]
Copper forms a very useful group of organic compounds known as Gilman

reagents.
Gilman reagents can react with alkyl halides via nucleophilic substitution to form
alkanes. An example is shown below:
Step 1:
2CH3Li
methyllithium
Step 2:
CH3CH2Cl
chloroethane
(i)
CuI
(CH3)2CuLi
Gilman reagent
(CH3)2CuLi
CH3CH2CH3
+ CH3Cu
LiI
+ LiCl
Suggest the structural formula of the final organic product formed when
, and bromoethane are used in a similar
phenyllithium,
two-step process.
(ii)
Gilman reagents can also react with acyl chlorides to form ketones.
An example is shown below:
O
C
(CH3)2CuLi
Cl
O
C
CH3 + CH3Cu + LiCl
It is observed that the reaction with acyl chlorides takes place much more
readily than that with alkyl chlorides. Explain why this is so.
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9647/02/Prelim 2012
[3]
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[Total: 11]
5.
(a)
The Green Fluorescent Protein (GFP) is a protein that can be isolated from the
jellyfish, Aequorea victoria, and it can exhibit bright green fluorescence when
exposed to ultraviolet light. The chromophore is the section of the GFP that
fluoresces and contains the amino acid sequence ser-tyr-gly.
H
H2N
H
COOH
CH2OH
H2N
H
COOH
H2N
CH2
COOH
OH
ser
tyr
gly
(i)
Draw the structure of this section of the GFP at pH 14.
(ii)
GFP has a beta barrel structure, consisting of one b-pleated sheet and
a-helices running through the centre of the barrel structure.
Sketch a labelled diagram to show how the -pleated sheet structure of
proteins is stabilised, showing clearly the stabilising bonds involved.
9647/02/Prelim 2012
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14
[4]
5.
(b)
A venomous jellyfish has tentacles containing stinging cells that inject venom
into the skin of a victim. The venom is made up of a diverse variety of proteins
and polypeptides capable of inflicting pain and swelling.
The most common first-aid treatment of jellyfish stings is to get the victim out of
water, scrape off any attached tentacles with a hard object and rinse the
affected area with hot seawater to deactivate the venom.
Explain how the application of heat is effective in treating jellyfish stings.
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(c)
[2]
Paracetamol is usually prescribed to the victim to reduce the pain from jellyfish
stings.
HO
NHCOCH3
Paracetamol
A student suggested that paracetamol can be synthesised from phenol, via a
three-step reaction sequence as proposed below.
OH
OH
OH
C
H3C
Step II
Step I
C
O
CH3
Step III
NO2
NH2
4-aminophenol
(i)
OH
ethanoic anhydride
NHCOCH3
paracetamol
What types of reaction take place in Step I, II and III?

Step I: ......................................................................
Step II: ....................................................................
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Step III: ...................................................................
5.
(c)
(ii)
State the reagents and conditions needed for Step I and II.
Step I: ........................................................................................................
Step II: .......................................................................................................
(iii)
In actual practice, 4-aminophenol is used instead as the starting material

and only Step III is carried out.
Given that both phenol and 4-aminophenol are easily available, suggest a
reason why phenol is not used as the starting material.
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[7]
[Total: 13]
6.
Lorcaserin (Trade name: Belviq) is a weight-loss drug developed by Arena

Pharmaceuticals in San Diego and is recently approved by the US Food and Drug
Administration in June 2012 for use in the treatment of obesity for adults.
Cl
H3C
(a)
Lorcaserin
Draw the structures of the organic compounds formed when Lorcaserin is

(i)
ethanoyl chloride
(ii)
excess CH3Cl
9647/02/Prelim 2012
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[2]
6.
(b)
An isomer of Lorcaserin (compound Y) is shown below.
H3C
Cl
compound Y
Suggest a chemical test that could be used to distinguish compound Y from

Lorcaserin. You should state what you would observe for each compound in
the test.
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[2]
(c)
NH2
phenylamine
Explain how the basicity of Lorcaserin might compare with that of phenylamine.
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[2]
[Total: 6]
9647/02/Prelim 2012
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Higher 2
CANDIDATE
NAME
EXAM INDEX
NUMBER
CLASS
CHEMISTRY
9647/02
14 September 2012
2 hours
Candidates answer on Question Paper.

Data Booklet

For Examiners Use
1
12
11
19
11
13
Total
72
This document consists of 16 printed pages and 1 blank pages.
[Turn over
2
1.
Planning (P)
You are to plan an investigation into the thermal decomposition of caesium nitrate, CsNO3.
You may make use of some or all of the following data when planning your investigation.
Data:
Group I element
cation
Ionic radius / nm
lithium
Li+
0.060
sodium
Na+
0.095
potassium
K+
0.133
rubidium
Rb+
0.148
caesium
Cs+
0.176
Equation for the thermal decomposition of lithium nitrate and sodium nitrate are given
below:
1.
4LiNO3(s) 2Li2O(s) + 4NO2(g) + O2(g)
2.
2NaNO3(s) 2NaNO2(s) + O2(g)

Nitrogen dioxide gas
Oxygen gas
NO2
O2
brown in colour
colourless
soluble in water
almost insoluble in water
poisonous
powerful oxidant
1 mol of any gas occupies a volume of approximately 24 dm3 at room temperature

and atmospheric pressure.
Ar: Cs, 133;
1.
N, 14.0;
O, 16.0
Planning (P)
(a)
Predict which of the equations below will represent the thermal decomposition of
caesium nitrate. Place a tick against the equation of your choice.
4CsNO3(s) 2Cs2O(s) + 4NO2(g) + O2(g)
2CsNO3(s) 2CsNO2(s) + O2(g)
[1m]
Use the data provided to explain your prediction.

As the size/ionic radius of Cs+ is larger than that of Na+, Cs+ has a
lower charge density and hence has a lower polarising power/less able
to polarise the large NO3- anion than Na+.
(b)
[1m]
You are to plan an experiment in which
caesium nitrate is heated

9647/02/Prelim 2012
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(i)
gas is collected
the volume of gas collected is measured
the experimental results are used in a calculation to confirm or reject your
prediction
Draw a diagram of the apparatus you would use in this experiment.
Your apparatus should use only standard items found in college laboratory.
Show clearly how the solid will be heated, the gas collected and its volume
measured.
Label each piece of apparatus used, indicating its size or capacity and state the
gas or gases collected on your diagram.
[1m] Heat solid CsNO3 in a hard glass tube or boiling tube with a stoppered
delivery tube. Must indicate Heat with or without arrow.
[1m] Collect gas over water into an inverted burette or a measuring cylinder;
or collect gas directly into a graduated frictionless gas syringe.
[1m] Connect the two apparatus (no gas loss), label the capacity of apparatus for
gas volume measurement, state the gas(es) collected in the set-up.
1.
(b)
(ii)
Calculate the volume of gas you would expect to collect in your apparatus if
1 mol of caesium nitrate completely decomposed according to your predicted
equation in (a).
Following equation 2, 2CsNO3 O2

Expected amount of O2 = x 1 = 0.5 mol
Expected volume of O2 gas at r.t.p. = 0.5 x 24 dm3 = 12 dm3
OR
[1m]
Following equation 1 (for direct collection), 4CsNO3 4NO2 O2

Expected amount of gases (NO2 and O2) = 5/4 x 1 = 1.25 mol
Following equation 1 (for collection of gas over water), 4CsNO3 O2
Expected amount of O2 gas = 1/4 x 1 = 0.25 mol
9647/02/Prelim 2012
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(c)
Use your answer to (b)(ii) and the size of the apparatus selected in (b)(i) to
calculate the maximum mass of CsNO3 that can be used in your experiment.
Following equation 2:
Mass of 1 mol of CsNO3 = 195 g
Using 100 cm3 measuring cylinder or graduated gas syringe,
Maximum volume of gas collected = 100 cm3
Maximum mass of CsNO3 = 100/12000 x 195 = 1.625 g 1.63 g (1-2 d.p.)
OR
[1m]
Or, Using 50.00 cm3 burette or graduated gas syringe,

Following equation 1 (for direct collection of gas):
Maximum mass of CsNO3 = 100/30000 x 195 = 0.65 g (1-2 d.p.)
OR

Following equation 1 (for collection of gas over water):
Maximum mass of CsNO3 = 100/6000 x 195 = 0.65 g (1-2 d.p.)
1.
(d)
Outline, in a series of numbered steps, the method to be used in the

experiment.
Make certain that the steps you describe are in the correct order.
You need not explain how the apparatus is assembled.
Indicate clearly how you will know when decomposed is complete.
1. Weigh accurately *1.50 g (should be slightly less than the maximum
mass) of solid CsNO3 into a dry boiling tube and record the mass.
[1m]
2. Stopper the boiling tube with a delivery tube. Measure and record
the initial volume reading on the gas syringe (or in the inverted
measuring cylinder or burette). ()
2()
[1m]
3. Heat the solid sample gently at first and then strongly until a
constant volume of gas is collected (or there is no movement of
piston of the gas syringe or no more gas bubbles is observed in
water).
[1m]
4. When the whole set-up has been cooled to room temperature, measure
9647/02/Prelim 2012
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5
and record the final volume reading on the gas syringe (or in the
inverted measuring cylinder or burette). ()
(e)
What should be done when decomposition is complete to ensure that the

volume of the gas measured in the apparatus is the correct volume.
The gas or whole set-up needs to be cooled to room temperature
before measuring the final volume (or repeat the whole experiment
with the same mass of solid and take the average readings)
(f)
[1m]
Identify a risk present in the method you have described and suggest how you
O2 is a powerful oxidant and support burning. Remove any oxidisable
material. (no mark if student commented that O2 is flammable..)
[1m]
Or,
Only for those who chose equation 1:
NO2 is poisonous gas. Conduct the experiment inside the fume
cupboard.)
Or,
Only for those who collected the gas over water:
Potential suck back may occur and crack the hot tube. Remove the
delivery tube from water when heating stops.
[Total: 12]
9647/02/Prelim 2012
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2.
(a)
Write an equation for the reaction between chlorine and cold aqueous
sodium hydroxide and state the type of reaction that occurs.
(i)
Type of reaction: Disproportionation
[1m]
Cl2 ( g ) + 2OH- ( aq )
Cl- ( aq ) + ClO- ( aq ) + H2O (l)
[1m]
Cl2 ( g ) + 2NaOH ( aq )
NaCl ( aq ) + NaClO ( aq ) + H2O (l)
OR
Ignore s.s
The resultant solution obtained in (a)(i) is heated and a further reaction

occurs. Write an equation for the overall reaction between chlorine and
sodium hydroxide.
(ii)
3Cl2 ( g ) + 6OH- ( aq )
5Cl- ( aq ) + ClO3- ( aq ) + 3H2O (l)
Overall eqn :
[1m]
3Cl2 ( g ) + 6NaOH ( aq )
5NaCl ( aq ) + NaClO3 ( aq) + 3H2O (l)
OR
Ignore s.s
(b)
Chlorine forms a variety of oxides and oxoanions. A series of standard reduction

potentials involving the chlorine oxoanions, in alkaline medium, are shown:
ClO
ClO2
ClO3
ClO4
+
+
+
+
Half-equation
H2O + 2e = Cl + 2OH
H2O + 2e = ClO + 2OH
H2O + 2e = ClO2 + 2OH
H2O + 2e = ClO3 + 2OH
E,/V
0.89
0.67
0.33
0.35
Using the above data and information in the Data Booklet, predict the final product
formed when excess zinc metal is added to an alkaline solution of chlorate(V), ClO3.
Support your answer with E,cell calculations.
Reaction of zinc metal with chlorate(V):
O
Ecell
= E O ClO3- /ClO2- - E O Zn2+ /Zn
= -0.33 - ( -0.76 )
= +0.43 V ()
Thus, Zn is able to reduce ClO3 to ClO2.
Reaction of zinc metal with chlorate(III):
O
Ecell
= E O ClO2- /ClO - - E O Zn2+ /Zn
= -0.67 - ( -0.76 )
= +0.09 V ()
Thus, Zn is able to reduce ClO2 to ClO.
Reaction of zinc metal with chlorate(I):
O
Ecell
= E O ClO - /Cl - - E O Zn2+ /Zn
3 () - 2 marks
1-2 () 1 mark
[4]
= -0.89 - ( -0.76 )
= -0.13 V ()
Rxn between ClO- and Zn2+ is not energetically feasible
[1m]
OR Zn is not able to reduce ClO to Cl .
Hence, zinc will be oxidised to Zn2+ and chlorate(V) will be reduced to

chlorate(I)/ClO-.
[1m] Can infer final product from conclusion
9647/02/Prelim 2012
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7
2.
(c)
Chlorine dioxide, ClO2, is a highly reactive gas that is used as a disinfectant to kill
water-borne bacteria, viruses and fungi.
Draw a dot-and-cross diagram to show the arrangement of electrons in the ClO2
molecule. Hence suggest why chlorine dioxide is highly reactive.
xx
x x Cl x x
[1m]
Chlorine dioxide has an unpaired electron/odd number of electrons.

Hence it is highly reactive.
[1m]
[2]
(d)
Despite having similar relative molecular mass, the boiling point of chlorine is 34 oC
and that of chlorine dioxide is 11 oC.
Give an explanation to account for this large difference in boiling points.
A larger amount of energy is required to break the stronger permanent
dipole-permanent dipole interactions between the ClO2 molecules than
that to break the weaker van der Waals forces between the Cl2
molecules.
[2]
[1m] for correct intermolecular forces identified bet. molecules

[1m] for pd-pd stronger than vdw (must compare bet. Correct I.M.F)
[Total: 11]
9647/02/Prelim 2012
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3.
(a)
Aluminium is obtained by electrolysis of molten Al2O3 using inert electrodes.

Give ion-electron equations, with state symbols, for the electrode
processes:
(i)
at the cathode: Al3+(l) + 3e Al(l)

at the anode:
[1m]
O2-(l) O2(g) + 2e
[1m]
s.s. required, reject =
for wrong or missing s.s. AND half-eqns are correct: 1m only

Calculate the mass of aluminium produced when a current of 8 A is
passed for 100 minutes through the molten Al2O3.
(ii)
(ignore sf)
[1m]
Mass of Al produced = 0.497/3 x 27.0 = 4.47 g

(1st mark ecf from (a)(i) for mole ratio)
(1 3 sf for final answer (2nd mark) + correct units)
[2m]
Amount of e transferred = 48000/96500 = 0.497 mol
(b)
[5]
The enthalpy change of formation of Al2O3 can be calculated from a BornHaber cycle.
Construct the Born-Haber cycle for the formation of Al2O3, using the following
data and relevant data from the Data Booklet. Hence, calculate the enthalpy
change of formation of Al2O3.
DH / kJ mol-1
+644
+702
13311
Enthalpy change of atomisation of aluminium

Lattice energy of Al2O3
2 Al(s)
3/2 O2(g)
2(+644)
enthalpy change
of f ormation
of Al2O3
Al2O3(s)
[1m] for balanced Al2O3(s)

formation equation
3/2(+496)
5: [3m]
4: [2m]
2-3: [1m]
0-1: [0m]
2 Al(g)
3 O(g)
-13311
2(+577
+1820
+2740)
3(+702)
2 Al3+(g)
Do not award
if + sign is
missing from
eqn
Do not double penalise:

Award 1 for L.E if student
miss out state symbols for
Al2O3 (first 1m is already
penalised)
[5]
3 O2-(g)
DHf(Al2O3(s)) = 2(644) + 2(5137) + (3/2(496)) + 3(702) 13311 = +1101 kJ mol1

[1m] for final answer (exact/3 sf), no ecf
Award each () only if

- equation is balanced
- state symbol of reactants and products are stated correctly
- process is labelled with correct DH value or symbol (ignore + sign)
Jurong
Junior
- Hf can
beCollege
accepted (infer to question)9647/02/Prelim 2012
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9
3.
(c)
Aluminium chloride exists in two different forms in the vapour state and the following
conversion exists between them:
Al2Cl6(g)
2AlCl3(g)
The conversion was studied using a fixed amount of Al2Cl6 in a reaction vessel. At
different times during the experiment, changes were made to the conditions in the
reaction vessel. The change in the concentrations in the equilibrium mixture with time
is given by the graph below.
Al2Cl6
Concentration
[1m] for correct

sketch (with ecf),
ignore magnitude,
show in students
answers reaching
new eqm at the same
time
T1
(i)
Do not accept:
AlCl3
T2
T3
time
Suggest the changes that caused the equilibrium shifts at time:

T1: decrease in total volume of reaction vessel/increase in pressure
[1m]
T2: addition of/increase in concentration/(partial) pressure of
Al2Cl6 (OWTTE) [1m]
Reject decrease in volume of (specific gas), accept decrease in
volume of gases.. Same for suggestions in pressure
Accept wrongly-written formula of Al2Cl6 (Benefit Of Doubt), and
reject AlCl3
9647/02/Prelim 2012
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10
(ii)
Explain whether the conversion of Al2Cl6 to AlCl3 is expected to be exothermic or

endothermic.
It is expected to be endothermic.
[1m]
This is because there is breaking of (dative covalent) bonding

between the Cl and Al atoms.
[1m]
Accept:
break molecule/ dimer
3.
(c)
Sketch on the same axes of the given graph on page 9, the changes in the
concentration of Al2Cl6 and AlCl3 when the mixture was cooled at time T3.
Explain your answer with reference to your conclusion made in (c)(ii).
(iii)
When temperature is lowered, the equilibrium position will shift to

the left, favouring the exothermic reaction, so as to increase
temperature.
[1m]
OR
When temperature is lowered, it favours the backward exothermic
reaction, so as to increase temperature.
Hence, yield of Al2Cl6 increases and yield of AlCl3 decreases.
Ecf from c(ii)
At a total pressure of 1 atm and 673 K, Al2Cl6 was 30% dissociated into AlCl3.
(iv)
Calculate the equilibrium constant, Kp, including its units, at 673 K.

Let p be the initial partial pressure of Al2Cl6 (g).
Al2Cl6(g)
Initial partial pressure/ atm
Eqm partial pressure/ atm
P
0.7p
2AlCl3(g)
0.6p
0.7p + 0.6p = 1 atm

p = 0.769 atm
At eqm, PAl2Cl6 = 0.7 0.769 = 0.538 atm
PAlCl3 = 0.6 0.769 = 0.462 atm (0.461 atm)
Kp =
[1m] ignore sf
[1m] ignore sf
[9]
0.4622
[1m]
0.538
for correct substitution (ecf from p.p.) in correct Kp expression
= 0.397 atm (0.395 atm or 0.396 atm)

[1m] correct answers + units + 3 sf (ecf only for correct Kp expression )
9647/02/Prelim 2012
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11
4.
(a)
Copper is a transition element that forms a rich variety of compounds with varying
oxidation states.
Aqueous copper(II) nitrate, Cu(NO3)2 is a blue solution which can undergo the
following reactions.
SO2
Cu(NO3)2(aq)
conc HCl
Cu2O(s)
D
white solid
NH3(aq)
excess
conc HCl
A
pale blue ppt
conc NH3(aq)
excess
NH3(aq)
E
colourless solution
oxidises in air
B
deep blue solution
C
colourless solution
B, C and E contain complex ions of copper. Both compound D and complex ion E
contain copper and chlorine only.
(i)
What are the formulae of the compound A and of the cation present in B?
A: Cu(OH)2
(ii)
B: [Cu(NH3)4(H2O)2]2+
[2m]
Suggest a balanced equation for the formation of B from A.

Cu(OH)2(s) +4NH3(aq) + 2H2O(l) [Cu(NH3)4(H2O)2]2+ + 2OH(aq)
[1m]
s.s not required

(iii)
State the role of SO2 in the conversion of Cu(NO3)2 to Cu2O.

Reducing agent/Reductant (mark for meaning)
(iv)
[1m]
The composition of complex ion C by mass is Cu, 65.1%, N, 28.7%, H, 6.2%.

Use the data to determine the empirical formula and identity of complex ion C.
Cu
65.1
28.7
6.2
63.5
14.0
1.0
1.025
2.05
6.2
[1m]
Working for empirical formula must be shown

Empirical Formula = CuN2H6 or Cu(NH3)2 (ignore charge if its given)
Identity: Cu(NH3)2+
9647/02/Prelim 2012
[1m]
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12
(v)
The oxidation number of copper in compound D and complex ion E are the same
as that in compound C, and both D and E contain copper and chlorine only.
Suggest the formulae of D and E.
D: CuCl
E: CuCl2-
[2m]
[8]
4.
(b)
Copper forms a very useful group of organic compounds known as Gilman reagents.
2CH3Li
CuI
in ether
methyllithium
(CH3)2CuLi
LiI
Gilman reagent
Alkyl halides (except fluorides) undergo nucleophilic substitution with Gilman reagents.
(CH3)2CuLi
CH3CH2Cl
CH3CH2CH3 + CH3Cu + LiCl
ethyl chloride
(i)
Suggest the structural formula of the final organic product formed when
, and bromoethane are used in a similar two-step
phenyllithium,
process.
CH2CH2CH3
accept C6H5CH2CH2CH3, reject -C3H7.

(ii)
[1m]
Gilman reagents can also react with acyl chlorides to form ketones. An example
is shown below:
O
C
(CH3)2CuLi
Cl
O
C
CH3 + CH3Cu + LiCl
It is observed that the reaction with acyl chlorides takes place much more readily
than that with alkyl chlorides. Explain why this is so.
It is because the carbonyl C atom/C in >C=O of acyl chlorides (the
electron-deficient C atom must be clearly specified in the answer) is
more/highly electron deficient, due to it being bonded to 2
electronegative/ electron-withdrawing atoms, O and Cl. Hence it is
more susceptible to nucleophilic attacks.
[1m]
[1m]
[3]
Or bonded to one more electronegative O atom

OR the trigonal planar sp2 hybridised C in COCl experience less
steric hindrance than the tetrahedral sp3 hybridised C in alkyl
chloride.
[1m] correct sp2 and sp2 assignment (or no. of alkyl groups)
[1m] steric hindrance comparison
[Total: 11]
9647/02/Prelim 2012
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13
5.
(a)
The Green Fluorescent Protein (GFP) is a protein that can be isolated from the
jellyfish, Aequorea victoria, and it can exhibit bright green fluorescence when exposed
to ultraviolet light. The chromophore is the section of the GFP that fluoresces and
contains the amino acid sequence ser-tyr-gly.
H
H2N
H
H2N
COOH
CH2OH
H
H2N
COOH
COOH
CH2
OH
tyr
ser
(i)
gly
Draw the structure of this section of the GFP at pH 14.

H
CH2OH
CH2
O-
[1m] for correct amino acid sequence and fragment of protein

drawing
[1m] for acid-base reaction with phenol, forming phenoxide
(ecf 2nd mark: if tripeptide is drawn and must accompany by acidbase reaction with any acidic groups: both phenol and COOH)
9647/02/Prelim 2012
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14
(ii)
GFP has a beta barrel structure, consisting of one b-pleated sheet and a-helices
running through the centre of the barrel structure.
Sketch a labelled diagram to show how two groups in a protein could be involved
in maintaining the structure of the b-pleated sheet.
C
d+
adjacent strand
O dhydrogen bonds
Hd
d-
d+
a strand of
polypeptide chain
O dH
d+
-
Nd
[1m] correct structure of b-pleated

sheet, showing C=O and N-H
groups involved in forming the
stabilising forces, N and C
must be on the polypeptide
backbone,
strands
of
polypeptide chain must be
labelled.
adjacent strand
[1m] at least 1 hydrogen bond correctly drawn Reject H-bond.

[4]
Accept anti-parallel/parallel diagrams and accept zigzag displayed

Accept polypeptide strand in place of a strand of polypeptide
chain
5.
(b)
A venomous jellyfish has tentacles containing stinging cells that inject venom into the
skin of a victim. The venom is made up of a diverse variety of proteins and
polypeptides capable of inflicting pain and swelling.
The most common first-aid treatment of jellyfish stings is to get the victim out of water,
scrape off any attached tentacles with a hard object and rinse the affected area with
hot seawater to deactivate the venom.
Explain how the application of heat is effective in treating jellyfish stings.
Heat will disrupt the weak interactions: van der Waals' forces in the
tertiary and quaternary structures and hydrogen bonds in the
secondary, tertiary and quaternary structures of the proteins in the
venom (and the nematocysts).
This alters the conformation/(3D) shape of the proteins which causes
the polypeptide chain folds differently/ this denatures the protein
[1m] : at least one correct R group interaction + structure disrupted
[2m] : for everything stated above(*without any other extra R group
interaction)
(c)
Paracetamol is usually prescribed to the casualty to reduce the pain from the
jellyfish sting.
HO
NHCOCH3
Paracetamol
A student suggested that paracetamol can be synthesised from phenol, via a
three-step reaction sequence as proposed below.
9647/02/Prelim 2012
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15
OH
OH
OH
C
H3C
Step II
Step I
C
O
CH3
Step III
NO2
NH2
4-aminophenol
(i)
OH
ethanoic anhydride
NHCOCH3
paracetamol
What types of reaction take place in Step I, II and III?

Step I: Electrophilic Substitution
[1m]
Step II: Reduction
[1m]
Step III:
Nucleophilic Substitution/Amide formation/Condensation [1m]
No spelling mistake allowed
5.
(c)
(ii)
State the reagents and conditions needed for Step I and II.
Step I: Dilute HNO3 (aq)
[1m] reject aqueous HNO3, heat
Step II: Concentrated HCl(aq), Sn, heat [1m],

followed by controlled amount of NaOH(aq) [1m]
Reject HCl(aq)
(iii)
In actual practice, 4-aminophenol is used instead as the starting material

and only Step III is carried out.
Given that both phenol and 4-aminophenol are easily available, suggest
a reason why phenol is not chosen to be the starting material to prepare
paracetamol in actual practice.
This is because 2 isomers will be produced (2-aminophenol & 4aminophenol)/mixture of isomers will be formed
[1m]
and separation of isomers/separation of 4-aminophenol from 2aminophenol is not easy/extra step for separation to carry out.
[7]
Thus, resulting in poor yield of product.

[Total: 13]
9647/02/Prelim 2012
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16
6.
Lorcaserin (Trade name: Belviq) is a weight-loss drug developed by Arena Pharmaceuticals

in San Diego and is recently approved by the US Food and Drug Administration in June 2012
for use in the treatment of obesity for adults.
N
Cl
H3C
Lorcaserin
(a)
Draw the structures of the organic compounds formed when Lorcaserin is treated with
the following reagents.
(i)
ethanoyl chloride
COCH3
Cl
[1m] correct product
H3C
(ii)
excess CH3Cl
+
N
CH3
CH3
Cl-
Cl
[2]
H3C
[1m] correct cation (if cation is given only)

[bonus 1m] correct product (with Cl-)
No double penalty for consistent structure mistake made in (a)(i) & (a)(ii)
6.
(b)
An isomer of lorcaserin (Compound Y) is shown below.

N
H3C
Cl
Compound Y
Suggest a chemical test (stating reagents and observations) that would distinguish
Compound Y from lorcaserin.
9647/02/Prelim 2012
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17
Test: 1. Add aqueous NaOH/KOH to each compound separately and heat.
2. Add (aqueous) dilute HNO3 to acidify the resulting mixtures
OR
Add (aqueous) dilute HNO3 to the resulting mixtures to remove

excess NaOH.
OR
Add EXCESS (aqueous) dilute HNO3 to the resulting mixtures
[1m]
3. Then, add (aqueous) AgNO3 to the resulting mixtures.

White precipitate / ppt. of AgCl is formed with Compound Y, but not
with lorcaserin. [1m] mark observations only when reagents (aq. NaOH
and aq. AgNO3) are correct
[2]
(c)
NH2
phenylamine
Suggest and explain how the basicity of lorcaserin might compare with that of
phenylamine.
Phenylamine will be less basic/a weaker base than lorcaserin.
[1m]
The p-p orbital overlap in phenylamine results in delocalisation of the lone

pair of electrons on N atom into the benzene ring, making the lone pair
less available for protonation, hence phenylamine is a weaker base.
[1m]
[2]
Reject .. making N less available
[Total: 6]
9647/02/Prelim 2012
[Turn over

Higher 2
CANDIDATE
NAME
EXAM
INDEX
NUMBER
CLASS
CHEMISTRY
9647/03
27 August 2012
2 hours

Answer Paper
Data Booklet

Begin your answer to each new question on a fresh sheet of writing paper.
At the end of the examination, arrange the answers in numerical order and attach the cover sheet on top.
1
2
3
4
5
This document consists of 10 printed pages and 0 blank pages.
[Turn over

1.
Use of the Data Booklet is relevant to the question.

(a)
Hydrogen can play an important role in the future by replacing the petroleum currently used
in automobiles. For example, electric cars can be powered by hydrogen-oxygen fuel cells,
with its hydrogen fuel kept at extremely high pressures in thick-walled storage tanks.
(i) State the half equations for the reactions occurring at each of the electrodes in a
hydrogen-oxygen fuel cell operating under acidic conditions.
(ii) Describe one disadvantage of using a hydrogen-oxygen fuel cell over internal
combustion engines in automobiles.
(iii) A quantity of hydrogen gas is confined in a chamber of constant volume. When the
chamber is placed at a temperature of 20C, the pressure of the gas is 3.29 105 Pa.
What will be the pressure of the gas, in Pa, if the chamber is now placed in a water bath
of boiling water to simulate the operating temperature of a certain automobile?
[5]
(b)
A student designed an ion-specific probe to determine the concentration of H+ ions in

solution. He connected a hydrogen electrode to a calomel reference electrode, which
comprises a paste of mercury(I) chloride and mercury in a saturated chloride electrolyte
solution. The porous glass frit acts as a salt bridge.
Measuring electrode
Reference electrode
1 atm, H2(g)
Pt wire
Pt electrode
coated with finely divided Pt
Test solution
of unknown
pH
Paste of Hg2Cl2 in Hg
Saturated Cl- electrolyte
Porous glass frit
(acts as salt bridge)
The hydrogen electrode, sensitive to H+ ion concentration, is the measuring electrode.

Therefore, this galvanic cell acts as a pH meter.
When both electrodes are in contact with the test solution, an electric current flows through
the wire and mercury(I) chloride reacts to form liquid mercury and chloride ion at the
reference electrode.
Under standard conditions, the E,cell of the pH meter is +0.28 V.
(i) Construct the half equation for the reaction occurring at the reference electrode.
(ii) Hence write an overall balanced equation for the pH meter.
(iii) Explain why the cell potential would increase when the pH meter is placed in a solution
of a higher pH.
[3]
9647/P3/Prelim 2012
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1.
(c)
The student used his probe to analyse a sample of 0.104 mol dm-3 solution of mandelic
acid, a bitter almond extract that is used as antibacterial treatment or an oral antibiotic.
The student obtained a cell potential reading, Ecell, of +0.41 V.
(i) The Nerst equation can be used to calculate the concentration of H+ ions detected by
the probe:
Ecell = Ecell -
[H+ ]2 [Cl - ]2
0.0592
log10
n
P
H
where n is the number of moles of electrons transferred in the overall reaction,

[H+] is the concentration of hydrogen ions detected
[Cl-] is the concentration of Cl- ions at the cathode.
PH2 is the pressure, in atm, of hydrogen gas passed into the probe,
Assuming that the concentration of Cl- is constant at 1 mol dm-3, use the Nerst equation
to calculate the concentration of H+ ions in the solution and the pH of the solution.
(ii) Hence calculate the value of acid dissociation constant, Ka, of mandelic acid.
(iii) How would you expect the value of Ka of mandelic acid to compare with that of
phenylacetic acid? Explain your answer.
CH(OH)COOH
mandelic acid
CH2COOH
phenylacetic acid
(iv) Suggest a chemical test (stating reagents and observations) that would distinguish
mandelic acid from phenylacetic acid.
(v) Suggest a synthetic route to form mandelic acid from starting material phenylmethanol.
CH2OH
CH(OH)COOH
phenylmethanol
[12]
[Total: 20]
9647/P3/Prelim 2012
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2.
(a)
Peppermint oil, also known as brandy mint and balm mint, is extracted from mentha piperita
of the Labiatae family. Menthol and menthone are the two main components of peppermint
oil.
Menthone can be reduced to menthol, which can be easily dehydrated to give 3-menthene
as the major product.
OH
O
step 1
menthone
step 2
menthol
3-menthene
Both menthone and menthol exhibit stereoisomerism but 3-menthene has no stereoisomer.
(i) Which compound, menthone or menthol, is expected to be more volatile? Give your
reasoning.
(ii) Menthol is insoluble in water but is freely soluble in ethers and alcohols. Explain why
menthol is insoluble in water.
(iii) Suggest the reagents and conditions required for step 1 and step 2.
(iv) An alkene M is also formed in step 2 in a much lower proportion than 3-menthene.
Suggest the structure for M and give the organic product when M is heated with
concentrated acidified KMnO4(aq).
(v) When HCl(g) is bubbled through a solution of 3-menthene, an addition reaction occurs
via a 2-stage mechanism.
Suggest the mechanism of this reaction by means of a diagram. Include all whole or
partial charges, and represent the movements of electron pairs by curly arrows.
(vi) What do you understand by the term stereoisomerism? Explain why 3-menthene does
not exhibit any stereoisomerism.
[12]
(b)
Magnesium nitrate is a hygroscopic salt. In air, it readily forms a hydrate with the formula
Mg(NO3)2.6H2O. Barium nitrate, however, does not form any hydrate in air. Both nitrates are
soluble in water. Like all soluble barium compounds, barium nitrate is toxic by ingestion.
Solutions of sulfate salts such as Epsom salt may be given as first aid for barium poisoning.
(i) Suggest reason(s) why magnesium nitrate readily forms a hydrate whereas barium
nitrate does not.
(ii) Describe what you would see when a sample of white crystals of Mg(NO3)2.6H2O is
heated in an open test-tube. Write a balanced equation for the reaction.
(iii) Explain why barium nitrate decomposes at a higher temperature than anhydrous
magnesium nitrate.
9647/P3/Prelim 2012
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2.
(b)
(iv) When water is added to the solid residue after barium nitrate has been heated, a
colourless solution is obtained. When water is added to the solid residue after
magnesium nitrate has been heated, a white suspension is obtained instead. Explain
these observations.
(v) Suggest how administering of Epsom salt solution, which contains magnesium sulfate,
helps to treat barium poisoning.
[8]
[Total: 20]
9647/P3/Prelim 2012
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3.
(a)
Amino acids, such as alanine and phenylalanine, are essential building blocks for making
proteins. They can be synthesised by a general 2-step reaction as exemplified below:
RCH2CO2H
Cl2
trace amount of phosphorus
excess NH3
II
RCH(NH2)CO2H
(i) Suggest the structure of the intermediate organic compound E.

(ii) What type of reaction is occurring in step I?
(iii) Phenylalanine is found naturally in the breast milk of
mammals. It is used in the manufacture of food and
drink products and is sold as a nutritional supplement.
Suggest the structural formula of the starting material
needed to synthesise phenylalanine by the above
2-step reaction.
COOH
NH2
phenylalanine
[3]
(b)
Solutions of amino acids are buffers important in maintaining optimal pH in our body. A food
chemist needs to ensure that all infant manufactured food products containing phenylalanine
and its salt, simulates the exact composition of human breast milk.
(i)
Draw the structural formula of the zwitterionic form of phenylalanine.

Hence suggest, with the aid of an equation, how phenylalanine behaves as a buffer
when small amount of base is added.
(ii)
In order to investigate the composition of a buffer solution of pH 7.4 containing

phenylalanine and its salt, the food chemist titrated a sample of this buffer solution
with NaOH(aq) and obtained the titration curve below.
pH
pHequivalence
7.4
X
Volume of
NaOH(aq) / cm3
39x
80x
The buffer solution operates at its maximum capacity when 39x cm3 of NaOH(aq) is
added and the equivalence point is attained when 80x cm3 of NaOH(aq) is added.
Show that the ratio of [phenylalanine] : [salt of phenylalanine] is 40 : 1 in the original
sample of buffer solution.
(iii) Hence determine the pH value at the maximum buffering capacity of the buffer
containing phenylalanine and its salt.
[6]
9647/P3/Prelim 2012
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3.
(c)
Chymotrypsin is a digestive enzyme produced by the pancreas to aid digestion in the small
intestine.
(i) A small peptide G was hydrolysed by chymotrypsin and gave three different amino
acids according to the following reaction.
COOH
COOH
NH2
COOH
NH2
NH
OH
tyrosine
M r = 181
NH2
phenylalanine
M r = 165
tryptophan
M r = 204
Calculate the Mr of peptide G.

(ii) During the hydrolysis of peptide G by chymotrypsin, the tyrosine residue of peptide G
must first bind to the active site on chymotrypsin.
active site on chymotrypsin
glycine residue
glycine residue
OH
CH2
serine residue
Copy this diagram onto your answer script and use it to illustrate how one tyrosine
residue of peptide G can bind to the active site on chymoptrypsin. Label the type(s) of
interaction that could be involved.
(iii) Vomiting is one of the immediate and observable effects of excessive alcohol
consumption as the presence of alcohol inhibits the digestive activity of chymotrypsin.
Suggest how the consumption of alcohol inhibits the digestive activity of chymotrypsin.
[5]
(d)
Compound H, an isomer of phenylalanine, with molecular formula C9H11NO2, is a basic

compound. When H is heated under reflux with NaOH(aq) followed by careful neutralisation,
compound J and ethanol are formed. Compound J reacts with aqueous sodium carbonate
and also dissolves in HCl(aq). 0.10 mol of compound J reacts completely with 0.20 mol of
aqueous bromine to give a white precipitate.
Suggest the structures of compounds H and J and explain all the reactions involved.
[6]
[Total: 20]
9647/P3/Prelim 2012
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4.
Under the influence of a dilute base or acid, two molecules of an aldehyde or a ketone may
combine in a process known as aldol reaction. An example of an aldol reaction between ethanal
molecules in dilute alkaline solution is shown below.
2 CH3CHO
OH-
CH3CH(OH)CH2CHO
3-hydroxybutanal
DH < 0
A chemist studied the kinetics of the above reaction at 298 K and obtained the following table of
results.
(a)
experiment
number
initial [CH3CHO]
/ mol dm-3
initial [OH-]
/ mol dm-3
initial rate
/ mol dm-3 s-1
0.10
0.10
0.0110
0.10
0.15
0.0165
0.30
0.20
0.0660
(i) Use these data to deduce the order of reaction with respect to both ethanal and OH-,
showing how you arrived at your answers.
(ii) Hence write the rate equation for the reaction and calculate the value of the rate
constant, stating its units.
(iii) The half-life of ethanal in experiment 1 is 9.0 s. Predict the half-life of ethanal in
experiment 3.
[6]
(b)
The following three-step mechanism has been proposed for the reaction between ethanal
molecules.
:
- :
:
- :
:
(i) Using your answers in (a), predict which of the three steps is the rate-determining step.
(ii) Sketch a labelled energy profile diagram for the above proposed mechanism.
You are only required to label the reactants, products and the activation energy of
forward reaction on your diagram.
9647/P3/Prelim 2012
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4.
(b)
(iii) Name the type of reaction occuring in Step 1.

(iv) Use a diagram to show how the product in Step 2 is formed. In your diagram, include
all whole or partial charges, and represent the movements of electron pairs by curly
arrows.
Hence explain why
3-hydroxybutanal.
the
overall
reaction
produces
racemic
mixture
of
[7]
(c)
In a similar three-step mechanism mentioned in (b), one molecule of 3-hydroxybutanal can

react further with one molecule of ethanal to give a mixture of products with six carbon
atoms each.
Deduce the structural formula of two possible products from this reaction.
[2]
(d)
The aldol reaction is a powerful means of forming carbon-carbon bonds and it combines
simple molecules to give a more complex one. Copper(I) and copper(II) complexes have
been developed successfully to catalyse some aldol reactions.
(i)
Write the electronic configuration of copper(I) and copper(II) ions using the
s,p,d,f notation.
(ii)
Explain why complexes of copper(II) are usually coloured and those of copper(I) are
colourless.
[5]
[Total: 20]
9647/P3/Prelim 2012
[Turn over
10
5.
The halogens and their compounds are useful laboratory reagents.

(a)
Iodine trichloride, ICl3, is a bright yellow solid formed by reaction of iodine and chlorine.
(i) Draw and suggest the shape of ICl3 molecule. Include all lone pairs in your diagram.
(ii) Unlike ICl3, the compound FCl3 does not exist. Suggest a reason for this difference.
(iii) Given the following enthalpy changes,
I2(s) + Cl2(g) 2ICl(s)
DH1O = +14 kJ mol1
2ICl(s) + 2Cl2(g) 2ICl3(s)
DH2O = 88 kJ mol1
construct an energy cycle to calculate the standard enthalpy change of formation of

solid iodine trichloride.
(iv) The standard entropy change of formation of solid iodine trichloride is
225 J mol-1 K-1. Explain why the formation of solid iodine trichloride has a negative
entropy change.
(v) Explain why the formation of solid iodine trichloride is spontaneous at low
temperatures.
(vi) Predict whether the reaction is spontaneous at 298 K.
[10]
(b)
Silver chloride and silver iodide are sparingly soluble in water at room temperature. Their
solubility products at 298K are given below.
(i)
Silver halide
AgCl
Solubility product, Ksp
AgI
8.52 x 10-17
1.77 x 10-10
Write an expression for the solubility product, Ksp, of silver iodide and hence calculate
[Ag+(aq)] in a saturated aqueous solution of silver iodide at 298K.
(ii) With the aid of relevant equations, suggest explanations for the following observations:
When aqueous silver nitrate is added to aqueous sodium chloride, a white precipitate
is formed which is soluble in excess aqueous ammonia, giving a colourless solution.
When aqueous sodium iodide is added to the resultant solution, a yellow precipitate is
formed immediately.
[5]
(c)
Solid halides such as sodium bromide or sodium chloride are commonly used in situ with
concentrated sulfuric acid to produce alkyl halides from alcohols.
(i) Describe what would be observed when concentrated sulfuric acid is added to
separate portions of NaCl(s) and NaBr(s). Write an equation for any reaction that
occurs and explain the differences in their reactions.
(ii) Suggest why sodium iodide is not used in situ with concentrated sulfuric acid to
produce alkyl iodide from alcohol.
[5]
[Total: 20]
9647/P3/Prelim 2012
9647/P3/Prelim 2012
Mark Scheme for 2012 JC2 Preliminary Examination Paper 3

Minus [1m] overall for P3 for lack of 3 sf. Indicate on Cover page when penalised.
General Comments for Q1
Many candidates probably left this question as their last attempted question, as they ran out of
time and thus
(i) did not manage complete answers or
(ii) did not have enough time to calculate their answers or
(iii) made a lot of careless mistakes.
Marks for this question varies greatly from 4-5 to 17-20.
1.
(a)
(i) Anode:
2H2(g) 4H+(aq) + 4eCathode: O2(g) + 4H+(aq) + 4e- 2H2O(l)
[1m] s.s not penalised

[1m] s.s. not penalised
Small handful of candidates still make the usual errors:

o Use of reversible arrows
o Use of [O] and [R]
o Wrong electrodes or no labelling of electrodes
A few wrote equations for alkaline medium
A few chose half eqn for H2O2 instead.
(ii) Requires a heavy storage tank of H2 gas on board a car / takes [1m] for any
relevant
up more storage space / must be kept under high pressure
ans. Do not
Difficult to refill H2 fuel due to lack of infrastructure
accept:
H2 gas is MORE explosive than fuels in internal combustion
explosive
engines.
only
More expensive due to the expensive catalysts etc
Explosive at high temperatures
Common Mistakes:
A few listed advantages instead
A small handful of candidates did not understand what to compare e.g.
thinking that the hydrogen-oxygen fuel cell is used together with the internal
combustion engine or to supply electricity to the internal combustion engine.
(iii)
Using
P1 P2
= ,
T1 T2
P
3.29 105
P1 = 2 T1 =
373
293
T2
= 4.19 105 Pa
[1m]: correct subst into

formula. Accept
293.15 and 373.15
[1m]: correct ans, 3 s.f.
Many candidates solved using PV=nRT, which is a longer method.
Common Mistake:
Wrong units for Temperature
Some gave a qualitative answer only, with no calculation.
Page 1
1.
(b)
(i) Reference electrode (cathode):

Hg2Cl2(s) + 2e 2Hg(l) + 2Cl-(aq)
[1m] full arrow
(ii) Measuring electrode (anode): H2(g) 2H+ (aq) + 2e

Overall: Hg2Cl2(s) + H2(g) 2Hg(l) + 2Cl-(aq) + 2H+ (aq)
[1m] full arrow
Common Mistakes for (i) and (ii):

Did not seem to understand Qn or were simply confused with Hg and H e.g.
o Mixed up Hg with H2 or Hg with H !
o wrote reduction of chlorine to chloride only
o wrote eqns for reaction between hydrogen and chlorine only
Did not notice formula of Hg2Cl2.
Did not check their equation for balancing of charges.
(iii) At a higher pH, there is lower [H+],
equilibrium in 2H+ (aq) + 2e = H2(g) shifts to the left
(OR eqm shifts to favour oxidation of H2) and thus
E(H+/H2) becomes (more) negative.
Thus Ecell becomes more positive.
[1m] No penalty for E,.

Just circle.
Common Mistakes:
Thought higher pH = higher [H+]
Did not write reversible arrow for the eqm equation.
Thought that a reaction between H+ & Cl- will result in an eqm shift!
(c)
(i)
Writing E value to represent E(H+/H2).
0
E = E cell
[H + ]2 [Cl - ]2
0.0592
log
n
PH 2
0.0592
log [H+ ] 2
2
0.0592
0.41 = 0.28 2log[H + ]
2
0.13
log[H + ] = 0.0592
0.41 = 0.28 -
[1m] correct
substitution & n=2
ecf for n from (b)
need work from both
half eqns
Solving, [H+] = 6.37 10-3 (or 6.38 10-3) mol dm-3

-3
pH = -log(6.37 10 ) = 2.20
[1m] 3sf, ecf

[1m] 3sf, ecf
About half of the candidates (who attempted this part) are able to solve and
calculate [H+], using whatever values substituted.
Common Mistakes:
Substituted n = amount of acid used (or any other strange number)
Substituted their answer in (a)(iii) for PH2
Substituted 1.01 x 105 for PH2
Page 2
1.
(c)
(ii)
Ka =
[H+ ]2 (6.37 10 -3 )2
= 3.90 10-4 mol dm-3
=
c
0.104
OR Ka =
[1m] for Ka,

3sf, ecf
[H+ ]2
(6.37 10 -3 )2
= 4.15 10-4 mol dm-3
=
+
c - [H ] 0.104 - 6.37 10 -3
(or 4.16 10-4 mol dm-3)
If students get [H+] = 6.38 10-3 mol dm-3,

Ka =
[H+ ]2
(6.38 10 -3 )2
= 4.17 10-4 mol dm-3
=
+
c - [H ] 0.104 - 6.38 10 -3
Ka =
[H+ ]2 (6.38 10 -3 )2
= 3.91 10-4 mol dm-3
=
c
0.104
Most candidates earned the ecf marks.
[H+ ]2
c
A few students got all previous calculations correct but were stuck at Ka.
Perhaps they did not notice that mandelic acid is a monobasic acid.
Most candidates (who got this part correct) solved for Ka using K a =
(iii) Mandelic acid, being the stronger acid, has a larger Ka value.
[1m] Not
awarded if
mandelic acid
is deduced as
weak acid
(contradiction)
The electron withdrawing O atom of the -OH group disperses the [1m] Anion
must be
CH(OH)COOclear
Accept:
negative charge and stabilises
,
CH2COO-
CH(OH)COO-
making
more stable than
- electron
withdrawing -OH
group
.
- electronegative
Common Mistakes:
Electron donating -OH group
Weaker acid has a larger Ka
stabilising negative charge
mandelic anion or anion or -COO- anion
Using it to describe the acid, the anion, the -OH group (basically everything!)
and thus making answers vague/unclear/misleading.
(iv) Add acidified K2Cr2O7 to each of the unknowns and heat in a hot [1m] Circle if
heat under
water bath. (Accept hot acidified K2Cr2O7)
reflux but no
penalty
Mandelic acid turns orange K2Cr2O7 green but not [1m]
phenylacetic acid.
Common Mistakes:
Using KMnO4
Using KMnO4 then Bradys reagent
Using KMnO4 (or K2Cr2O7), followed by Tollens reagent.
Using PCl5
Page 3
1.
(c)
(v)
Acidified K2Cr2O7(aq),
distil ()
CH2OH
HCN, trace amt of

NaCN/base ()
CHO
CH(OH)CN
dilute H2SO4, heat

or H2SO4(aq), heat
or dilute HCl, heat
or HCl(aq), heat ()
CH(OH)COOH
OR the less recommended way:

Limited Cl2,
uv light ()
NaCN in ethanol, heat

under reflux ()
CH2OH
CHOH
Cl
CHOH
CN
dilute H2SO4, heat

or H2SO4(aq), heat
or dilute HCl, heat
or HCl(aq), heat ()
CH(OH)COOH
[1m] for each correct intermediate structure

2(): 1m ; 3(): 2m , only awarded if corresponding structures are correct
Award marks proportionately, for any other long synthesis method suggested.
1m max for any haywire synthesis method but correct cyano-intermediate &
reagent and conditions for hydrolysis to get the end product
-1m
if answers are correct but not clearly presented
Have to remind students that Free Radical Substitution is not a recommended

way of synthesis. It gives a mixture of products.
Common Mistakes:
Some only listed the sequence of reagents & conditions required w/o giving
intermediates for synthetic route
Suggested step to convert -OH group to -CN group (MANY STUDENTS)

Suggested step to convert -OH group to -COOH group (MANY STUDENTS)
Using KMnO4/K2Cr2O7 and heat under reflux to oxidise alcohol to aldehyde
Confused on when to use HCN and NaCN (for nuclephilic sub & addition)
Listed a mixture of two acids for hydrolysis e.g. H2SO4, HCl, heat under reflux
Did not use dilute or aq for acid hydrolysis (i.e. simply H2SO4, heat)
Used conc acid for hydrolysis.
Page 4

Part (a) was generally well attempted and the average score is 7 out of 12. Students generally lost
most marks in (a)(i)(ii)(vi).
Part (b) was poorly attempted and the average score is 3 out of 8. Students generally scored all
marks in (b)(iii)(v).
For details, please see the comments under individual subparts.
2.
(a)
(i)
Menthone is expected to be more volatile.

(or Menthol is expected to be less volatile)
[1m]
Less energy is required to overcome the *weaker permanent dipole[1m]

permanent dipole interaction **between menthone molecules than the
*stronger hydrogen bonds **between menthol molecules.
Reject:
Just mention menthol has a higher boiling point.
Methanol/Menthanol as Menthone/Menthol
Common mistakes:
(ii)
Menthone and Menthol were spelt wrongly.

C=O bond is stronger than O-H bond..
.van der waals forces between menthone molecules
between molecules is often missing
higher b.p..therefore more volatile
Menthol is insoluble in water due to the presence of large/bulky non- [1m]

polar/hydrophobic cyclic alkyl chain/group in menthol molecule which
*prevents/hinders effective hydrogen bonding with water molecules.
Reject:
mention steric hindrance without relating to the large alkyl group
and hydrogen bonding.
Common mistakes:
Menthol is non-polar/hydrophobic.cannot form ion-dipole
interaction or hydrogen bonding with water .
DHsoln is highly endothermic.
Lone pair on O atom of OH not available for hydrogen bonding as it
is delocalised into the benzene ring.
Page 5
(iii)
Step 1: LiAlH4, dry ether or NaBH4, methanol or H2, Ni, heat/200 oC
[1m]
Step 2: concentrated H2SO4, heat at 170/180 oC or Al2O3, heat/350 oC
[1m]
Reject:
heat under reflux for both steps
(aq)/wrong state symbol of reagent.
Except for conc. H2SO4(aq) (to cancel (aq) on students script)
AlLiH4 as LiAlH4
Common mistakes:
Did not state 170 oC in step 2 when conc. H2SO4 is used.
Quoted acidified KMnO4/K2Cr2O7 in step 1.
Quoted ethanolic KOH/NaOH, heat under reflux in step 2.
(iv)
M:
or
(or correct fully expanded structural formula)
CH3C
[1m]
CH3
Oxidised product:
HOCO COOH
or
COOH
CH3CHCHCH2CH2CH2COOH
CH3
Common mistakes:
One missing carbon/one extra carbon atom in the oxidized product.
Leave out one of more H atoms in the fully expanded structural
formula of M/oxidised product.
Some gave ketone/aldehyde/CO2 as the oxidised product
Page 6
[1m]
2.
(a)
(P)
(v)
d+
H
dCl
(P)
slow
+
(P)
+ :Cl -
fast
Cl
(P)
(P)
(P) full arrow pointing from p bond to d+H

(P) full arrow pointing from H-Cl bond towards d-Cl
*(P) correct carbocation structure
(P) full arrow pointing from lone pair on Cl - towards C+
*(P) correct addition product
3-4(P): [1m]
5(P): [2m]
Common mistakes:
Leave out one or more H atoms in the expanded structural formula of
3-menthene.
Put (d+, d-) on the C=C bond. Penalise under 1st (P).
Dissociate H-Cl into H+ and Cl - in the first step, then proceed with p
electrons attacking the H+ and Cl - attacking the carbocation.
Lone pair on Cl - is often missing.
Arrow point from the electrophile (d+H) to C=C bond.
(iv)
Stereoisomerism occurs when compounds/molecules have the same [1m]

molecular formula and same structural formula but the *atoms/groups of
atoms of the molecules are directed/arranged differently in 3-dimensional
space.
3-menthene **has no chiral centre (or no carbon atom with four different
[1m]
groups/groups of atoms attached) and so it does not exhibit optical
isomerism.
***One form of the geometric isomer (or E-isomer/trans-isomer) is
unstable (or does not exist) due to ring strain (or angle strain in the ring). [1m]
Therefore it only exists in one stable form.
Reject:
***One form/isomer is unstable . without linking to geometric
isomerism
Due to ring strain, 3-menthene does not exhibit geometric isomerism
3-menthene has ring strain and cannot exhibit geometric isomerism
Common mistakes:
For definition of stereoisomerism:
- molecules with 4 different groups attached to C/has chiral
centre/give rise to optical isomers that rotate plane polarised light.
- different arrangement of molecules/functional group in space.
- same molecular/chemical formula but different structural formula.
Did not use ring strain but mentioned twisting/distortion of ring and
failed to relate to unstability of one geometric/trans isomer.
No geometric isomerism as each C of C=C is bonded to the same
group/due to cyclic ring.
Mostly did not discuss both optical and geometric isomerism.
Page 7
2.
(b)
(i)
The charge density of Mg2+ is greater than that of Ba2+, therefore *Mg2+ has [1m]
a higher/greater tendency to attract the polar water molecules to itself to
form hydrate as compared to Ba2+.
Reject:
...greater polarising power.
Common mistakes:
Many did not know what is a hydrate and discussed solubility of
compound in water or reaction of compound with water instead.
Discussed DHhyd/oxidising power of Mg2+.
Discussed high polarising power of Mg2+ and polarises the water
molecule to great/greater extent.
High charge density Mg2+ favours formation of dative covalent bond
with water molecules/readily accepts lone pair of electrons from water
molecule to form dative covalent bond...
Page 8
2.
(b)
(ii)
When white crystals of Mg(NO3)2.6H2O is heated in an open test-tube, [1m]

water droplets condense at the top (P) of the test-tube, followed by evolution 3(P)
of a pungent brown NO2 gas/fumes (P) and a colourless odourless O2 gas
which relights a glowing splint . A *white residue/solid/powder (P) of MgO is
obtained after heating.
[1m]
Mg(NO3)2.6H2O(s) MgO(s) + 2NO2(g) + O2(g) + 6H2O(g)
ignore
s.s.
or, 2Mg(NO3)2.6H2O(s) 2MgO(s) + 4NO2(g) + O2(g) + 12H2O(g)
Reject:
*White precipitate/ppt.
Common mistakes:
Many thought that this was a combustion reaction and wrote
- Mg(NO3)2.6H2O(s) + O2(g)
- burns with a __________ flame
Some gave Mg (instead of MgO) as the product.
Equation not balanced and O2 in the product or .6H2O in the
reactant were often missing.
MgO residue is black.
Water droplets form/condense at the top was often missing.
Water vapour is seen.
(iii)
The charge density of Ba2+ is lower than that of Mg2+ since Ba2+ has a larger [1m]
size/ionic radius/radius (or is bigger) than Mg2+.
Ba2+ has a lower polarising power (or *Ba2+ has a lower ability to distort [1m]
the (large) NO3-/anion). Hence, Ba(NO3)2 is thermally more stable and
requires a higher temperature to decompose than Mg(NO3)2.
Reject:
polarising power/Charge density of BaNO3
atomic radius of Ba/Ba2+/BaNO3
size/ionic radius/radius of Ba/BaNO3
Ba/BaNO3...lower ability to distort/polarise anion etc
(Basically, the subject must be Ba2+/Mg2+, not Ba/Mg or BaNO3/MgNO3)
Common mistakes:
As mentioned in Reject.
Page 9
(iv)
The solid residue after barium nitrate has been heated is BaO.
BaO is soluble/dissolves/reacts () readily in water to form a strongly
alkaline solution of Ba(OH)2. () Hence a colourless solution is observed.
The solid residue after magnesium nitrate has been heated is MgO. MgO is
only sparingly/partially/slightly soluble/not very soluble (or MgO dissolves
to a small extent) () and reacts with water to a small extent to form a weakly
alkaline solution of Mg(OH)2. Hence a white suspension of MgO () is
observed.
2-3(P): [1m]
4(P): [2m]
Common mistakes:
Many did not discuss solubility of MgO and BaO, but comment on
solubility of Mg(OH)2 and Ba(OH)2.
Extent of reactivity with water i.e. BaO reacts readily/completely..
MgO reacts only to a small extent was not discussed.
MgO reacts to give Mg(OH)2 which is sparingly soluble to give white
Mg(OH)2 suspension.
2.
(b)
(v)
Epson salt contains SO42- ions which form an insoluble BaSO4 precipitate with
aqueous solution containing Ba2+.
Hence, administering of Epson salt helps *to remove Ba2+ ions/reduce [Ba2+]
[1m]
from the solution through precipitation of BaSO4.
Common mistakes:
Many are not aware that Ba2+(aq) is toxic whereas insoluble barium
compounds are not.
Some thought that the barium poisoning is caused by the presence of
Ba and discussed
- reducing power of Mg/Ba
- displacement reaction: Ba + MgSO4 Mg + BaSO4
form soluble BaSO4 and therefore easier to remove (eg. as urine)
stronger MgSO4 salt displaces out weaker BaSO4 salt.
Page 10

This question was one of the popular question that student would choose, however many
students made a lot of careless mistakes especially in the proteins section.
Marks for this question varies greatly from 2-10, very few students had more than 15. (no full
marks)
Part (a) and (b) was generally well attempted and the average score is 5 out of 9. Students
generally lost most marks in (b)(iii).
Part (c) was poorly attempted and the average score is 4 out of 11. Students generally scored full
marks in (c)(i) only.
3.
(a)
(i)
RCHClCO2H
(ii)
substitution
[1m]
[1m]
COOH
(iii)
[1m]
or C6H5CH2CH2COOH
COOH
H
Accept
COOH
C
H
reject
(b)
(incomplete structure)
-
COO
(i)
[1m]
NH3+
-
COO
COO
-
+ OH
+ H2O
NH3+
NH2
[1m]
The small amount of OH added is removed through acid-base reaction,

maintaining the pH (or resisting changes in pH) of the buffer mixture.
A few of candidates still make the usual error of using reversible arrows for
the acid-base rxn.
COOH
Small handful of candidates chose

present in the buffer to remove the base added.
Page 11
NH3+
as the species
(b)
(ii)
The solution is a buffer at the start of the titration.
When 39x cm3 of NaOH(aq) is added

the buffer solution is at its maximum
buffering capacity
COO
NH3+
Mole ratio of
COO
NH2
= 1: 1
A further 41x cm3 of NaOH(aq) is added to reach equivalence point.

41x cm3 of NaOH(aq) was required to neutralise all the acid left in the
buffer at the maximum buffering capacity.
i.e. at max. buffering capacity,
-
COO
NH3+
amt of
COO
NH2
= 41x : 41x
Working backwards, at start of the titration :

-
COO
Mole ratio of
NH3+
COO
NH2
80x : 41x 39x
[1m]
80x : 2x
40 : 1 (shown)
(iii)
In the original sample of buffer,

pH = pKa + lg
[salt]
[acid]
40
7.4 = pKa + lg
[1m] correct substitution
Solving, pKa = 9.00

Or, Ka = 10
-7.4
[1m] pH can be calculated

directly, with clear working
( ) [1m]
1
40
Ka = 9.95 x 1010 [1m]

At the maximum buffering capacity, pH = pKa = 9.00
(c)
(i)
[1m]
Since 7 amino acids are formed, 6 amide bonds were

broken in peptide G with the release of 6 mol of H2O.
Mr of G = (2 x 181) + (2 x 204) + (3 x 165) 6(18)
= 1157
[1m] no units
Page 12
active site on chymotrypsin
(ii)
van der Waals forces [1m] label & drawing

glycine residue
d-
OH
d+
..
d- OH d+
(iii)
glycine residue
hydrogen bond [1m] label & drawing
CH2
1m max if both interactions are correct but

drawing is incomplete.
serine residue
0m if drawing is complete but wrong label
Majority of candidates still make the usual errors:

o Drew the free NH2 and COOH groups from the tyrosine amino acid.
o Drew hydrogen bonding between the free NH2 and COOH groups
from the tyrosine to the serine residue.
o indicated hydrogen bonding for the H atoms of the glycine residue.
Many did not have complete hydrogen bonding diagram.
The presence of alcohol reacts with the polar groups/ alcohol and disrupts the
hydrogen bonds in the secondary, tertiary and quaternary structures of the
protein/enzyme/ chymotrypsin.
[1m]
Thus, the conformation (or shape) of the active site of the enzyme is
altered/change/destroyed and inhibits its digestive activity.
[1m]
Reject : Alcohol interacts/reacts with the serine residue, hence this inhibits
the tyrosine from binding to the serine residue
(inhibitor only works if the structure of the inhibitor is almost the same as the
substrate, alcohol does not have a structure like tyrosine-so such inhibiting
of substrate does not work)
alcohol disrupts the hydrogen bonds in the secondary, tertiary and
quaternary structures present in the active site of chymotrypsin.
Small handful of candidates still make the usual error of stating that the
active site is altered, without mentioning that it is the conformation/shape of
the active site that is altered.
Page 13
3.
(d)
Formatted Table
NH2
basic
H : presence of amine
or phenylamine
C
OCH2CH3
[1m]
H : C9H11NO2
Since J and ethanol are
produced after hydrolysis
H : presence of ester()
H : C:H ratio = 1: 1
presence of benzene ring
NaOH
heat under reflux alkaline/base hydrolysis ()
f ollowed by neutralisation
NH2
C
+
OH
[1m]
CH3CH2OH
Na CO aq
2
3( )
HCl(aq)
acid-base reaction()
Br aq
2( )
acid-carbonate/
acid-base ()
reaction
reacts
J : presence of
carboxylic acid ()
dissolves
electrophilic substitution
J : presence of amine/phenylamine
()
white ppt
J : presence of phenylamine
since 0.1 mol of J reacts with 0.2 mol of Br2(aq)
J : presence of one substituent group on 2 or 4 or
6th position wrt -NH2 group of phenylamine. ()*
OR J contains
NH2
can be inferred from the

drawn structure- wrt NH2
only if phenylamine is shown.
NH2
R
side-chain structure
or
()*
R
OR Alternative answers:
2 - 3 () : [1m]
C
OCH2CH3
H:
H2N
[1m] : mentions
phenylamine in H or J
4 - 5 () : [2m]
OH
J:
6 - 7 () : [3m]
H2N
A few of the candidates concludes for rxn with HCl(aq) that J is a polar molecule
Some of the candidates concludes for rxn with Br2(aq) that J has a benzene ring or J
has a benzene ring with more than 2 positions unoccupied (but forgets about 3,5
position wrst NH2 group is also unoccupied)
Page 14

Many students attempted this question. Generally well-done and answers are well-presented.
Most students can achieve at least a pass for this question. Main problem is finding the t1/2 for
expt 3 (4aiii) and energy profile diagram (4bii).
4
(a)
(i) Compare Expt. 1 and 2:

When [OH-] is increases to 1.5/Error! Objects cannot be created from editing
field codes. times of its original value (or by 1.5 /Error! Objects cannot be
created from editing field codes. times), rate increases to 1.5 times of its
original value (or by 1.5 /Error! Objects cannot be created from editing field
codes. times).
Hence, the order of reaction with respect to (or w.r.t.) OH- is one.
[1m]
OR:
Accept: [OH-] 1.5 X, rate 1.5 X
Hence, the order of reaction with respect to (or w.r.t.) OH- is one.
OR rate [OH-]
Compare Expt. 1 and 3:
Let the order of reaction w.r.t CH3CHO be a.
Error! Objects cannot be created from editing field codes.= 6
Error! Objects cannot be created from editing field codes.= 3
[1m]
a=1
Hence, the order of reaction with respect to (or w.r.t.) CH3CHO is one.
OR rate [CH3CHO]
OR Alternatively:
Compare Expt 1 and 3:
When [CH3CHO] increases to 3 times of its original value(or by 3 times
or 3 X) and the [OH-] increases to 2 times of its original value(or by 2
times or 2 X), rate increases to 6 times of its original value(or by 6 times
or 6 X).
Hence, the order of reaction with respect to (or w.r.t.) CH3CHO is one .
Specific Comments:
Generally well-done. Students who attempted this part
mostly achieve full marks. A few made careless mistakes in
the calculations. The indices method was the most
commonly seen when students compare expt 1(or 2) and 3.
Page 15
(ii) Rate = k [CH3CHO] [OH-]
[1m] e.c.f from a(i)

-
Reject: R(or r)ate eqn is k [CH3CHO] [OH ]

OR R(or r)ate eqn = k [CH3CHO] [OH-]
--
k = Rate / [CH3CHO] [ OH ]
From Expt 1: k = 0.0110 / [(0.10)(0.10)] = 1.10 mol-1 dm3 s-1
OR From Expt 2: k = 0.0165 /{(0.10)(0.15)} = 1.10 mol-1 dm3 s-1
OR From Expt 3: k = 0.0660/{(0.30)(0.20)} = 1.10 mol-1 dm3 s-1
ECF: If student obtains rate = k [CH3CHO]2 [OH-],
[1m] correct ans

(accept 2-3 s.f.),
e.c.f from rate
eqn
Accept 1.1(exact
value)
[1m] for units,
e.c.f from
rate eqn
k = Rate / [CH3CHO]2 [ OH--]

From Expt 1: k = 0.0110 / [(0.10)2(0.10)]
Accept 11(exact
value)
= 11.0 mol-2 dm6 s-1
Specific Comments:
-
A few still gave rate equation = k [CH3CHO] [OH ]. Some

miss out answering this part and move on to the
calculations straight away. A small number made mistakes
in the units.
Page 16
(a)
(iii) Half-life of CH3CHO in expt 3 = (9) = 4.5 s (or sec./seconds)
[1m] No e.c.f
Explanation not
reqd.
{Explanation:
From Rate = k [CH3CHO][OH-]
Rate = k [CH3CHO] where k = k[OH-]

and t1/2 of CH3CHO = ln 2/k = 9 s in expt 1
Comparing expt 1 & 3:

[CH3CHO] is tripled but this has no effect on the half-life of
CH3CHO since the t1/2 of CH3CHO is independent of
[CH3CHO]. The rxn is first order with respect to CH3CHO.
When [OH-] is doubled, k is doubled.
Thus t1/2 of CH3CHO is halved.
\ Half-life of CH3CHO in expt 3 = (9) = 4.5 s}

Specific Comments:
Not well-done. Many cannot give the correct answers. Only
a small number got this right. Students seem to have
problem with this type of question asking for t1/2.
Many incorrectly deduce 27s (as well as 9s) as the answer,
seeing that the the [CH3CHO] is tripled.
Another common value seen was 1.5s. This was due to
students pointing out that [CH3CHO] is tripled and [OH-] is
doubled.
(b)
(i) Step 1
[1m]
The rate determining step involves only one molecule of CH3CHO reacting
with/and/+ one OH- ion.
[1m]
ECF: If student obtains rate = k [CH3CHO]2 [OH-] in 4a(ii), accept Step 2

supported with appropriate reasoning or derive from equations.
Specific Comments:
A small number achieve full marks for the explanation. They miss out
one molecule and one ion. None manage to get this part correct if they
got the wrong rate equation from the previous part. Some still regard OHion as a molecule.
The only ECF allowed mentioned above was earned by a small no. of
students. This was usually due to them concluding incorrectly
rate = k [CH3CHO]2 [OH-] in 4a(ii).
Page 17
(b)
(ii)
Energy(/kJ mol-1)
()()
3 humps
3 humps
() Axes labeled
()()
Reactants
and products labelled
Axes labeled
() Energy level of pdt < rxt.
nd
rd
()()
Ea Reactants
of 1st step and
>> Eproducts
/3labelled
step + label Ea
a of 2
Allow ecf from (b)(i) r.d.s. tied to 1st ()
5()
- [2m]
5()
- [2m]
() E f 1st t
E f 2nd /3rd t
l b3-4()
l E - [1m]
3-4()
- [1m]
0-2()
- [0m]
0-2()
- [0m]1m if energy
Penalise
of reactants is shown
as 0
Penalise
1m5ifth()
energy
Penalise
if
of reactants
is shown
student label
Ea1, Ea2,
Ea3 unless justified
Ea
2CH3CHO (+OH)
CH3CH(OH)CH2CHO (+OH)
2CH3CHO (+OH)
Accept: reactants
Accept: reactants
Accept: products
Specific Comments:
Reaction
pathway/coordinate
or Extent/progress
of reaction
Many students
gave
one (or two) humps
in their sketch with
the labelling
of Ea, reactants and products., wrong label of x-axis as time or no of
molecules (confusing with Boltzmann distribution).
The concept of (overall) Ea of a reaction may need to be reinforced since
many students use Ea1, Ea2, Ea3 in their labelling, without recognising that
Ea1 is the (overall) Ea of the forward reaction.
A number of students drew the following energy profile. Students were
penalised 1m. It should be reiterated that intermediates, being less stable
than reactants and products, usually exist for short period of time (or
usually instantaneously) and as such, by drawing the following profile, it
seems to indicate that intermediates exist for a significant period of time
in the reaction.
(b)
(X) 3 humps
(ii)
Energy(/kJ mol-1)
() Axes labeled
() Reactants and products labelled
(X) 3 humps
5() - [2m]
Axes
Energy(/kJ mol ) ()()
E labeled
f 1st t
E f 2nd /3rd t
l b lE
3-4() - [1m]
st
nd
rd
() Ea of 1 step >> Ea of 2 /3 step + label
Ea - [0m]
0-2()
Allow ecf from (b)(i) r.d.s.
5() - [2m]
3-4() - [1m]
0-2()
- [0m]
Penalise
1m if energy
-1
Ea
2CH3CHO (+OH)
2CH3CHO (+OH)
Accept: reactants
Penalise 1m if energy
as 0
Penalise 5th() if
student label Ea1, Ea2,
Accept: reactants
Accept: products
Page 18
Reaction pathway/coordinate or Extent/progress of reaction

(b)
(ii)
OR
Energy(/kJ mol-1)
(X) 3 humps
() 3Axes
labeled
(X)
humps
level of pdt < rxt.
() Energy
Axes labeled
(X) Ea of 1st step >> Ea of 2nd + label Ea
Allow ecf from
(b)(i) r.d.s.
tied to 1st ()
() Reactants
and products
labelled
(X) E
f 1st t
Ea
2CH3CHO (+OH)
2CH3CHO (+OH)
Accept: reactants
f 2nd
5() - [2m]
l b l E 3-4() - [1m]
3-4()
0-2() - [1m]
[0m]
0-2()
- [0m]
Penalise
1m if energy
as 0
5th()
if
Penalise 1m
if energy
student
f
t label
t i Ea1h, Ea2,
Accept: reactants
(ii)
Accept: products
(X) 3 humps
OR
Energy(/kJ mol-1)
() 3Axes
labeled
(X)
humps
() Axes labeled
(X) Ea of 1st step >> Ea of 2nd + label Ea
5()
5() -- [2m]
[2m]
1st ()
st
(X) Allow
E f 1ecf
tfrom (b)(i)
E r.d.s.
f 2nd tied
l btol E
3-4() - [1m]
3-4()
0-2() -- [1m]
[0m]
Ea
2CH3CHO (+OH)
2CH3CHO (+OH)
Accept: reactants
0-2()
- [0m]
Penalise
1m if energy
as 0
Penalise
if energy
Penalise 1m
5th()
if
student
f
t label
t i Ea1h, Ea2,
Accept: reactants
Accept: products
(iii)
Acid-base/ Neutralisation reaction

Specific Comments:
A large number gave nucleophilic substitution. A small number gave
free-radical substitution.
Page 19
[1m]
(b)
d+
d-
forbe C
and from
O editing field codes.
cannot
created
(iv) Error! Objects (P)
(P)
Accept if :CH2COH is drawn in place of :CH2CHO. Circle!
In Step 2, there is an equal probability/possibility/chance of the
:CH2CHO/CH2CHO/nucleophile attacking either side (or top or bottom)

of the trigonal planar >C=O group, producing an equimolar mixture of the two
optical isomers. (P)
3(P) [1m]
0 2 (P) [0m]
From Organic Summary Handbk (Section 2 pg. 19):
[1m]
Arrangement around carbonyl C atom is trigonal planar. Hence there is
equal probability of :CH2CHO nucleophile attacking either side of the
plane, producing a racemic mixture (50:50 proportion of each optical
isomer).
50%
CH3
d+
d-
Formatted Table
Formatted: Space After: 0 pt, Line spacing: single
: CH2CHO can attack from the top
:CH2CHO
50%
OR
: CH2CHO can attack from the bottom
Specific Comments:
Some students gave carbocation as intermediate and wrote a 2-step
mechanism instead. For the explanation, many students give planar
carbonyl compound/molecule. A number drew the wrong nucleophile or
the carbonyl compound (replace CHO with -COOH).
Page 20
(c)

Objects cannot be created from editing field codes.
Error!
[1m] for each correct structure for ANY 2 of the 3 structures below
Specific Comments:
A very small number got full marks. Most earned at least 1 mark. Many gave repetition
of answers (mirror image of their 1st structure), or give wrong bond linkage. This
question involved students using the 3-step mechanism given to deduce the possible
products from this reaction.
Page 21
(d)
(i) Cu+
Cu
2+
1s22s22p6 3s23p63d10 Reject: [Ar] 3d10 unless [Ar] is defined
[1m]
1s22s22p6 3s23p63d9 Reject: [Ar] 3d9 unless [Ar] is defined
Specific Comments:
Generally well-done. Most students achieve full marks. There were still
some who removed electrons from the 3d first before the 4s orbitals.
(ii) Cu(II) / Cu2+ ion has partially-filled d orbitals in its 3d9
configuration. Cu(II) / Cu2+ complexes are coloured because
electron transition between d orbitals is possible.
In a Cu(II) / Cu2+ complex, the presence of ligands causes the
3d orbitals to split into 2 sets of different energies. (P)*
5(P) [3m]
The difference in energies (DE) between these two sets of d 3 4 (P) [2m]
orbitals is so small (P)* such that radiation from the visible
2 (P) [1m]
region/ visible light/ visible spectrum of the electromagnetic
spectrum
is
absorbed
(P)#
when
an
electron 0 1 (P) [0m]
moves/transits/excites/promotes/shifts/travels from a d orbital
of lower energy to a partially filled/incompletely filled/
unfilled (or vacant) d orbital of higher energy. [1m] Hence, (P)* [1m]
copper(II) complexes are coloured.
(P)# [1m]
The colour seen/reflected/transmitted will be the complement/
complementary of the colours absorbed. (P)#
Cu(I) / Cu+ ion has fully/completely/totally filled 3d orbitals
OR no empty or partially filled 3d orbitals.
Thus electron transitions between d-orbitals are not possible.
Hence, copper(I) complexes are colourless.
[1m]
Specific Comments:
Students generally score full marks for this part, if they have
studied. Those who did not do well obviously did not study
the topic well, especially on the aspect of ligands causing
the splitting of d-orbitals.
There were a no. of rather short ans merely describing that
Cu(I) / Cu+
ion has fully/completely filled 3d orbitals
OR no empty or partially filled 3d orbitals
and Cu(II) / Cu2+ ion has partially-filled d orbitals in its 3d9
configuration.
Students need to recognize the question clearly asks them
to explain and take note of the mark allocation in this
part of the qns.
Formatted: Font: Times New Roman, 10 pt, Not Bold, No

underline, Font color: Auto, English (United States)
Formatted: Space After: 0 pt, Line spacing: single
Page 22

This is one of the most popular questions. Most students who attempted this question gained
close to ten marks.
In this question, we found that most students could correctly identify the concept being tested in
each part. However, they are unable to express their ideas using the correct scientific terms. See
comments for individual parts for details.
Some students also make careless/ spelling mistakes in this question which caused them to lose
a number of marks. Questions in which students demonstrated their carelessness include (a)(v);
(b)(i).
5.
(a)
(i)
Cl
Cl
[dotted plane must be drawn]
[1m]
Cl
Shape: T-Shaped/T shape [do not accept t]

Common mistakes:
1. Many students drew the lone pairs of electrons on the axial
position instead of the equatorial positions. Could they have
forgotten their year ones work on shapes of molecules?
2. In addition, a number of students actually written out the number
of bond-pairs and lone-pairs correctly (3 bp, 2 lp), yet they
cannot produce the correct molecular shape.
3. For those who got the shape right, they drew imprecise dotted
lines.
4. Others left out drawing the dotted lines. A few left out the lobes
for the lone pairs.
5. A large number of students drew dot-and-cross diagram for the
ICl3 molecule instead of shape of the molecule. Could it be they
did not understand the requirement of the question or they do
not know the shape at all?
Page 23
[1m]
(a)
(ii)
F is from Period 2 while I is from Period 5.

I can expand its octet structure/accommodate more than 8 electrons in [1m]
its outer shell because it has energetically accessible vacant d orbitals but
F cannot expand its octet structure. Thus FCl3 does not exist.
[Note: circle wrong period no.]
OR F does not have energetically accessible vacant d orbitals and
hence it does not allow expansion of octet/ accommodation of more
than 8 electrons. Thus FCl3 does not exist.
Common mistakes:
1. Instead of stating that F does not have energetically accessible
vacant 3d orbitals to expand its octet structure, students stated
FCl3.
2. Students omit the word octet or configuration or structure in
their explanation.
3. This is the part with the most types of spelling mistakes. Octet
was frequently spelled as octect, expand was spelt wrongly too.
4. Students describe the vacant 3d orbitals as energetically
feasible instead of accessible.
5. In addition, many students wrote energetically accessible d
orbitals and forgot to add the word vacant.
6. Two common misconceptions from students to account for why
FCl3 does not exist are (a) that F is a very small atom, so it
cannot accommodate three Cl atoms around it as the resulting
FCl3 will be unstable or (b) F is very electronegative, hence, F
does not share its electrons, unlike iodine.
(iii)
DHf (ICl3(s))
1
2
I2(s) +
+
3
2
[1m] correct energy

cycle (all equations
are balanced with
correct state symbols
and correctly labeled
ICl3 (s)
Cl2(g)
14
88
2
ICl(s) + Cl2(g)
By Hess Law:
DHf ,(ICl3) = +
14
2
+ (-
88
2
) = 37 or 37.0 kJ mol1
Common mistakes:
1. The energy cycle is very often not balanced. One common type of
wrong energy cycle is shown below (where Cl2 (of various coefficients)
is inserted at the arrows):
1
2
I2(s) +
3
2
1
1
Cl2(g)
ICl3 (s)
Cl2(g)
(+14)
ICl(s)
(-88)
Cl2(g)
In the above cycle, we can see another common mistake, that is

students did not label DHf(ICl3) although there is no penalty here.
2. One or more state symbols were also left out.
3. A good number of students did not realize that they need to half the
value of the enthalpy changes, resulting in many leaving the answer
as -74.0 kJ mol-1.
4. A typical area for careless mistakes where the subtraction is
incorrectly done for DHf(ICl3).
Page 24
[1m]
(a)
(iv)
S, is negative due to a decrease in disorder as reaction proceeds with [1m]

decrease/drop in the number of gaseous particles/molecules from 1.5
mol to 0 mol.
Common mistakes:
1. Many students missed out on stating there was a decrease in
disorder when there is a negative entropy change.
2. A common misconception was that some students reasoned that
the decrease in disorder is due the change of states from
gaseous reactants to solid products or due to mixing.
3. We did not mark for the numerical value of changes in the
amount of gas particles. However, we note that many students
got the mark for part (iv) although they have used the wrong
equation to deduce the answer. For instance, they often wrote
that the decrease in disorder.from 2 mol to 0 mol. It is
highly likely that they are referring to this equation for their
answer: 2ICl(s) + 2Cl2(g) 2ICl3(s) instead of the formation of
solid trichloride.
4. A small number of students wrote gaseous ions or gaseous
atoms instead of gaseous molecules.
(v)
DH < 0, DS < 0, TDSf >0

DGf, = DHf, TDSf,
At low temperature, |TDS |<|DH | (or magnitude TDS < DH ) and
[1m]
thus DGf < 0 (or DGf is negative). Since DGf < 0, reaction is spontaneous at
low temperature.
Common mistakes:
1. Many did not state the first point, i.e. -TDS > 0 or simply just
state the sign of TDS is positive, the second of which is not
helpful in their explanation.
2. Many misused the modulus sign, e.g., they stated that |DH| is
negative.
3. A good number did not include the - sign when they are
comparing DH with -TDS
(vi)
DGf, (ICl3) = DHf, (ICl3) TDSf,(ICl3)

= 37 (298)(225 103) [1m] correct subst in kJ mol1 or J mol1 ecf(iii)
= +30.1 kJ mol1 [1m] 2 4 sf, in kJ mol1 or J mol1
Since DGf > 0, formation of ICl3 is not spontaneous at 298K. [1m] e.c.f from
Reject:
1. Conclusion on whether the reaction is spontaneous or not if a value for DGf
is not computed by students.
2. energetically feasible in place of spontaneous
Note:
2 marks are lost if the students substitute values that are not of the same
units:
e.g. DGf, (ICl3) = 37 (298)(225 103)
There is ecf from (a)(iii) if the units are consistent for all the values
substituted.
Common mistakes:
1. Some did not convert 225 to kJ mol-1 K-1, some carelessly
substituted 255 instead of 225.
2. Some thought that a positive DG meant spontaneous reaction!
Page 25
DGf,
3. Some used the term, energetically feasible instead of

spontaneous
4. Some did not know the requirement of the question despite
being a similar question to their tutorial on Entropy. These
students did not calculate any value for DG to predict
spontaneity of the reaction. Instead, they gave a qualitative
explanation.
5.
(b)
(i)
Ksp = [Ag+][ I-]
[1m]
Let y mol dm3 be the solubility of AgI at 25C.

AgI(s) = Ag+(aq) +
y
I- (aq)
y
Ksp = [Ag ][ I ]
+
8.52 10-17 = y2
y = 9.23 10-9
[Ag+] = 9.23 x 10-9 mol dm3 [1m] ecf from expression + 3sf
Reject:
1. Ksp [AgI]
Common mistakes:
1. Students wrote expression for AgCl instead of AgI.
2. Even if expression is correct, students substituted wrong Ksp
value for calculation.
3. Some also substituted wrong power in the Ksp value for
calculation, e.g. 10-7 was used instead of the correct 10-17.
(ii)
White ppt:
AgCl
Yellow ppt:
AgI
[1m] for the identities of ppt, which can be

inferred from eqn/answer
When AgNO3(aq) is added to NaCl(aq), the white ppt formed is AgCl.

Ag+(aq)+ 2NH3(aq) Ag(NH3)2+(aq)
accept =
OR AgCl(s) + 2NH3(aq) [Ag(NH3)2]+ (aq) + Cl(aq)

AgCl(s) = Ag+(aq) + Cl-(aq) ------(*)
When NH3(aq) is added, Ag+ forms a soluble colorless complex [1m]
Ag(NH3)2+, resulting in a decrease of [Ag+(aq)] causing the
equilibrium position of (*) to shift to the right. Thus AgCl dissolves
when excess NH3(aq) is added.
When NaI(aq) is added to [Ag(NH3)2]+, the yellow ppt formed is AgI(s).
AgI is formed since
Ksp of AgI is much smaller than Ksp of AgCl [1m]
the ionic product of [Ag+][I] will be greater than Ksp of AgI.
Common mistakes:
1. Students did not state the identities of white and yellow
ppt explicity. They probably did not understand from the
question that they need to give the identities of the two
ppt in their answers.
2. The second mark is also difficult to award to students as
very few of them knew how to explain why the white ppt
dissolves.
3. They also got the formula of the complex wrong, common
Page 26
wrong formulae include AgOH, AgNH3 (without the

charge), AgNH4, AgNO3
4. For the third mark, instead of quoting the difference in
Ksp values for the two silver halides as a reason for the
different behaviours with ammonia, students said that the
reason was because iodide ions was a stronger reducing
agent than chloride ions/iodide is a stronger ligand than
chloride.
5. Good students generally can answer the dissolving of
AgCl in excess NH3 but lost that mark due to missing state
symbols in the equilibrium equation.
(c)
(i)
Misty/White fumes(or gas) of HCl will be observed.

Orange-red/Orange/Orange-brown/Red-brown/brown fumes(or gas) of Br2
with pungent misty HBr(g) will be observed.
[1m]
NaX + H2SO4 NaHSO4 + HX where X = Cl, Br [accept ionic eqn]
[1m]
2HBr + H2SO4 2H2O + SO2 + Br2
[1m]
HBr/Br is a stronger reducing agent (or has greater reducing power) than
HCl/Cl.
[1m]
Hence HBr can reduce conc. H2SO4 (O.S. of S = +6) to SO2 (O.S. of S = +4)
and itself oxidised to Br2. But HCl cannot reduce conc. H2SO4.
Common mistakes:
1. More students gave the correct observations here.
2. A few of them stated brown solution/liquid instead of brown
fumes.
3. Some left out the word, gas , in their description and hence, lost
the mark as it is not clear if the student meant solution or gas.
4. A number of them said that bromide ion is a stronger oxidising
agent, instead of it being a stronger reducing agent.
5. Many did not even give an explanation for the difference in
observations.
6. Some students wrote Na2SO4 in place of NaHSO4 when trying
to balance the first equation. A few incorrectly wrote H2S in
place of SO2 for the 2nd eqn for Br.
(ii)
Very little HI left for the reaction with alcohol since most of the HI formed will [1m]
be oxidised to I2.
OR
Most of the HI formed will be oxidised to I2 as HI is an even stronger
reducing agent than HBr, while concentrated sulfuric acid is reduced to give
mainly H2S and SO2. Thus the remaining HI will not be enough (or too little HI
left) to react with alcohol to give alkyl iodide.
Common mistakes:
1. Many did not conclude that very little HI is left for the reaction
even though they gave a reasonable explanation as to why the
specified reaction is not used to prepare alkyl iodides. One logical
reason that students propsed is that HI is unstable and hence,
decomposes to H2 and I2 readily, and hence is hardly available to
react with alcohol to give alkyl iodide.
2. Some students commented on the reducing power of HI instead
and did not explain clearly how this could lead to the specified
reaction not being used to prepare alkyl iodide.
Page 27
Class
Adm No
Candidate Name:
2012 Preliminary Examination II

Pre-university 3
H2 CHEMISTRY
9647 / 01
Paper 1
20 Sept 2012
1 hour
OMR
Data Booklet

1.
Do not turn over this question paper until you are told to do so.
2.
Write your name, class and admission number in the spaces provided at the top of
this page and on the OMR provided.
3.
Answer ALL questions and shade the correct answers on the OMR provided using a
soft pencil.
4.
No extra time will be given for shading.
5.
Hand in the question paper and the OMR separately.
INFORMATION FOR CANDIDATES

Marks will not be deducted for wrong answers; your total score will be the number of correct
answers given.
FOR EXAMINERS USE

TOTAL (40 marks)
This question paper consists of 16 printed pages.
[Turn over]
Answer all questions on the OMR form provided (40 Marks)

For each question, there are four possible answers, A, B, C and D.
Choose the one you consider correct.
Zn reacts with VO3- ions to give Vn+.

3.9 g of Zn was required to react completely with 40.0 cm3 of 1.0 mol dm-3 of KVO3.
What is the value of n?
In which of the following pairs do the species have different shapes?

A
AlCl3 and CO32-
NH4+ and CH4
NH3 and H3O+
SeF4 and SO42-
The following graph shows how ionic radius changes across Period 3 for seven elements.
Ionic radius
Unknown
Property
11
12
13
14
15
16
17
Atomic Number
The sharp increase in ionic radius between the 4th and 5th element is due to an
increase in the number of principal quantum shells.
There is a decrease in ionic radius for the first 4 elements in Period 3 due to
decreasing shielding effect.
There is a decrease in ionic radius for the last 3 elements due to decreasing proton
to electron ratio.
The first 4 elements form anions and hence have lower ionic radii than the last 3
elements which form cations.
In which of the following reactions is the acid acting as an oxidant?

A
KBr + H3PO4 HBr + KH2PO4

MgO + H2SO4 MgSO4 + H2O
12HClO4 + P4O10 6Cl2O7 + 4H3PO4
Cu + 4HNO3 Cu(NO3)2 + 2H2O + 2NO2
A 1 dm3 flask containing helium at 2 kPa pressure is connected (at constant temperature)
to a 2 dm3 flask containing neon at 1 kPa pressure.
What is the final pressure after connection?
A
B
C
D
4
3
3
2
5
3
kPa
kPa
kPa
2 kPa

Phosphorus, P4, has the following molecular structure:
P
P
P
Imagine that nitrogen were to form a similar molecule N4 shown in the reaction below:
2N2(g) N4(g)
What would be the value of H (in kJ mol1) for the above reaction?
A
1028
1348
1954
2628
[Turn over
Which gas shows the greatest deviation from ideal gas behavior?
A
HCl
He
CH4
N2
The use of the data booklet is relevant to this question.

In many areas, tap water is slightly acidic due to dissolved carbon dioxide. Which metal
will not be dissolved by tap water containing carbon dioxide?
10
11
Cr
Fe
Cu
Pb
Which of the following mixtures is not an acid/conjugate base pair?

A
H2O/OH-
NaH/Na
H2PO4-/HPO42-
NH3/NH2-
Which of the following pairs of solutions would form an acidic buffer when mixed?
A
HCN and NaCN
HNO3 and NaNO3
NaOH and NaCl
HCl and NaOH
Bleaching solutions are manufactured by dissolving chlorine gas in sodium hydroxide

solution to give the following reaction.
Cl2 (g) + 2OH- (aq)
OCl- (aq) + Cl- (aq) + H2O (l)
Users are warned not to mix the bleach with other cleaning solutions to prevent evolution
of hazardous chlorine gas. Which of the following actions will lead to liberation of chlorine
gas?
A
Addition of water to bleach
Mixing of an alkali with bleach
Shaking bleach with table salt, NaCl
Subjecting bleach to high pressure
12
Given that,
Equilibrium I:
Equilibrium II:
Equilibrium III:
C (s) + O2 (g)
CO2 (g)
C (s) + O2 (g)
CO (g)
CO (g) + O2 (g)
CO2 (g)
Kc1 = 3
Kc2 = 2
Kc = ?
What is the numerical Kc value for the Equilibrium III?

A
13
2
3
2
3
3
2
3
2
The rate of removal of the pain-killing drug paracetamol from the body is a first order
reaction with a rate constant, k, of 0.26 h-1.
How long will it take for 6.25% of the paracetamol ingested to remain in the body?
14
2.7 hours
8.1 hours
10.6 hours
13.5 hours
Sulfates of Group II metals exist as crystalline form as follows:

MgSO4.7H2O
CaSO4.2H2O
SrSO4
BaSO4
Which one of the following accounts for this trend in hydration?
15
The atomic radius of the elements increases down the group.
The ionic character of these sulfates increases down the group.
The ionisation energy of the elements decreases down the group.
The radius of the cation increases down the group.
X is a mixture of two compounds. When X is treated with an excess of dilute hydrochloric

acid, a colour gas is evolved and some, but not all of the mixture dissolves.
Which one of the following mixtures could be X?
A
Ba(NO3)2 and Ca(OH)2
Ag2SO4 and CaCO3
CaCO3 and MgSO4
Ca(OH)2 and MgCO3
[Turn over
16
A yellow precipitate of cadmium(II) sulfide is formed when H2S is passed into an aqueous
solution of cadmium(II) ions, Cd2+. This precipitate is also obtained in the presence of
dilute hydrochloric acid but not in the presence of concentrated hydrochloric acid nor in
excess potassium chloride.
Which explanation accounts for all these observations?
The presence of a high concentration of H+ (aq) suppresses the ionisation of H2S

(aq).
17
The concentration of S2- (aq) is reduced by the formation of SCl42- (aq).
CdS (s) is insoluble in concentrated HCl (aq).
Cd2+ (aq) ions react with Cl- (aq) to form the complex ion [CdCl4]2- (aq).
A current of 2.0 A is used to plate Ni(s) from 500 cm3 of a 1.00 mol dm-3 Ni2+(aq) solution.
What is the concentration of Ni2+(aq) after 3.0 hours?
18
0.39 mol dm-3
0.46 mol dm-3
0.78 mol dm-3
0.89 mol dm-3
Which one of the following statements is correct about a reaction for which the equilibrium
constant is independent of temperature?
A
The enthalpy change of reaction is zero.
Its rate constants do not vary with temperature.
There are equal numbers of moles of reactants and products.
The activation energies for both the forward and reverse reactions are zero.
19
Magnesium iodate(V) undergoes thermal decomposition to yield products as shown by

the equation below. The other Group II iodates(V) also undergo similar thermal
decomposition.
2Mg(IO3)2(s) 2MgO(s) + 2I2(g) + 5O2(g)
The three graphs given below show the change in mass when 2.00 g each of three
Group II iodates(V) are heated separately at a temperature T.
mass/g
Graph
Graph(1)
(1)
2.00
mass/g
mass/g
Graph(2)(2)
Graph
2.00
1.00
1.00
time
Graph
(3)
Graph (3)
2.00
1.00
time
time
Which three Group II iodates(V) give rise to these graphs?
20
21
Graph (1)
Graph (2)
Graph (3)
Ca(IO3)2
Mg(IO3)2
Ba(IO3)2
Mg(IO3)2
Ba(IO3)2
Sr(IO3)2
Ca(IO3)2
Mg(IO3)2
Sr(IO3)2
Sr(IO3)2
Ba(IO3)2
Ca(IO3)2
A compound X exhibits structural isomerism, the isomers being members of different

homologous series.
To which pair of isomers could X belong?
A
acyl chlorides and carboxylic acids
carboxylic acids and esters
amino acids and ammonium salts
amides and amino acids
What is the total number of structural and geometrical isomers for a compound with
molecular formula C3H5F, excluding cyclic structures?
A
6
[Turn over
22
1,2-dibromo-3-chloropropane (DBCP) has been used in the control of earthworms in

agricultural land. The structure of DBCP is shown below.
Br
Br
Cl
Which of the following reactions will lead to the highest yield of DBCP?
23
CH2=CHCH2Cl + Br2 / CCl4 DBCP
CH2=CHCHBr2 + HCl (g) DBCP
CH3CH2CH2Cl + 2Br2 / uv light DBCP + 2HBr
CH3CHBrCH2Br + BrCl / uv light DBCP + HCl
Compound J, C5H11Cl undergoes the following reaction.

Ethanolic KOH
C5H11Cl
C5H10
Which of the following cannot be Compound J?

A
1-chloropentane
2-chloropentane
2 chloro-3-methylbutane
1-chloro-2,2-dimethlypropane
24
A polypeptide was digested using two different enzymes. The fragments obtained were
separated using electrophoresis. Analysis of the fragments from each digestion gave the
following results:
Digestion using enzyme N:
thr-phe-leu
cys-glu-val
ser-glu-cys
asp-cys
Digestion using the enzyme O:
val-asp-cys-thr
phe-leu-ser
glu-cys
cys-glu
What is the correct sequence of the polypeptide structure?
A
B
C
D
cys-glu-val-ser-glu-cys-asp-cys-thr-phe-leu
cys-glu-val-asp-cys-thr-phe-leu-ser-glu-cys
glu-cys-glu-val-asp-cys-thr-phe-leu-ser-glu
ser-glu-cys-glu-val-asp-cys-thr-phe-leu-ser
[Turn over
10
25
Methylbenzene and bromine, in the ratio of 1:6 were mixed and left under the sun and
compound Q was isolated.
After which, iron fillings were added to the mixture at room temperature and Compound R
was identified to be the final product.
Which of the following is likely to be Compounds Q and R?
Compound Q
Compound R
CH2Br
A
CH2Br
Br
CH2Br
Br
CH2Br
Br
CBr3
C
CBr3
Br
CBr3
D
CBr3
Br
Br
11
26
One industrial preparation of ethanoic acid is the direct carbonylation of methanol using a
rhodium catalyst.
CH3OH + CO
rhodium
CH3CO2H
catalyst
CO2H
Which compound could be used to produce HC
CH2CO2H by this method?
CH2CO2H
A
OH
HC CH2CO2H
CO2H
CO2H
HC CO2H
CH2OH
OH
HC CH2OH
CH2OH
CH2OH
HC CH2OH
CH2OH
27
Tamoxifen is widely used in the treatment of breast cancer.

CH3
CH2
C
C
CH3
N
CH2
O
CH2
CH3
Tamoxifen
What is the number of sp2 and sp3 carbon atoms respectively after subjecting Tamoxifen
to hydrogen gas under heat and in the presence of nickel?
sp2
sp3
20
18
18
20
6
[Turn over
12
28
The reduction of a nitrile produces a compound of formula C3H7NH2.

Which of the following would be produced if the same nitrile is heated with hydrochloric
acid?
29
CH3CONH2
CH3CH2COOH
(CH3)2CHCOOH
CH3CH2OH
GABA has the structural formula, H2NCH2CH2CH2CO2H. It is a neuro-transmitter

released by red algae to encourage shellfish larvae to settle on the ocean bed.
How does GABA differ from amino acids obtained by the hydrolysis of proteins?
30
It does not form zwitterions.
It is not a 2-aminocarboxylic acid.
It is insoluble in water.
It cannot form a polyamide linkage.
Which property enables proteins to function as a pH buffer?
Proteins contain the carboxyl and amino groups.
Proteins are soluble.
Proteins have high molecular mass.
Proteins possess secondary and tertiary structures.
13
For questions 31 40, the responses A to D should be selected on the basis of
1,2 and 3
1 and 2
2 and 3
1 only
are correct
only are correct
only are correct
is correct
No other combination of statements is to be used as a correct response.
Which of the following is/are correct statement(s) about a 12.0 g sample of 12C?
31
32
The number of atoms is 6.02 x 1023.
The number of atoms is the same as the number of atoms in 4.0 g of 4He.
The number of atoms is the same as the number of atoms in 2.0 g of 1H2.
The enthalpy change of reaction, DHr, between sodium and water (in excess) to produce
sodium hydroxide and hydrogen gas can be measured in the laboratory.
2Na(s) + 2H2O(l)
DHr
2NaOH(aq) + H2(g)
Other than temperature change of the solution, what information is/are needed to
calculate a value for the enthalpy change of this reaction?
33
Mass of water
Mass of sodium
Pressure
0.1 mol of each of the following is separately added to 100 cm3 of water.
Which of the following resulting solution(s) show an increasing order of pH values?
1
2
PCl3, AlCl3, NaCl

NH3, NaOH, Ba(OH)2
HCl, CH3CO2H, CH3CH2OH
[Turn over
14
34
35
Which of the following reaction(s) is/are always endothermic?

1
Hydration of a gaseous ion
The dissociation of a diatomic molecule into atoms
The sublimation of a solid
The table below shows the solubility product, in mol dm3 for three metal sulfides. In an
acidic solution, [S2]saturated = 1018 mol dm3.
Metal ion
Mn2+
Ni2+
Ag+
Ksp of sulfide
1016
1021
1036
Which of the metal sulfide(s) would be precipitated from the acidic solution containing
0.010 mol dm3 of the metal ion when the solution is saturated with hydrogen sulfide?
36
Mn2+
Ni2+
Ag+
The compound 2-ethylhexyl-p-methoxycinnamate (MOC) is used as a sunscreen.
CH3O
CH
CHCO2C8H17
Which of the following statement(s) is/are correct?

1
A brown precipitate is formed with cold alkaline KMnO4.
A racemic mixture is produced when it is boiled with HCl (g).
It is insoluble in organic solvents.
15
37
A hydrocarbon, on heating with acidified KMnO4 gives

CH3CH2COCH2CH2CH2CH2COOH.
Which of the following is/are possible structure(s) of the hydrocarbon?
1
2
OH
3
O
38
39
Which of the following reaction(s) could have the same intermediate?

1
CH3CH=CH2 intermediate
CH3CH=CH2 intermediate CH3COCH3
CH3CO2CH(CH3)2 intermediate CH3CHBrCH3
CH3CH(NH2)CH3
Psilocin is a psychedelic mushroom alkaloid. It is the active compound that produces

hallucinations from ingesting magic mushrooms and amplifies sensory experience.
Compound Y is a derivative of Psilocin.
NH
OH
CH3
N
H
Y
Which of the following statement(s) is/are true about Y?
1
It gives white fumes with CH3COCl.
It dissolves in both aqueous acids and alkalis.
The nitrogen-containing group in the ring has a lower pKb than the nitrogencontaining group in the side chain.
[Turn over
16
40
The Grignard reaction is a very important tool in organic reactions involving the formation
of carbon-carbon bond. Grignard reagents are formed by reacting halogenoalkane, R-X,
with magnesium in dry ether.
For example, reaction of CH3Cl with Mg,
CH3Cl + Mg
dry ether
H3C
d-
Mg
d+
Cl
d-
Grignard Reagent
Grignard reagents allow the carbon chain of carbonyl compounds to be lengthened.

For example,
OH
O
CH3CH
1. CH3MgCl, ether
2. H3O+
CH3CH
CH3
Which compounds could be made from a ketone and a Grignard reagent?

1
CH3C(CH2CH3)2OH
CH3CH2CH2CH2OH
(CH3CH2)2CHOH
END OF PAPER
Class
Adm No
Candidate Name:

Pre-university 3
H2 CHEMISTRY
9647 / 01
Paper 1
20 Sept 2012
1 hour
OMR
Data Booklet

1.
2.
Write your name, class and admission number in the spaces provided at the top of
this page and on the OMR provided.
3.
Answer ALL questions and shade the correct answers on the OMR provided using a
soft pencil.
4.
No extra time will be given for shading.
5.
Hand in the question paper and the OMR separately.

Marks will not be deducted for wrong answers; your total score will be the number of correct
answers given.
FOR EXAMINERS USE

TOTAL (40 marks)
[Turn over
Answer all questions on the OMR form provided (40 Marks)

For each question, there are four possible answers, A, B, C and D.
Choose the one you consider correct.
Zn reacts with VO3- ions to give Vn+.

3.9 g of Zn was required to react completely with 40.0 cm3 of 1.0 mol dm-3 of KVO3.
What is the value of n?
In which of the following pairs do the species have different shapes?

A
AlCl3 and CO32-
NH4+ and CH4
NH3 and H3O+
SeF4 and SO42-
The following graph shows how ionic radius changes across Period 3 for seven elements.
Ionic radius
Unknown
Property
11
12
13
14
15
16
17
Atomic Number
The sharp increase in ionic radius between the 4th and 5th element is due to an
increase in the number of principal quantum shells.
There is a decrease in ionic radius for the first 4 elements in Period 3 due to
decreasing shielding effect.
There is a decrease in ionic radius for the last 3 elements due to decreasing proton
to electron ratio.
The first 4 elements form anions and hence have lower ionic radii than the last 3
elements which form cations.
In which of the following reactions is the acid acting as an oxidant?

A
KBr + H3PO4 HBr + KH2PO4
MgO + H2SO4 MgSO4 + H2O
12HClO4 + P4O10 6Cl2O7 + 4H3PO4
Cu + 4HNO3 Cu(NO3)2 + 2H2O + 2NO2
A 1dm3 flask containing helium at 2 kPa pressure is connected (at constant temperature)
to a 2 dm3 flask containing neon at 1 kPa pressure.
What is the final pressure after connection?
A
B
C
D
4
3
3
2
5
3
kPa
kPa
kPa
2 kPa

Phosphorus, P4, has the following molecular structure:
P
P
P
Imagine that nitrogen were to form a similar molecule N4 shown in the reaction below:
2N2(g) N4(g)
What would be the value of H (in kJ mol1) for the above reaction?
A
1028
1348
1954
2628
[Turn over
Which gas shows the greatest deviation from ideal gas behavior?
A
HCl
He
CH4
N2
The use of the data booklet is relevant to this question.

In many areas, tap water is slightly acidic due to dissolved carbon dioxide. Which metal
will not be dissolved by tap water containing carbon dioxide?
10
11
Cr
Fe
Cu
Pb
Which of the following mixtures is not an acid/conjugate base pair?

A
H2O/OH-
NaH/Na
H2PO4-/HPO42-
NH3/NH2-
Which of the following pairs of solutions would form an acidic buffer when mixed?
A
HCN and NaCN
HNO3 and NaNO3
NaOH and NaCl
HCl and NaOH
Bleaching solutions are manufactured by dissolving chlorine gas in sodium hydroxide

solution to give the following reaction.
Cl2 (g) + 2OH- (aq)
OCl- (aq) + Cl- (aq) + H2O (l)
Users are warned not to mix the bleach with other cleaning solutions to prevent evolution
of hazardous chlorine gas. Which of the following actions will lead to liberation of chlorine
gas?
A
Addition of water to bleach
Mixing of an alkali with bleach
Shaking bleach with table salt, NaCl
Subjecting bleach to high pressure
12
Given that,
Equilibrium I:
Equilibrium II:
Equilibrium III:
C (s) + O2 (g)
CO2 (g)
CO (g)
C (s) + O2 (g)
CO (g) + O2 (g)
CO2 (g)
Kc1 = 3
Kc2 = 2
Kc = ?
What is the numerical Kc value for the Equilibrium III?

A
13
2
3
2
3
3
2
3
2
The rate of removal of the pain-killing drug paracetamol from the body is a first order
reaction with a rate constant, k, of 0.26 h-1.
How long will it take for 6.25% of the paracetamol ingested to remain in the body?
14
2.7 hours
8.1 hours
10.6 hours
13.5 hours
Sulfates of Group II metals exist as crystalline form as follows:

MgSO4.7H2O
CaSO4.2H2O
SrSO4
BaSO4
Which one of the following accounts for this trend in hydration?
15
The atomic radius of the elements increases down the group.
The ionic character of these sulfates increases down the group.
The ionisation energy of the elements decreases down the group.
The radius of the cation increases down the group.
X is a mixture of two compounds. When X is treated with an excess of dilute hydrochloric

acid, a colour gas is evolved and some, but not all of the mixture dissolves.
Which one of the following mixtures could be X?
A
Ba(NO3)2 and Ca(OH)2
Ag2SO4 and CaCO3
CaCO3 and MgSO4
Ca(OH)2 and MgCO3
[Turn over
16
A yellow precipitate of cadmium(II) sulfide is formed when H2S is passed into an aqueous
solution of cadmium(II) ions, Cd2+. This precipitate is also obtained in the presence of
dilute hydrochloric acid but not in the presence of concentrated hydrochloric acid nor in
excess potassium chloride.
Which explanation accounts for all these observations?
The presence of a high concentration of H+ (aq) suppresses the ionisation of H2S

(aq).
17
The concentration of S2- (aq) is reduced by the formation of SCl42- (aq).
CdS (s) is insoluble in concentrated HCl (aq).
Cd2+ (aq) ions react with Cl- (aq) to form the complex ion [CdCl4]2- (aq).
A current of 2.0 A is used to plate Ni(s) from 500 cm3 of a 1.00 mol dm-3 Ni2+(aq) solution.
What is the concentration of Ni2+(aq) after 3.0 hours?
18
0.39 mol dm-3
0.46 mol dm-3
0.78 mol dm-3
0.89 mol dm-3
Which one of the following statements is correct about a reaction for which the equilibrium
constant is independent of temperature?
A
The enthalpy change of reaction is zero.
Its rate constants do not vary with temperature.
There are equal numbers of moles of reactants and products.
The activation energies for both the forward and reverse reactions are zero.
19
Magnesium iodate(V) undergoes thermal decomposition to yield products as shown by

the equation below. The other Group II iodates(V) also undergo similar thermal
decomposition.
2Mg(IO3)2(s) 2MgO(s) + 2I2(g) + 5O2(g)
The three graphs given below show the change in mass when 2.00 g each of three
Group II iodates(V) are heated separately at a temperature T.
mass/g
Graph
Graph(1)
(1)
2.00
mass/g
mass/g
Graph(2)(2)
Graph
2.00
1.00
1.00
time
Graph
(3)
Graph (3)
2.00
1.00
time
time
Which three Group II iodates(V) give rise to these graphs?
20
21
Graph (1)
Graph (2)
Graph (3)
Ca(IO3)2
Mg(IO3)2
Ba(IO3)2
Mg(IO3)2
Ba(IO3)2
Sr(IO3)2
Ca(IO3)2
Mg(IO3)2
Sr(IO3)2
Sr(IO3)2
Ba(IO3)2
Ca(IO3)2
A compound X exhibits structural isomerism, the isomers being members of different

homologous series.
To which pair of isomers could X belong?
A
acyl chlorides and carboxylic acids
carboxylic acids and esters
amino acids and ammonium salts
amides and amino acids
What is the total number of structural and geometrical isomers for a compound with
molecular formula C3H5F, excluding cyclic structures?
A
6
[Turn over
22
1,2-dibromo-3-chloropropane (DBCP) has been used in the control of earthworms in

agricultural land. The structure of DBCP is shown below.
Br
Br
Cl
Which of the following reactions will lead to the highest yield of DBCP?
23
CH2=CHCH2Cl + Br2 / CCl4 DBCP
CH2=CHCHBr2 + HCl (g) DBCP
CH3CH2CH2Cl + 2Br2 / uv light DBCP + 2HBr
CH3CHBrCH2Br + BrCl / uv light DBCP + HCl
Compound J, C5H11Cl undergoes the following reaction.

Ethanolic KOH
C5H11Cl
C5H10
Which of the following cannot be Compound J?

A
1-chloropentane
2-chloropentane
2 chloro-3-methylbutane
1-chloro-2,2-dimethlypropane
24
A polypeptide was digested using two different enzymes. The fragments obtained were
separated using electrophoresis. Analysis of the fragments from each digestion gave the
following results:
Digestion using enzyme N:
thr-phe-leu
cys-glu-val
ser-glu-cys
asp-cys
Digestion using the enzyme O:
val-asp-cys-thr
phe-leu-ser
glu-cys
cys-glu
What is the correct sequence of the polypeptide structure?
A
B
C
D
cys-glu-val-ser-glu-cys-asp-cys-thr-phe-leu
cys-glu-val-asp-cys-thr-phe-leu-ser-glu-cys
glu-cys-glu-val-asp-cys-thr-phe-leu-ser-glu
ser-glu-cys-glu-val-asp-cys-thr-phe-leu-ser
[Turn over
10
25
Methylbenzene and bromine, in the ratio of 1:6 were mixed and left under the sun and
compound Q was isolated.
After which, iron fillings were added to the mixture at room temperature and Compound R
was identified to be the final product.
Which of the following is likely to be Compounds Q and R?
Compound Q
Compound R
CH2Br
A
CH2Br
Br
CH2Br
Br
CH2Br
Br
CBr3
C
CBr3
Br
CBr3
D
CBr3
Br
Br
11
26
One industrial preparation of ethanoic acid is the direct carbonylation of methanol using a
rhodium catalyst.
CH3OH + CO
rhodium
CH3CO2H
catalyst
CO2H
CH2CO2H by this method?
Which compound could be used to produce HC
CH2CO2H
A
OH
HC CH2CO2H
CO2H
CO2H
HC CO2H
CH2OH
OH
HC CH2OH
CH2OH
CH2OH
HC CH2OH
CH2OH
27
Tamoxifen is widely used in the treatment of breast cancer.

CH3
CH2
C
C
CH3
N
CH2
O
CH2
CH3
Tamoxifen
What is the number of sp2 and sp3 carbon atoms respectively after subjecting Tamoxifen
to hydrogen gas under heat and in the presence of nickel?
sp2
sp3
20
18
18
20
6
[Turn over
12
28
The reduction of a nitrile produces a compound of formula C3H7NH2.

Which of the following would be produced if the same nitrile is heated with hydrochloric
acid?
29
CH3CONH2
CH3CH2COOH
(CH3)2CHCOOH
CH3CH2OH
GABA has the structural formula, H2NCH2CH2CH2CO2H. It is a neuro-transmitter

released by red algae to encourage shellfish larvae to settle on the ocean bed.
How does GABA differ from amino acids obtained by the hydrolysis of proteins?
30
It does not form zwitterions.
It is not a 2-aminocarboxylic acid.
It is insoluble in water.
It cannot form a polyamide linkage.
Which property enables proteins to function as a pH buffer?
Proteins contain the carboxyl and amino groups.
Proteins are soluble.
Proteins have high molecular mass.
Proteins possess secondary and tertiary structures.
13
For questions 31 40, the responses A to D should be selected on the basis of
1,2 and 3
1 and 2
2 and 3
1 only
are correct
only are correct
only are correct
is correct
Which of the following is/are correct statement(s) about a 12.0 g sample of 12C?
31
32
The number of atoms is 6.02 x 1023.
The number of atoms is the same as the number of atoms in 4.0 g of 4He.
The number of atoms is the same as the number of atoms in 2.0 g of 1H2.
The enthalpy change of reaction, DHr, between sodium and water (in excess) to produce
sodium hydroxide and hydrogen gas can be measured in the laboratory.
2Na(s) + 2H2O(l)
DHr
2NaOH(aq) + H2(g)
Other than temperature change of the solution, what information is/are needed to
calculate a value for the enthalpy change of this reaction?
33
Mass of water
Mass of sodium
Pressure
0.1 mol of each of the following is separately added to 100 cm3 of water.
Which of the following resulting solution(s) show an increasing order of pH values?
1
2
PCl3, AlCl3, NaCl

NH3, NaOH, Ba(OH)2
HCl, CH3CO2H, CH3CH2OH
[Turn over
14
34
35
Which of the following reaction(s) is/are always endothermic?

1
Hydration of a gaseous ion
The dissociation of a diatomic molecule into atoms
The sublimation of a solid
The table below shows the solubility product, in mol dm3 for three metal sulfides. In an
acidic solution, [S2]saturated = 1018 mol dm3.
Metal ion
Mn2+
Ni2+
Ag+
Ksp of sulfide
1016
1021
1036
Which of the metal sulfide(s) would be precipitated from the acidic solution containing
0.010 mol dm3 of the metal ion when the solution is saturated with hydrogen sulfide?
36
Mn2+
Ni2+
Ag+
The compound 2-ethylhexyl-p-methoxycinnamate (MOC) is used as a sunscreen.
CH3O
CH
CHCO2C8H17
Which of the following statement(s) is/are correct?

1
A brown precipitate is formed with cold alkaline KMnO4.
A racemic mixture is produced when it is boiled with HCl (g).
It is insoluble in organic solvents.
15
37
A hydrocarbon, on heating with acidified KMnO4 gives

CH3CH2COCH2CH2CH2CH2COOH.
Which of the following is/are possible structure(s) of the hydrocarbon?
1
2
OH
3
O
38
39
Which of the following reaction(s) could have the same intermediate?

1
CH3CH=CH2 intermediate
CH3CH=CH2 intermediate CH3COCH3
CH3CO2CH(CH3)2 intermediate CH3CHBrCH3
CH3CH(NH2)CH3
Psilocin is a psychedelic mushroom alkaloid. It is the active compound that produces

hallucinations from ingesting magic mushrooms and amplifies sensory experience.
Compound Y is a derivative of Psilocin.
NH
OH
CH3
N
H
Y
Which of the following statement(s) is/are true about Y?
1
It gives white fumes with CH3COCl.
It dissolves in both aqueous acids and alkalis.
The nitrogen-containing group in the ring has a lower pKb than the nitrogencontaining group in the side chain.
[Turn over
16
40
The Grignard reaction is a very important tool in organic reactions involving the formation
of carbon-carbon bond. Grignard reagents are formed by reacting halogenoalkane, R-X,
with magnesium in dry ether.
For example, reaction of CH3Cl with Mg,
CH3Cl + Mg
dry ether
H3C
d-
Mg
d+
Cl
d-
Grignard Reagent
Grignard reagents allow the carbon chain of carbonyl compounds to be lengthened.

For example,
OH
O
CH3CH
1. CH3MgCl, ether
2. H3O+
CH3CH
CH3
Which compounds could be made from a ketone and a Grignard reagent?

1
CH3C(CH2CH3)2OH
CH3CH2CH2CH2OH
(CH3CH2)2CHOH
END OF PAPER
Class
Adm No
Candidate Name:

Pre-university 3
H2 CHEMISTRY
9647/02
Paper 2
18 Sept 2012
2 hours
Data Booklet

1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
Write your name, class and index number in the spaces provided at the top of
this page.
Write in dark blue or black pen in the spaces provided on the Question Paper.
You may use a soft pencil for any diagrams or graphs.
DO NOT use paper clips, highlighters, glue or correction fluid or tape.
Answer ALL the questions.
Give non-exact numerical answers correct to 3 significant figures, or 1 decimal
place in the case of Mr and Ar, unless a different level of accuracy is specified in
the question.
The number of marks is given in brackets [ ] at the end of each question or part
question.
You are reminded of the need for clear presentation in your answers and to
show all working in calculations.
The use of a calculator is expected, where appropriate.
Paper 2
Question No
1
(12m)
2
(9m)
3
(10m)
4
(16m)
5
(10m)
6
(15m)
72
Marks Obtained

[Turn over
Planning
The benzenediazonium ion, C6H5N2+, reacts with water as shown in the equation.
C6H5N2+ (aq) + H2O (l) C6H5OH (aq) + N2 (g) + H+ (aq)
At temperatures below 10 C, the reaction is very slow. However, nitrogen gas is evolved
at a measureable rate at temperatures of 20 C and above.
In this experiment, you are provided with an aqueous solution containing 0.100 mol dm-3 of
the benzenediazonium ion at a temperature below 10 C.
You are required to design an experiment to deduce the order of reaction with respect to
C6H5N2+ of an aqueous solution at 20 C and an atmospheric pressure of 101 kPa.
(a) Define the term order of reaction.
[1]
................................................................................................................................................
................................................................................................................................................
(b)
Outline the steps you would take to determine the order of reaction with respect to
C6H5N2+ (aq) at 20 C. In your plan, include the following details:
-
a suitable volume of C6H5N2+ (aq) used,
measurement(s) to be taken,
plotting of a suitable graph, if any.
[5]
(c)
Draw a labelled diagram of the experimental set-up.

[You may assume that you are given common apparatus found in a school laboratory.]
(d)
[2]
Describe how you will use the results obtained to determine the order of reaction with
respect to C6H5N2+ (aq).
[2]
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
(e)
Identify one potential hazard in this experiment and suggest the safety precaution you
[2]
would take to overcome this.
................................................................................................................................................
................................................................................................................................................
[Total: 12 marks]
[Turn over
2 (a)
A lower secondary Science student described an atom of Silicon as having fourteen bees
buzzing around a space the size of a football stadium, as though they are being trapped.
(i)
Explain using Chemistry concepts, what do the bees in the description represent and what
stopped the bees from flying away from the stadium?
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
(ii)
The teacher commented that the students description of Silicon was incomplete. What is
missing from the students description of Silicon?
................................................................................................................................................
................................................................................................................................................
(iii)
28Si, 29Si, 30Si
are isotopes of Silicon.
Explain why isotopes of Silicon undergo identical chemical reactions?
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
[3]
(b)
Amongst all the elements in Period 3 of the periodic table, Silicon has the highest melting
point. Sketch a graph to illustrate the trend of the melting points of elements in Period 3.
Explain your sketch.
[4]
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
[Turn over
(c)
Silicon reacts with oxygen to form silicon dioxide as a possible product.

In dentistry, a composite material based on SiO2 has been developed to be used as dental
fillings.
(i)
State one property of SiO2 that makes it suitable for use as dental fillings.
................................................................................................................................................
................................................................................................................................................
(ii)
Draw a diagram to illustrate the type of bonding involved in SiO2.
[2]
[Total: 9 marks]
Ammonia gas decomposes into nitrogen and hydrogen when passed over a platinum
gauze. The rate of decomposition is found to be independent of the partial pressure of

ammonia at very high pressures, but the rate was directly proportional to the partial
pressure of ammonia at low pressures.
(a)
Explain this observation as far as you can.
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
[2]
(b)
Given that 45% of ammonia dissociated into nitrogen and hydrogen at moderately high
temperatures, and a total pressure of 1 atm, calculate the value of Kp, stating its units.
(c)
Ammonia, nitrogen and hydrogen are non-ideal gases.
(i)
State two assumptions of the kinetic theory as applied to an ideal gas.
[3]
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
(ii)
Which of these three gases deviates the most from an ideal gas? Explain your answer.
.
...............................................................................................................................................
................................................................................................................................................
(iii)
For a given fixed mass of an ideal gas, sketch graphs of:

I: P against V at constant T (where P represents pressure)
II: V against pV at constant T (where p represents density)
[5]
[Total: 10 marks]
[Turn over
The reaction between phenol and benzoyl chloride produces an ester with the formula
C6H5COOC6H5. Hydrogen chloride is also formed in this reaction.
Name of Compound
Chemical formula
Mr
Phenol
C6H5OH
94.0
Benzoyl chloride
C6H5COCl
140.5
C6H5COOC6H5
198.0
The crude (impure) ester produced in the reaction can be purified by recrystallisation in
ethanol. A typical yield, based on benzoyl chloride is 70%.
[Additional info:
Melting point of ester: 68- 70 C
Boiling point of ester: 298- 299 C]
(a)
State the name of the ester that is produced in the reaction.
[1]
(b)
Explain why this reaction will not occur if benzoic acid was used instead of benzoyl
chloride.
................................................................................................................................................
................................................................................................................................................
(c)
In this experiment, only 70% of benzoyl chloride is converted into to the ester.
(i)
Calculate the minimum mass of benzoyl chloride needed to form 5 g of the ester.
[1]
(ii)
Hence, calculate the minimum mass of phenol needed in the reaction.
[2]
(d)
Briefly describe how the crude (impure) ester produced can be purified by recrystallisation
(i)
in ethanol.
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
(ii)
Suggest and explain a method that can be used to check the purity of the ester produced.
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
[Turn over
[4]
10
(e)
Another ester, P (Mr = 116) used in synthetic fruit flavors, is subjected to hydrolysis to give
a monoprotic acid, Q and an alcohol, R.
When 1.00 g of Q is titrated with 0.500 mol dm-3 NaOH, 33.0 cm3 of NaOH is required for
neutralization. R reacts with alkaline aqueous iodine to give a precipitate S. Compound R
exists as a pair of isomers, both of which are oxidized to give T which also reacts with
alkaline aqueous iodine to give the same precipitate S, and a solution U.
Identify the structures P, Q, R, S, T and U, explaining your deductions clearly.
[Total: 16 marks]
[8]
11
This question discusses metals in Group I and Group II of the Periodic table.
5
(a)
For a group I element, the ease with which the following reaction occurs is indicated by its
electrode potential, E.
M(s) M+ (aq) + e-
---------- Reaction (I)
Calculate the enthalpy change of Reaction (I) for Li and Na, using values given below as
well as relevant data from the data booklet.
(b)
Element (M)
Hat (M) / kJ mol-1
Hhydration (M+) / kJ mol-1
Li
159
-957
Na
107
-841
[3]
Comment on the relationship between the enthalpy change of Reaction (I) obtained in (a)
and the E values given in the data booklet for Li and Na.
[2]
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
[Turn over
12
(c)
The melting points of Group II oxides are given in the table below.
Oxide
Melting point / C
MgO
2852
CaO
2614
SrO
2430
BaO
1918
Explain the trend in the melting points.
[2]
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
(d)
Describe the reactions, if any, for magnesium and calcium with cold water, writing
equations, with state symbols, for any reactions taking place.
[3]
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
[Total: 10 marks]
13
Synthetic detergents (anionic, cationic and non-ionic) consist of a hydrocarbon chain and
polar group. As a surfactant, the synthetic detergent is more effective than conventional
soap in hard water water that contains dissolved minerals such as Ca2+ and Mg2+.
Anionic detergents
Anionic detergents contain groups with a negative charge such as Na+SO3-. An example of
synthesis of a detergent sodium-n-dodecylbenzenesulfonate is as follows:
H2SO4
Reaction I
HO 3S
Na O 3 S
Cationic detergents
Cationic detergents contain positively charged groups and can be found in hair
conditioners. Keratin, a protein which contains negatively-charged groups which can be
found on the surface of hair, binds strongly to the hydrophilic ends of cationic detergents.
The hydrophobic ends of the surfactant molecules then act as the new hair surface. One
example
of
such
detergent
is
trimethylhexadecylammonium
chloride,
[CH3(CH2)15N(CH3)3]+ Cl-.
Non-ionic detergents
Non-ionic detergents are commonly used in dish-washing liquids. An example is
pentaerythrityl palmitate:
H2C
O
CH3 (CH2)14 C
O CH2
OH
C CH2 OH
H2C OH
[Turn over
14
(a)
State possible reagents and conditions to synthesize [CH3(CH2)15N(CH3)3]+ from
(i)
CH3(CH2)15NH2.
................................................................................................................................................
................................................................................................................................................
(ii)
Name and draw the mechanism for the following synthesis.
(b)
HO 3S
Suggest why non-ionic detergents are commonly used in dish-washing liquids.
................................................................................................................................................
................................................................................................................................................
[5]
[1]
15
(c)
Describe a chemical test that can be used to distinguish between sodium-ndodecylbenzenesulfonate and pentaerythrityl palmitate.
[2]
You are to include all reagents, conditions and expected observations.
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
(d)
Apart from detergents or soap, cleaning products may also contain enzymes to degrade
protein-based stains. Enzymes are proteins with a specific biological activity that are
determined by their primary, secondary, tertiary and quaternary structures.
(i)
Apart from its function as an enzyme, state one other function of proteins.
................................................................................................................................................
(ii)
Briefly describe with a well-labeled diagram, one example of a secondary structure of a

protein.
[3]
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
[Turn over
16
(e)
The effectiveness of enzymes can be reduced by the addition of heavy metal ions such as
Hg+ or Pb2+.
(i)
Explain this phenomenon.
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
(ii)
Pb2+ typically forms complexes that are coloured. Explain why this is so.
[4]
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
................................................................................................................................................
[Total: 15 marks]
END OF PAPER
Class
Adm No
Candidate Name:

Pre-university 3
H2 CHEMISTRY
9647/02
Paper 2
18 Sept 2012
2 hours
Data Booklet

1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
Write your name, class and index number in the spaces provided at the top of
this page.
Write in dark blue or black pen in the spaces provided on the Question Paper.
DO NOT use paper clips, highlighters, glue or correction fluid or tape.
Answer ALL the questions.
place in the case of Mr and Ar, unless a different level of accuracy is specified in
the question.
question.
You are reminded of the need for clear presentation in your answers and to
show all working in calculations.
Paper 2
Question No
1
(12m)
2
(9m)
3
(10m)
4
(16m)
5
(10m)
6
(15m)
72
Marks Obtained

[Turn over
Planning
The benzenediazonium ion, C6H5N2+, reacts with water as shown in the equation.
C6H5N2+ (aq) + H2O (l) C6H5OH (aq) + N2 (g) + H+ (aq)
At temperatures below 10 C, the reaction is very slow. However, nitrogen gas is evolved
at a measureable rate at temperatures of 20 C and above.
In this experiment, you are provided with an aqueous solution containing 0.100 mol dm-3 of
the benzenediazonium ion at a temperature below 10 C.
You are required to design an experiment to deduce the order of reaction with respect to
C6H5N2+ of an aqueous solution at 20 C and an atmospheric pressure of 101 kPa.
(a) Define the term order of reaction.
[1]
Order of reaction with respect to a reactant is the power of the concentration of that
reactant in the experimentally determined rate equation.
(b)
Outline the steps you would take to determine the order of reaction with respect to
C6H5N2+ (aq) at 20 C. In your plan, include the following details:
-
a suitable volume of C6H5N2+ (aq) used,
measurements to be taken,
plotting of a suitable graph, if any.
[5]
Assume 50 cm3 of nitrogen gas to be collected. (Volume chosen has to be large enough
for sufficient volume of C6H5N2+ solution used)
Using pV = nRT,
Amount of nitrogen gas to be collected = 0.002074 mol
= Amount of C6H5N2+ required
Thus, minimum volume of C6H5N2+ needed = 0.002074 / 0.1 = 20.7 cm3
(To use 25 cm3 of C6H5N2+ )
Use a water bath (no naked flame) to maintain a temperature of 20 C for the reaction
mixture.
Record the volume of nitrogen produced over regular time intervals of 5 minutes.
A graph of volume of nitrogen produced against time is plotted.
(c)
Draw a labelled diagram of the experimental set-up.

[You may assume that you are given common apparatus found in a school laboratory.]
[2]
1 mark for suitable apparatus (use of well-greased gas syringe to collect nitrogen gas),
well-labeled.
1 mark for feasibility of set-up
(d)
Describe how you will use the results obtained to determine the order of reaction with
respect to C6H5N2+ (aq).
[2]
From the graph of volume of nitrogen produced against time plotted, determine the time
taken for nitrogen to be produced. (time taken for of total volume, then of total
volume, then all of nitrogen produced)

If the time taken is constant, order of reaction with respect to C6H5N2+ (aq) is one.
(e)
Identify one potential hazard in this experiment and suggest the safety precaution you
[2]
would take to overcome this.

The organic compounds are toxic and may cause irritation when in contact with the skin.
Gloves should be worn during the experiment.
OR
Conduct the experiment in a fume cupboard to present inhaling of toxic fumes.
[Total: 12 marks]
[Turn over
2 (a)
A lower secondary Science student described an atom of Silicon as having fourteen bees
buzzing around a space the size of a football stadium, as though they are being trapped.
(i)
Explain using Chemistry concepts, what do the bees in the description represent and what
stopped the bees from flying away from the stadium?
The bees represent electrons and the electrostatic attraction of the positively charged
protons in the nucleus for the electrons presents the electrons from being lost.
(ii)
The teacher commented that the students description of Silicon was incomplete. What is
missing from the students description of Silicon?
The positively charged nucleus.
(iii)
28Si, 29Si, 30Si
are isotopes of Silicon.
Explain why isotopes of Silicon undergo identical chemical reactions?
[3]
Chemical reactions depend on the electronic configuration of the substance.
Since isotopes have the same number of electrons but different number of neutrons, they
still have identical chemical properties.
(b)
Amongst all the elements in Period 3 of the periodic table, Silicon has the highest melting
point. Sketch a graph to illustrate the trend of the melting points of elements in Period 3.
Explain your sketch.
[4]
Na to Al
giant metallic structure
strong electrostatic forces of attraction between metal cations and delocalised
electronlarge amount of energy required to overcome those forces
\ high m.p.
delocalised electrons , size of cations , (charge on cation )
strength of metallic bond
;
\m.p.
Si
giant covalent structure
large amount of energy required to break strong covalent bonds between Si atoms.
\ high m.p.
P to Ar
Simple molecular structure
weak temporary dipole induced dipole forces of attraction between molecules
relatively smaller amount of energy required to overcome those forces
\ low m.p.
size of electron cloud of molecules varies, S8>P4>Cl2>Ar
size of electron cloud of molecules , strength of temporary dipole induced dipole forces
of attraction .
\ m.p.: S8>P4>Cl2>Ar
(c)
Silicon reacts with oxygen to form silicon dioxide as a possible product.

In dentistry, a composite material based on SiO2 has been developed to be used as dental
fillings.
(i)
State one property of SiO2 that makes it suitable for use as dental fillings.
SiO2 is hard and resistant to chemical attack (Unreactive towards acids in food or saliva)
(ii)
Draw a diagram to illustrate the type of bonding involved in SiO2.
[2]
Tetrahedral, similar to diamond.
Each Si is bonded to 4 O atoms, and each O is bonded to 2 Si atoms

[Total: 9 marks]
Ammonia gas decomposes into nitrogen and hydrogen when passed over a platinum
gauze. The rate of decomposition is found to be independent of the partial pressure of

ammonia at very high pressures, but the rate was directly proportional to the partial
pressure of ammonia at low pressures.
(a)
Explain this observation as far as you can.
[2]
2NH3 N2 + 3H2
When the pressure is high enough, the catalyst surface would be saturated with adsorbed
ammonia molecules (By LCP, equilibrium shifts left at high pressure). Any decomposition
products that are desorbed from the surface would immediately be replaced by incoming
[Turn over
adsorbed ammonia. Hence, rate of decomposition is constant.

At low pressure, the catalyst surface is not saturated with adsorbed ammonia molecules.
Hence, rate of decomposition depends on the partial pressure of ammonia.
(b)
Given that 45% of ammonia dissociated into nitrogen and hydrogen at moderately high
temperatures, and a total pressure of 1 atm, calculate the value of Kp, stating its units.
[3]
2NH3 N2 + 3H2
I / mol
C/ mol
-0.9
E / mol
1.1
+0.45 +1.35
0.45
1.35
Total amount at eqm = 2.90

PNH3 = 1.1 / 2.9 = 0.3793 atm
PN2 = 0.1552 atm
PH2 = 0.4655 atm
Kp = (0.1552) (0.4655)3 / 0.37932 = 0.109 atm-2 (3s.f.) (with units stated)
(c)
Ammonia, nitrogen and hydrogen are non-ideal gases.
(i)
State two assumptions of the kinetic theory as applied to an ideal gas.
(ii)
Gas particles have negligible volume as compared to the volume of the whole gas.
Gas particles have negligible intermolecular forces of attraction.
Which of these three gases deviates the most from an ideal gas? Explain your answer.
Ammonia, due to formation of hydrogen bonding (strongest intermolecular force) between
its molecules. Thus, the intermolecular forces of attraction are significant.
(iii)
For a given fixed mass of an ideal gas, sketch graphs of:

I: P against V at constant T (where P represents pressure)
II: V against pV at constant T (where p represents density)
[5]
constant T
V
;;
pV
[Total: 10 marks]
The reaction between phenol and benzoyl chloride produces an ester with the formula
C6H5COOC6H5. Hydrogen chloride is also formed in this reaction.
Name of Compound
Chemical formula
Mr
Phenol
C6H5OH
94.0
Benzoyl chloride
C6H5COCl
140.5
C6H5COOC6H5
198.0
The crude (impure) ester produced in the reaction can be purified by recrystallisation in
ethanol. A typical yield, based on benzoyl chloride is 70%.
[Additional info:
Melting point of ester: 68- 70 C
Boiling point of ester: 298- 299 C]
(a)
State the name of the ester that is produced in the reaction.
[1]
Phenyl Benzoate
(b)
Explain why this reaction will not occur if benzoic acid was used instead of benzoyl
chloride.
[1]
Phenol is weakly acidic. In the presence of a stronger acid (benzoyl acid), phenol can act
as a base to react with benzoyl chloride to form esters.
(c)
In this experiment, only 70% of benzoyl chloride is converted into to the ester. Calculate
(i)
the minimum mass of benzoyl chloride needed to form 5 g of the ester.

Amount of ester = 5 / 198 = 0.02525 mol = amount of benzoyl chloride
Minimum mass of benzoyl chloride required = 100/70 x 0.02525 x 140.5 = 5.07 g (3s.f)
(ii)
Hence, calculate the minimum mass of phenol needed in the reaction.
[2]
Mass of phenol required = 100/70 x 0.02525 x 94.0 = 3.39 g (3s.f)
(d)
Briefly describe how the crude (impure) ester produced can be purified by recrystallisation
(i)
in ethanol.
[Turn over
Dissolve the crude ester in hot ethanol, until a saturated solution is obtained. ;
Filter and allow the hot solution to cool. Crystals will form upon cooling. Dry the crystals
using filter paper. ;
(ii)
Suggest and explain a method that can be used to check the purity of the ester produced.
[4]
Use of melting point to check purity of the ester.
If a pure ester is obtained, a sharp and distinct melting point will be obtained. If the ester is
impure, the ester will melt over a range of temperatures.
(e)
Another ester, P (Mr = 116) used in synthetic fruit flavors, is subjected to hydrolysis to give
a monoprotic acid, Q and an alcohol, R.
When 1.00 g of Q is titrated with 0.500 mol dm-3 NaOH, 33.0 cm3 of NaOH is required for
neutralization. R reacts with alkaline aqueous iodine to give a precipitate S. Compound R
exists as a pair of isomers, both of which are oxidized to give T which also reacts with
alkaline aqueous iodine to give the same precipitate S, and a solution U.
Identify the structures P, Q, R, S, T and U, explaining your deductions clearly.
Observations
Mol of acid = mol of NaOH = 0.0165
Deductions
Q is CH3CO2H
Mr of Q = 1 / 0.0165 = 60.6
Calculating Mr:
R is an alcohol with 4 carbon atoms.
116 +18.0 = R + 60.0.6

Mr of R = 73.4
R oxidizes to give T, and both react S is CHI3 (yellow ppt) and solution U
with alkaline aqueous iodine to give a contains a sodium salt with 3 carbon
yellow ppt S and a solution U.
atoms.
R contains a 2 alcohol and T
contains a ketone.
R exists as a pair of isomers
R contains a chiral center (optical

isomers)
P: CH3COOCH(CH3)CH2CH3
Q: CH3CO2H
[8]
R: CH3CH2CH(OH)CH3
S: CHI3
T: CH3CH2COCH3
U: CH3CH2COO-Na+
(1 mark for each unknown, a maximum of two marks for each pair of correct observations
and deductions)
[Total: 16 marks]
This question discusses metals in Group I and Group II of the Periodic table.
5
(a)
For a group I element, the ease with which the following reaction occurs is indicated by its
M(s) M+ (aq) + e-
electrode potential, E.
---------- Reaction (I)
Calculate the enthalpy change of reaction (I) for Li and Na, using values given below as
well as relevant data from the data booklet.
Element (M)
Hat (M) / kJ mol-1
Hhydration (M+) / kJ mol-1
Li
159
-957
Na
107
-841
[3]
M(s) M+ (aq) + eHat
Hhyd
Hhyd
M (g) M+ (g) + e-
st
1 IE
By Hess Law,
H = Hat + 1st IE Hhyd
For Li, H = 159 + 519 957 = -279 kJ mol-1
For Na, H = 107 + 494 841 = -240 kJ mol-1
(b)
;
;
Comment on the relationship between the enthalpy change of Reaction (I) obtained in (a)
and the E values given in the data booklet for Li and Na.
Li+ (aq) + e- Li (s)
[2]
E = -3.04 V
[Turn over
10
Na+ (aq) + e- Na (s)
E = -2.71 V
The E values mirror the calculated H values.
The more exothermic H value for Li calculated in (a) shows that the reaction is
energetically more favourable to form Li+. The more negative E value also indicates that Li
;
is readily oxidized to Li+.
(c)
The melting points of Group II oxides are given in the table below.
Oxide
Melting point / C
MgO
2852
CaO
2614
SrO
2430
BaO
1918
Explain the trend in the melting points.
[2]
The melting point of the oxides decrease down the group.
L.E.
q+ qr+ + r-
Down the group, cationic size increases, thus lattice energy decreases.
This results in decreasing electrostatic forces of attraction between the cation and O2-,
;
hence melting point decreases.
(d)
Describe the reactions, if any, for magnesium and calcium with cold water, writing
equations, with state symbols, for any reactions taking place.
[3]
Mg does not react with cold water.
Calcium reacts vigorously with cold water to give effervescence of hydrogen gas and a
white ppt of Ca(OH)2.
Ca (s) + H2O (aq) Ca(OH2) (s) + H2 (g)
;
[Total: 10 marks]
Synthetic detergents (anionic, cationic and non-ionic) consist of a hydrocarbon chain and
polar group. As a surfactant, the synthetic detergent is more effective than conventional
soap in hard water water that contains dissolved minerals such as Ca2+ and Mg2+.
Anionic detergents
11
Anionic detergents contain groups with a negative charge such as Na+SO3-. An example of
synthesis of a detergent sodium-n-dodecylbenzenesulfonate is as follows:
H2SO4
Reaction I
HO 3S
Na O 3 S
Cationic detergents
Cationic detergents contain positively charged groups and can be found in hair
conditioners. Keratin, a protein which contains negatively-charged groups which can be
found on the surface of hair, binds strongly to the hydrophilic ends of cationic detergents.
The hydrophobic ends of the surfactant molecules then act as the new hair surface. One
example
of
such
[CH3(CH2)15N(CH3)3]+
detergent
is
trimethylhexadecylammonium
chloride,
Cl .
Non-ionic detergents
Non-ionic detergents are commonly used in dish-washing liquids. An example is
pentaerythrityl palmitate:
H2C
O
CH3 (CH2)14 C
O CH2
OH
C CH2 OH
H2C OH
(a)
State possible reagents and conditions to synthesize [CH3(CH2)15N(CH3)3]+ from
(i)
CH3(CH2)15NH2.
(ii)
Name and draw the mechanism for the following synthesis.
[5]
HO 3S
[Turn over
12
Reagents: Add excess CH3Cl

Conditions: Heat
; (without stating excess, no marks)
Mechanism: Electrophilic substitution
1 mark for correct intermediate

1 mark for clearly shown arrows
1 mark for indicating that the electrophile is HSO3+
(students need not know how to generate the electrophile)
(b)
Suggest why non-ionic detergents are commonly used in dish-washing liquids.

They do not possess charges and thus do not react with hard water.
(c)
[1]
Describe a chemical test that can be used to distinguish between sodium-ndodecylbenzenesulfonate and pentaerythrityl palmitate.
You are to include all reagents, conditions and expected observations.
[2]
Reagent: PCl5
Conditions: room temperature
Observations: white fumes of HCl gas evolved for pentaerythrityl palmitate, absence of
white fumes for sodium-n-dodecylbenzenesulfonate
(d)
Apart from detergents or soap, cleaning products may also contain enzymes to degrade
protein-based stains. Enzymes are proteins with a specific biological activity that are
determined by their primary, secondary, tertiary and quaternary structures.
(i)
Apart from its function as an enzyme, state one other function of proteins.
Transport and storage OR structure and shape OR regulation and defense OR Receptors
(ii)
Briefly describe with a well-labeled diagram, one example of a secondary structure of a

protein.
Either a diagram of b-sheet or a-helix with a brief description.
a-helix:
Helix is stabilized by hydrogen bonds which are arranged such that the O of the C=O
group of the nth residue points along the helix axis towards the N of the N-H group of the (n
+ 4)th residue
Parallel b-sheet:
Formed when segments of polypeptide chains lie adjacent to one another. Hydrogen
bonds are formed between the C=O and N-H groups of adjacent chains, and are
perpendicular to the direction of the sheet. R groups of adjacent amino acid residues
points up or down of the sheet
[3]
13
(e)
The effectiveness of enzymes can be reduced by the addition of heavy metal ions such as
Hg+ or Pb2+.
(i)
Explain this phenomenon.

Heavy metal ions disrupt salt bridges (in R groups) that are held together by opposite
charges, thus causing the protein structure to unfold.

(ii)
Pb2+ typically forms complexes that are coloured. Explain why this is so.
[4]
Transition element complexes are coloured because of electron transition between d

orbitals
In a complex, the presence of ligands causes the 3d orbitals to split into 2 sets of different
energies. Radiation from the visible region of the electromagnetic spectrum is absorbed
when an electron moves from a d orbital of lower energy to another partially filled / unfilled
d orbital of higher energy.
Hence, transition element complexes are coloured.
The colour seen is the complement of the colours absorbed.
[Total: 15 marks]
END OF PAPER
[Turn over
;
;
Class
Adm No
Candidate Name:

Pre-university 3
H2 CHEMISTRY
9647/03
Paper 3
14 Sept 2012
2 hours
Writing Paper
Data Booklet
Graph Paper

1.
2.
Write your name, class and index number in the spaces provided at the top of this
page and on all the work you hand in.
3.
4.
5.
DO NOT use staples, paper clips, highlighters, glue or correction fluid or tape.
6.
7.

place in the case of Mr and Ar, unless a different level of accuracy is specified in the
question.
8.
question.
9.
You are reminded of the need for good English and clear presentation in your
answers and to show all working in calculations.
10.

[Turn over
Answer ANY FOUR questions

1
(a)
When studying Hydrocarbons, we recognised the environmental consequences of

carbon monoxide, oxides of nitrogen and unburnt hydrocarbons arising from the
internal combustion engine.
Because of these environmental concerns, alongside with high oil prices and oil
being a limited natural resource, development of cleaner alternative fuels and
advanced power systems for vehicles has become a high priority for many
governments and vehicle manufacturers around the world.
An alternative fuel vehicle is a vehicle that runs on a fuel other than "traditional"
petroleum fuels (petrol or diesel); and also refers to any technology of powering an
engine that does not involve solely petroleum (e.g. electric car, hybrid electric
vehicles, solar powered).
One such source of alternative fuel is the hydrogen / oxygen fuel cell, which is
increasingly used in space crafts.
Describe, providing details, the hydrogen / oxygen fuel cell.

Include the following in your answer:
Draw a well-labeled diagram for the cell.
Outline the reactions taking place at each electrode, assuming an alkaline

medium.
(b)
[6]
State one advantage of using this fuel cell.
Cyanogen is a highly toxic gas, composing of 46.2% carbon and 53.8% nitrogen by
mass. At 25 C and 1 atm, 1.05 g of cyanogen occupies 0.500 dm3.
(i)
Determine the molecular formula of cyanogen.
(ii)
Draw the dot-and-cross diagram for cyanogen. Hence, state its shape.
(iii)
Cyanogen is soluble in ethanol. Explain this statement with the aid of a suitable
diagram.
(c)
[7]
Sketch and explain the trend observed for the atomic and ionic radii of the elements
[4]
(from Na to Cl) in Period 3.

(d)
Phosphine, PH3, a gas at room temperature can be prepared by action of sodium

hydroxide on phosphonium iodide, PH4I. When 1.00 g of phosphonium iodide
reacted with solid sodium hydroxide, 0.925 g of white solid was formed, together
with steam and 150 cm3 of PH3 gas.
All measurements were taken at room temperature and pressure.
Identify the white solid and use the information given to write a balanced equation
[3]
with state symbols, for the preparation of PH3.

[Total: 20 marks]
-2-
(a)
Halogen derivatives can be used to synthesize alcohols.

The overall reaction is shown below:
CH3CH2Br + NaOH CH3CH2OH + NaBr
State the type of reaction mechanism for the above reaction and illustrate how the
reaction proceeds via the mechanism you stated.
(b)
[3]
Describe the reactions of chloride, bromide and iodide ions with the following
reagents:
I.
Aqueous silver nitrate, followed by aqueous ammonia
II. Concentrated sulfuric acid

You are required to write equations where appropriate and give explanations for the
[7]
differences in their reactions.
(c)
When a primary aromatic amine is treated with nitrous acid in a cool solution, the
product is unstable compound, known as a diazonium salt.
5 C
+ HNO2 + HCl
+ H2O
One reaction the diazonium cation undergoes is the substitution of halides.

diazonium salt
The reaction is shown below, where X represents the halogen.
C6H5N2+ + KX C6H5X + K+ + N2
diazonium ion
Compound P can be synthesised from benzoic acid in the reaction shown below.
Suggest a synthetic route for the conversion of benzoic acid to compound P.
In each case, identify all the intermediate compounds and state clearly the reagents
and conditions used for each transformation.
[*Note: In your proposed synthesis route, two of the stages of the synthesis
requires the formation of the diazonium ion and the substitution of the halide.]
[5]
(d)
Arrange the following halogen containing compounds according to increasing pKa

values. Explain your answer.
CH3CHClCOOH , CH3CCl2COOH , CH3CHBrCOOH
-3-
[3]
(e)
Explain the following physical property trends of transition metals across the Period.
I: relatively constant atomic radius
II: very high melting point
[2]
[Total: 20 marks]
-4-
(a)
An Ellingham diagram shows how the change in Gibbs free energy for a particular
reaction varies with temperature.
The following shows a sketch of an Ellingham diagram for three reactions:
I:
2C (s) + O2 (g) 2CO (g)
G = (-223 0.18T) kJ mol-1
II:
2Fe (s) + O2 (g) 2FeO (s)
G = (-525 + 0.13T) kJ mol-1
III:
(i)
Al (s) + O2 (g) Al2O3 (s)
G = (-1116 + 0.21T) kJ mol-1
Predict and explain what will happen to the value of G when the pressure of the system
in reaction I is reduced.
(ii)
Explain why the gradient for reaction I is negative (downward sloping), while the gradient
for reactions II and III are positive (upward sloping)?
(iii)
Calculate G of the following reaction at 1000K:

FeO (s)+ C (s) Fe (s) + CO (g)
(iv) Hence, what is the minimum temperature at which the reduction of iron (II) oxide by
carbon becomes thermodynamically feasible?
(v)
Aluminium oxide and carbon have high melting points. With reference to the Ellingham
diagram, explain why carbon is not used to line vessels that are used to contain molten
steel saturated with oxygen.
[The melting point of steel is 1800 K]
(b)
[14]
The manipulation and rearrangement of the Gibbs free energy equation shows a relation
between the change in Gibbs free energy and the standard electrode potential of a cell.
(i)
Define the term standard electrode potential of a cell.
(ii)
With the use of relevant data from the data booklet, state and illustrate how the relative
stabilities of the Fe (II) / Fe (III) oxidation states are affected by the following changes:
I. CN- ligands
[6]
II. pH
[Total: 20 marks]
-5-
(a)
Compound K is formed when phenylhydroxylamine, C6H5NHOH, is warmed with dilute

sulfuric acid. Compound K has the following properties:
K is not very soluble in water, but dissolves in HCl (aq)
K dissolves in NaOH (aq) but not in Na2CO3 (aq)
K reacts with 1 mol of ethanoyl chloride to give compound L, C8H9O2N, which is

not soluble in HCl (aq), but is soluble in NaOH (aq).
L reacts with Br2 (aq) to give compound M, C8H7O2NBr2.
K reacts with 2 mol of ethanoyl chloride to give compound N, C10H11O3N, which is

not soluble in HCl (aq) or NaOH (aq).
(i)
Suggest structures for compounds K, L, M and N.

Present your reasoning clearly by explaining the Chemistry involved.
(ii)
Write balanced chemical equations for each of the bullet points above to show how the
reactions proceeded.
(b)
[12]
A student was given 4 unlabelled bottles and each bottle contains one of the following
organic compounds with a different functional group:
2o Alcohol
Aldehyde
Ketone
1o Amide
Outline a sequence of simple chemical tests by which you could identify each of the
above organic substances.
[Note: you are not allowed to identify the substances by elimination. You must give a
positive test to prove the presence of each functional group present.]
[8]
[Total: 20 marks]
-6-
5 (a)
To study the rate of reaction between sodium and ethanol, a student added a freshly cut
piece of sodium (of known mass) to a large excess of ethanol and measured the total
volume of gas liberated every minute. The results obtained are given below:
Time / min
23.0
36.5
46.0
51.0
54.5
57.0
58.5
58.5
Total vol. of
gas produced /
cm3
(i)
Write an equation with state symbols for the above reaction.
(ii)
Give two reasons why sodium must be freshly cut?
(iii)
By plotting a suitable graph on graph paper, explain why the experimental results indicate
that the overall kinetics is first order.
(iv) Hence, suggest why the reaction appears to be zero order with respect to ethanol in this
experiment.
(v)
The student modified the experiment by changing the concentration of ethanol.

With the aid of a suitable equation, explain why water should not be used to dilute
ethanol.
[8]
(b)
A solution containing ethanoic acid and sodium ethanoate functions as a buffer.
(i)
Explain what is meant by the term buffer solution, and write suitable equations to show
how this solution functions as a buffer.
(ii)
Calculate the pH of the resulting solution when 25 cm3 of 0.10 mol dm3 of ethanoic acid
was added to 10 cm3 of 0.20 mol dm3 of NaOH.
[Ka of ethanoic acid = 1.8 x 10-5 mol dm-3]
[7]
(c)
A solution X is saturated with the soluble salts, NaNO3 and Mg(NO3)2.
(i)
When solution X is heated strongly, the salts start to decompose. State which salt will
begin to decomposes first, and the expected observations you will see to indicate that
decomposition has taken place. Explain your answer.
(ii)
A student conducted an experiment to dissolve magnesium carbonate in solution X.

She noted down her observations as follows: The solubility product of magnesium
carbonate decreased in solution X. Only a small amount of magnesium carbonate
dissolved.
Discuss in detail the validity of this statement, making corrections to the observations
where necessary.
[5]
[Total: 20 marks]
END OF PAPER
-7-
Class
Adm No
Candidate Name:

Pre-university 3
H2 CHEMISTRY
9647/03
Paper 3
14 Sept 2012
2 hours
Writing Paper
Data Booklet
Graph Paper

1.
2.
Write your name, class and index number in the spaces provided at the top of this
page and on all the work you hand in.
3.
4.
5.
DO NOT use staples, paper clips, highlighters, glue or correction fluid or tape.
6.
7.

place in the case of Mr and Ar, unless a different level of accuracy is specified in the
question.
8.
question.
9.
answers and to show all working in calculations.
10.

[Turn over
Answer ANY FOUR questions

1
(a)
When studying Hydrocarbons, we recognised the environmental consequences of

carbon monoxide, oxides of nitrogen and unburnt hydrocarbons arising from the
internal combustion engine.
Because of these environmental concerns, alongside with high oil prices and oil
being a limited natural resource, development of cleaner alternative fuels and
advanced power systems for vehicles has become a high priority for many
governments and vehicle manufacturers around the world.
An alternative fuel vehicle is a vehicle that runs on a fuel other than "traditional"
petroleum fuels (petrol or diesel); and also refers to any technology of powering an
engine that does not involve solely petroleum (e.g. electric car, hybrid electric
vehicles, solar powered).
One such source of alternative fuel is the hydrogen / oxygen fuel cell, which is
increasingly used in space crafts.
Describe, providing details, the hydrogen / oxygen fuel cell.

Include the following in your answer:
Draw a well-labeled diagram for the cell.
Outline the reactions taking place at each electrode, assuming an alkaline

medium.
State one advantage of using this fuel cell.
(1 mark for correct electrolyte, 1 mark for labelled anode, 1 mark for labelled
[6]
;;;
cathode)
In alkaline electrolyte
Reaction at anode:
Reaction at cathode:
Overall cell reaction:
H2(g) + 2OH(aq) 2H2O(l) + 2e

O2(g) + H2O(l) + 2e 2OH(aq)
H2(g) + O2(g) H2O(l)
-2-
;
;
Advantage:
Clean products are produced. OR
Water produced in hydrogen-oxygen fuel cell used in spacecraft can be used for
drinking and washing.
(b)
Cyanogen is a highly toxic gas, composing of 46.2% carbon and 53.8% nitrogen by
mass. At 25 C and 1 atm, 1.05 g of cyanogen occupies 0.500 dm3.
(i)
Determine the molecular formula of cyanogen.
% mass
46.2
53.8
Mole ratio
3.85
3.84
Simple ratio
1
;
Empirical formula of cyanogen is CN.
Using PV = nRT
1.01 x 105 x 0.5 x 10-3 = (1.05 / Mr) x 8.31 x 298
(ii)
Mr = 51.5 (1 d.p)
Thus, molecular formula of Cyanogen = C2N2
Draw the dot-and-cross diagram for cyanogen. Hence, state its shape.
NC-CN , linear
(iii)
;;
Cyanogen is soluble in ethanol. Explain this statement with the aid of a suitable
diagram.
[7]
Cyanogen can form hydrogen bonds with ethanol as it has a lone pair of electrons
on nitrogen, thus soluble in ethanol.
;
(lone pairs on N and O, +, - must all be clearly shown)
(c)
Sketch and explain the trend observed for the atomic and ionic radii of the elements
[4]
(from Na to Cl) in Period 3.
-3-
Atomic Radius:
Across the period,
nuclear charge as proton number
change in the screening effect is negligible (Same no. of inner shells of e-s across
the period). Thus the outer e-s are more strongly attracted by the nucleus
\ atomic radii
Cations (Na+ to Si4+)
cations have one shell less than neutral atoms. Thus, the outer e-s are more
strongly attracted by the nucleus therefore having a smaller radius than its parent
atoms.
Anions (P3- to Cl-)
anions have more e-s than protons and so, the effective attractive force on the
outer e-s is less than that in neutral atoms.
the outer e-s are less strongly attracted by the nucleus, thus having a radius that
is larger than its parent atoms.
(d)
Phosphine, PH3, a gas at room temperature can be prepared by action of sodium

hydroxide on phosphonium iodide, PH4I. When 1.00 g of phosphonium iodide
reacted with solid sodium hydroxide, 0.925 g of white solid was formed, together
with steam and 150 cm3 of PH3 gas.
All measurements were taken at room temperature and pressure.
Identify the white solid and use the information given to write a balanced equation
[3]
with state symbols, for the preparation of PH3.

The white solid is NaI.
Molar mass of PH4I = 162.0

Amount of PH4I = 1 / 162 = 0.00617 mol
Amount of Na I = 0.925 / (23.0 + 127.0) = 0.00617 mol
Amount of PH3 = 150 / 24000 = 0.00625 mol
Mole ratio of PH4 I : PH3 : Na I 1 : 1 : 1
Thus,
PH4 I (s) + NaOH (s) Na I (s) + PH3 (g) + H2O (g)
;
(state symbols must be correct to earn this mark)
[Total: 20 marks]
-4-
(a)
Halogen derivatives can be used to synthesize alcohols.

The overall reaction is shown below:
CH3CH2Br + NaOH CH3CH2OH + NaBr
State the type of reaction mechanism for the above reaction and illustrate how the
reaction proceeds via the mechanism you stated.
[3]
Nucleophilic Substitution, SN2

-
OH
d+
H C
H3C
d-
Br
slow
w
H
d-
HO
d+
d-
Br
HO
CH3
H + Br
CH3
1 mark for name of mechanism SN2

1 mark for clearly shown arrow pushing
1 mark for correct intermediate and the final product must have the structure of an
inverted umbrella
(b)
Describe the reactions of chloride, bromide and iodide ions with the following
reagents:
I.
Aqueous silver nitrate, followed by aqueous ammonia
II.
Concentrated sulfuric acid
You are required to write equations where appropriate and give explanations for the
[7]
differences in their reactions.
Ppt
Colour
Reaction with NH3 (aq)

AgCl(s) + 2NH3 (aq) [Ag (NH3)2]+ (aq) +Cl- (aq)
diamine silver (I) ion
AgCl
White
;
White precipitate readily dissolves in NH3 (aq) to give a
colourless solution, diamine silver (I) ion.
AgBr (s) + 2NH3 (aq) [Ag (NH3)2]+ (aq) + Br- (aq)
diamine silver (I) ion
Pale
AgBr
yellow/
Cream
Cream precipitate ONLY dissolves in Conc. NH3

solution.
AgI
Deep
Precipitate insoluble in NH3 (aq)
yellow
-5-
NaCl + H2SO4 HCl + NaHSO4
NaBr + H2SO4 HBr + NaHSO4

2HBr + H2SO4 Br2 + SO2 + 2H2O
NaI + H2SO4 HI + NaHSO4

6HI + H2SO4 3I2 + S + 4H2O OR
;
8HI + H2SO4 4I2 + H2S + 4H2O

The ease of oxidation of halide ions, X- X2, increases from Cl- to I- (as the
reducing power of the halides increases from Cl- to I-). Hence, I- is readily oxidised
by conc. sulphuric acid to I2, Br- is oxidised to Br2 to a lesser extent and Cl- is not
oxidised at all.
(Students can also quote E values to substantiate their answers)
(c)
When a primary aromatic amine is treated with nitrous acid in a cool solution, the
product is unstable compound, known as a diazonium salt.
+
N2 Cl
NH2
+ HNO2 + HCl
5 C
+ H2O
diazonium salt
One reaction the diazonium cation undergoes is the substitution of halides.
The reaction is shown below, where X represents the halogen.
C6H5N2+ + KX C6H5X + K+ + N2
diazonium ion
Compound P can be synthesised from benzoic acid in the reaction shown below.
Suggest a synthetic route for the conversion of benzoic acid to compound P.
In each case, identify all the intermediate compounds and state clearly the reagents
and conditions used for each transformation.
[*Note: In your proposed synthesis route, two of the stages of the synthesis
requires the formation of the diazonium ion and the substitution of the halide.]
[5]
-6-
CO2H
CO2H
conc. HNO3
conc. H2SO4
heat under
reflux
NO2
NO2
CO2H
CO2H
Sn,
conc. HCl
heat under
reflux
CO2H
NaNO2
dilute HCl
Cl
NH2
5C
NH2
KClCuBr
/ KBr (aq)
ClN2+
N2+
Cl
Br
(1 mark for every underlined answer)
(d)
Arrange the following halogen containing compounds according to increasing pKa

values. Explain your answer.
CH3CHClCOOH , CH3CCl2COOH , CH3CHBrCOOH
[3]
Increasing pKa value: CH3CCl2COOH , CH3CHClCOOH , CH3CHBrCOOH
CH3CCl2COOH has the smallest pKa (thus most acidic) as there is the presence of
two electron withdrawing Cl atoms. This, the negative charge on the O atom in
(CH3CCl2COO-) is more dispersed than in (CH3CHClCOO-). Thus the CH3CCl2COO;
anion is more stable, and the acid is more willing to donate a proton, increasing the
acidity of the solution.
CH3CHBrCOOH has the largest pKa value (least acidic) as Br is less electronegative
than Cl. Thus, the electron withdrawing ability of Br is less than Cl. Thus the
CH3CHBrCOO- anion is less stable, and the acid is less willing to donate a proton,
decreasing the acidity of the solution.

(no marks for correct arrangement without explanation)
(e)
Explain the following physical property trends of transition metals across the Period.
I: relatively constant atomic radius
[2]
II: very high melting point

Electrons are being added to inner 3d subshell.
Screening effect of 3d electrons effectively cancels almost all increase in nuclear
charge across series.
Hence, there is a relatively small difference in the effective nuclear charge and
atomic radius remains relatively constant.
;
Strong metallic bonding in transition elements due to availability of both the 4s
and 3d electrons for delocalisation, thus melting point increases.
[Total: 20 marks]
-7-
(a)
An Ellingham diagram shows how the change in Gibbs free energy for a particular
reaction varies with temperature.
The following shows a sketch of an Ellingham diagram for three reactions:
I:
2C (s) + O2 (g) 2CO (g)
G = (-223 0.18T) kJ mol-1
II:
2Fe (s) + O2 (g) 2FeO (s)
G = (-525 + 0.13T) kJ mol-1
III:
(i)
4
3
Al (s) + O2 (g) Al2O3 (s)

3
G = (-1116 + 0.21T) kJ mol-1
Predict and explain what will happen to the value of G when the pressure of the system
in reaction I is reduced.
When pressure in reaction I is reduced, By LCP the system will counteract by increasing
pressure, thus equilibrium will shift to the right where more amount of gas will be
produced. Thus, S > 0.
Since G = H -TS, and S > 0,

G then becomes more negative, as pressure is reduced.
(ii)
Explain why the gradient for reaction I is negative (downward sloping), while the gradient
for reactions II and III are positive (upward sloping)?
The gradient of the graph represents -S.
In reaction I, there is an increase in the disorderliness as number of moles of gaseous

increased from 1 to 2 moles. Thus, S > 0 and the overall gradient is negative.
In reactions II and III, there is an increase in the orderliness of the system as number of
moles of gases decreased from 1 to 0 moles. Thus, S<0, and the overall gradient is
;
positive.
(iii)
Calculate G of the following reaction at 1000K:

FeO (s)+ C (s) Fe (s) + CO (g)
-8-
;;
;
;
(iv) Hence, what is the minimum temperature at which the reduction of iron (II) oxide by
carbon becomes thermodynamically feasible?
For the minimum temperature in which the extraction can occur, this happens at
the intersection point.
G = -223 0.18T = -525 + 0.31T

;
Solving, T = 974 K
(v)
Aluminium oxide and carbon have high melting points. With reference to the Ellingham
diagram, explain why carbon is not used to line vessels that are used to contain molten
steel saturated with oxygen.
[14]
[The melting point of steel is 1800 K]

From the Ellingham diagram, at T=1800K, reaction I is still thermodynamically feasible.
G = -223 0.18 (1800) = -547 kJ mol-1
Thus oxygen can react with carbon to form CO since G < 0 and reaction is spontaneous.
Thus carbon is not used as a lining material at such a high temperature in the presence of
;
oxygen gas.
(b)
The manipulation and rearrangement of the Gibbs free energy equation shows a relation
between the change in Gibbs free energy and the standard electrode potential of a cell.
(i)
Define the term standard electrode potential of a cell.

Standard electrode potential, E of a cell is the relative potential of this cell under
standard conditions compared with the standard hydrogen electrode whose electrode
potential is assigned as zero.
(ii)
With the use of relevant data from the data booklet, state and illustrate how the relative
stabilities of the Fe (II) / Fe (III) oxidation states are affected by the following changes:
I. CN- ligands
[6]
II. pH
Fe3+ is stabilised with respect to Fe2+ when complexed with CN-, resulting in a less
positive reduction potential.
-9-
Fe3+ is stabilised with respect to Fe2+ by an alkaline medium, resulting in a less positive
;
reduction potential.
[Total: 20 marks]
- 10 -
(a)
Compound K is formed when phenylhydroxylamine, C6H5NHOH, is warmed with dilute

sulfuric acid. Compound K has the following properties:
K is not very soluble in water, but dissolves in HCl (aq)
K dissolves in NaOH (aq) but not in Na2CO3 (aq)
K reacts with 1 mol of ethanoyl chloride to give compound L, C8H9O2N, which is not
soluble in HCl (aq), but is soluble in NaOH (aq).
L reacts with Br2 (aq) to give compound M, C8H7O2NBr2.
K reacts with 2 mol of ethanoyl chloride to give compound N, C10H11O3N, which is not
soluble in HCl (aq) or NaOH (aq).
(i)
Suggest structures for compounds K, L, M and N.

Present your reasoning clearly by explaining the Chemistry involved.
(ii)
Write balanced chemical equations for each of the bullet points above to show how the
reactions proceeded.
OH
[12]
OH
Br
K:
NH2
L:
NHCOCH3
NHCOCH3
NHCOCH3
M:
Br
OH
Observations
N:
OCOCH3
Deductions
K is not very soluble in water,
K contains a hydrophobic group.
but dissolves in HCl (aq)
K contains a basic group.
K dissolves in NaOH (aq) but
K contains an acidic group that is not a
not in Na2CO3 (aq)
carboxylic group. Hence, K contains a

phenol group.
K reacts with 1 mol of ethanoyl
L is acidic (contains the phenol group
chloride to give compound L,
from K) and also contains an amide.
C8H9O2N, which is not soluble

in HCl (aq), but is soluble in
NaOH (aq).
L reacts with Br2 (aq) to give
Electrophilic substitution occurs readily
compound M, C8H7O2NBr2.
as the benzene ring is activated by the

phenol group.
K reacts with 2 mol of ethanoyl
N is neutral and N contains both ester
chloride to give compound N,
and amide functional groups.
C10H11O3N, which is not soluble

in HCl (aq) or NaOH (aq).
- 11 -
Balanced Equations:
OH
OH
+ HCl
NH2
NH3 Cl
OH
O Na
+ NaOH
+ H2O
NH2
NH2
OH
OH
+ HCl
+ CH3COCl
NHCOCH3
NH2
OH
NHCOCH3
+ 2Br2
+ 2HBr
Br
NHCOCH3
Br
OH
NHCOCH3
OH
+ 2 CH3COCl
+ 2 HCl
OCOCH3
NH2
1mark for each unknown structure

3 marks (max) for explaining the deductions
1 mark for each equation for each bullet point.
- 12 -
(b)
A student was given 4 unlabelled bottles and each bottle contains one of the following
organic compounds with a different functional group:
2o Alcohol
Aldehyde
Ketone
1o Amide
Outline a sequence of simple chemical tests by which you could identify each of the above
organic substances.
[Note: you are not allowed to identify the substances by elimination. You must give a positive
test to prove the presence of each functional group present.]
[8]
1. Test for aldehyde

;
Add tollens reagent to 4 test tubes each of the unknown, warm.
;
Silver mirror will be formed in the test tube containing the aldehyde only.
2. Test for ketone
;
Add bradys reagent to new samples of the remaining 3 unknowns, warm.
Orange ppt observed in the test tube containing the ketone only.
3. Test for 2 alcohol.
Add KrCr2O7 / H2SO4 to the remaining two unknowns. Heat under reflux.
Orange solution of Cr2O72- decolorize for test tube containing the 2 alcohol only.
(KMnO4 accepted, iodoform test not accepted)

4. Test for 1o amide
;
Add NaOH (aq) to a new sample of the remaining test tube. Warm.
;
Effervescence, colourless, pungent gas evolved that turned moist red litmus blue.
[Total: 20 marks]
- 13 -
5 (a)
To study the rate of reaction between sodium and ethanol, a student added a freshly cut
piece of sodium (of known mass) to a large excess of ethanol and measured the total
volume of gas liberated every minute. The results obtained are given below:
Time / min
Total vol. of
23.0
36.5
46.0
51.0
54.5
57.0
58.5
58.5
gas produced /
cm3
(i)
Write an equation with state symbols for the above reaction.

Na (s) + C2H5OH (l) C2H5O-Na+ (aq) + H2 (g)
(ii)
Give two reasons why sodium must be freshly cut?

Na must be freshly cut because it rapidly oxidised by O2 in air to form a layer of oxide (Na2O)
on its surface.
Na also reacts with the water vapour present in air.

(iii)
By plotting a suitable graph on graph paper, explain why the experimental results indicate
that the overall kinetics is first order.
1 mark for correct axis chosen (graph of total volume of gas produced against time)
1 mark for collect plotting
1 mark for indicating on graph that half-life of the reaction is first order (must state the value
of half-life to be 1.5min)
(half-life measured from 0 - 29.3 cm3, and from 29.3 - 43.9 cm3 of H2)
70
60
50
40
30
20
10
0
1.5 2
10
(iv) Hence, suggest why the reaction appears to be zero order with respect to ethanol in this
experiment.
Since ethanol is present in large excess, the concentration of ethanol does not change. Thus
rate is independent on concentration of ethanol / reaction is zero order with respect to
ethanol.
(v)
The student modified the experiment by changing the concentration of ethanol.

With the aid of a suitable equation, explain why water should not be used to dilute ethanol.
[8]
Na (s) + H2O (l) NaOH (aq) + H2 (g)
- 14 -
(b)
A solution containing ethanoic acid and sodium ethanoate functions as a buffer.
(i)
Explain what is meant by the term buffer solution, and write suitable equations to show how
this solution functions as a buffer.
A buffer solution is a solution whose pH remains relatively unchanged when a small amount
of acid or alkali is added to it.

When a small amount of base is added,
CH3COOH + OH- CH3COO- + H2O
When a small amount of acid is added,

CH3COO- + H+ CH3COOH
(ii)
Calculate the pH of the resulting solution when 25 cm3 of 0.10 mol dm3 of ethanoic acid was
added to 10 cm3 of 0.20 mol dm3 of NaOH.
[Ka of ethanoic acid = 1.8 x 10-5 mol dm-3]
[7]
Amount of ethanoic acid = 0.00250 mol

Amount of NaOH = 0.00200 mol
The limiting reagent is NaOH.
Amount of CH3COO- formed = 0.00200 mol

[CH3COO-]eqm = 0.002 / 0.035 = 0.05714 mol
[CH3COOH]eqm = (0.0025-0.002) / 0.035 = 0.01428

pH = pKa + lg(0.05714)/(0.01428)
= -lg (1.8x10-5) + lg(0.05714)/(0.01428)
= 5.35 (3s.f)
(c)
A solution X is saturated with the soluble salts, NaNO3 and Mg(NO3)2.
(i)
When solution X is heated strongly, the salts start to decompose. State which salt will begin
to decomposes first, and the expected observations you will see to indicate that
decomposition has taken place. Explain your answer.
Mg(NO3)2 will decompose first.
Mg2+ has a higher charge density as compared to Na+ due to its higher charge and smaller
ionic radius. Thus, its polarising power increases.
Mg2+ will polarise the electron cloud of NO3-, distorting the N-O bonds, releasing O2 and N2.
Brown fumes of N2 will be observed to indicate that the reaction has occurred.
;
(ii)
A student conducted an experiment to dissolve magnesium carbonate in solution X.

She noted down her observations as follows: The solubility product of magnesium
carbonate decreased in solution X. Only a small amount of magnesium carbonate dissolved.
Discuss in detail the validity of this statement, making corrections to the observations where
necessary.
[5]
- 15 -
The statement recorded by the student is wrong.

The solubility product of magnesium carbonate does not decrease in Solution X. The
solubility product remains the same in solution X, as solubility product is only affected by
changes in temperature.
However, in solution X, due to the presence of the common ion, Mg2+, the solubility of
magnesium carbonate decreases.
[Total: 20 marks]
END OF PAPER
- 16 -
Calculator Model / No.
Name ________________________
Class: ___________
Reg Number: _____
MERIDIAN JUNIOR COLLEGE

JC2 Preliminary Examination
Higher 2
_________________________________________________________________________
Chemistry
9647/1
20 September 2012
1 hour
Additional Materials: OMR Sheet

Data Booklet
___________________________________________________________________
Write your name, class and register number in the spaces provided at the top of this page.
Write your calculator brand and model/number in the box provided above.
There are forty questions in this section. Answer all questions. For each question, there are
four possible answers labelled A, B, C and D. Choose the one you consider correct and
record your choice in soft pencil on the OMR answer sheet.
Read very carefully the instructions on the use of the OMR answer sheet.
You are advised to fill in the OMR Answer Sheet as you go along; no additional time will be
given for the transfer of answers once the examination has ended
Use of OMR Answer Sheet

Ensure you have written your name, class register number and class on the OMR Answer
Sheet.
Use a 2B pencil to shade your answers on the OMR sheet; erase any mistakes cleanly.
Multiple shaded answers to a question will not be accepted.
For shading of class register number on the OMR sheet, please follow the given examples:
If your register number is 1, then shade 01 in the index number column.
If your register number is 21, then shade 21 in the index number column.
Section A
For each question there are for possible answers, A, B, C and D. Choose the one you
Which of the following statements contains one mole of the stated particle?
A
Molecules in 19.0 g of fluorine gas.
Electrons in 24.0 dm3 of hydrogen gas at room temperature and pressure.
Neutrons in 1.00 g of helium gas.
Protons in 2.02 g of neon gas.
Which of the following diagrams correctly describes the behaviour of a fixed

mass of an ideal gas at constant T?
pV
T
p
pV
pV
T
pV
Two elements X and Y have the following properties.
X and Y form ionic compounds Na2X and Na2Y respectively.

Element Y forms YF6 molecule whereas X is unable to do so.
Which pair of electronic configurations of X and Y is correct?
[He]2s22p2
[Ne]3s23p2
[He]2s22p2
[Ne]3s23p4
[He]2s22p4
[Ne]3s23p2
[He]2s22p4
[Ne]3s23p4
Ions of the two most common isotopes of zinc are shown below:
64
30
Zn2+
66
30
Zn2+

A
Both these Zn2+ ions have the same number of electrons but different
number of protons.
Both these Zn2+ ions

1s22s22p63s23p63d84s2.
The
64
30
Zn2+ ion has fewer neutrons in its nucleus than the
The
66
30
Zn2+ ion will be deflected more than the
have
the
same
64
30
electron
66
30
configuration
Zn2+ ion.
Zn2+ ion in an electric field
of the same strength.
For the pairs of species shown below, in which does the first species have a
larger bond angle than the second?
A
PH3, NH3
SO32-, CO32-
CH2Cl2, OCl2
BrF2-, BeCl2
In an experiment, a radioactive sample of the sodium thiosulfate, Na2S2O3 was

prepared by boiling solid sulfur containing 35S with sodium sulfite, Na232SO3.
Adding HCl (aq) to this sample causes all the 35S to precipitate as sulphur,
leaving a resulting solution that contains non-radioactive sulfite ions.
Which of the following depicts the correct displayed formula of the thiosulfate ion
produced?
2-
O
A
32
32
2-
2-
O
D
32
32
O
O 35
S
35
O
O 35
S
2-
35
An experiment is conducted to investigate the kinetics of reaction between

bromopropane and 0.1 mol dm-3 sodium hydroxide.
The rate equation is as follows:
Rate = k [bromopropane] [OH-]
The half-life of bromopropane in one of the experiments is t minutes.
What is the new half-life (in minutes) of bromopropane when the concentration of
bromopropane is doubled and concentration of sodium hydroxide is reduced to
0.01 mol dm-3?
A
0.05t
0.1t
5t
10t
4
Consider the following equilibrium system:

H2 (g) + I2 (g)
2HI (g)
DH = +53 kJ mol-1
Which of the following change is incorrect?
Numerical value of Kp is not equal to Kc at 25 C.
Increasing the mass of H2 will not cause the equilibrium constant to

increase.
Increasing temperature increases the rate constant and equilibrium

constant.
Rate of forward reaction is equal to rate of backward reaction when

equilibrium is reached.
The graph shows the change in pH when 0.25 mol dm-3 acid is gradually added
to V cm3 of 0.25 mol dm-3 base.
pH
14
Volume of acid
added /cm3
Which pair of solutions will give the result as shown in the graph?
A
HNO3 and NH3
H2SO4 and CH3NH2
CH3COOH and Ca(OH)2
CH2(COOH)2 and NaOH

5
10
The solubility product of iron(II) carbonate is 2.1 1011 while that of silver
carbonate is 8.1 1012 at 25C.
11
Addition of silver nitrate increases the solubility of silver carbonate.
Addition of sulfuric acid to a solution containing iron(II) carbonate

increases the solubility product of iron(II) carbonate.
Iron(II) carbonate precipitates first when sodium carbonate is added to a

solution containing equal concentrations of iron(II) and silver ions.
The solubility of iron(II) carbonate is higher than the solubility of silver

carbonate.
Liquid E has an DHq of vapourisation of +10.0 kJ mol-1 and a boiling point of

266 K.
What is the DSq of condensation of vapour E?
12
26.6 J mol-1 K-1
37.6 J mol-1 K-1
+26.6 J mol-1 K-1
+37.6 J mol-1 K-1
Which of the following has an exothermic enthalpy change?

Ca2+ (g) + 2e
Ca (g)
CaO (s) Ca2+ (g) + O2- (g)
O2 (g)
O (g) + e O- (g)
O (g)
13
When a solution of concentrated sodium carboxylate is electrolysed, the equation

for the reaction is
2RCO2Na (aq) + 2H2O (l)
RR (l) + 2CO2 (g) + 2NaOH (aq) + H2 (g)
Which statement regarding the electrolysis is correct?
14
Carbon dioxide is liberated at the cathode.
Hydrogen is liberated at the cathode.
RR is liberated at the cathode.
The solution around the anode turns red litmus blue.
When a large current was passed through acidified aqueous copper(II) sulfate,
there was simultaneous liberation, at the cathode, of x mol of copper and y dm3
of hydrogen (measured at s.t.p.).
How many moles of electrons passed through the solution?
A
B
15
y
11.2
y
x+
22.4
x+
y
11.2
y
2x +
22.4
2x +
C
D
Two cells, one containing a molten chloride of manganese and the other
containing molten chromium(II) chloride were connected in series. 11.0 g of
manganese and 15.6 g of chromium were deposited.
What is the oxidation state of manganese ion in the chloride?
A
+2
+3
+4
+5
16
Element G is in the third period of the Periodic Table. The chloride of G has a
simple molecular structure while the oxide of G has a giant ionic structure.
Which of the following statements is true about G?
17
The atomic radius of G is smaller than that of Cl.
The first ionisation energy of G is higher than that of Mg.
The chloride of G dissolves in water to give a neutral solution.
The oxide of G reacts with excess aqueous sodium hydroxide to form a

colourless complex.
J, K and L are elements in Period 3. K has a larger ionic radius than J, and L
has a less endothermic first ionisation energy than K.
What are elements J, K and L?
18
Cl
Al
Mg
Al
Mg
Si
Al
Beryllium is a Group II metal and has the smallest ionic radius among the
Group II metals.
Which of the following statements is incorrect?
A
Beryllium chloride has the highest melting point among the Group II
chlorides.
Beryllium ions have the highest charge density amongst the Group II
metals ions.
Beryllium has the highest melting point among the Group II metals.
Beryllium has the highest electronegativity among the Group II metals.

8
19
20
21
Which of the following statements is most likely to be true for astatine, the
element below iodine in Group VII of the Periodic Table?
A
Astatine reacts with aqueous iron(II) ions to give iron(III) ions.
Astatine reacts with aqueous sodium bromide to given aqueous sodium

astatide and bromine.
Hydrogen iodide is more acidic than hydrogen astatide.
Silver astatide has a lower Ksp value than silver iodide.
Which process is not involved in the catalytic hydrogenation of ethene?

A
Absorption
Activation
Desorption
Diffusion
How many stereoisomers does this organic molecule have?

CH3
CH3
COOH
HO
CH3
16
32
64
22
2-methylpropane can react with bromine in the presence of sunlight to give two
monosubstituted halogenoalkanes, 1-bromo-2-methylpropane and 2-bromo-2methylpropane.
Given the relative rates of abstracting H atoms are:
Type of H atom
primary
secondary
tertiary
Relative rate of abstraction
What is the expected ratio of 1-bromo-2-methylpropane to 2-bromo-2methylpropane formed?
23
9 : 1
6 : 1
3 : 2
1 : 1
Why does hydrogen cyanide undergo addition reaction with propanone but not
with propene?
A
Propanone is more susceptible to CN- attack than propene.
Propene is less susceptible to H+ attack than propanone.
The addition product formed with propene would not be stable.
The two methyl groups in propanone exert a stronger electron-donating

effect than the single methyl group in propene.
10
24
The following compound was heated with ethanolic sodium hydroxide.

CH3
CH3
HO
Cl
Cl
Which of the following represents the structure of the organic product?

CH3
H2C
CH3
CH3
HO
OH
Cl
Cl
OH
CH3
H3C
CH3
CH3
HO
D
Cl
Cl
11
25
Esters can be converted to alcohols using lithium aluminium hydride followed by

the addition of water.
O
O
C
C2H5
O
C
H
C2H5
H
O
OH
H
H2O
+ HO
H
+
C2H5
C2H5
Which of the following reaction does not occur in this process?
26
Hydrolysis
Hydrogenation
When organic compounds P, Q, R and S are added separately to water,

solutions of increasing pH values are obtained. The possible identities of the
compounds P to S (not necessarily in that order) are given.
CH3CH2COOH
CH3CH2COCl
(CH3)2CHNH2
H2NCH2CH2COOH
Which is the correct set of identities of compounds P to S?

P
CH3CH2COCl
CH3CH2COOH
H2NCH2CH2COOH
(CH3)2CHNH2
CH3CH2COCl
CH3CH2COOH
(CH3)2CHNH2
H2NCH2CH2COOH
CH3CH2COOH
CH3CH2COCl
H2NCH2CH2COOH
(CH3)2CHNH2
CH3CH2COOH
CH3CH2COCl
(CH3)2CHNH2
H2NCH2CH2COOH
12
27
One of the chemicals giving blue cheese its unique aroma is heptan-2-one.
The diagram shows reactions involving heptan-2-one.
Cr2O72- / H+
Cr2O72- / H+
reflux apparatus
distillation apparatus
T
U
Which is the correct identification of compound T, reagent U and compound V?
28
compound T
reagent U
compound V
heptane
NaBH4
heptanoic acid
heptan-2-ol
NaBH4
heptanoic acid
heptanal
hydrogen gas
heptan-2-one
heptan-2-ol
LiAlH4 in dry ether
heptan-2-one
The compound C4H6O2 gives butter its distinctive flavour.

It reacts with hydrogen cyanide to form C6H8N2O2 but does not form a silver
mirror with ammoniacal silver nitrate.
What is the structural formula of this compound in butter?
A
CH3COCH2CHO
CH3COCOCH3
CH3COCH=CHOH
CH2=CHCOCH2OH
13
29
The two-stage reaction sequence given shows a possible mechanism for the
reaction between hydroxide and ethanoyl chloride.
CH3
CH3
HO
HO
CH3
O
Cl
Cl
HO
Cl
In what way should the overall reaction be classified?
30
After the reduction of nitrobenzene to phenylamine, using tin and concentrated

hydrochloric acid, an excess of sodium hydroxide is added.
What is the purpose of the sodium hydroxide?
A
to dry the product
to liberate phenylamine
to lower the boiling point for subsequent distillation
to precipitate tin(II) hydroxide
14
Section B
For each of the questions in this section, one or more of the three numbered statements
1 to 3 may be correct.
Decide whether each of the statements is or is not correct (you may find it helpful to put
a tick against the statements which you consider to be correct).
A
1, 2 and 3 are
correct
B
1 and 2 only are
correct
C
2 and 3 only are
correct
D
1 only is correct
31
32
In which sequences are the molecules quoted in order of decreasing boiling

points?
1
CH3(CH2)3CH3, (CH3)2CHCH2CH3, CH3C(CH3)2CH3
AlBr3, AlCl3, AlF3
SO2, SiO2, CO2
Beryllium difluoride reacts readily with trimethylamine, (CH3)3N to form a stable

addition product. Nitrogen trifluoride has no reaction with trimethylamine.
1
Nitrogen trifluoride does not react as the nitrogen atom lacks energetically
accessible orbitals for reaction.
The bond angle in the addition product is 109.5o.
The molar ratio for the reaction between beryllium difluoride and (CH3)3N is
1:1.
15

A
1, 2 and 3 are
correct
B
1 and 2 only are
correct
C
2 and 3 only are
correct
D
1 only is correct

33
The graph for the equilibrium,

W (g) + X (g)
3Y (g)
H < 0
is given below:
% yield
of Y
Graph 1
Graph 2
Progress of reaction
Which of the following changes could account for the change from Graph 1 to
Graph 2?
34
Addition of catalyst
Increase in temperature
Increase in pressure
A cell consisting of a V2+ (aq), V3+ (aq) | Pt (s) half-cell and a Au3+ (aq) | Au (s)
half-cell is shown below using conventional notation.
Pt (s) | V2+ (aq), V3+ (aq) || Au3+ (aq) | Au (s)
Eqcell = +1.76 V

1
The mass of the Au electrode increase.
The negative electrode is the Pt electrode.
The standard electrode potential for Au3+ (aq) | Au (s) is +2.02 V.

16

A
1, 2 and 3 are
correct
B
1 and 2 only are
correct
C
2 and 3 only are
correct
D
1 only is correct
35
The graph shows the first thirteen ionisation energies for element Z.
Ionisation
energy
Number of electrons removed
What can be deduced about element Z from the graph?
36
An oxide of Z dissolves in water to form an alkaline solution.
A chloride of Z undergoes hydrolysis to form a solution of pH 3.
The element Z reacts with steam to form an oxide.
Which of the following statements are correct with respect to the trend of the
thermal stability of hydrogen halides, HX?
1
The enthalpy change of atomisation of the halogens becomes more

endothermic from chlorine to iodine.
The enthalpy change of formation of the hydrogen halides becomes less

exothermic from hydrogen chloride to hydrogen iodide.
The bond energy of the HX bond becomes less endothermic from

hydrogen chloride to hydrogen iodide.
17

A
1, 2 and 3 are
correct
B
1 and 2 only are
correct
C
2 and 3 only are
correct
D
1 only is correct
37
Alkanes can be prepared from chloroalkanes by heating under reflux with sodium
(in ether) according to the equation:
2RCl + 2Na RR + 2NaCl
Which alkanes will be produced if a mixture containing equal amounts of
CH3CH2Cl and CH3CHClCH3 are used?
38
CH3CH2CH2CH3
CH3CH2CH(CH3)2
CH3CH(CH3)CH(CH3)2
Oxytetracycline is a class of broad-spectrum antibiotics used to treat a variety of

infections.
O
OH
OH
OH
OH
OH
C
H2N
HO
NH2
Which of the following statements about oxytetracycline is correct?

1
One mole of oxytetracycline reacts with three moles of thionyl chloride.
One mole of oxytetracycline reacts with two moles of hot sodium hydroxide
to liberate one mole of ammonia gas.
One mole of oxytetracycline reacts with six moles of ethanoyl chloride.
18

A
1, 2 and 3 are
correct
B
1 and 2 only are
correct
C
2 and 3 only are
correct
D
1 only is correct
39
Benzoylglycine (hippuric acid) was first isolated from stallions urine.
CONHCH2CO2H
.
Which of the following reactions about hippuric acid are correct?
40
It can be made by reacting benzoyl chloride with aminoethanoic acid.
It can be made by reacting hot benzoic acid with aminoethanoic acid.
It can be hydrolysed with cold aqueous sodium hydroxide to produce an

amino acid.
Amylase is an enzyme that converts complex carbohydrates into simple sugars.

Which conditions will inhibit the action of amylase?
1
High pH
Low temperatures
Presence of electrolytes
End of paper
19
2012 H2 Chemistry Prelim Paper 1 MCQ Key
11
21
31
12
22
32
13
23
33
14
24
34
15
25
35
16
26
36
17
27
37
18
28
38
19
29
39
10
20
30
40
20
Name ________________________
Class: ___________
Reg Number: ______

Higher 2
____________________________________________________________________________
Chemistry
9647
10 September 2012
2 hours

____________________________________________________________________________
Write your calculator brand and model/number in the box provided above.
Answer all questions in the spaces provided on the question paper.
All working must be shown clearly.
FOR EXAMINERS USE
Q1
/ 12
Q2
/8
The number of marks is given in brackets [ ] at the end of each

question or part question.
Q3
/ 12
Q4
/ 12
Q5
/9
Q6
/ 19
Total
/ 72
You are reminded of the need for good English and clear
presentation in your answers.

copyright chem dept @ meridian jc
1 Planning (P)
(a)
The solubility of a substance in aqueous solution is defined as the mass of

anhydrous solid that will dissolve in and just saturate 100 g of water at a fixed
temperature.
solubility
solubility =
mass of solid in a saturated solution

100
mass of water in the saturated solution
A solution that is saturated at a particular temperature is one in which no

more solid may be dissolved.
A saturated solution can be recognised by undissolved solid in equilibrium

with aqueous solution.
For example, a saturated solution of potassium chlorate(V) can be

represented by the equilibrium:
KClO3(s)
KClO3(aq)
You are provided with solid potassium chlorate(V), KClO3, and distilled water. In
addition to the standard apparatus present in a laboratory you are provided with
the following materials:
(i)
evaporating basin
measuring cylinders
Use the information given above to plan an experiment to describe how
you would prepare a saturated solution of potassium chlorate(V) at room
temperature.
(ii)
Hence, describe an experiment to determine the solubility of the

potassium chlorate(V) prepared in (a)(i).
(iii)
Create specimen results for your experiment and show how you would use
these results to calculate the solubility of potassium chlorate(V) at room
temperature.
(iv)
Identify a potential safety hazard in the experiment and state how you
[7]
(b)
Sodium bromide crystallises as NaBr.2H2O at low temperatures and as NaBr at

higher temperatures.
Temperature / oC
10
20
30
Solubility of
sodium bromide
/g per 100g H2O
84.2
90.5
97.2
40
50
60
70
80
90
100
105.8 116.0 116.9 117.4 118.3 119.8 121.2
Plot the solubility temperature data for sodium bromide and draw one line for
the solubility of NaBr.2H2O and another line for the solubility of NaBr. Draw
two separate lines and extrapolate them to a point of intersection. The line at
higher temperatures represents the solubility of NaBr. The line at lower
temperatures represents the solubility of NaBr.2H2O.
[2]
(i)
Read from the graph the temperature where the two lines intersect. This
is the transition temperature.
Estimated transition temperature = ______________________
(ii)
Describe the difference in the variation of solubility with temperature
above the transition temperature,
below the transition temperature.
The solubility curve represents equilibrium conditions between solid sodium

bromide and dissolved sodium bromide.
The position of equilibrium can be influenced by temperature change and
whether a change is exothermic or endothermic.
From the shape of your graph, comment on the likely enthalpy change for solid
sodium bromide dissolving under equilibrium conditions. Explain your answer.
[3]
[Total: 12]
2 A ketene is an organic compound of the form RR'C=C=O.

Ketenes can be prepared from acyl chlorides.
base
RR'CHCOCl
(a)
RR'C=C=O + HCl
Suggest the type of reaction that might occur during the preparation of ketenes
from acyl chlorides.
[1]
Ketene is a reactive compound which readily undergoes addition reaction, for example
RR'C=C=O + H2O RR'CHCOOH
Ketenes also undergo cycloaddition reaction with unsaturated compounds to form fourmembered or larger rings.
R
C C O
R'
R
C C O
R'
+
R
R'
O
+
O
O
C
O
R
R'
The simplest ketene is ethenone, CH2=C=O, where R and R' are hydrogen atoms.
(b)
(i)
Describe the mechanism for the reaction between ethenone and water.
(ii)
Ethenone reacts with ethanoic acid to give compound R, C4H6O3, which

reacts with phenylamine to give compound S, C8H9NO. Compound S
yields phenylamine and sodium ethanoate with hot aqueous sodium
hydroxide.
Suggest the structures of R and S.
(iii)
Compound T, an ester, is formed when two molecules of ethenone react

with one molecule of hydrogen cyanide.
2CH2=C=O + HCN C5H5NO2
T
Suggest a structure for the compound T using the given information on the
addition and cycloaddition reactions of ketenes.
(iv)
State the type of hybridisation and sketch the hybrid orbitals present at
C-1 in ethenone.
1
CH2=C=O
[7]
[Total: 8]
3 a-Terpineol, C10H18O, contains an alcoholic group which is not easily oxidised.

(a)
Identify compounds A to E in the following reaction scheme.
CH3
HO
CH3
acidified KMnO4
heat
warm alkaline
aqueous iodine
CH3
HCl
a-terpineol
H2, Ni, 10 atm
yellow ppt
A
excess conc. H2SO4
170C
,
C
C9H16O
warm alkaline
aqueous iodine
B
acidified KMnO4
heat
yellow ppt
H2, Ni, 10 atm

CH3
CH3
CH3
[3]
(b)
The conversion of a-terpineol to compound D uses HCl as the reagent.

(i)
Suggest how you prepare gaseous HCl in the laboratory using sodium
chloride as one of the reactants.
(ii)
Explain, with aid of balanced equations, why small amounts of gaseous HI

is produced when sodium iodide is used instead of sodium chloride in
(b)(i).
(iii)
Gaseous HI can also be prepared by another two-step method. Firstly,

iodine is directly combined with red phosphorous to form phosphorus
triiodide. In the next step, water is added to phosphorus triiodide to form
gaseous HI and H3PO3 as a by-product.
Write balanced equations for the reactions above.
[5]
(c)
Compound F can also be formed by using compound G.
H2, Ni, 200C, 30 atm
Suggest why compound B undergoes reduction with hydrogen over a nickel

catalyst at room temperature and slight pressure, but compound G requires
elevated temperature and pressure to form compound F.
[1]
(d)
Compound G is oxidised by hot potassium manganate(VII) to form compound H,

C8H6O4.
(i)
Draw the displayed formula of compound H.
(ii)
Two isomers of compound G undergo oxidation with hot potassium

manganate(VII) to give compound H in (d)(i).
Suggest the structures of the two isomers.
[3]
[Total: 12]
10
4 (a)
Electrophoresis can be used to separate amino acids produced by hydrolysing

proteins. The amino acids are placed in a buffered solution in an electric field.
In an experiment, a spot of a solution containing a mixture of the 4 amino acids
(tyr, lys, asp and phe) was placed in the middle of the plate in a buffered solution
of pH 7. Following electrophoresis, the amino acids move to a new position
under the influence of the electric charge.
Table 1: Amino acid data. This data is repeated on page 12.
Amino acid
Isoelectric
point
Structure
Tyrosine
(tyr)
Lysine
(lys)
Aspartic Acid
(asp)
Phenylalanine
(phe)
5.66
9.74
2.77
5.48
O
H2N
CH
OH
H2N
CH2
H2N
CH
OH
H2N
CH
CH
OH
OH
CH2
(CH2)4NH2
CH2
COOH
OH
(i)
Draw the structure of tyrosine formed in the buffered solution of pH 7.
11
This data is repeated from page 11.

Amino acid
Tyrosine
(tyr)
Lysine
(lys)
Aspartic Acid
(asp)
Phenylalanine
(phe)
5.66
9.74
2.77
5.48
Isoelectric
point
Structure
O
H2N
CH
OH
H2N
CH2
H2N
CH
OH
H2N
CH
CH
OH
OH
CH2
(CH2)4NH2
CH2
COOH
OH
mixture of amino acids

Before electric
+
current is applied
(ii)
Using the information provided, indicate on the diagram below the new
position of the 4 amino acids when an electric current is applied.
After electric
+
current is applied
(iii)
Explain the relative position of the tyrosine and aspartic acid after the
electric current is applied.
[3]
12
(b)
Aspartame is an artificial sweetener which is about 200 times sweeter than

sucrose.
NH2
HO2CCH2CHCONHCHCO2CH3
CH2
Aspartame
(i)
Aspartame is a high melting point crystalline white solid.

Explain the bonding in this solid that accounts for the high melting
point.
(ii)
A disadvantage of using aspartame as a sweetener is that it undergoes a

chemical reaction and breaks up at a fast rate in acidic soft drinks.
1
Suggest a possible reason for the breaking up of aspartame in soft

drinks.
13
NH2
HO2CCH2CHCONHCHCO2CH3
CH2
Aspartame
Hence, suggest the structure of all the organic products formed in

the reaction.
[4]
14
(c)
One possible synthesis route of aspartic acid is shown below.

Identify structures X and Y, and suggest the reagent(s) and conditions for steps I,
II and III.
Cl
II
NH3(g) heat
in sealed
tube
COOH
III
HOOC
NH 2
Y
Step
Reagent(s) and conditions
II
III
[5]
[Total: 12]
15
5 Tris is an abbreviation for tris(hydroxymethyl)aminomethane with the formula

(HOCH2)3CNH2. In biochemistry, Tris is widely used as a component of buffer
solutions especially for solutions of nucleic acids.
(a)
Describe and explain why the basicity of Tris differs from that of tert-butylamine,
(CH3)3CNH2.
[2]
(b)
A solution containing Tris and Tris-Hydrochloride, (HOCH2)3CNH3+Cl can resist

pH changes on addition of small amounts of acid and base.
Write two relevant equations to illustrate how this occurs.
[2]
16
(c)
Calculate the final pH, at 298 K, after a 5.00 cm3 portion of 1.00 mol dm3
hydrochloric acid is added separately to
(i)
100 cm3 of 1.00 104 mol dm3 sodium hydroxide solution.
(ii)
100 cm3 of solution X that contains 0. 200 mol dm3 Tris, (HOCH2)3CNH2,
and 0.200 mol dm3 Tris-Hydrochloride, (HOCH2)3CNH3+Cl.
(Given that pKb for Tris is 5.93 at 298 K)
[4]
(d)
Solution Y contains 1.00 mol dm3 Tris, (HOCH2)3CNH2, and 1.00 mol dm3
Tris-Hydrochloride, (HOCH2)3CNH3+Cl.
State which solution, X or Y, has a larger buffering capacity and explain why.
[1]
[Total: 9]
17
6 Iron is the most common element (by mass) on Earth. It exists in a wide range of
oxidation states, although +2 and +3 are the most common states.
The chemical equation below shows the reaction of chlorine gas and iron(II) ion.
Cl2(g) + 2Fe2+(aq)
(a)
2Cl -(aq) + 2Fe3+(aq)
(i)
Draw a diagram to show the apparatus needed to measure the Ecell for the
above reaction. Label the chemicals and concentration of the chemicals
used in the diagram. Indicate the direction of the electron flow.
(ii)
Use the Data Booklet to calculate the Ecell for this reaction.
[5]
18
(b)
On the other hand, ruthenium is a rare transition metal with oxidation states
ranging from 0 to +8. The most common oxidation states are also +2 and +3.
The standard electrode potentials for Ru(III)/Ru(II) and Fe(III)/Fe(II) are given
below.
[Ru(H2O)6]3+ + e-
[Ru(H2O)6]2+
E = +0.23 V
[Fe(H2O)6]3+ + e-
[Fe(H2O)6]2+
E = +0.77 V
Comment on the relative stability of the +2 and +3 oxidation state of ruthenium

compared to that of iron using the data above.
[1]
(c)
When ruthenium(III) ions are treated with aqueous ammonia, an aqueous

complex A is formed. Zinc is added to complex A and the resulting solution is
treated with NaCl. Orange crystals of compound B are formed which contains
37% of ruthenium by mass.
(i)
Suggest a formula for complex A and compound B.
Complex A .. Compound B ..
(ii)
Aqueous ammonia is added to iron(III) chloride solution. The resulting

mixture is treated with Zn metal to form compound C. Using the Data
Booklet, suggest with reasoning the identity of compound C.
[4]
19
The following table lists some iron complexes together with their colours and their
equilibrium constants, Kc.
Complex
[Fe(SCN)(H2O)5]2+(aq)
[FeF6]3- (aq)
[Fe(CN)6]4- (aq)
[Fe(CN)6]3- (aq)
[Fe(edta)]2- (aq)
[Fe(edta)]- (aq)
Colour
Deep red
Colourless
Pale yellow
Orange
Colourless
Yellow
Kc
1 102
2 1015
1 1024
1 1031
2 1014
1 1025
[edta = (-O2CCH2)2NCH2CH2N(CH2COO2-)2]
(d)
Write down the equation for the formation of the complex ion formed when Fe3+ is
mixed with F- ions.
[1]
(e)
Write an expression for the equilibrium constant, Kc, of [FeF6]3-.
[1]
(f)
Use the data in the table to predict and explain:

(i)
the effect of adding edta on the colour of a solution containing

[Fe(SCN)(H2O)5]2+,
20
(ii)
the effect of adding edta on the E value for the Fe3+ + esystem.
Fe2+
[4]
(g)
Explain why [Fe(CN)6]3- is orange in colour.
[3]
[Total: 19]
End of paper
21
BLANK PAGE
22
Meridian JC 2012 H2 Chemistry Paper 2 Suggested Answers

1.
(ai)
1.
2.
3.
4.
5.
Using a measuring cylinder, measure 100 cm3 of water and place it

in a 250 cm3 beaker.
Add solid KClO3 to water and stir with a glass rod to dissolve the
solids.
Add more solid KClO3 to the water until excess solids remains / no
more solid dissolves.
Allow the mixture to stand for a period of time (eg. 30 min) to
establish equilibrium.
Filter the solution to mixture to obtain the saturated solution as a
filtrate.
(ii)
1.
2.
3.
4.
5.
6.
Weigh an empty evaporating basin using a mass balance.

Using a measuring cylinder, transfer 20 cm3 of the saturated solution
from (b)(i) into the weighed evaporating basin. (Any volume from 20
50 cm3)
Weigh the evaporating basin and saturated solution.
Evaporate the water from the solution by placing the evaporating
basin on top of a beaker of boiling water.
Cool and reweigh the evaporating basin.
Repeat the heating, cooling and weighing until a constant mass is
obtained.
(iii)
Mass of evaporating basin = m1 g

Mass of evaporating basin and 20 cm3 saturated solution = m2 g
Final mass of solid KClO3 and evaporating basin = m3 g
Mass of water in saturated KClO3 solution = m2 m3 g
Mass of solid KClO3 in saturated solution = m3 m1 g
m -m
Solubility of KClO3 = 3 1 100
m2 -m3
(iv)
KClO3 solid is corrosive or caustic.

Wear gloves when handling the reagent.
(b)
Solubility of sodium
bromide
/ g per 100g H2O
130
120
50
60
70
80
110
x
100
x
x
90
x
80
70
60
10
20
30
40
90
100
Temperature / oC
(i)
52.0 oC
(ii)
above the transition temperature,

The solubility of NaBr increases gradually with temperature.
below the transition temperature.
The gradient of the graph is steeper, hence the solubility of NaBr.2H2O
increases more rapidly with temperature.
Dissolving sodium bromide under equilibrium conditions is endothermic.
2 (a)
(b)
Elimination
(i)
slow
CH2=C=O
CH3C=O
+ :OH+
CH3COOH
d+ d-
H-OH
(ii)
HN
CH3
R
(iii)
H
H
N
C
H
(iv)
H
O
C
O
sp
3 (a)
CH3
H2C
HO C
CH3
CH3
H3C
CH3
H3C
B
C
O
CH3
Cl
Cl C
CH3
CH3
D
CH3
H3C
HO C
H3C
OH
CH3
O
E
3
(b)
(i)
Add concentrated sulfuric acid to sodium chloride.
(ii)
I- is a stronger reducing agent than ClMost of the HI can be oxidised by concentrated H2SO4 to form violet
fumes of I2 gas.
NaI (s) + H2SO4 (l)
HI (g)
8 HI (g) + H2SO4 (l) 4 I2 (g)

(iii)
+ NaHSO4 (s)
+ H2S (g) + 4 H2O (l)
P (s) + 3/2 I2 (s) PI3 (s)

or
P4 (s) + 6 I2 (s) 4 PI3 (s)
PI3 (s) + 3 H2O (l)
H3PO3 (aq) + 3 HI (g)
(c)
Benzene in G is more resonance stabilized than alkene in B
(d)
(i)
H
H
(ii)
H2C
H3C
CH2 CH2
H2C
CH3
4 (a)
CH3
CH3
(i)
O
H2 N
CH
CH 2
(ii)
Asp
After electric
+
current applied
(iii)
Tyr
Phe
Lys
Aspartic acid and tyrosine formed negative ions and they migrate
towards the positive terminal.
Aspartic acid is nearer to the positive terminal than tyrosine as the aspartic
acid has a negative charge (-2) and a lower molecular mass than tyrosine.
(b)
(i)
Aspartame exist as zwitterions. A large amount of energy needed to break

the ionic bonds between the oppositely charged ions
(ii)
acidic hydrolysis
2
O
H3N+ CH
OH
CH2
NH3+ O
HOOC
H2C
HC
OH
CH3OH
(c)
Cl
OH
5 (a)
NH2
Step
Reagent(s) and conditions
Aqueous Cl2
II
(Excess) conc. H2SO4 170oC
III
KMnO4 , dilute H2SO4, heat
The electron withdrawing hydroxyl grp decreases the electron density on

the lone pair of N atom. Hence, the lone pair on N atom is less available to
accept a proton
Hence, Tris is less basic than tert-butylamine.
(b)
(c)
(HOCH2)3CNH2 + H+
(HOCH2)3CNH3+
(HOCH2)3CNH3+ + OH-
(HOCH2)3CNH2 + H2O
(i)
No. of mole of (unreacted) HCl in 105 cm3 = 4.99 10-3

[H+] = 4.99 10-3/0.105 = 0.04752 mol dm-3
pH = 1.32
(ii)
(0.025/)
pOH = 5.93 + lg (0.015/) where V = total volume

= 6.15
pH = 7.85
(d)
Solution Y has a larger buffering capacity and will much better resist changes in
pH upon the addition of a strong acid or base as the concentrations of its buffer
components are much larger than that of solution X.
6 (a)
(i)
Pt(s)
Pt (s)
Cl2 (g) at 298K

and 1 atm
[Cl - (aq)] = 1 mol dm-3
[Fe3+ (aq)] = 1 mol dm-3

[Fe2+ (aq)] = 1 mol dm-3
Pt (s)
(ii)
(b)
(c)
EqFe3+/Fe2+ is more positive than EqRu3+/Ru2+, the relative stability of +2 oxidation

state compared to +3 oxidation state is larger for iron than ruthenium.
(i)
(ii)
(d)
(g)
Complex A [Ru(NH3)6]3+
Compound B [Ru[(NH3)6]2+.2Cl- or Ru[(NH3)6].2Cl or Ru(NH3)6Cl2
Ecell = -0.56 (-0.76) = +0.20V
C is Fe(OH)2
Since Fe(OH)3 can be reduced by Zn, the compound
Fe3+ + 6F-
(e)
(f)
Ecell = +1.36 (+0.77)= +0.59 V
[FeF6]3-Or [Fe(H2O)6]3+ + 6F-
[FeF6]3[F-]6
[FeF6]3- + 6H2O
[[FeF6]3-]
[[Fe(H2O)6]3+] [F-]6
(i)
Kc of [Fe(edta)]- is larger than Kc of [Fe(SCN)(H2O)5]2+. Edta is a stronger

ligand than H2O and SCN- and the deep red [Fe(SCN)(H2O)5]2+ solution
changes to yellow [Fe(edta)]-
(ii)
Addition of edta results in forming [Fe(edta)]2- and [Fe(edta)]-.

Since Kc of [Fe(edta)]- is greater Kc of [Fe(edta)]2-, edta ligand stabilises
Fe(III) relative to Fe(II) to a larger extent than water ligand. Hence Eo
value is less than +0.77V/decreases.
[Fe(CN)6]3- has a partially-filled d orbitals; undergoes d-orbital splitting. During

the transition, the d electron absorbs the blue wavelength of light from the visible
region of the electromagnetic spectrum and emits the remaining wavelengths
which appear as the orange colour of [Fe(CN)6]3- observed.
Class
Reg Number
Candidate Name _____________________________

Preliminary Exam
Higher 2
___________________________________________________________________
H2 Chemistry
9647/3
18 Sep 2012
2 hours
Data Booklet
Writing paper
___________________________________________________________________
Write your name, class and register number in the spaces provided at the top
of this page.
Answer 4 out of 5 questions in this paper.

Begin each question on a fresh page of writing paper.
Fasten the writing papers behind the given Cover Page for Questions 1 & 2 and
Cover Page for Questions 3, 4 & 5 respectively.
Hand in Questions 1 & 2 and 3, 4 & 5 separately.
You are advised to spend about 30 min per question only.
The number of marks is given in brackets [
question.
] at the end of each question or part
answers.
___________________________________________________________________
This document consists of 14 printed pages (including the cover pages)
Answer any 4 out of 5 questions in this paper.

Begin each question on a fresh sheet of writing paper.
1
Sugars, or saccharides, are the most abundant bio-molecules found on the

planet and play many important biological roles. A simple sugar, a derivative
of a straight chain polyhydroxyl alcohol and glycerol, is considered to be the
parent of all sugars.
(a)
2-chloropropane-1,3-diol can be synthesised from glycerol via the reaction

scheme below.
OH
OH
CH 2-CH-CH 2
OH
KMnO4, dilute H2SO4

heat
glycerol
HOOC C COOH
O
Step I
Step II
H2O
O
O
HO C CH C OH
Cl
Step III
OH
OH
CH2 CH CH2
Cl
2-chloropropane-1,3-diol
Suggest reagents and conditions for steps I to III, and draw the structural
formula of intermediates A and B.
[5]
(b)
Glucose, an important simple sugar or monosaccharide, is required by the

cells in our body as a source of energy and metabolic intermediate.
A common source of glucose is sucrose or table sugar. In humans and other
mammals, sucrose is broken down into its constituent monosaccharides,
glucose and fructose as shown below.
CH 2 OH
HO
CH 2OH
O
O
HO
CH 2 OH
CH2 OH
O
OH
HO
sucrose
HO
HO
OH
CH2 OH
O
+
OH
OH
glucose
CH 2 OH
HO
HO
OH
fructose
(i)
Name the functional group, other than ether (R-O-R), present in

sucrose.
(ii)
Suggest the type of reaction undergone by sucrose.

[2]
(c)
Glucose undergoes complete combustion to form carbon dioxide and water.

(i)
Write a balanced equation for the complete combustion of glucose.
(ii)
The standard enthalpy change of formation of CO2, H2O and glucose is

-394 kJ mol-1, -286 kJ mol-1 and -1275 kJ mol-1 respectively.
Use your answer in (c)(i) and the data given to calculate the energy
released when 9.0 g of glucose undergoes complete combustion.
(iii)
In a calometric experiment, 9.0 g of glucose was burnt completely and

the energy released raised the temperature of 650 cm3 of water by
44oC.
Calculate the energy released by the combustion of 9.0 g of glucose in
the experiment.
(iv)
Suggest a reason for the discrepancy between the answers in (c)(ii)

and (c)(iii).
[5]
(d)
(e)
Group II nitrates and sugars undergo decomposition when heated.

(i)
Write an equation for the thermal decomposition of Group II nitrates.
(ii)
Suggest why the numerical value of the entropy change is very similar
for the decomposition reaction of all the Group II nitrates.
(iii)
Predict, with reasoning, whether magnesium nitrate or barium nitrate

has a higher decomposition temperature.
[4]
Chlorophyll is an extremely important bio-molecule which allows plants to

absorb energy from light. It consists of a chlorin ring with a magnesium ion,
Mg2+, at the centre of the ring.
With the aid of an energy cycle, calculate the enthalpy change of hydration of
Mg2+ using the following data and appropriate data from the Data Booklet.
enthalpy change of solution of MgCl2
enthalpy change of hydration of Clenthalpy change of formation of MgCl2
enthalpy change of atomization of Mg
first electron affinity of Cl
= - 153 kJ mol-1
= - 362 kJ mol-1
= - 642 kJ mol-1
= + 148 kJ mol-1
= - 364 kJ mol-1
[4]
[Total: 20]
2(a)
Halogens react readily with hydrogen.

X2(g) + H2(g) 2HX(g)
(b)
(where X = Cl, Br or I)
(i)
Describe how you could carry out this reaction using chlorine.
(ii)
Describe two observations you would make if this reaction was carried
out with bromine.
(iii)
Describe and explain the trend observed in the reactions of the

elements chlorine, bromine and iodine with hydrogen.
[6]
Some halogens also react readily with alkanes. Consider the following
sequence of reactions.
Reaction 1
C6H14
alkane W
Reaction 2
C6H13X
C6H13OH
(i)
State the reagent and conditions needed for reaction 1 when X is

bromine, Br.
(ii)
Use bond energy data from the Data Booklet to calculate the Ho of
reaction 1 when X is iodine, I.
(iii)
Hence, suggest why it is not possible to synthesise iodoalkane by

reaction 1.
(iv)
In another separate experiment using reaction 1, alkane W, C6H14,

produced only two isomeric monobromo compounds Y and Z, with the
molecular formula C6H13Br. Compound Z is chiral.
Suggest the structures of W, Y and Z.
[6]
(c)
Both isomers Y and Z with formula C6H13Br can undergo reaction 2 with
aqueous sodium hydroxide solution to form alcohols. When the reaction of
one of these isomers with aqueous sodium hydroxide was investigated, the
following kinetic data was obtained.
Initial [C6H13Br] /
Experiment
mol dm-3
Initial [OH-] /
mol dm-3
Initial rate of reaction /

mol dm-3 min-1
1.30
2.60
13.0
2.60
1.30
26.0
3.90
2.60
39.0
7.80
5.20
78.0
(i)
Use these data to deduce the order of reaction with respect to each of
the reagents, showing how you arrive at your answers. Hence, write
the rate equation for the above reaction.
(ii)
Suggest which isomer Y or Z was being investigated in the above

reaction and explain your choice.
(iii)
Hence, using the isomer you have suggested in (c)(ii), describe a

mechanism that is consistent with your rate equation, and indicate
which step in the mechanism is the rate determining step.
(iv)
Draw a labeled energy profile diagram of the mechanism you described

in (c)(iii).
[8]
[Total: 20]
3(a)
Iron metal has traditionally been extracted from its ore using a Blast furnace.
The process uses coke (carbon) and haematite (Fe2O3) in three stages,
whereby
coke is first oxidised by air to form carbon dioxide;

the carbon dioxide formed further reacts with more coke to form carbon
monoxide;
the haematite is reduced to obtain the iron metal
New research proposes that iron could be recovered via electrolysis. This
involves passing current via inert platinum electrodes into a mixture of molten
Fe2O3. This new process is thought to be more advantageous than using the
current Blast furnace method.
(b)
(i)
Draw a diagram to illustrate the electrolysis set-up, showing clearly the

polarity of the electrodes and the species attracted to and formed at
each electrode.
(ii)
Give the equations, including state symbols, for the reactions occurring
at each electrode.
(iii)
An initial pilot production plant using the new method yields 5 kg of iron
per day. Calculate the current to be supplied per day if the pilot plant
runs continuously for 24 hours each day.
(iv)
Construct the equations for the reactions occurring at each stage of the
Blast furnace extraction of iron.
(v)
Suggest an advantage of the new electrolysis method over the Blast

furnace method.
[8]
Solutions of iron(II) compounds are commonly prepared in the laboratory.

(i)
By selecting two appropriate half-equations from the Data Booklet,

explain why iron(II) solutions are normally made up and stored in the
presence of acids instead of bases.
(ii)
With the aid of suitable equations, explain why iron(II) solutions can
catalyse the reaction involving iodide ions with peroxodisulfate(VI)
ions.
2I- (aq) + S2O82- (aq) I2 (aq) + 2SO42- (aq)
[5]
(c)
Iron compounds can be used to catalyse a number of organic reactions. One

such organic reaction is the Michael reaction as shown below.
H
R''
R'
E.g. of R or R' groups

=
base / catalyst
R''
E.g. of R'' groups
R'
The reaction can also be carried out using sodium ethoxide (CH3CH2O-Na+)
as a catalyst, whereby the labelled hydrogen H reacts with the ethoxide ion as
a proton and is eventually transferred to its new position on the product.
(i)
Explain how the ethoxide ion is able to remove the proton in the
Michael reaction.
(ii)
State the type of reaction which occurs in the Michael reaction.
The Michael reaction can be used to synthesise a useful blood anticoagulant

known as Warfarin. The synthesis of Warfarin can give rise to two possible
isomers.
OH
base / catalyst
+
O
OH
O
O
O
W ar f ar i n
(iii)
Suggest the structure of compound A used to form Warfarin.
(iv)
State the type of isomerism present in Warfarin and sketch the

structures of these two isomers. [You may use R to represent a part of
the molecule in your answer]
(v)
Draw the structure of the product formed when 2,4-DNPH is reacted

with Warfarin.
[7]
[Total: 20]
Oxygen reacts with various Period III elements to produce compounds of

numerous uses. Examples are Al2O3 which is often used as a refractory
material and chlorine oxides which act as oxidising agents used in water
treatments and in bleaching.
(a)
Element X forms a white oxide that is soluble in cold water.

dissolves in water to form a neutral solution.
Its chloride
Element Y forms two oxides. 0.09 mol of one of the two oxides produces
12.3 g of white precipitate when shaken with excess calcium hydroxide
solution. A solution containing 1 mol of the oxide of element Y forms a neutral
solution when the same amount of the oxide of element X is added to it.
Given that X and Y are Period III elements, identify the element X and the
oxide of Y in the above reactions. Explain the observations with the help of
relevant equations.
[4]
(b)
(c)
When a sample of an oxide of chlorine, ClmOn, was vapourised in a suitable

apparatus at 250 oC and 101 kPa, the density of the gas was found to be
1.60 g dm-3.
(i)
Calculate the molar mass of the gas and hence suggest the value of m
and n.
(ii)
Explain why the molar mass obtained in (b)(i) is different from the
theoretical value.
[4]
A to F are consecutive elements having atomic numbers between 10 to 20.

(i)
Write an equation that represents the third ionisation energy of

aluminium.
(ii)
From the graph below, identify which element, A to F, is aluminium.

[3]
(d)
Other than its use as a refractory material, Al2O3 is also used in chemical
reactions involving organic compounds. In the reaction scheme below, Al2O3
is used to dehydrate chloramphenicol-X to form compound D.
H2N
A
CH3COCl
NHCOCHCl2
CH
CH
OH
CH2OH
B+C
hot alkaline
KMnO4
chloramphenicol-X
Step I
Al2O3
D
Step II
OH
H2N
NHCOCHCl2
CH
OH
CH3
(i)
Identify the lettered compounds A to D.
(ii)
Suggest the reagent and condition used in step II. State the type of
reaction occurring in step II.
(iii)
Describe a simple chemical test to distinguish

chloramphenicol-X and its isomer shown below.
H2N
CH
OH
COCH2NH
between
CCl2
CH2OH
[9]
[Total: 20]
Fluoxetine is an anti-depressant drug or mood elevator commonly used to

treat depression and other mental illness like obsessive compulsive
behaviour.
The structure of Fluoxetine is shown below:
H
N
CF3
Fluoxetine
(a)
(b)
(i)
Draw a diagram to show how hydrogen bonding occurs between one

molecule of Fluoxetine and two molecules of water.
(ii)
Suggest why Fluoxetine is insoluble in water despite the formation of

hydrogen bonding between Fluoxetine and water molecules.
(iii)
Fluoxetine is manufactured and merchandised as Fluoxetine

hydrochloride. Explain, in terms of structure and bonding, why this is
so.
[5]
Bupropion is another type of anti-depressant.

It is synthesised from
3-chloropropiophenone as shown in the pathway below.
O
Cl.
Step I
Cl.
Br
Step II
N
H
NH
Cl.
C(CH3)3
3-chloropropiophenone
intermediate X
Bupropion
(i)
State the type of reaction that occurs in step I.
(ii)
Suggest the reagents and conditions for step II.
(iii)
Draw the structure of the product obtained by heating intermediate X

with aqueous potassium hydroxide.
[3]
(c)
Compound A, C11H15NO3, has potential to treat certain mental disorders.

Compound A reacts with aqueous bromine to form compound B,
C11H13NO3Br2. 1 mole of compound A reacts with 2 mole of aqueous sodium
hydroxide at room temperature. No decolourisation is observed upon heating
compound A with acidified potassium manganate(VII). Compound A reacts
with iodomethane to form compound C, C12H18NO3I, which yields a yellow
precipitate with aqueous silver nitrate at room temperature.
Suggest the structure of each lettered compound and explain the reactions
involved.
[8]
(d)
In some cases of mental illness, lithium ion, Li+, can also be administered in
the form of lithium salt as a mood-stabilizing drug.
(i)
Explain why Li has the lowest first ionisation energy among the Period
2 elements.
(ii)
All Group I halides dissolve in water to give neutral solutions containing

hydrated ions.
Suggest why lithium forms Li(H2O)4+ ions, whereas the other Group I
halides form mainly M(H2O)6+ ions.
[4]
[Total: 20]
END OF PAPER
Cover Page for Question 1 & 2

Class
Reg Number
Candidate Name _____________________________

2012 JC 2 Preliminary Examination
H2 Chemistry 9647
H
2
18 September 2012
INSTRUCTION TO CANDIDATES
Answer any 4 out of 5 questions in Paper 3.
Fasten your answers for Question 1 and 2 behind this Cover Page.
You are advised to spend about 30 min per question.
Circle the questions that you attempted.

You are reminded the need for good English and clear presentation in your answers.
FOR EXAMINERS USE
Paper 3
Q1
/ 20
Q2
/ 20
Cover Page for Question 3, 4 & 5

Class
Reg Number
Candidate Name _____________________________

2012 JC 2 Preliminary Examination
H2 Chemistry 9647
H
2
18 September 2012
INSTRUCTION TO CANDIDATES
Answer any 4 out of 5 questions in Paper 3.
Fasten your answers for Question 3, 4 and 5 behind this Cover Page.
You are advised to spend about 30 min per question.
Circle the questions that you attempted.
You are reminded the need for good English and clear presentation in your answers.
FOR EXAMINERS USE

Q3
/ 20
Q4
/ 20
Q5
/ 20
Paper 3
2012 Meridian JC H2 Chemistry Prelim P3 Suggested Answers

1
(a)
Reaction I : NaBH4 in ethanol , rtp

Reaction II : PCl5 , rtp
Reaction III : LiAlH4 in dry ether , rtp
H
HOOC-C-COOH
OH
(b)
(c)
Cl C-CH-C Cl
Cl
(i)
1o and 2o alcohols
(ii)
Hydrolysis
(i)
C6H12O6 + 6O2 6CO2 + 6H2O
(ii)
Hrxn = = [6(-394) + 6(-286)] [-1275] = - 2805 kJ mol-1

Energy released = 2801 x 0.0500 = 140 kJ
(d)
(iii)
Energy released by combustion = 650 x 4.18 x 44 = 120 kJ
(iv)
Some heat was lost to the surrounding.
(i)
M(NO3)2 MO + 2NO2 + O2
(ii)
Each mole of Group II nitrates release the same amount of gaseous

molecules.
(iii)
Ionic size of cation: Mg2+ < Ba2+

charge density hence polarizing effect of cation: Mg2+ > Ba2+
Therefore Ba(NO3)2 has a higher decomposition temperature.
Hsoln (MgCl2)
(e)
MgCl2 (s)
Mg2+ (aq) + 2Cl- (aq)
-Hf (MgCl2)
Mg(s) + Cl2(g)
Hat (Mg)
BE(Cl Cl)
Hhyd (Mg2+)
2 x Hhyd (Cl-)
Mg(g) + 2Cl(g)
1st IE + 2nd IE (Mg)
Mg2+(g) + 2Cl(g) + 2e-
2 x 1st EA (Cl)
Mg2+(g) + 2Cl-(g)
Hhyd (Mg2+) = -148 - 244 - 736 - 1450 - 2 x (-364) - 2 x (-362) + (-642)

+ (-153) hence Hhyd (Mg2+) = -1921 kJ mol-1
2(a)
(i)
Shine uv light on the mixture of hydrogen and chlorine gas.
(ii)
Decolorisation of reddish brown bromine ; white fumes of HBr seen.
(iii)
Reactivity of halogens with hydrogen decreases down the group.

The total bond energy released in forming H-X decreased down the
group more significantly than the total bond energy absorbed in
breaking X-X and H-H bonds. DHrxn becomes more endothermic down
the group, reactivity decrease down the group
(b)
(i)
Limited Br2 gas and uv light
(ii)
DH = 410 + 151 240 - 299 = + 22.0 kJ mol-1
(iii)
Endothermic due to the weak C-I bond formed.
(iv)
CH3 CH3
W:
H3C
CH3
CH3 CH3
CH3 CH3
Y:
(c)
(i)
H3C
Br
CH3
Z:
H3C
CH2Br
Comparing experiments 1 & 3, when [C6H13Br] was tripled, the initial

rate of reaction increased by 3 times, order of reaction wrt C6H13Br is 1.
Comparing experiments 1 & 2
13.0 [1.30][ 2.60]
=
26.0 [ 2.60][1.30]b
b
2.60
1=
1.30
b=0
Rate = k[C6H13Br]
(ii)
It should be isomer Y since it is a tertiary bromoalkane, it will form a

stable carbocation in the slow step of the mechanism due to the
presence of three electron donating alkyl group
(iii)
Mechanism : SN1
CH3
CH3
slow
(CH3)2CH
C
d+
Br
d-
CH3
CH3
(CH3)2CH
C+
d+
CH3
: OH-
CH3
fast
C
(CH3)2CH
CH3
(iv)
+ Br-
C+
d+
(CH3)2CH
OH
CH3
(CH3)2CHC(CH3)2+ + Br- + OH-
Marking points:
(CH3)2CHC(CH3)2Br + OH Axes
are correctly labeled
(CH3)2CHC(CH3)2OH + Br-
3(a)
(i)
(Pt cathode)
(Pt anode)
+
O2 (g)
formed
Fe (s)
formed
O2- (l)
Fe3+ (l)
(ii)
Cathode: Fe3+ (l) + 3e Fe (s); Anode:
(iii)
5 1000 I 24 60 60
=
; I = 300 A.
55.8
3 96500
2O2- (l) O2 (g) + 4e
(iv)
C + O2 CO2 ; CO2 + C 2CO ; Fe2O3 + 3CO 2Fe + 3CO2
(v)
Less / no pollutants of CO or CO2 are formed.
(b)(i) Fe(II) is stabilised with respect to Fe(III) in acidic medium compared to

basic medium. Fe2+ in acidic medium is a weaker reducing agent
compared to Fe(OH)2 in basic medium.
(ii)
Fe2+ acts as a homogeneous catalyst

Step 1: 2Fe2+ + S2O82- 2SO42- + 2Fe3+
Step 2: 2Fe3+ + 2I- 2 Fe2+ + I2
(c)
(i)
Ethoxide ion acts as a base
(ii)
(Nucleophilic) Addition
(iii)
(iv)
Optical isomerism
R
H
(v)
NO2
H
N
OH
NO2
OH
4(a)
R:
Element X : Sodium / Na
Na2O + H2O 2NaOH
Formula of the oxide of Element Y: SO3

Upon addition of Ca(OH)2, white ppt formed could be CaSO4
No of mol of CaSO4 = = 0.09 mol
SO3 + Ca(OH)2 CaSO4 + H2O
white ppt
SO3 +H2O H2SO4
H2SO4 + Na2O Na2SO4 + H2O
(b)
(i)
1.60 x 103 x 8.31 (250+273)
101 x 1000 M =
Molar mass of gas = 68.8 g mol-1 67.5 g mol-1

Hence m = 1, n = 2
(c)
(d)
(ii)
There is significant van der Waals forces of attraction between the

ClO2 molecules.
(i)
Al2+ (g) Al3+ (g) + e
(ii)
C is aluminium, as it has the lowest 3rd IE. The removal of the third
electron will lead to the formation of the stable noble gas configuration
hence a small amount of energy is required to remove the valence
electron.
(i)
A:
O
H3C
NH
CH
CH
NHCOCHCl2
CH2
CH3
CH3
B, C:
NH2
O-
Na-O
O-Na+
D:
NH2
(ii)
CH
OH
CH2
NHCOCHCl2
H2O (g) or steam , conc. H3PO4, 65 atm , 300C

Electrophilic Addition
(iii)
5(a)
Add 2,4-DNPH to each compound separately and heat.

Chloramphenicol-X will not produce orange ppt of hydrazine;its isomer
will produce orange ppt of hydrazone.
(i)
Hydrogen bond
- O
+
H
+ H
N
F
F
C
F
(b)
(ii)
Due to the presence of a large hydrophobic benzene rings.
(iii)
Formation of ion-dipole interaction with water molecules causes

solvation hence drug is better is better absorbed.
(i)
Free radical substitution
(ii)
excess (CH3)3CNH2 , heat
(iii)
O
Cl
OH
(c)
COOH
A:
H3C
CH3
CH3
Or A can also be 1, 2 di-substituted isomer
OH
COOH
B:
H3C
CH3
CH3
Br
Br
OH
C:
COOH
H3C
CH3
+N
Br -
CH3
CH3
OH
(d)(i)
Effective nuclear charge increases.The electrostatic force of attraction

between nucleus and valence electrons increases hence energy
required to remove the valence electrons increases.
(ii)
Li+ has the smallest ionic radius among the group I metal ion
Less H2O ligands can be datively bonded to Li+ cation, thus the
coordination number is 4 and Li(H2O)4+ ions is formed.
NATIONAL JUNIOR COLLEGE

SH2 PRELIMINARY EXAM
Higher 2
CANDIDATE
NAME
SUBJECT
CLASS
REGISTRATION
NUMBER
CHEMISTRY
9647/01
Fri 21 Sept 2012

1 hour
Data Booklet

Write your name, subject class and registration number on the Answer Sheet in the spaces
provided unless this has been done for you.
There are 40 questions on this paper. Answer all questions. For each question there are four
Answer Sheet.
This paper consists of 18 printed pages and 0 blank page.
NJC/H2 Chem/01/2012
[Turn over
Section A
For each question there are four possible answers A, B, C, and D. Choose the one you
1
Which atom has the highest ratio of unpaired electrons to paired electrons in its ground
state?
A boron
B carbon
C nitrogen
D oxygen
Bombardment of 14N with a-particles (helium nuclei) produces a hydrogen nucleus and
another nucleus. This other nucleus is
A
14C
6
14N
7
17O
8
18Ne
10
The successive ionisation energies (kJ mol 1) of two elements are given below:
X
Y
1012
1251
1907
2298
2914
3822
4964
5159
6274
6542
21267
9362
26431
11108
29876
33604
35905
38860
Which of the following statements is false?
The formula of the compound formed between X and Y is XY3.
The compound formed between X and Y is covalent.
X has a giant covalent structure.
Y exists as diatomic molecules.
When the N2+ ion is formed from N2, a bonding electron is removed.
Which statement is correct?
A The bond order decreases so N2+ has a stronger, shorter bond than N2.
B The bond order decreases so N2+ has a weaker, longer bond than N2.
C The bond order increases so N2+ has a stronger, shorter bond than N2.
D The bond order increases so N2+ has a weaker, longer bond than N2.
NJC/H2 Chem/01/2012
[Turn over
In which pair of species are the values of the bond angles the closest?
A BF3 and NH3
B CH3 and BF3
C H2O and C2H4
D NH4+ and SO42
10 cm3 of hydrocarbon is burnt in 100 cm3 of excess oxygen at room temperature. The
final volume of gas mixture is 85 cm3. When the gas mixture is bubbled through
aqueous sodium hydroxide solution, the volume of gas mixture decreases to 55 cm3.
What is the formula of the hydrocarbon?
A C3H6
B C3H8
C C6H12
D C6H14

The graph represents the variation of a property of the Group II elements.
property
What is this property?

A ionic radius
B ionisation energy
C neutron / proton ratio
D rate of reaction with water
NJC/H2 Chem/01/2012
[Turn over
The diagram shows bond energies in halogen molecules.
Why does the value for fluorine not follow the trend shown by chlorine, bromine and
iodine?
A Fluorine is more electronegative than the other halogens.
B Lone electron pairs in fluorine repel more strongly than those in the other halogens.
C The bonds in fluorine are more polar than those in the other halogens.
D The bonds in fluorine have some -character.
What is the pressure (in Pa) of a sample of hydrogen gas that has density of 8 gm3 at
300 C?
A
573 4 22.4 101 10 3

273
573 8 22.4 101

273
273 4 11.2 101 10 3

573
573 8 11.2 101

273
NJC/H2 Chem/01/2012
[Turn over
10
The rate equation for the reaction

S2O82 (aq) + 2 I (aq) 2SO42 (aq) + I2(aq)
is rate = k[S2O82][I] where k, the rate constant is found to be 0.2 mol1 dm3 s1 at
temperature t.
What is the half-life of the reaction when S2O82 is present in a large excess at a
concentration of 0.5 mol dm3 at the same temperature t?
A 0.7 s
B 1.4 s
C 3.5 s
D 6.9 s
11
Hesss Law can be used to calculate the average CH bond energy in methane.
DHoat = standard enthalpy change of atomisation
DHof = standard enthalpy change of formation
DHoc = standard enthalpy change of combustion
Which values of the following data are needed in order to perform the calculation?
A DHoc (C), DHoc (H2), DHoc (CH4)
B DHoat (C), DHoat (H2), DHof (CH4)
C DHoc (C), DHoc (H2), DHof (CH4)
D DHof (CH4) only as DHof (C) and DHof (H2) are defined as zero.
12
In a car engine, non-metallic element X forms a pollutant oxide Y.

Further oxidation of Y to Z occurs spontaneously in the atmosphere. In this further
oxidation, 2 mol of Y reacts with 1 mol of gaseous oxygen. Z can dimerise at specific
conditions.
Which statement about X, Y and Z is incorrect?
A
X forms a basic hydride.
Y is a diatomic molecule.
Z is a polar molecule.
Z contributes to global warming.
NJC/H2 Chem/01/2012
[Turn over
13
The diagram below represents the reaction profile of the monomer-dimer system:
2NO 2 (g)
brown
kf
kb
N2O 4 (g)
colourless
Enthalpy
Progress of reaction
Which statement about the equilibrium is correct?
A The equilibrium constant Kc will be larger at higher temperatures.
B kf increases and kb decreases when the equilibrium mixture is heated.
C Doubling the total pressure of the system reduces the percentage dissociation to
half.
D At higher temperature, the colour intensity of the mixture increases.
14
Which of the following statements about the spontaneity of the gas-phase reaction
shown is true at 25 C?
2 O=NCl(g) 2 N=O(g) + Cl2(g)
A The reaction cannot be spontaneous.
B The reaction will be spontaneous regardless of the magnitude of DH and DS.
C The reaction will be spontaneous only if the magnitude of DH is large enough to
overcome the unfavorable entropy change.
D The reaction will be spontaneous only if the magnitude of DS is large enough to
overcome the unfavorable enthalpy change.
NJC/H2 Chem/01/2012
[Turn over
15
When a mineral was heated in a Bunsen flame to constant mass, a colourless gas that
turned limewater milky was evolved. The remaining solid was cooled and then added
to aqueous hydrochloric acid. Vigorous effervescence was seen.
What was the mineral?
A Dolomite, CaCO3.MgCO3
B Barytocalcite, BaCO3.CaCO3
C Aragonite, CaCO3
D Artinite, MgCO3.Mg(OH)2.3H2O
16
The following two experiments are carried out with anhydrous potassium chloride and
observations X and Y are made at the end of each experiment.
Concentrated sulfuric acid is added to the potassium chloride and the fumes produced
are bubbled into aqueous potassium iodide solution - observation X.
The potassium chloride is dissolved in aqueous ammonia and this is then added to
aqueous silver nitrate - observation Y.
What are the observations X and Y?
17
Brown solution
Colourless solution
Brown solution
White precipitate
Colourless solution
Colourless solution
Colourless solution
White precipitate
The unbalanced equation below involves manganese species in acid medium.

MnO42
Mn2+ + MnO4
Which of the following statements is false?

A This is a disproportionation reaction.
B MnO4 ions are purple due to the presence of dd electronic transition.
C Unequal amounts of Mn2+ and MnO4 ions are formed.
D The 3d electrons in Mn2+ ions are unpaired.
NJC/H2 Chem/01/2012
[Turn over
18
The oxide and chloride of an element X are separately mixed with water. The two
resulting solutions have the same effect on litmus.
What is element X?
A Sodium
B Magnesium
C Aluminum
D Phosphorus
19
Under similar conditions, carbon monoxide competes 200 times more effectively than
oxygen for haemoglobin available in blood. The effects in the body of
carboxyhaemoglobin are detectable when it reaches 5 % of the concentration of
oxyhaemoglobin in the blood. Air contains 20 % of oxygen by volume.
By using these data, it can be deduced that the minimum concentration
(parts per million, ppm) of carbon monoxide in the atmosphere that will result in
detectable effects in the body is
A 10 ppm
B 50 ppm
C 250 ppm
D 500 ppm
20
Which of the following compounds is not made up of 6.90 % and 51.7% by mass of
hydrogen and carbon respectively?
A
S
O
B
O
CH3CSCH(CH3)CHO
CH3CO(CH2)2CO2H
NJC/H2 Chem/01/2012
[Turn over
21
A halogenoalkane is reacted with NH3 in the following reaction.

Which of the statements is correct?
R
RX
NH3
RX
R
Step 1
NH2
NH R
Step 2
R
RX
RX
Step 3
Step 4
A Rate of reaction of step 2 is faster than step 3 as RNH2 is a stronger nucleophile.

B Rate of reaction of step 3 is faster than step 2 as RNH2 is a stronger nucleophile.
C R4N+ will be the major product when excess RX is used.
D R4N+ will be the major product when excess NH3 is used.
22
Aspartic acid, HO2CCH2CH(NH2)CO2H, is an essential amino acid. Its anion, aspartate

is an important metabolite in the urea cycle. Aspartic acid can be used to make
polymers.
O
O
reagent A
Br
aspartic acid
H 2N
O
O
compound B
OK
reaction III
reaction II
Br
H
O
CO2K
N
H
polymer X

A A white precipitate is formed when aqueous silver nitrate is added to compound B.
B Reagent A is aqueous thionyl bromide.
C One mole of hot aqueous KOH is required to react with one mole of polymer X in
reaction III.
D The imide (the CONRCO- group present in the polymer X) has a higher pKb value
than an average amide.
23
Which of the following gives the compounds in order of decreasing Ka?

A CH3CH2OH > C6H5OH > CH3CO2H
B CH3CF2CO2H > FCH2CHFCO2H > F2CHCH2CO2H
C CH3CH2CO2H > CH2(OH)CH2COOH > CH3CH(OH)CO2H
D CH3CH2CO2H > CH3CH(OH)CO2H > CH2(OH)CH2COOH
NJC/H2 Chem/01/2012
[Turn over
10
24
A chloroalkane G with molecular formula C5H11Cl exhibits optical activity. On warming

G with alcoholic NaOH, two alkenes E and F are formed, E being the major product.
One of the products of the reaction between E and hot acidified potassium
manganate(VII) gives a yellow precipitate with alkaline aqueous iodine.
Which of the following could be G?
A CH3CHClCH2CH2CH3
B CH3CH2CHClCH2CH3
C CH3CH(CH3)CHClCH3
D CH3CCl(CH3)CH2CH3
25
Which of the following compounds can be prepared by the apparatus shown?
water out
water in
heat
A 1,2-dibromoethane by using bromine and ethene.

B Ethanoic acid by using ethanol, sodium dichromate(VI) and sulfuric acid.
C Bromoethane by using ethanol, sodium bromide and concentrated sulfuric acid.
D Phenyl ethanoate by using phenol and ethanoyl chloride.
NJC/H2 Chem/01/2012
[Turn over
11
26
It has been estimated that for every atom of chlorine or bromine generated from a
halogenoalkane in the stratosphere, one hundred thousand molecules of ozone may
be destroyed.
Which of the following organic compounds is most destructive to ozone?
A CF2ClCH2CF2Cl
B CCl2BrCH2Br
C CHCl2CBr3
D CCl4
27
What is the total number of stereoisomers that can be obtained from the major product
of the reaction between compound H and NaOH in ethanol?
Br
CH3
CH2CH2CH=CHCH3
compound H
A 2
B 4
C 8
D 12
NJC/H2 Chem/01/2012
[Turn over
12
28
When a nonapeptide (containing nine amino acid residues) isolated from rat brains was
hydrolysed, it gave the following smaller peptides as identifiable products:
Gly-Ala-Phe
Ala-Leu-Val
Gly-Ala-Leu
Phe-Glu-His
His-Gly-Ala
What is the amino acid sequence in the nonapeptide?
A Gly-Ala-Leu-Val-Phe-Glu-His-Gly-Ala
B Phe-Glu-His-Gly-Ala-Leu-Val-Gly-Ala
C Gly-Ala-Phe-Glu-His-Gly-Ala-Leu-Val
D His-Gly-Ala-Phe-Glu-His-Leu-Val-Gly
29
A tripeptide, cys-ala-his, was analysed using electrophoresis. The tripeptide was

hydrolysed and the resulting solution was then placed at the centre of the plate in a
buffer solution of pH 6.5. A potential difference was then applied across the plate.
Amino acid
Isoelectric point
cysteine (cys)
alanine (ala)
histidine (his)
5.05
6.00
7.60
With reference to the above table, which of the following statements is correct?
A Alanine would remain at the centre of the plate.
B Cysteine would migrate towards the cathode.
C Histidine would migrate towards the anode.
D Alanine would migrate towards anode.
NJC/H2 Chem/01/2012
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13
30
The sequence below is the repeat unit of a polypeptide chain in egg albumin.
H
CH3
CH2C6H5
CH2OH
Which of the following will cause this part of the protein to coagulate?
I.
II.
III.
IV.
Addition of Pb(NO3)2(aq)
Heating in a frying pan
Addition of H2SO4(aq)
Whisking with an egg beater
A II and IV only
B I, II and III only
C II, III and IV only
D I, II, III and IV
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14
Section B
3 may be correct. Decide whether each of the statements is or is not correct (you may find it
helpful to put a tick against the statements that you consider to be correct.)
A
1,2, and 3 are

correct
1 and 2 only are

correct
2 and 3 only are

correct
1 only is correct
31
The table below gives the percentage of HX dissociated into H2 and X2 at different
temperatures.
Temperature/ oC
HF
HCl
HBr
HI
200
13
600
4 x 102
22
2000
6 x 105
4 x 101
30
Which of the following statements explain the data given?
32
The polarity of the HX bond becomes weaker on going down the group.
The s-p overlap in the HX bond is less efficient on going down the group.
The dissociation of HX is an endothermic reaction.
All the statements below are true.

Which of these can be explained, at least in part, by reference to hydrogen bonding?
1
Ice floats on water.
The boiling point of propan-2-ol is 82 C. The boiling point of propanone is 56 C.
At a specific temperature, the apparent relative molecular mass of ethanoic acid is

90.
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33
34
In which of the following does statement II give a correct explanation for statement I?
Statement I
Statement II
Ethanamide, CH3CONH2 is a
weaker base than methylamine,
CH3NH2.
The electronegativity of the oxygen atom of

the carbonyl group reduces the availability
of the lone pair of electrons on the nitrogen
atom in ethanamide.
The boiling point of ethanol is

higher than that of ethanethiol,
C2H5SH.
The ethanethiol molecule has a larger

electron cloud than ethanol.
The ionic product of water, Kw

increases
with
increasing
temperature.
H+(aq)
and
exothermically.
OH(aq)
ions
react

The graph below shows the variation in electromotive force (emf) of the
electrochemical cell with lg [ M+(aq) ] at 298 K.
Cu(s) | Cu2+ (aq, 1 mol dm-3) || M+ (aq) | M(s)
emf /V
(0, +0.46)
(0, 0)
lg [ M+(aq) ]
(-0.80, 0)
1
The Cu2+(aq)Cu(s) half cell is the negative pole.
The emf of the given cell under standard conditions will be +0.46V.
The standard electrode potential of the half cell M+(aq) | M(s) is +0.80V.
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16

A
1,2, and 3 are

correct
1 and 2 only are

correct
2 and 3 only are

correct
1 only is correct

35
The following two equations show two different partial ligand substitution reactions of
the hexaaquacopper(II) ion. (en represents 1,2-diaminoethane, H2NCH2CH2NH2)
DH= -54 kJ mol-1
I: [Cu(H2O)6]2+(aq) + en(aq) [Cu(en)(H2O)4]2+(aq) + 2H2O(l)
II: [Cu(H2O)6]2+(aq) + 2NH3(aq) [Cu(NH3)2(H2O)4]2+(aq) + 2H2O(l) DH= -46 kJ mol-1

Which of the following statements are correct?
36
The entropy change, DS, for reaction I is more positive than that for reaction II.
The stability constant of [Cu(en)(H2O)4]2+ is larger than that of [Cu(NH3)2(H2O)4]2+.
The cation formed in reaction II exhibits geometric isomerism.

The cell shown in the diagram below is set up under standard conditions.
V
X
Pt(s)
Y
Pt(s)
Salt Bridge
Q
1.0 mol dm3 Cr2O72(aq) in H+(aq)
1.0 mol dm3 Cr3+(aq)
1.0 mol dm3 Fe2+(aq)

1.0 mol dm3 Fe3+(aq)

1
Electrons will flow from Y to X through the meter.
The voltmeter reading will increase when aqueous KCN is added to beaker R.
The voltmeter reading will decrease when water is added to beaker Q.
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37

The methanoate anion and carbon dioxide can be simultaneously reduced to the
tartrate anion in alkaline medium. The standard electrode potential of this half-cell is
+ 0.20 V.
HO
O
2
+ 2CO2 + 4H2O + 6e
H3C
H
methanoate
OH
+ 6OH
-
O *C
C* O
O O
tartrate
38
The oxidation states of carbon are +4 and +2 in carbon dioxide and methanoate
respectively.
Tartrate can be oxidised to methanoate and carbon dioxide using aqueous iodine.
When 14CO2 is used in place of CO2, the asterisked carbon atoms (C*) in the
tartrate will be replaced with 14C.
Deuterium, D, is an isotope of hydrogen.

Which mixtures, on heating, produce an alkaline gas containing deuterium?
1
CH3CH2CONHCH3 and NaOD in D2O
(ND2H2)2SO4 and NaOD in D2O
C6H5CH2CN and DCl in D2O
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18

A
1,2, and 3 are

correct
1 and 2 only are

correct
2 and 3 only are

correct
1 only is correct
39
Pravastatin is a drug used to lower cholesterol in the blood.

O
HO
OH
OH
O
C
OH
CH3
40
It reacts with liquid bromine in tetrachloromethane to form a compound with 12

chiral centres.
It reacts with acidified potassium manganate(VII) under reflux to form one organic
product.
It reacts with 3 moles of hydrogen gas in the presence of nickel catalyst and heat.
Which of the following groups of compounds show an increasing rate of hydrolysis?

1
CH3CH2Cl, CH3CH2Br, CH3CH2I
CH3COONa, C6H5ONa, CH3CH2ONa
CH3CONH2, CH3COOCH3, CH3COCl
End of Paper
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19
SH2 Prelim Paper 1 Answers
11
21
31
12
22
32
13
23
33
14
24
34
15
25
35
16
26
36
17
27
37
18
28
38
19
29
39
10
20
30
40
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PRELIMINARY EXAMINATIONS
Higher 2
CANDIDATE
NAME
REGISTRATION
NUMBER
SUBJECT
CLASS
CHEMISTRY
9647/02
Paper 2 Structured
Fri 14 Sept 2012
Answer on the Question Paper.
2 hours
READ THE INSTRUCTIONS FIRST
For Examiners Use
Write your subject class, registration number and

name on all the work you hand in.
Write in dark blue or black ink in the spaces
provided.
You may use a soft pencil for any diagrams, graphs
or rough working.
Do not use paper clips, highlighters, glue or
correction fluid.
/12
/10
/18
/11
/6
/15
Total
/72
Answers all questions.
The number of marks is given in brackets [ ] at the

end of each question or part question.
2
1
Planning (P)
The hydroxides of Group I metals (LiOH, NaOH, KOH, RbOH, CsOH) are highly
corrosive white solids which rapidly absorb water vapour on exposure to the
atmosphere.
All of these solids dissolve exothermically in water.
The enthalpy change of solution, Hsoln, is the energy change associated with the
following reaction.
MOH(s) + (aq) M+(aq) + OH(aq)
where M represents the Group I metal.
Both lattice energy and hydration enthalpy play an important part in determining the
magnitude of Hsoln.
Lattice energy and hydration enthalpy are both more exothermic when ions carry higher
charges and/or ions have smaller radii.
When comparing Group I hydroxides, changes in Hhydration are more significant than
changes in lattice energy.
(a) Sketch the likely trend in Hsoln from LiOH to CsOH and explain your answer.
Hsoln
LiOH
NaOH
KOH
RbOH
CsOH
Explanation:
....
.......
. .....
[2]
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(b) Without considering heat loss, based on the information given, identify one possible
source of error in the experiment to determine Hsoln of the hydroxides of Group I
metals. State how you would minimise the effect of this source of error.
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[1]
(c) Identify a safety risk in the experiment and suggest how you would minimise it when
carrying out the experiment.
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[1]
(d) Given the enthalpy change of solution of lithium hydroxide is approximately

-21 kJ mol-1, describe the procedure you would carry out to find its enthalpy change of
solution.
Your plan should give a step-by-step description of the method, including appropriate
masses and volumes of reagents. You may use the apparatus normally found in a
school or college laboratory.
The following data may be of use in planning the details of your experiment.
Ar: Li, 6.9; O, 16.0; H, 1.0
4.3 J are required to raise the temperature of 1.0 cm3 of any solution by 1C.
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[4]
(e) A student was interested to investigate how the enthalpy change of neutralisation,
DHneutralisation, varies when acids such as hydrochloric acid, HCl and ethanedioic acid,
(CO2H)2 are neutralised with aqueous solutions of a Group I hydroxide such as RbOH.
The student proposed measuring the temperature change when each of the given acids
reacts with 30.0 cm3 of 2.0 mol dm-3 rubidium hydroxide.
Identify one aspect of the experimental procedure that must be kept the same to ensure
comparable results.
.............................................................................................................................................
.............................................................................................................................................
[1]
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5
(f)
(i) In each experiment, 30.0 cm3 of 2.0 mol dm3 RbOH is to be used.
There is to be an excess of rubidium hydroxide, RbOH.
For
Examiners
Use
Suggest appropriate volumes and concentrations for each of the acids to be used in
the individual experiments such that the experiments are equivalent.
Justify your answer with respect to ethanedioic acid with relevant working.
Complete the table below.
Acid
Volume
/ cm3
Concentration
/ mol dm-3
Hydrochloric acid
HCl
Ethanedioic acid
(CO2H)2
[2]
(ii) Show the mathematical expression for the enthalpy change of neutralisation of
rubidium hydroxide with ethanedioic acid, using the volume and concentration from
(f) (i) and T to represent the temperature change.
[1]
[Total:12]
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6
2
The Dissolved Oxygen Concentration (DOC) in rivers and lakes is important for aquatic
life. If DOC falls below 5 mg dm3, most species of fish cannot survive.
Environmental chemists can determine the DOC in water using the procedure below.
A sample of water is shaken with aqueous Mn2+ and aqueous alkali. The dissolved
oxygen oxidises the Mn2+ to Mn3+, forming a pale brown precipitate of Mn(OH)3.
O2(aq) + Mn2+ (aq) + 8 OH(aq) + 2 H2O(l) 4 Mn(OH)3 (s)
The Mn(OH)3 precipitate is then reacted with an excess of aqueous potassium iodide,
which is oxidised to iodine, I2.
2 Mn(OH)3 (s) + 2I I2(aq) + 2 Mn(OH)2 (s) + 2 OH(aq)
The iodine formed is then determined by titration using aqueous sodium thiosulfate,
Na2S2O3 (aq).
(a) A student decided to analyse the National Junior Colleges pond water using the above
procedure. The student found that a 20.0 cm3 sample of the pond water required
18.60 cm3 of 0.00100 mol dm3 of Na2S2O3 (aq) for titration.
(i) Calculate the DOC of the sample of pond water, in mg dm3.
DOC = mg dm3
(ii) Comment on whether there is enough dissolved oxygen in the pond water for the
carps to survive.
....
....
[4]
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(b) Another d-block element, rhenium is similar in many ways to manganese. The standard
electrode potential E for the change between 2 oxidation states of rhenium is + 0.3V.
ReO4 (aq) + 4H+(aq) + 3e
ReO2(s) + 2H2O(l)
ReO4(aq) is colourless while ReO2 is a dark solid.

(i)
Draw a fully labelled diagram for the apparatus that can be used to determine this
standard electrode potential.
[3]
(ii) Using the Data Booklet, show that a reaction occurs when an aqueous solution
containing sodium sulfite, Na2SO3 is added to aqueous ammonium perrhenate,
NH4ReO4.
Describe the observation(s) and write a balanced equation for the reaction.
....
....
....
....
[3]
[Total: 10]
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8
3
Copper, silver and gold share certain attributes: they have one s-orbital electron in
addition to a filled d-shell. The filled d-shells in these elements do not contribute much to
the interatomic interactions, which are dominated by the s-electrons through metallic
bonds. Contrary to metals with incomplete d-shells, metallic bonds in copper are
relatively weak. Thus pure copper is soft and malleable.
Alloys are made to alter the mechanical properties of copper, to induce hardness and
ductility. Brass and bronze are typical substitutional alloys in which some of the copper
atoms are substituted by zinc in the former, and by tin in the latter.
The table below gives the hardness of copper and these two alloys as measured on the
Brinell Scale.
Hardness
copper
brass
bronze
42
114
241
(a) Using relevant information from the Data Booklet, account for the difference in the
hardness of copper, brass and bronze.
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[3]
(b) Although both copper and zinc are 3-d elements, zinc is not classified as a transition
metal. Explain why zinc is not classified as a transition metal.
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[1]
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9
(c)
Copper forms compounds with variable oxidation states. Copper(I) compounds are
unstable in water. The following flow scheme shows the reactions between different
compounds of copper.
copper(I) sulfate
white solid
H2O,
filter
pink solid
D
blue solution
E
conc. HCl
yellow solution
G
excess RNH2 (aq),

where R is an alkyl group
deep blue solution

F
(i)
State the type of reaction between copper(I) sulfate and water. Using relevant data
from the Data Booklet, explain why this reaction occurs.
....
....
....
....
(ii) Give the formulae of the complex ions in F and G.

F:
G:
(iii) When solution G was diluted with water, it changed from yellow to green and finally
blue. Explain the colour changes.
....
....
....
[7]
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10
(iv) Describe what you would observe when potassium iodide solution is added to
solution E. Write an equation for the reaction that occurs.
....
....
....
(v) Explain why solution E is blue.

....
....
....
....
....
....
....
[5]
(d)
Copper has remarkable resistance to corrosion. However, many well-known architectural

structures built with copper, such as the Statue of Liberty in the United States and the
Royal Observatory in Edinburgh, on centuries of exposure to the elements, appear
green due to the formation of the basic carbonate, Cu(OH)2.CuCO3.
Explain the formation of the basic copper carbonate.
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[2]
[Total:18]
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11
4 (a) Aspartic acid, HO2CCH2CH(NH2)CO2H, is one of the two acidic essential amino acids.
A 25.0 cm3 solution of fully protonated aspartic acid, HO2CCH2CH(NH3+)CO2H, is titrated
with 0.500 mol dm3 NaOH (aq). The titration curve is shown below. The label E1, E2
and E3 denotes equivalence point 1, 2 and 3 respectively.
Vol of NaOH(aq)
added / cm3
(i)
The species present at E1 is HO2CCH2CH(NH3+)CO2 . Identify the species present

at E2 and E3.
(ii) The equation for the first acid dissociation constant, Ka1, of the fully protonated
aspartic acid can be written as follows:
HO2CCH2CH(NH3+)CO2H
HO2CCH2CH(NH3+)CO2 + H+
Using the titration curve, determine Ka1.
Ka1 = mol dm3

NJC/H2 Chem/02/2012
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12
For
Examiners
Use
(iii) Explain why the shape of the graph at E3 differs from that at E1.
....
....
....
....
(iv) At pH = 4.0, the mixture can act as a buffer. Identify the two species present in this
buffer and calculate the ratio of the concentrations of these two species at this pH.
[8]
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13
(b) Papain, an enzyme in fresh papaya juice is used as a meat tenderiser. It is responsible
for catalysing the hydrolysis of certain proteins in muscle tissues, causing the tough
meats to soften during the cooking process.
Papain is a relatively heat resistant enzyme, with an optimal temperature range of
60-70 C. The three main amino acids involved in the catalytic activity of papain are
His48, Asp102 and Ser185.
The first stage in the mechanism of the action of papain is illustrated in the figure below.
peptide chain
N
N
asp
O-
his
papain enzyme
ser
OH
NH
asp
his
R'
O-
ser
papain enzyme
(i) Name the region of the papain enzyme that is illustrated above.
....
(ii) With reference to the figure above, explain why the action of this enzyme would be
inhibited if the pH was too low.
....
....
....
....
....
[3]
[Total:11]
NJC/H2 Chem/02/2012
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14
5
OH
O
CH3
For
Examiners
Use
O
CH2
CH2NH2
CH2CH3
Q
(i)
Name the four functional groups in compound Q, other than the phenyl group.
1)
2)
3)
4)
(ii) Draw the structural formulae of the compound(s) when compound Q is treated with
o
Cold HCl(aq)
Hot NaOH (aq)
[6]
[Total:6]
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15
6 (a) 2-methylpropane reacts with Br2 to give a mixture in which the major products are two
monobrominated alkanes.
CH3
CH3
CH3
CH3
(i)
CH3
CH3
CH2Br
CH3
Br
63%
37%
CH3
State the conditions required for this reaction.

....
(ii) Outline the mechanism for the formation of 1-bromo-2-methylpropane from

2-methylpropane under the conditions stated in (i).
(iii) Discuss two factors which are responsible for the observed percentages of the two
monobrominated alkanes.
....
....
....
....
....
[6]
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16
(b) 1-bromo-2-methylpropane undergoes a series of reactions as shown by the given flow
scheme.
CH3
compound V
CH3
CH2Br
compound S
Step 1
Step 2
hot KMnO4/ H+
OH
COOH
compound T
compound U
C13H10O2
(i)
Step 3
NaOH
State the conditions needed for step 1.

....
(ii) Explain as fully as you can why the conditions you stated in (i) are required.
....
....
....
(iii) Draw the structures of compounds S, T and U in the boxes provided below.
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17
(iii) When an alkaline solution of complexed Cu2+(aq) is added to compound V, a
reddish-brown precipitate is observed.
Propose a 2-step synthesis for compound V from 1-bromo-2-methylpropane.
[9]
[Total:15]
End of Paper
NJC/H2 Chem/02/2012
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18
NJC/H2 Chem/02/2012
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NJC H2 Chemistry Prelim Solutions

Solutions to Paper 2
1
(a)
(i)
LiOH NaOH KOH RbOH CsOH
[1/2]
Size of cations increases down Group II, heat of hydration of cation less
exothermic [1/2]
Most students can score these two marks. The students who drew an increasing line
above the x-axis were awarded one upon two.
Common mistakes
It is clearly stated in the question that all of the heats of solution are exothermic.
Many students did not seem to notice that, judging from their answers. Their lines
were above the x-axis.
It is nH(hyd), not just nH(hyd)!
A lot of students, while getting the full credit for the graph, failed to include the
equation in their explanation.
(b)
The group I hydroxides are all hygroscopic. [1/2] Weigh the solid out promptly so as to
minimise its exposure to air. [1/2]
(c)
Wear gloves. [1/2] The chemicals are corrosive. [1/2]

Common mistakes
(d)
Toxicity is not the same as corrosiveness!

Grammar! A pair of gloves, not just a glove! If you were to use just one glove, wont
your other hand get corroded? A pair of googles, not just a goggle! If you were to
use just one goggle, how are you going to wear it? Hold it over your eye?
Procedure
Major points [1/2 each, maximum 2]
Measure the initial temperature of the temperature of the water.

Measure the highest/maximum temperature reached. (No marks if temperature is
lowest/minimum; ECF according to answer to (a)).
Measuring cylinder to measure out the water.
Weigh mass of the residue and weighing bottle after adding the LiOH into the cup.
Minor points [1/2 each, maximum 1]
Weigh out LiOH using a weighing bottle.

Cup to be supported with a beaker.
Repeat the experiment until two
values are within 5 % of each other. m has to
be specified as the mass of the solid.

Preliminary calculations [1]
Justify mass of LiOH weighed out. [NOTE: The capacity of the cup must be
stated, otherwise at most half a mark will be awarded.]
[Set
]
where m is between 50 to 90 % of the stated capacity of cup.
Simplifying,
If the capacity of the cup is 100 cm3 and filling 90 % of it, then
(e)
Volumes of the two solutions are the same/same setup/same apparatus [1]
(f)
(i)
for both experiments.

and
(Check:
(a)(i)
n(O2) =
[O2] = (
[O2] = (
(a)(ii)
no. of moles of H2SO4 half that of CH3COOH.

total volume not more than 90% of capacity of cup and not less than 50% of
capacity of cup.
acids are the limiting reagents i.e. C1V1 < 60 and C2V2 < 30.
n(S2O32-) =
(
)
)
)=
=
[2]
moldm-3 [1/2]
= 7.44 mgdm-3 [1/2]
The carps will be able to survive. (Justification).

(b)(i)
(ii)
2H+ + 3SO32- + 2ReO4-
H2O + 3SO42- + 2ReO2
[1]
Ecell0 = (0.3 0.17) V = 0.13 V > 0 [1]

Dark solid forms. [1]
3(a) Copper, brass and bronze all have metallic bonds. Copper is a pure metal made up of Cu2+ ions
(0.069nm) arranged in a orderly metallic lattice. Brass and bronze are alloys and the presence of
metal ions of different sizes disrupts the orderly metallic lattice. Ionic radius of Sn2+ ion (0.112nm) is
bigger than ionic radius of Zn2+ ions (0.074nm) and the bigger ions Sn2+ will disrupt the orderly
metallic lattice more significantly. The greater extent of disruption of the orderly lattice makes it more
difficult for the layers of atoms to slide over each other, leading to greater hardness.
Or
Copper gives out 1 electron to the sea of electron, zinc gives out 2 while tin gives out 4. Ionic radius of
Cu+ is approximately 0.069nm, Zn2+ is 0.074nm and Sn4+ is approximately 0.112nm. Charge/size of
Cu+ is lowest, followed by Zn2+ and Sn4+. The metallic bond is weakest in Cu followed by Zn and Sn.
Therefore, greater force is needed for the layers of atom to slide over each other in Brass and bronze.
3(b) Zinc does not form any ions that have partially filled 3d orbital.
3(c) (i) Type of reaction: Disproportionation

Cu+
Cu+ + e
Cu2+ + e
Eox = 0.15V
Cu
Ered = +0.52V
Ecell = +0.520.15 = 0.37V > 0, reaction is feasible.

(ii) F: [Cu(RNH2)4]2+
G: [CuCl4]2
(iii) [CuCl4]2 + 6H2O
[Cu(H2O)6]2+ + 4Cl
(iv) Cream precipitate in brown solution.

2Cu2+ + 4I
2CuI + I2
(v) Cu2+ has partially filled 3d orbitals. When ligands approach, the 3d orbitals of Cu2+ are splitted into
2 different energy levels. When an electron is promoted from lower energy 3d orbital to higher energy
3d orbital, an energy corresponding to the wavelength in the visible region is absorbed. The
complementary colour of the wavelength absorbed is blue.
(d) When copper is exposed to air, it is oxidized to CuO. When CuO reacts with the moisture in the
air, Cu(OH)2 is formed. Some of the Cu(OH)2 reacts with CO2 in the air to form CuCO3. This leads to
the formation of Cu(OH)2.CuCO3.
or
When copper is exposed to air, it is oxidized to CuO. Some of the CuO reacts with the moisture in the
air forming Cu(OH)2 while some of the CuO reacts with CO2 in the air forming CuCO3. This leads to
the formation of Cu(OH)2.CuCO3.
4(a) (i) E2: O2CCH2CH(NH3+)CO2
E3: O2CCH2CH(NH2)CO2
(ii) pKa1 = 2.11

Ka1 = 102.11 = 7.76 x 103
(iii) E1: The solution present at E1 can act as a buffer and the pH change is relatively small when
small amount of NaOH(aq) is added.
E3: The solution present at E3 is a salt and when small amount of NaOH(aq) is added, there is a
large increase in pH due to OH from NaOH.
Or
E1: At E1, the species still have H+ available to neutralize OH, however, at E3, the species present
does not have any H+ to neutralize OH from NaOH, hence, the large increase in pH is due to the OH
from NaOH.
(iv) the two species present are HO2CCH2CH(NH3+)CO2 and O2CCH2CH(NH3+)CO2
Salt: O2CCH2CH(NH3+)CO2
Acid: HO2CCH2CH(NH3+)CO2
[salt ]
)
[acid]
[salt ]
4 =3.86 lg(
)
[acid]
[salt ]
) = 1.38
[acid]
pH = pKa lg(
(b) (i) Active site

(ii) When pH is low, the concentration of H+ from the solution is high, COO of asp will be protonated
to form COOH. Therefore, no lone pair is available to abstract H+ from his and subsequent electron

transfer cannot happen. The will not be O: on ser to act as a nucleophile to attack the + C of the
peptide bond to bring about hydrolysis.
5(i)
1. Primary amine
2. Tertiary alcohol
3. amide
4. ester
(ii) cold HCl(aq)
OH
O
H3C
CH2 N
CH2NH3
CH2CH3
Hot NaOH(aq)
CH3CO2Na
CH3CH2CO2Na
OH
NaO
CH2 NH2
CH2NH2
6 (a) (i)
Limited Br2 or excess alkane and ultraviolet light/ sunlight/ heat
(ii) Free radical substitution [1]

Initiation
Br
uv
Br
2 Br
Propagation
CH3
CH3 H
CH3
H +
Br
CH3
HBr
Br
CH3 Br
CH3
CH3
H +
Br2
CH3
Termination

CH3
2 CH3
2 Br
CH3
CH3 H
CH3
CH3
Br2
(iii) There are 9 primary H atoms available for substitution to form 1-bromo-2-methylpropane
compared to 4 secondary H atoms to form 2-bromo-2-methylpropane.By equal probability of
substitution, expected ratio of 1-bromo-2-methylpropane : 2-bromo-2-methylpropane is 9 : 1
However, a tertiary radical, C(CH3)3, is more stable than a primary radical, CH2CH(CH3)2 due to
the electro-donating effects of the alkyl groups. More tertiary radicals are formed, giving rise to
more 2-bromo-2-methylpropane formed. Thus the observed percentages.
(b) (i)
(ii)
AlBr3 or FeBr3 or AlCl3 or FeCl3 , anhydrous

The Lewis acid catalyst is required to form a strong electrophile (CH3)2CHCH2+ [1] to react
with the aromatic /resonance stabilised benzene.
AlBr3 use a vacant orbital of Al to accept/extract a lone pair/ Br. [1]
OR
OR
AlBr3 + R-Br AlBr4 + R+ [1]

AlCl3 or AlBr3 will dissolve in water and be hydrolysed, hence unable to act as a Lewis acid
catalyst.
(iii)
CH3
H
CH3
O
Cl
O
O C
(iv)
CH3
CH3
CH3 O
K2Cr2O7, dil H2SO4
NaOH(aq), heat
CH3
C
H
CH2Br
CH3
C
H
CH2OH
heat with immediate

distillation
CH3

Higher 2
CANDIDATE
NAME
REGISTRATION
NUMBER
SUBJECT
CLASS
CHEMISTRY
9647/03
Paper 3 Free response
Tues 18 Sep 2012

2 hours

Start your answer to each question on a fresh piece of paper.
The number of marks is given in brackets [
question.
] at the end of each question or part
At the end of the examination, fasten all your work securely behind the cover page.
This paper consists of 13 printed pages including 1 blank page.
2
1 (a)
The graph below shows the variation of pV versus p for NH3, which exists as a gas under
normal room conditions.
pV / J
D
NH3
Ideal gas
C
B
p / atm
Explain the shape of the graph, commenting on the behaviour of NH3 gas as an ideal gas at
A, B, C and D.
[3]
(b)
Ammonia is manufactured by the Haber Process, using gaseous nitrogen and hydrogen.
3H2(g) + N2(g)
2NH3(g)
DH = 92.4 kJ mol1
In an experiment starting with a 3:1 ratio of H2 and N2 mixture at 400 oC and a constant
total pressure of 200 atm in the presence of iron catalyst, the equilibrium mixture was found
to contain 36.3 % by volume of ammonia.
(i)
Justify the conditions of temperature and pressure used.
(ii)
Write an expression for Kp of this reaction.
(iii) Calculate the partial pressures of each of these three gases at equilibrium, and hence
calculate Kp at this temperature, stating its units.
[6]
(c)
Hydrazine, NH2NH2 , is a flammable liquid with ammonia-like odour. It has basic chemical
properties like ammonia.
Compound
NH2NH2
NH3
Kb / mol dm3
1.3 x 106
1.8 x 105
Explain the difference in the Kb values of these two compounds.

[2]
NJC/H2 Chem/03/2012
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3
1 (d)
Hydrazine is miscible with water but immiscible with trichloromethane.

(i)
Explain, in terms of bonding, and with appropriate diagrams to illustrate, the

difference in the miscibilities of hydrazine with the two stated solvents.
(ii)
Hydrazine hydrate, made from hydrazine, takes part in the following reaction:
NH2NH2.H2O + IO3 + 2H+ + Cl N2 + ICl + 4H2O
Calculate the change in the oxidation states of the species oxidised.
[4]
(e)
Hydrazines are part of many organic syntheses and undergo condensation reactions with
carbonyl compounds. Below is a scheme showing some reactions of phenylethanone,
which includes the reaction mentioned.
COCH3
CompoundEA
Compound
NH2NH2
H2 /Ni
high
T,temp
P and
pressure
Compound CG
Compound
phenylethanone
phenylethanone
ReagentX X
Reagent
sodium
benzoate
Compound
sodium
benzoate
+ Compound
F B
(i)
Draw the structural formulae of Compounds E, F and G.
(ii) State what Reagent X is, and give the conditions under which the reaction will take
place.
[4]
(f)
Hydrazine reacts in a similar way with an isomer of phenylethanone, H. H is also a

monosubstituted benzene like phenylethanone. Suggest the identity of H.
[1]
[Total: 20]
NJC/H2 Chem/03/2012
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4
The Group II element, barium, was first isolated by Sir Humphry Davy, a British chemist
and inventor in the nineteenth century. Besides being used widely in pyrotechnics, barium
is also used in the production of hydrogen peroxide, a colourless liquid with a boiling point
of 150 C.
Hydrogen peroxide was originally produced commercially in a two-stage process. In the

first stage, barium was heated in air to form barium peroxide. In the second stage, barium
peroxide was added to aqueous nitric acid. The equations for the reactions are shown
below.
(a)
Stage 1:
Ba(s) + O2(g) BaO2(s)
Stage 2:
BaO2(s) + 2HNO3(aq) H2O2(aq) + Ba(NO3)2(aq)
(i)
Suggest one method of separating hydrogen peroxide from the reaction mixture in
Stage 2.
(ii) Suggest one reason why nitric acid was eventually replaced by sulfuric acid in Stage 2
to lower the cost of this commercial production.
(iii) Draw the dot-and-cross diagram for barium peroxide.
[3]
(b)
(i)
Write an equation for the reaction of barium with water.
(ii) Would the reaction in (i) occur more or less vigorously than that for magnesium?
Justify your answer by quoting relevant data from the Data Booklet.
[3]
(c)
Although Group II elements can form many compounds, the standard enthalpy of formation
of solid barium chloride cannot be obtained directly.
(i)
Define the term standard enthalpy of formation of barium chloride.
(ii) Given the standard enthalpy change of solution of barium chloride is

-13.2 kJ mol-1, write a thermochemical equation to represent the standard enthalpy
change of solution of barium chloride.
NJC/H2 Chem/03/2012
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5
2 (c) (iii) Using the information from (ii) and the following data:
DH / kJ mol-1
Reaction
Ba(OH)2(aq) + 2HCl(aq) BaCl2(aq) + 2H2O(l)
-114.4
H2(g) + O2(g) H2O(l)
-285.9
H2(g) + Cl2(g) HCl(g)
-92.3
HCl(g) + aq HCl(aq)
-71.9
Ba(s) + O2(g) + H2(g) + aq Ba(OH)2(aq)
-1002
draw an appropriate energy cycle and use it to calculate the enthalpy change of
formation of solid barium chloride.
(iv) Use the following entropy data and your answer to (iii),
S /J K-1 mol-1
BaCl2 (s)
Ba(s)
Cl2(g)
124
63
223
calculate the lowest temperature at which the following reaction becomes feasible.
BaCl2(s) Ba(s) + Cl2(g)
[9]
(d)
Catalytic poisoning is normally undesirable as it results in a loss of the usefulness of

expensive metals like platinum and palladium. However, poisoning of a catalyst can be
used to enhance selectivities of some reactions.
An example of such practice is seen in the Rosenmund reduction where carbonyl
compounds are produced. The palladium catalyst required for this reduction reaction is
poisoned with barium sulfate.
The scheme below shows a 4step synthesis of compound G which has the molecular
formula C3H9ON. One of the steps involves the Rosenmund reduction.
CH3COOH
SOCl2
H2 /Pd
BaSO4
HCN
Step (i)
G
C3H9ON
Give the structural formulae of compounds D G and the reagent(s) and conditions
required for Step (i).
[5]
[Total: 20]
NJC/H2 Chem/03/2012
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6
3 (a) In the Clemmensen reaction, zinc is used, along with hydrochloric acid, for the reduction of
a carbonyl compound into an alkane.
H
O
Zn, HC
HCll
Zn,
C
heat
R'
R'
Clemmensen reaction
W and X are carbonyl compounds which undergo Clemmensen reaction to form the same
alkane, Y. W is an optically active compound but X and Y are not. Only W forms a silver
mirror with Tollens reagent. 0.3 mol of Y burns in excess oxygen to produce 33.6 dm3 of
CO2 at standard temperature and pressure.
Calculate the number of moles of CO2 produced, and hence deduce the possible structures
of W, X and Y.
[4]
(b) Compound J has molecular formula of C4H7Cl and exhibits the following properties:
-
J reacts with acidified potassium manganate(VII), giving effervescence of a

colourless gas.
J reacts with ethanolic potassium cyanide to produce compound K with molecular

formula C5H7N.
J rotates plane-polarised light.
Draw the displayed formula for J. Explain how the identity you suggest for J fits in with the
reactions described above.
[3]
(c)
A number of experiments were carried out at constant pressure and temperature in which
compound J was reacted with ethanolic potassium cyanide. The concentrations of
compound J and ethanolic potassium cyanide were varied and the results are as shown
below:
Experiment
Number
[J]
/ mol dm-3
[KCN]
/ mol dm-3
Initial rate of formation of product

/ mol dm-3 min-1
1
2
3
0.10
0.30
0.20
0.10
0.10
0.20
0.015
0.045
0.030
NJC/H2 Chem/03/2012
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7
3 (c) (i) Deduce the rate equation for the reaction between J and potassium cyanide.
Hence, describe the mechanism for this reaction, showing any relevant charges, lone
pairs of electrons and movement of electrons.
(ii) It is common to plot a graph of concentration against time to determine the rate law for
a reaction. This approach works well for simple systems with numerically exact data.
However, in practice, experimental data suffers from random errors, making it difficult
to determine the gradient or slope accurately.
A better approach is to make characteristic kinetics plots based on the integrated rate
law:
Reaction order
Integrated rate law
zero
[A] = [A]o - kt
first
ln [A] = ln [A]o - kt
second
1
1
=
+ kt
[A] o
[A]
Note:
[A] = conc of a reactant at any moment of time
[A]o = initial concentration of that reactant
t = time since reaction started
Based on the information given and your answer to c(i), sketch a graph for the reaction
of J with potassium cyanide and show how the rate constant for the reaction could be
determined from it.
[7]
(d) In the above reaction between J and potassium cyanide, ethanol was used as the solvent.
Another similar reaction was carried out using propanone as the solvent and the rate
constant, k, for this experiment was found to be 1.50 mol1 dm3 min1.
(i) State the overall order of reaction when propanone is used as the solvent.
(ii) Explain why the mechanism described in c(i) was favoured when ethanol was used as
the solvent instead of propanone.
[3]
(e) With the aid of a suitable diagram, state and explain how the rate of a reaction will change
when temperature is decreased.
[3]
[Total: 20]
NJC/H2 Chem/03/2012
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8
4
(a)
This question describes two methods for the syntheses of organic compounds which have
one carbon atom fewer than the starting material.
One method is the Hoffmann degradation whereby treating a primary amide with aqueous
alkaline bromine produces a primary amine.
R-CONH2
Br2+ OH-
R-NH2
The Hoffmann degradation can be used as the last step in the following synthesis of
phenylamine from benzoyl chloride.
COCl
NH2
Step I
Br2+ OHStep II
benzoyl chloride
(i)
phenylamine
Suggest reagents and conditions for Step I and the structure of compound P.
(ii) Suggest a route to prepare phenylamine from benzene.

(iii) Give a test (stating reagents and observations) that would enable you to distinguish
phenol from phenylamine.
[6]
(b)
Another method is decarboxylation whereby a carboxylic acid loses CO2.

In 1849, the German chemist Kolbe first published a method describing the preparation of
an alkane from the electrolysis of the sodium or potassium salt of a carboxylic acid. The
reaction occurs via the formation of radicals.
The following steps summarise the preparation of ethane using an aqueous solution of
potassium ethanoate:
Step 1
CH3COO CH3COO + e
Anode reaction
Step 2
CH3COO CH3 + CO2
Decarboxylation
Step 3
2 CH3 CH3CH3
Dimerization
(i)
What do you understand by the term radical ?
(ii) Draw the dot-and-cross diagram of the radical in Step 1, and predict the OCO bond
angle.
(iii) Write the half equation for the cathode reaction.
NJC/H2 Chem/03/2012
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9
(b) (iv)
In the electrolysis of an aqueous solution containing 2.43 g of potassium ethanoate at

1 atm pressure and 28 oC, 200 cm3 of ethane gas was collected. Calculate
(I)
the percentage yield of ethane in this electrolysis.
(II) the time for this electrolysis if a current of 0.5 A was used.
[9]
(c)
In the electrolysis of potassium butanoate solution, hexane (b.p. 63 oC) was formed
together with its isomer P (b.p. 58 oC). Account for
(i)
the identity of P and its formation.
(ii) the difference in the boiling points of the isomers.

[4]
(d)
Another electrolysis was carried out using a mixture of potassium ethanoate and potassium
methanoate solution.
Draw the structure(s) of the organic product(s) formed.
[1]
[Total: 20]
NJC/H2 Chem/03/2012
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10
5 (a) The typical oxides of tin and lead are SnO, SnO2, PbO and PbO2.
The following two generalisations can be made about the oxides of the elements in
Group IV of the Periodic Table.
As the metallic character of the elements increases down the Group, the oxides become
more basic.
The oxides of the elements in their higher oxidation states are more acidic than the oxides
of the elements in their lower oxidation states.
(i)
Use these generalisations to suggest which of the above oxides of tin or lead is
the most
acidic
basic
(ii) PbO is found to be amphoteric. Write a balanced equation, with state symbols, for its
reaction with aqueous NaOH.
[3]
(b)
0.00425g of lead(II) sulfate can dissolve in 100 cm3 of deionised water at 25 C.

(i) What is the solubility, in mol dm3, of lead(II) sulfate in deionised water at 25 C?
(ii) Determine the solubility product of lead(II) sulfate at 25 C.
(iii) How would you expect the solubility of lead(II) sulfate to differ from the calculated
value in (i) when it is dissolved in potassium sulfate solution? Explain your answer.
[5]
(c)
The table below gives the melting points of CO2, SiO2 and PbO.
Melting point/ C
CO2
-78
SiO2
1610
PbO
888
In terms of structure and bonding, explain the difference in the melting points of
(i)
CO2 and SiO2
(ii) SiO2 and PbO

[3]
NJC/H2 Chem/03/2012
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11
(d) Styrene is used for making polystyrene, a common plastic material.
CH
CH2
polystyrene
The pathway below shows the production of styrene from compound R.
Cl
Cl
NaOH(aq)
heat
Compound S + H2O
NaBH4
in methanol
R
II
Step II
Compound T
I
Step I
CH2CHCl2
CH
CH2
NO2
styrene
CH3Cl, AlCl3
Compound U
(i)
Suggest reagents and conditions for steps I and II and the structures of compounds
S and T.
(ii)
Give the structural formula for U. Explain clearly why you placed the new functional
group in its particular position.
(iii)
Suggest how styrene will react with cold alkaline KMnO4, giving the observations and
the organic product(s) formed.
(iv)
What is the major product formed when styrene reacts with iodine monochloride,
ICl?
[9]
[Total: 20]
NJC/H2 Chem/03/2012
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12
Blank Page
NJC/H2 Chem/03/2012
[Turn over
13

Higher 2
CANDIDATE NAME
REGISTRATION NUMBER
SUBJECT CLASS
H2 CHEMISTRY
9647/03
Tues 18 Sep 2012

TIME: 2 hour
Cover page for Paper 3

Staple this cover page in front of your writing paper.
Please circle the question numbers which you have attempted.
Question
For Examiners Use
Total
NJC/H2 Chem/03/2012
[Turn over
NJC SH2 Preliminary Examinations Paper 3 Solutions
1(a)
Pressure is approximately zero at A

Volume occupied by gas particles is small compared to the volume of the
container
\NH3 is almost an ideal gas.
Low pressure at B, intermolecular attractions are dominant, thus NH3
molecules are pulled closer together. This reduces the impact on wall collisions
and makes them softer. PNH3 < Pideal , hence the negative deviation. Volume
occupied by gas particles is still relatively small compared to container.
High pressure at D, mainly repulsion between particles. The volume of the
molecules becomes a significant fraction of the volume of the container, and
thus is no longer negligible. VNH3> Videal, hence the positive deviation.
At C, NH3 appears to follow the ideal gas equation, because the two deviations
balance out.
1(b)(i)
A relatively low temperature of 400 oC is used to increase the yield of the

exothermic reaction. Iron catalyst is used to compensate for any reduction in
rate due to the low temperature used.
A high pressure of 200 atm caters to the forward reaction, which is
accompanied by a reduction in volume. Pressure exceeding 200 atm would
increase the cost of production.
1(b)(iii) PNH3 = 0.363 x 200 = 72.6 atm

PH2 = 0.47775 x 200 = 95.55 atm
PN2 = 0.15925 x 200 = 31.85 atm
Kp = = 1.90 x 10-4 atm-2
1(c)
1(d)(i)
The - NH2 in hydrazine has a stronger electron-withdrawing effect than the H

in ammonia
\the lone pair of electrons in ammonia is more available for donation to a
proton
\ the stronger base & the bigger Kb value
Hydrazine and water form a miscible mixture
Free intermingling of the molecules of hydrazine & water through mutual
H-bonding
\ Exists as a homogeneous phase
d+
H
d
dH
N N
d
d+
H
d
H
O
d
d
H
H
H
N N
dH
d+
H
O d+
H
d H
d+
H
d
H
d+ H
d
H
H
d
H
O d+
d N d
H
H
H
d+
H-bond
Hydrazine and trichloromethane are immiscible

Segregation between the molecules of hydrazine & trichloromethane into 2
distinct layers
NH2NH2 have strong H-bond with one another
CHCl3 have van der Waals attraction for one another

Each cannot establish any significant attraction for the other and will be
squeezed out from one anothers layer
H
H
N
H
H
N
H
N
H-bond
H
N
H
N
H
_________________________________________Phase boundary
H
Cl
d+
C
Cl Cl
d-
Van der Waals forces
1(d)(ii)
-2 oxidation state in N of hydrazine is oxidized to 0 in N2
1(e)(i)
H2NN
CH(OH)CH3
CH3
CHI3
Compound E
Compound F
Compound G
1(e)(ii) Reagent X is I2(aq) with NaOH(aq); and the reaction mixture is warmed.
1(f)
CH2CHO
Compound H
a (i) Distillation and collect the distillate that boils over at 150 OC.
(ii) Solid BaSO4 will be formed and it can be removed by filtration.
(iii)
2
Ba +
2
o O O o

b (i) Ba + 2H2O Ba(OH)2 + H2

(ii) Reaction in b(i) involves the reduction of water by the group II metals.
Reaction is more vigorous with barium as barium is a stronger reducing
agent than magnesium as evidenced by the following data:
Mg Mg2+ + 2e
Ba Ba2+ + 2e
Eooxid = +2.38V
Eooxid = +2.90V
c (i) Standard enthalpy of formation of barium chloride is the heat change or

enthalpy change when 1 mole of solid barium chloride is formed from its
elements in their standard states ( 25oC and 1 atmosphere) i,e, formed from
barium solid and chlorine gas.
(ii) BaCl2(s) + aq Ba2+(aq) + 2Cl-(aq)
(iii)
Ba(s) + Cl2(g) + O2(g) + 2H2(g)
DHf
DH = -13.2 kJ mol-1
BaCl2(s) + O2(g) + 2H2(g)
+ aq
(-1002
)
2
(-285.9)
BaCl2(s) + 2H2O(l)
Ba(OH)2(aq) + Cl2(g) +
H2(g)
2 (-92.3)
+aq
(-13.2)
Ba(OH)2(aq) + 2HCl(g)
+aq
2 (-71.9)
Ba(OH)2 (aq) + 2HCl(aq)
(-114.4)
BaCl2 (aq) + 2H2O(l)
Using Hess Law,

DHf + 2(-285.9) + (-13.2) = (-1002) + 2(-92.3) + 2(-71.9) + (-114.4)
DHf = - 859.8 kJ mol-1
= - 860 kJ mol-1
(iii)
BaCl2(s) Ba(s) + Cl2(g)

Using DS = SSproducts - Sreactants
= (63 + 223) - (124) = + 162 JK-1 mol-1
For the reaction to be feasible, DG = DH - TDS must be less than zero.
= 5307K
Lowest temp for the reaction to be feasible is 5307K.
D: CH3COCl
E: CH3CHO
H
F: CH3C CN
G: CH3C CH2NH2
OH
OH
Reagents and conditions for step (i):

LiAlH4 in dry ether or H2 with Pt as catalyst
(a)
W contains chiral carbon.

W is an aldehyde.
No of moles of CO2 =
33.6
= 1.50 mol
22.4
nY : n CO2
0.3 : 1.50
1:5
Y contains 5 carbon atoms.
Structure of W:
CH3
Structure of Y:
CH3 H
Structure of X:
(b)
CH3
Observations
J has molecular formula of C4H7Cl.
J reacts with acidified potassium
manganate(VII), giving effervescence
of a colourless gas.
J reacts with ethanolic potassium
cyanide to produce compound K with
molecular formula C5H7N.
Deductions
J is a halogenoalkane.
J undergoes oxidative cleavage.
J contains terminal alkene.
J undergoes nucleophilic substitution
of Cl with CN.
J contains a chiral carbon.
Displayed formula of J:
H
H
C
C
Cl
H
H
C
C
(c)
(i) Comparing Expt 1 & 2, when [J] triples while [KCN] is kept constant, initial
rate of formation of product triples. Hence, reaction is first order wrt J.
Comparing Expt 1 & 3, when [J] doubles and [KCN] doubles, initial rate of
formation of product only doubles. Hence, reaction is zero order wrt KCN.
Rate = k[J]
Mechanism:
Nucleophilic Substitution (SN1)
Step 1:
CH3
CH3
slow
d+
C
d- Cl
C
H
Cl
H
CHCH2
CHCH2
Step 2:
CH3
CH3
fast
+
C
H
CHCH2
CN
C
CN
CHCH2
(ii)
In[J]
In[J]o
Time
In[J] = In[J]o kt
In[J] = kt + In[J]o
[y = mx + c]
Hence, rate constant = gradient
(d)
(i) overall order = 2
(ii)
Ethanol is more polar than propanone, stabilizes carbocation to a greater

extent through formation of stronger ion-dipole interactions. Hence SN1
mechanism is favoured when ethanol is used as the solvent.
(e)
Fraction of molecules
T2
where T2 < T1
T1
Energy
Ea
Legend:
fraction of molecules having energy Ea at T1

fraction of molecules having energy Ea at T2
At a lower temperature T2, the fraction of molecules having energy greater than
or equal to Ea decreases, from
to
Hence, the number of effective collisions decreases and rate of reaction
decreases.
(i)
NH3 in ethanol, in sealed tube

P:
CONH2
(ii)
c.HNO3
c. H2SO4
55oC
NO2
NH2
Sn, c.HCl ,reflux
followed by
NaOH(aq)
(iii)
Add neutral aqueous iron(III) chloride to both.

An intense violet complex will be observed for phenol.
No violet complex for phenylamine.
Or Add sodium metal to both.
Effervescence will be observed for phenol. Gas evolved extinguished burning
splinter with a pop sound.
No gas evolved for phenylamine.
(b)
(i)
a radical contains a lone/unpaired electron or odd number of electrons.
(ii)
H O

H C C O
H
OCO bond angle = 120o
(iii) 2 H2O + 2e H2 + 2OH
(b) (iv) (I) Mr of CH3COOK = 98.1

Amt of CH3COOK in 2.43g = 0.02477 mol
1 mol of CH3COOK gives rise to 1 mol of CH3 radical.
2 mol of CH3 gives rise to 1 mol of CH3CH3 molecule.
Step 1
CH3COO CH3COO + e
Anode reaction
Step 2
CH3COO CH3 + CO2
Decarboxylation
Step 3
2 CH3 CH3CH3
Dimerization
Theoretical amt of CH3CH3 to be produced =
0.02477
= 0.01238 mol
2
Theoretical volume of CH3CH3 to be produced :

pV = nRT
(101000)V = (0.01238)(8.31)(28 + 273)
V= 3.065 104 m3
Percentage yield of CH3CH3 =
200 10 -6
100% = 65.2%
3.065 10 -3
OR
pV=nRT
(101000)(200 106) = n (8.31)(28 + 273)
n = 8.075 103
8.075 103 mol of CH3CH3 produced.
10
Percentage yield of CH3CH3 =
8.075 10 -3
100% = 65.2%
0.01238
electron : CH3COO
1
:
1
(II)
Amt of electrons required = 0.02477 mol

Q = It
(0.02477)(96500) = 0.5 t
t = 4778s
= 79.6min
(c) (i)
CH3
P:
CH3
CH3
CH3
CH3
CH3
CH2CH2CH3
or
Step 1
CH3CH2CH2COO CH3CH2CH2COO + e
Step 2
CH3CH2CH2COO CH3CH2CH2 + CO2
Step 3
2 CH3CH2CH2 CH3CH2CH2CH2CH2CH3
In step 2, once the primary radical is formed. It immediately forms a more stable
secondary radical by rearrangement of radical/ hydride shift.
H
CH3
1 radical
CH3
2 radical
Collision of 2 secondary radicals give rise to P.

(ii)
Hexane has a higher boiling point than P as hexane is straight-chain with a higher
surface area of contact between its molecules compared to P which is branched.
More energy is required to overcome the stronger temporary dipole induced dipole
between hexane molecules.
11
(d)
Potassium ethanoate
CH3COOK
Potassium methanoate
HCOOK
Mixture of
CH3COOK + HCOOK
Radical
CH3
Product
CH3CH3
H2
H , CH3
CH3CH3 [ ]
CH4 [ ]
Potassium methanoate :
Step 1
HCOO HCOO + e
Step 2
HCOO H + CO2
Step 3
H H2
(a)
(i) SnO2
PbO
(ii) PbO(s) + 2NaOH(aq) + H2O(l) Na2Pb(OH)4(aq)
(b)
(i) Amount of PbSO4 dissolved in 100 cm3=
0.00425
207 + 32.1 + 4(16.0)
= 1.402 x 10-5 mol

Solubility = 1.402 x 10-5 mol x
1000
= 1.402 x 10-4 mol dm-3
100
(ii) Ksp = [Pb2+][SO42-] = (1.402 x 10-4)2

= 1.97 x 10-8 mol2dm-6
(iii) PbSO4(s)
Pb2+(aq) + SO42-(aq)
The solubility will be lower due to common ion effect. By LCP, equilibrium above
shifts to LHS due to a higher concentration of SO42- ion.
(c)
(i) CO2 has a simple covalent structure whereas SiO2 has a giant covalent
structure. A greater amount of energy is required to break the strong
covalent bonds between Si and O atoms as compared to the weak van der
Waals forces between CO2 molecules.
(ii) SiO2 has a giant covalent structure and PbO has a giant ionic structure. Both
12
covalent and ionic bonds are strong. The covalent bonds between Si and O
atom is stronger than the ionic bonds between the Pb2+ and O2- ions in this
case. Hence a greater amount of energy is required to break the covalent
bonds in SiO2.
(d)
(i) Step I: excess conc.H2SO4, 170C

Step II: conc.H2SO4, conc.HNO3, 55C
S:
T:
CH2CH2OH
CH2CHO
(ii) U:
CH2CHCl2
CH3
NO2
The CH2CHCl2 group is 2,4-directing whereas the NO2 group is 3-directing.

Hence the next substitution will occur on position 2 relative to the CH2CHCl2
group or the 3rd position relative to the NO2 group. Both are essentially the
same position.
(iii) Mild oxidation occurs. KMnO4 decolourised with the formation of brown
MnO2 ppt.
CH(OH)CH2OH
(iv)
Cl
13
NANYANG JUNIOR COLLEGE

Higher 2
CHEMISTRY
9647/01
21 September 2012
1 hour

Data Booklet

Write your name, class and tutors name on the Answer Sheet in the spaces provided unless
this has been done for you.
There are forty questions on this paper. Answer all questions. For each question there are
four possible answers A, B, C and D.
Choose the one you consider correct and record you choice in soft pencil on the separate
Answer Sheet.

[Turn over
2
Section A
For each question there are four possible answers, A, B, C and D. Choose the one
you consider to be correct.
1
The mass percentage of magnesium in a mixture of magnesium chloride and

magnesium nitrate was found to be 21.25%. What mass of magnesium chloride
is present in 100 g of the mixture?
A
47 g
51 g
53 g
56 g

The successive ionisation energies, in kJ mol1, of an element X are given below.
870
1800 3000 3600 5800 7000 13200
What is X?
8O
33As
52Te
53I
Iodine and phosphorus each form a trifluoride. What are the shapes of these two
molecules?
IF3
PF3
trigonal planar
trigonal pyramidal
B T-shaped
trigonal pyramidal
C trigonal pyramidal
trigonal planar
D T-shaped
trigonal planar
H2 Chemistry 9647/01 NYJC J2/12 PX
3
4
Which of the following diagrams correctly describes the behavior of a fixed mass
of an ideal gas? (T is measured in K.)
A
constant T
B
constant T
C
pV
constant T
0
D
V
constant p
[Turn over
4
Questions 5 and 6 refer to the OXO reaction shown below.
The OXO reaction shown below is industrially important for making alcohols,
aldehydes and carboxylic acids. For example, butanal can be synthesised from
propene, C3H6, according to the following scheme. It can then be converted to
butan-1-ol and butanoic acid.
CH3CH=CH2(g) + CO(g) + H2(g) CH3CH2CH2CHO(g)
propene
butanal
5
The value of G for this reaction is negative. What is the sign of S and H for
the above reaction?
S

Taking the bond energy for the CO bond in carbon monoxide to be 1077 kJ
mol1 and using other appropriate bond energies, what is the numerical value of
H for the above OXO reaction?
137 kJ mol1
213 kJ mol1
573 kJ mol1
623 kJ mol1
The radioactive decay is a first order reaction. If the rate of decay of a radioactive
isotope decreases from 200 counts per minute to 25 counts per minute after 21.6
hours, what is its half-life?
A
2.4 hours
6.5 hours
7.2 hours
7.8 hours
5
8
Which of the following statements correctly explains why a small increase in

temperature leads to a significant increase in the rate of a gaseous reaction?
A
The average kinetic energy of the molecules is slightly greater at a higher

temperature.
B The proportion of molecules with any given energy increases.
The frequency of collisions between molecules is greater at a higher

temperature.
The frequency of collisions between molecules with kinetic energy greater

than the activation energy is greater at a higher temperature.
An equilibrium can be represented by the following equation:

P(aq) + Q(aq) 2R(aq) + S(aq)
In a certain mixture, the equilibrium concentration of Q is 10 mol dm3.
What will be the new equilibrium concentration of Q if 5 mol of pure Q is
dissolved in the mixture?
A 15 mol dm3
B between 10 mol dm3 and 15 mol dm3
C 10 mol dm3
D between 5 mol dm3 and 10 mol dm3
10 Which of the following correctly lists 0.10 mol dm3 solutions of HCl, KCl, NH4Cl,
KOH and KCN in order of increasing pH?
A HCl, KCl, KCN, NH4Cl, KOH
B HCl, NH4Cl, KCl, KCN, KOH
C HCl, KCl, NH4Cl, KCN, KOH
D KCl, KCN, KOH, HCl, NH4Cl
11 Thorium hydroxide, Th(OH)4, is a sparingly soluble salt. Which of the following

shows the correct expression of its molar solubility s (mol dm3) in terms of its
solubility product Ksp?
A
s = (Ksp)1/5
s = (Ksp/4)1/2
s = (Ksp)1/5/256
s = (Ksp/256)1/5
[Turn over
6
12 Use of the Data Booklet is relevant to this question.
Using inert electrodes, a current was passed through two beakers containing
aqueous silver sulfate and aqueous copper(II) nitrate, connected in series under
standard conditions.
A
At 25oC, 1 atm
1.00 mol dm-3

Cu(NO3)2(aq)
0.50 mol dm-3

Ag2SO4(aq)
What is the ratio of the mass of silver to copper deposited after the current was
passed for t minutes?
A
0.59
0.85
1.70
3.40
13 Use of the Data Booklet is relevant to this question.

The circuit shown in the diagram was set up.
battery
At 25oC, 1 atm
impure Cu containing
Ag and Fe impurities
pure Cu
1.00 mol dm-3

CuSO4(aq)
sludge
What are the products formed at the anode and cathode and what is the
substance present in the sludge after some time?
A
B
C
D
anode
Cu2+
Fe2+
Ag+, Fe2+
Cu2+, Fe2+
cathode
Cu
Cu2+
Cu2+
Cu
sludge
Ag
Ag
Zn
Ag
7
14 On descending Group II from magnesium to barium, which of the following
statements is true?
A The enthalpy change of hydration of the M2+ ion becomes more exothermic.
B The first ionisation energy increases.
C The nitrates is less easily decomposed by heat to give brownish fumes.
D The solubility of the Group II oxides decreases.
15 What is observed when aluminium chloride is added to excess water?
solubility in water
pH of resulting solution
insoluble
7.0
very slightly soluble
6.5
dissolves
5.0
dissolves
3.0
16 Which of the following compounds has the highest melting point?

A
NaCl
MgCl2
AlCl3
SiCl4
17 Both aqueous bromine and aqueous chlorine appear as yellow solutions. Which
of the following reagents can be used to distinguish the two solutions?
A aqueous chlorine
B aqueous sodium chloride
C aqueous sodium thiosulfate
D aqueous iron(II) sulfate, followed by aqueous sodium hydroxide
[Turn over
8
18 In the laboratory, there are three bottles labeled A, B and C. Each bottle contains
one of the following reagents: CaCl2(aq), FeCl2(aq) and AgNO3(aq).
The tests were carried out using these reagents and the results were
summarised in the table below:
Tests
Observations
Mixing reagents A and B, followed by
A white ppt soluble in NH3(aq)
addition of NH3(aq)
Mixing reagents A and C, followed by
A grey precipitate insoluble in NH3(aq)
addition of NH3(aq)
What are the identities of the reagents A, B and C?
A
CaCl2
AgNO3
FeCl2
FeCl2
AgNO3
CaCl2
AgNO3
FeCl2
CaCl2
AgNO3
CaCl2
FeCl2
19 Letters written on paper using aqueous ammonium thiocyanate are invisible until
turned blood-red by brushing the paper with aqueous iron(III) chloride. If the
ammonium thiocyanate is first made alkaline, the letters are orange and less
clear.
Which of the following substances, when formed on the paper in these reactions,
best explains these observations?
with aqueous ammonium
thiocyanate
with alkaline aqueous

ammonium thiocyanate
Fe-NH3 complex
Fe(OH)3
Fe-CNS complex
Fe-NH3 complex
Fe-CNS complex
Fe(OH)3
Fe-CNS complex
Fe-OH complex
9
20 The table shows the possible oxidation states of five d-block elements in the
Periodic Table. (The elements are represented by letters which are not their
symbols.)
element
possible oxidation numbers
Which of the following ions is likely to exist?

A PO2+
B QO3
C RO42+
D SO22+
21 Warfarin is used as a rat poison.
OH
Warfarin
2
How many sp hybridised carbon atoms are present in the Warfarin molecule?
A 4
B 12
C 14
D 16
[Turn over
10
22 The structure of vitamin D2 is shown below.
CH3
CH3
CH3
HO
CH3
CH3
CH2
When it is completely reacted with hydrogen in the presence of a palladium
catalyst at room temperature, how many chiral centres does the product
molecule possess?
A7
B8
C9
D 10
23 Limonene is an oil formed in the peel of citrus fruits.
limonene
Which of the following is the major product formed when hydrogen bromide
reacts with limonene at room temperature?
A
CH2Br
Br
B
CH2Br
Br
Br
Br
D
Br
Br
11
24 A sample of ethylbenzene is quantitatively oxidised to the corresponding
carboxylic acid.
What is the mass of product formed from 1.00 g of ethylbenzene?
A 1.15 g
B 1.28 g
C 1.32 g
D 1.38 g
25 The Hofmann elimination is a process where an amine undergoes treatment with
excess methyl iodide to form a tertiary amine intermediate followed by treatment
with silver oxide, water and heat to form an alkene.
CH3
H
CH3
excess CH3I
CH3
CH3
Ag2O, H 2O
H3C
heat
+
NH2
N (CH3)3 I
H3C
+
(CH3)3N
What is the structure of the alkene formed when a cyclic amine, piperidine,
undergoes the Hofmann elimination?
NH
Piperidine
A CH2=CHCH2CH2CH2N(CH3)2
B CH2=CHCH2CH2CH3
N
CH3
[Turn over
12
26 When sodium iodide in propanone is added to an optically active sample of 2bromobutane, a sodium bromide precipitate formed after 13 minutes upon
heating.
NaI + CH3CHBrCH2CH3 CH3CHICH2CH3 + NaBr(s)
The experiment was repeated several times and the rate equation was found to
be
Rate = k[CH3CHBrCH2CH3][NaI]
Which of the following statements is incorrect?
A A racemic mixture is formed.

B The reaction involves nucleophilic substitution.
C The reaction is bimolecular.
D A similar experiment, using 1-bromobutane, will produce precipitate in less
than 13 minutes.
27 The following compound contains 4 chlorine atoms (labelled 1, 2, 3 and 4).
COCl
Cl
COCl
Cl
What is the relative order of increasing ease of hydrolysis of the chlorine atoms?
A 1, 2, 3, 4
B 2, 1, 3, 4
C 1, 2, 4, 3
D 2, 1, 4, 3
13
28 Compound Z can be obtained via the 2-step synthesis from compound V.
CHO
CO 2H
H2 gas
Na metal
X
Pt
OH
CN
V
What is the change in gas volume if 96 dm3 of H2 gas was reacted with one mole
of compound V, followed by excess sodium metal, at room conditions?
A Gas volume contracted by 60 dm3

B Gas volume contracted by 36 dm3
C Gas volume expanded by 60 dm3
D Gas volume expanded by 36 dm3
29 Which of the following compound can be used, in a 1-step conversion, to

produce the following cyclic structure?
O
A
B
HO2CCH2NH2 and HO2CCH2OH

HO2CCH2CONHCH2OH
ClOCCH2COCl and H2NCH2OH
ClOCCH2OH and H2NCH2CO2H
N
H
[Turn over
14
30 The thermal decomposition of calcium ethanoate produces its metal carbonate
and a carbonyl compound.
(CH3CO2)2Ca CaCO3 + (CH3)2CO
When a mixture of calcium ethanoate and calcium methanoate was heated, a
mixture of three carbonyl compounds X, Y and Z were obtained. Both X and Y
give a silver mirror with Tollens reagent but not Z. Both X and Z give yellow
precipitate in aqueous alkaline iodine but not Y.
Based on the above, which of the following statements are incorrect?
A Only X and Y can decolourise aqueous potassium manganate(VII).

B The ratio of X to Y to Z formed is 2:1:1.
C Only X reacts with HCN to produce an optically active product.
D All three compounds can form an orange precipitate with 2,4-DNPH.
15
Section B
For each of the questions in this section one or more of the three numbered
statements 1 to 3 may be correct.
Decide whether each of the statements is or is not correct (you may find it helpful to
put a tick against the statements which you consider to be correct).
1, 2 and 3
are
correct
1 and 2
only are
correct
2 and 3
only are
correct
1 only
is
correct
31
10 cm3 of a gaseous hydrocarbon X is mixed with 100 cm3 oxygen and ignited.
After the reaction the gases produced are shaken with aqueous KOH solution.
The final volume of gases is 25 cm3. Which of the following hydrocarbons could
be X?
(All volumes are measured at room temperature and pressure.)
1 C4H8
2 C5H10
3 C6H6
32
1 dm3 of gas X weighs 1 g and 1 dm3 of gas Y weighs 5 g under the same
conditions of temperature and pressure. Which of the following statements are
correct?
1 The ratio of the Mr of X to Y is 1:5.

2 The average velocity of the molecules in gas X and gas Y are the same at
the same temperature.
3 The number of molecules of Y in 1 dm3 is five times the number of molecules
of X in 1 dm3.
[Turn over
16
1, 2 and 3
are
correct
1 and 2
only are
correct
2 and 3
only are
correct
1 only
is
correct
33 In the reaction between iodide and peroxodisulfate, iron(III) is used as a catalyst.

Which of the statements are incorrect?
1 The rate of both the forward and backward reaction increases to the same
extent, but the rate constant remains the same.
2 One of the equations involve: 2Fe3+ + 2S2O32 2Fe2+ + S4O62.
3 This reaction is an example of a homogeneous catalysis.
34 Ammonia is manufactured in the Haber process.

N2 (g) + 3H2 (g) 2NH3 (g) H
= 92 kJ mol1
Given that Kp for the above reaction is 3.375 at T K, which of the following
statements involving the reaction is correct?
1 The partial pressure of H2 (g) at equilibrium at T K can be expressed as

2
-1
2
PNH3 3 PN2 3 .
3
) ( )
H
.
S
3 When pressure is increased, the yield of ammonia and the equilibrium
constant increases.
2 When equilibrium is established, temperature, T K, is given by T=
17
1, 2 and 3
are
correct
1 and 2
only are
correct
2 and 3
only are
correct
1 only
is
correct
35 The Group II metals have higher melting points than the Group I metals. Which
of the following factors could contribute towards the higher melting points?
1 There are smaller interatomic distances in the metallic lattices of the Group II
metals.
2 Two valence electrons are available from each Group II metal atom for
bonding the atom into the metallic lattice.
3 Group II metals have higher first ionization energies.
36 Chromium and its compounds undergo the following reactions.
NaOH(aq)
in excess
A
H2O2
green
solution
B
yellow
solution
H+
C
NH4SCN
orange
solution
D
NH4[Cr(SCN)x(NH3)y]
CrK(SO4)2
D has the following composition by mass: Cr, 15.5%; S, 38.1%; N, 29.2%

Which of the following can be deduced from the above reaction scheme?
The values of x and y in D are 4 and 2 respectively.
The types of reactions that occur are ligand exchange and redox only.
The formula of A is Cr(OH)2(H2O)6.
[Turn over
18
1, 2 and 3
are
correct
1 and 2
only are
correct
2 and 3
only are
correct
1 only
is
correct
37 A hydrocarbon, on heating with an excess of hot concentrated acidic KMnO4(aq),

produces CH3COCH3 and (CH3)2CHCO2H as the only organic products.
What could the hydrocarbon be?
CH3
H
C
C
CH
CH3
CH3
CH3
CH3
C
CH3
CH3
C
CH3
CH3
3
CH3
CH2
CH2
CH3
C
CH3
38 Which reagents can be used to distinguish between the following compounds?
CH3
C
CH3
CH3
OH
1 PCl5
2 Na2Cr2O7
3 NaHCO3
C
Cl
CH3
19
1, 2 and 3
are
correct
1 and 2
only are
correct
2 and 3
only are
correct
1 only
is
correct
39
The following are structures of 3 amino acids.

H
CH2
H2N
CH
CH2
H2C
CO2H
H2 N
CH
CH2
CO2H
CO 2H
CH
CO 2H
CH 2CONH 2
Which of the following represents dipeptides formed from these amino acids?
O
CH2
1
HO2C
CO2H
CH
CH
CONH2
NH
CH2
NH2
CO2H
CH
NH2
HO2C
CH
CH2
CH2
CH2
O
CH2
CH
H2C
CH2
CH2
NH
CO 2H
H2C
CH
NH2
[Turn over
20
1, 2 and 3
are
correct
1 and 2
only are
correct
2 and 3
only are
correct
1 only
is
correct
40
Lysine is an essential amino acid found in the body. It has three pKa values
associated with it: 2.2, 9.0 and 10.5
CO2H
H2N
H
(CH2)4NH2
When one mole of protonated lysine was titrated against hydroxide ions, the
following pH curve is obtained:
pH
14
12
10
A
2
0
0
0.5
1.0
1.5
2.0
2.5
3.0
Moles of
hydroxide
added
Which of the following statements are true with respect to the curve above?
Equal amounts of H3N+CH(CO2H)(CH2)4NH3+ and H3N+CH(CO2H)(CH2)4NH2

are present at point A.
The major species present at point C has no net charge.
The major species present at point B will migrate towards the cathode of an
electrolytic cell.

JC 2 PRELIMINARY EXAMINATION 2012
H2 Chemistry
1
2
3
4
5
6
7
8
9
10
C
C
B
D
D
A
C
D
B
B
11
12
13
14
15
16
17
18
19
20
D
D
D
C
D
A
D
D
C
D
21
22
23
24
25
26
27
28
29
30
D
C
C
A
A
A
C
B
D
C
31
32
33
34
35
36
37
38
39
40
C
D
B
B
B
D
B
D
D
C

Higher 2
CANDIDATE
NAME
CLASS
1 1
INDEX
NO.
TUTOR
CHEMISTRY
9647/02
Paper 2 Structured
10 September 2012
2 hours

Data Booklet

Answer all questions in the spaces provided.
For Examiners Use
/12
/ 8
/ 7
/ 14
/ 6
/ 4
/ 8
/ 9
/ 4
/60

[Turn over
For
Examiner's
Use

1
Planning (P)
Paracetamol (acetaminophen) is commonly used for the relief of headaches and is a major
ingredient in numerous cold and flu medicine.
It is a white solid (m.p. = 169 oC) which can be prepared by a reaction between
4-aminophenol and ethanoic anhydride.
HOC6H4NH2
4-aminophenol
(Mr = 109)
(CH3CO)2O
ethanoic anhydride
(Mr = 102)
CH3CONHC6H4OH
paracetamol
(Mr = 151)
A typical yield, based on 4-aminophenol, is 70%.

The crude product can be purified by recrystallisation from water.
The purity of the recrystallised product can be confirmed by determining its melting point.
Ethanoic anhydride can cause irritation of tissue, especially in nasal passages.
4-aminophenol is a skin irritant and is toxic.
(a)
Using the information above:

(i) Write a balanced equation for the formation of paracetamol;
(ii)
Calculate the minimum masses of reactants needed to prepare 5 g of pure

paracetamol.
[3]
[Turn over
3
(b)
For
Examiner's
Use
Write a full description of the purification of the crude paracetamol. List the essential
apparatus you would use in the process.
You do not have to describe the preparation of paracetamol.
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
.............................................................................................................................. [6]
(c)
Write a brief description showing how you would use the melting point of the
purified product to confirm its purity. You do not have to describe how you would
obtain the melting point.
..................................................................................................................................
.............................................................................................................................. [1]
(d)
Identify two potential safety hazards in this experiment and the relevant safety
precautions you would take.
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
.............................................................................................................................. [2]
[Total: 12]
[Turn over
4
2
Given the following thermochemical data:

H
/ kJ mol1
Reaction
(a)
For
Examiner's
Use
C(graphite) + 2H2(g) CH4(g)
75.0
C(graphite) + O2(g)
CO2(g)
393.5
H2(g)
H2O(l)
285.9
O2(g)
With the aid of an energy cycle, calculate the

the reaction
CH4(g) + 2O2(g) 2H2O(l) + CO2(g)
enthalpy
change
for
Energy
[3]
[Turn over
5
(b)
For
Examiner's
Use
The experimental enthalpy change is 801.7 kJ mol1 for the following reaction
CH4(g) + 2O2(g) 2H2O(g) + CO2(g) ..(I)
(i)
Calculate the enthalpy change of vaporisation of water at 298K.
[2]
(ii)
Using bond energy data from the Data Booklet, calculate another value for
H for reaction (I) in (b). Account for any differences between your answer
and the given experimental value in (b).
.......................................................................................................................
.......................................................................................................................
.......................................................................................................................
[3]
[Total: 8]
[Turn over
For
Examiner's
Use
Mixtures of citric acid, C5H7O4CO2H (Ka = 7.40 x 104 mol dm3), and its sodium salt
are often used as acidity regulators for food. The mixture regulates the pH of food
by acting as a buffer.
(a)
Prove that the pH of a mixture formed from 25.0 cm3 of 0.200 mol dm3 citric acid
and 2.48 g of sodium citrate (Mr = 198) is 3.53.
[2]
(b)
When 0.059 g of an unknown solid was added to the mixture prepared in (a), the pH
of the resultant solution is 3.73. Determine the molar mass of the solid and hence
suggest its identity.
[3]
[Turn over
7
(c)
For
Examiner's
Use
Determine the volume of 0.100 mol dm-3 of HCl(aq) that needs to be added to the
solution in (a) to obtain a buffer at its maximum buffering capacity.
[2]
[Total: 7]
4
Cobalt and vanadium are transition metals.
(a)
Give one characteristic chemical property of cobalt and vanadium which shows that
they are transition metals.
..................................................................................................................................
.............................................................................................................................. [1]
(b)
Aqueous cobalt(II) chloride, CoCl2 is a pink solution. When a mixture of the pink
solution and tartaric acid, HO2CCH(OH)CH(OH)CO2H, is added to aqueous
hydrogen peroxide, the following changes take place.
The initially pink solution turns green and then oxygen is vigorously evolved. Finally,
the solution turns pink again.
Suggest a role for the CoCl2(aq) and for the tartaric acid. Write an equation for the
overall reaction.
CoCl2(aq):..................................................................................................................
Tartaric acid: .............................................................................................................
Equation: ...................................................................................................................
[3]
[Turn over
8
(c)
For
Examiner's
Use
Aqueous CoCl2 also undergoes the following reaction.

I
CoCl2(aq)
NH4Cl, NH3
and O2
(i)
Crystals of
salt K
Crystals of salt, K has the following composition by mass:

Co, 22.0%; N, 31.4%; H, 6.7%; Cl, 39.8%
On adding an excess of AgNO3(aq) to an aqueous solution containing
0.01 mol of K, 4.29 g of AgCl(s) is precipitated.
Calculate the empirical formula of K, and draw the structure of the cation
present in K to show the geometry around the central ion.
(ii)
State the types of reactions occurring in step I.

.......................................................................................................................
.......................................................................................................................
[Turn over
9
(iii)
For
Examiner's
Use
Eo data for some cobalt complex ions are given below.

[Co(C2O4)3]3(aq) + e [Co(C2O4)3]4(aq)
Eo = +0.57 V
[Co(NH3)6]3+(aq) + e [Co(NH3)6]2+(aq)
Eo = +0.11 V
Use the Eo data given above to predict the reaction, if any, of adding C2O42
to K. Explain your prediction.
.......................................................................................................................
.......................................................................................................................
.......................................................................................................................
.......................................................................................................................
.......................................................................................................................
.......................................................................................................................
[7]
(d)
Some of the ions of vanadium and their corresponding colours are shown in the
table below.
formula of vanadium ion
colour of aqueous solution
VO3
yellow
VO2+
blue
V3+
green
V2+
violet
The colour of the reaction mixture changes from yellow to green when a transition
metal is added to an aqueous solution containing the salt of a vanadium ion.
By reference to the Data Booklet, suggest a possible identity of the transition metal
and explain the colour change observed.
Identity of the transition metal: ..................................................................................
Explanation:
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
.............................................................................................................................. [3]
[Total: 14]
[Turn over
10
5
The standard enthalpy change of fusion (Hfus) is the energy required to convert
one mole of a substance in the solid state to the liquid state under standard
pressure. The table below shows numerical values of standard enthalpy change of
fusion for the respective elements:
Element
Na
Al
Si
Cl
(a)
For
Examiner's
Use
Hfus / kJ mol1
2.60
10.7
50.2
6.41
Explain, in terms of structure and bonding, the difference in the Hfus between:
(i)
Si and Cl
.......................................................................................................................
.......................................................................................................................
.......................................................................................................................
.......................................................................................................................
.......................................................................................................................
................................................................................................................... [2]
(ii)
Na and Al
.......................................................................................................................
.......................................................................................................................
.......................................................................................................................
.......................................................................................................................
.......................................................................................................................
................................................................................................................... [2]
(b)
Experimental results show that the first ionisation energies for the elements
phosphorus and iodine are similar. Suggest an explanation for the observations.
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
.............................................................................................................................. [2]
[Total: 6]
[Turn over
11
6
For
Examiner's
Use
X2 and Y2 are halogens and they are known to be more soluble in organic solvents.
In an experiment, excess X2 was mixed with Na2S2O3(aq). When hexane was
added, two immiscible layers were observed and was later separated using a
separatory funnel. A reddish brown organic layer was obtained and the aqueous
layer was divided into 2 portions.
To one portion of the aqueous layer, Y2(aq) was added and shaken. When CCl4
was added, a violet organic layer was obtained.
To another portion of the aqueous layer, AgNO3(aq) was added. The precipitate
formed does not dissolve in aqueous NH3.
(a)
Suggest a suitable identity of X2 and Y2.

X2: Y2: [1]
(b)
Write a balanced ionic equation for the reaction between Na2S2O3 and X2.
.............................................................................................................................. [1]
(c)
Explain in energy terms, why halogens are more soluble in organic solvent than in
water.
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
.............................................................................................................................. [2]
[Total: 4]
[Turn over
12
7
For
Examiner's
Use
Keratin refers to a family of fibrous proteins which is the key component of hair and
nails. The keratins in hair consist of -helically coiled single protein strands, further
twisted into superhelical ropes that may be further coiled. The presence of keratins
determines the strength and structure of hair i.e. straight or wavy. Nails, which are
less flexible and elastic, contains keratins which have -pleated sheets twisted
together, stabilised and hardened by R-group interactions.
The table below shows the amino acid composition of 2 samples of keratins. One
sample was extracted from nails, the other sample from hair.
Amino acid composition
Acid
R group
asp
asn
thr
ser
glu
CH2CO2H
CH2CONH2
CH(OH)CH3
CH2OH
CH2CH2CO2H
tyr
pro
CH2
CH2
OH
CH2 (cyclic)
Sample A
Sample B
3.0
3.0
6.9
11.7
6.1
3.0
2.0
4.5
8.5
6.1
1.9
4.2
3.6
3.2
6.5
4.8
17.5
5.9
0.5
2.7
6.1
6.0
5.6
3.2
28.2
5.9
3.5
2.7
6.0
5.8
1.4
4.5
3.7
3.0
2.3
3.8
0.8
2.1
5.6
6.2
CH2
gly
ala
cys
val
met
ile
leu
gln
phe
H
CH3
CH2SH
CH(CH3)2
CH2CH2SCH3
CH(CH3)CH2CH3
CH2CH(CH3)2
CH2CH2CONH2
CH2
trp
CH2
C
NH
lys
CH2CH2CH2CH2NH2
+
NH
his
CH2
C
N
H
arg
CH2CH2CH2NHC(NH2)=NH2+
[Turn over
13
(a)
For
Examiner's
Use
Draw a diagram representing the secondary structure of keratins found in nails. In

your diagram, show clearly the bonding that is involved in stabilising the secondary
structure. You may represent the R groups using the symbol R.
[3]
(b)
By referring to the amino acid composition data, answer the questions below:
(i)
State the R group interaction that is mainly responsible for the stabilisation of
the tertiary structure of keratins. Write an equation to support your answer.
.......................................................................................................................
.......................................................................................................................
(ii)
In order to straighten wavy hair permanently, using a heating iron is

insufficient. Instead, one will need to go to the hairdresser to undergo a
treatment of chemicals. Explain why.
.......................................................................................................................
.......................................................................................................................
.......................................................................................................................
(iii)
Which sample belongs to keratins extracted from a nail sample? Explain.

.......................................................................................................................
.......................................................................................................................
.......................................................................................................................
.......................................................................................................................
[5]
[Total: 8]
[Turn over
14
8(a)
For
Examiner's
Use
There are four stereoisomers of compound P.
CH
CHCH2CH
CHOH
OH
P
What is the type of stereoisomerism exhibited by P? Draw the stereoisomers of P.
Type of stereoisomerism: ........................................................................................
[4]
[Turn over
15
(b)
For
Examiner's
Use
Q is a structural isomer of P in (a).

Suggest the structures of Q, R, S, T and U in the reaction scheme below.
aqueous HCl
R (C3H6O2)
+
heat
Q (C11H12O2)
S
H2
Ni catalyst
heat
aqueous
bromine
U (C8H7OBr3)
T
[5]
[Total: 9]
[Turn over
16
For
Examiner's
Use
When methylbenzene is nitrated by a mixture of concentrated nitric acid and

concentrated sulfuric acid, the product consists largely of two isomers, V and W, of
formula C7H7NO2. V has a plane of symmetry perpendicular to the plane of the
benzene ring in its molecule, while W does not. The formation of V proceeds via an
organic intermediate X.
(a)
Draw the displayed formulae of V and X, showing clearly the geometry of the bonds
around the carbon atom bonded to the nitrogen atom.
isomer V
organic intermediate X
[2]
(b)
What is the name of the mechanism of the reaction for the formation of V? Briefly
outline the mechanism of this reaction using equations.
Name of mechanism: .................................................................................................
Mechanism:
[2]
[Total: 4]
over
[End[Turn
of Paper]

Higher 2
CANDIDATE
NAME
CLASS
Answers
1 1
INDEX
NO.
TUTOR
CHEMISTRY
9647/02
Paper 2 Structured
10 September 2012
2 hours

Data Booklet

For Examiners Use
/12
/ 8
/ 7
/ 14
/ 6
/ 4
/ 8
/ 9
/ 4
/60

[Turn over
For
Examiner's
Use

1
Planning (P)
Paracetamol (acetaminophen) is commonly used for the relief of headaches and is a major
ingredient in numerous cold and flu medicine.
It is a white solid (m.p. = 169 oC) which can be prepared by a reaction between
4-aminophenol and ethanoic anhydride.
HOC6H4NH2
4-aminophenol
(Mr = 109)
(CH3CO)2O
ethanoic anhydride
(Mr = 102)
CH3CONHC6H4OH
paracetamol
(Mr = 151)
A typical yield, based on 4-aminophenol, is 70%.

The crude product can be purified by recrystallisation from water.
The purity of the recrystallised product can be confirmed by determining its melting point.
Ethanoic anhydride can cause irritation of tissue, especially in nasal passages.
(a)
Using the information above:

(i) Write a balanced equation for the formation of paracetamol;
HOC6H4NH2 + (CH3CO)2O CH3CONHC6H4OH + CH3CO2H
(ii)
Calculate the minimum masses of reactants needed to prepare 5 g of pure

paracetamol.
Mass of 4-aminophenol required =
5 100
109 = 5.16 g
151 70
Mass of ethanoic anhydride required =
5 100
102 = 4.82 g
151 70
[3]
[Turn over
3
(b)
For
Examiner's
Use
Write a full description of the purification of the crude paracetamol. List the essential
apparatus you would use in the process.
You do not have to describe the preparation of paracetamol.
Apparatus:
Conical flask for dissolving crude solid (accept beaker)
Hot plate for heating (accept oil bath but not water bath or heating mantle)
Filter funnel/ conical flask for hot filtration
Buchner apparatus for collecting pure crystals.
Method:
Dissolve crude solid in minimum amount of hot water
Filter solution while hot
Cool hot solution (in ice bath)
Collects crystals using vacuum filtration/ reduced pressure (using Buchner
apparatus)
Wash with small amounts of cold water
Dries crystals between filter paper/ under IR lamp.
.............................................................................................................................. [6]
(c)
Write a brief description showing how you would use the melting point of the
purified product to confirm its purity. You do not have to describe how you would
obtain the melting point.
-
Melts sharply/ over small temperature range

Melting point agrees with data value (i.e. 169 oC)
.............................................................................................................................. [1]
(d)
Identify two potential safety hazards in this experiment and the relevant safety
precautions you would take.
Hazard
Ethanoic acid is corrosive
Precaution
Avoid skin contact; wear personal protective
equipment (gloves, goggles); flood affected
areas if there is spillage.
Ethanoic anhydride can cause irritation of Perform experiment in fume cupboard.
tissue, especially in nasal passages.
Ethanoic anhydride is flammable
Do not use naked flames.
-
Precautions must be relevant to the hazard

Do not allow use fume cupboard as a precaution for toxicity.
Do not allow do not eat/ consume, do not breathe in as precautions
.............................................................................................................................. [2]
[Total: 12]
[Turn over
4
2
For
Examiner's
Use
Given the following thermochemical data:

H
/ kJ mol1
Reaction
(a)
C(graphite) + 2H2(g) CH4(g)
75.0
C(graphite) + O2(g)
CO2(g)
393.5
H2(g)
H2O(l)
285.9
O2(g)
With the aid of an energy cycle, calculate the

the reaction
CH4(g) + 2O2(g) 2H2O(l) + CO2(g)
enthalpy
change
for
Energy
0
C(graphite) + 2H2(g) + 2O2(g)

75
CH4(g) + 2O2(g)
(
393.5) + 2(
285.9)
H
CO2(g) + 2H2O(g)
By Hess Law:
285.9) + (
393.5)}
H = +75.0 + {2(
= 890.3 kJ mol1
[3]
[Turn over
5
(b)
For
Examiner's
Use
The experimental enthalpy change is 801.7 kJ mol1 for the following reaction
CH4(g) + 2O2(g) 2H2O(g) + CO2(g) ..(I)
(i)
Calculate the enthalpy change of vaporisation of water at 298K.

890.3
CH4(g) + 2O2(g) 2H2O(l) + CO2(g)
801.7
2
Hvap
2H2O(g) + CO2(g)
2
801.7)
Hvap = +890.3 + (
2
Hvap = +88.6
Hvap = +44.3 kJ mol1
[2]
(ii)
Using bond energy data from the Data Booklet, calculate another value for
H for reaction (I) in (b). Account for any differences between your answer
and the given experimental value in (b).
H
= 4(410) + 2(496) 4(460) 2(740)

= 688 kJ mol1
The value obtained from bond energy calculations is different because

bond energies are only average values obtained from different molecules.
They may not be the actual values for the molecules used.
[3]
[Total: 8]
[Turn over
For
Examiner's
Use
Mixtures of citric acid, C5H7O4CO2H (Ka = 7.40 x 104 mol dm3), and its sodium salt
are often used as acidity regulators for food. The mixture regulates the pH of food
by acting as a buffer.
(a)
Prove that the pH of a mixture formed from 25.0 cm3 of 0.200 mol dm3 citric acid
and 2.48 g of sodium citrate (Mr = 198) is 3.53.
pH = pKa + log [C5H7O4CO2Na]/[C5H7O4CO2H]
pH = - log (7.40 x 104) + log
2.48/198
0.025 0.200
= 3.53
[2]
(b)
When 0.059 g of an unknown solid was added to the mixture prepared in (a), the pH
of the resultant solution is 3.73. Determine the molar mass of the solid and hence
suggest its identity.
Since pH is raised on addition of the solid, the solid added must be a base.
C5H7O4CO2H + OH C5H7O4CO2 + H2O
3.73 = - log (7.40 x 104) + log [C5H7O4CO2Na]/[C5H7O4CO2H]
[C5H7O4CO2Na]/[C5H7O4CO2H] = 3.97
Let the molar mass of the solid be M
ncitric acid
= 0.025 x 0.200 0.059/M
ncitrate = 2.48/198 + 0.059/M
2.48/198 + 0.059/M
= 3.97
0.025 0.200 0.059/M
M = 40.0
Solid is sodium hydroxide.
[3]
[Turn over
7
(c)
For
Examiner's
Use
Determine the volume of 0.100 mol dm-3 of HCl(aq) that needs to be added to the
solution in (a) to obtain a buffer at its maximum buffering capacity.
pH at max. buffering capacity = 3.13
C5H7O4CO2 + H3O+ C5H7O4CO2H + H2O
Let the volume of 0.100 mol dm-3 HCl required be V
ncitric acid
= 0.025 x 0.200 + 0.100V
ncitrate = 2.48/198 0.100V

At max. buffering capacity,
[C5H7O4CO2H] = [C5H7O4CO2]
ncitric acid = ncitrate
0.025 x 0.200 + 0.100V = 2.48/198 0.100V
V = 0.0376 dm3 = 37.6 cm3
[2]
[Total: 7]
Cobalt and vanadium are transition metals.
(a)
Give one characteristic chemical property of cobalt and vanadium which shows that
they are transition metals.
variable oxidation state or catalytic activity or complex ion formation or

..................................................................................................................................
formation of coloured ions
.............................................................................................................................. [1]
(b)
Aqueous cobalt(II) chloride, CoCl2 is a pink solution. When a mixture of the pink
solution and tartaric acid, HO2CCH(OH)CH(OH)CO2H, is added to aqueous
hydrogen peroxide, the following changes take place.
The initially pink solution turns green and then oxygen is vigorously evolved. Finally,
the solution turns pink again.
Suggest a role for the CoCl2(aq) and for the tartaric acid. Write an equation for the
overall reaction.
catalyst
CoCl2(aq): .................................................................................................................
Ligand
Tartaric acid: .............................................................................................................
2H2O2 2H2O + O2
Equation: ...................................................................................................................
[3]
[Turn over
8
(c)
For
Examiner's
Use
Aqueous CoCl2 also undergoes the following reaction.
I
NH4Cl, NH3
CoCl2(aq)
and O2
(i)
Crystals of
salt K
Crystals of salt, K has the following composition by mass:

Co, 22.0%; N, 31.4%; H, 6.7%; Cl, 39.8%
On adding an excess of AgNO3(aq) to an aqueous solution containing
0.01 mol of K, 4.29 g of AgCl(s) is precipitated.
Calculate the empirical formula of K, and draw the structure of the cation
present in K to show the geometry around the central ion.
ratio of Co:N:H:Cl =
22.0 31.4 6.7 39.8

:
:
:
= 0.3735:2.243:6.7:1.121
58.9 14.0 1.0 35.5
= 1:6:18:3
CoN6H18Cl3
empirical formula of K ..
structure of the cation in K
(ii)
State the types of reactions occurring in step I.
Ligand
exchange and redox
.......................................................................................................................
.......................................................................................................................
[Turn over
9
(iii)
For
Examiner's
Use
Eo data for some cobalt complex ions are given below.

[Co(C2O4)3]3(aq) + e [Co(C2O4)3]4(aq)
Eo = +0.57 V
[Co(NH3)6]3+(aq) + e [Co(NH3)6]2+(aq)
Eo = +0.11 V
Use the Eo data given above to predict the reaction, if any, of adding C2O42
to K. Explain your prediction.
Co3+ is more stable when NH3 is the ligand as seen from the smaller Eo value
.......................................................................................................................
for the reduction of [Co(NH3)6]3+ to [Co(NH3)6]2+.
.......................................................................................................................
The ligand C2O42 is unable to displace the ammonia ligands in K.
.......................................................................................................................
No
ligand exchange reaction takes place when C2O42 is added to K.
.......................................................................................................................
[7]
(d)
Some of the ions of vanadium and their corresponding colours are shown in the
table below.
formula of vanadium ion
colour of aqueous solution
VO3
yellow
VO2+
blue
V3+
green
V2+
violet
The colour of the reaction mixture changes from yellow to green when a transition
metal is added to an aqueous solution containing the salt of a vanadium ion.
By reference to the Data Booklet, suggest a possible identity of the transition metal
and explain the colour change observed.
Co, Fe or Ni
Identity of the transition metal: ..................................................................................
Explanation:
VO3 + 4H+ + e VO2+ + 2H2O
VO2+ + 2H+ + e V3+ + H2O
V3+ + e V2+
Co2+ + 2e Co
Fe3+ + 3e Fe
Ni2+ + 2e Ni
Co reducing V(+5) to V(+3)
E = + 1.00 V
E = + 0.32 V
E = 0.26 V
E = 0.28 V
E = 0.04 V
E = 0.25 V
Ecell = +1.00 (0.28) = 1.28 V > 0

Ecell = +0.32 (0.28) = 0.60 V > 0
Ecell = 0.26 (0.28) = 0.02 V > 0 but too small
Fe reducing V(+5) to V(+3)
Ecell = +1.00 (0.04) = 1.04 V > 0
Ecell = +0.32 (0.04) = 0.36 V > 0
Ecell = 0.26 (0.04) = 0.22 V < 0
[Turn over
10
For
Examiner's
Use
Ni reducing V(+5) to V(+3)

Ecell = +1.00 (0.25) = 1.25 V > 0
Ecell = +0.32 (0.25) = 0.57 V > 0
Ecell = 0.26 (0.25) = 0.01 V > 0 but too small
The E potential for Co2+/Co (Fe3+/Fe or Ni2+/Ni) is bigger(less negative/more
positive) than that for V3+/V2+.
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
..................................................................................................................................
.............................................................................................................................. [3]
[Total: 14]
[Turn over
11
5
The standard enthalpy change of fusion (Hfus) is the energy required to convert
one mole of a substance in the solid state to the liquid state under standard
pressure. The table below shows numerical values of standard enthalpy change of
fusion for the respective elements:
Element
Na
Al
Si
Cl
(a)
For
Examiner's
Use
Hfus / kJ mol1
2.60
10.7
50.2
6.41
Explain, in terms of structure and bonding, the difference in the Hfus between:
(i)
Si and Cl
Silicon has a giant covalent structure while chlorine has a simple molecular
structure.
Melting of silicon requires breaking the numerous strong covalent bonds
between the atoms while melting of chlorine requires overcoming the weak
dispersion forces between the molecules.
Hence, more energy is required for silicon.
................................................................................................................... [2]
(ii)
Na and Al
Both aluminium and sodium have giant metallic structures with strong
metallic bonds between the cations and delocalised sea of electrons.
Aluminium contributes more electrons for metallic bonding than sodium and
the cation has smaller ionic radius. Hence the metallic bonds in aluminium
are stronger and more energy is required for the fusion process.
................................................................................................................... [2]
(b)
Experimental results show that the first ionisation energies for the elements
phosphorus and iodine are similar. Suggest an explanation for the observations.
Iodine has more protons has a higher nuclear charge.
However, valence electrons are further away from the nucleus experiences
greater screening effect.
As a result, the valence electron in I experiences similar effective nuclear effect as
that in P requires similar energies to remove the electron.
.............................................................................................................................. [2]
[Total: 6]
[Turn over
12
6
For
Examiner's
Use
X2 and Y2 are halogens and they are known to be more soluble in organic solvents.
In an experiment, excess X2 was mixed with Na2S2O3(aq). When hexane was
added, two immiscible layers were observed and was later separated using a
separatory funnel. A reddish brown organic layer was obtained and the aqueous
layer was divided into 2 portions.
To one portion of the aqueous layer, Y2(aq) was added and shaken. When CCl4
was added, a violet organic layer was obtained.
To another portion of the aqueous layer, AgNO3(aq) was added. The precipitate
formed does not dissolve in aqueous NH3.
(a)
Suggest a suitable identity of X2 and Y2.

X2: Bromine
(b)
Y2: Iodine
[1]
Write a balanced ionic equation for the reaction between Na2S2O3 and X2.
4Br2(l) + S2O32-(aq) + 5H2O(l) 2SO42-(aq) + 8Br(aq) + 10H+(aq)
.............................................................................................................................. [1]
(c)
Explain in energy terms, why halogens are more soluble in organic solvent than in
water.
In order for halogens to be soluble in organic solvents,
o Interactions between the halogen molecules and the solvent molecules
must be formed,
o Since the intermolecular forces are similar in both halogen molecules and
the solvent molecules are similar (e.g. van der Waals forces),
o The energy evolved in bond formation is likely able to compensate the
energy that is needed to break the interactions. Hence, it is energetically
favourable.
.............................................................................................................................. [2]
[Total: 4]
[Turn over
13
7
For
Examiner's
Use
Keratin refers to a family of fibrous proteins which is the key component of hair and
nails. The keratins in hair consist of -helically coiled single protein strands, further
twisted into superhelical ropes that may be further coiled. The presence of keratins
determines the strength and structure of hair i.e. straight or wavy. Nails, which are
less flexible and elastic, contains keratins which have -pleated sheets twisted
together, stabilised and hardened by R-group interactions.
The table below shows the amino acid composition of 2 samples of keratins. One
sample was extracted from nails, the other sample from hair.
Amino acid composition
Acid
R group
asp
asn
thr
ser
glu
CH2CO2H
CH2CONH2
CH(OH)CH3
CH2OH
CH2CH2CO2H
tyr
pro
CH2
CH2
OH
CH2 (cyclic)
Sample A
Sample B
3.0
3.0
6.9
11.7
6.1
3.0
2.0
4.5
8.5
6.1
1.9
4.2
3.6
3.2
6.5
4.8
17.5
5.9
0.5
2.7
6.1
6.0
5.6
3.2
28.2
5.9
3.5
2.7
6.0
5.8
1.4
4.5
3.7
3.0
2.3
3.8
0.8
2.1
5.6
6.2
CH2
gly
ala
cys
val
met
ile
leu
gln
phe
H
CH3
CH2SH
CH(CH3)2
CH2CH2SCH3
CH(CH3)CH2CH3
CH2CH(CH3)2
CH2CH2CONH2
CH2
trp
CH2
C
NH
lys
CH2CH2CH2CH2NH2
+
NH
his
CH2
C
N
H
arg
CH2CH2CH2NHC(NH2)=NH2+
[Turn over
14
(a)
For
Examiner's
Use
Draw a diagram representing the secondary structure of keratins found in nails. In

your diagram, show clearly the bonding that is involved in stabilising the secondary
structure. You may represent the R groups using the symbol R.
..
Hydrogen
bond
[3]
(b)
By referring to the amino acid composition data, answer the questions below:
(i)
State the R group interaction that is mainly responsible for the stabilisation of
the tertiary structure of keratins. Write an equation to support your answer.
Disulfide bonds
(ii)
In order to straighten wavy hair permanently, using a heating iron is

insufficient. Instead, one will need to go to the hairdresser to undergo a
treatment of chemicals. Explain why.
Disulfide bonds are covalent and strong, hence not easily broken by heating.
Treatment with chemicals is required.
(iii)
Which sample belongs to keratins extracted from a nail sample? Explain.

Nails are less flexible implying that there are more disulfide bonds (i.e. cross
linkages) formed between the R groups.
Hence the sample with greater amount of cys residues is probably keratins
from nail.
[5]
[Total: 8]
[Turn over
15
8(a)
For
Examiner's
Use
There are four stereoisomers of compound P.
CH
CHCH2CH
CHOH
OH
P
What is the type of stereoisomerism exhibited by P? Draw the stereoisomers of P.
Type of stereoisomerism: cis-trans / geometric ........................................................
OH
OH
OH
H
H
H
OH
H
OH
H
H
HO
OH
H
HO
[4]
[Turn over
16
(b)
For
Examiner's
Use
Q is a structural isomer of P in (a).

Suggest the structures of Q, R, S, T and U in the reaction scheme below.
CH3CH2CO2H
R (C3H6O2)
+
aqueous
HCl
heat
Q (C11H12O2)
H2
Ni catalyst
heat
aqueous
bromine
U (C8H7OBr3)
[5]
[Total: 9]
[Turn over
17
For
Examiner's
Use
When methylbenzene is nitrated by a mixture of concentrated nitric acid and

concentrated sulfuric acid, the product consists largely of two isomers, V and W, of
formula C7H7NO2. V has a plane of symmetry perpendicular to the plane of the
benzene ring in its molecule, while W does not. The formation of V proceeds via an
organic intermediate X.
(a)
Draw the displayed formulae of V and X, showing clearly the geometry of the bonds
around the carbon atom bonded to the nitrogen atom.
isomer V
organic intermediate X
[2]
(b)
What is the name of the mechanism of the reaction for the formation of V? Briefly
outline the mechanism of this reaction using equations.
Name of mechanism: Electrophilic substitution ..........................................................
Mechanism:
HNO3 + 2H2SO4 NO2+ + H3O+ + 2HSO4
[2]
[Total: 4]
[End[Turn
of Paper]
over

Higher 2
CHEMISTRY
9647/03
18 September 2012
2 hours
Candidates answer Section A on the Question Paper

Answer Paper
Data Booklet

Section B
Answer all questions on separate answer paper.
For Examiners Use

1
2
3
4
5
Total
[Turn over
2
Answer any four questions
1
Aldehydes and ketones react with primary amines in slightly acidic solution to form
imines which have the C=N functional group. For example, propanal reacts with
methylamine to give N-methyl-1-propanimine.
CH3CH2
CH3NH2
CH3CH2
H+
CH3
H
N-methyl-1-propanimine
propanal
(a) Aldehydes and ketones also react with 2,4-dinitrophenylhydrazine (2,4-DNPH) to

give compounds that are closely related to imines.
(i) Write a balanced equation for the reaction between benzaldehyde and 2,4DNPH.
(ii) State what you would observe in the reaction with 2,4-DNPH. What is the
type of reaction?
[4]
(b) The mechanism for the reaction between benzaldehyde and methylamine is
shown below.
H
H
step I
+
C
H
C
N
CH3
+ CH3NH2
O
O H
step II
CH3
OH
carbinolamine
step III + H+
step V
G
imine
H+
G
iminium ion
step IV
H2O
CH3
OH2
[Turn Over
3
(i) What is the type of reaction in step I?
(ii) The positive charge on the iminium ion, G+, does not reside on a carbon
atom. Suggest the structure of G+.
(iii) Write equations for step I and step IV to show the movement of electrons,
using curved arrow notation. Show the lone pairs of electrons, if any, that are
involved in each step.
(iv) The maximum rate of formation of imines occurs at a pH of about 4.5.
Explain why the rate is slow under very acidic conditions and under alkaline
conditions.
[6]
(c) Acrylamide is a carcinogen. It is formed when potato chips are heated to above
120 C. Its formation has been linked to the presence of glucose (C6H12O6) and
an -amino acid L found in relatively high amounts in potato.
H
C
H
OH OH OH OH OH
glucose
C
CONH2
acrylamide
Glucose reacts with L to form an imine M. At high cooking temperatures, M

decomposes to produce only three compounds in equimolar amounts: acrylamide,
carbon dioxide and compound N (C6H13NO5).
(i) Name the functional groups in acrylamide.

(ii) Deduce the structure of L. Show clearly how you obtained your answer.
[5]
(d) Suggest the reagents and conditions required to synthesise the following imine
derivative. Identify all the intermediate compounds.
O
N
N
[5]
[Total: 20]
[Turn Over
4
2
(a) A container holds a gaseous mixture of nitrogen and propane. The pressure in
the container at 200 C is 4.5 atm. At 40 C, the propane completely
condenses and the pressure drops to 1.5 atm. Calculate the mole fraction of
propane in the original gaseous mixture.
[3]
(b) The graph below shows the variation in electromotive force (e.m.f.) of the
following electrochemical cell with lg [Ag+(aq)] at 298 K.
Cu(s) | Cu2+(aq) || Ag+(aq) | Ag(s)
0.6
0.5
0.4
0.3
e.m.f / V
0.2
0.1
0
-8.0
-7.0
-6.0
-5.0
-4.0
-3.0
-2.0
-1.0
0.0
lg [Ag+(aq)]
(i) Using the information from the graph, calculate the standard electrode
potential of the half-cell, Ag+(aq) | Ag(s), at 298 K.
(ii) If the Ag+(aq) solution of the electrochemical cell is replaced by a saturated
solution of silver bromate(V), AgBrO3, in 0.1 mol dm3 potassium bromate(V)
and the e.m.f. of the cell measured at 298 K is +0.27 V, determine
(I)
(II)
the concentration of Ag+(aq) ions in the saturated solution, and

the solubility product of silver bromate(V) at 298 K.
[5]
[Turn Over
5
(c) Solid silver nitrate was slowly dissolved in a solution Q containing ethanedioate,
C2O42, and chromate(VI), CrO42, ions of concentrations 2.50 x 102 mol dm3
and 1.44 x 105 mol dm3 respectively.
(i) When a permanent precipitate of silver ethanedioate first appeared, the
concentration of silver ions in the solution was 2.10 x 105 mol dm3.
Calculate the solubility product of silver ethanedioate.
(ii) The dissolving of solid silver nitrate in Q was continued until a permanent red
precipitate of silver chromate(VI) first appeared. Calculate the concentrations
of silver ions and ethanedioate ions at that instant.
(Ksp of silver chromate(VI) is 1.2 x 1012 mol3 dm9.)
3
(iii) What is the amount of silver ethanedioate precipitated from 1.00 dm of the
solution?
[7]
(d) An electrochemical cell containing an oxygen cathode and a hydrogen anode is
shown below. The pistons above the gas chambers are frictionless.
high resistance
voltmeter
pistons
H2
O2
1 atm
25 C
Pt
Pt
1 mol dm3 H2SO4
(i) Write balanced equations for the half reactions and for the overall reaction in
the cell.
(ii) How does the concentration of sulfuric acid affect the equilibria of the half
reactions?
(iii) If weights are added to the pistons of both chambers, how would the reading
of the voltmeter change? Explain your answer.
[5]
[Total: 20]
[Turn Over
6
3
(a)
(i) Alkanes are generally considered to be unreactive compounds, showing an

inertness to common reagents such as NaOH, H2SO4 and K2Cr2O7.
Suggest a reason why these reagents do not attack an alkane such as CH4.
(ii) It is found by experiment that, during free-radical substitution of alkane,
primary, secondary and tertiary hydrogen atoms are replaced by chlorine
atoms at different rates, as shown in the following table.
type of hydrogen atom
primary
secondary
tertiary
reaction
RCH3 RCH2Cl
R2CH2 R2CHCl
R3CH R3CCl
relative rate
1
7
21
Using this information, and considering the number and type of hydrogen
atoms within the molecule, predict the relative ratio of the two possible
products J and K from the monochlorination of 2-methylpropane. Explain
your answer.
[3]
(b)
Compounds A and B are amines with the same molecular formula. Both have a
molecular mass of 73.0 and the following composition by mass: C, 65.8 % and H,
15.1 %.
Compound A has a pKb of 3.23 and contains a tri-substituted N atom.
The pH of an aqueous solution of 0.0100 mol dm3 of compound B is 11.5. When
B undergoes free-radical substitution reaction, it only gives one mono-substituted
organic product.
(i) Calculate the molecular formulae of compounds A and B.

(ii) Calculate the pKb of compound B.
(iii) Suggest the structural formulae of compounds A and B.
(iv) State and explain the relative basicity of compounds A and B.
[7]
[Turn Over
7
(c)
(i) The hydrolysis of 2-bromo-2-methylpropane takes place as follows.

(CH3)3CBr + H2O (CH3)3COH + H+ + Br
An experiment was conducted to determine the order of reaction with respect
to 2-bromo-2-methylpropane. The following results were obtained.
time/s
[(CH3)3COH]/mol dm3
19
28
50
69
154
0.0030 0.0040 0.0060 0.0072 0.0095
It was found that the order of reaction with respect to 2-bromo-2methylpropane is one and the half-life of the reaction is 34.5 s.
Using a non-graphical method, show that the concentration of 2-bromo-2methylpropane at the start of the experiment is 0.0096 mol dm3.
(ii) Hence, deduce how long the reaction has proceeded when concentration of
(CH3)3COH obtained is 0.0084 mol dm3.
(iii) The following two mechanisms are both consistent with the reaction being
overall first order.
mechanism X
mechanism Y
(CH3)3CBr (CH3)3C+ + Br
(CH3)3C+ + H2O (CH3)3COH + H+
slow
fast
Explain why both mechanisms X and Y show overall first order kinetics.
(iv) The rate of reaction for the hydrolysis of 2-bromo-2-methylpropane increases

when the temperature is increased. Explain this observation with the aid of a
suitable diagram.
(v) The rate of reaction for the hydrolysis of 2-bromo-2-methylpropane is R at
T oC. What is the new rate if temperature is increased to (T+50) oC?
[10]
[Total: 20]
[Turn Over
8
4
This question is about thermal decomposition reactions of Group II compounds.
(a)
A student investigates the thermal decomposition of some Group II nitrates. He

separately heats equal amounts of the nitrates of magnesium, calcium and
barium for one minute, passes the gases produced through aqueous sodium
hydroxide and measures the volume of the remaining gas. The following table
shows the results:
Element of nitrate
Volume of remaining gas / cm3
Mg
90
Ca
19
Ba
9
(i) Explain the purpose of sodium hydroxide and identify the remaining gas.
(ii) Draw an appropriate experimental set-up that allows the student to perform
the experiment and measure the volume of the remaining gas.
(iii) Using suitable data from the Data Booklet, explain the results obtained by the
student.
(iv) Hence, estimate the volume of remaining gas produced after 1 min if the
student were to heat zinc nitrate.
(b)
(v) The student heats a 10.0 g mixture of magnesium nitrate and calcium nitrate
till no further changes. The volume of remaining gas produced was 780 cm3
at room temperature. Calculate the mass of magnesium nitrate present.
[12]
The decomposition of calcium carbonate is as follows.
In order to determine the enthalpy change of decomposition, two pieces of
calcium carbonate were selected, each with a mass of 1.25 g. The first piece was
placed in 20 cm3 of excess dilute hydrochloric acid and the temperature rose by
2 C. The second piece was heated strongly for ten minutes to decompose it
thoroughly. It was then allowed to cool to room temperature before it was added
to 20 cm3 of dilute hydrochloric acid. The temperature rose by 26 C. The two
experiments were estimated to be 90% efficient.
(i) By using the information above and drawing a suitable energy cycle,
calculate the enthalpy change of decomposition of calcium carbonate, in
kJ mol1, to 3 significant figures.
When calcium carbonate is heated in a sealed tube at its thermal decomposition
temperature, the reaction eventually reaches an equilibrium.
(ii) Given that S = +161 J mol1 K1 and your answer in part (i), calculate the
thermal decomposition temperature, in K.
(iii) Hence sketch the graph of G against T, labelling clearly the thermal
decomposition temperature.
[8]
[Total: 20]
[Turn Over
9
5
Iron is the sixth most abundant element in the Universe and the most common
refractory element.
(a) Iron(III) oxide has a high melting point and is a good conductor of electricity when
molten. Explain, in terms of its bonding and structure, why iron(III) oxide has
these properties.
[3]
(b) Samples of iron(III) oxide and iron(III) chloride are added, with stirring, to
separate beakers of pure water. Suggest the pH value of the resulting solution in
each beaker after stirring, giving a reason for your choice. Write equations for any
reactions occurring.
[4]
(c) Give the ion-electron equations for the electrode reactions in the electrolysis of
aqueous iron(III) chloride using inert electrodes.
[2]
(d) When water reacts with iron(III) ions, it acts as a ligand in the formation of the
complex ion, [Fe(H2O)6]3+ to give a coloured solution.
(i) Explain what is meant by the term ligand.
(ii) Explain why solutions containing iron(III) ions are coloured but those
containing zinc ions are colourless.
[5]
(e) A solution contains a mixture of iron(III) and zinc ions. You are provided with
NaOH(aq) and HNO3(aq). You are to propose a series of test-tube experiments
to separate the two cations so that each cation is present as its aqueous ions.
(i) Give a description of your proposed sequence of steps to separate the two
cations, numbering each step.
(ii) With the aid of appropriate equations, explain the reactions involved.
[6]
[Total: 20]
[End
of Paper]
[Turn
Over

Higher 2
Answers
CHEMISTRY
9647/03
18 September 2012
2 hours
Candidates answer Section A on the Question Paper

Answer Paper
Data Booklet

Section B
Answer all questions on separate answer paper.
For Examiners Use

1
2
3
4
5
Total
[Turn over
2
1
Aldehydes and ketones react with primary amines in slightly acidic solution to form
imines which have the C=N functional group. For example, propanal reacts with
methylamine to give N-methyl-1-propanimine.
CH3CH2
CH3NH2
CH3CH2
H+
CH3
H
N-methyl-1-propanimine
propanal
(a) Aldehydes and ketones also react with 2,4-dinitrophenylhydrazine (2,4-DNPH) to

give compounds that are closely related to imines.
(i) Write a balanced equation for the reaction between benzaldehyde and 2,4DNPH.
O 2N
C
H2N
NO2
N
H
O2 N
C
H
NO2
H2O
(ii) State what you would observe in the reaction with 2,4-DNPH. What is the
type of reaction?
orange precipitate
condensation
[4]
[Turn Over
3
(b) The mechanism for the reaction between benzaldehyde and methylamine is
shown below.
H
H
step I
+
C
H
C
N
CH3
+ CH3NH2
O
O H
step II
CH3
OH
carbinolamine
step III + H+
step V
G
imine
G
iminium ion
H+
step IV
H2O
CH3
OH2
(i) What is the type of reaction in step I?

nucleophilic addition
(ii) The positive charge on the iminium ion, G+, does not reside on a carbon
atom. Suggest the structure of G+.
H
CH3
[Turn Over
4
(iii) Write equations for step I and step IV to show the movement of electrons,
using curved arrow notation. Show the lone pairs of electrons, if any, that are
involved in each step.
(iv) The maximum rate of formation of imines occurs at a pH of about 4.5.

Explain why the rate is slow under very acidic conditions and under alkaline
conditions.
acidic: amine protonated; no nucleophile (Step I)
alkaline: very low H+ conc; no catalyst (Step III)
[6]
(c) Acrylamide is a carcinogen. It is formed when potato chips are heated to above
120 C. Its formation has been linked to the presence of glucose (C6H12O6) and
an -amino acid L found in relatively high amounts in potato.
H
C
H
OH OH OH OH OH
glucose
C
CONH2
acrylamide
Glucose reacts with L to form an imine M. At high cooking temperatures, M

decomposes to produce only three compounds in equimolar amounts: acrylamide,
carbon dioxide and compound N (C6H13NO5).
(i) Name the functional groups in acrylamide.

alkene , amide
[Turn Over
5
(ii) Deduce the structure of L. Show clearly how you obtained your answer.
H
L : H2N
CO2H (asparagine).
CH2CONH2
Accept other possible alternatives.
[5]
(d) Suggest the reagents and conditions required to synthesise the following imine
derivative. Identify all the intermediate compounds.
O
N
N
OH
O
aq NaBH4
xs conc. H2SO4
heat
OH
aq Br2
OH
Br
NH2
xs ethanolic NH3
heat in sealed tube
O
acidified K2Cr2O7
NH2
H+
warm
N
N
[5]
[Total: 20]
[Turn Over
6
2
(a) A container holds a gaseous mixture of nitrogen and propane. The pressure in
the container at 200 C is 4.5 atm. At 40 C, the propane completely
condenses and the pressure drops to 1.5 atm. Calculate the mole fraction of
propane in the original gaseous mixture.
[3]
Let the amount of nitrogen and propane be n1 and n2 respectively. Since the
gas constant, R, and volume of container, V, are constants, the gas equation
becomes:
P = nR = kn where k = R
T
V
V
4.5 = k (n1 + n2) = 9.513 x 103
473
and 1.5 = kn1 = 6.437 x 103
233
kn2 = 9.513 x 103 6.437 x 103 = 3.076 x 103
mole fraction of propane = 3.076 x 103 = 0.323
9.513 x 103
(b) The graph below shows the variation in electromotive force (e.m.f.) of the
following electrochemical cell with lg [Ag+(aq)] at 298 K.
Cu(s) | Cu2+(aq) || Ag+(aq) | Ag(s)
0.6
0.5
0.4
0.3
e.m.f / V
0.2
0.1
0
-8.0
-7.0
-6.0
-5.0
-4.0
-3.0
-2.0
-1.0
0.0
lg [Ag (aq)]
(i) Using the information from the graph, calculate the standard electrode
potential of the half-cell, Ag+(aq) | Ag(s), at 298 K.
[Turn Over
7
Let the standard electrode potential of Ag+(aq) | Ag(s) half-cell be x.
+
When [Ag+(aq)] = 1.00 mol dm3, lg [Ag (aq)] = 0
E
cell = +0.46 = x (+0.34)
x = +0.46 + (+0.34) = +0.80 V
(ii) If the Ag+(aq) solution of the electrochemical cell is replaced by a saturated
solution of silver bromate(V), AgBrO3, in 0.1 mol dm3 potassium bromate(V)
and the e.m.f. of the cell measured at 298 K is +0.27 V, determine
the concentration of Ag+(aq) ions in the saturated solution, and
(I)
From the graph, when e.m.f. of cell is +0.27 V, lg [Ag (aq)] = 3.2.
+
[Ag (aq)] = 6.309 x 104 mol dm3

(II)
the solubility product of silver bromate(V) at 298 K.

2
Ksp = 6.309 x 104 x 0.1 = 6.309 x 105 mol dm6

[5]
(c) Solid silver nitrate was slowly dissolved in a solution Q containing ethanedioate,
C2O42, and chromate(VI), CrO42, ions of concentrations 2.50 x 102 mol dm3
and 1.44 x 105 mol dm3 respectively.
(i) When a permanent precipitate of silver ethanedioate first appeared, the
concentration of silver ions in the solution was 2.10 x 105 mol dm3.
Calculate the solubility product of silver ethanedioate.
2
Ksp(Ag2C2O4) = (2.10 x 105) x 2.50 x 102

3
= 1.10 x 1011 mol dm9
(ii) The dissolving of solid silver nitrate in Q was continued until a permanent red
precipitate of silver chromate(VI) first appeared. Calculate the concentrations
of silver ions and ethanedioate ions at that instant.
(Ksp of silver chromate(VI) is 1.2 x 1012 mol3 dm9.)
3
Given: Ksp(Ag2CrO4) is 1.2 x 1012 mol dm9.

1.2 x 1012 = [Ag+]2 x 1.44 x 105
[Ag+]2 = 8.333 x 108
+
[Ag ] = 2.89 x 104 mol dm3
1.102 x 1011 = (2.886 x 104)2 x [C2O42]
[C2O42] = 1.32 x 104 mol dm3
3
(iii) What is the amount of silver ethanedioate precipitated from 1.00 dm of the
solution?
[Turn Over
8
n(C2O42) removed from solution = 2.50 x 102 1.322 x 104
= 0.02486 mol
amount of silver ethanedioate ppted = 0.0249 mol.
[7]
(d) An electrochemical cell containing an oxygen cathode and a hydrogen anode is

shown below. The pistons above the gas chambers are frictionless.
high resistance
voltmeter
pistons
H2
O2
1 atm
25 C
Pt
Pt
1 mol dm3 H2SO4
(i) Write balanced equations for the half reactions and for the overall reaction in
the cell.
Half reactions:
Overall reaction:
H2 2H+ + 2e
(anode)
+
O2 + 4H + 4e 2H2O (cathode)
2H2 + O2 2H2O
(ii) How does the concentration of sulfuric acid affect the equilibria of the half
reactions?
2H+ + 2e H2
O2 + 4H+ + 4e 2H2O
0.00V (anode)
+1.23V (cathode)
Increase in concentration of sulfuric acid will increase [H+] and by

Le Chateliers Principle, cause the position of equilibrium of anode and
cathode reactions to shift right.
[Turn Over
9
(iii) If weights are added to the pistons of both chambers, how would the reading
of the voltmeter change? Explain your answer.
If weights are added, the pressure will increase, resulting in position of
equilibrium of anode reaction shifting left to remove excess pressure
on hydrogen gas. The electrode potential will decrease to less than
zero volt.
The position of equilibrium of the cathode reaction will shift right,
resulting in a more positive electrode potential for the cathode. As a
result, the reading on the voltmeter will be greater than 1.23 V.
[5]
[Total: 20]
[Turn Over
10
3
(a)
(i) Alkanes are generally considered to be unreactive compounds, showing an

inertness to common reagents such as NaOH, H2SO4 and K2Cr2O7.
Suggest a reason why these reagents do not attack an alkane such as CH4.
Alkanes are non-polar or have no dipole or CH bonds are strong
or C and H have similar electronegativities.
(ii) It is found by experiment that, during free-radical substitution of alkane,

primary, secondary and tertiary hydrogen atoms are replaced by chlorine
atoms at different rates, as shown in the following table.
type of hydrogen atom
primary
secondary
tertiary
reaction
RCH3 RCH2Cl
R2CH2 R2CHCl
R3CH R3CCl
relative rate
1
7
21
Using this information, and considering the number and type of hydrogen
atoms within the molecule, predict the relative ratio of the two possible
products J and K from the monochlorination of 2-methylpropane. Explain
your answer.
J:K = 2.3 : 1 or 7:3 or 21:9
reason: straightforward relative rate suggests 21:1, but there are 9 primary to
1 tertiary, so divide this ratio by 9. 21/9 = 2.33
[3]
(b)
Compounds A and B are amines with the same molecular formula. Both have a
molecular mass of 73.0 and the following composition by mass: C, 65.8 % and H,
15.1 %.
Compound A has a pKb of 3.23 and contains a tri-substituted N atom.
The pH of an aqueous solution of 0.0100 mol dm3 of compound B is 11.5. When
B undergoes free-radical substitution reaction, it only gives one mono-substituted
organic product.
(i) Calculate the molecular formulae of compounds A and B.

C:H:N ratio: 65.8/12 : 15.1/1 : 19.1/14 = 4 : 11 : 1
Empirical Formula: C4H11N
Let the molecular formula be C4nH11nNn
4n(12.0) + 11n(1.0) + n(14.0) = 73.0
n=1
Hence molecular formula is C4H11N
[Turn Over
11
(ii) Calculate the pKb of compound B.
10(14-11.5) = (0.0100 * Kb)1/2
Kb = 1 x 103 mol dm3
pKb = lg (1 x 103) = 3
(iii) Suggest the structural formulae of compounds A and B.

CH3
H3C
CH3
A: H3C
CH2CH3
B:
NH2
CH3
(iv) State and explain the relative basicity of compounds A and B.

[7]
pKb (A) = 3.23
pKb (B) = 3
B (1o amine) is more basic than A (3o amine).

Although A has 3 electron-donating alkyl groups bonded to the N atom while
B has only one electron-donating group, the presence of 3 bulky
substituents in A hinder the approach of H+ to form dative bond with
the lone pair of electrons on N.
(c)
(i) The hydrolysis of 2-bromo-2-methylpropane takes place as follows.

An experiment was conducted to determine the order of reaction with respect
to 2-bromo-2-methylpropane. The following results were obtained.
time/s
[(CH3)3COH]/mol dm3
19
28
50
69
154
0.0030 0.0040 0.0060 0.0072 0.0095
It was found that the order of reaction with respect to 2-bromo-2methylpropane is one and the half-life of the reaction is 34.5 s.
Using a non-graphical method, show that the concentration of 2-bromo-2methylpropane at the start of the experiment is 0.0096 mol dm3.
The first t1/2 corresponds to the time taken for half the final [(CH3)3COH] to be
formed while the sum of two t1/2 corresponds to the time taken for of the
final [(CH3)3COH] to be formed.
The [(CH3)3COH] at time = 34.5 s is not given in the table but the
[(CH3)3COH] at time = 2 x 34.5 = 69 s is given.
Hence, x final [(CH3)3COH] = 0.0072 mol dm3 ,
final [(CH3)3COH] = 4/3 x 0.0072 = 0.0096 mol dm3
[Turn Over
12
Since the mole ratio of (CH3)3CBr : (CH3)3COH = 1:1 and assuming that the
total volume of the reaction mixture remains constant,
[(CH3)3CBr] at the start of the experiment = final [(CH3)3COH]
= 0.0096 mol dm3
(ii) Hence, deduce how long the reaction has proceeded when concentration of
(CH3)3COH obtained is 0.0084 mol dm3.
0.0084 = 7/8 x 0.0096
Hence, three half-lives have passed by.
Reaction has proceed for 3 x 34.5 = 103.5 s.
(iii) The following two mechanisms are both consistent with the reaction being
overall first order.
mechanism X
mechanism Y
(CH3)3CBr (CH3)3C+ + Br
(CH3)3C+ + H2O (CH3)3COH + H+
slow
fast
Explain why both mechanisms X and Y show overall first order kinetics.
H2O is usually present in excess, hence its concentration is kept relatively
constant. Since the given equation in mechanism 1 shows 1 molecule of
(CH3)3CBr participating in the reaction, the reaction is overall first order
kinetics.
In mechanism 2, the slow step involves 1 molecule of (CH3)3CBr. Hence the
rate equation is rate = k[(CH3)3Br] which shows that the reaction is overall
first order kinetics.
[Turn Over
13
(iv) The rate of reaction for the hydrolysis of 2-bromo-2-methylpropane increases
when the temperature is increased. Explain this observation with the aid of a
suitable diagram.
(v) The rate of reaction for the hydrolysis of 2-bromo-2-methylpropane is R at

T oC. What is the new rate if temperature is increased to (T+50) oC?
Rate doubled when temperature increased by 10oC. Since temperature
increased by 20oC, rate increased by 25 times. Hence the new rate is 32R.
[10]
[Total: 20]
[Turn Over
14
4
This question is about thermal decomposition reactions of Group II compounds.
(a)
A student investigates the thermal decomposition of some Group II nitrates. He

separately heats equal amounts of the nitrates of magnesium, calcium and
barium for one minute, passes the gases produced through aqueous sodium
hydroxide and measures the volume of the remaining gas. The following table
shows the results:
Element of nitrate
Volume of remaining gas / cm3
Mg
90
Ca
19
Ba
9
(i) Explain the purpose of sodium hydroxide and identify the remaining gas.
NaOH: absorb NO2. O2 is remaining gas.
(ii) Draw an appropriate experimental set-up that allows the student to perform
the experiment and measure the volume of the remaining gas.
Sealed boiling tube and Bunsen burner, connected to U-tube containing
NaOH, connected to gas syringe.
(iii) Using suitable data from the Data Booklet, explain the results obtained by the
student.
Ionic radii Mg2+(0.065 nm), Ca2+(0.099 nm), Ba2+(0.135 nm)
Down the group, as ionic radii increases, charge density of the cation
decreases, hence polarizes the nitrate anion to a lesser extent.
Nitrate becomes more thermally stable and produces lesser gas after 1 min.
(iv) Hence, estimate the volume of remaining gas produced after 1 min if the
student were to heat zinc nitrate.
Ionic radii of Zn2+ is 0.074 nm, in between that of Mg2+ and Ca2+.
Hence, volume of gas produced is approximately 60 cm3.
(v) The student heats a 10.0 g mixture of magnesium nitrate and calcium nitrate
till no further changes. The volume of remaining gas produced was 780 cm3
at room temperature. Calculate the mass of magnesium nitrate present.
Let mass of magnesium nitrate be x.
Mg(NO3)2 MgO + 2NO2 + O2
Ca(NO3)2 CaO + 2NO2 + O2
n(Mg(NO3)2) = x / 148.3
n(O2) produced by Mg(NO3)2 = x / 296.6
V(O2) = 24000x / 296.6
n(Ca(NO3)2) = (10.0 x) / 164.1
n(O2) produced by Ca(NO3)2 = (10.0 x) / 328.2
m(Mg(NO3)2) = 24000(10.0 x) / 328.2
Total volume = [24000x / 296.6] + [24000(10.0 x) / 328.2] = 780
328.2x + 296.6(10.0 x) = 0.0325(296.6)(328.2)
x = 6.26 g
[12]
[Turn Over
15
(b)
The decomposition of calcium carbonate is as follows.

In order to determine the enthalpy change of decomposition, two pieces of
calcium carbonate were selected, each with a mass of 1.25 g. The first piece was
placed in 20 cm3 of excess dilute hydrochloric acid and the temperature rose by
2 C. The second piece was heated strongly for ten minutes to decompose it
thoroughly. It was then allowed to cool to room temperature before it was added
to 20 cm3 of dilute hydrochloric acid. The temperature rose by 26 C. The two
experiments were estimated to be 90% efficient.
(i) By using the information above and drawing a suitable energy cycle,
calculate the enthalpy change of decomposition of calcium carbonate, in
kJ mol1, to 3 significant figures.
CaCO3 + 2HCl CaCl2 + CO2 + H2O H1
H1 = [(20 x 4.18 x 2) / 0.9 ] / (1.25 / 100.1) = 14.9 kJ mol-1
CaO + 2HCl CaCl2 + H2O H2
H2 = [(20 x 4.18 x 26) / 0.9 ] / (1.25 / 100.1) = 193.4 kJ mol-1
H
H2
H1
+2HCl
+2HCl
CaCl2(aq) + H2O(l) + CO2(g)
H = 193.4 14.9 = 179 kJ mol-1

When calcium carbonate is heated in a sealed tube at its thermal decomposition
temperature, the reaction eventually reaches an equilibrium.
(ii) Given that S = +161 J mol1 K1 and your answer in part (i), calculate the
thermal decomposition temperature, in K.
G = 0 = 179 T(161/1000)
T = 1112 K
(iii) Hence sketch the graph of G against T, labelling clearly the thermal
decomposition temperature.
G
T/K
1112
[8]
[Total: 20]
[Turn Over
16
5
Iron is the sixth most abundant element in the Universe and the most common
refractory element.
(a) Iron(III) oxide has a high melting point and is a good conductor of electricity when
molten. Explain, in terms of its bonding and structure, why iron(III) oxide has
these properties.
[3]
Fe2O3 has giant ionic structure with strong ionic bonds between oppositely
charged ions.
Large amount of energy required to overcome the strong ionic bonds hence it
has a high melting point.
In molten state, there are free mobile ions to carry charges hence it can conduct
electricity.
(b) Samples of iron(III) oxide and iron(III) chloride are added, with stirring, to
separate beakers of pure water. Suggest the pH value of the resulting solution in
each beaker after stirring, giving a reason for your choice. Write equations for any
reactions occurring.
[4]
pH 7 (Fe2O3). pH 3 (FeCl3)
Fe2O3 is insoluble in water due to the very exothermic lattice energy.
FeCl3 undergoes hydrolysis due to the high charge density of Fe3+.
FeCl3 + 6H2O Fe(H2O)63+ + 3ClFe(H2O)63+ + H2O Fe(H2O)5(OH)2+ + H3O+
(c) Give the ion-electron equations for the electrode reactions in the electrolysis of
aqueous iron(III) chloride using inert electrodes.
[2]
Cathode: Fe3+ + e Fe2+
Anode: 2H2O O2 + 4H+ + 4e
(d) When water reacts with iron(III) ions, it acts as a ligand in the formation of the
complex ion, [Fe(H2O)6]3+ to give a coloured solution.
(i) Explain what is meant by the term ligand.
Ligand is a molecule or anion with at least one lone pair of electrons that it
can use to form a coordinate bond to the central metal atom/ion in a complex
ion.
(ii) Explain why solutions containing iron(III) ions are coloured but those
containing zinc ions are colourless.
In an octahedral iron(III) complex ion, the ligands cause a split in the

energies of the 3d orbitals.
The energy difference, o = h, corresponds to wavelengths in the visible
spectrum.
An electron is promoted from a d orbital of lower energy to one of higher
energy by absorbing a photon with energy o.
Unabsorbed wavelengths are transmitted.
[Turn Over
17
The colour of the complex is complementary to the colour absorbed.

Zn2+ has completely filled d orbitals and no d-d transition can take place
[5]
(e) A solution contains a mixture of iron(III) and zinc ions. You are provided with
NaOH(aq) and HNO3(aq). You are to propose a series of test-tube experiments
to separate the two cations so that each cation is present as its aqueous ions.
(i) Give a description of your proposed sequence of steps to separate the two
cations, numbering each step.
1. To 2 cm depth of solution in a test tube, add NaOH(aq) dropwise till in
excess.
2. Filter the mixture
3. Add excess HNO3 to the filtrate. (Zn2+)
4. Add excess HNO3 to the residue. (Fe3+)
(ii) With the aid of appropriate equations, explain the reactions involved.
Precipitation reaction:
Fe3+(aq) + 3OH-(aq) Fe(OH)2(s)
(I)
2+
(I)
Zn (aq) + 2OH (aq) Zn(OH)2(s)
Formation of soluble complex:
Excess NaOH(aq): Zn(OH)2(s) + 2OH-(aq) Zn(OH)42-(aq) (II)
H+ added will react with OH- present and cause [OH-] to decrease in
equilibrium (I) POE will shift left to replace the removed OH- hence Fe3+(aq)
and Zn2+(aq) are formed.
[6]
[Total: 20]
[End of Paper]
[Turn Over
Name:
Index No.:
CT Group: 11
PIONEER JUNIOR COLLEGE

JC2 PRELIMINARY EXAMINATION
HIGHER 2
CHEMISTRY
9647/01
20 September 2012
1 hour

Data Booklet

Write your name, Centre number and index number on the Answer Sheet in the spaces provided
unless this has been done for you.
Answer Sheet.
2
Section A
For each question, there are four possible answers labelled A, B, C and D. Choose the
one you consider to be correct.
1
Acidified, aqueous potassium manganate(VII) oxidises ethanedioate ions, C2O42-, to

CO2.
2MnO4-(aq) + 5C2O42-(aq) + 16H+(aq) 2Mn2+(aq) + 10CO2(g) + 8H2O(l)
What is the concentration of potassium manganate(VII), in mol dm3, if 20 cm3 is
required to completely oxidise 2.0 x 10-3 mol of the salt KHC2O4.H2C2O4?
5 1000
x
x 2.0 x 10 -3
2
20
5 1000
x
x 4.0 x 10 -3
2
20
2 1000
x
x 2.0 x 10 -3
5
20
2 1000
x
x 4.0 x 10 -3
5
20
The radioactive decay of polonium,

following equation.
210
84
Po
210
84
206
82
Po , can be simply represented by the
Pb + + 2e-
What would be the path taken by the alpha particle, , when it is passed through an
electric field?
1
H+
source
A
+
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3
3
What are the values of angle x, y and z in a molecule of Disperse Yellow?

H
x
CH3
O
C
z
O
NH
CH3
Disperse Yellow
angle x
angle y
angle z
90
115
105
90
180
180
120
115
105
120
180
115
Which of the following pairs of graphs share the same general shape according to
ideal gas law for a fixed mass of gas?
A
p against V (at constant T)
and
V/T against T (at constant p)
pV against V (at constant T)
and
V/T against T (at constant p)
p against T (at constant V)
and
pV against p (at constant T)
V against T (at constant p)
and
pV against p (at constant T)
Travellers to countries with cold climate may sometimes use heat packs to keep
warm. One example is the sodium ethanoate heat pack. This consists of a
supersaturated solution of sodium ethanoate and a small metal disc containing very
small crystals of sodium ethanoate.
When the disc is broken, the small crystals of sodium ethanoate are released into
the solution and act as nucleation sites to catalyse the crystallisation reaction of
sodium ethanoate.
Which line gives the signs of H, S and G for the overall process?
H
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4
6
Barium reacts with water to form barium hydroxide and hydrogen.

Ba(s) + 2H2O(l) Ba(OH)2(aq) + H2(g)
The standard enthalpy change for this reaction can be measured in the laboratory.
What further information is needed to calculate the standard enthalpy change of
formation of solid barium hydroxide?
I
II
III
IV
Standard enthalpy change of formation of water

Standard enthalpy change of solution of barium hydroxide
Standard enthalpy change of hydration of barium ion
Standard enthalpy change of hydration of hydroxide ion
I only
I and II
III and IV
I, II, III and IV
The distribution of the number of molecules with energy E is given in the sketch for
two temperatures, T1 and a higher temperature T2. The letters P, Q, R refer to the
separate and differently shaded areas. The activation energy is marked on the
energy axis.
Legend
Number of
molecules
with energy E
T1
region P
T2
region Q
region R
energy E
activation energy
Which expression gives the fraction of the molecules present which have at least
the activation energy at the higher temperature T2?
Q
A P
PJC 2012
Q+R
P
Q+R
P +Q
9647/01/JC2 PRELIM/2012
Q+R
P +Q + R
5
8
Aspirin is an analgesic often used to relieve minor aches and pains. The chemical
stability of aspirin is of great importance since it becomes less effective when
exposed to high temperature and moisture.
A kinetic study on the reaction of aspirin and water was conducted.
O
O
O
CH3
OH
+ H2O
O
OH
+ CH3COOH
OH
aspirin
The graph below shows the concentration of aspirin against time for this reaction.
[aspirin]
time
What does the shape of the graph suggest about this reaction?
A
It is exothermic.
It is endothermic.
It shows first order kinetics.
It produces its own catalyst.
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6
9

A cell is set up by connecting a Cu2+/Cu half-cell and an acidified Cr2O72/Cr3+ halfcell under standard conditions.
Which of the following correctly describes the effect on the e.m.f of the cell when the
corresponding change is made?
Change
10
Effect on e.m.f of cell
replace copper with an alloy of copper and silver
increases
addition of concentrated H2SO4 into reduction half-cell
decreases
addition of dilute NaOH into oxidation half-cell
decreases
addition of water into oxidation half-cell
increases
When a dilute sulfate solution of a metal J is electrolysed, the metal J and a

diatomic gas K are produced at the cathode and the anode respectively in the molar
ratio 2:1. In another experiment, the same quantity of electricity is used to
electrolyse a saturated sodium chloride solution and a gas L is evolved at the
anode.
What is the molar ratio of J:K:L?
A
2:1:1
2:1:2
4:2:1
4:2:3
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7
11
The following equation represents the conversion of Y2 to Y.

Y2(g) 2Y(g)
The conversion was studied using a fixed amount of Y2 in a reaction vessel. At
different times during the experiment, changes were made to the conditions in the
reaction vessel. The change in the concentrations in the equilibrium mixture with
time is given by the graph below:
Which one of the following statements is correct?
12
A catalyst was added at T1.
There was a decrease in volume of the reaction vessel at T2.
There was an increase in temperature at T2.
More Y2 was introduced at T2.
A pure sample of dinitrogen tetraoxide at an initial pressure of 1 atm is allowed to

reach equilibrium in a vessel of constant volume and constant temperature.
N2O4
2NO2
What is the equilibrium constant, Kp, for this reaction, given that the equilibrium
pressure is 1.5 times greater than the initial pressure?
A 1 atm
PJC 2012
2 atm
3 atm
9647/01/JC2 PRELIM/2012
4 atm
8
13
The table below shows the values of the ionic product of water, Kw, at two different
temperatures.
Temperature / oC
Kw / mol2 dm-6
25
62
1.00 10-14
1.00 10-13
Which of the following statements is correct for pure water?
14
The ionic dissociation of water is an exothermic process.
At 62 oC, pH = 14 pOH.
At 62 oC, pH < pOH.
At 62 oC, it is neutral and pH < 7.
A sample of waste solution at pH 1 is found to contain 0.100 mol dm-3 zinc sulfate
and 0.100 mol dm-3 lead(II) sulfate. Solid sodium hydroxide is slowly added until the
pH is 5.
The solubility product of zinc hydroxide is 3.00 x 10-17 mol3 dm-9 and that of lead(II)
hydroxide is 1.42 x 10-20 mol3 dm-9.
Which statement describes what happens in the solution?
15
No precipitate is formed.
Only lead(II) hydroxide is precipitated.
Only zinc hydroxide is precipitated.
Both zinc hydroxide and lead(II) hydroxide are precipitated.
P, Q and R are elements of the third period of the Periodic Table. The oxide of P is
amphoteric, the oxide of Q is basic and oxide of R is acidic.
What is the order of decreasing ionic radius?
A RQP
B RPQ
C QPR
D PQR
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9
16
17
Which property of the Group II elements (magnesium to barium) and their

compounds increases with increasing proton number?
A
The ease of thermal decomposition of the carbonate
The pH of the aqueous chloride
The solubility of hydroxide in water
The magnitude of the enthalpy change of hydration of the metal ion
The ash from burnt seaweed contains chlorides and iodides of some Group I and
Group II elements. Some seaweed ash was treated with concentrated sulfuric acid
and the resulting fumes passed first through a cold tube and then bubbled through
aqueous silver nitrate.
What would be observed during the experiment?
inside the cold tube
with aqueous silver nitrate
no deposit
white precipitate
no deposit
yellow precipitate
black deposit
white precipitate
black deposit
yellow precipitate
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10
18
Nickel(II) ion forms a red complex with ligand L (shown below) at room temperature.
H
C
N
O
CH3
L
The graph below was obtained when the colour intensities of mixtures of a
4 x 103 mol dm3 solution of L and a 3 x 103 mol dm3 solution of nickel(II) chloride
were measured using a colorimeter at room temperature
Which one of the following statements regarding the ligand L or the nickel(II)
complex is correct?
A
L is a monodentate ligand.
The nickel(II) complex is negatively charged.
The nickel(II) complex absorbs red light strongly.
The co-ordination number of nickel in the complex is 4.
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11
19
What is the total number of possible isomers that can be formed when the following
compound reacts with hot excess concentrated H2SO4?
HO
Cl
HO
A 2
20
How many esters with molecular formula C4H8O2 react with hot, acidified potassium
manganate(VII) to give carbon dioxide?
A 2
21
When excess BrCl is added to the methylbenzene in the presence of uv light, which
organic compound will be produced in the smallest proportion?
A
CH2Br
CHBr2
CH2Cl
CH2
CH2
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12
22
23
Which of the following statements regarding compound Z is incorrect?
There is only one sp hybridised carbon atom in a molecule of Z.
A molecule of Z contains four p bonds.
After Z reacts with LiAlH4, all the carbon atoms in the product formed are sp3
hybridised.
After Z reacts with HCl(g), all but one carbon atom in the product formed are
sp3 hybridised.
Compound V may be synthesised from benzene.

Br
HO 2C
NH2
V
Which of the following synthetic routes will yield compound V?
A
alkylation nitration oxidation bromination reduction
bromination nitration reduction alkylation oxidation
nitration alkylation reduction bromination oxidation
nitration reduction bromination alkylation oxidation
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13
24
Putrescine is used in the production of Nylon-4,6. It can be synthesised from

ethene by the following reactions.
I
II
CH2=CH2
III
NCCH2CH2CN
H2NCH2CH2CH2CH2NH2
Putrescine
Which of the following gives the correct reagents and conditions for steps I to III?
25
26
II
III
Br2
KCN in ethanol, heat
H2, Ni, 200 C
Br2
HCN, trace NaCN, 15 C
LiAlH4, dry ether
cold, alkaline KMnO4
KCN in ethanol, heat
LiAlH4, dry ether
cold, alkaline KMnO4
HCN, trace NaCN, 15 C
H2, Ni, 200 C
Which of the following compounds would not give sodium ethanoate when treated
with hot, aqueous sodium hydroxide?
A
CH3CONHCH3
C6H5OCOCH3
CH3CH2CN
CH3COCl
When treated with concentrated potassium hydroxide, benzaldehyde undergoes

disproportionation.
What compounds are produced in this reaction?
A
C6H5O-K+ and C6H5CO2-K+
C6H5O-K+ and C6H5CH2OH
C6H5CH2O-K+ and C6H5CO2-K+
C6H5CH2OH and C6H5CO2-K+
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14
27
Which of the following compounds

(i) does not decolourise hot, acidified KMnO4(aq) and
(ii) gives a salt when reacted with NaOH(aq)?
A
CH3CO2CH2CO2H
CH2(OH)COCH2CO2H
(CH3)2C(OH)CH2COOH
CH3
D
OH
28
Compounds X, Y and Z all react with PCl5 to release hydrogen chloride, but only
one reacts with Fehlings solution.
Which one of the following combinations could be X, Y and Z?
X
CH2OH
CH2OH
CHO
CH2CH2OH
CH2CHO
CH2CHO
CH2OH
CHO
CH2OH
CH2CH2OH
CH2OH
CH2CHO
CO 2H
CH2OH
CO 2H
CO 2H
CH2CHO
CH2CHO
CO 2H
CH2OH
CO 2H
CO 2H
CHO
CH2CH2OH
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15
29
Morphine is an effective pain killer.

N
HO
CH3
OH
morphine
Which of the following statements about morphine is correct?
30
It contains 4 chiral centres.
It reacts with Br2(aq) to incorporates up to 3 atoms of bromine atoms in each

molecule.
It decolourises Baeyers reagent (alkaline KMnO4) at room temperature.
With excess PCl5, 1 mole of morphine reacts with excess PCl5 to give 2 moles
of HCl.
A mixture of amino acids can be separated using electrophoresis. The solution of

amino acids is buffered at a specific pH and placed in a well in a gel conducting
current between two electrodes.
At a buffer pH of 8, which of the following amino acids will appear closest to the
anode at the end of electrophoresis?
NH2
A
HO2C CH CH2CH2OH
NH2
B
HO2C
CH
CH2CO2H
NH2
C
HO2C
CH
CH2CONH2
NH2
D
PJC 2012
HO2C
CH
CH2
OH
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16
Section B
For each of the questions in this section, one or more of the three numbered statements 1
to 3 may be correct.
A
1, 2 and 3 are
correct
B
1 and 2 only are
correct
C
2 and 3 only are
correct
D
1 only is correct
31
Gases A and B are both gaseous hydrocarbons. When a 30 cm3 mixture of A and B
in the ratio of 1:2 is sparked continuously with excess oxygen gas, 70 cm3 of the
residual gas is absorbed by aqueous sodium hydroxide.
Which of the following pairs of hydrocarbons could be A and B?
32
33
A
methane
B
propane
propane
ethane
pentane
methane
Which of the following pairs of elements have the same number of unpaired
electrons in their ground state?
1
carbon and titanium
nitrogen and cobalt
fluorine and copper
Which of the following could act as acidic buffers?

1
A 1:2 mixture of NaOH and C6H5COOH
A 1:2 mixture of HCl and NaHCO3
A 1:2 mixture of HCl and CH3CO2Na
PJC 2012
9647/01/JC2 PRELIM/2012
17
A
1, 2 and 3 are
correct
B
1 and 2 only are
correct
C
2 and 3 only are
correct
D
1 only is correct
34
A chloride and an oxide of two elements were dissolved in water.

Only one of the solutions can dissolve Al2O3 but both solutions cannot dissolve
SiO2.
Which of the following could be the chloride and the oxide?
35
NaCl and SO3
SiCl4 and P4O10
PCl5 and Na2O
The hexa-aquairon(III) ion hydrolyses as shown.

[Fe(H2O)6]3+(aq) + H2O(l) [Fe(H2O)5OH]2+(aq) + H3O+(aq)
36
The corresponding iron(II) ion [Fe(H2O)6]2+ is less likely to undergo hydrolysis.
The iron undergoes a change in oxidation state.
This hydrolysis is favoured by low pH values.
Which of the following statements about the chemical reactions of cyclohexane,

cyclohexene and methylbenzene are correct?
1
Upon reduction under suitable conditions, one mole each of cyclohexene and
methylbenzene will react with one mole and three moles of hydrogen gas
respectively.
All the three compounds decolourise bromine under uv light.
Only cyclohexene and methylbenzene will react with hot, acidified potassium
dichromate(VI).
PJC 2012
9647/01/JC2 PRELIM/2012
18
A
1, 2 and 3 are
correct
B
1 and 2 only are
correct
C
2 and 3 only are
correct
D
1 only is correct
37
For the reaction,

(CH3)3CX + CH3CH2O- (CH3)3COCH2CH3 + X- (where X = Cl, Br or I)
which of the following statements are likely to be correct?
38
The reaction involves a nucleophilic attack by CH3CH2O-.
The rate determining step involves the formation of a carbocation.
The reaction will take place more rapidly when X is I than when X is Cl.
In some organic reactions, the reactive carbon atom is not tetrahedral in the
reactant molecule but becomes tetrahedral in the organic intermediate.
To which of the following reactions does this statement apply?
NO 2
H2SO4
1
+
HNO 3
H2O
NaCN
CH3CHO
+ HCN
CH3CH(OH)CN
CH3
PJC 2012
CH2Br
Br2
uv light
+ HBr
9647/01/JC2 PRELIM/2012
19
A
1, 2 and 3 are
correct
B
1 and 2 only are
correct
C
2 and 3 only are
correct
D
1 only is correct
39
Which of the following pairs of compounds can be distinguished using the stated
reagents and conditions?
O
CH3
NaOH(aq) and heat
CH3
NH2
CH3
and
CH3
CH3
CH3
CH3
OH
CH3
CH3
and
O
O
CH3
CH3
40
NH
HCl(aq)
NH2
CH3
and
NaOH(aq), I2(aq), warm

CH3
a-aminobutyric acid and g-aminobutyric acid are isomers.

O
O
NH2
OH
CH3
OH
NH2
g-aminobutyric acid
a-aminobutyric acid

1
Both are soluble in water.
Both can form zwitterions.
Both can be obtained from the hydrolysis of protein.
END OF PAPER
PJC 2012
9647/01/JC2 PRELIM/2012
20
Answers
1
2
3
4
5
6
7
8
9
10
PJC 2012
D
B
C
B
A
B
C
D
D
B
11
12
13
14
15
16
17
18
19
20
D
B
D
B
A
C
C
D
C
B
21
22
23
24
25
26
27
28
29
30
9647/01/JC2 PRELIM/2012
D
C
C
A
C
D
C
B
B
B
31
32
33
34
35
36
37
38
39
40
A
A
A
D
D
B
A
B
A
B

HIGHER 2
CANDIDATE
NAME
CT
GROUP
INDEX
NUMBER
CHEMISTRY
9647/02
Paper 2 Structured
10 September 2012
2 hours
Data Booklet

Write your Centre number, index number and name on all work you hand in.
You may use a soft pencil for any diagrams, graphs or rough workings.
FOR EXAMINERS USE

Paper 2
1
/ 12
/ 12
/ 9
/ 9
/ 15
/ 7
Penalty
/ 8
Total
sf
units
/ 72
2
Answer all the questions in the spaces provided.
1 Planning (P)
You are provided with solutions FA 1, FA 2 and FA 3.
FA 1 and FA 2 are either
1.0 mol dm3 nitric acid or
1.0 mol dm3 ethanoic acid
whereas FA 3 is 2.0 mol dm3 sodium hydroxide.
You are to plan an experiment that will enable you to identify FA 1 and FA 2, and
hence, calculate the enthalpy change of neutralisation for the reaction between
ethanoic acid and sodium hydroxide.
You are provided with the following apparatus:
a thermometer,
a polystyrene cup,
other common apparatus in the laboratory
(a)
State the independent and dependent variables when determining the identity of
each solution, FA 1 and FA 2.
[1]
Independent variable
Dependent variable ...
(b)
Plan an experiment to identify which of the two solutions, FA 1 and FA 2,

is 1.0 mol dm3 nitric acid and which is 1.0 mol dm3 ethanoic acid.
Your plan must identify the acids solely based on the change in temperature.
Mathematical processing of the temperature change is thus not required.
Your plan should give a step by step description of the method including:
the apparatus used for measurement
appropriate volumes of reagents
how you would measure the various variables
[3]
.............
................................................................................................................................
................................................................................................................................
................................................................................................................................
PJC 2012
9647/02/JC2 Prelim/2012
................................................................................................................................
................................................................................................................................
................................................................................................................................
.............
................................................................................................................................
................................................................................................................................
................................................................................................................................
.............
................................................................................................................................
................................................................................................................................
(c)
Either a burette with 0.1 cm3 interval or a measuring cylinder with 1 cm3 interval
can be used to measure the volume of FA 3 required.
It is known that the error (or uncertainty) that is associated with each reading
when using a measuring cylinder with 1 cm3 interval is 0.5 cm3, while that using
a burette with 0.1 cm3 interval is 0.05 cm3.
Assuming that the volume of FA 3 measured is V cm3, calculate the maximum
total percentage error (or uncertainty) in the measurement of the volume of
FA 3, in terms of V, when using:
(i)
a measuring cylinder with 1 cm3 interval,
(ii)
a burette with 0.1 cm3 interval.
[2]
PJC 2012
9647/02/JC2 Prelim/2012
4
(d)
Explain clearly how you could determine the identity of the acids using the
difference in temperature rise in the experiment proposed in (b).
[2]
.............
................................................................................................................................
................................................................................................................................
................................................................................................................................
(e)
(i)
Define the term standard enthalpy change of neutralisation.
....
........................................................................................................................
........................................................................................................................
(ii)
Show the mathematical expression for the enthalpy change of

neutralisation between ethanoic acid and sodium hydroxide, using the
volumes proposed in (b).
The temperature change measured in (b) should be represented by T.
[You may assume that 4.2 J of heat energy raised the temperature of 1 cm3
of any solution by 1oC.]
[3]
PJC 2012
9647/02/JC2 Prelim/2012
5
(f)
A student suggests titrating FA 3 against FA 1 and FA 2 separately, using

phenolphthalein as indicator, to identify two acids. Explain why this proposed
method cannot work.
[1]
.............
................................................................................................................................
................................................................................................................................
................................................................................................................................
[Total: 12]
2 Nitrogen dioxide, NO2 undergoes dimerisation to form dinitrogen tetraoxide, N2O4.

2NO2(g) N2O4(g)
(a)
(i)
Draw the dot-and-cross diagram of NO2.
(ii)
State the shape and bond angle of the ONO bond in NO2.
Shape
Bond angle
PJC 2012
9647/02/JC2 Prelim/2012
6
(iii)
Draw the dot-and-cross diagram of NO2- ion. With reference to your

answer in (a)(i) and (ii), suggest a bond angle of the ONO in NO2- ion,
as compared to NO2. Explain your answer.
..
.....................................................................................................................
.....................................................................................................................
.....................................................................................................................
.....................................................................................................................
[5]
The general rate equation for the dimerisation of nitrogen dioxide can be represented
as:
Rate = k(pNO2)n,
where n represents the order of reaction with respect to nitrogen dioxide.
To determine the value of n, an experiment was carried out to collect experiment data
on the partial pressure of nitrogen dioxide (pNO2) measured at a constant temperature
of 500 K. The results were given below.
Time/ s
pNO2 / atm
Rate / atm s-1
0.917
9.48 x 10-5
1000
0.827
7.75 x 10-5
2000
0.753
6.45 x 10-5
3000
0.691
5.45 x 10-5
4000
0.638
4.67 x 10-5
Table 1
(b)
(i)
PJC 2012
Given that n is 2, process the results in the Table 1 to produce data that
would enable you to plot a straight line graph.
9647/02/JC2 Prelim/2012
7
(ii)
Hence, use the processed data above to plot the graph on the grid below.
(iii)
A student repeated the experiment at the temperature of 250 K. Sketch,

on the same axes in (ii), the graph obtained by this student. Label this
graph as 250 K.
[4]
[Total: 9]
PJC 2012
9647/02/JC2 Prelim/2012
8
3 The following reaction scheme shows the chemistry of some chromium-containing
species in aqueous solution.
SO2
2-
Cr22O
O772-
Zn
A
green solution
[Cr(H
O)66]2+
]2+
[Cr(H22O)
II
blue solution
(aq)
Na22CO
CO33(aq)
III Na
H2H
SO
VII dil
2SO
4
4(aq)
CO22
CO
grey-green ppt
NaOH(aq)
excess
NH3 (aq)
NH3(aq)
IV
H2O2
C
yellow
solution
VI
[Cr(OH)
[Cr(OH)66]3-3-
3+
[Cr(NH
[Cr(NH33))66]]3+ violet solution
..
D
(a)
(i)
Write the formulae of the following chromium-containing species.

A: ...............................................................................
B: ...............................................................................
C: ...............................................................................
PJC 2012
..
VIII excess H2NCH2CH2NH2
9647/02/JC2 Prelim/2012
9
(ii)
State the type of reaction that has occurred in VIII. Construct a balanced
equation to represent the reaction.
....
.......................................................................................................................
.......................................................................................................................
(iii) Hence, using your knowledge of Gibbs free energy, explain why the
reaction in (a)(ii) occurs spontaneously.
....
.......................................................................................................................
.......................................................................................................................
....
.......................................................................................................................
.......................................................................................................................
....
[7]
(b)
Explain why carbon dioxide is evolved when Na2CO3(aq) is added to A in III.

Include any relevant equations in your answer.
[2]
.............
................................................................................................................................
.............
................................................................................................................................
................................................................................................................................
PJC 2012
9647/02/JC2 Prelim/2012
10
(c)
Explain why aqueous solutions of chromium ions are coloured.
[3]
.............
................................................................................................................................
.............
................................................................................................................................
.............
.............
................................................................................................................................
.............
(d)
In a separate experiment, a chemist prepared two compounds with the general

formula CrCl3.6H2O. Upon adding AgNO3(aq) to aqueous solutions of
compounds E and F separately, he noted the following:
Solution containing
Amount of AgCl precipitated per mole of

compound
compound E
compound F
Based on these observations, deduce the formula of compounds E and F in the

solutions. Explain your answer.
[3]
.............
................................................................................................................................
.............
................................................................................................................................
.............
.............
................................................................................................................................
[Total: 15]
PJC 2012
9647/02/JC2 Prelim/2012
11
4 In the vapour phase, ethanoic acid associates to form dimers and an equilibrium is
established as shown.
2CH3COOH(g) (CH3COOH)2(g)
At 177 C and 1 atm, 0.084 g of the equilibrium mixture occupies 37.8 cm3.
(a)
(i)
Calculate the average relative molecular mass of the gaseous mixture,

giving your answer to 1 decimal place.
(ii)
Calculate the proportion of ethanoic acid and its dimer in the equilibrium
mixture.
(iii) Hence, calculate the value of Kp for the dimerisation of ethanoic acid at
177 C, giving its units.
[4]
PJC 2012
9647/02/JC2 Prelim/2012
12
(c)
State and explain the effect of an increase in temperature on the average Mr of

the equilibrium mixture.
[3]
.............
................................................................................................................................
.............
................................................................................................................................
................................................................................................................................
[Total: 7]
5 Cinnamaldehyde is an essential oil with the distinctive odour of cinnamon.

CH CH CHO
cinnamaldehyde
(a)
Sketch the shapes of the hybrid orbitals around one carbon atom in the
cinnamaldehyde molecule, indicate clearly the hybridisation of the carbon atom.
[1]
(b)
A yellow oil is suspected to be cinnamaldehyde.

(i)
Assuming the oil is cinnamaldehyde, complete the table below, giving the
reagent and conditions to confirm the presence of the two functional
groups. Give the expected observation for each test.
Functional
group
Reagent
and conditions
Alkene
Aldehyde
PJC 2012
9647/02/JC2 Prelim/2012
Expected observation
13
(ii)
Write an equation for the reaction between cinnamaldehyde with the

reagent you have chosen to test for presence of the aldehyde.
...
[3]
(c)
Cinnamaldehyde undergoes electrophilic addition with hydrogen bromide

according to the equation as shown.
CH CH CHO
CHBr CH2 CHO
+ HBr
Draw the mechanism of the reaction and explain why the product obtained does
not rotate the plane of polarised light.
[4]
.............
................................................................................................................................
.............
................................................................................................................................
................................................................................................................................
[Total: 8]
PJC 2012
9647/02/JC2 Prelim/2012
14
6 (a)
Tyrosine, one of the 20 -amino acids commonly found in proteins, was

discovered 1846 by German chemist Justus von Liebig in the protein casein from
cheese. It has the following structure.
H
CH2
HO
CO 2H
NH2
tyrosine
The Hell-Volhard-Zelinskii reaction is the one of oldest methods of -amino acids
synthesis. It involves bromination of a carboxylic acid by treatment with Br2
and PBr3, followed by the conversion of the -bromo acid to the -amino acid.
II
1. Br2, PBr3
R-CH2CO2H
2. H2O
R-CHBrCO2H
R-CH(NH2)CO2H
(i)
Give the structure of the carboxylic acid that could be converted to

tyrosine by the above reaction scheme.
(ii)
Suggest reagent and condition for step II.
..
The yield of the amino acid obtained in step II of the above reaction scheme
tends to be low. A better method is to carry out the Gabriel amine synthesis,
which involves the use of phthalimide as shown.
A
O
+
K
N
KOH
ethanol
RCHBrCO2H
CH
CO 2H
phthalimide
NaOH(aq)
RCH(NH2)CO2H
PJC 2012
9647/02/JC2 Prelim/2012
15
(iii)
State the role of KOH in step A.
..
(iv)
What is the type of reaction in step B?
..
(v)
Suggest a reason for the low yield of the amino acid obtained in step II of
Hell-Volhard-Zelinskii the reaction. Hence, explain how the use of
phthalimide in Gabriel amine synthesis would give a higher yield.
..
......................................................................................................................
..
......................................................................................................................
......................................................................................................................
(vi)
The protons of amide (-CONH2) are not known to be acidic (pKa > 500).
Explain why the proton of phthalimide is acidic (pKa = 8.3).
..
......................................................................................................................
..
......................................................................................................................
......................................................................................................................
(vii)
Give the structure of the other organic product obtained when alkaline
hydrolysis is carried out in step C of the Gabriel amine synthesis.
[9]
PJC 2012
9647/02/JC2 Prelim/2012
16
(b)
The three pKa values associated with tyrosine are 2.20, 9.11 and 10.13.
Make use of these pKa values to suggest the major species present in solutions
of tyrosine with the following pH values.
pH 1
pH 6
pH 11
[3]
[Total: 12]
PJC 2012
9647/02/JC2 Prelim/2012
17
7 Benzoic acid can be prepared by the oxidation of benzaldehyde using alkaline
potassium manganate(VII) as described below.
Data about the benzaldehyde and benzoic acid are given below.
compound
density / g cm-3
melting point / C
boiling point / C
benzaldehyde
1.05
-26
179
benzoic acid
1.27
122
229
Preparation of impure benzoic acid

1
Place 2.00 g of solid potassium manganate(VII), 30 cm3 of 1 mol dm-3 sodium

hydroxide and 1.5 cm3 of benzaldehyde in a round-bottomed flask. Swirl the
flask carefully to mix the contents thoroughly.
Fit a reflux condenser onto the round-bottomed flask and boil the mixture gently
for 10 minutes.
Filter off the brown precipitate of manganese(IV) oxide formed, collect the filtrate
in a 100 cm3 beaker and allow the filtrate to cool.
Carefully add concentrated hydrochloric acid, with constant swirling, to the filtrate
till the mixture is acidic enough to precipitate the benzoic acid.
(a)
By means of two ion-electron half-equations, write an equation for the

oxidation of benzaldehyde by alkaline potassium manganate(VII).
[2]
(b)
Show by calculation, which

manganate(VII), is in excess.
PJC 2012
reagent,
9647/02/JC2 Prelim/2012
benzaldehyde
or
potassium
[2]
18
(c)
Draw a diagram of the assembled apparatus for heating under reflux.

Indicate clearly how water enters and leaves the condenser.
[2]
Purification of impure benzoic acid

5
Filter the benzoic acid that has been precipitated and wash it once with cold
water.
The crude benzoic acid product is purified by recrystallisation from water.
Filter the recrystallised solid, wash with water and dry the solid by pressing it
under several layers of filter paper.
Weigh the solid obtained.
(d)
Give a description of the procedure you would use to purify the crude benzoic
acid.
[1]
.............
.............
................................................................................................................................
PJC 2012
9647/02/JC2 Prelim/2012
19
(e)
Explain how you would check for purity of the benzoic acid.
[1]
.............
.............
................................................................................................................................
(f)
Given that 1.40 g of benzoic acid is obtained from the preparation, calculate the
percentage yield of the reaction.
[1]
[Total: 9]
END OF PAPER
PJC 2012
9647/02/JC2 Prelim/2012

HIGHER 2
CANDIDATE
NAME
SUGGESTED ANSWERS
CT
GROUP
INDEX
NUMBER
CHEMISTRY
9647/02
Paper 2 Structured
10 September 2012
2 hours
Data Booklet

FOR EXAMINERS USE

Paper 2
1
/ 12
/ 12
/ 9
/ 9
/ 15
/ 7
Penalty
/ 8
Total
sf
units
/ 72
2
Answer all the questions in the spaces provided.
1 Planning (P)
You are provided with solutions FA 1, FA 2 and FA 3.
FA 1 and FA 2 are either
1.0 mol dm3 nitric acid or
1.0 mol dm3 ethanoic acid
whereas FA 3 is 2.0 mol dm3 sodium hydroxide.
You are to plan an experiment that will enable you to identify FA 1 and FA 2, and
hence, calculate the enthalpy change of neutralisation for the reaction between
ethanoic acid and sodium hydroxide.
You are provided with the following apparatus:
a thermometer,
a polystyrene cup,
other common apparatus in the laboratory
(a)
State the independent and dependent variables when determining the identity of
each solution, FA 1 and FA 2.
[1]
Independent variable Strength of acid
Dependent variable Rise in temperature
(b)
Plan an experiment to identify which of the two solutions, FA 1 and FA 2,

is 1.0 mol dm3 nitric acid and which is 1.0 mol dm3 ethanoic acid.
Your plan must identify the acids solely based on the change in temperature.
Mathematical processing of the temperature change is thus not required.
Your plan should give a step by step description of the method including:
the apparatus used for measurement
appropriate volumes of reagents
how you would measure the various variables
[3]
Step 1: Using a 100 cm3 measuring cylinder, measure out 25 cm3 of FA 3
into the polystyrene cup and record its initial temperature using a
thermometer. Rinse the thermometer.
Step 2: Using ANOTHER 100 cm3 measuring cylinder, measure 50 cm3 of
FA 1. Record its initial temperature.
Step 3: The initial temperature is given by the average of the initial
temperature of FA 1 and FA 3.
PJC 2012
9647/02/JC2 Prelim/2012
3
Step 4: Carefully transfer the 50 cm3 of FA 1 into the polystyrene cup
containing FA 3, stir with the thermometer and record the highest
temperature reached. Rinse the cup.
Step 5: Repeat steps 1 to 4, this time replacing FA1 with FA2.
(c)
Either a burette with 0.1 cm3 interval or a measuring cylinder with 1 cm3 interval
can be used to measure the volume of FA 3 required.
It is known that the error (or uncertainty) that is associated with each reading
when using a measuring cylinder with 1 cm3 interval is 0.5 cm3, while that using
a burette with 0.1 cm3 interval is 0.05 cm3.
Assuming that the volume of FA 3 measured is V cm3, calculate the maximum
total percentage error (or uncertainty) in the measurement of the volume of
FA 3, in terms of V, when using:
(i)
a measuring cylinder with 1 cm3 interval,

Percentage error in measuring V cm3
= (0.5/ V) x 100% = 50/V %
(ii)
a burette with 0.1 cm3 interval.

Percentage error in measuring V cm3
= [(0.05/ V) x 100%] x 2 = 10/V %
[2]
(d)
Explain clearly how you could determine the identity of the acids using the
difference in temperature rise in the experiment proposed in (b).
[2]
Ethanoic acid is a weak acid and nitric acid is a strong acid.
The temperature rise will be lower when 1.0 mol dm-3 ethanoic acid is used
compared to 1.0 mol dm-3 nitric acid for the same number of moles of water
formed.
This is because some of the energy evolved from the neutralisation
process is used to further dissociate the ethanoic acid completely.
(e)
(i)
Define the term standard enthalpy change of neutralisation.

The heat evolved when one mole of water is formed when an acid
neutralises a base under standard conditions of 298K and 1 atm.
(ii)
Show the mathematical expression for the enthalpy change of

neutralisation for the reaction between ethanoic acid and sodium
hydroxide, using the volumes proposed in (b).
The temperature change measured in (b) should be represented by T.
[You may assume that 4.2 J of heat energy raised the temperature of 1 cm3
of any solution by 1oC.]
PJC 2012
9647/02/JC2 Prelim/2012
4
Heat evolved by neutralisation reaction
= mcT
= (vol. of FA1 or FA2 + vol of FA3) x c x T
= (50 + 25) x 4.2 x T
= 315T J
Hneutralisation = 315T / amount of water formed
= 315T / 0.050
= 6300T J mol-1
[3]
(f)
A student suggests titrating FA 3 against FA 1 and FA 2 separately, using

phenolphthalein as indicator, to identify the acids. Explain why this proposed
method cannot work.
[1]
Both FA 1 and FA 2 are of the same concentration and basicity
(monobasic).
Both acids would hence require the same amount of NaOH for a complete
reaction, and hence same volume. The volume of FA 3 (NaOH) required at
end point would hence be the same.
[Total: 12]
2 Nitrogen dioxide, NO2 undergoes dimerisation to form dinitrogen tetraoxide, N2O4.

2NO2(g) N2O4(g)
(a)
(i)
Draw the dot-and-cross diagram of NO2.
.. ..
.. ..
O .. xx N xx O ..
NO2 molecule
(ii)
State the shape and bond angle of the ONO bond in NO2.
Shape of NO2: Bent
Bond angle: accept any value where 110o < angle < 120o
(iii)
Draw the dot-and-cross diagram of NO2- ion. With reference to your

answer in (a)(i) and (ii), suggest a bond angle of the ONO in NO2- ion,
as compared to NO2. Explain your answer.
PJC 2012
9647/02/JC2 Prelim/2012
.. .
.. . x xx
O . x N x O ..
..
NO2- ion
Bond angle of NO2- ion: bond angle must be smaller than NO2, but
still within range of 110o < angle < 120o
Lone pair of electrons present in NO2- ion occupies a larger volume
of space than the single lone electron present in NO2 molecule.
Hence, lone pair-bond pair repulsion in NO2- ion is greater than lone
electron-bond pair repulsion in NO2, causing NO2- ion to have a
smaller bond angle than NO2.
[5]
The general rate equation for the dimerisation of nitrogen dioxide can be represented
as:
Rate = k(pNO2)n,
where n represents the order of reaction with respect to nitrogen dioxide.
To determine the value of n, an experiment was carried out to collect experiment data
on the partial pressure of nitrogen dioxide (pNO2) measured at a constant temperature
of 500 K. The results were given below.
Time/ s
pNO2/ atm
Rate /atm s-1
(pNO2)2/ atm2
0.917
9.48 x 10-5
0.841
1000
0.827
7.75 x 10-5
0.683
2000
0.753
6.45 x 10-5
0.567
3000
0.691
5.45 x 10-5
0.477
4000
0.638
4.67 x 10-5
0.407
Table 1
(b)
(i)
PJC 2012
Given that n is 2, process the results in the Table 1 to produce data that
would enable you to plot a straight line graph.
9647/02/JC2 Prelim/2012
6
(ii)
Hence, use the processed data to plot the graph on the grid below.
Rate / atm s-1
500 K
250 K
0
(iii)
(pNO2)2 /atm2
A student repeated the experiment at the temperature of 250 K. Sketch,

on the same axes in (ii), the graph obtained by this student. Label this
graph as 250 K.
Straight line graph still obtained, with y-intercept = 0.
Gradient (k) decreases.
[4]
[Total: 9]
PJC 2012
9647/02/JC2 Prelim/2012
7
3 The following reaction scheme shows the chemistry of some chromium-containing
species in aqueous solution.
SO2
2Cr22O
O772-
Zn
A
green solution
[Cr(H
O)66]2+
]2+
[Cr(H22O)
II
blue solution
(aq)
Na22CO
CO33(aq)
III Na
H2H
SO
VII dil
2SO
4
4(aq)
CO22
CO
grey-green ppt
NaOH(aq)
excess
NH3 (aq)
NH3(aq)
IV
H2O2
C
yellow
solution
VI
[Cr(OH)
[Cr(OH)66]3-3-
3+
[Cr(NH
[Cr(NH33))66]]3+ violet solution
..
..
VIII excess H2NCH2CH2NH2
D
(a)
(i)
Write the formulae of the following chromium-containing species.

A: [Cr(H2O)6]3+ or Cr3+ or Cr2(SO4)3
B: Cr(OH)3
C: CrO42 or Na2CrO4
(ii)
State the type of reaction that has occurred in VIII. Construct a balanced
equation to represent the reaction.
Ligand exchange has taken place.
[Cr(NH3)6]3+ + 3 H2NCH2CH2NH2 [Cr(H2NCH2CH2NH2)3]3+ + 6 NH3
(iii) Hence, using your knowledge of Gibbs free energy, explain why the
reaction in (a)(ii) occurs spontaneously.
PJC 2012
9647/02/JC2 Prelim/2012
8
[Cr(NH3)6]3+ + 3 en [Cr(en)3]3+ + 6 NH3
This ligand exchange proceeds with the breaking and formation of
similar chemical bonds (N: Cr dative bonds). H of reaction is
hence approximately zero.
However, displacement of monodentate NH3 ligands by bidentate en
ligands causes an increase in number of molecules in the system,
resulting in an increase in disorderliness and hence S is positive.
Since G = H - TS, G is always negative, accounting for
spontaneity of ligand exchange.
[7]
(b)
Explain why carbon dioxide is evolved when Na2CO3(aq) is added to A in III.

Include any relevant equations in your answer.
[2]
Cr3+ ion has a high charge density and high polarising power. Hence
[Cr(H2O)6]3+ can undergo hydrolysis in water, polarising and weakening the
O-H bonds of surrounding H2O molecules, to release H+ ions. H+ ions react
with carbonate ions via acid-base reaction to form CO2.
[Cr(H2O)6]3+(aq) [Cr(OH)(H2O)5]2+(aq) + H+(aq)
2H+(aq) + CO32-(aq) CO2 + H2O
(c)
Explain why aqueous solutions of chromium ions are coloured.
[3]
In the presence of ligands, the partially filled, originally degenerate 3d

orbitals of Cr split into two different sets of energy, separated by a small
energy gap E. An electron from the lower energy d-orbital absorbs a
specific wavelength of light from the visible light spectrum corresponding
to E and is promoted to a higher energy d-orbital, undergoing d to d
electron transition. The colour absorbed is complementary to colour
observed.
(d)
In a separate experiment, a chemist prepared two compounds with the general

formula CrCl3.6H2O. Upon adding AgNO3(aq) to aqueous solutions of
compounds E and F separately, he noted the following:
Solution containing
Amount of AgCl precipitated per mole of

compound
Compound E
Compound F
Based on these observations, deduce the formula of compounds E and F in the

solutions. Explain your answer.
[3]
PJC 2012
9647/02/JC2 Prelim/2012
9
Formula of E: [Cr(H2O)4Cl2]Cl.2H2O
Formula of F: [Cr(H2O)5Cl]Cl2.H2O
Only free chloride ions can be precipitated as AgCl. Chloride ions
coordinated to Cr3+ as ligands cannot be precipitated.
OR:
E contains 1 free Cl ion, which can be precipitated as AgCl by Ag+.
F contains 2 free Cl ions, which can be precipitated as AgCl by Ag+.
[Total: 15]
4 In the vapour phase, ethanoic acid associates to form dimers and an equilibrium is
established as shown.
2CH3COOH(g) (CH3COOH)2(g)
At 177 C and 1 atm, 0.084 g of the equilibrium mixture occupies 37.8 cm3.
(a)
(i)
Calculate the average relative molecular mass of the gaseous mixture,

giving your answer to 1 decimal place.
(101000)(37.8 x 10-6) =
0.084
(8.31)(177 + 273)
average Mr
Average Mr = 82.3
(ii)
Calculate the proportion of ethanoic acid and its dimer in the equilibrium
mixture.
Let fraction of CH3COOH in mixture be x and that of (CH3COOH)2 be
(1 x).
60x + 120(1 x) = 82.3
x = 0.628
Fraction of CH3COOH in mixture = 0.628
Fraction of (CH3COOH)2 in mixture = 0.372
(iii) Hence, calculate the value of Kp for the dimerisation of ethanoic acid at
177 C, giving its units.
Kp =
P( CH3COOH)2
(PCH3COOH ) 2
0.372 1
(0.628 1) 2
= 0.943 atm-1
=
PJC 2012
9647/02/JC2 Prelim/2012
10
[4]
(c)
State and explain the effect of an increase in temperature on the average Mr of

the equilibrium mixture.
[3]
The dimerisation of CH3COOH is an exothermic process as it involves the
formation of two hydrogen bonds.
According to Le Chateliers Principle, increasing the temperature favours
an endothermic reaction. Thus, position of equilibrium shifts to the left.
There will be a greater proportion of CH3COOH in the reaction mixture,
causing the average Mr of the reaction mixture to decrease.
[Total: 7]
5 Cinnamaldehyde is an essential oil with the distinctive odour of cinnamon.

CH CH CHO
cinnamaldehyde
(a)
Sketch the shapes of the hybrid orbitals around one carbon atom in the
cinnamaldehyde molecule, indicate clearly the hybridisation of the carbon atom.[1]
sp2 hybridised
(b)
A yellow oil is suspected to be cinnamaldehyde.

(i)
Assuming the oil is cinnamaldehyde, complete the table below, giving the
reagent and conditions to confirm the presence of the two functional
groups. Give the expected observation for each test.
Functional group
Reagent and conditions

Br2(aq)
alkene
aldehyde
PJC 2012
Tollens reagent
warm
Or
Fehlings solution
warm
9647/02/JC2 Prelim/2012
Expected observation
Orange/ reddishbrown Br2(aq)
decolourises.
and Silver mirror

observed.
Or
and Brick red precipitate
observed.
11
(ii)
Write an equation for the reaction between cinnamaldehyde with the

reagent you have chosen to test for presence of the aldehyde.
C6H5CH=CHCHO + 2Ag+ + 3OH- C6H5CH=CHCOO- + 2Ag + 2H2O
Or
C6H5CH=CHCHO + 2Cu2+ + 5OH- C6H5CH=CHCOO- + Cu2O + 3H2O
[3]
(c)
Cinnamaldehyde undergoes electrophilic addition with hydrogen bromide

according to the equation as shown.
CHBr CH2 CHO
CH CH CHO
+ HBr
Draw the mechanism of the reaction and explain why the product obtained does
not rotate the plane of polarised light.
[4]
Br dH d+
slow
CH CH CHO
CH2 CHO
Br
Br
: Br
CH2 CHO
fast
H
+
CH2 CHO
H
CH2 CHO
fast
: Br
Br
The reaction takes place with the formation of a carbocation. The C atom
bearing the positive charge has a trigonal planar arrangement. There is
equal likelihood of the Br- attacking from above and below the plane. Thus,
resulting in the formation of a racemic mixture (equimolar quantities of the
two enantiomers) in which the optical activity cancels out.
[Total: 8]
PJC 2012
9647/02/JC2 Prelim/2012
12
6 (a)
Tyrosine, one of the 20 -amino acids commonly found in proteins, was

discovered in 1846 by German chemist Justus von Liebig in the protein casein
from cheese. It has the following structure.
H
CH2
HO
CO 2H
NH2
tyrosine
The Hell-Volhard-Zelinskii reaction is the one of oldest methods of -amino acids
synthesis. It involves bromination of a carboxylic acid by treatment with Br2
and PBr3, followed by the conversion of the -bromo acid to the -amino acid.
I
1. Br2, PBr3
R-CH2CO2H
(i)
II
R-CH(NH2)CO2H
Give the structure of the carboxylic acid that could be converted to

tyrosine by the above reaction scheme.
CH2
HO
(ii)
R-CHBrCO2H
2. H2O
CH2
CO 2H
Suggest reagent and condition for step II.

Excess NH3 in ethanol, heat in sealed tube
The yield of the amino acid obtained in step II of the above reaction scheme
tends to be low. A better method is to carry out the Gabriel amine synthesis,
which involves the use of phthalimide as shown.
A
O
+
K
N
KOH
ethanol
RCHBrCO2H
CH
CO 2H
phthalimide
NaOH(aq)
RCH(NH2)CO2H
(iii)
State the role of KOH in step A.

KOH acts as a base to deprotonate the phthalimide.
PJC 2012
9647/02/JC2 Prelim/2012
13
(iv)
What is the type of reaction in step B?

(v)
Suggest a reason for the low yield of the amino acid obtained in step II of
Hell-Volhard-Zelinskii the reaction. Hence, explain how the use of
phthalimide in Gabriel amine synthesis would give a higher yield.
Multiple substitution (alkylation) may occur, giving a mixture of 2
amine, 3 amine and possibly an quaternary ammonium salt, instead
of the desired 1 amine. By having N bonded to two CO groups,
multiple alkylation cannot take place, hence a higher yield is
obtained.
(vi)
The protons of amide (-CONH2) are not known to be acidic (pKa > 500).
Explain why the proton of phthalimide is acidic (pKa = 8.3).
The presence of the two electron withdrawing CO group helps to
disperse the negative charge on the anion / the negative charge of
the anion formed from deprotonation can be delocalised with the pi
electron system of the two CO groups. This stabilises the anion,
making it acidic.
(vii)
Give the structure of the other organic product obtained when alkaline
hydrolysis is carried out in step C of the Gabriel amine synthesis.
O
-
O Na
-
O Na+
O
[9]
(b)
The three pKa values associated with tyrosine are 2.20, 9.11 and 10.13.
Make use of these pKa values to suggest the major species present in solutions
of tyrosine with the following pH values.
pH 1
H
HO
CH2
CO 2H
+
NH3
PJC 2012
9647/02/JC2 Prelim/2012
14
pH 6
HO
CH2
NH3
pH 11
O
CH2
NH2
[3]
[Total: 12]
7 Benzoic acid can be prepared by the oxidation of benzaldehyde using alkaline

potassium manganate(VII) as described below.
Data about the benzaldehyde and benzoic acid are given below.
compound
benzaldehyde
benzoic acid
density / g cm-3
1.05
1.27
melting point / C
-26
122
boiling point / C
179
229
Preparation of impure benzoic acid

1
Place 2.00 g of solid potassium manganate(VII), 30 cm3 of 1 mol dm-3 sodium
hydroxide and 1.5 cm3 of benzaldehyde in a round-bottomed flask. Swirl the
flask carefully to mix the contents thoroughly.
2
Fit a reflux condenser onto the round-bottomed flask and boil the mixture gently
for 10 minutes.
Filter off the brown precipitate of manganese(IV) oxide formed, collect the filtrate
in a 100 cm3 beaker and allow the filtrate to cool.
Carefully add concentrated hydrochloric acid, with constant swirling, to the filtrate
till the mixture is acidic enough to precipitate the benzoic acid.
(a)
By means of two ion-electron half-equations, write an equation for the oxidation

of benzaldehyde by alkaline potassium manganate(VII).
[2]
C6H5CHO + 3OH- C6H5CO2- + 2H2O + 2e
MnO4- + 3e + 2H2O MnO2 + 4OH3C6H5CHO + OH- + 2MnO4- 3C6H5CO2- + 2MnO2 + 2H2O
PJC 2012
9647/02/JC2 Prelim/2012
15
(b)
Show by calculation, which

manganate(VII), is in excess.
reagent,
benzaldehyde
or
potassium
[2]
Amount of benzaldehyde used = (1.5 x 1.05) / 106

= 0.0149 mol
Amount of KMnO4 used = 2.00 / 158
= 0.0127 mol
2 mol of KMnO4 3 mol C6H5CHO
0.0127 mol of KMnO4 0.01905 mol of C6H5CHO
Potassium manganate(VII) is in excess.
(c)
Draw a diagram of the assembled apparatus for heating under reflux. Indicate
clearly how water enters and leaves the condenser.
[2]
Purification of impure benzoic acid

5
Filter the benzoic acid that has been precipitated and wash it once with cold
water.
6
The crude benzoic acid product is purified by recrystallisation from water.
Filter the recrystallised solid, wash with water and dry the solid by pressing it
under several layers of filter paper.
Weigh the solid obtained.
PJC 2012
9647/02/JC2 Prelim/2012
16
(d)
Give a description of the procedure you would use to purify the crude benzoic
acid.
Dissolve the crude benzoic acid in a minimum volume of hot water. Cool
the hot saturated solution to obtain the crystallised product.
(e)
Explain how you would check for purity of the benzoic acid.
Purity of benzoic acid can be checked by melting point determination.
Pure benzoic acid should melt very sharply at 122C.
(f)
Given that 1.40 g of benzoic acid is obtained from the preparation, calculate the
percentage yield of the reaction.
Theoretical yield = 0.0149 x 122
= 1.818 g
Percentage yield = (1.40 / 1.818) x 100
= 77.0%
[Total: 9]
END OF PAPER
PJC 2012
9647/02/JC2 Prelim/2012
Name:
Index No.:
CT Group: 11

HIGHER 2
CHEMISTRY
9647/03
14 September 2012
2 hours
Answer Paper
Data Booklet
Cover Page

Answer any four out of five questions.
State the question number of the questions that you have attempted on the cover page provided.
The question numbers should be stated in sequence.
2
1 Enzymes are biological molecules that catalyse chemical reactions. Almost all
chemical reactions in a biological cell need enzymes in order to occur at rates sufficient
for life.
(a) Acquired Immuno-Deficiency Syndrome (AIDS) is a disease of the human immune
system caused by the Human Immunodeficiency Virus (HIV). HIV-1 Protease is
an enzyme which speeds up the reproduction of HIV. In the development of antiHIV drugs, scientists often study the amino acid sequence of the HIV-1 Protease
to understand how this enzyme displays its biological properties in the human
body.
(i)
A segment of the polypeptide structure of HIV-1 Protease, containing 10

amino acids, was digested using an enzyme and the following fragments
were obtained.
leu asn phe
ile gly cys thr leu
leu thr glu ile gly
Deduce the primary structure of this segment of HIV-1 Protease.
(ii)
A segment of the HIV strand acts as a substrate, which binds to the active
site of the HIV-1 Protease which speeds up the reproduction of the HIV
virus. The rate of this enzyme-catalysed reaction is investigated and can be
represented by the following graph.
rate
substrate concentration
Explain the difference in the rate of reaction at high and low concentrations
of substrate.
PJC 2012
9647/03/JC2 Prelims/2012
3
(iii) The structural formulae of the three most common amino acids present in
the protein chain in HIV-1 Protease are shown below.
NH2
COOH
NH2
CH2
CH2
CH2
CH
COOH
CH3
glutamic acid
(glu)
COOH
NH2
COOH
CH2
CH3
SH
leucine
cysteine
(leu)
(cys)
In how many different ways can these three amino acids be coupled by
peptide bonds to form a tripeptide? Draw the structural formula of one such
peptide.
(iv) The side chains of these three amino acids are responsible for maintaining
the tertiary structure of HIV-1 Protease.
State and draw the type of side-chain interaction between two cysteine (cys)
residues.
State the type of reaction that is involved in the formation of the side-chain
interaction.
(v)
Since its discovery in 1981, scientists have studied the protein structure of
HIV in order to prevent its transmission. The World Health Organisation
recommends heat treatment of breast-milk prior to giving it to the child, as a
way to reduce the risk of HIV transmission to the baby in sub-Saharan
Africa.
Explain how this treatment of breast-milk reduces the risk of HIV infection in
infants.
[9]
PJC 2012
9647/03/JC2 Prelims/2012
4
(b) An example of a copper-containing enzyme is superoxide dismutase (SOD) that
aids in the disproportionation of the strongly oxidising superoxide ion, O2- to
oxygen and hydrogen peroxide. Thus, they are an important antioxidant defense
in nearly all cells exposed to oxygen, thereby protecting the body from harm.
2O2- + 2H+
(i)
O2
H2O2
The activity of SOD hinges on the active site Cu2+ ion.

By referring to the following E data, suggest a mechanism for the catalysis
of the disproportionation of O2- by SOD.
You may represent the oxidised and reduced forms of the enzyme as
SOD-Cu2+ and SOD-Cu+ respectively.
O2 + eO2O2- + e- + 2H+
H2O2
2+
SOD-Cu + e
SOD-Cu+
(ii)
E/ V
-0.33
+0.89
+0.42
State the type of catalysis and explain how SODCu2+ can act as a catalyst.
(iii) With the aid of a sketch of the Boltzmann distribution, explain how the
presence of a catalyst affects the rate of reaction.
(iv) The secondary structure of SOD is composed mainly of beta-pleated sheets,
as well as some regions of alpha-helices.
Draw a diagram of the beta-pleated sheet, showing the bonding which
maintains the structure of the secondary structure of the enzyme.
[11]
[Total: 20]
PJC 2012
9647/03/JC2 Prelims/2012
5
2
Ginger has been used as a natural remedy for many ailments for centuries.
Researchers around the world are finding that ginger works wonders in the treatment
of everything from cancer to migraines. Ginger consists of many chemicals. Vitamin C
and chlorogenic acid are two of the chemicals present in ginger.
(a) The structure of vitamin C and its reaction pathway is shown below.
HO
HO
O
HO
HO
HO
OH
HO
OH
compound A
vitamin C
specific controlled
elimination
HO CH2 CH
HO CH CH
+
HO
OH
compound B
HO
OH
compound D
(i)
Draw the structural formula of the compound formed when vitamin C reacts
with hot acidified potassium dichromate(VI).
(ii)
Compound A undergoes elimination to produce compounds B and D.

State and explain which compound is the major product.
(iii) Determine the maximum number of stereoisomers of compound D. Draw

the pair that has the same boiling point.
[4]
PJC 2012
9647/03/JC2 Prelims/2012
6
(b) The structure of chlorogenic acid and its reaction pathway is shown below.
O
O
HO
OH
HO
OH
OH
OH
step 1
HO
O
HO
OH
OH
OH
compound F
OH
chlorogenic acid
step 2
step 3
O
HO
OH
OH
OH
H2N
NH2
HO
OH
NH2
compound G
(i)
Compound F can be converted to compound G in two steps.

Suggest reagents and conditions for steps 2 and 3.
(ii)
Draw the structures of compounds formed when compound G reacts with

I
H2, Ni(s), 200oC
II
NaBH4 in methanol
[4]
(c) Ginger also contains nutrients like magnesium. Magnesium is a vital component
of a healthy human diet. Magnesium taken in the proper amount plays a role in
preventing both stroke and heart attack.
(i)
Describe what is observed when a piece of magnesium ribbon is burnt in air.
(ii)
The product obtained in (i) is placed in a beaker of water containing a few

drops of universal indicator. State the observation(s) and write equations for
the reaction(s) that occur.
[4]
PJC 2012
9647/03/JC2 Prelims/2012
7
(d) Sketch a graph of the pH of the solution when the chlorides of the elements from
sodium to phosphorus are added separately to water. Label your graph clearly. [2]
(e) Hydrofluoric acid dissociates in water according to the following equation:
DHodissociation
HF(aq)
H+(aq) + F-(aq)
The following are some enthalpy changes related to hydrogen fluoride.

First electron affinity of fluorine/ kJ mol-1
Standard enthalpy change of hydration of fluoride ion / kJ mol-1
Standard enthalpy change of reaction, HF(aq) HF(g) / kJ mol-1
Standard enthalpy change of hydration of hydrogen ion / kJ mol-1
-328
-506
+39
-1090
(i)
By using the data provided and other relevant data from the Data Booklet,
construct an energy cycle and calculate the standard enthalpy change of
dissociation of hydrofluoric acid.
(ii)
Aqueous hydrofluoric acid is a weak acid under standard conditions. One

explanation for the relatively weaker acid strength of hydrofluoric acid is its
negative standard entropy change of dissociation, Sdissociation. Account for
the sign of Sdissociation.
[6]
[Total: 20]
PJC 2012
9647/03/JC2 Prelims/2012
8
3 (a) Hydrazine (N2H4) is a colourless liquid with a slight odour like ammonia. However,
the solubility of hydrazine in water is very much higher than that of ammonia.
Draw a diagram to show the bonding between a molecule of hydrazine and a
molecule of water. Account for the difference in solubility of hydrazine and
ammonia in water.
[2]
(b) The Italian catalyst manufacturer Acta proposed using hydrazine as an alternative
to hydrogen in fuel cells. The chief benefit of using hydrazine is that it can produce
more energy than a similar hydrogen-oxygen cell.
The following diagram shows a typical hydrazine-oxygen fuel cell system
incorporated with an anion exchange membrane between the electrodes.
(i)
Write the two ion-electron half equations for the reactions that take place at
each electrode. Hence, write an overall equation for the cell reaction.
(ii)
Given that Eo(N2/N2H4) is -1.16 V, calculate the cell e.m.f. if the process
takes place under standard conditions.
(iii) The hydrazine-oxygen fuel cell that is used to power a satellite produces an
average current of 5 A per day. Assuming that the fuel cell is only 70%
efficient, calculate the mass of hydrazine required in a day.
(iv) Based on the physical properties of hydrazine, suggest an advantage of the
hydrazine-oxygen fuel cell over the hydrogen-oxygen fuel cell.
[6]
(c) Wolff-Kishner reaction was discovered independently in 1911 by Ludwig Wolff in
Germany and N. M. Kishner in Russia. It is a valuable synthetic method for
converting ketones or aldehydes into alkanes using hydrazine in the presence of
potassium hydroxide.
R
H
C
R
PJC 2012
H
N
KOH
C
H
9647/03/JC2 Prelims/2012
N2
H2O
9
Indene (C9H8) is a colourless organic liquid obtained from coal tar and used in
preparing synthetic resins. It can be synthesised from phenylethene by the
following route, incorporating Wolff-Kishner reaction.
Br2(aq)
CH2
A
Step 1
B
Step 2
phenylethene
H2SO4(aq)
heat
Step 3
COOH
COOH
Step 4
OH
Step 5
COCl
H2NNH2
KOH
anhydrous
FeCl3
D
Step 6
Step 7
indene
(i)
Give the structures of compounds A, B and D.
(ii)
State the reagents and conditions for Steps 2, 4 and 5.
(iii) State the types of reaction occurring in Steps 6 and 7.

(iv) When aqueous silver nitrate is added to compound C, a white precipitate is
observed immediately. The precipitate dissolves when dilute aqueous
ammonia is added to it. The addition of aqueous sodium iodide to the
resulting mixture produces a yellow precipitate. Identify the precipitates
formed and account for the observation.
[12]
[Total: 20]
PJC 2012
9647/03/JC2 Prelims/2012
10
4
(a) A solution of carbonate reacts with H+ in two stages.
CO 3
2-
+H+
pKb1
HCO 3
+H+
pKb2
CO 2
H2O
The pH changes during the addition of 0.200 mol dm-3 nitric acid to a 20.0 cm3
solution of sodium carbonate and sodium hydrogencarbonate are shown below.
(i)
A list of indicators and their pKa values is given below.

indicator
pKa
thymol
blue
1.7
methyl
yellow
3.1
methyl
red
5.1
cresol
red
8.3
thymolphthalein
9.2
From the given list of indicators, choose two suitable indicators that can be
used to determine the two end-points in the titration. Explain your choice.
(ii)
Calculate the concentration, in g dm-3, of sodium carbonate present in the

original solution, given that the end-point between B and C occurs after
8.40 cm3 of nitric acid is added.
(iii) Calculate the concentration, in g dm-3, of sodium hydrogencarbonate

present in the original solution, given that the end-point between D and E
occurs after 18.80 cm3 of nitric acid is added.
[4]
PJC 2012
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11
(b) Dicarboxylic acids ionise in two stages.
HO 2C (CH2)n
CO 2H
-H+
pKa1
HO 2C (CH2)n
-H+
CO 2-
pKa2
-O C
2
(CH2)n
CO 2-
The following table compares the pKa values of three dicarboxylic acids.
acid
formula
pKa1
pKa2
oxalic
HO2CCO2H
1.25
4.27
malonic
HO2CCH2CO2H
2.85
5.70
succinic
HO2C(CH2)2CO2H
4.21
5.64
(i)
Explain why succinic acid has the highest pKa1 value.
(ii)
An amphiprotic species is one that reacts with an acid and a base. The
monocarboxylate ion of a dicarboxylic acid, HO2C(CH2)nCO2, is an
amphiprotic species.
The pH of an amphiprotic species is given by the following expression.
pH = (pKa1 + pKa2)
Using malonic acid as an example, write two equations to show that its
monocarboxylate ion is an amphiprotic species.
(iii) The pH-volume added curve when 55 cm3 of 0.20 mol dm-3 NaOH is added
to 25 cm3 of 0.20 mol dm-3 oxalic acid is shown below.
Calculate the pH of the curve at points X, Y and Z.

[6]
PJC 2012
9647/03/JC2 Prelims/2012
12
(c) Thermal decomposition of the calcium salt of oxalic acid, calcium oxalate,
produces calcium oxide and oxides of carbon.
The graph below is an Ellingham diagram, which shows the variation in the
standard Gibbs free energy change of formation, Gfq, with temperature, T, for
various oxides.
(i)
Which oxide, calcium oxide, zinc oxide or silver(I) oxide, could be

decomposed by heat at 1000 K? Explain your choice.
(ii)
What does the gradient of the graph in the Ellingham diagram represent?
Hence, explain why the gradient for 2C + O2 2CO is as shown.
(iii) From the Ellingham diagram, find the G values of the following reactions
at 1500 K.
I
2C(s) + O2(g) 2CO(g)
II
2Zn(s) + O2(g) 2ZnO (s)
(iv) Use your answer in (iii) to calculate Gq value for the reaction in which
carbon reduces zinc oxide at 1500 K.
2ZnO + 2C 2Zn + 2CO
Hence, comment on the feasibility of the reaction at 1500 K.
[5]
PJC 2012
9647/03/JC2 Prelims/2012
13
(d) In no more than 3 steps, suggest how each of the following transformations can
be achieved. You are required to state the reagents and conditions for each step
and give the structures of the intermediate compounds.
OH
(i)
HO
OH
OH
O
Br
(ii)
CH3
O
O
COOH
NO 2
[5]
[Total: 20]
PJC 2012
9647/03/JC2 Prelims/2012
14
5
(a) Magnesium carbonate occurs naturally in several forms. Due to its hygroscopic
properties, anhydrous magnesium carbonate is used in organic reactions to
remove moisture.
The decomposition temperature of magnesium carbonate is 540 C. Explain how
you would expect the decomposition temperature of barium carbonate to differ
from magnesium carbonate.
[3]
(b) The solubility of magnesium carbonate is 0.267 g dm-3.
(i)
Calculate the solubility product, Ksp, of magnesium carbonate.
(ii)
To a 1.0 dm3 saturated solution of magnesium carbonate, 50.0 cm3 of

1.00 mol dm-3 aqueous magnesium chloride was added. Find the mass of
precipitate formed.
[4]
(c) Compound A (C11H22) decolourises aqueous bromine. Compound A was heated

with a mixture of aqueous sodium hydroxide and potassium manganate(VII).
After the reaction was completed (assuming 100% yield), the reaction mixture
was extracted several times with an organic solvent.
The aqueous and organic layers were then collected separately. Acidification of
the aqueous layer yielded compound B (Mr = 102), which rotated the plane of
polarised light. Compound B produced a colourless gas with sodium metal.
(i)
Use all of the information to determine the identity of functional group

present in
I
II
compound A,
compound B.
For each functional group you identify, explain how you came to your
decision.
(ii)
Deduce the molecular formula of compound B and hence, draw its

displayed formula.
(iii)
Explain why the salt of compound B was found in the aqueous layer after
the separation of the reaction mixture.
The organic layer was then distilled to give compound C (C6H12O). Warming
compound C with aqueous alkaline iodine, followed by controlled addition of
concentrated hydrochloric acid produced compound B.
(iv)
Propose the structure of compound C and give a balanced equation for its
reaction with aqueous alkaline iodine.
(v)
Hence or otherwise, deduce the structure of compound A.
PJC 2012
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15
Compound C was converted to compound E via the following reaction scheme.
Compound C 1. HCN(aq), NaCN, 10-20 oC
(C6H12O)
2. H2SO4(aq)
Compound D
(C7H14O3)
concentrated H2SO4,
heat under reflux
Compound E
(C14H24O4)
(vi)
Draw the structures of compounds D and E.
(vii)
Describe a simple chemical test to distinguish between compounds C

and D, clearly stating how each compound behaves in the test. You should
not use any of the reagents and conditions outlined in this question.
[13]
[Total: 20]
End of Paper
PJC 2012
9647/03/JC2 Prelims/2012
Name: SUGGESTED ANSWERS
Index No.:
CT Group: 11

HIGHER 2
CHEMISTRY
9647/03
14 September 2012
2 hours
Answer Paper
Data Booklet
Cover Page

Answer any four out of five questions.
2
1 Enzymes are biological molecules that catalyse chemical reactions. Almost all
chemical reactions in a biological cell need enzymes in order to occur at rates sufficient
for life.
Acquired Immuno-Deficiency Syndrome (AIDS) is a disease of the human
immune system caused by the Human Immunodeficiency Virus (HIV). HIV-1
Protease is an enzyme which speeds up the reproduction of HIV. In the
development of anti-HIV drugs, scientists often study the amino acid
sequence of the HIV-1 Protease to understand how this enzyme displays its
biological properties in the human body.
(a)
(i)
A segment of the polypeptide structure of HIV-1 Protease, containing 10

amino acids, was digested using an enzyme and the following fragments
were obtained.
leu asn phe
ile gly cys thr leu
leu thr glu ile gly
Deduce the primary structure of this segment of HIV-1 Protease.
leu thr glu ile gly cys thr leu asn phe
(ii)
A segment of the HIV strand acts as a substrate, which binds to the active
site of the HIV-1 Protease which speeds up the reproduction of the HIV
virus. The rate of this enzyme-catalysed reaction is investigated and can be
represented by the following graph.
rate
substrate concentration
Explain the difference in the rate of reaction at high and low concentrations
of substrate.
At low substrate concentration,
Rate of reaction increases linearly / reaction is first order wrt the

substrate concentration as active sites of the enzyme are not fully
occupied.
At high substrate concentration,
Rate of reaction is constant / rate is independent of substrate

concentration / reaction is zero order wrt the substrate
concentration as all active sites occupied.
PJC 2012
9647/03/JC2 Prelims/2012
3
(iii) The structural formulae of the three most common amino acids present in
the protein chain in HIV-1 Protease are shown below.
NH2
H
NH2
COOH
CH2
CH2
CH2
CH
COOH
CH3
glutamic acid
(glu)
NH2
COOH
COOH
CH2
SH
CH3
leucine
cysteine
(leu)
(cys)
In how many different ways can these three amino acids be coupled by
peptide bonds to form a tripeptide? Draw the structural formula of one such
peptide.
3! = 6 ways
H
H2N
C
CH2
O
C
CH2
CH2
CH
COOH
CH3
O
C
CH3
CH2
COOH
SH
**Accept other correct tripeptides

(iv) The side chains of these three amino acids are responsible for maintaining
the tertiary structure of HIV-1 Protease.
State and draw the type of side-chain interaction between two cysteine (cys)
residues.
State the type of reaction that is involved in the formation of the side-chain
interaction.
PJC 2012
9647/03/JC2 Prelims/2012
Type of reaction: oxidation

(v)
Since its discovery in 1981, scientists have studied the protein structure of
HIV in order to prevent its transmission. The World Health Organisation
recommends heat treatment of breast-milk prior to giving it to the child, as a
way to reduce the risk of HIV transmission to the baby in sub-Saharan
Africa.
Explain how this treatment of breast-milk reduces the risk of HIV infection in
infants.
Heating leads to denaturation of protein. When temperature increases,
molecular vibrations agitate the polypeptide chains sufficiently to
overcome the weak interactions that stabilise protein conformation.
(Also accept loss of 3d conformation)
As the secondary and tertiary structures are broken down, it results in
the loss of function of the HIV protein.
[9]
(b) An example of a copper-containing enzyme is superoxide dismutase (SOD) that

aids in the disproportionation of the strongly oxidising superoxide ion, O2- to
oxygen and hydrogen peroxide. Thus, they are an important antioxidant defense
in nearly all cells exposed to oxygen, thereby protecting the body from harm.
(i)
2O2- + 2H+
O2 + H2O2
The activity of SOD hinges on the active site Cu2+ ion.
By referring to the following E data, suggest a mechanism for the catalysis
of the disproportionation of O2- by SOD.
You may represent the oxidised and reduced forms of the enzyme as
SOD-Cu2+ and SOD-Cu+ respectively.
E/ V
O2 + e- Error! Objects cannot be
created from editing field codes. O2O2- + e- + 2H+ Error! Objects cannot
be created from editing field codes.
H2O2
SOD-Cu2+ + e- Error! Objects cannot
PJC 2012
9647/03/JC2 Prelims/2012
-0.33
+0.89
+0.42
5
be created from editing field codes.
SOD-Cu+
Step 1: SOD-Cu2+ + O2- O2 + SOD-Cu+

Ecell = +0.42 (-0.33) = +0.75V (> 0, hence feasible)
Step 2: SOD-Cu+ + O2- + 2H+ H2O2 + SOD-Cu2+
Ecell = +0.89 (+0.42) = +0.47V (> 0, hence feasible)
(ii)
State the type of catalysis and explain how SOD-Cu2+ can act as a catalyst.
Homogenous catalysis
The catalytic effect is due to the ability of Cu to have variable oxidation
states.
(iii) With the aid of a sketch of the Boltzmann distribution, explain how the
presence of a catalyst affects the rate of reaction.
When a catalyst is used in a reaction, it:
increases the rate of the reaction by providing an alternative
reaction pathway with lower activation energy
increases the number of reacting particles with energy Ea
increases the number of effective collisions per unit time
increases the rate of reaction.
[1] diagram
PJC 2012
9647/03/JC2 Prelims/2012
(iv) The secondary structure of SOD is composed mainly of beta-pleated sheets,

as well as some regions of alpha-helices.
Draw a diagram of the beta-pleated sheet, showing the bonding which
maintains the structure of the secondary structure of the enzyme.
H
H
Hydrogen
H bond
H C
N H
w::
deedd vviieew
EExxppaannd
dd++
H
H
dd--
dd++
H
dd--
[11]
[Total: 20]
PJC 2012
9647/03/JC2 Prelims/2012
Ginger has been used as a natural remedy for many ailments for centuries.
Researchers around the world are finding that ginger works wonders in the treatment
of everything from cancer to migraines. Ginger consists of many chemicals. Vitamin C
and chlorogenic acid are two of the chemicals present in ginger.
(a) HO
HO
O
HO
HO
HO
OH
HO
OH
compound A
vitamin C
specific controlled
elimination
HO
HO CH CH
+
HO
OH
compound B
(i)
PJC 2012
HO
OH
compound D
Draw the structures of compounds formed when vitamin C reacts with hot
acidified potassium dichromate(VI).
9647/03/JC2 Prelims/2012
8
O
O
HO
HO
O
O
HO
(ii)
OH
Compound A undergoes elimination to produce compounds B and D.

State and explain which compound is the major product.
Compound B should be the major product.
Alkene B is more highly substituted than alkene D. By Satyzevs rule,
the more highly substituted alkene is the major product.
OR
Alkene B is a more stable product as it has an extended conjugate
system (involving both alkenes and the ketone group).
(iii) Determine the maximum number of stereoisomers of compound D. Draw

the pair that has the same boiling point.
Maximum no. of stereoisomers = 22 = 4
O
HO
H
OH
HO
HO
OH
OH
or
HO
OH
HO
HO
OH
OH
[4]
(b) The structure of chlorogenic acid and its reaction pathway is shown below.
PJC 2012
9647/03/JC2 Prelims/2012
9
O
O
HO
OH
HO
OH
OH
OH
step 1
HO
O
HO
OH
OH
OH
compound F
OH
chlorogenic acid
step 2
step 3
O
HO
OH
OH
OH
H2N
NH2
HO
OH
NH2
compound G
(i)
Compound F can be converted to compound G in two steps.

Suggest reagents and conditions for steps 2 and 3.
Step 2 dilute HNO3 / HNO3(aq)
Step 3 Sn, concentrated HCl, heat,
followed by controlled addition of NaOH(aq)
(ii)
Draw the structures of the compounds formed when compound G reacts

with
I
H2, Ni(s), 200oC
O
OH
HO
OH
HO
OH
HO
II
PJC 2012
HO
NaBH4 in methanol
9647/03/JC2 Prelims/2012
10
O
OH
HO
OH
HO
OH
HO
HO
[4]
(c) Ginger also contains nutrients like magnesium. Magnesium is a vital component
of a healthy human diet. Magnesium taken in the proper amount plays a role in
preventing both stroke and heart attack.
(i)
Describe what is observed when a piece of magnesium ribbon is burnt in air.

Mg burns to give a bright white flame. A white solid residue (of MgO)
is left behind.
(ii)
The product obtained in (i) is placed in a beaker of water containing a few

drops of universal indicator. State the observation(s) and write equations for
the reaction(s) that occur.
MgO + H2O Mg(OH)2
Magnesium oxide is sparingly soluble in water.
Mg(OH)2(s) Mg2+(aq) + 2OH-(aq)
Green solution turns blue.
[4]
(d) Sketch a graph of the pH of the solution when the chlorides of the elements from
sodium to phosphorus are added separately to water. Label your graph clearly. [2]
pH
7
NaCl MgCl2 AlCl3 SiCl4 PCl3/PCl5
PJC 2012
9647/03/JC2 Prelims/2012
11
(e) Hydrofluoric acid dissociates in water according to the following equation:
DHodissociation
H+(aq) + F-(aq)
HF(aq)
The following are some enthalpy changes related to hydrogen fluoride.

First electron affinity of fluorine/ kJ mol-1
Standard enthalpy change of hydration of fluoride ion / kJ mol-1
Standard enthalpy change of reaction, HF(aq) HF(g) / kJ mol-1
Standard enthalpy change of hydration of hydrogen ion / kJ mol-1
(i)
-328
-506
+39
-1090
By using the data provided and other relevant data from the Data Booklet,
construct an energy cycle and calculate the standard enthalpy change of
dissociation of hydrofluoric acid.
D Hodissociation
+
HF (aq)
F (aq)
H (aq)
D Hohyd (F-)
D Ho1
DH
o
hyd
(H+)
F (g)
1st E.A.(F)
B.E.(H-F)
HF (g)
1st I.E.(H)
H (g)
F (g)
H (g)
F (g)
Hdissociation (HF)
= H1 + BE(H-F) + 1st I.E(H) + 1st E.A.(X) + Hhyd(H+) + Hhyd(F-)
= + 39 + (+562) + (+1310) + (-328) + (-1090) + (-506)
= -13.0 kJ mol-1
(ii)
Aqueous hydrofluoric acid is a weak acid under standard conditions. One

explanation for the relatively weaker acid strength of hydrofluoric acid is its
negative standard entropy change of dissociation, Sdissociation. Account for
the sign of Sdissociation.
A negative sign of Sdissociation indicates a decrease in disorderliness
of the system.
Small anionic radius of F- ion leads to a high charge density, resulting
in a more regular arrangement of water molecules around the F- ions.
[6]
[Total: 20]
PJC 2012
9647/03/JC2 Prelims/2012
12
3 (a) Hydrazine (N2H4) is a colourless liquid with a slight odour like ammonia. However,
the solubility of hydrazine in water is very much higher than that of ammonia.
Draw a diagram to show the bonding between a molecule of hydrazine and a
molecule of water. Account for the difference in solubility of hydrazine and
ammonia in water.
Each hydrazine molecule has two -NH2 groups, which allow it to form more
extensive hydrogen bonds with water molecules than ammonia. Hence,
hydrazine has a higher solubility than ammonia.
H
H
N
H
d+ H
d- O
hydrogen
bond
H
[2]
(b) The Italian catalyst manufacturer Acta proposed using hydrazine as an alternative
to hydrogen in fuel cells. The chief benefit of using hydrazine is that it can produce
more energy than a similar hydrogen-oxygen cell.
The diagram below shows a typical hydrazine-oxygen fuel cell system
incorporated with an anion exchange membrane between the electrodes.
(i)
Write the two ion-electron half equations for the reactions that take place at
each electrode. Hence, write an overall equation for the cell reaction.
Anode:
PJC 2012
N2H4 (l) + 4OH- (aq) N2(g) + 4 H2O(l) + 4 e9647/03/JC2 Prelims/2012
13
Cathode: O2(g) + 2 H2O(l) + 4 e- 4OH- (aq)
Overall: N2H4 (l) + O2 (g) N2 (g) + 2H2O(l)
(ii)
Given that Eo(N2/N2H4) is -1.16 V, calculate the cell e.m.f. if the process
takes place under standard conditions.
Ecell = E (Reduction) + E (Oxidation)
= + 0.40 V + (+ 1.16)
= + 1.56 V
(iii) The hydrazine-oxygen fuel cell that is used to power a satellite produces an
average current of 5 A per day. Assuming that the fuel cell is only 70%
efficient, calculate the mass of hydrazine required in a day.
Total charge generated per day = I x t x
100
70
= 5 x (24 x 60 x 60) x
100
70
= 617100 C
Q
F
617100
=
= 6.40 mol
96500
Amount of electron transferred =
1 mol N2H4 4 mol of e-
6.40
= 1.60 mol
4
Mass of N2H4 required = 1.60 x [2(14.0)+4(1.0)]
= 51.2 g (3sf)
Amount of N2H4 required =
(iv) Based on the physical properties of hydrazine, suggest an advantage of the

hydrazine-oxygen fuel cell over the hydrogen-oxygen fuel cell.
Hydrazine is a liquid at room temperature and can be handled and
stored more easily than hydrogen gas.
[6]
(c) Wolff-Kishner reaction was discovered independently in 1911 by Ludwig Wolff in
Germany and N. M. Kishner in Russia. It is a valuable synthetic method for
converting ketones or aldehydes into alkanes using hydrazine in the presence of
potassium hydroxide.
R
H
C
H
N
KOH
C
H
N2
H2O
Indene (C9H8) is a colourless organic liquid obtained from coal tar and used in
preparing synthetic resins. It can be synthesised from phenylethene by the
PJC 2012
9647/03/JC2 Prelims/2012
14
following route, incorporating Wolff-Kishner reaction.
Br2(aq)
CH2
Step 1
Step 2
phenylethene
H2SO4(aq)
heat
Step 3
COOH
COOH
Step 4
OH
Step 5
COCl
H2NNH2
KOH
anhydrous
FeCl3
D
Step 7
Step 6
indene
C
(i)
Give the structures of compounds A, B and D.

Br
OH
(ii)
OH
State the reagents and conditions for Steps 2, 4 and 5.

Step 2: KCN in ethanol, heat
Step 4: excess concentrated H2SO4, 170C
Step 5: PCl5
*Also accept PCl3, warm
OR SOCl2, warm
PJC 2012
CN
9647/03/JC2 Prelims/2012
15
(iii) State the types of reaction occurring in Steps 6 and 7.
Step 6: Electrophilic substitution
Step 7: Reduction
(iv) When aqueous silver nitrate is added to compound C, a white precipitate is
observed immediately. The precipitate dissolves when dilute aqueous
ammonia is added to it. The addition of aqueous sodium iodide to the
resulting mixture produces a yellow precipitate. Identify the precipitates
formed and account for the observation.
White precipitate formed is AgCl is formed.
In the presence of aqueous ammonia, aqueous Ag+ ions react to form
the diamminesilver(I) complex, Ag(NH3)2+. The formation of the
complex, decreases [Ag+(aq)], lowering its ionic product. Thus, ionic
product falls below the Ksp of AgCl, causing it to dissolve.
When aqueous sodium iodide is added to the resulting solution, a
yellow precipitate of AgI is formed. As the Ksp (AgI) is extremely small,
the ionic product exceeds its Ksp, accounting for the formation of the
precipitate.
[12]
[Total: 20]
(a) A solution of carbonate reacts with H+ in two stages.

CO 3
2-
+H+
pKb1
HCO 3
+H+
pKb2
CO 2
H2O
The pH changes during the addition of 0.200 mol dm-3 nitric acid to a 20.0 cm3
solution of sodium carbonate and sodium hydrogencarbonate are shown below.
PJC 2012
9647/03/JC2 Prelims/2012
16
(i)
A list of indicators and their pKa values is given below.

indicator
thymol
blue
1.7
pKa
methyl
yellow
3.1
methyl
red
5.1
cresol
red
8.3
thymolphthalein
9.2
From the given list of indicators, choose two suitable indicators that can be
used to determine the two end-points in the titration. Explain your choice.
1st indicator: cresol red
2nd indicator: methyl yellow
both correct
pKa of indicator matches the pH change at equivalence point

OR
Equivalence point pH lies within the working range of the indicator.
(ii)
Calculate the concentration, in g dm-3, of sodium carbonate present in the

original solution, given that the end-point between B and C occurs after
8.40 cm3 of nitric acid is added.
CO32-
H+
HCO3-
amount of Na2CO3 = amount of HNO3 = 0.00168 mol

concentration of Na2CO3 =
0.00168
x106 = 8.90 g dm-3
20.0
1000
(iii) Calculate the concentration, in g dm-3, of sodium hydrogencarbonate

present in the original solution, given that the end-point between D and E
occurs after 18.80 cm3 of nitric acid is added.
HCO3-
H+
CO2
H2O
volume of HNO3 used to react with the total amount of HCO3 PJC 2012
9647/03/JC2 Prelims/2012
17
= 18.80 - 8.40 = 10.40 cm3
total amount of HCO3- = amount of HNO3 used = 0.00208 mol
At first end-point, 1CO32- 1HCO3-,
amount of HCO3- formed from Na2CO3 = 0.00168 mol
\ original amount of HCO3- = 0.00208 0.00168 = 0.0004 mol
concentration of NaHCO3 =
0.0004
x 84.0 = 1.68 g dm-3
20.0
1000
[4]
(b) Dicarboxylic acids ionise in two stages.

HO 2C (CH2)n
CO 2H
-H+
pKa1
HO 2C (CH2)n
-H+
CO 2-
pKa2
-O C
2
(CH2)n
CO 2-
The following table compares the pKa values of three dicarboxylic acids.
acid
oxalic
malonic
succinic
(i)
formula
HO2CCO2H
HO2CCH2CO2H
HO2C(CH2)2CO2H
pKa1
1.25
2.85
4.21
pKa2
4.27
5.70
5.64
Explain why succinic acid has the highest pKa1 value.

In succinic acid, the two CO2H groups are unable to form
intramolecular hydrogen bond to stabilise the negative charge of the
monoanion formed after the first dissociation.
(ii)
An amphiprotic species is one that reacts with an acid and a base. The
monocarboxylate ion of a dicarboxylic acid, HO2C(CH2)nCO2, is an
amphiprotic species.
The pH of an amphiprotic species is given by the following expression.
pH = (pKa1 + pKa2)
Using malonic acid as an example, write two equations to show that its
monocarboxylate ion is an amphiprotic species.
HO2CCH2CO2 +
HO2CCH2CO2 +
PJC 2012
H+ HO2CCH2CO2H
OH- -O2CCH2CO2- +
9647/03/JC2 Prelims/2012
H2O
18
(iii) The pH-volume added curve when 55 cm3 of 0.20 mol dm-3 NaOH is added
to 25 cm3 of 0.20 mol dm-3 oxalic acid is shown below.
C
B
l
55
55
Calculate the pH of the curve at points X, Y and Z.

X - Initial pH = 0.974
[H3O+]2 = Ka1[acid] = (101.25)(0.20) = 0.01124 mol2 dm6
pH = lg[H3O+] = lg (0.01124) = 0.974 (3 s. f.)
Y - pH at 1st equiv. point = (pKa1 + pKa2)= (1.25 + 4.27) = 2.76
(HO2CCO2- is an amphiprotic species)
Z - pH at MBC2 (when [HO2CCO2] = [O2CCO2]) = pKa2 = 4.27
[6]
(c) Thermal decomposition of the calcium salt of oxalic acid, calcium oxalate,
produces calcium oxide and oxides of carbon.
The graph below is an Ellingham diagram, which shows the variation in the
standard Gibbs free energy change of formation, Gf q, with temperature, T, for
various oxides.
PJC 2012
9647/03/JC2 Prelims/2012
19
(i)
(ii)
Which oxide, calcium oxide, zinc oxide or silver(I) oxide, could be

decomposed by heat at 1000 K? Explain your choice.
Silver(I) oxide
G < 0 for the decomposition of 2Ag2O 4Ag + O2
What does the gradient of the graph in the Ellingham diagram represent?
Hence, explain why the gradient for 2C + O2 2CO is as shown.
Gradient represents DSq (equation of line is DGq = TDSq + DHq).
A negative gradient implies that DSq is positive. An increase in
disorderliness of the system (DSq > 0) is due to an increase in amount
of gases (from 1 to 2 mol) as the reaction proceeds.
_
(iii) From the Ellingham diagram, find the G values of the following reactions
at 1500 K.
I
II
2C(s) + O2(g) 2CO(g)

2Zn(s) + O2(g) 2ZnO (s)
2C + O2 2CO
DGq = 500 kJ mol-1 (1)
2Zn + O2 2ZnO
DGq = 300 kJ mol-1 ........... (2)
(iv) Use your answer in (iii) to calculate Gq value for the reaction in which
carbon reduces zinc oxide at 1500 K.
2ZnO + 2C 2Zn + 2CO
PJC 2012
9647/03/JC2 Prelims/2012
20
Hence, comment on the feasibility of the reaction at 1500 K.
2ZnO 2Zn + O2
DGq = + 300 kJ mol-1 ........(3)
(1) + (3) gives 2ZnO + 2C 2Zn + 2CO and DGq = 200 kJ mol-1
The reaction is thermodynamically feasible at 1500 K.
[5]
(d) In no more than 3 steps, suggest how each of the following transformations can
be achieved. You are required to state the reagents and conditions for each step
and give the structures of the intermediate compounds.
OH
(i)
HO
OH
OH
O
Br
HO
OH
Excess conc H2SO4

170 oC
Br
Br
OH
(ii)
CH3
heat
OH
KMnO4(aq), H2SO4(aq)
heat
OH
COOH
NO 2
PJC 2012
NaOH (aq)
9647/03/JC2 Prelims/2012
21
CH3
COOH
NO 2
H2SO4(aq),
KMnO4(aq), heat
concentrated HNO3,
COOH
concentrated H2SO4,
>55oC
[5]
[Total: 20]
PJC 2012
9647/03/JC2 Prelims/2012
22
5
(a) Magnesium carbonate occurs naturally in several forms. Due to its hygroscopic
properties, anhydrous magnesium carbonate is used in organic reactions to
remove moisture.
The decomposition temperature of magnesium carbonate is 540 C. Explain how
you would expect the decomposition temperature of barium carbonate to differ
from magnesium carbonate.
Ba2+ ion has a smaller ionic radius compared to Mg2+. Ba2+ ion has a lower
charge density and hence is less polarising/ lower polarising power. Ba2+
ion polarises and weakens the C-O bond in CO32- to a smaller extent than
Mg2+. Thus, the C-O bond in BaCO3 is stronger. More energy is required to
break the bond and hence the decomposition temperature of barium
carbonate would be higher.
[3]
-3
(b) The solubility of magnesium carbonate is 0.267 g dm .

(i)
Calculate the solubility product, Ksp, of magnesium carbonate.

Mr MgCO3
= 24.3 + 12.0 + 3(16.0)

= 84.3
Solubility
= 0.267 / 84.3
= 3.17 x 10-3 mol dm-3
Ksp
(ii)
= (3.17 x 10-3)2
= 1.00 x 10-5 mol2 dm-6
To a 1.0 dm3 saturated solution of magnesium carbonate, 50.0 cm3 of

1.00 mol dm-3 aqueous magnesium chloride was added. Find the mass of
precipitate formed.
Let the solubility of MgCO3 in MgCl2 be s mol dm-3.
Total volume
= 1.0 + 0.0500
= 1.05 dm3
1 50
/ 1.05)
1000
= s + 0.04762
[Mg2+] = s + (
s(s + 0.04762)
s (0.04762)
s
= 1 x 10-5
1 x 10-5 (since 0.04762 >>> s)
= 2.100 x 10-4 mol dm-3
Amount of MgCO3 extracted
Mass extracted
PJC 2012
= (3.17 x 10-3)
(2.100 x 10-4 x 1.05)
= 2.950 x 10-3 mol
= 2.950 x 10-3 x 84.3

= 0.249 g
9647/03/JC2 Prelims/2012
23
[4]
(c) Compound A (C11H22) decolourises aqueous bromine. Compound A was heated
with a mixture of aqueous sodium hydroxide and potassium manganate(VII).
After the reaction was completed (assuming 100% yield), the reaction mixture
was extracted several times with an organic solvent.
The aqueous and organic layers were then collected separately. Acidification of
the aqueous layer yielded compound B (Mr = 102), which rotated the plane of
polarised light. Compound B produced a colourless gas with sodium metal.
(i)
Use all of the information to determine the identity of functional group

present in
I compound A
II compound B.
For each functional group you identify, explain how you came to your
decision.
Compound A contains an alkene.
It has one degree of unsaturation and undergoes electrophilic addition
with aqueous bromine. A undergoes oxidative cleavage/ strong
oxidation with KMnO4.
Compound B contains a carboxylic acid.
Alkenes undergo oxidative cleavage/ strong oxidation to form carbon
dioxide, ketones or carboxylic acids.
Only carboxylic acid can react with sodium metal via redox reaction.
(ii)
Deduce the molecular formula of compound B and hence, draw its

displayed formula.
C5H10O2
H
C
H
C
O
H
H
H
H
(iii)
Explain why the salt of compound B was found in the aqueous layer after
the separation of the reaction mixture.
The carboxylate anion, produced by strong oxidation of alkene A, can
form favourable ion-dipole interactions with water, and is hence highly
soluble in water.
PJC 2012
9647/03/JC2 Prelims/2012
24
The organic layer was then distilled to give compound C (C6H12O). Warming
compound C with aqueous alkaline iodine, followed by controlled addition of
concentrated hydrochloric acid produced compound B.
(iv)
Propose the structure of compound C and give a balanced equation for its
reaction with aqueous alkaline iodine.
CH3
O
CH
CH3
CH2
CH3
(v)
CH3
CH3
O
CH
CH3
CH2
3I2
O
CH
4OH
CH3
CH3
CH2
C
O
CHI3
3I-
+ 3H2O
Hence or otherwise, deduce the structure of compound A.

CH3 CH2
CH3
C
H
H
C
CH3
C
CH3
H
CH2 CH3
Compound C was converted to compound E via the following reaction scheme.

Compound C 1. HCN(aq), NaCN, 10-20 oC
(C6H12O)
2. H2SO4(aq)
Compound D
(C7H14O3)
concentrated H2SO4,
heat under reflux
Compound E
(C14H24O4)
PJC 2012
9647/03/JC2 Prelims/2012
25
(vi)
Draw the structures of compounds D and E.

OH
C
HO
CH3
CH3
CH3
CH
CH3
CH3 CH2 CH3

O
(vii)
CH3
CH3
O
CH3
Describe a simple chemical test to distinguish between compounds C and

D, clearly stating how each compound behaves in the test. You should not
use any of the reagents and conditions outlined in this question.
Test: Aqueous sodium carbonate, room temperature. Bubble any gas
evolved into limewater.
Observation for C: No effervescence observed.
Observation for D: Effervescence observed. Gas evolved forms a
white precipitate with limewater.
OR
Test: 2, 4- dinitrophenylhydrazine, room temperature.
Observation for C: Orange precipitate/ orange crystalline solid
observed.
Observation for D: No orange precipitate observed.
[13]
[Total: 20]
End of Paper
PJC 2012
9647/03/JC2 Prelims/2012
RIVER VALLEY HIGH SCHOOL

YEAR 6 PRELIMINARY EXAMINATION
CANDIDATE
NAME
CLASS
CENTRE
NUMBER
INDEX
NUMBER
H2 CHEMISTRY
9647/01
21 September 2012
1 hour

Data Booklet

Write your name, class, centre number and index number on the Answer Sheet in the spaces
provided.
Sheet.
________________________________________________________________________

Prelim Examination 2012
9647/01/PRELIM/12
[Turn over
Year 6 H2 Chemistry 9647 Paper 1
2
Section A
1
Methane was burned with a faulty Bunsen burner. As a result, a mixture of carbon
dioxide and carbon monoxide was produced in a ratio of 98:2, together with water
vapour.
What was the volume of oxygen gas used when y dm3 of methane was burned?
0.01
y) dm3
2
(2 y -
(2 y - 0.01y) dm3
(y -
( y - 0.01y) dm3
0.01
y) dm3
2
An ion of metal M can be oxidised by potassium manganate(VII) in acid solution to

form MO3. In an experiment, 1.25 103 mol of the ion of M required 37.5 cm3 of
0.0200 mol dm3 potassium manganate(VII) for complete reaction.
What is the initial oxidation state of the ion of M?
+1
+2
+3
+4
Which of the following statements best explains why the boiling point of
CH3CH2CH2NH2 is higher than that of (CH3)3N?
A
There are hydrogen bonds between CH3CH2CH2NH2 molecules but no

hydrogen bonds between (CH3)3N molecules.
The covalent bonds between atoms in CH3CH2CH2NH2 are stronger than those
between atoms in (CH3)3N.
CH3CH2CH2NH2 molecule has a larger surface area than (CH3)3N molecule.
CH3CH2CH2NH2 molecule is polar but (CH3)3N molecule is not.

9647/01/PRELIM/12
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Which of the following electrostatic attraction is not present in a sample of CH3F?

A
permanent dipole-permanent dipole interactions
instantaneous dipole-induced dipole interactions
hydrogen bonds
covalent bonds
Which of the following graph is obtained when density () is plotted against

temperature (T) for an ideal gas under constant pressure?
T / C
T / C
T / C
T / C
Which of the following oxides is unlikely to dissolve in aqueous sodium hydroxide?

A
MgO
Al2O3
SiO2
SO2

9647/01/PRELIM/12
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4
7
Nitrogen dioxide decomposes on heating according to the following equation.

2NO2(g) 2NO(g) + O2(g)
When 2 mol of nitrogen dioxide is placed in a 4 dm3 container and heated, the
equilibrium mixture contained 0.8 mol of oxygen.
What is the numerical value of the equilibrium constant, Kc, at the temperature of the
experiment?
0.0889
0.800
3.20
12.8
Which statement about the effect of a catalyst on a reversible reaction is correct?

A
It increases the yield of product in an equilibrium.
It increases the equilibrium constant for the forward reaction.
It increases the rate of the forward reaction and decreases the rate of the
reverse reaction.
It increases the rate constant for both the forward and the reverse reaction.
Which expression represents the solubility product of iron(III) hydroxide?

A
[Fe3+][OH]
[Fe3+][OH]3
[Fe3+][3OH]
[Fe3+][3OH]3

9647/01/PRELIM/12
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5
10
H2SO4(aq) was added to Ba(OH)2(aq) until the acid was in excess.

Which graph shows the variation in the total number of ions in solution?
No. of ions
Vacid
0
No. of ions
Vacid
0
No. of ions
Vacid
11
No. of ions
Vacid
The product of the concentrations of X and Y, [X][Y], is plotted against time, t, for the
following second-order reaction.
X+YZ
Which graph would be obtained?
[X][Y]
0
[X][Y]
[X][Y]

9647/01/PRELIM/12
[X][Y]
[Turn over
6
12
13
Which one of the following elements has the same oxidation state in all of its known
compounds?
A
beryllium
bromine
nitrogen
sulfur
X is obtained by reacting aqueous cobalt(III) chloride with ammonia. The coordination number of cobalt is 6 and when the complex is treated with an excess of
aqueous silver nitrate, only of the total chloride is precipitated as AgCl.
What is the formula of X?
14
15
Co(NH3)6Cl3
Co(NH3)5Cl3
Co(NH3)4Cl3
Co(NH3)3Cl3
Using relevant E values from the Data Booklet, determine which of the following
statements is correct.
A
No reaction occurs when V3+(aq) is added to Fe3+(aq).
VO2+(aq) can reduce Fe2+(aq) to Fe3+(aq).
Zn2+(aq) can reduce VO2+(aq) to V3+(aq).
Zn(s) can reduce V3+(aq) to V2+(aq).
A current of 8 A is passed for 100 min through molten aluminium oxide using inert
electrodes.
What will be the approximate volume of gas liberated, measured at s.t.p.?
16
2.8 dm3
3.0 dm3
11.2 dm3
12.0 dm3
Which one of the following products is not obtained commercially by the electrolysis
of concentrated brine?
A
chlorine
oxygen
sodium chlorate(V)
sodium hydroxide

9647/01/PRELIM/12
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7
17

In the construction of pacemakers for the heart, a tiny magnesium electrode can be
used to create an electrical cell with the inhaled oxygen. The relevant half-equations
are as shown:
Mg2+ + 2e Mg
O2 + 2H+ + 2e H2O
In the body, a potential of 3.20 V is usually obtained. What is the best explanation for
this e.m.f.?
18
The small size of the magnesium electrode
The low concentration of Mg2+ surrounding the magnesium electrode
The high resistance of the body fluids surrounding the electrodes
The physiological pH of between 7 and 8 of the body fluid surrounding the

electrodes

The enthalpy changes for three reactions are given below:
Na(s) Na(g)
DH1 = +107 kJ mol1
H+(aq) + OH(aq) H2O(l)
DH2 = 58 kJ mol1
2Na+(g) + 2H+(aq) + 2e 2Na+(aq) + H2(g)
DH3 = 1700 kJ mol1
What is the enthalpy change for the following reaction?

Na(s) + H2O(l) Na+(aq) + OH(aq) + H2(g)
19
191 kJ mol1
307 kJ mol1
685 kJ mol1
1041 kJ mol1
The bond dissociation energy of HCl is 431 kJ mol1. In which of the following
processes is 431 kJ of energy released?
A
HCl(g) H(g) + Cl(g)
H(g) + Cl(g) HCl(g)
HCl(g) H2(g) + Cl2(g)
H2(g) + Cl2(g) HCl(g)

9647/01/PRELIM/12
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8
20
Vitamin E acts as an antioxidant as well as an enzymatic activity regulator. There are

8 forms of Vitamin E, of which a-tocopherol is the most biologically active form. The
diagram shows the structure of a-tocopherol.
CH3
HO
CH3
H3C
CH3
CH3
CH3
CH3
O
CH3
How many chiral carbon centres are there in one molecule of a-tocopherol?
A
21
22
Which of the following could be best used to distinguish between hex-1-ene and
methylbenzene?
A
acidified K2Cr2O7
Br2 in CCl4
I2 in NaOH(aq)
concentrated sulfuric acid
Samples of the gases CH3Cl and Cl2 are mixed together and irradiated with light.
Which compound is produced by a termination stage in the chain reaction?
23
HCl
CH2=CH2
CH3CH3
CH2Cl2
Which hydrocarbon, on treatment with hot acidified potassium manganate(VII),

would give ethanoic acid as one of the products?
A

9647/01/PRELIM/12
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9
24
25
Which of the following compounds would undergo electrophilic substitution most

readily?
A
Cl
CHO
CH3
N(CH3)2
A reaction sequence is given below.
CHBrCH3
KCN,
CH3CH2OH
HCl(aq)
P
Heat under
reflux
Br
Which of the following structures represents the product Q?
CHCH3
CHCH3
CO2H
CO2H
Br
HOOC
CHCH3
CHCH3
D
Cl
CO2H
Br
Cl

9647/01/PRELIM/12
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10
26
Citronellol is a colourless oily liquid with a rose-like smell. It is the active ingredient in
over 30 essential oils and is a major component in perfumes, cosmetics and soaps. It
may be prepared synthetically from compound S using reagent T.
OH
Citronellol
Which of the following could S and T most likely be?
S
KOH in ethanol
Cl
aqueous NaOH
Cl
LiAlH4 in dry ether

O
D
concentrated H2SO4 at 170 C
OH
OH
27
One mole of compound R reacts with excess sodium metal to give one mole of
hydrogen gas. One mole of ammonia gas is also evolved when one mole of
compound R is heated with aqueous sodium hydroxide.
What is the identity of R?
A
HOCH2CH(NH2)CO2H
HOCH2CH(OH)CN
HOCH2CH2CONH2
HOCH2CH(NO2)CO2H

9647/01/PRELIM/12
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11
28
The reaction scheme below shows the formation of compound V.

Br
NaOH(aq)
NC
Heat under
reflux
CONHCH3
1. H+
2. PCl5
What is the structure of V?

Br
O
CONHCH3
Cl
Cl
O
NC
CONHCH3
Cl
O
NC
Cl
Br
Cl
29
Cl
Which of the following statements explains why ethylamine has a lower pKb value
than ammonia? (pKb of ethylamine = 3.2; pKb of ammonia = 4.8)
A
The nitrogen atom in ammonia is bonded to more hydrogen atoms than that in
ethylamine.
The conjugate acid of ethylamine is less stable than that of ammonia.
Ethyl group in ethylamine increases the electron density of the nitrogen atom.
The lone pair on the nitrogen atom of ammonia is less delocalised than that on
ethylamine.

9647/01/PRELIM/12
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12
30
Denaturation of proteins occurs due to the destruction of the tertiary structure where
various R group interactions are disrupted by external factors such as extreme pH
and heavy metal ions.
Which of the following incorrectly shows the R group interactions that will be
affected by such external factors?
R group interactions
External factor
hydrogen bonds
extreme pH
disulfide bridges
extreme pH
disulfide bridges
heavy metal ions
ionic interactions
heavy metal ions

9647/01/PRELIM/12
[Turn over
13
Section B
3 may be correct.
Decide whether each of the statements is or is not correct. (You may find it helpful to put a
31
32
1, 2 and 3 are
1 and 2 only are
2 and 3 only are
1 only is
correct
correct
correct
correct
Which statements about the electronegativity of elements in the Periodic Table are
correct?
1
In Period 3, it decreases from sodium to chlorine.
In Group II, it decreases from beryllium to barium.
In Group VII, it decreases from fluorine to iodine.
When light is shown for a fixed period into a solution of CH2ICH2I and I2 in
tetrachloromethane at 100 C, the following reaction occurs.
CH2ICH2I CH2=CH2 + I2
Experiment
Relative
concentrations
Relative light
intensity
Relative initial rate of

formation of iodine
CH2ICH2I
I2
From the data above, the rate of formation of iodine is

1
independent of the initial concentration of I2
proportional to the initial concentration of CH2ICH2I
proportional to the square root of light intensity

9647/01/PRELIM/12
[Turn over
14
33
34
1, 2 and 3 are
1 and 2 only are
2 and 3 only are
1 only is
correct
correct
correct
correct
Why is the addition of concentrated sulfuric acid to solid potassium iodide

unsuitable for the preparation of hydrogen iodide?
1
Hydrogen iodide is not displaced by sulfuric acid
Iodide ions are oxidised to iodine
The product is contaminated by sulfur-containing compounds
When a paramagnetic object is placed in a strong magnetic field, it is attracted to the

field. Paramagnetism is associated with unpaired electrons, and many transition
elements are often paramagnetic because they contain unpaired d-electrons.
Which of the following transition metal atoms or ions would you expect to be
paramagnetic?
35
Cr
Mn
Cu+
The enthalpy changes of formation of carbon monoxide and carbon dioxide are given
below.
DHf (CO) = 110 kJ mol1
DHf (CO2) = 393 kJ mol1
1
The enthalpy change of combustion of carbon monoxide is exothermic.
Carbon dioxide is energetically more stable than carbon monoxide.
The enthalpy change of combustion of carbon is 110 kJ mol1.

9647/01/PRELIM/12
[Turn over
15
36
37
1, 2 and 3 are
1 and 2 only are
2 and 3 only are
1 only is
correct
correct
correct
correct
What are the conditions usually quoted for the standard electrode potential of
hydrogen to be 0.00 V?
1
temperature is 25 C
pH of the acid solution is 1.0
atmospheric pressure is exactly 1 atm

When nitric acid is added to iron filings, a brown gas that turns moist blue litmus red
is observed.
Which statements are correct?
1
Iron acts as a reducing agent.
The standard cell potential of the reaction between iron filings and nitric acid is
+0.04 V.
38
Addition of potassium cyanide to the reaction vessel of nitric acid and iron filings
will result in a decrease in the standard cell potential.
By varying the conditions of the reaction between 1,2-dibromoethane and sodium

hydroxide, which of the following compounds can be obtained?
OH
OH
Br
OH
H
C

C
Br
9647/01/PRELIM/12
[Turn over
16
39
1, 2 and 3 are
1 and 2 only are
2 and 3 only are
1 only is
correct
correct
correct
correct
Ethanal can react with HCN in a nucleophilic addition reaction catalysed by NaCN.
Which of the following statements about the reaction mechanism are true?
40
The shape of the intermediate is planar.
In the intermediate, the oxygen carries a negative charge.
A new carbon-carbon bond is formed.
In which of the following reactions is the inorganic reagent acting as a nucleophile?

1
CH3CH2Cl + KCN CH3CH2CN + KCl
CH3COCl + NH3 CH3CONH2 + HCl
CH3CH2NH2 + HCl CH3CH2NH3+Cl
End of Paper 1

9647/01/PRELIM/12
[Turn over
Answer key for Prelim Paper 1

1.
11.
21.
31.
2.
12.
22.
32.
3.
13.
23.
33.
4.
14.
24.
34.
5.
15.
25.
35.
6.
16.
26.
36.
7.
17.
27.
37.
8.
18.
28.
38.
9.
19.
29.
39.
10.
20.
30.
40.

CANDIDATE
NAME
CLASS
CENTRE
NUMBER
INDEX
NUMBER
H2 CHEMISTRY
9647/02
11 September 2012
2 hours

Data Booklet

Write your name, class, Centre number and index number on all the work you hand in.
A Data Booklet is provided. Do NOT write anything on it.
For Examiners Use

Paper 2
Question
Number
Marks
12
Paper 1
7
40
10
Paper 3
9
80
13
Total
8
Total
72
192
____________________________________________________________________________

Preliminary Examination 2012
9647/02/PRELIM/12
[Turn over
Planning (P)
Calcium salts are used in many industrial processes. Calcium oxide is used
in the production of cement while calcium nitrate is sometimes used to
accelerate the setting of concrete.
Calcium oxide is a white hygroscopic solid. Calcium oxide can react with
water and as such can cause severe irritation when in contact with skin,
eyes or if inhaled.
Calcium nitrate is also a white hygroscopic solid. Calcium nitrate
decomposes on heating to form the oxide, nitrogen dioxide and oxygen.
(a)
Write a balanced equation, including state symbols, for the thermal

decomposition of calcium nitrate.
.....................
(b)
[1]
Calculate the change in mass of the solid you would expect if 1.00 mol
of calcium nitrate underwent thermal decomposition.
[1]
(c)
A container of calcium nitrate was contaminated with calcium oxide.

Design an experiment to determine the percentage purity of calcium
nitrate by a gravimetric method. You are provided with about 2 g of the
impure calcium nitrate.
(In gravimetric methods, the objective is to form a thermally stable
solid so that the mass can be determined accurately for analysis.)
Your plan should include the following:
A full description of the procedure.
Details of how you would calculate the percentage purity from

the measurements made.
[Mr of Ca(NO3)2 = 164]

......................
......................
......................
......................
......................
......................
9647/02/PRELIM/12
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......................
......................
......................
......................
......................
......................
......................
......................
......................
......................
......................
......................
......................
......................
......................
......................
......................
(d)
[8]
State and explain clearly one precaution you would take to improve
the accuracy of your results.
......................
......................
......................
(e)
[1]
Identify one potential safety hazard in this experiment and state how
you would minimise the risk.
......................
......................
[1]
[Total: 12]

9647/02/PRELIM/12
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Titanium(IV) oxide, TiO2, is the naturally occurring oxide of titanium. It is the

main ingredient in sunscreen lotion due to its high refractive index and
strong UV-light absorbing capability.
(a)
Using the following information as well as relevant data from the Data
Booklet, draw a Born-Haber cycle for the formation of TiO2(s) and
calculate the lattice energy of TiO2(s).
Standard enthalpy change of formation of TiO2(s)
945 kJ mol1
Standard enthalpy change of atomisation of Ti
+471 kJ mol1
1st electron affinity of oxygen
142 kJ mol1
2nd electron affinity of oxygen
+844 kJ mol1
[3]

9647/02/PRELIM/12
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(b)
Crude titanium(IV) oxide is purified via the Chloride process. In this

two-step process, the crude ore (containing at least 70% titanium(IV)
oxide) is first reacted with carbon and chlorine, represented by the
equation shown below.
TiO2(s) + C(s) + 2Cl2(g) TiCl4(l) + CO2(g)
Standard enthalpy change of formation of TiCl4(l)
804 kJ mol1
Standard enthalpy change of formation of CO2(g)
394 kJ mol1
Standard molar entropy of TiO2(s)
+49.9 J mol1 K1
Standard molar entropy of C(s)
+5.7 J mol1 K1
Standard molar entropy of Cl2(g)
+223 J mol1 K1
Standard molar entropy of TiCl4(l)
+252 J mol1 K1
Standard molar entropy of CO2(g)
+214 J mol1 K1
Using the above information, as well as relevant data from (a) and the
Data Booklet, calculate, for the first step of the Chloride process,
(i)
the standard enthalpy change of reaction,
(ii)
the standard entropy change of reaction.

Note: DS, = SS,(products) SS,(reactants)
[2]

9647/02/PRELIM/12
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(c)
Using your answers in (b), determine if the first step of the Chloride
process is spontaneous at 2000 K.
[1]
(d)
The second step of the Chloride process involves the titanium(IV)

chloride being distilled off and oxidised in a pure oxygen flame to give
pure titanium(IV) oxide and chlorine gas.
Write an equation for the reaction in the second step.
.....................
[1]
[Total: 7]
Neidong Forest Recreation National Park, located in the Wulai District in

Taipei, has the highest concentration of anions in Taiwan due to the
numerous waterfalls and lush forestation in the park. Anions are said to help
boost the immune system, among other health benefits.
(a)
Bromide ions are thought to be one of the anions present in

abundance. The concentration of bromide ions in the river waters can
be used as an estimate of the concentration of the ions in the park.
A 25.0 cm3 sample of river water was collected and 50.0 cm3 of
1.00 mol dm3 Pb(NO3)2 was added. The precipitate formed was
filtered off and 3.00 g of precipitate was collected. The filtrate can be
regarded as a saturated solution of PbBr2.
(i)
Calculate the concentration of Pb2+ ions in the filtrate.

9647/02/PRELIM/12
[Turn over
(ii)
Write an expression for the solubility product, Ksp, of PbBr2.

............
(iii)
The numerical value for the Ksp of PbBr2 is 3.9 105. Determine
the concentration of bromide ions in the sample of river water.
[5]
(b)
Another anion, W, found in Neidong National Park can be formed

when the oxide of a Period 3 element reacts with an alkali. When
dilute nitric acid is added to a solution containing W, a colourless and
pungent gas that turns acidified potassium dichromate(VI) from
orange to green is evolved.
(i)
Suggest an identity for anion W.

............
(ii)
Write an equation for the formation of W from the reaction of a

Period 3 oxide with an alkali.
............
[2]
[Total: 7]

9647/02/PRELIM/12
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The leadacid accumulator is a storage battery used in cars because it can

be recharged. It consists of a series of cells containing lead plate anodes,
lead dioxide plate cathodes and an electrolyte of 6 mol dm3 sulfuric acid.
When it is operating, the reactions that occur at the electrodes are
Pb2+(aq) + 2e = Pb(s)
E, = 0.13 V
PbO2(s) + 4H+(aq) + 2e = Pb2+(aq) + 2H2O(l)
E, = +1.47 V
(a)
Write the overall equation for the reaction during discharge and
calculate the voltage delivered by the battery.
Equation: .............
[2]
(b)
However, it is noted that the actual voltage is 2.0 V as compared to

the value that you have calculated in (a). Explain why the actual
voltage differs from the calculated voltage.
.............................
.............................
.............................
.............................
.............................
(c)
[2]
Explain why the battery is rechargeable.

.............................
.............................
.............................

9647/02/PRELIM/12
[1]
[Turn over
(d)
State one disadvantage of the lead-acid accumulator battery.

.............................
.............................
.............................
[1]
[Total: 6]
5
This question is about the chemistry of halogens and halide ions.

(a)
Aqueous bromine is decolourised when added to aqueous sodium

thiosulfate. When excess of aqueous barium nitrate is added to the
resulting solution, a white precipitate is observed. This precipitate is
filtered off, leaving a colourless filtrate.
(i)
Write a balanced ionic equation for the reaction between

bromine and sodium thiosulfate.
....................
(ii)
To the colourless filtrate in (i), aqueous silver nitrate is added,

followed by concentrated ammonia solution.
Describe what is observed and write balanced equations for any
reaction that occur.
....................
....................
....................
....................
....................
....................

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[4]
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10
(b)
In a separate experiment, aqueous bromine is added to aqueous

potassium iodide. To the resulting mixture, an equal volume of an
organic solvent is added.
What will be the colour of the organic layer? Write equations for any
reactions that occur.
.....................
.....................
(c)
[2]
Iodide ions react with peroxodisulfate ions in the presence of Fe3+

catalyst. The overall equation for the reaction is shown below.
2I -(aq) + S2O82-(aq) I2(aq) + 2SO42-(aq)
(i)
Fe3+ ions are added to lower the high activation energy so that
the reaction can proceed at a higher rate. Explain why the
activation energy is high for the reaction between the iodide and
peroxodisulfate ions if no Fe3+ ions are added.
............
............
............
(ii)
With reference to the Data Booklet, suggest a mechanism for

this reaction in the presence of Fe3+.
[4]
[Total: 10]

9647/02/PRELIM/12
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11
Chromium is a hard grey metal which is widely used in the manufacture of

stainless steel due to its good corrosion-resistant properties.
Calcium is a fairly soft, silvery grey metal which tarnishes quickly in air.
(a)
The melting point of calcium is 843 C while chromium melts at a

much higher temperature of 1907 C.
Explain this difference in terms of the type and strength of bonding in
each metal.
.............................
.............................
.............................
.............................
.............................
.............................
(b)
Write the electronic

chromium(III) ions.
configuration
of
chromium
atoms
[3]
and
Cr ..............................
Cr3+..............................
(c)
[2]
When aqueous sodium hydroxide was added to aqueous

chromium(III) nitrate, a blue-green precipitate was observed. Upon
addition of excess aqueous sodium hydroxide, the precipitate
dissolved to give a dark green complex.
When aqueous sodium carbonate was added
chromium(III) nitrate, effervescence was observed.
(i)
to
aqueous
State the formula of the blue-green precipitate.

............
(ii)
Suggest a reason why effervescence was observed when

aqueous sodium carbonate was added to aqueous
chromium(III) nitrate.
............
............

9647/02/PRELIM/12
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12
(iii)
Given that the formula of the soluble dark green complex is

Na3CrO6H6, state the formula of the complex ion formed.
............
(iv)
Draw the structure of the complex ion.
[4]
[Total: 9]

9647/02/PRELIM/12
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13
Hydrocarbons are commonly used as combustible fuel sources as well as

feed materials in the petrochemical industry.
(a)
Describe a simple chemical test to distinguish between but-1-ene and

but-2-ene. State clearly what would be observed with each compound.
.............................
.............................
.............................
.............................
.............................
(b)
[2]
But-2-ene is able to exist as 2 isomers.

(i)
State the type of isomerism exhibited by but-2-ene.

............
(ii)
Draw the displayed structural formulae for the 2 isomers of

but-2-ene.
[3]

9647/02/PRELIM/12
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14
(c)
Benzene is an aromatic hydrocarbon present in many compounds.

A reaction scheme involving benzene derivatives is given below. Draw
the structures of A to D and give the reagents and conditions for steps
I to IV.
OH
H2SO4(aq)
heat under
reflux
CH2CH2COOH
OH
OH
IV
ethanolic
NaCN
NaOH(aq)
C
heat under
reflux
heat under
reflux
CH2CH2Br
CH2CH2CH(OH)CH3
acidified K2Cr2O7(aq),
heat
II
LiAlH4 in
dry ether
III
OH
OH
OH
CH2CHO
CH2CH2CH2NH2

9647/02/PRELIM/12
CH=CH2
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15
A:
B:
C:
D:
Step I: .....
Step II:
Step III:
Step IV:
[8]
[Total: 13]

9647/02/PRELIM/12
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16
Students often complain of headaches when faced with a tough problem

they cannot solve. A very common over-the-counter drug to combat
headaches is paracetamol. The synthesis of paracetamol is shown below:
Paracetamol
(a)
Draw the structure of compound X.
[1]
(b)
Step I is actually a two-stage process. State the reagents and

conditions for the two stages.
Stage 1: .......
Stage 2: .......
(c)
[2]
Step II involves a condensation reaction. An organic side-product, Y,

can be formed along with paracetamol.
(i)
State the reagent for this step.

............
(ii)
Suggest a structure for Y.
[2]

9647/02/PRELIM/12
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17
(d)
Suggest the structures of all the organic products formed when

paracetamol reacts with
(i)
NaOH(aq) at room temperature
(ii)
NaOH(aq) with heating
[3]
[Total: 8]

9647/02/PRELIM/12
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18
BLANK PAGE

9647/02/PRELIM/12
[Turn over

CANDIDATE
NAME
MARK SCHEME
CLASS
CENTRE
NUMBER
INDEX
NUMBER
H2 CHEMISTRY
9647/02
11 September 2012
2 hours

Data Booklet

Write your name, class, Centre number and index number on all the work you hand in.
A Data Booklet is provided. Do NOT write anything on it.
For Examiners Use

Paper 2
Question
Number
Marks
12
Paper 1
7
40
Paper 3
9
80
13
Total
8
Total
72
192
____________________________________________________________________________

9647/02/PRELIM/12
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Planning (P)
Calcium salts are used in many industrial processes. Calcium oxide is used
in the production of cement while calcium nitrate is sometimes used to
accelerate the setting of concrete.
Calcium oxide is a white hygroscopic solid. Calcium oxide can react with
water and as such can cause severe irritation when in contact with skin,
eyes or if inhaled.
Calcium nitrate is also a white hygroscopic solid. Calcium nitrate
decomposes on heating to form the oxide, nitrogen dioxide and oxygen.
(a)
Write a balanced equation, including state symbols, for the thermal

decomposition of calcium nitrate.
Ca(NO3)2(s) CaO(s) + 2NO2(g) + O2(g)
(b)
[1]
Calculate the change in mass of the solid you would expect if 1.00 mol
of calcium nitrate underwent thermal decomposition.
Loss in mass = Mass of NO2 and O2
= 2(14.0 + 2(16.0)) + (2(16.0))
= 108 g
(c)
[1]
A container of calcium nitrate was contaminated with calcium oxide.

Design an experiment to determine the percentage purity of calcium
nitrate by a gravimetric method. You are provided with about 2 g of the
impure calcium nitrate.
(In gravimetric methods, the objective is to form a thermally stable
solid so that the mass can be determined accurately for analysis.)
Your plan should include the following:
A full description of the procedure.
Details of how you would calculate the percentage purity from

the measurements made.
[Mr of Ca(NO3)2 = 164]

1. Weigh accurately a clean and dry crucible (Accept: hard glass
tube). Add the sample and weigh the crucible with its contents.
2. Heat the crucible strongly for about five minutes to decompose
the calcium nitrate.
3. Place crucible in a dessicator to cool. Then weigh the crucible
and its contents.
4. Repeat the heating, cooling and weighing process until the
mass of the crucible and its contents is consistent within 0.05 g
in difference.
Loss in mass = initial mass of crucible and contents final mass of
crucible and contents after final heating
9647/02/PRELIM/12
[8]
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Amount of Ca(NO3)2 = loss in mass / 108

Mass of Ca(NO3)2 = amount of Ca(NO3)2 164
% purity = mass of Ca(NO3)2 / initial mass of solid 100%
(d)
State and explain clearly one precaution you would take to improve
the accuracy of your results.
Sample should be stored in dessicator while cooling to prevent
absorption of water from the air.
(e)
[1]
Identify one potential safety hazard in this experiment and state how
you would minimise the risk.
NO2 is toxic. Perform experiment in fume cupboard.
OR
CaO causes skin / eye irritation / irritation if inhaled. Wear gloves,
mask etc.
[1]
[Total: 12]
2
Titanium(IV) oxide TiO2 is the naturally occurring oxide of titanium. It is the

main ingredient in sunscreen lotion due to its high refractive index and
strong UV-light absorbing capability.
(a)
Using the following information as well as relevant data from the Data
Booklet, draw a Born-Haber cycle for the formation of TiO2(s) and
calculate the lattice energy of TiO2(s).
Standard enthalpy change of formation of TiO2(s)
945 kJ mol1
Standard enthalpy change of atomisation of Ti
+471 kJ mol1
1st electron affinity of oxygen
142 kJ mol1
2nd electron affinity of oxygen
+844 kJ mol1
Ti(s)
+661 + (+1310) +
(+2720) + (+4170)
Ti4+(g)
945
TiO2(s)
+496
+471
Ti(g)
O2(g)
2O(g)
2[(142) +
(+844)]
Lattice energy
of TiO2
2O2(g)
[3]

9647/02/PRELIM/12
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By Hess Law,
945 = +471 + (+661) + (+1310) + (+2720) + (+4170) + (+496) +
2[(142) + (+844)] + LE(TiO2)
LE(TiO2) = 12177 kJ mol1
= 1.22 104 kJ mol1
(b)
Crude titanium(IV) oxide is purified via the Chloride process. In this

two-step process, the crude ore (containing at least 70% titanium(IV)
oxide) is first reacted with carbon and chlorine, represented by the
equation shown below.
TiO2(s) + C(s) + 2Cl2(g) TiCl4(l) + CO2(g)
Standard enthalpy change of formation of TiCl4(l)
804 kJ mol1
Standard enthalpy change of formation of CO2(g)
394 kJ mol1
Standard molar entropy of TiO2(s)
+49.9 J mol1 K1
Standard molar entropy of C(s)
+5.7 J mol1 K1
Standard molar entropy of Cl2(g)
+223 J mol1 K1
Standard molar entropy of TiCl4(l)
+252 J mol1 K1
Standard molar entropy of CO2(g)
+214 J mol1 K1
Using the above information, as well as relevant data from (a) and the
Data Booklet, calculate, for the first step of the Chloride process,
(i)
the standard enthalpy change of reaction,

Standard enthalpy change of reaction
= [(804) + (394)] [(945) + 0 + 2(0)]
= 253 kJ mol1
(ii)
the standard entropy change of reaction.

Note: DS, = SS,(products) SS,(reactants)
Standard entropy change of reaction
= [(+252) + (+214)] [(+49.9) + (+5.7) + 2(+223)]
= 35.6 J mol1 K1

[2]
9647/02/PRELIM/12
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(c)
Using your answers in (b), determine if the first step of the Chloride
process is spontaneous at 2000 K.
DG = H TDS
DG = (253) (2000)(35.6/1000)
DG = 182 kJ mol1 < 0
Hence, the reaction is spontaneous at 2000 K.
(d)
[1]
The second step of the Chloride process involves the titanium(IV)

chloride being distilled off and oxidised in a pure oxygen flame to give
pure titanium(IV) oxide and chlorine gas.
Write an equation for the reaction in the second step.
TiCl4 + O2 TiO2 + 2Cl2
[1]
[Total: 7]
Neidong Forest Recreation National Park, located in the Wulai District in

Taipei, has the highest concentration of anions in Taiwan due to the
numerous waterfalls and lush forestation in the park. Anions are said to help
boost the immune system, among other health benefits.
(a)
Bromide ions are thought to be one of the anions present in

abundance. The concentration of bromide ions in the river waters can
be used as an estimate of the concentration of the ions in the park.
A 25.0 cm3 sample of river water was collected and 50.0 cm3 of
1.00 mol dm3 Pb(NO3)2 was added. The precipitate formed was
filtered off and 3.00 g of precipitate was collected. The filtrate can be
regarded as a saturated solution of PbBr2.
(i)
Calculate the concentration of Pb2+ ions in the filtrate.

Amount of PbBr2 collected =
3.00
207 + 2(79.9)
= 8.18 103 mol
50
1.00 - ( 8.18 10 -3 )
Amount of Pb2+ in filtrate =
1000
= 0.0418 mol

9647/02/PRELIM/12
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[Pb2+] in filtrate =
0.0418
0.075
= 0.557 mol dm3

(ii)
Write an expression for the solubility product, Ksp, of PbBr2.

Ksp = [Pb2+][Br ]2
(iii)
The numerical value for the Ksp of PbBr2 is 3.9 105. Determine
the concentration of bromide ions in the sample of river water.
[Br ] in filtrate =
3.9 10 -5
0.557
= 8.37 103 mol dm3

Total amount of Br in sample of river water
= Amount of Br in filtrate + Amount of Br in ppt
= (8.37 103
75
) + (8.18 103 2)
1000
= 0.0170 mol
[Br ] in sample of river water = 0.0170
25
1000
= 0.680 mol dm3

(b)
[5]
Another anion, W, found in Neidong National Park can be formed

when the oxide of a Period 3 element reacts with an alkali. When
dilute nitric acid is added to a solution containing W, a colourless and
pungent gas that turns acidified potassium dichromate(VI) from
orange to green is evolved.
(i)
Suggest an identity for anion W.

SO32/HSO3
(ii)
Write an equation for the formation of W from the reaction of a

Period 3 oxide with an alkali.
SO2 + 2OH SO32 + H2O
OR
SO2 + OH HSO3
[2]
[Total: 7]

9647/02/PRELIM/12
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The leadacid accumulator is a storage battery used in cars because it can

be recharged. It consists of a series of cells containing lead plate anodes,
lead dioxide plate cathodes and an electrolyte of 6 mol dm3 sulfuric acid.
When it is operating, the reactions that occur at the electrodes are
Pb2+(aq) + 2e = Pb(s)
E, = 0.13 V
PbO2(s) + 4H+(aq) + 2e = Pb2+(aq) + 2H2O(l)
E, = +1.47 V
(a)
Write the overall equation for the reaction during discharge and
calculate the voltage delivered by the battery.
Pb(s) + PbO2(s) + 4H+(aq) 2Pb2+(aq) + 2H2O(l)
[2]
E,cell = 1.47 (0.13) = +1.60V

(b)
However, it is noted that the actual voltage is 2.0 V as compared to the

value that you have calculated in (a). Explain why the actual voltage
differs from the calculated voltage.
During discharging, Pb2+(aq) is removed as it precipitates out as
PbSO4(s).
This
cause
the
equilibrium
position
of
PbO2 + 4H+ + 2e- = Pb2+ + 2H2O to shift to the right, hence,
E(PbO2/Pb2+) is more positive than +1.47 V.
On the other hand, as PbSO4 is precipitated out, the equilibrium
position of Pb2+ + 2e- = Pb shifts to the left, resulting in E(Pb2+/Pb) to
be more negative than -0.13 V.
Hence actual voltage is 2.0V
[2]
(c)
Explain why the battery is rechargeable.

When an external current is applied, it will recharge the battery by
driving the cell reaction in the reverse direction.
(d)
[1]
State one disadvantage of the lead-acid accumulator battery.

1) Rather large and heavy due to the lead, hence produces low power
for its mass.
2) PbSO4 deposits on the electrodes in a finely divided form during
discharge. If a discharged battery stands for a long time, the small
grains of PbSO4 may grow into large crystals that fall from the
electrodes. If too much PbSO4 is lost, the cell cannot be recharged
and results in a loss of capacity.
3) Lead is toxic.
[1]
[Total: 6]

9647/02/PRELIM/12
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This question is about the chemistry of halogens and the halide ions.
(a)
Aqueous bromine is decolourised when added to aqueous sodium

thiosulfate. When excess of aqueous barium nitrate is added to the
resulting solution, a white precipitate is observed. This precipitate is
filtered off, leaving a colourless filtrate.
(i)
Write a balanced ionic equation for the reaction between

bromine and sodium thiosulfate.
4Br2 + S2O32 + 5H2O 8Br + 2SO42 + 10H+
(ii)
To the colourless filtrate in (i), aqueous silver nitrate is added,

followed by concentrated ammonia solution.
Describe what is observed and write balanced equations for the
reaction that occur.
Cream ppt formed when AgNO3 is added.
Upon adding concentrated NH3, cream ppt is soluble in
concentrated NH3
Ag+(aq) + Br(aq) AgBr(s)
AgBr(s) + 2NH3(aq) [Ag(NH3)2]+(aq) + Br(aq)
(b)
In a separate experiment, aqueous bromine is added to aqueous

potassium iodide. To the resulting mixture, an equal volume of an
organic solvent is added.
What will be the colour of the organic layer? Write equations for any
reactions that occur.
Colour: Purple
[6]
Equation: Br2(aq) + 2KI(aq) 2KBr(aq) + I2(aq)

(c)
Iodide ions react with peroxodisulfate ions in the presence of Fe3+

catalyst. The overall equation for the reaction is shown below.
2I -(aq) + S2O82-(aq) I2(aq) + 2SO42-(aq)
(i)
Fe3+ ions are added to lower the high activation energy so that
the reaction can proceed at a higher rate. Explain why the
activation energy is high for the reaction between the iodide and
peroxodisulfate ions if no Fe3+ ions are added.
Energy is required to overcome the repulsion between two
reactant anions before the ions can react.
(ii)
With reference to the Data Booklet, suggest a mechanism for

9647/02/PRELIM/12
[4]
[Turn over
this reaction in the presence of Fe3+.

S2O82(aq) + 2e- = SO42(aq)
E, = +2.01 V
Fe3+(aq) + e- = Fe2+(aq)
E, = +0.77 V
I2(aq) + 2e- = 2I(aq)
E, = +0.54 V
Step 1: 2Fe3+(aq) + 2I -(aq) 2Fe2+(aq) + I2(aq)

E,cell = +0.77 - (+0.54) = + 0.23 V > 0 V
Reaction in step 1 is energetically feasible.
Step 2: 2 Fe2+(aq) + S2O82-(aq) 2Fe3+(aq) + 2SO42-(aq)
E,cell = +2.01 - (+0.77) = + 1.24 V > 0 V
Reaction in step 2 is energetically feasible.
[Total: 10]
Chromium is a hard grey metal which is widely used in the manufacture of

stainless steel due to its good corrosion-resistant properties.
Calcium is a fairly soft, silvery grey metal which tarnishes quickly in air.
(a)
The melting point of calcium is 843 C while chromium melts at a

much higher temperature of 1907 C.
Explain this difference in terms of the type and strength of bonding in
each metal.
Both elements have metallic bonding. In Cr, both the 4s and 3d
electrons can be contributed to form mobile charge cloud as they are
very close in energy. The resulting chromium ion has a higher positive
charge and a smaller ionic radius. This leads to stronger metallic
bonds in Cr as compared to Ca, which only contributes 2 valence
electrons per Ca atom to form Ca2+.
[3]
(b)
Write the electronic

chromium(III) ions.
configuration
of
chromium
atoms
and
Cr: 1s2 2s2 2p6 3s2 3p6 3d5 4s1

Cr3+: 1s2 2s2 2p6 3s2 3p6 3d3
(c)
[2]
When aqueous sodium hydroxide was added to aqueous

chromium(III) nitrate, a blue-green precipitate was observed. Upon
addition of excess sodium hydroxide, the precipitate dissolved to give
a dark green complex.

9647/02/PRELIM/12
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10
When aqueous sodium carbonate was added

chromium(III) nitrate, effervescence was observed.
(i)
to
aqueous
State the formula of the blue-green precipitate.

Cr(OH)3
(ii)
Suggest a reason why effervescence was observed when

aqueous sodium carbonate was added to aqueous
chromium(III) nitrate.
Aqueous chromium(III) solutions are acidic (and an acidcarbonate reaction occurred forming carbon dioxide).
(iii)
Given that the formula of the soluble dark green complex is

Na3CrO6H6, state the formula of the complex ion formed.
[Cr(OH)6]3
(iv)
Draw the structure of the complex ion.

3-
OH
HO
OH
Cr
HO
OH
OH
[4]
[Total: 9]
Hydrocarbons are commonly used as combustible fuel sources as well as

feed materials in the petrochemical industry.
(a)
Describe a simple chemical test to distinguish between but-1-ene and

but-2-ene. State clearly what would be observed with each compound.
Heat with acidified KMnO4 and test the gas evolved with limewater.
But-1-ene would (turn purple KMnO4 colourless and) produce a gas
that forms a white ppt with limewater, while but-2-ene (would turn
purple KMnO4 colourless but) would not produce a gas.
(b)
[2]
But-2-ene is able to exist as 2 isomers.

(i)
State the type of isomerism exhibited by but-2-ene.

9647/02/PRELIM/12
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11
Geometric(al) isomerism / cis-trans isomerism
(ii)
Draw the displayed structural formulae for the 2 isomers of

but-2-ene.
H
H
H
C
H
H
H
C
C
C
C
H
H H
H
C
C
C
H
H H
H
H
H
[3]
(c)
Benzene is an aromatic hydrocarbon present in many compounds.

A reaction scheme involving benzene derivatives is given below. Draw
the structures of A to D and give the reagents and conditions for steps
I to IV.

9647/02/PRELIM/12
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12
A:
B:
O Na+
CH2CH2OH
C:
D:
O Na+
CH2CH2COO Na+
Step I: NaOH(aq)/KOH(aq), heat under reflux

Step II: acidified K2Cr2O7(aq), heat and distil
Step III: alcoholic NaOH/KOH, heat under reflux
Step IV: I2, NaOH(aq), warm
[8]

9647/02/PRELIM/12
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13
[Total: 13]
Students often complain of headaches when faced with a tough problem

they cannot solve. A very common over-the-counter drug to combat
headaches is paracetamol. The synthesis of paracetamol is shown below:
Paracetamol
(a)
Draw the structure of compound X.
[1]
(b)
Step I is actually a two-stage process. State the reagents and

conditions for the two stages.
Stage 1: ........
Sn, conc. HCl, heat
Stage 2: ........
NaOH(aq)
(c)
[2]
Step II involves a condensation reaction. An organic side-product, Y,

can be formed along with paracetamol.
(i)
State the reagent for this step.

CH3COCl
(ii)
Suggest a structure for the side-product, Y.

9647/02/PRELIM/12
[2]
[Turn over
14
OR
(d)
Suggest the structues of all the organic products formed when

paracetamol reacts with
(i)
NaOH(aq) at room temperature
(ii)
NaOH(aq) with heating
and CH3COONa+
[3]
[Total: 8]

9647/02/PRELIM/12
[Turn over

CANDIDATE
NAME
CLASS
CENTRE
NUMBER
INDEX
NUMBER
H2 CHEMISTRY
9647/03
18 September 2012
2 hours

Answer Paper
Cover Page
Data Booklet

Write your name, class, centre number and index number on all the work you hand in.
Write in dark blue or black pen on both sides of paper.
Begin each question on a fresh sheet of paper.
A Data Booklet is provided. Do not write anything on it.
At the end of the examination, fasten all your work securely together, with the cover page on top.
_______________________________________________________________________________

9647/03/PRELIM/12
[Turn over

1
(a)
One common characteristic of transition elements is the ability to form

complexes. Transition elements react with carbon monoxide to form a
class of complexes known as metal carbonyls. One aspect of metal
carbonyls that is unusual for metallic compounds is that they are often
volatile.
Nickel carbonyl was first synthesised in 1890 by Ludwig Mond by
passing carbon monoxide over nickel metal. Nickel carbonyl has a
boiling point of 43 C and is extremely poisonous.
(i) Draw the dot-and-cross diagram of carbon monoxide.
(ii) Explain in terms of structure and bonding why nickel carbonyl
has a low boiling point.
(iii) A 2.00 g sample of nickel carbonyl was vaporised and found to
occupy a volume of 314 cm3 at 50 C and 1 atmosphere
pressure.
Determine the Mr of nickel carbonyl.
(iv) Nickel carbonyl has the general formula Ni(CO)x. Using the
answer in (iii), determine the coordination number of nickel in
nickel carbonyl and suggest the shape of the complex.
(b)
[7]
Transition metal compounds are often coloured.

(i) Explain why transition metal compounds are often coloured.
(ii) When a solution of dilute sulfuric acid was electrolysed using
copper electrodes, a blue solution was obtained. On heating this
solution to dryness, an anhydrous white solid was eventually
obtained.
When concentrated hydrochloric acid was electrolysed using
copper electrodes in a separate experiment, a yellow solution
was obtained. On adding water, the colour of the solution turned
from yellow to green and eventually blue.
Explain these observations. State clearly the formula of any
coloured species.

9647/03/PRELIM/12
[9]
[Turn over
(c)
Menthol, menthone and limonene are members of a class of

compounds called isoprenoids which are derived from isoprene,
CH2=C(CH3)CH=CH2.
Limonene and menthone are intermediates in the biosynthesis of
menthol. The many reactions in the biosynthesis of menthol are
catalysed by different enzymes. In the laboratory, transition metal
catalysts can be used to catalyse many of these reactions instead of
enzymes.
limonene
menthone
OH
menthol
Describe how you would distinguish these three compounds by means

of simple chemical tests.
[4]
[Total: 20]

9647/03/PRELIM/12
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(a)
Hydrocarbons like alkanes are commonly used for fuels. Increasingly,

biofuels are gaining increased public and scientific attention, driven by
concerns over oil prices and greenhouse gas emission. Biofuels, like
methanol and butan-1-ol, which can be produced by the fermentation
of biomass, are increasingly being used for fuels over hydrocarbons.
(i) Using common oxidation numbers for H and O, calculate the
oxidation number of carbon in methanol, CH3OH.
(ii) Using only the elements C, H and O, suggest the structural
formulae of two compounds, each containing a single carbon
atom with an oxidation number of zero and +2 respectively.
In an experiment to determine the standard enthalpy change of
combustion of butan-1-ol, DHc,, a quantity of the fuel was burned
underneath a 200 g copper can containing 515 g of water. It was found
that the temperature of water rose from 23 C to 58 C after 2.30 g of
butan-1-ol has been burned completely.
(iii) Write an equation for the complete combustion of butan-1-ol.
(iv) Using the experimental results and relevant data from the Data
Booklet, calculate the apparent DHc, of butan-1-ol. You can
ignore the heat capacity of the copper can.
(v) The true value of DHc, of butan-1-ol is -2670 kJ mol-1. Compare
this value to the one you have calculated in (iv) and suggest a
reason for the discrepancy.
(b)
[7]
The following table compares the pKa values of two dicarboxylic acids.
HO2C-(CH2)n-CO2H
pK 1
HO2C-(CH2)n-CO2-
pK 2
O2C-(CH2)n-CO2
acid
formula
pK1
pK2
propanedioic acid
HO2CCH2CO2H
2.85
5.70
butanedioic acid
HO2CCH2CH2CO2H
4.20
5.60
(i) Suggest a reason why the pK1 value of propanedioic acid is so

much less than the pK1 of butanedioic acid.
(ii) Suggest a reason why the pK2 value of propanedioic acid is
higher than its pK1 value.
(iii) Calculate the pH of 0.25 mol dm-3 of butanedioic acid (ignoring
the effect of pK2 on the pH).

9647/03/PRELIM/12
[Turn over
(iv) Sketch the pH-volume added curve you would expect to obtain
when 60 cm3 of 0.25 mol dm-3 NaOH is added to 20 cm3 of
0.25 mol dm-3 butanedioic acid. On your curve, include all
relevant information and highlight any buffer regions.
(c)
[7]
When chlorine gas is passed over heated aluminium in a hard glass

tube, a vapour is produced which condenses to a yellow-white solid. At
low temperatures, the vapour has the empirical formula AlCl3 and an
Mr of 267.
(i) Suggest the molecular formula of the vapour, and draw a
dot-and-cross diagram to describe the bonding.
The yellow-white solid reacts with water in two different ways. When a
few drops of water are added to the solid, steamy white fumes are
evolved and a white solid remains, which is insoluble in water. When a
large volume of water is added to the solid, a clear, weakly acidic
solution is produced.
(ii) Write equations, including state symbols, for these two reactions
and explain the observations.
[6]
[Total: 20]

9647/03/PRELIM/12
[Turn over
Alcohols and ketones are two classes of organic compounds with great
importance in both industrial processes and in biological systems.
(a)
The iodination of propanone under acidic conditions is shown by the

following equation:
CH3COCH3(aq) + I2(aq) CH3COCH2I(aq) + H+(aq) + I (aq)
The rate of the reaction was studied via a colorimetric method, in
which the colour intensity of iodine was measured at regular intervals.
Three sets of separate experiments were performed in which the initial
concentration of iodine, propanone and acid was varied in turn, with
the other two being kept constant. The results are shown in Graphs 1
and 2 below:
[I2]/ mol dm3
Graph 1
[CH3COCH3] = 0.10 mol dm3

time/ min
[I2]/ mol dm3
Graph 2
[H+] = 0.20 mol dm3

[H+] = 0.40 mol dm3
[H+] = 0.60 mol dm3
time/ min

9647/03/PRELIM/12
[Turn over
(i) Suggest another method, other than a colorimetric method, that

can be used to investigate the rate of the reaction. Include the
variables to be measured.
(ii) Using the graphs above, deduce the orders of reaction with
respect to propanone, iodine and H+.
(iii) Hence, write the rate equation for this reaction.
A mechanism for the reaction is suggested as below:
CH3COCH3
H+ as catalyst
stage 1
CH2 C(OH)CH3
I2
stage 2
CH3COCH2I
(iv) From your answers from (iii), what can be deduced about the
relative rate of the two stages given in the mechanism above?
(b)
[8]
Ketone bodies are three water-soluble organic compounds that are

produced as by-products when fatty acids are broken down for energy
in the liver. The three ketone bodies found in humans are propanone,
3-oxobutanoic acid and 3-hydroxybutanoic acid.
O
OH
OH
OH
3-oxobutanoic acid
3-hydroxybutanoic acid
(i) 3-oxobutanoic acid can be converted to 3-hydroxybutanoic acid

in a chemistry laboratory. State the reagents required for this
conversion and the type of reaction undergone.
(ii) Under suitable conditions, 3-hydroxybutanoic acid can be
converted to 3-bromobutanoic acid.
Compare the acid strength of 3-bromobutanoic acid and
butanoic acid. Explain your answer.
(iii) The accumulation of ketone bodies in blood can cause an
alarming decrease in the pH of blood. Suggest how this is
prevented in the human body.

9647/03/PRELIM/12
[5]
[Turn over
(c)
Compound P is a drug used to treat narcolepsy, a condition where a

person falls asleep uncontrollably. P has a molecular formula of
C4H8O3 and is structurally related to one of the ketone bodies. P can
be oxidised to give compound Q, which then reacts with alkaline
copper(II) ions to give a brick-red precipitate and the salt of an acid, R.
1 mole of P and R will each react with sodium metal to produce 1 mole
of hydrogen gas.
When P is warmed with a few drops of concentrated sulfuric acid, a
neutral compound S, with the molecular formula C4H6O2, can be
isolated.
Deduce the structures of P, Q, R and S. Explain your reasoning.
[7]
[Total: 20]

9647/03/PRELIM/12
[Turn over
Organic compounds containing halogens are widely used in industry and

society as flame retardants, refrigerants, propellants, solvents and
pharmaceuticals.
(a)
Methylbenzene can be converted to 1-chloro-2-methylbenzene.

(i) State the reagents and conditions required for the conversion.
(ii) State the type of reaction and describe the mechanism for the
conversion of methylbenzene to 1-chloro-2-methylbenzene.
(iii) Calculate the percentage yield of the conversion given that
92.4 g of 1-chloro-2-methylbenzene was obtained from 118 g of
methylbenzene.
(b)
(c)
(iv) Another mono-chlorinated compound was also formed in

significant amounts. Suggest the structure of this other
compound.
[7]
Suggest a two-step synthesis to convert 1-chloropropane to butanoic

acid, giving the structure of the intermediate.
[3]
Compound A is an optically active compound with molecular formula

C10H13Br. When heated with aqueous sodium hydroxide, compound A
gives compound B which forms a yellow precipitate when warmed with
alkaline iodine.
When compound A is heated under reflux with sodium hydroxide
dissolved in ethanol, it forms compound C which has molecular
formula C10H12. When cold, alkaline potassium manganate(VII) is
added to compound C, compound D with molecular formula, C10H14O2,
is formed. On the other hand, when compound C is heated with
acidified potassium manganate(VII), the products are compound E
with molecular formula, C8H6O4, and ethanoic acid.
Deduce the structures of compounds A, B, C, D and E. Explain the
chemistry of the reactions involved.
[10]
[Total: 20]

9647/03/PRELIM/12
[Turn over
10
Sulfur is a chemical element with the symbol S and an atomic number of 16.
It is an abundant, multivalent non-metal. It can be found in amino acids and
as a precursor to other chemicals such as H2SO4. H2SO4 is a common
mineral acid with many uses. It can be used as an electrolyte and an
oxidising agent.
(a)
Anodising is a process used to increase the thickness of the natural

oxide, on the surface of metal parts. Aluminium is a common metal
which can be anodised as aluminium is a reactive metal and is readily
oxidised by oxygen in air. This forms a layer of aluminium oxide
(Al2O3), making it resistant to corrosion.
(i) Using H2SO4(aq) as the electrolyte and an inert electrode, draw
an electrolysis set-up to show how an iPod Nano, which is
made of Al, can be anodised.
(ii) Write chemical equations to show the reactions at the anode
and cathode during anodisation.
(iii) The iPod Nano has a surface area of 29.21 cm2 which can be
anodised. How long will it take to form a 0.2 mm protective layer
of Al2O3 on the iPod Nano if a current of 2.0 A is passed
through the set-up?
(density of Al2O3 is 3.95 g cm-3)
(b)
[10]
Heating solid halides with concentrated H2SO4 is one of the ways to

obtain hydrogen halides.
However, the halides have different
reactivity with concentrated H2SO4.
(i) Write an equation to show the reaction of NaCl with
concentrated H2SO4.
(ii) With reference to the Data Booklet, explain why chlorine cannot
be isolated by the action of concentrated sulfuric acid with
sodium chloride.

9647/03/PRELIM/12
[3]
[Turn over
11
(c)
Sulfur is an essential element for all life, and is widely used in

biochemical processes. Sulfur is a component of some amino acids
such as cysteine.
(i) Using the cysteine residue, as shown in the diagram below,
construct an equation to show the formation of the disulfide
bridge between two cysteine residues.
O
N
CH
CH2SH
(ii) Denaturation of proteins involves the disruption and possible

destruction of the tertiary structure of the protein. Addition of
heavy metal ions can cause denaturation through the disruption
of R group interactions.
State and explain, in chemical terms, how R group interactions
are disrupted by the addition of heavy metal ions.
(d)
[4]
Group II elements are shiny, silvery-white reactive metals. Down the

group, reactivity of the elements changes.
(i) With reference to the Data Booklet, state and explain the trend
in reactivity, in terms of reducing power, from Mg to Ba.
(ii) State the differences in reactivity of Mg and Ba with water.
[3]
[Total: 20]

9647/03/PRELIM/12
[Turn over
12
BLANK PAGE

9647/03/PRELIM/12
[Turn over
H2 Chemistry (9647) Prelims 2012 Paper 3

1
(a)
(i)
C O
(ii) Nickel carbonyl has a simple covalent structure with weak

intermolecular forces which require little energy to overcome.
(iii)
(iv)
2.00 8.31 (273 + 50)

1.01 105 314 10 -6
= 169
Mr =
58.7 + (12.0 + 16.0)x = 169

x = 3.93
= 4 (nearest whole number)
Coordination number is 4
Tetrahedral (accept square planar)
(b)
[7]
(i) In transition metal compounds, the presence of ligands causes

the 3d orbitals to split into 2 sets of non-degenerate orbitals. The
difference in energies (DE) between these 2 sets of 3d orbitals is
small and radiation from the visible region of the electromagnetic
spectrum is absorbed when an electron moves from a lower
energy d-orbital to another unfilled/partially-filled d orbital of
higher energy. The colour observed correspond to the
complement of the absorbed colours. Hence, transition metal
compounds are often coloured.
[3]
(ii) Blue solution [Cu(H2O)6]2+

Yellow solution CuCl42Blue solution was formed from the oxidation of Cu (to Cu2+(aq)).
Blue solution formed a white solid on heating to due to loss of
water ligands. / Splitting of 3d orbitals into 2 sets of different
energy no longer occurs.
CuCl42- + 6H2O = [Cu(H2O)6]2+ + 4Cl On addition of water, position of equilibrium of CuCl42- + 6H2O =
[Cu(H2O)6]2+ + 4Cl - shifts to the right, forming blue [Cu(H2O)6]2+
[6]
(c)
Limonene:
aqueous bromine
cold alkaline KMnO4
Menthone:
2,4-DNPH
Menthol:
PCl5 / SOCl2
Acidified potassium dichromate, heat
Acidified KMnO4, heat; followed by test with limewater
(a)
[4]
(i) Oxidation number = 0 (-2) 4(+1)

= -2
(ii) Zero
O
HO
C
H
OH
C
OR
OR
C%O
+2
O
C
HO
(iii) CH3CH2CH2CH2OH(l) + 6O2(g) 4CO2(g) + 5H2O(l)

(iv) Temperature increase = 58 - 23
= 35 C
Heat evolved = 35 515 4.18
= 7.53 104 J
Amount of butan-1-ol = 2.30 (4 12.0 + 10 1.0 + 16.0)
= 3.11 10-2 mol
7.53 10 4
DHc, = -
-2
3.11 10
= -2.42 106 J mol-1

2
= -2.42 103 kJ mol-1

(v) The calculated value is less negative (less exothermic) than the
true value as there is heat loss to the surroundings and copper
can calorimeter.
(b)
(i) Propanedioic acid is a stronger acid than butanedioic acid due to

the stabilisation of the anion by hydrogen bonding with the
unionised CO2H group.
O
O
H
CO2H +
HO2C
H2O
H2C
+ H3O+
(ii) Removal of H+ from an anion (A) that already carries a negative

charge is electrostatically unfavourable.
OR
The stabilising hydrogen bonding would be destroyed by the
ionisation of the second CO2H group.
(iii) Let the acid be HA and the concentration of H+(aq) be x.
Ka =
[H+ ][A - ]
[HA]
10-4.20 =
x2
0.25 - x
Since x is small,
10
-4.20
x2
=
0.25
x = 3.97 10-3 mol dm-3

pH = -lg (3.97 10-3)
= 2.40
[7]
(iv)
pH
Buffer Region
pH
=pK2
=5.60
pH
=pK1
=4.20
Buffer Region
2.40
0
(c)
10
20
30
40
VNaOH
(i) Al2Cl6
Cl
Cl Al Cl
Cl Al Cl
Cl
(ii) AlCl3(s) + 3H2O(l) Al(OH)3(s) + 3HCl(g)
OR 2AlCl3(s) + 3H2O(l) Al2O3(s) + 6HCl(g)
(When a few drops of water is added, AlCl3 undergoes hydrolysis
to form white fumes of HCl(g) and white insoluble solid of
Al(OH)3.)
AlCl3(s) + 6H2O(l) [Al(H2O)6]3+(aq) + 3Cl -(aq)
[Al(H2O)6]3+(aq) + H2O(l) = [Al(OH)(H2O)5]2+(aq) + H3O+(aq)
AlCl3 undergoes dissolves readily in water to form
hydrated/aqueous Al3+ / Al3+(aq) ions which undergoes hydrolysis
due to the high charge density of the polarising cation to give a
weakly acidic solution.
(a)
(i)
Determine the [I2] at regular time intervals by quenching the

sample of the solution and titrating with aqueous sodium
thiosulfate.
OR Measure the electrical conductivity of solution at different
time intervals.
OR Measure the pH of the solution at regular time intervals
using a pH meter.
(ii)
The graph of [I2] against time is a straight line, indicating that

rate is constant despite decreasing [I2]. Hence, the reaction is
zero order with respect to iodine.
From graph 1, when [CH3COCH3] is increased from
0.10 mol dm3 to 0.25 mol dm3, gradient/rate of reaction is
increased from 1.0 104 mol dm3 min1 to 2.5 104 mol dm3
min1. Gradient/rate is 2.5 times the original gradient/rate when
[CH3COCH3} is 2.5 times the original concentration. Hence, the
reaction is first order with respect to propanone.
From graph 2, when [H+] is doubled from 0.20 mol dm3 to
0.40 mol dm3, gradient/rate of reaction is also doubled from
1.67 104 mol dm3 min1 to 3.33 104 mol dm3 min1.
Hence, the reaction is first order with respect to H+.
(iii) Rate = k[CH3COCH3][H+]

(iv) Stage 1 is relatively slower than stage 2. / Stage 1 is the slow
step. / Stage 1 is the rate determining step.
Rate equation suggests that the slow step/ rate determining step
involves only one molecule of propanone and a H+ ion.
(b)
[8]
(i) NaBH4 (in aqueous ethanol) OR H2, Ni, (heat)

Reduction
(ii) The electron-withdrawing bromine atom in 3-bromobutanoate
ion disperses the negative charge on the COO- group,
making the 3-bromobutanoate ion more stable than the
butanoate ion. Hence, 3-bromobutanoic acid is a stronger
acid.
(iii)
(c)
An increase in concentration of 3-oxobutanoic acid and

3-hydroxybutanoic acid is buffered by the CO2/HCO3- buffer
system present in blood. OR
Excess ketone bodies are excreted from the human body in
urine (since they are water-soluble).
[5]
P undergoes oxidation to give Q, which is further oxidised by

Fehlings solution/gives positive Fehlings tes to form the salt of R
[7]
Q is an aldehyde and P is a primary alcohol.

Both P and R undergoes acid-metal reaction with sodium to give 1
mole of hydrogen gas
Both P and R contain 2 OH groups.
P undergoes (intramolecular) condensation when warmed with
concentrated sulfuric acid to produce S S is a (cyclic) ester.
Structures:
P:
Q:
O
O
H
HO
OH
OH
O
S:
R:
O
HO
OH
(a)
(i) Cl2, AlCl3

OR
Cl2, FeCl3
OR
Cl2, Fe
(ii) Electrophilic substitution

Cl2 + AlCl3 Cl+ + AlCl4-
CH3
CH3
CH3
Cl+
Cl
AlCl4-
Cl
H
+
AlCl3
HCl
(iii) Amount of methylbenzene in 118 g

= 118 (7 12.0 + 8 1.0)
= 1.28 mol
Amount of 1-chloro-2-methylbenzene produced
= 92.4 (7 12.0 + 7 1.0 + 35.5)
= 0.730 mol
Percentage yield =
0.730
100
1.28
= 57.0%
(iv)
CH3
Cl
(b)
CH3CH2CH2Cl
[8]
KCN(alc)
heat under reflux
CH3CH2CH2CN
dilute H2SO4(aq)
heat under reflux
CH3CH2CH2COOH
[3]
(c)
Compound A is optically active

compound A contains chiral carbon
C:H ratio in Compound A is close to 1:1
compound A contains benzene ring
Compound A undergoes nucleophilic substitution with NaOH(aq) to
form compound B
compound B is an alcohol
compound A is an alkyl bromide/alkyl halide
[10]
7
Positive iodoform test with Compound B

compound B contains CH(OH)CH3
Compound A undergoes elimination to form compound C
compound A is an alkyl bromide/alkyl halide
compound C contains C$C bond / alkene functional group
Compound C undergoes mild oxidation to form compound D
compound D is a diol
Compound C undergoes vigorous oxidation to form compound E and
ethanoic acid
compound C is not a terminal alkene
Br
OH
H3C
H3C
OH
H3C
OH
C
H3C
D
COOH
HOOC
E
(a)
(i)
Pt/graphite (cathode)
Ipod Nano
dilute H2SO4(aq)
(ii)
Reactions at anode: 2H2O(l) O2(g) + 4H+(aq) + 4e2Al(s) + 3/2O2(g) Al2O3(s)

Reaction at cathode: 2H+(aq) + 2e- H2(g)
(iii) Volume of Al2O3 layer = 29.21 0.02

= 0.584 cm3
Mass of Al2O3 = 3.95 0.584
= 2.31 g
Amount of Al2O3 =
2.31
2 27.0 + 3 16.0
= 0.0226 mol
Amount of O2 = 0.0226 3/2
= 0.0339 mol
Amount of electrons passed through the cathode = 0.0339 4
= 0.136 mol
Q = 0.136 96500
= 13100 C
Time needed =13100 2.0
= 6550 s
(b)
(i)
[10]
NaCl(s) + H2SO4(l) NaHSO4(s) + HCl(g)

9
(State symbols not required)

(ii)
2Cl - + SO42- + 4H+ Cl2 + SO2 + 2H2O

E,cell = +0.17 - (+1.36)
= -1.19 V
As E,cell < 0 V, reaction is energetically non-feasible.
(c)
(i)
O
N
CH
CH2
CH
CH2
SH
+ 2[H]
SH
CH2
CH
CH2
CH
C
O
O
(ii)
Heavy metal ions form ionic interactions with -COO-, which

brings about the formation of insoluble protein salts (i.e.
precipitation of protein). This disrupts the ionic interactions in the
tertiary structure, and hence leads to denaturation.
Heavy metal ions have a high affinity for sulfur and will bind
tightly to the -SH group. This disrupts the disulfide bridges in the
tertiary structure, and hence leads to denaturation.
(d)
(i)
Electrode reaction
E,(M2+/M)/ V
Mg2+ + 2e- = Mg
2.38
Ca2+ + 2e- = Ca
2.87
Ba2+ + 2e- = Ba
2.90
Down the group, E,(M2+/M) becomes more negative. Therefore,

the reducing power increases from Mg to Ba.
Element
1st IE/ kJ mol-1
2nd IE/ kJ mol-1
10
[4]
Mg
736
1450
Ca
590
1150
Sr
548
1060
Ba
502
966
OR Quote 1st and 2nd IE values

This is because the atomic radius increases from Mg to Ba and
as a result, ionisation energy decreases. Thus, reducing power
increases from Mg to Ba.
(ii)
Mg reacts with cold water slowly/Mg reacts with steam readily

while Ba reacts with cold water vigorously.
11
[3]
ST ANDREWS JUNIOR COLLEGE
JC2 Preliminary Examinations

Chemistry
Higher 2
9647/01
19 September 2012
1 hour
Additional Materials: Multiple Choice Answer Sheet, Data Booklet

Write in soft pencil. Do not use staples, paper clips, highlighters, glue or correction fluid.
There are 40 questions on this paper. Answer all questions. For each question there are
four possible answers A, B, C and D. Chose the one you consider correct and record your
choice in soft pencil on the separate Answer Sheet.
Each correct answer will score one mark. A mark will not be deducted for a wrong
answer. Any rough working should be done in this booklet.
This document consists of 22 printed pages including this page.

[Turn Over
Section A
1.
Group I and Group II ionic hydrides react with water.

H- + H2O OH- + H2
In an experiment, 1 g of a sample of an ionic hydride is dissolved in excess H2O. The

resulting solution required 24.00 cm3 of a 2.0 mol dm-3 HCl solution for complete
neutralisation.
What is the formula of the hydride?
2.
LiH
NaH
MgH2
CaH2
Which species is oxidised and which species is reduced in the following reaction?
4TiCr2O4 + 8Rb2CO3 + 7O2 8Rb2CrO4 + 2Ti2O3 + 8CO2
Species oxidised
Species reduced
Chromium only
Carbonate ion only
Chromium only
Carbonate ion and oxygen
Chromium and titanium
Oxygen only
Chromium and titanium
Carbonate ion and oxygen
[Turn Over
3.
The graph below shows how pressure varies with temperature when 1 mole of helium
is heated in an enclosed volume.
p
T/ C
Similar relationship between pressure and temperature was examined for 1 mole of
gaseous XY2 which dissociates according to the following equation.
X (g) + Y2 (g) H > 0
XY2 (g)
Which graph best represents how pressure varies with temperature of the gas?
A
T/ C
T / oC
T / oC
T / oC
[Turn Over
4.
5.
Which of the following particles has a half-filled p subshell after losing two electrons?
Ga-
As2+
Se-
Te+
Which of the following isomers is likely to have the highest boiling point?
B
O
C
OH
OH
6.
In which of the following reactions is the HNH bond angle in ammonia smaller than
that in the product?
2NH3 (l) + 2Na (s)
2NaNH2 (s) + H2 (g)
NH3 (g) + HCl (g)
NH4Cl (s)
2NH3 (g)
H2NNH2 (l) + H2 (g)
2NH3 (g) + O2 (g)
2NH2OH (l)
[Turn Over
7.
When water vaporises, 51.6 kJ mol-1 of heat enthalpy is required. What is the entropy
change when 54 g of water boils at 1 atm?
8.
+ 138 J K-1
+ 415 J K-1
+ 516 J K-1
+ 1548 J K-1
Ellingham diagrams are plots of G against temperature, T. An Ellingham diagram for

two reactions involving the oxidation of S and SO2 is as shown below:
Given that, G = H - TS, which of the following correctly shows the two reactions
corresponding to reactions I and II in the above Ellingham diagram?
II
2S + 3O2 2SO3
2SO2 + O2 2SO3
2SO2 + O2 2SO3
S + O2 SO2
S + O2 SO2
2S + 3O2 2SO3
2SO2 + O2 2SO3
2S + 3O2 2SO3
[Turn Over
In the conversion of compound X into compound Z, it was found that the reaction
proceeded according to the rate equation below:
Rate = k [X]
The intermediate Y can be isolated. Which reaction profile fits these data?
Y
energy
energy
A
Y
X
D
energy
Y
energy
9.
X
Z
Z
X
Y
[Turn Over
10.
A solution of vanadium (V) ions in 1 mol dm-3 H2SO4 slowly oxidises arsenic (III) oxide
to arsenic (V) oxide, according to the following equation.
As2O3 + 4 VO2+ + 4 H+ As2O5 + 4 VO2+ + 2 H2O
To find the rate equation for the above reaction, two experiments were carried out,
starting with different concentrations of arsenic (III) oxide and the concentration of
VO2+ was monitored.
The rate equation is most likely to be
rate = k [As2O3][VO2+]
rate = k [As2O3][VO2+]2
rate = k [As2O3]2[VO2+]
rate = k [As2O3]
[Turn Over
11.
The graphs below show the variation of the percentage of gaseous products present at
equlibrium, with pressure and two temperatures, T oC and (T + z) oC.
% products at
equilibrium
(T + z) oC
T oC
Pressure
Which one of the following systems could the graphs represent?
12.
DH = - 92 kJ mol-1
N2(g) + 3H2(g)
3O2(g) + 4NH3(g)
2N2(g) + O2(g)
2N2O (g)
DH = + 82 kJ mol-1
CO2(g) + C(s)
2CO (g)
DH = + 173 kJ mol-1
2NH3(g)
2N2(g) + 6H2O(g)
DH = - 1248 kJ mol-1
Solutions E, F, G and H contain a strong monobasic acid, a weak monobasic acid HX,
a strong base and a salt of HX, but not necessarily in the same order. The
concentration and pH for each solution are shown below.
Solution
E
F
G
H
Concentration /mol dm-3

1.0
1.0
0.01
0.01
pH
4.0
9.4
12.0
2.0
Which one of the following statements is false?

A
E contains a weak acid while H contains a strong acid.
Mixing 10 cm3 of E and 50 cm3 of G produces a buffer solution.
Mixing 10 cm3 of E and 50 cm3 of H produces a buffer solution.
Mixing 10 cm3 of F and 1 dm3 of H produces an acidic solution.
[Turn Over
13.
At a temperature T K, 0.60 mol dm-3 of CO and 0.30 mol dm-3 of O2 were introduced
into a 5 dm3 vessel and allowed to reach equilibrium.
2 CO (g) + O2 (g)
2CO2 (g)
H < 0
The graph below shows the changes in the concentration of CO and CO2 in the system
with time. A change was made to the system at time, t1 and t2.
What were the changes made at time, t1 and t2?
t1
t2
A catalyst was added
Volume of the system is increased
The temperature was increased
Volume of the system is decreased
More CO2 was added
An inert gas was added at constant volume
The temperature was decreased
More O2 was added
[Turn Over
10
14.
Use of the data booklet is relevant to this question.
Two cells are connected in series as shown in the diagram where P, Q, R and S are
electrodes. Which of the following correctly shows the products formed at each
electrode?
Cu
Pt
P
HCl (aq)
15.
Fe2(SO4)3 (aq)
Cu2+
H2
O2
Fe2+
O2
Cu
SO2
H2
Cl2
H2
O2
Fe
Cu2+
Cu
SO2
Fe2+
Use of the data booklet is relevant to this question.
Ladles are often made from sterling silver. Which aqueous solution should not be
stirred with a silver ladle because a reaction could occur?
KCl
(NH4)2S4O6
Na2SO4
PbBr4
[Turn Over
11
16.
The oxide and chloride of an element F are separately mixed with water. The two
resulting solutions have the same effect on methyl orange and can also be used to
dissolve BeO. What is element F?
17.
Magnesium
Aluminium
Silicon
Phosphorus
Which of the following statements about the elements strontium and barium is correct?
The elements react with cold water liberating hydrogen gas.
Aqueous solutions of their chlorides have a pH greater than 7.
The hydroxide of barium is less stable to heat.
The enthalpy change of hydration of the cations becomes less endothermic from
strontium to barium.
18.
Which statement is likely to be true for astatine which is below iodine in group VII of
the Periodic Table?
Potassium astatide and hot dilute sulfuric acid react to form astatine.
Silver astatide reacts with excess dilute aqueous ammonia to form a soluble
complex.
Sodium astatide and hot concentrated phosphoric acid react to form white fumes
of hydrogen astatide.
Hydrogen astatide is stable to heat.
[Turn Over
12
19.
Transition metals such as iron are often used as a catalyst in reactions such as the
Haber process. Which of the following statements best explains the role of transition
metals in this use?
Transition metals have good electrical conductivity as both 4s and 3d electrons

are involved in metallic bonding.
Transition metals have available and partially filled 3d orbitals for adsorption of
reactant molecules.
Transition metals form coloured ions due to the absorption of energy in the
visible light region to promote an electron from a lower to a higher energy 3d
orbital.
Transition metals can exhibit variable oxidation states due to the close proximity
in energy between the 3d and 4s electrons.
20.
X is a transition metal. In aqueous solution, it forms the coloured complex ion,

[X(H2O)6]4+. On oxidation of [X(H2O)6]4+ to [X(H2O)6]5+, the solution turned colourless.
Which of the following is the electronic configuration of the transition metal X?
21.
[Ar] 3d2 4s2
[Ar] 3d3 4s2
[Ar] 3d5 4s1
Ar] 3d10 4s2
How many cyclic hydrocarbons are there with the molecular formula C4H6?
A
[Turn Over
13
22.
Warfarin is used as a pesticide against rodents. The structural formula of warfarin is

given below.
O
OH
Which of the following reactants will not react with warfarin?
23.
Alkaline aqueous iodine
Acidified potassium manganate (VII)
Ethanoyl chloride
Neutral FeCl3
In which of the following reactions would the intermediate behave as a nucleophile?

Reaction 1: CH3CH2CHO intermediate CH3CH2CH(OH)(CN)
Reaction 2: C(CH3)3Cl intermediate C(CH3)3NH2
OH
OH
Reaction 3:
intermediate
Cl
Reaction 1
Reaction 2
Reactions 1 and 2
Reactions 2 and 3
[Turn Over
14
24.
Which of the following reaction scheme is able to prepare compound G from

methylbenzene?
NH2
O
NH2
Compound G
25.
Nitration, Side-chain oxidation, Condensation
Nitration, Reduction, Side-chain oxidation, Condensation
Side-chain oxidation, Condensation, Nitration
Side-chain oxidation, Condensation, Nitration, Reduction
Diels-Alder reaction is a conjugate addition reaction which is best exemplified by the

reaction below.
Which of the following pairs of starting materials will give the following compound H?
Compound H
Cyclopentene and ethene
Cyclopentadiene and ethene
Cyclobutene and ethene
Cyclobutadiene and ethene
[Turn Over
15
26.
Which of the following compounds is formed when compound M is dissolved in

aqueous sodium hydroxide under standard conditions?
OH
NHCOCH3
OCOCH2OH
Compound M
O-Na+
O-Na+
NH2
NH2
O-Na+
OCOCH2OH
O-Na+
O-Na+
NHCOCH3
OCOCH2O-Na+
27.
NHCOCH3
OCOCH2OH
In which sequence is it correctly stated that the value of pKb decreases continuously?
CH3CH2CONHCH3, CH3CH2NH2, CH2ClCH2NH2, C6H5NH2
CH3CH2CONHCH3, C6H5NH2, CH2ClCH2NH2, CH3CH2NH2
CH3CH2NH2, CH2ClCH2NH2, C6H5NH2, CH3CH2CONHCH3
CH2ClCH2NH2, CH3CH2NH2, C6H5NH2, CH3CH2CONHCH3
[Turn Over
16
28.
Compound J exhibits the following characteristics:
1 mol of J reacts with excess sodium metal to form 1 mol of hydrogen gas.
Yellow precipitate is formed when J reacts with aqueous alkaline iodine.
Orange precipitate is formed when J reacts with 2,4-DNPH, but no reaction with
alkaline silver diammine solution.
What could compound J be?

OH
OH
OH
OH
D
O
OH
OH
O
HO
O
29.
Which one of the following alcohols will give the most number of products when it is
heated with concentrated H2SO4 at 170C?
CH3CH2CH2OH
C(CH3)3OH
CH3CH2CH(OH)CH3
CH3CH2C(CH3)2OH
[Turn Over
17
30.
Polypeptides can be enzymatically hydrolysed to form shorter peptide chains. When a

nanopeptide was hydrolysed by enzymes, the following tripeptides were obtained.
gly-ala-leu
tyr-ser-leu
leu-gly-tyr
lys-gly-ala
ser-leu-gly
Which of the following could this nanopeptide be?
lys-gly-ala-leu-gly-tyr-ser-leu-gly
gly-ala-leu-gly-tyr-ser-leu-gly-tyr
lys-gly-ala-tyr-ser-leu-gly-tyr-ser
gly-ala-leu-gly-ser-tyr-leu-gly-tyr
[Turn Over
18
Section B
3 may be correct. Decide whether each of the statements is or is not correct (you may find it
helpful to put a tick against the statements that you consider to be correct).
1, 2 and 3 are
1 and 2 only are
2 and 3 only are
1 only is correct
correct
correct
correct
31.
For the elements R and S with atomic number 14 and 15 respectively, which of
the following statements are true?
32.
The fifth ionisation energy of R is higher than that of S.
They can form RCl4 and SCl3 respectively.
The atomic radius of R is smaller than that of S.
For the following chlorine-containing species,
ICl2-, ClF3, ClO3Which of the following statements is correct?
All atoms achieve stable octet configuration.
ICl2- is linear, ClF3 is T-shaped while ClO3- is trigonal pyramidal.
The bond angles increase in the order of ClF3 , ClO3- , ICl2-
[Turn Over
19
1, 2 and 3 are
1 and 2 only are
2 and 3 only are
1 only is correct
correct
correct
correct
33.
When a few drops of calcium nitrate solution is added to a saturated calcium hydroxide
solution, a white precipitate is observed. Which of the following provides the correct
explanation?
[Ca2+] and [OH-] are high enough such that the ionic product exceeds the Ksp.
The precipitate is formed because of the common ion, NO3- , and its effect on the
equilibrium.
34.
The Ksp has decreased due to the addition of calcium nitrate.
When a current of 2.05 A was passed through J(NO3)3 (aq) for 1 hour and 13 minutes,
1.73 g of metal J was deposited at the cathode. Which of the following statements
about the above electrolysis are correct?
J is iron.
A colourless gas, which turned acidified KMnO4 from purple to colourless, was
evolved at the anode.
35.
Increasing the [NO3-] decreased the rate of formation of J.
Which of the following can act as ligands?
BF4-
CH3CH2NH2
H2S
[Turn Over
20
1, 2 and 3 are
1 and 2 only are
2 and 3 only are
1 only is correct
correct
correct
correct
36.
In black and white photographic film, light converts silver chloride into metallic silver.
After the film has been produced, the unreacted silver chloride is removed by reaction
with sodium thiosulfate. Given that the function of the thiosulfate ion is similar to that of
ammonia, what are the functions of the thiosulfate ion?
37.
To oxidise the chloride ions to chlorine.
To form complexes with silver ions.
To lower the concentration of silver ions.
Salbutamol is used in the treatment of asthma.

OH
H
N
HO
HO
Salbutamol
Which of the following statements about salbutamol are correct?
It reacts with SOCl2 to form a product with three Cl atoms.
It has one chiral carbon.
One mole of salbutamol reacts with four moles of ethanoyl chloride.
[Turn Over
21
1, 2 and 3 are
1 and 2 only are
2 and 3 only are
1 only is correct
correct
correct
correct
38.
Saffron and vanilla beans are often used to flavour foods. Safranal and vanillin are
organic molecules which are responsible for the aromas of saffron and vanilla beans
respectively.
O
O
H
CH3
HO
Safranal
Vanillin
Which of the following reagents show identical observations when reacted with both
compounds?
Aqueous bromine
Ammonical silver nitrate
Acidified potassium dichromate (VI)
[Turn Over
22
1, 2 and 3 are
1 and 2 only are
2 and 3 only are
1 only is correct
correct
correct
correct
39.
Which of the following statements are true for all amino acids from natural sources?
They can undergo condensation with one another to form peptide linkages.
They can exist as zwitterions which have high melting points.
When placed in buffer solutions with pH lower than their isoelectric points, amino
acids will move towards the negative plate when electricity is applied.
40.
Collagen is the main component of connective tissues in our body. The more common
amino acids in collagen are listed in the table below.
Amino acid
R-group
Glycine
-H
Alanine
-CH3
Glutamic acid
-CH2CH2COOH
Arginine
-CH2CH2CH2NHC(NH2)=NH
Aspartic acid
-CH2COOH
Which of the following statements about collagen are true?
pH changes will denature collagen.
Hydrogen bonds are responsible for forming the secondary and tertiary structures
in collagen.
The R-groups of alanine and arginine interact with each other through induced
dipole-induced dipole interactions.
~~~ END ~~~
[Turn Over
SAJC 2012 PRELIMS PAPER 1 SOLUTIONS

1
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
Name:
Class:

Chemistry
Higher 2
Paper 2
9647/02
10 September 2012
2 hours
Candidates answer in the spaces provided on the question paper.


question.
For Examiners Use:

Question
Marks
1
2
3
4
5
Total
BLANK PAGE
[Turn Over
3
1
Planning (P)
Four aqueous solutions are provided. Each solution contains one of the following:
Aluminium bromide, Zinc sulfate, Silver nitrate, Barium hydroxide
You are to plan a series of test-tube experiments using only the four solutions and solid
potassium carbonate, in order to deduce which compound is present.
No other reagents should be used.
You should commence your plan by adding potassium carbonate to each of the solutions.
Your completed plan should include observations, deductions and balanced equations for
positive tests.
[12]
No.
Experiment
1.
Add spatula of solid

potassium carbonate to each
separate samples (1 cm3) of
the 4 solutions in clean, dry
test tubes.
Observations
Deductions with relevant

balanced equations
2.
[Turn Over
4
3
[Turn Over
5
2 (a)
Transition metals are often used to produce ornamental stained-glass windows.

Ironbased colours and pigments have been used since ancient times for stained-glass
windows in European churches.
(i)
Explain why iron compounds are usually coloured.
(ii)
Explain why the melting point of iron is significantly higher than that of calcium.
Stained-glass windows are darkened from corrosion and age. Microprobe analysis showed
that the tiny cracks and defects on the glass surface were enriched with insoluble MnO2.
(iii)
Using the Data Booklet, suggest a suitable reducing agent to dissolve MnO2 without
reducing iron (III) to iron (II).
[7]
[Turn Over
6
2 (b)
Iron (III) chloride is often used as a catalyst in the conversion of benzene to produce carbonyl
compounds.
CO / HCl
CHO
FeCl3
(i)
Write an equation to show the generation of the electrophile to form benzaldehyde.
(ii)
Explain why iron (III) chloride must be anhydrous in order to generate the
electrophile.
[3]
[Turn Over
7
2 (c)
By making use of the reaction in 2(b) and suitable starting materials, suggest a synthetic
pathway (in no more than 4 steps) to convert benzene into the following compound. State
clearly the reagents and conditions for each stage, and draw the structural formulae of
every intermediate formed.
[4]
[Turn Over
8
2 (d)
Iron (III) chloride can also be used in the alkylation of benzene to yield alkyl benzene, for
example methylbenzene (toluene). Toluene is less toxic than benzene, and thus can
replace benzene as an aromatic solvent in chemical preparation.
Using the following data,

H/ kJ mol-1
Enthalpy change of formation of CO2 (g)
- 393.5
Enthalpy change of formation of H2O (l)
- 285.8
Enthalpy change of combustion of C6H5CH3 (l)
- 3910
Enthalpy change of vaporisation of C6H5CH3 (l)
+ 38
(i)
Calculate the standard enthalpy change of formation of toluene, HfC6H5CH3 (l).
(ii)
Using your answer to 2 (d)(i), relevant data from the table above and the Data
Booklet, draw an appropriate energy cycle to determine the enthalpy change of
formation of benzyl radical C6H5CH2 (g).
[Turn Over
9
2 (d)
(iii)
Hence, deduce the thermodynamic stability of the product, benzyl radical C6H5CH2
as compared to its reactants. Explain.
[7]
[Total: 21 marks]
3 (a)
Chelation is the formation of coordinate bonds between a ligand and a single central atom
or metal ion. The ethanedioate ion (C2O42) is an example of a chelating ligand. Two
complexes which are successfully synthesised are [Al(C2O4)3]3 and [Al(C2O4)2].
(i)
Draw a dot-and-cross diagram for C2O42. Hence, suggest the bond angle about
either carbon atom.
(ii)
State the coordination number of aluminium in the complex [Al(C2O4)3]3.
[3]
[Turn Over
10
3 (b)
Aluminium is able to form ethanedioate complex such as K2n-3[Al(C2O4)n]. To determine

the identity of the complex, the complex is first decomposed in an acidic solution to give
ethanedioic acid and then titrated against potassium manganate (VII).
Al(C2O4)n(3-2n) + n H2SO4 n H2C2O4 + Al3+ + n SO42 (n = 2 or 3)
2 H+ + 2 CO2 + 2 e H2C2O4
E = - 0.49 V
Volumetric Analysis for ethanedioate content

Step 1
Weigh 1.77 g of the complex, K2n-3[Al(C2O4)n], in a 50 cm3 beaker.
Step 2
Dissolve it in deionised water and transfer to a 250 cm3 volumetric flask

and top up to the mark with deionised water.
Step 3
Pipette 25.0 cm3 of the solution into a conical flask and add about 40 cm3
of aqueous H2SO4.
Step 4
Warm the solution to about 50 0C.
Step 5
Titrate the contents of the flask with potassium manganate (VII) from a
burette until the first pink colour appears.
(i)
Use the Data Booklet to explain how the results of titration would differ when HCl is
used instead of H2SO4 in Step 3.
(ii)
By using collision theory of reaction kinetics, explain why the solution needs to be
warmed in Step 4.
[4]
[Turn Over
11
3 (b)
(iii)
Given that 27.50 cm3 of 0.0213 mol dm3 potassium manganate (VII) is needed to
reach equivalence point, calculate the % by mass of ethanedioate ion in the
aluminium complex.
(iv)
Hence, determine the value of n.
[4]
[Turn Over
12
3 (c)
Other chelating ligands such as F-, H2O and NH3 can also be used to form cobalt
complexes.
The UV-visible absorption spectra of the three aqueous solutions are shown below:
Relative Absorbance
[Co(NH3)6]3+
[Co(H2O)6]3+
400
450
500
550
[CoF6]3-
600
650
700
Wavelength / nm
(i)
With the aid of the spectrum above, account for the difference in the wavelength for
each complex.
(ii)
With the addition of another chelating ligand such as EDTA4- to [Co(H2O)6]2+,

[CoEDTA]2- complex is formed according to the following equation:
[Co(H2O)6]2+(aq) + EDTA4-(aq)
[CoEDTA]2-(aq) + 6H2O (l)
Explain why this reaction is spontaneous at all temperatures.
[5]
[Total: 16 marks]
[Turn Over
13
4 (a)
Acetal is relatively inert and can be made from a carbonyl compound. The carbonyl
functional group may be restored by adding aqueous acid.
Formation of Acetal
O
Step I
CH3CH2OH,
OH- catalyst
OH
OCH2CH3
Carbonyl Compound
Step II
CH3CH2OH,
OH- catalyst
OCH2CH3
OCH2CH3
H2O
An Acetal
Carbonyl functional group is restored by adding aqueous H+

OCH2CH3
OCH2CH3
An Acetal
H+
Carbonyl Compound
(i)
Suggest the type of reaction which occurs in Step I.
(ii)
Suggest why OH catalyst is needed in Step I.
(iii)
Outline a mechanism for Step I. In your answer, show any relevant charges, lone
pairs of electrons and movement of electrons.
[Turn Over
14
4 (a)
(iv)
Explain why anhydrous calcium chloride is added after Step II.
[7]
(b)
Thiols (RSH) are sulfur analogs of alcohols.
HS
(i)
CH3SH
H+ catalyst
Final organic product, X
Compound X has the following composition by mass.

C: 51.2%; H: 7.7%; S: 27.4%; O:13.7%
Using the given data, calculate the empirical formula of the final organic
product X.
(ii)
When a sample of 0.219 g of compound X was vaporised using a suitable

apparatus, the vapour occupied 38.2 cm3 at 95 0C and 150 kPa.
Calculate the Mr of compound X.
[3]
[Total: 10 marks]
[Turn Over
15
5 (a)
The rate of the reaction between A and Cl2 (l) has the following rate law:
Rate = k[A]m [Cl2]
O
Where A =
and
k is the rate constant with units of mol-2dm6s-1.
Two experiments to study the kinetics of this reaction were carried out and the data
obtained are tabulated below.
Experiment
Initial [A]
[Cl2]
Initial rate
/ mol dm-3
/ mol dm-3
/ mol dm-3 s-1
0.40
0.08
0.20
(i)
What is the value of y in Experiment 2?
(ii)
Given that the half-life of Cl2 in Experiment 1 was 4.5 seconds, predict a value for
the half-life of Cl2 in Experiment 2, giving your reasoning.
[3]
(b)
(i)
Predict the products formed when BaCl2 reacts with concentrated H2SO4.
[Turn Over
16
5 (b)
(ii)
Hence, identify the structural formula for the organic product formed when
O
reacts with BaCl2 and concentrated H2SO4.
[2]
(c)
The
reaction
scheme
below
shows
how
an
ester
is
generated
from
Complete the reaction scheme below by writing the structural formulae of the
organic products and the reagents and conditions in the spaces provided.
O
I
A
hot
alumina
II
NC
III
D
NaBH4
in methanol
IV
[Turn Over
17
5 (c)
Step
Reagents and conditions
II
III
IV
[8]
[Total: 13]
~~~ END ~~~
[Turn Over
Date: 11 September 2012

SAJC 2012 Prelims P2 Solutions
1
No.
1.
2.
Experiment
Observation
Add spatula of Effervescence OR gas evolved.

solid potassium
carbonate to
each separate
samples (1 cm3)
of the 4
solutions in
clean, dry test
tubes.
White precipitate formed
Add each
unknown sample
to 1 cm3 of AlBr3
solution till
excess in clean,
dry test tubes.
Deductions with relevant

equation
Al(H2O)63+(aq)
Al[(OH)(H2O)5]2+(aq) +
H+(aq)
2H+(aq) + CO32-(aq)
H2O(l) + CO2 (g)
AlBr3 identified
ZnCO3, Ag2CO3, CaCO3
No precipitate formed
ZnSO4 identified
Off-white precipitate formed
Ag+(aq) + Br (aq)
AgBr(s)
AgNO3 identified
Al3+(aq) + 3 OH(aq)
Al(OH)3(s)
White ppt soluble in excess
Al(OH)3(s) + OH(aq)
Al(OH)4(aq)
Ba(OH)2 identified
3.
Add Ba(OH)2
dropwise till
excess to 1 cm3
of the last
unknown
solution
Ba2+(aq) + SO42(aq)
BaSO4(s)
ZnSO4 identified
2(a)
(i)
The iron ion has incompletely filled d-orbitals.

In the isolated gas phase atoms, all 5 d orbitals of the iron ion are
degenerate
In forming complexes, the d orbitals split into 2 groups with a small energy
gap between them.
When a d-electron from the lower energy group is promoted to the higher
energy group, energy from the visible region is absorbed.
The light energy not absorbed will be seen as the colour of the complex.
(ii)
The melting point of iron is significantly higher than that of calcium due to
the stronger metallic bonding present in iron and thus more energy needed
which is attributed to the following reasons:
- more delocalised electrons contributed from 3d and 4s electrons
- higher charge density
(iii)
Fe3+ + e
Fe2+
MnO2 + 4H+ + 2e
+0.77V
Mn2+ + H2O
+1.23V
Ag metal
Student can choose any reducing agent as long as the electrode potential is
+0.77V < x < +1.23V.
OR student show calculation of Ecell
Ecell >0 for Ag/MnO2.
Ecell = 1.23- 0.80 = + 0.43V >0 reaction is feasible.
Ecell of Ag/Fe3+ < 0V, no reaction, Ag only reduces MnO2.
Ecell = 0.77 -0.80
= -0.03V <0
2(b)
(i)
CO + HCl + FeCl3 +CHO + FeCl4--
(ii)
FeCl3 will hydrolyse with water to yield [Fe(H2O)5(OH)]2+ and Cl- ions. OR
dissolve in water to form [Fe(H2O)6]3+. Fe in [Fe(H2O)5(OH)]2+ or Fe in
[Fe(H2O)6]3+ has no vacant d-orbitals to accept electron pair from Cl- to
generate the electrophile.
2(c)
(i)
O
CO/ HCl
FeCl 3
Heat with reflux
O
CHO
Heat with reflux
LiAlH4, in dry ether

r.t.p
CH2Cl
CH2OH
PCl5, r.t.p
OR
PCl3, Heat
OR
SOCl2 r.t.p
(d)
(i)
Hc C6H5CH3 = nDHformationo(products)nDHformationo(reactants)
(-3910)
= 7 (-393.5) + 4(-285.8) - Hf C6H5CH3
Hf C6H5CH3 = +12.3 kJ/mol

(ii)
Hformation of C6H5CH2
7 C(s) + 4 H2 (g)
C6H5CH2 (g) + H2 (g)
Hf = +12.3
C6H5CH3 (l)
Hvapouration = + 38.00
C6H5CH3 (g)
+ 410
C6H5CH2 (g) + H (g)

Hf C6H5CH2 (g) = +12.3 + 38 + 410 218
= +242.3 kJ/mol
= + 242 kJ/mol
B.E. (H-H) = +218
(iii)
Benzyl radical C6H5CH2 is less stable than its reactant, Hf C6H5CH2 (g) is
endothermic. The radical is very reactive as it requires only 1 more electron
to form a stable configuration.
[Total marks : 21]
3(a)
(i)
1200
3(b)
(ii)
Coordination no: 6
(i)
Cl 2
+ 2e
2Cl -
MnO4- + 8H+ + 5e
+1.36V
Mn2+ + 4H2O
+1.52V
MnO4 is able to oxidise Cl to Cl2. Ecell = +0.16V, reaction is feasible.

Hence more MnO4 will be used for the titration.
(ii)
When temperature is increased, the molecules gain kinetic energy and move
about faster. This increases the number of molecules having energy E EA.
Thus, the frequency of effective collisions increases. Reaction rate increases.
3(b)
(iii)
Calculation of % weight of C2O42-ion Al complex

H+ + 2 CO2 + 2 e H2C2O4
MnO4- + 8H+ + 5e Mn2+ +4H2O
5H2C2O4 2MnO4
Amt of MnO4 = 27.50/1000 x 0.0213 = 5.86 x 10-4 mol
Amt of H2C2O4 in 25 ml = 5.86 x 10-4 x 5/2 = 1.466 x 10-3 mol
Amt of H2C2O4 in 250 ml = 1.466 x 10-3 x 10 = 1.466 x 10-2 mol
Mass C2O42- = 1.466 x 10-2 x 88.0 = 1.29 g
% of C2O42- in complex = 1.29/1.77 x 100% = 72.9%
(iv)
If n =2, K[Al(C2O4)2]
% of C2O42- in complex = 176/242.1 x 100% = 72.7%
If n =3, K3[Al (C2O4)3]
% of C2O42- in complex = 264/408.3 x 100% = 64.7%
Since the value obtained is closer to n = 2, the complex is K[Al(C2O4)2]
3(c)
(i)
Due to the presence of different ligand, the d orbitals are split to different
extent/ energy gap, DE.
Rank of the d-orbital splitting NH3 > H2O > F-
(ii)
Since EDTA is able to displace H2O, hence it will form a stronger dative bond
to Co2+. Hence, H is negative.
S is positive as there is an increase in entropy due to more molecules at the
product side, 7 molecules vs 2 molecules.
Using G =H -TS, Since S >0 and H is <0,
-TS would always be <0 G would be always <0 at all temperature.
[Total marks:16]
4(a)
(i)
(ii)
OH- will react with ethanol to generate a stronger nucleophile CH3CH2O-.
(iii)
(iv)
Generation of Nucleophile
Slow
Intermediate
Arrow
Partial charges + lone pair
OH
OCH2CH3
Step II
OCH2CH3
+ H2O
CH3CH2OH,
H+ catalyst
OCH2CH3
An Acetal
Calcium chloride is a drying agent, which help to remove water. Hence the
position equilibrium will shift right to increase the yield of the product.
4(b)
(i)
Percentage by
mass / %
Mole ratio
Simplest ratio
C
51.2
H
7.7
O
13.7
S
27.4
4.3
5
7.7
9
0.86
1
0.85
1
`
Empirical formula = C5H9OS
(ii)
Using the ideal gas equation, pV = nRT = (m/Mr)RT

Mr = (mRT)/pV
= [0.219 X 8.31 X (95 + 273)]/(150 X 103 X 38.2 X 10-6) = 116.9
[Total: 10 marks]
5(a)
(i)
0.160
(ii)
Experiment 2: 18 seconds.
Since r = k [Cl2], hence t1/2 = ln 2 / k.
O
Where k = k [
]2, thus when
halves, the
time x 4 .
(b)
(i)
HCl + BaSO4 or HCl + Ba(HSO4)2
(ii)
OR
Cl
Cl
(c)
Step
Reagents and conditions
X2 (aq)
II
Ethanolic KCN heat with reflux
III
Aqueous H2SO4, heat with reflux
IV
PCl5 or SOCl2 (with pyridine) or PCl3 (heat)
Br
Br
OH
A
O
D
O
HOOC
Cl
C
O
[Total: 13 marks]

Chemistry
Higher 2
9647/03
Paper 3
18 September 2012
2 hours

Additional Materials: Writing paper, Data Booklet
READ THESE INSTRUCTIONS FIRST:
Write your name and civics group on all the work you hand in.
[Turn Over
Answer any 4 questions.

1.
Paracetamol and aspirin are well known drugs to treat pain and to reduce fever.
(a)
The following are structures of paracetamol and aspirin:

H
COOH
CH3
CH3
HO
Paracetamol
Aspirin
pKa = 9.5
pKa = 3.5
Mr = 151.0
Mr = 180.0
(i)
Explain the difference in the pKa values of aspirin and paracetamol.
(ii)
Phenacetin is an analgesic whose use has largely declined due to its carcinogenic
properties. Starting from paracetamol, show the steps involved in the synthesis of
phenacetin. In your answer, include the reagents and conditions required for each
step, as well as the structure of the intermediate involved.
H
N
CH3
C
O
CH3CH2
O
Phenacetin
(iii)
Salicin is an anti-inflammatory agent that is closely related in chemical make-up to

aspirin. Suggest a chemical test that could be used to distinguish salicin from
aspirin. Write a balanced equation for the reaction that occurred.
CH2OH
OH
O
O
CH2OH
OH
OH
Salicin
[Turn Over
1.
(a)
(iv)
Aspirin is supplied as a crystalline solid. A standard solution of aspirin may be

made by dissolving aspirin in an organic solvent. Explain why water is not used as
a suitable solvent.
[9]
(b)
(i)
Write an expression for the acid dissociation constant, Ka, of aspirin.
(ii)
A tablet of aspirin is swallowed into the stomach. Given that the pH of the
stomach is 1, calculate the percentage of aspirin molecules that remain
undissociated in the stomach.
[3]
(c)
0.270 g of aspirin and 0.121 g of paracetamol are dissolved in 30 cm3 of ethanol and
titrated against 0.100 mol dm-3 aqueous sodium hydroxide, using 1 to 2 drops of two
indicators, methyl red and phenolphthalein.
x cm3 of aqueous sodium hydroxide is required to change the colour of the methyl red
and a further y cm3 of aqueous sodium hydroxide is needed to change the colour of
phenolphthalein.
(i)
Explain why both indicators are added in small amounts.
(ii)
Calculate the initial pH of the mixture, assuming the initial pH is from aspirin
only.
(iii)
Calculate the values of x and y.
(iv)
Sketch the shape of the pH curve during this titration.

[8]
[Total 20]
[Turn Over
2. (a)
In an effort to provide a sustainable system for waste treatment and energy

production, scientists are currently working in the area of microbial fuel cell (MFC)
technology. MFC is a device that converts chemical energy to electrical energy by
the catalytic reaction of microorganisms such as bacteria. A typical microbial fuel
cell consists of an anode and a cathode separated by a cation exchange membrane
which only allows cations to pass through. Copper has been used extensively as
electrodes in MFCs as shown in the following diagram.
Copper anode
electron flow
Copper cathode
Air
Sucrose
Bacteria
cation exchange membrane
On the anode side, bacteria grow and proliferate, forming a dense cell aggregate
known as a biofilm that adheres to the MFCs anode. In the course of their microbial
metabolism, the bacteria act as catalysts for converting the organic substrate such
as sucrose, C12H22O11, into carbon dioxide. At the cathode, in the presence of air,
steam is produced.
(i)
Write balanced half-equations, occurring at each electrode, when the

MFC discharges.
(ii)
Given the electromotive force of the MFC is 1.25 V, calculate the

reduction potential of the carbon dioxide / sucrose half-cell.
(iii)
Suggest with a reason, the effect on the standard cell potential if the pH of
the electrolyte at the cathode is increased.
[5]
[Turn Over
2. (b) Copper reacts with 50% nitric (V) acid, HNO3, to give a blue solution, containing
complex ion A and a brown gas B. If the solution containing A is diluted and sodium
hydroxide solution added cautiously, a gelatinous blue precipitate C is obtained,
which if heated, forms a black solid D.
Addition of concentrated aqueous ammonia solution to A gives a deep blue solution
that contains the ion E. Addition of concentrated hydrochloric acid to E gives a
yellow solution of the ion F, which on dilution with water gives a solution containing
the same ion A.
If the brown gas B is passed into water, a mixture of acids G and H is formed in a
disproportionation reaction.
(i)
Identify A H. Construct balanced equations, with state symbols, for the

formation of C, D, E and F.
(ii)
Draw a dot-and-cross diagram of nitric (V) acid, HNO3. With reference to

the Valence Shell Electron Repulsion theory, explain the shape about the
nitrogen atom.
[15]
[Total 20]
[Turn Over
3.
Hydrazine, N2H4, is a colourless, volatile and corrosive liquid with an ammonia-like odour.
It is well known for its use in various rocket fuels and to prepare gas precursors used in air
bags.
(a)
Hydrazine decomposes thermally, liberating a large amount of heat and a large

volume of gaseous products in the following ways:
3 N2H4 (l) 4NH3 (g) + N2 (g)
N2H4 (l) N2 (g) + 2H2 (g)
(i)
Hr = +111.8 kJ mol-1
Hr = z kJ mol-1
Write the equation that corresponds to the enthalpy change of formation of

ammonia.
(ii)
Hence, using your answer to (a)(i), the above reactions and relevant data from
the Data Booklet, construct an energy cycle to calculate z.
[3]
(b)
Hydrazine can be synthesised by the Raschig process, where Cl2 gas and NH3 gas
are heated under certain conditions in the presence of sodium hydroxide.
(i)
State the change in oxidation number of nitrogen atom during the Raschig
process.
(ii)
Predict the product of Cl2 in the process.
(iii)
Construct an ionic equation for the Raschig process.

[3]
[Turn Over
3.
(c)
The WolffKishner reduction is a chemical reaction that reduces a carbonyl

compound (ketone or aldehyde) to its corresponding alkane. Condensation of the
carbonyl compound with hydrazine forms a hydrazone intermediate, and treatment
with a base induces the formation of the corresponding alkane.
Below shows the synthesis of propane from propanone via the Wolff-Kishner
reduction.
CH3
H2NNH2
C
hydrazone
intermediate
KOH
CH3CH2CH3
CH3
Carbonyl compounds A and B both undergo the Wolff-Kishner reduction

separately forming ethylbenzene.
A is found to give a silver mirror with Tollens reagent but B does not.
Draw the displayed formulae of A, B and the hydrazone intermediate formed with A.
[3]
[Turn Over
3.
(d)
Ethylbenzene undergoes the following reaction scheme producing C.

CH2CH3
CH2CH3
CH2CH3
HNO3 + BF3
Step I
NO2
Step II
NH
NH2
Step III
C
For Step I,
(i)
outline the mechanism of the reaction.
(ii)
with reference to the structure of BF3, explain how BF3 helps in the
mechanism.
For Step II,

(iii)
state the reagents and conditions required.
For Step III,

(iv)
an intermediate is involved. Draw the structure of the intermediate.
(v)
state the reagents and conditions required to form the intermediate.
(vi)
name the two types of reactions involved.
(vii)
explain why the yield of C is low.

[11]
[Total 20]
[Turn Over
4.
(a)
A 25.0 cm3 solution containing 0.00500 mol dm-3 of potassium chloride, KCl, and
0.800 mol dm-3 of potassium chromate (VI), K2CrO4, was titrated against
0.100 mol dm-3 aqueous silver nitrate. White precipitate was first formed.
When v cm-3 of aqueous silver nitrate was added, a trace amount of red precipitate,
Ag2CrO4, was observed.
Ksp for AgCl = 1.6 x 10-10 mol2 dm-6
Ksp for Ag2CrO4 = 9.0 x 10-12 mol3 dm-9
(i)
Assuming no dilution was caused by the addition of aqueous silver nitrate,

calculate the concentration of chloride present in the mixture when the first
trace of red precipitate was observed.
(ii)
Calculate the percentage of chloride precipitated when the first trace of red
precipitate was observed.
Hence, suggest the role of potassium chromate (VI) in the solution.
[4]
Potassium chlorate (I), KClO, and potassium chlorate (V), KClO3, can be easily made by
the electrolysis of saturated potassium chloride solution under different conditions.
During the electrolysis, inert electrodes are used and the products at the electrodes are
allowed to mix.
(b)
(i)
Using the Data booklet, describe and explain the reactions occurring at the
cathode and the anode.
(ii)
Write a balanced equation to show the formation of KClO3.
(iii)
How do you ensure that potassium chlorate (I), KClO, is not formed.
(iv)
A current of 3 A was passed through the electrolytic cell. Calculate the time
required to obtain 30 g of KClO3.
[9]
[Turn Over
10
4.
(c)
2.12 g of potassium chlorate, KClOx, was heated and decomposed completely to

give oxygen gas and potassium chloride as shown in the diagram below.
The oxygen gas produced was collected over water at 22 oC at a total pressure of
100525 Pa. The volume of gas collected was 650 cm3, and the vapour pressure of
water at 22 oC is 2800 Pa.
Oxygen gas and water vapour
KClOx
(i)
Write the balanced equation, with state symbols, of the decomposition

reaction of KClOx.
(ii)
Calculate the amount of O2 produced. Hence, deduce the value of x in

KClOx.
[5]
(d)
Compare and explain the ease of decomposition between KBrOx and KClOx.
[2]
[Total 20]
[Turn Over
11
5.
The following information was taken from the side of a carton of milk.
How long does your milk keep?
(a)
(i)
30C
day
18C
1 day
5C
4 days
The souring of milk is a chemical reaction. How is the rate of this reaction
related to the length of time the milk keeps?
(ii)
Explain how this rate varies with temperature. Draw an energy distribution
diagram to illustrate your answer.
[4]
(b)
(i)
For each of the following cases, explain with the help of a diagram, how the
following types of side chain interactions are affected during each
denaturation process.
I.
AgNO3 is used as disinfectants to prevent gonorrhea infections in the

eyes of new born infants.
O
CH2CH2CH2CH2NH3+
CH2CH2
glutamic acid
lysine
polypeptide chain of gonorrhea
II. Ethanol solutions are used as disinfectants on the skin as it can

penetrate the bacterial cell wall and denature the proteins inside the
cell.
O
CH2C
O-
CH2
HO
aspartic acid
tyrosine
polypeptide chain of bacterial cell
[Turn Over
12
5.
(b)
(ii)
Which of the treatments, AgNO3 in case I or ethanol in case II, is likely to

affect the alpha helix structure? Explain.
[6]
(c)
Compound B (C10H14O2) is optically active and does not react with aqueous sodium
carbonate. However, it dissolves slowly in aqueous sodium hydroxide.
B reacts with hydrogen bromide but will not decolourise acidified potassium
dichromate (VI). B decolourises aqueous bromine to form white precipitate C
(C10H12O2Br2), together with dense white fumes.
Upon treatment with concentrated sulfuric acid at 170oC, B gives compound D
(C10H12O) which exists as a pair of geometric isomers. D gives compound E
(C10H14O3) on addition of cold, dilute alkaline potassium manganate (VII) solution.
E reacts with phosphorus pentachloride to give copious fumes and compound F

(C10H12OCl2).
Suggest a structure for each lettered compound, B F, and explain the reactions
involved.
[10]
[Total 20]
~~~ END ~~~
[Turn Over
SAJC Prelim 2012 P3 solutions

No.
1(a)(i)
(ii)
1 SAJC PRELIM 2012 P3 solutions
Solutions
Aspirin has a lower pKa hence a higher Ka thus aspirin is a stronger acid
Aspirin has a RCOOH group and the conjugate base that is formed is more stable as the
negative charge on the carboxylate ion is delocalised over O-C-O bond (charge delocalised over
two oxygen atoms) by resonance effect.
The conjugate base of phenol is less stable as the negative charge (lone pair of electrons on O)
of the phenoxide ion is only delocalised into the benzene ring.
H
N
H
CH3
N
C
O
HO
CH3
C
O
Na(s)
or
NaOH(aq)
CH3CH2Br/I/Cl
heat
H
N
CH3
C
O
CH3CH2
O
Phenacetin
(iii)
Add aqueous sodium carbonate / sodium hydrogen carbonate

Aspirin gives bubbles that will form white ppt. with aqueous calcium hydroxide. Salicin does not
give white ppt or bubbles.
OR
K2Cr2O7 (aq), aq H2SO4, heat OR Add aqueous KMnO4 (aq), aq H2SO4, heat.
Salicin decolourises purple KMnO4 OR turns K2Cr2O7 from orange to green.
Aspirin remains purple OR remains orange.
(iv)
Water is not a suitable solvent as the solute-solvent interaction (pd-pd, id-id, H-bonding)
cannot overcome the H-bonding between water and id-id between aspirin.
(b)(i)
Ka =
COOH
CH3
O
C
O
Where HA =
COO-
O
C
(ii)
CH3
and A- =
10-3.5 =
Hence,
= 3.16 x 10-3
Percentage ionised = (3.16 x 10-3 / 1) x 100 % = 0.316 %

Percentage unionised = 100 0.316 = 99.7 %
(c)(i)
(ii)
Indicators are weak acids hence if added in large amount, the amount of NaOH required will be
higher than expected / titration is inaccurate.
[aspirin] =
= 0.05 mol dm-3
Using Ka =
(iii)
[H+]2 = 3.98 x 10-3

pH = 2.40
Using [aspirin] = 0.05 mol dm-3
x=
[paracetamol] =
y=
= 15.00 cm3
= 0.0267 mol dm-3
= 8.00 cm3
(iv)
2(a)(i)
(ii)
Cathode: O2 + 4H+ + 4e 2H2O

Anode: 13H2O + C12H22O11 12CO2 + 48H+ + 48e
Using data booklet: Eq O2 + 4H+ + 4e 2H2O + 1.23 V
Using Eqcell = Eqcathode - Eqanode
+ 1.25 = + 1.23 (Eqanode)
Eqcathode = 0.02 V
(iii)
(b)(i)
O2 + 4H+ + 4e 2H2O + 1.23 V

When the pH increases, the cathodic reaction shifts to the left to replenish H+.
Hence, the Eqcell becomes more negative.
A: [Cu(H2O)6]2+
E: [Cu(NH3)4(H2O)2]2+
B: NO2
F: [CuCl4]2-
C: Cu(OH)2
D: CuO
G/H: HNO2 and HNO3
Equations:
C: [Cu(H2O)6]2+(aq) + 2OH- (aq) Cu(OH)2 (s) + 6H2O (l)
OR Cu(NO3)2 (aq) + 2NaOH (aq) Cu(OH)2 (s) + 2NaNO3 (aq)
D: Cu(OH)2 (s) CuO (s) + H2O (l)/ (g)
E: [Cu(H2O)6]2+(aq) + 4NH3 (aq) [Cu(NH3)4(H2O)2]2+ (aq) + 4H2O (l)
F: [Cu(NH3)4(H2O)2]2+ (aq) + 4HCl (aq) [CuCl4]2- (aq) + 2H2O(l) + 4NH4+ (aq)
OR [Cu(NH3)4(H2O)2]2+ (aq) + 4Cl- (aq) [CuCl4]2- (aq) + 2H2O(l) + 4NH3 (aq)
(ii)
3 bond pairs of electrons repels each other equally OR lp-lp>lp-bp>bp-bp

Hence, the shape is trigonal planar.
3(a)(i)
(ii)
N2 (g) +
H2 (g) NH3 (g)

+ 111.8
3N2H4 (l)
4NH3 (g)
N2 (g)
3z
y
3N2 (g) + 6H2 (g)
Using bond energy from the data booklet:

y = [2BE (NN) + 6BE (H-H)] 12 BE (N-H)]
y = - 76 kJ mol-1
(b)(i)
(ii)
(iii)
Using energy cycle:

3z + y = 111.8
Z = +62.6 kJ mol-1
-3 to -2
N is oxidised, Cl- is formed or NaCl where Cl2 must be reduced.
Note: HCl not accepted given that NaOH is the medium.
2OH- + 2NH3 + Cl2 N2H4 + 2Cl- + 2H2O
Note: No spectator ions.
(c)
A:
B:
Hydrazone:
H
N
3(d)(i)
HNO3 + BF3 NO2+ + [BF3OH]-
H+ + [BF3OH]- BF3 + H2O

(ii)
(iii)
(iv)
B has an empty orbital. Hence, B can accept a lone pair of electrons from OH- via dative
bonding.
Sn and concentrated HCl with heat followed by aq NaOH
CH2
CH2Cl
NH2
(v)
(vi)
(vii)
4(a)(i)
(ii)
(b)(i)
Limited chlorine gas / in CCl4 + UV OR by heating.

Free radical substitution
Difficult to control the position and number of substitution by Cl during FRS.
OR difficult to control NS.
Using Ksp for Ag2CrO4 = [Ag+]2[CrO42-] = 9 x 10-12
[Ag+] needed to form the red ppt = [(9 x 10-12)/(0.8)]1/2 = 3.35 x 10-6 mol dm-3
Using Ksp for AgCl = [Ag+][Cl-] = 1.6 x 10-6
[Cl-] = (1.6 x 10-10)/( 3.35 x 10-6) = 4.78 x 10-5 mol dm-3
Percentage of Cl- precipitated =
= 99.0 %
Since almost all of the Cl- is precipitated when the first trace of red ppt appears, CrO4- acts as an
indicator for the titration.
At the cathode (negative electrode),
K+ and H2O compete to be reduced.
K+ + e K
-2.92 V
2H2O + 2e H2 + 2OH
- 0.83 V
Since the Eq (H2O/OH-) = - 0.83 V is more positive than Eq (K+/K) = - 2.92 V
H2O is preferentially reduced.
Cathode: 2H2O + 2e H2 + 2OHAt the anode (positive electrode),
Cl- and H2O compete to be oxidised.
Cl2 + 2e Cl- + 1.36 V
(ii)
(iii)
(iv)
(c)(i)
(ii)
O2 + 4H+ + 4e 2 H2O +1.23 V

Although the Eq (Cl2/Cl-) = + 1.36 V is more positive than Eq (O2/H2O) = +1.23 V
Cl- is preferentially oxidised due to its high concentration.
Anode: 2Cl- Cl2 + 2e
3Cl2 + 6KOH KClO3 + 5KCl + 3H2O
Note: Ionic eqn accepted.
High temperature of electrolyte must be used.
Cl- + 3H2O ClO3- + 6H+ + 6e
OR Thus, 1 mole of ClO3- is formed from 6F.
122.6 g of KClO3 = 1 mole of KClO3 = 579 000 C
30 g of KClO3 = 0.245 moles = 141 680 C
Using Q = It
t = (141 680) / 3 = 47227 seconds OR 13.1 hours.
KClOx (s) KCl (s) + x/2 O2 (g)
Poxygen gas = Ptotal Pwater vapour = 100525 2800 = 97725 Pa
Using PV = nRT
97725 x 650 x 10-6 = noxygen x 8.314 x (22 + 273)
noxygen = 0.0260 mol.
=
(d)
5(a)(i)
(ii)
x = 2.99 3
KBrO3 is more easily decomposed than KClO3 OR KBrO3 is thermally less stable.
BrO3- has a larger electron cloud than ClO3- hence K+ is more able to polarise the larger electron
cloud more easily due to weakening of Br-O bond.
Rate a 1/ time
When temperature is increased, the molecules gain kinetic energy and move about faster. This
increases the number of molecules having energy E Ea. As a result, the frequency of effective
collisions increases. Reaction rate thus increases.
b(i)
I. Ag+ will compete with the cation of lysine to form ionic interaction with the anion of glutamic
acid. OR NO3- will compete with the anion of glutamic acid to form ionic interaction with the
cation of lysine.
polypeptide chain
II. A polar solvent such as ethanol will disrupt the ion dipole interactions between Asp and Tyr to
form ion-dipole interaction with the anion of aspartic acid OR hydrogen bonding with tyrosine.
polypeptide chain
(ii)
Ethanol in case II.

Ethanol can disrupt the hydrogen bonding between peptide linkages which maintain the alpha
helix structure OR by forming hydrogen bonds with the peptide linkages.
Note: OR ethanol can form hydrogen bonding with the secondary structure.
OR
polypeptide chain
(c)
OH
OH
Br
CH3
CH3
B:
C:
CH2CH3
CH2CH3
OH
OH
Br
OH
OH
CH3
CH3
D:
E:
CHCH3
CHCH3
OH
OH
OH
CH3
F:
CHCH3
Cl
Cl
ES substn at 2, 4 or 6.
Information
B is optically active.
B dissolves slowly in aq. NaOH
B reacts with HBr
B does not decolourise potassium dichromate.
Deduction
B has a chiral carbon
B has phenol.
B undergoes neutralisation
B undergoes N.S
B forms alkyl bromide
B has alcohol group.
B is a tertiary alcohol.
B decolourises aq. Bromine to form white ppt.
B is a phenol.
B undergoes E.S.
From molecular formula of C, one of
the 2,4 or 6 positions is occupied.
B reacts with concentrated sulfuric acid at

170oC
D reacts with cold alkaline KMnO4
B undergoes elimination.
D is an alkene.
D undergoes mild oxidation.
D forms a diol.
E undergoes NS.
E reacts with PCl5 to give white fumes
END
SERANGOON JUNIOR COLLEGE

General Certificate of Education Advanced Level
Higher 2
Candidate Name
Class
CHEMISTRY
9647/01
24 August 2012
1 hour
Data Booklet
Optical Mark Sheet (OMS)

On the separate multiple choice OMS given, write your name, FIN/NRIC and class in the
spaces provided.
Shade correctly your class and FIN/NRIC number.
Eg. If your NRIC is S9306660Z, shade S9306660Z for the item index number.
There are forty questions in this paper. Answer all questions.
For each question there are four possible answers A, B, C and D.
Choose the one you consider correct and record your choice using a soft pencil on the
separate OMS.
You are advised to fill in the OMS as you go along; no additional time will be given for the
transfer of answers once the examination has ended.
Any rough working should be done in this question paper.
This document consists of 19 printed pages and 1 blank page
SRJC PRELIM 9647 P1
Turn Over]
2
Section A
1
To determine the percentage of nitrogen present in a snack, 1.0 g of the snack was
boiled with concentrated sulphuric acid to convert all the nitrogen into ammonium
sulphate. The ammonium salt obtained was then boiled with excess aqueous sodium
hydroxide to liberate the ammonia, which was passed into 25.0 cm3 of 0.20 mol dm3
hydrochloric acid. The unreacted hydrochloric acid required 20.0 cm3 of 0.10 mol dm3
aqueous sodium hydroxide for complete neutralisation.
What is the percentage by mass of nitrogen in the snack?
2.8%
4.2%
7.2%
8.4%
In an experiment, 25.0 cm3 of 0.20 mol dm3 solution of K2AO4 reacted exactly with
25.0 cm3 of 0.10 mol dm3 aqueous sodium sulfate(IV). The half-equation for the
oxidation of the sulfate(IV) ion is shown below.
SO32 (aq) + H2O (l) SO42 (aq) + 2H+ (aq) + 2e
Calculate the final oxidation state of A.
+2
+3
+4
+5
Two elements D and E have the following properties.
D and E form ionic compounds Na2D and Na2E respectively.

Element E forms EF6 molecules whereas D is not able to do so.
Which pair of electronic configurations for D and E is correct?
A
B
C
D
D
[He] 2s2 2p2
[He] 2s2 2p2
[He] 2s2 2p4
[He] 2s2 2p4
SRJC PRELIM 9647 P1
E
[Ne] 3s2 3p4
[Ne] 3s2 3p2
[Ne] 3s2 3p2
[Ne] 3s2 3p4
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3
4
The diagram below shows liquid trichloromethane and liquid benzene flowing from
burettes 1 and 2 respectively.
Burette 1
Liquid
trichloromethane
Burette 2
Liquid Benzene
What would happen to the flow of the liquids trichloromethane and benzene when a
negatively-charged rod is brought near to each of them?
A
B
C
D
Liquid trichloromethane
Deflected towards the rod
Undeflected
Undeflected
SRJC PRELIM 9647 P1
Liquid benzene
Undeflected
Undeflected
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4
5
The value of pV is plotted against p for two gases, G and H, where p is the pressure
and V is the volume of the gas.
Gas G
pV
Gas H
2x
x
Which of the following could be the identities of the gases?

Gas G
Gas H
0.5 mol of H2 at 25 C
1 mol of SO2 at 25 C
0.5 mol of SO2 at 25 C
1 mol of H2 at 25 C
During an inspection, a small spacecraft of capacity 20 m3 was connected to another of

capacity 50 m3. Before connection, the pressure inside the smaller craft was 40 atm
and that inside the larger one was 150 atm.
Given that all measurements were made at the same temperature, What is the
pressure of the system after the connection?
A
78 atm
SRJC PRELIM 9647 P1
95 atm
119 atm
190 atm
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5
7
In which of the following pairs of compounds will compound II have a higher boiling
point than compound I?
II
CH3CH2CH2CH2CH3
C(CH3)4
CH3CH2CH2COOH
CH3CH2CH2OH
CH2Cl
C
CH3
Cl
Br
CH2Cl
CH2Cl
C
C
CH2Cl
CH3
C
H
The conversion of compound X into Z was exothermic and proceeded by two steps,
where Y was the intermediate. The steps involved were:
Step 1:
XY
Step 2:
YZ
It was found that Step 1 is the rate-determining step. Which diagram represents the
energy level diagram for the reaction?
SRJC PRELIM 9647 P1
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6
9
Pure nitrosyl chloride, NOCl gas, was heated at 320C in a 2.0 dm3 vessel. At
equilibrium, 30% of the NOCl gas had dissociated according to the equation below and
the total pressure was p atm.
2NOCl (g)
2NO (g) + Cl2 (g)
What is value of the equilibrium constant, Kp?

A
17.9
41.7
0.0120p
0.0130p
10 The pH change when 0.10 mol dm3 CH3COOH is added drop-wise to 10.0 cm3 of
0.10 mol dm3 NaOH (aq) is shown below.
At which point on the graph does pH = pKa, where Ka is the acid dissociation constant of
the weak acid?
B
pH
C
Volume of 0.10 mol dm-3 CH3COOH added/ cm3
SRJC PRELIM 9647 P1
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7
11
In an experiment, 70 cm3 of water at 25C was brought to boiling point by burning

butane in excess oxygen. Given that the standard enthalpy change of combustion of
butane is 2877 kJ mol1, calculate the volume of butane needed if this process is only
85% efficient.
Assume that the specific heat capacity of water is 4.2 J g1 K1 and that 1 mole of gas
occupies 24 dm3 under the given conditions.
A
12
13
0.0721 dm3
0.156 dm3
0.184 dm3
0.216 dm3
Which of the following changes does not alter the Eq value measured for a Cl2/Cl halfcell that is under standard conditions?
A
Adding water into the half-cell.
Placing the half-cell in an ice bath.
Adding copper(II) ions into the half-cell.
Introducing an inert gas into the half-cell at a pressure of 1 atm through a

separate inlet from the Cl2 gas inlet.
Which statement concerning the chlorine-containing compounds of elements in the third

period, sodium to argon, is correct?
A
NaCl dissolves easily in water due to favourable ion-dipole interactions and the
compound with the highest electrical conductivity in molten state is AlCl3.
PCl3 and Cl2O7 are both acidic in nature due to hydration of the compounds in
water.
The low boiling points of PCl3 and Cl2O7 are due to the weak bond energies
involved in the P-Cl bonds and the Cl-O bonds.
The different oxidation states of chlorine in NaCl and Cl2O7 are due to the relative
electronegativities of the pairing element and chlorine.
SRJC PRELIM 9647 P1
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8
14
The diagram represents the melting points of four consecutive elements in the third
period of the Periodic Table.
melting point / K
proton number
The sketches below represent another two properties of the elements.

property K
property J
proton number
proton number
What are properties J and K?
property J
property K
third ionisation energy
electronegativity
number of valence electrons
boiling point
ionic radius
nuclear charge
electrical conductivity
atomic radius
SRJC PRELIM 9647 P1
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9
15
16
17
Which of the following is true about the thermal decomposition of magnesium nitrate?
A
Sodium nitrate is thermally unstable as compared to magnesium nitrate.
Every 1 mol of magnesium nitrate burnt gives 2.5 mol of gaseous products.
The decomposition temperature of magnesium nitrate is higher than that of

barium nitrate.
The solid product of the thermal decomposition of magnesium nitrate readily

dissolves in water to give an alkaline solution.
Which of the following gives the best description of the reactions of Group II metals and
their compounds?
A
All Group II metals react with steam to give hydrogen gas.
Barium oxide is stored in oil due to its explosive reaction with oxygen gas in air.
All Group II oxides undergo neutralisation with hot acids to give a salt and water.
Beryllium hydroxide is amphoteric due to the high charge density of the Be2+ ion.
The table below shows the results of experiments in which the halogens, P2, Q2 and R2
were added to separate aqueous solutions containing P, Q and R ions.
P (aq)
Q (aq)
R (aq)
P2
no reaction
no reaction
R2 formed
Q2
P2 formed
no reaction
R2 formed
R2
no reaction
no reaction
no reaction
In which sequence is the solubility of the silver halides in aqueous ammonia arranged in
increasing order?
A
AgP < AgQ < AgR
AgQ < AgP < AgR
AgQ < AgR < AgP
AgR < AgP < AgQ
SRJC PRELIM 9647 P1
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10
18
Aqueous sodium hydroxide was added to a pale green solution of a mixture of two
metal cations. The resulting precipitate was treated with excess ammonia solution
giving an intense deep blue mixture. The mixture was filtered giving a reddish-brown
residue and a deep blue filtrate. The residue was washed with deionised water and
treated with excess acidified ammonium thiocyanate giving a blood red solution.
Which of the following substances best explains these observations?
reddishbrown residue
19
20
deep blue filtrate
Fe(OH)2
Cu(OH)2
Fe(OH)3
[Cu(NH3)4]
Fe(OH)2
[Cu(H2O)6]
Fe(OH)3
[Cu(NH3)4]
bloodred solution
[Fe(H2O)6]
2+
[Fe(H2O)6]
2+
2+
3+
[Fe(H2O)5SCN]
2+
[Fe(H2O)5SCN]
2+
2+
Rhodium and its compounds are used as catalysts in many important reactions. Which
of the following properties makes rhodium a suitable heterogeneous catalyst?
A
Rhodium has vacant d orbitals of suitable energy.
Rhodium exhibits variable oxidation states.
Rhodium is able to form stable complexes.
Rhodium is able to form coloured compounds.
Compound S was used in the following synthesis route.
COCH
CH2
HCN,
trace KCN
Compound T
Br2 (aq)
Compound U
Compound S
What are the respective numbers of sp, sp2 and sp3 hybridised carbon atoms in
compound U?
A
0, 6, 4
1, 6, 3
0, 7, 3
1, 7, 2
SRJC PRELIM 9647 P1
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11
21
Carvone is the main active ingredient found in spearmint and has the following
structure.
Carvone
Carvone can be reduced to compound V by heating with hydrogen gas in the presence
of nickel.
How many stereoisomers do the molecules of carvone and V each have?
Carvone
22
23
Compound V
How many alcohols (including both structural isomers and stereoisomers) can have the
molecular formula C4H10O?
A
A sample of ethene was added to a solution of Br2 (aq) and NaCl (aq). Which of the
following products is not likely to be found in the reaction mixture?
A
CH2(OH)CH2Br
CH2(OH)CH2Cl
CH2BrCH2Cl
CH2BrCH2Br
SRJC PRELIM 9647 P1
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12
24
Hydrocortisone is a steroid hormone produced by the adrenal gland and is released in

response to stress. It is commonly used as an active ingredient in anti-inflammatory
creams.
O
HO
OH
HO
H
Hydrocortisone
Which of the following statements about hydrocortisone is true?

A
When treated with an excess of hot concentrated acidified KMnO4, it forms a

compound containing seven carbonyl groups.
When warmed with aqueous alkaline iodine, a yellow precipitate is observed.
When treated with cold dilute KMnO4, it forms a compound containing two
hydroxy groups.
When treated with NaBH4 in the presence of methanol, it forms a compound

containing five hydroxy groups.
SRJC PRELIM 9647 P1
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13
25
Deuterium, D, is an isotope of hydrogen, 1 H .
OH
HO
OH
HO
OH
Which of the following is the product formed when the above compound reacts with hot
K2Cr2O7 in aqueous D2SO4 under controlled conditions?
A
OH
OH
CHO
CDO
O
OH
OH
HO
OH
OD
DO
COOH
HO
26
COOD
DO
OH
OD
Which of the following shows the correct sequence in order of increasing ease of
hydrolysis for the compounds below?
Cl
Cl
X
X<W<Y<Z
Z<X<W<Y
Z<Y<X<W
W<X<Y<Z
SRJC PRELIM 9647 P1
Br
Y
COCl
Z
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14
27
Which of the following statements about compound A is true?
OH
O
Cl
OH
OH
Compound A
28
When treated with alkaline Tollens reagent, it forms a compound with molecular
formula, C15H13O5Cl.
When reacted with PCl5, 1 mole of HCl (g) is formed.
When heated with H2 (g) in the presence of Ni catalyst, it forms a compound

containing three hydroxy groups.
When treated with sodium hydroxide, hydrolysis occurs.
What is the ratio of sodium iodide formed when each of the three compounds reacts
with alkaline aqueous iodine?
OH
A
1:1:1
5:0:6
5:0:3
1:1:2
SRJC PRELIM 9647 P1
OH
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15
29
Compound B can be converted to compound C as shown below.
O
CH2CH2OH
OH
O
Y
II
III
Compound B
Compound C
Which of the following statements is correct with regards to the given reaction scheme?
30
Step I may involve the use of PCl5.
Step I may involve the use of hot acidified potassium manganate(VII).
Step III may involve the use of aqueous sodium hydroxide.
Step III may involve the use of hot concentrated sulfuric acid.
A polypeptide was partially hydrolysed using two different enzymes and the fragments
were separated. Analysis of the fragments gave the following results:
Using enzyme D:
glu-val-phe
glu-asp-leu
ala-ser
val-ala
Using enzyme E:
val-phe
ala-glu-asp
val
ser-glu
leu-ala
What is the amino acid sequence of the polypeptide?
A
leu-ala-ser-glu-val-phe-val-ala-glu-asp
ala-glu-asp-leu-ala-ser-glu-val-phe-val
glu-val-phe-ala-glu-asp-leu-ala-ser-val
val-ala-glu-asp-leu-ala-ser-glu-val-phe
SRJC PRELIM 9647 P1
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16
Section B
For questions 31-40, one or more of the numbered statements 1 to 3 may be correct.
Decide whether each of the statements is or is not correct. The responses A to D should be
selected on the basis of:
A
1, 2 and 3
are correct
1 and 2 only
are correct
2 and 3 only
are correct
1 only
is correct

31
32
33
The compound ammonium sulfate is primarily used as a fertiliser for alkaline soils.
Which type(s) of bonding is/are found in the compound?
1
ionic
covalent
dative bond
The rate of reaction of a strip of magnesium ribbon and 45 cm3 of 1.5 mol dm3 HNO3 is
determined at 25 C. Which of the following cases would both conditions contribute to
an increase in the rate of reaction?
1
Mg powder and 90 cm3 of 1.5 mol dm3 HNO3
45 cm3 of 2.0 mol dm3 HNO3 at 35C
Which of the following statements is/are correct for the following equilibrium?
3H2 (g) + N2 (g)
DH < 0
2NH3 (g)
Condition
Position of
equilibrium
Kp
Rate of
formation of NH3
Right
No change
Increase
Decrease in temperature
Right
Increase
Decrease
Left
No change
Increase
SRJC PRELIM 9647 P1
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17
34
35
1, 2 and 3
are correct
1 and 2 only
are correct
2 and 3 only
are correct
1 only
is correct
Which of the following indicators can be used for the titration between ethylamine and
hydrochloric acid?
Indicator
pH transition range
Naphtholphthalein
7.3 8.7
Congo red
3.0 5.0
Azolitmin
4.5 8.3
In which of the following pairs will compound I and compound II give the same number
of cis-trans isomers after reaction with hot ethanolic potassium hydroxide?
II
Br
Br
CH2CHCH3
Br
Br
CH2Br
CH3
Br
CH2Br
C CH2CH3
CH3
Br
CH2CH3
Br
BrCH2
C CH2CH2Br
H
36
Which of the following processes lead(s) to an increase in entropy?

1
Diffusion of CFCs into the stratosphere.
Combustion of a piece of charcoal to form CO2 (g) and H2O (g).
Desalination of sea water by reverse osmosis (solvent passes from a more

concentrated solution to a more dilute solution).
SRJC PRELIM 9647 P1
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18
37
1, 2 and 3
are correct
1 and 2 only
are correct
2 and 3 only
are correct
1 only
is correct
The diagram shows the structure of salicylic acid:

COOH
OH
salicylic acid
Which compound(s) give(s) salicylic acid on acidic hydrolysis?
1
CO2CH3
OCOCH3
CONH2
Cl
COCl
CN
SRJC PRELIM 9647 P1
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19
38
1, 2 and 3
are correct
1 and 2 only
are correct
2 and 3 only
are correct
1 only
is correct
In which of the following sequences does the value of pKb decrease?

1
NH2
NH2
CH2NH2
NO2
CH3
CH3CHCH2NH2 CH2CH2CH2NH2
OH
, OH
COOH
CH3CH2CH2NH2
OH
COOH
Cl
Cl
Cl
39

A student set up an electrolytic cell for the purpose of purifying copper metal. However,
the set-up did not lead to successful purification of copper.
Which of the following could explain the failure of the set-up?
40
The electrolyte used was aqueous chromium(III) chloride.
The impure copper was used as the cathode and the anode was made of pure
copper metal.
The Eqcell for the reaction is a negative value.
Vanadium has the electronic structure 1s22s22p63s23p63d34s2. Which of the following

vanadium compounds is/are likely to exist?
1
V2O5
VOCl
K2V2O7
END
SRJC PRELIM 9647 P1
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20
BLANK PAGE
BLANK PAGE
SRJC PRELIM 9647 P1
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Higher 2
Candidate Name
Class
CHEMISTRY
9647/01
24 August 2012
1 hour
Data Booklet
Optical Mark Sheet (OMS)

On the separate multiple choice OMS given, write your name, FIN/NRIC and class in the
spaces provided.
Shade correctly your class and FIN/NRIC number.
Eg. If your NRIC is S9306660Z, shade S9306660Z for the item index number.
There are forty questions in this paper. Answer all questions.
For each question there are four possible answers A, B, C and D.
Choose the one you consider correct and record your choice using a soft pencil on the
separate OMS.
Each correct answer will score one mark.
A mark will not be deducted for a wrong answer.
You are advised to fill in the OMS as you go along; no additional time will be given for the
transfer of answers once the examination has ended.
Any rough working should be done in this question paper.
Section A
Answer all questions
1
To determine the percentage of nitrogen present in a snack, 1.0 g of the snack was
boiled with concentrated sulphuric acid to convert all the nitrogen into ammonium
sulphate. The ammonium salt obtained was then boiled with excess aqueous sodium
hydroxide to liberate the ammonia, which was passed into 25.0 cm3 of 0.20 mol dm3
hydrochloric acid. The unreacted hydrochloric acid required 20.0 cm3 of 0.10 mol dm3
aqueous sodium hydroxide for complete neutralisation.
What is the percentage by mass of nitrogen in the snack?
A
2.8%
4.2%
7.2%
8.4%
Answer: B
25
20
Amt of NH3 =(
x 0.20) (
x 0.10) = 0.003 mol
1000
1000
2NH3 1(NH4)2SO4 2N
Mass of nitrogen in snack = 0.003 x 14.0 = 0.042 g
0.042
% by mass =
x 100 = 4.2%
1.0
In an experiment, 25.0 cm3 of 0.20 mol dm3 solution of K2AO4 reacted exactly with
25.0 cm3 of 0.10 mol dm3 aqueous sodium sulfate(IV). The half-equation for the
oxidation of the sulfate(IV) ion is shown below.
SO32 (aq) + H2O (l) SO42 (aq) + 2H+ (aq) + 2e
Calculate the final oxidation state of A.
A
+2
+3
+4
Answer: D
2K2AO4 SO32
No. of e gained by A in K2AO4 = No. of e lost by S in SO32 = 2e
2A6+ + 2e 2An+
12 2 = 2n
n = +5
+5
Two elements D and E have the following properties.
D and E form ionic compounds Na2D and Na2E respectively.

Element E forms EF6 molecules whereas D is not able to do so.
Which pair of electronic configurations for D and E is correct?

D
E
[He] 2s2 2p2
[Ne] 3s2 3p4
A
[He] 2s2 2p2
[Ne] 3s2 3p2
B
[He] 2s2 2p4
[Ne] 3s2 3p2
C
2
4
[He] 2s 2p
[Ne] 3s2 3p4
D
Answer: D
The diagram below shows liquid trichloromethane and liquid benzene flowing from
burettes 1 and 2 respectively.
Burette 1
Liquid
trichloromethane
Burette 2
Liquid Benzene
What would happen to the flow of the liquids trichloromethane and benzene when a
negatively-charged rod is brought near to each of them?
Liquid trichloromethane
Liquid benzene
A
Undeflected
B
Undeflected
C
Undeflected
Undeflected
D
Answer: C
Liquid trichloromethane is polar. The partial positive charge can be attracted by the
negatively charged rod.
Benzene is non-polar and does not have partial charges.
The value of pV is plotted against p for two gases, G and H, where p is the pressure
and V is the volume of the gas.
Gas G
pV
Gas H
2x
x
Which of the following could be the identities of the gases?

Gas G
Gas H
1 mol of SO2 at 25 C
1 mol of H2 at 25 C
Answer: D
Amount of gas H should be twice the amount of gas G.
According to the shape of the curves, gas G should be a less ideal gas than gas H.
During an inspection, a small spacecraft of capacity 20 m3 was connected to another of

capacity 50 m3. Before connection, the pressure inside the smaller craft was 40 atm
and that inside the larger one was 150 atm.
Given that all measurements were made at the same temperature, What is the
pressure of the system after the connection?
A
78 atm
95 atm
119 atm
Answer: C
pV (40)(20) 800
=
=
RT
RT
RT
pV (150)(50) 7500
Amt of gas in large spacecraft =
=
=
RT
RT
RT
800 + 7500 8300
total amt of moles of gas =
=
RT
RT
8300
RT
nRT
RT
Pressure in the combined arrangement =
=
= 119atm
(20 + 50)
V
Amt of gas in small spacecraft =
190 atm
In which of the following pairs of compounds will compound II have a higher boiling
point than compound I?
I
A
II
Cl
Br
CH3CH2CH2CH2CH3
C(CH3)4
CH3CH2CH2COOH
CH3CH2CH2OH
CH2Cl
C
CH3
CH2Cl
CH2Cl
C
CH2Cl
CH3
C
H
Answer: D
A: I has higher Mr than II and hence has more extensive intermolecular VDW forces of
attraction and a higher boiling point.
B: I is linear and II is branched and hence has more extensive intermolecular VDW
forces of attraction and a higher boiling point.
C: I has more extensive intermolecular hydrogen bonding than II and hence a higher
boiling point.
D: I is non-polar and has temporary dipole-induced dipole interactions while II is polar
and has permanent dipole-dipole interactions. Hence II has a higher boiling point.
The conversion of compound X into Z was exothermic and proceeded by two steps,
where Y was the intermediate. The steps involved were:
Step 1:
XY
Step 2:
YZ
It was found that Step 1 is the rate-determining step. Which diagram represents the
energy level diagram for the reaction?
Answer: A
Pure nitrosyl chloride, NOCl gas, was heated at 320C in a 2.0 dm3 vessel. At
equilibrium, 30% of the NOCl gas had dissociated according to the equation below and
the total pressure was P atm.
2NOCl (g)
2NO (g) + Cl2 (g)
What is value of the equilibrium constant, Kp?

17.9
Answer: C
41.7
2NOCl (g)
Initial partial
pressure/atm
Change in
partial
pressure /
atm
Equilibrium
partial
pressure /
atm
0.7x + 0.3x + 0.15x = p

x = 0.8696p
Kp =
(0.2609)(0.1304)2
(0.6087)2
= 0.01197
= 0.0120p
0.0120p
0.0130p
2NO (g) + Cl2 (g)
-0.3x
+0.3x
+0.15x
0.7x
0.3x
0.15x
0.6087p
0.2609p
0.1304p
10 The pH change when 0.100 mol dm-3 CH3COOH is added drop-wise to 10.0 cm3 of
0.100 mol dm-3 NaOH (aq) is shown below.
At which point on the graph does pH = pKa, where Ka is the acid dissociation constant of
the weak acid?
Answer: D
Regions C and D are where there is an excess of weak acid CH3COOH as well as the
salt CH3COO-Na+ that is formed. Hence, buffer region.
At Region D,
10
x 0.100 = 0.001 mol
1000
(20 - 10)
Amt of excess CH3COOH added =
x 0.100 = 0.001mol
1000
Amt of CH3COO-Na+ formed =
Amt of CH3COO-Na+ and CH3COOH is the same, hence this is the point where there is
maximum buffering capacity and pH = pKa.
11
In an experiment, 70 cm3 of water at 25C was brought to boiling point by burning

butane in excess oxygen. Given that the standard enthalpy change of combustion of
butane is -2877 kJ mol-1, calculate the volume of butane needed if this process is only
85% efficient.
Assume that the specific heat capacity of water is 4.2 J g-1 K-1 and that 1 mole of gas
occupies 24 dm3 under the given conditions.
A
0.0721 dm3
0.156 dm3
0.184 dm3
0.216 dm3
Answer: D
Since Q = mcT = 70 4.2 (100.0 - 25.0) = 22050 J
Apparent amount of heat absorbed by water, Q
85
Q (Actual amount of heat evolved by burning butane)
100
100
Actual amount of heat evolved, Q =
x 22050 = 25941 J
85
25941
Hc(CH3CH2CH2CH3) = = -2877 x 103
n
=
Amount of butane = 9.017 x 10-3 mol

Volume of butane = 9.017 x 10-3 x 24 = 0.216 dm3
12
Which of the following changes does not alter the Eq value measured for a Cl2/Cl- halfcell that is under standard conditions?
A
Adding water into the half-cell.
Placing the half-cell in an ice bath.
Adding copper(II) ions into the half-cell.
Introducing an inert gas into the half-cell at a pressure of 1 atm through a

separate inlet from the Cl2 gas inlet.
Answer: D
A: Dilution causes the concentration of Cl- ions to be lower than 1 mol dm-3.
B: The ice bath lowers the temperature of the half-cell to less than 298 K.
C: Cu2+ ions will form a complex with Cl- ions and lower the concentration of Cl- ions to
less than 1 mol dm-3.
D: Introducing an inert gas through a separate inlet does not affect the pressure of Cl2
gas hence doing so does not affect the Eq value of the half-cell.
13
Which statement concerning the chlorine-containing compounds of elements in the third

period, sodium to argon, is correct?
NaCl dissolves easily in water due to favourable ion-dipole interactions and the
compound with the highest electrical conductivity in molten state is AlCl3.
PCl3 and Cl2O7 are both acidic in nature due to hydration of the compounds in
water.
The low boiling points of PCl3 and Cl2O7 are due to the weak bond energies
involved in the P-Cl bonds and the Cl-O bonds.
The different oxidation states of chlorine in NaCl and Cl2O7 are due to the relative
electronegativities of the pairing element and chlorine.
Answer: D
A: AlCl3 is a simple molecular structure, it does not conduct electricity.
B: PCl3 and Cl2O7 are both acidic in nature due to hydrolysis of the compounds in
water.
C: The low boiling points of PCl3 and Cl2O7 are due to the weak intermolecular forces of
attraction present and not related to bond energy.
14
The diagram represents the melting points of four consecutive elements in the third
period of the Periodic Table.
melting point / K
proton number
The sketches below represent another two properties of the elements.

property K
property J
proton number
proton number
What are properties J and K?
property J
property K
third ionisation energy
electronegativity
number of valence electrons
boiling point
ionic radius
nuclear charge
electrical conductivity
atomic radius
Answer: A
15
Which of the following is true about the thermal decomposition of magnesium nitrate?
A
Sodium nitrate is thermally unstable as compared to magnesium nitrate.
Every 1 mole of magnesium nitrate burnt gives 2.5 moles of gaseous products.
The decomposition temperature of magnesium nitrate is higher than that of

barium nitrate.
The solid product of the thermal decomposition of magnesium nitrate readily

dissolves in water to give an alkaline solution.
Answer: B
A: Sodium nitrate is more thermally stable than magnesium nitrate due to the lower
charge density, and hence lower polarising power, of Na+ as compared to Mg2+, leading
to a smaller polarising effect on the NO3- electron cloud.
B: 2Mg(NO3)2 (s) 2MgO (s) + 4NO2 (g) + O2 (g)
C: The decomposition temperature of magnesium nitrate is lower than that of barium
nitrate due to the higher charge density, and hence greater polarising power, of Mg2+ as
compared to Ba2+, leading to a greater polarising effect on the NO3- electron cloud.
D: MgO (s) dissolves very slowly, if at all, in water.
16
Which of the following gives the best description of the reactions of Group II metals and
their compounds?
A
All Group II metals react with steam to give hydrogen gas.
Barium oxide is stored in oil due to its explosive reaction with oxygen gas in air.
All Group II oxides undergo neutralisation with hot acids to give a salt and water.
Beryllium hydroxide is amphoteric due to the high charge density of the Be2+ ion.
Answer: C
A: Be (s) does not react with steam.
B: Ba (s), not barium oxide, is explosive in air.
D: The acidic nature of Be(OH)2 can be explained by its high charge density but not its
basic nature.
17
The table below shows the results of experiments in which the halogens, P2, Q2 and R2
were added to separate aqueous solutions containing P, Q and R ions.
P (aq)
Q (aq)
R (aq)
P2
no reaction
no reaction
R2 formed
Q2
P2 formed
no reaction
R2 formed
R2
no reaction
no reaction
no reaction
In which sequence is the solubility of the silver halides in aqueous ammonia arranged in
increasing order?
A
AgP < AgQ < AgR
AgQ < AgP < AgR
AgQ < AgR < AgP
AgR < AgP < AgQ
Answer: D
From the table R2 is the weakest oxidising agent while Q2 is the strongest oxidising
agent.
A logical deduction means Q2 is chlorine, and R2 is iodine.
Solubility of silver halides in NH3 (aq) in increasing order is AgR, AgP and AgQ.
18
Aqueous sodium hydroxide was added to a pale green solution of a mixture of two
metal cations. The resulting precipitate was treated with excess ammonia solution
giving an intense deep blue mixture. The mixture was filtered giving a reddishbrown
residue and a deep blue filtrate. The residue was washed with deionised water and
treated with excess acidified ammonium thiocyanate giving a blood red solution.
Which of the following substances best explains these observations?
reddishbrown residue
deep blue filtrate
Fe(OH)2
Cu(OH)2
Fe(OH)3
[Cu(NH3)4]
Fe(OH)2
[Cu(H2O)6]
Fe(OH)3
[Cu(NH3)4]
Answer: D
bloodred solution
[Fe(H2O)6]
2+
2+
2+
[Fe(H2O)6]
2+
3+
[Fe(H2O)5SCN]
[Fe(H2O)5SCN]
2+
2+
19
Rhodium and its compounds are used as catalysts in many important reactions. Which
of the following properties makes rhodium a suitable heterogeneous catalyst?
A
Rhodium has vacant d-orbitals of suitable energy.
Rhodium exhibits variable oxidation states.
Rhodium is able to form stable complexes.
Rhodium is able to form coloured compounds.
Answer: A
The only answer to explain the feature of transition elements which allow them to
function as heterogeneous catalyst.
Statement B is more for homogeneous catalyst.
20
Compound S was used in the following synthesis route.
COCH
CH2
HCN,
trace KCN
Br2 (aq)
Compound U
Compound T
Compound S
What are the numbers of sp, sp2 and sp3 hybridised carbon atoms in compound U?
A
0, 6, 4
1, 6, 3
0, 7, 3
1, 7, 2
Answer: C
Compound U is
sp2
sp
sp2
sp2
C
C
sp2
sp2
sp3
sp3
CH CH2
OH Br
sp2
sp3
OH
21
Carvone is the main active ingredient found in spearmint and it has the following
structure:
Carvone
Carvone can be reduced to compound V by heating with hydrogen gas in the presence
of nickel.
How many stereoisomers do the molecules of carvone and V each have?
Carvone
Compound V
Answer: D
Carvone has one chiral carbon as shown:
hence is will have 21 = 2 optical isomers
Compound V has 3 chiral carbon as shown:
HO
hence is will have 23 = 8 optical isomers
22
How many alcohols (including both structural and stereoisomers) can have the
molecular formula C4H10O?
A
Answer: C
23
CH3CH2CH2CH2OH
CH3CH2CH(OH)CH3 (presence of chiral carbon 2 isomers)
CH3C(CH3)CH2OH
CH3C(CH3)(OH)CH3
A sample of ethene was added to a solution of Br2 (aq) and NaCl (aq). Which of the
following products is not likely to be found in the reaction mixture?
A
CH2(OH)CH2Br
CH2(OH)CH2Cl
CH2BrCH2Cl
CH2BrCH2Br
Answer: C
In the electrophilic substitution of ethane and Br2(aq), the first step is:
H
C
d+
Br
dBr
H H
slow
H C+ C H
Br
carbocation
intermediate
Hence, the product must contain at least one Br.
24
Hydrocortisone is a steroid hormone produced by the adrenal gland and is released in

response to stress. It is commonly used as an active ingredient in anti-inflammatory
creams.
O
HO
OH
HO
H
Hydrocortisone
Which of the following statement about hydrocortisone is true?

A
When treated with an excess of hot concentrated acidified KMnO4, it forms a

compound containing 7 carbonyl groups.
When warmed with aqueous alkaline iodine, a yellow precipitate is observed.
When treated with cold dilute KMnO4, it forms a compound containing 2 hydroxy
groups.
When treated with NaBH4 in the presence of methanol, it forms a compound

containing 5 hydroxy groups.
Answer: D
Ketone undergoes reduction to form:
HO
HO
OH
OH
H
H
HO
A: C=C, primary and secondary alcohol undergo oxidation to form a compound with 4
carbonyl groups.
B: No CH3CO- or -CH(CH3)(OH) group observed.
C: Only alkene undergoes mild oxidation to form a diol, a compound with 5 hydroxy
groups is formed.
25
Deuterium, D, is an isotope of hydrogen, 1 H .
OH
HO
OH
HO
OH
Which of the following is the product formed when the above compound reacts with hot
K2Cr2O7 in aqueous D2SO4 under controlled conditions?
A
OH
OH
CDO
O
CHO
O
OH
OH
HO
OH
OD
DO
COOD
COOH
HO
DO
OH
OD
Answer: C
26
Which of the following shows the correct sequence in order of increasing ease of
hydrolysis for the compounds below?
Cl
W
Cl
X
X<W<Y<Z
Z<X<W<Y
Z<Y<X<W
Br
Y
COCl
Z
W<X<Y<Z
D
Answer: A
Acyl chloride, Z undergoes hydrolysis readily at rtp.
Strength of C-X bond: C-Cl >C-Br
Ease of hydrolysis: R-Cl < R-Br
For X, presence of double bond strengthen C-Br bond making nucleophilic sub less
readily to happen.
27
Which of the following statement about compound A is true?
OH
O
Cl
OH
OH
Compound A
When treated with alkaline Tollens reagent, it forms a compound with molecular
formula, C15H13O5Cl.
When reacted with PCl5, 1 mole of HCl (g) are formed.
When heated with H2 (g) in the presence of Ni catalyst, it forms a compound

containing 3 hydroxy groups.
When treated with sodium hydroxide, hydrolysis occurred.
Answer: B
A: Compound with formula, C15H11O5Cl is formed as phenol undergoes neutralisation
with alkaline Tollens reagent.
B: Only 1 mole of HCl(g) is formed as phenol do not react with PCl5
C: After reduction of ketone and C=C, a compound containing 5 hydroxy groups is
formed.
D: Neutralisation occurred not hydrolysis.
28
What is the ratio of sodium iodide formed when each of the three compounds reacts
with alkaline aqueous iodine?
OH
A
1:1:1
5:0:6
5:0:3
1:1:2
Answer: B
OH
29
Compound B can be converted to compound C as shown below.
O
CH2CH2OH
OH
O
Y
II
III
Compound B
Compound C
Which of the following statements is correct with regards to the given reaction scheme?
A
Step I may involve the use of PCl5.
Step I may involve the use of hot acidified potassium manganate(VII).
Step III may involve the use of aqueous sodium hydroxide.
Step III may involve the use of hot concentrated sulfuric acid.
Answer: C
Compound C
O
Compound B
CH2CH2OH
CH2COOH
OH
CH2COCl
OH
OH
II
Step I: hot, acidified K2Cr2O7

Step II: PCl5, rtp
Step III: NaOH (aq), rtp (to form phenoxide)
III
30
A polypeptide, was partially hydrolysed using two different enzymes and the fragments
were separated. Analysis of the fragments gave the following results:
Using enzyme D:
glu-val-phe
glu-asp-leu
ala-ser
val-ala
Using enzyme E:
val-phe
ala-glu-asp
val
ser-glu
leu-ala
What is the amino acid sequence of the polypeptide?
A
leu-ala-ser-glu-val-phe-val-ala-glu-asp
ala-glu-asp-leu-ala-ser-glu-val-phe-val
glu-val-phe-ala-glu-asp-leu-ala-ser-val
val-ala-glu-asp-leu-ala-ser-glu-val-phe
Answer: D
Section B
For questions 31-40, one or more of the numbered statements 1 to 3 may be correct.
Decide whether each of the statements is or is not correct. The responses A to D should be
selected on the basis of:
A
1, 2 and 3
are correct
1 and 2 only
are correct
2 and 3 only
are correct
1 only
is correct

31
The compound ammonium sulfate is primarily used as a fertiliser for alkaline soils.
Which type(s) of bonding is/are found in the compound?
1
ionic
covalent
dative bond
Answer: A (1, 2 and 3)
2
H
32
N H
H
O
O
2-
S O
O
The rate of reaction of a strip of magnesium ribbon and 45 cm3 of 1.5 mol dm3 HNO3 is
determined at 25C. Which of the following cases would both conditions contribute to
an increase in the rate of reaction?
1
45 cm3 of 2.0 mol dm3 HNO3 at 35C
Answer: C (2 and 3 only)

1: Use of Mg powder increases rate of reaction due to increase in surface area of
reaction but increase in volume does not increase rate of reaction.
2: Use of Mg powder increases rate of reaction due to increase in surface area of
reaction and increase in concentration of HNO3 increases rate of reaction due to
increase in effective collisions.
3: Increase in concentration and temperature increases rate of reaction due to increase
in effective collisions.
33
Which of the following statements is/are correct for the following equilibrium?
3H2 (g) + N2 (g)
DH < 0
2NH3 (g)
Condition
Position of
equilibrium
Kp
Rate of
formation of NH3
Right
No change
Increase
Right
Increase
Decrease
Left
No change
Increase
Answer: B (1 and 2 only)
Condition
1
Increase in
pressure
Decrease in
temperature
Addition of
catalyst
Position of
equilibrium
Kp
Rate of forward reaction
Right ()
No change ()
Increase ()
Position of eqm
will shift to
decrease amt of
gases.
Kp is
independent of
pressure
results in increase number
of effective collisions.
Right ()
Increase ()
Decrease ()
Position of eqm
will shift to
forward
exothermic
reaction.
Forward rate
constant will
decrease less
than backward
rate constant,
hence Kp
increases
leads to lower kinetic
energy and decrease in
number of effective
collisions.
Left (x)
Increase (x)
Increase ()
Catalyst does
not affect eqm
position
Kp is
independent of
catalyst
Catalyst increases rate of

reaction.
34
Which of the following indicators can be used for the titration between ethylamine and
hydrochloric acid?
Indicator
pH transition range
Naphtholphthalein
7.3 8.7
Congo red
3.0 5.0
Azolitmin
4.5 8.3
Answer: C (2 and 3 only)

For the titration between ethylamine and hydrochloric acid, it is a strong acid/weak base
titration. Hence, at equivalence point of titration, pH increases sharply from 3 to 7.
Only Congo red and Azolitmin pH transition range) lies within the rapid pH change ( 3
to 7) over the equivalence point
35
In which of the following pairs will compound I and compound II give the same number
of cis-trans isomers after reaction with hot ethanolic potassium hydroxide?
II
Br
Br
CH2CHCH3
Br
Br
CH2Br
CH3
Br
CH2Br
C CH2CH3
CH3
Br
CH2CH3
Br
BrCH2
C CH2CH2Br
H
Answer: A (1, 2 and 3)

Pair 1 both give 2 cis-trans isomers.
Pair 2 and 3 both give 0 cis-trans isomers.
36
Which of the following processes lead(s) to an increase in entropy?

1
Diffusion of CFCs into the stratosphere.
Combustion of a piece of charcoal to form CO2 (g) and H2O (g).
Desalination of sea water by reverse osmosis (solvent passes from a more

concentrated solution to a more dilute solution).

For option 3, there is an increase in orderliness as the solvent passes from a more
concentrated solution to a more diluted solution. Hence, entropy will decrease.
37
The diagram shows the structure of salicylic acid:

COOH
OH
salicylic acid
Which compound(s) give(s) salicylic acid on acidic hydrolysis?
1
CO2CH3
OCOCH3
CONH2
Cl
COCl
CN
Answer: D (1 only)
2: Halogenoarenes do not undergo nucleophilic substitution.
COOH
COOH
3:
will be formed instead.
38
In which of the following sequences does the value of pKb decrease?

1
NH2
NH2
CH2NH2
NO2
CH3
OH
, OH
COOH
OH
COOH
Cl
Cl
Cl
CH3CH2CH2NH2
Answer: B (1 and 2)
pKb decreases means weakest base to strongest base or strongest acid to

weakest acid.
NH2
NH2
CH2NH2
1:
NO2
CH3
The electron donating alkyl group increases the availability of the lone pair of
CH2NH2
electrons on N atom to accept a proton via a dative bond. Hence,

the strongest base.
is
4-methylphenylamine is a stronger base than 4-nitrophenylamine.

The presence of the electron-donating methyl group in 4-methylphenylamine
reduces the delocalization of the lone pair of electrons on N into benzene ring.
This increases the availability of lone pair of electrons to accept a proton via
dative bond.
2:
OH
, OH
CH3CH2CH2NH2
The electron donating alkyl group increases the availability of the lone pair of
electrons on N atom to accept a proton via a dative bond. Hence,
CH3CH2CH2NH2
is the strongest base.
Proximity of withdrawing OH substituent to NH2 group:

CH3CHCH2NH2
OH
CH2CH2CH2NH2
>
OH
CH3CHCH2NH2
CH2CH2CH2NH2
OH
Electron withdrawing effect:
> OH
Availability of the lone pair of electrons on N atom to accept a proton via a
CH3CHCH2NH2
CH2CH2CH2NH2
dative bond:
>
OH
OH
CH3CHCH2NH2
CH2CH2CH2NH2
Strength of base:
OH
>
OH
3: The order of the acidity is already incorrect to begin.
39

A student set up an electrolytic cell for the purpose of purifying copper metal. However,
the set-up did not lead to successful purification of copper.
Which of the following could explain the failure of the set-up?
The electrolyte used was aqueous chromium(III) chloride.
The impure copper was used as the cathode and the anode was made of pure
copper metal.
The Eqcell for the reaction is a negative value.

1: Chromium metal would be deposited on the cathode before copper metal, hence
leading to the failure of the purification of copper.
2: Impure copper should be the anode and the cathode should be pure copper metal.
When the polarities are switched, the pure copper anode would be oxidised and copper
metal would be deposited on the impure copper cathode, leading to the failure of the
purification of copper.
3: Even if Eqcell is a negative value, the reaction can still occur because electricity is the
source of energy for a chemical reaction to take place in an electrolytic cell.
40
Vanadium has the electronic structure 1s22s22p63s23p63d34s2. Which of the following

vanadium compounds is/are likely to exist?
1
V2O5
VOCl
K2V2O7

Oxidation of Vanadium in V2O72- is expected to be 6 which is not possible.

Higher 2
CANDIDATE
NAME
CLASS
CHEMISTRY
9647/02
Paper 2 Structured Questions (SPA)
17 August 2012
2 hours
Data Booklet

You may use a soft pencil for any diagrams, graphs or rough work.
The number of marks is given in the brackets [ ] at the end of each question or part questions.
For Examiners Use
/40
P1
P2
/72
P3
/80
GRAND
TOTAL
%
/192
For Examiners Use

/12
1(P)
2
/8
/18
/10
/12
6 (P)
/12
GRADE
TOTAL
P2
/72
This document consist of 16 printed pages and 0 blank page

SRJC PRELIM 9647 P2
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2
1
(a)
For
Planning
In the presence of hydrogen ions, bromate(V) ions, BrO3 , oxidise bromide ions to Examiners
Use
bromine.
BrO3 (aq) + 5Br (aq) + 6H+ (aq) 3Br2 (aq) + 3H2O (l)
The reaction is relatively slow and can be followed by adding aqueous phenol and
the indicator methyl orange to the reaction mixture. As bromine is formed, it reacts
rapidly with the phenol present until the latter is used up. The free bromine in
solution now bleaches the methyl orange indicator.
The initial rate of the reaction can be investigated by measuring the time taken for
the methyl orange indicator to be bleached.
You are to plan a series of experiments to determine the order of reaction with
respect to the bromide ion.
In addition to the standard apparatus present in a laboratory, you are provided with
the following:
FA 1 0.01 mol dm 3 aqueous KBr.
FA 2 1.0 mol dm 3 potassium bromate(V), KBrO3.
FA 3 1.0 mol dm 3 sulfuric acid, H2SO4.
Aqueous phenol containing methyl orange indicator
Distilled water
(i) Complete the table below and outline, by means of a series of numbered steps,
the apparatus to be used
the experimental procedure
the measurements to be taken to collect the required data.
Expt
.
Volume of
phenol/methyl
orange
indicator
solution / cm3
Volume of
FA1 / cm3
Volume of
FA2 / cm3
Volume of
FA3 / cm3
Volume of
distilled
water / cm3
20.0
50.0
50.0
20.0
0.0
20.0
40.0
20.0
30.0
20.0
20.0
20.0
10.0
SRJC PRELIM 9647 P2
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3
Outline of experiment:
.
For
Examiners
Use
.
.
.
...
...
...
...
....
....
(ii)
In order to find the order of reaction with respect to bromide, a graph of log10( )
t
against log10(volume of KBr (aq)) can be plotted. Use the general rate equation to
1
derive a relationship between log10( ) and log10(volume of KBr (aq)). Hence, explain
t
how the order of reaction with respect to bromide can be found from the plotted
graph.
(iii)
The concentration of phenol used in the experiment is very low. Suggest why this is
so.
[7]
SRJC PRELIM 9647 P2
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4
(b)
An experiment was carried out to measure the enthalpy change for the reaction of For
Examiners
zinc with aqueous copper(II) sulfate.
Use
Zn (s) + CuSO4 (aq) ZnSO4 (aq) + Cu (s)
A measuring cylinder was used to transfer separate 50 cm3 samples of

1.25 mol dm-3 copper(II) sulfate solution into polystyrene cups.
Different weighed amounts of zinc powder were added to each sample of
copper(II) sulfate.
Each mixture was stirred thoroughly and the temperature rise noted.
The results of the experiment is summarised on the graph below.

70.0
60.0
50.0
DT/ oC
40.0
30.0
20.0
10.0
0.0
(i)
0.00
1.00
2.00 3.00 4.00 5.00 6.00 7.00

Mass of zinc / g
Explain the shape of the graph.
(ii)
Using the data from the graph, calculate the Hreaction.
(iii)
Suggest a simple practical change to the method that will make the
experiment more accurate.
.
.
[5]
Total 12 marks
SRJC PRELIM 9647 P2
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5
2
(a)
Pyruvic acid is an important component in living cells as it is involved in the aerobic For
process of supplying energy. The flow chart shows a series of reactions starting Examiners
Use
with compound A, which has an empirical formula of CH2.
A
H2O /
Cr2O72- / H+
distilation
H+
Ethanal
HCN, NaCN, cold
H+, heat
C
O
CH3CCOOH
Pyruvic acid
II
Ethanedioic acid
(i)
Draw the structures of compounds A, B and C in the boxes above.
(ii)
State the reagents and conditions for steps I and II.

Step I: .
Step II:
[5]
SRJC PRELIM 9647 P2
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6
(b)
Element D can form two different chlorides. The two chlorides of element D is For
commonly used in Organic Chemistry qualitative analysis to test for a specific Examiners
Use
functional group. When dissolved in a solution containing methyl orange, chlorides
of element D turn the solution red.
10 cm3 of liquid organic compound E, CnH2n+2O, is vaporised and burnt in
excess oxygen. After the reaction is cooled to 25oC, a contraction of
20 cm3 in the gas volume was observed. When the resultant gases from the
combustion were passed through aqueous sodium hydroxide, the gas volume
decreased a further 20 cm3. The vapour of E is also observed to react with the
same reagents and conditions of step II mentioned in (a).
(i)
State the identities of element D and organic compound E.

D: ..
E: .
(ii)
Hence write an equation, if any, between one of the chlorides of element D

and organic compound E.
.
[3]
Total 8 marks
SRJC PRELIM 9647 P2
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7
3
(a)
(i)
Both strontium and manganese are silvery metals. Complete the electronic For
Examiners
configurations of manganese and strontium below.
Use
Mn: [Ar]
Sr: [Kr] .
(ii)
Manganese and strontium both contribute two electrons into the sea of
delocalised electrons.
Explain if strontium or manganese has a higher melting point.
.
.
.
.
(iii)
Manganese is particularly important in the manufacturing of stainless steel. A

reaction scheme involving manganese-containing compounds is shown
below. F undergoes a reaction to form G and H.
Solution F containing Mnn+
Mn in stainless steel
Nitric acid
Pale pink solution G

FeCl2
Purple
solution J
Black/brown
solid H
NaOH + O2
Na2FeO4
Green
crystal K
Using the information provided, state the oxidation number of manganese in

F and K. (Manganese and its compounds have different oxidation states).
.
(iv)
Suggest a chemical formula for the purple solution J.

.
SRJC PRELIM 9647 P2
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8
(v)
Suggest the type of reaction that takes place when F forms G and H.
Write a balanced chemical equation, including state symbols, for this reaction.
For
Examiners
Use
.
.
.
[10]
(b)
Strontium compounds such as SrF2 and SrSO4 are sparingly soluble in water. Their
solubility products at 298 K are given in the table below:
Strontium compound
Numerical value of Ksp
SrF2
2.5 x 10 9
SrSO4
3.2 x 10 7
(i)
Suggest, using quantitative calculations, which of the two compounds is less

soluble in water at 298 K.
(ii)
A sample of strontium(II) fluoride is dissolved in a solution of sodium fluoride.

Predict qualitatively the effect, if any, on the solubility and solubility product of
strontium(II) fluoride.
[4]
SRJC PRELIM 9647 P2
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9
(c)
Propose chemical test(s) to differentiate between the following organic compounds.

You are to state clearly in your answer the reagents and conditions used and
observations made. Write chemical equation(s) for any reactions that occur.
O
H 2N
For
Examiners
Use
O
N
and
[4]
Total 18 marks
SRJC PRELIM 9647 P2
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10
4(a)
Amino acids serve as the building blocks of proteins. They can be linked together in For
varying sequences to form a vast variety of proteins. An example of a segment of a Examiners
Use
protein is shown below.
O H H
O H H O
N
C C N C
CH2
C C N
(CH2)2
COOH
OH
(i)
In the space provided below, draw the structural formulae of the amino acids
formed from the hydrolysis of the above protein with aqueous sodium hydroxide.
(ii)
Amino acids can be separated using electrophoresis. With reference to the

isoelectric point of the amino acids provided, indicate the positions of the amino
acids on the gel at a pH of 5.96.
Amino acid
Structure
Isoelectric point
O H
Aspartic acid
HO C C
H C
2.77
NH2
H
COOH
Proline
HO C
Valine
H
H 2N C C
CH3
C H
6.30
5.96
OH
CH3
Anode
SRJC PRELIM 9647 P2
Cathode
Turn Over]
11
(iii)
A common secondary structure of proteins is the alpha helix. With the aid of a For
diagram and your knowledge in chemical bonding, describe the alpha helix Examiners
Use
structure.
[7]
(b)
(i)
Methamphetamine, C10H15N, is a psychostimulant. It has high potential for abuse

and addiction. In high doses, it can induce euphoria and anxiety. Under the
Misuse
of
Drugs
Act
in
Singapore,
a
person
who
carries
500 grams of methamphetamine will be sentenced to the Mandatory Death
Penalty. Its structure is as shown:
H
N
Methamphetamine
A 25.0 cm3 sample of 0.500 mol dm3 methamphetamine was titrated with
aqueous hydrochloric acid of the same concentration.
Would you expect the pH at equivalence point to be above or below 7? Explain
your answer.
.
.
(ii)
State the formula of the organic product formed when methamphetamine was
reacted with sulfuric acid instead of hydrochloric acid.
[3]
Total 10 marks
SRJC PRELIM 9647 P2
Turn Over]
12
5
Elements L to S are consecutive Period 3 elements with proton number less than 20. The For
Examiners
following graph shows the third ionisation energies of these elements.
Use
[L to S are not specific elements from the Periodic Table].
3rd Ionisation Energy / kJ mol
-1
lg 9000
(3rd I.E.)
8000
7000
6000
5000
4000
3000
2000
1000
0
A
(a)
Elements
Identify the group that element P belongs to.

..
[1]
(b)
Sketch a graph to show the successive ionisation energies of element P when the
first eight electrons are removed from it.
lg I.E.
No of
electrons
removed
1
SRJC PRELIM 9647 P2
[1]
Turn Over]
13
(c)
Explain the drop in the third ionisation energy from N to P.

.
For
Examiners
Use
[2]
(d)
Write down the equations for the reactions of the oxide of M with aqueous
hydrochloric acid and aqueous sodium hydroxides separately.
.
[2]
(e)
Describe the reactions, if any, of the chlorides of M and P with water, suggesting the
pH of the resulting solutions and writing equations where appropriate.
.
..
.
.
.
.
.
[6]
Total 12 marks
SRJC PRELIM 9647 P2
Turn Over]
14
6
(a)
Nitrogen monoxide in the air can be converted to nitric acid, which results in acid rain. For
Both nitrogen monoxide and nitrogen dioxide participate in ozone layer depletion. One Examiners
Use
way of forming nitrogen monoxide is through the dissociation of nitrogen dioxide.
2NO2 (g) 2NO (g) + O2 (g)
At 494 oC, the value of Kp for the above reaction is 36.9 kPa.
When a certain partial pressure of nitrogen dioxide is put into an empty vessel at
494 oC, equilibrium is reached when 45% of the original nitrogen dioxide has
decomposed.
(i)
Write an expression for the equilibrium constant, Kp, for the reaction.
(ii)
Calculate the original partial pressure of nitrogen dioxide before any dissociation
occurred.
[3]
SRJC PRELIM 9647 P2
Turn Over]
15
(b) Draw the structural formula of the organic products formed when compound T reacts For
Examiners
with the following reagents.
Use
OH
OH
O
C
NH2
C CH2
CH3
OH
NH2
Compound T
(i)
Alkaline aqueous KMnO4, heat
(ii)
Br2 in CCl4, absence of UV light
[5]
SRJC PRELIM 9647 P2
Turn Over]
16
(c)
Compound U has the molecular formula C9H12O.

It reacts with chlorine gas in the presence of light to form compound V, C9H11OCl,
which is optically active.
For
Examiners
Use
On addition of bromine water at room temperature, U forms a white precipitate W,

C9H10OBr2.
When treated with acidified potassium manganate(VII) under reflux, U forms
compound X, C8H6O5. 1 mol of X reacts with 2 mol of thionyl chloride.
Draw the structures for compounds U to X.
[4]
Total 12 marks
END
SRJC PRELIM 9647 P2
Turn Over]

Higher 2
CHEMISTRY
9647/02
Paper 2 Structured Questions (SPA)
Suggested Solutions
1
(a)
Planning
In the presence of hydrogen ions, H+, bromate(V) ions, BrO3- , oxidise bromide
ions, Br, to bromine, Br2.
BrO3(aq) + 5Br (aq) + 6H+(aq) 3Br2(aq) + 3H2O(l)
The reaction is relatively slow and can be followed by adding aqueous phenol and
the indicator methyl orange to the reaction mixture. As bromine is formed, it reacts
rapidly with the phenol present until the latter is used up. The free bromine now in
solution bleaches the methyl orange indicator.
The initial rate of the reaction can be investigated by measuring the time taken to
bleach the methyl orange indicator.
You are to plan a series of experiments, to determine the order of reaction with
respect to the bromide ion.
In addition to the standard apparatus present in a laboratory, you are provided with
the following:
FA 1 0.01 mol dm-3 aqueous KBr.
FA 2 1.0 mol dm-3 potassium bromate(V), KBrO3.
FA 3 1.0 mol dm3 sulfuric acid, H2SO4.
Aqueous phenol containing methyl orange indicator
Distilled water
(i) Complete the table below and outline, by means of a series of numbered steps,
the apparatus to be used
the experimental procedure
the measurements to be taken, to collect the required data.
Expt
.
Volume of
phenol/methyl
orange
indicator
solution / cm3
Volume of
FA1 / cm3
Volume of
FA2 / cm3
Volume of
FA3 / cm3
Volume of
distilled
water / cm3
20.0
50.0
50.0
20.0
0.0
20.0
40.0
50.0
20.0
10.0
20.0
30.0
50.0
20.0
20.0
20.0
20.0
50.0
20.0
30.0
20.0
10.0
50.0
20.0
40.0
1. Using a measuring cylinder, add 20.0 cm3 of the phenol/indicator solution into a
clean, dry conical flask.
2. Using different measuring cylinders, place 50.0 cm3 of FA 1 and 20.0 cm3 of FA
3 into the conical flask.
3. Place the conical flask on a white tile.
4. From another measuring cylinder, measure 50.0 cm3 of FA 2.
5. Add FA 2 into the conical flask, simultaneously starting the stopwatch.
Swirl the conical flask carefully.
6. Stop the stopwatch when the colour of the indicator just disappears to leave a
colourless solution. Record the time taken.
7. Repeat procedure 1 to 6 for experiments 2 to 5.
(ii)
In order to find the order of reaction with respect to bromide, a graph of

1
log10( ) against log10(volume of KBr(aq)) can be plotted.

t
Use the rate equation to derive a relationship between log10( ) and

log10(volume of KBr(aq)).
Hence, explain how the order of reaction with respect to bromide can be
found from the plotted graph.
In these experiments, the total volume has been kept constant and only the
concentration of FA 1 in the reaction mixture has been changed. The rate
equation, where n is the rate order with respect to FA 1, can be simplified to
rate = k[Br-]n (where k = k[BrO3-]m[H+]n)
taking logarithms of the factors in this equation gives
lg(rate) = n lg ([Br-]) + lg (k)

Hence, by finding the gradient of the plotted graph, order of reaction wrt Brcan be found.
(iii)
The concentration of the phenol used in the experiment is very low. Suggest
why this is so.
[7]
If too much phenol was present, it is possible that the reaction could have
taken longer OR if a large amount of phenol was added the mixture may
not have decolourised at all as all the bromine formed would have
reacted with the phenol present.
(b)
An experiment was carried out to measure the enthalpy change for the reaction of
zinc with aqueous copper (II) sulfate.
Zn (s) + CuSO4 (aq) ZnSO4 (aq) + Cu (s)
A measuring cylinder was used to transfer separate 50 cm3 samples of 1.25

mol dm-3 copper (II) sulfate solution into polystyrene cups.
Different weighed amounts of zinc powder were added to each sample of
copper (II) sulfate.
Each mixture was stirred thoroughly and the temperature rise noted.
The results of the experiments are summarised on the graph below.

70.0
60.0
50.0
40.0
Temperature / oC
30.0
20.0
10.0
0.0
0.00
1.00
2.00 3.00 4.00 5.00 6.00 7.00

Mass of zinc / g
(i)
Explain why the graph shows an initial rise in temperature and then levels off.
(ii)
Initially CuSO4 in excess so amount of reaction depends on amount of Zn

Or more CuSO4 reacts (as more Zn added)
Graph levels off because all CuSO4 used up
(reject just Reaction is complete)
Using the data from the graph, calculate the Hreaction.
Q = 50 x 63.5 x 4.18 =13271.5 J
Amount of CuSO4 = 50 x
H = -
(iii)
13271.5
0.0625
1.25
1000
= 0.0625 mol
= - 212 x 103 J mol-1
Suggest a simple practical change to the method that will make the
experiment more accurate.
[5]
Use a lid on the cup (to reduce heat loss), extra insulation for cup,
weigh CuSO4 solution, use burette/pipette to measure volumes
(Reject Repeat experiments OR use more accurate balance OR Smaller
mass intervals)
Total 12 marks
(a)
Pyruvic acid is an important component in living cells as it is involved in the aerobic

process of supplying energy. The flow chart shows a series of reactions starting
with compound A, which has an empirical formula of CH2.
A
H2O /H+
Cr2O72- / H+,
distilation
Ethanal
HCN, NaCN, cold
H+, heat
C
O
I
CH3CCOOH
Pyruvic acid
II
Ethanedioic acid
(i)
Draw the structures of compounds A, B and C in the boxes above.
H
C C
CH3
C OH
CH3
CN
(ii)
C OH
COOH
State the reagents and conditions for Steps I and II.

[5]
Step I: methanolic NaBH4 or H2 nickel catalyst, heat or
H2 platinum, rtp
Step II: I2 (aq), NaOH (aq), warm, followed by H+(aq)
(b)
Element D can form two different chlorides. The two chlorides of element D is
commonly used in Organic Chemistry qualitative analysis to test for a specific
functional group. When dissolved in a solution containing methyl orange, chlorides
of element D turn the solution red.
10 cm3 of liquid organic compound E, CnH2n+2O, is vaporised and burnt in
excess oxygen. After the reaction is cooled to 25 oC, a contraction of
20 cm3 in the gas volume was observed. When the resultant gases from the
combustion was passed through aqueous sodium hydroxide, the gas volume
decreased a further 20 cm3. The vapour of E is also observed to react with the
same reagents and conditions of step II mentioned in (a).
(i)
State the identities of element D and organic compound E.

D is phosphorus.
E is ethanol.
(Since 10 cm3 of vapour E combusted to give 20 cm3 of CO2, by Avogadros
and volume ratio, n =2 C2H6O
(ii)
Hence, write an equation, if any, between one of the chlorides of element D

and organic compound E.
CH3CH2OH + PCl5 CH3CH2Cl + POCl3 + HCl
or
3CH3CH2OH + PCl3 3CH3CH2Cl + H3PO3
Total 8 marks
(a)
(i)
Both strontium and manganese are silvery metals. Write the electronic
configurations of manganese and strontium.
Mn: [Ar]3d54s2
Sr: [Kr]5s2
(ii)
Manganese and strontium both contribute two electrons into the sea of
delocalised electrons.
Suggest if strontium or manganese has a higher melting point.
Cationic radius of manganese is smaller as compared to strontium
ions.
Electrostatic forces of attraction b/w the cations and sea of
delocalised electrons(metallic bonding) is stronger in Mn than in Sr.
Thus more energy is required to overcome these forces of attraction. Mn
has a higher melting point than Sr.
(For your information m.p. of strontium is 777oC and manganese is
1246oC)
(iii)
Manganese is particularly important in the manufacturing of stainless steel.

Below shows a reaction schematic of manganese containing compounds.
F undergoes a reaction to form G and H.
Solution F containing Mnn+
Mn in stainless steel
Nitric acid
Pale Pink Solution G

FeCl2
Purple
solution J
Black/brown
solid H
KOH + O2
Na2FeO4
Green
crystal K
Using the information provided, state the oxidation number of manganese

in F and K. (All Mn and its compounds have different oxidation state).
F: +3
(iv)
K: +6
Suggest the formula of purple solution J.

NaMnO4
(v)
Suggest the type of reaction when F forms G and H.

Write a balanced chemical equation, including state symbols, for this
reaction.
[10]
Disproportionation reaction
Reduction: Mn3+ + e Mn2+
Oxidation: 2H2O + Mn3+ MnO2 + 4H+ + e
Overall: Mn3+ (aq) + 2H2O (l) Mn2+ (aq) + MnO2 (s) + 4H+ (aq)
(b)
Strontium compounds such as SrF2 and SrSO4 are sparingly soluble in water.
Their solubility products at 298 K are given in the table below:
(i)
Strontium compound
Numerical value of Ksp
SrF2
2.5 x 10-9
SrSO4
3.2 x 10-7
Suggest, using quantitative calculations, which of the two compounds is

less soluble in water at 298 K.
Sr2+ (aq) + 2F- (aq)

SrF2 (s)
Ksp(SrF2) = [Sr2+][F-]2
2.5 x 10-9 = (s)(2s)2
s = 8.55 x 10-4 mol dm-3

SrSO4 (s)
Sr2+ (aq) + SO42- (aq)
Ksp(SrSO4) = [Sr2+][SO42-]
3.2 x 10-7 = (s)2
s = 5.66 x 10-4 mol dm-3
Based on the calculated solubilities, SrSO4 is less soluble than SrF2.
(ii)
A sample of strontium(II) fluoride is dissolved in a solution of sodium

fluoride. Predict qualitatively the effect (if any) on the solubility and
solubility product of strontium(II) fluoride.
[4]
Sr2+ (aq) + 2F- (aq)
SrF2 (s)
NaF (s)
Na+ (aq) + F- (aq)
There will be common ion effect due to the increase in [F-].

By Le Chateliers Principle, position of equilibrium will shift to the left to
decrease [F-]. The solubility of SrF2 is reduced.
The solubility product of SrF2 is not affected as it is only dependent on
temperature.
(c)
Propose chemical test(s) to differentiate the following organic compounds.

You are to state clearly in your answer the reagents and conditions used
and observations made. Write chemical equation(s) for any reactions that
have occurred.
H 2N
O
N
and
[4]
Test: Add NaOH (aq), heat

Observation:
O
H 2N
: effervescence
O
H
O
N
: No effervescence
Equation:
O
H 2N
O
H
O
+ 2 NaOH
O
N
O
O-Na+ + NH3
Na O
OH
H
C C C
+ 2NaOH
Na+O-
O
O-Na+
OH
(Test for NH3: Moist red litmus paper turns blue)

Total 18 marks
4(a)
Amino acids serve as the building blocks of proteins. They can be linked together in
varying sequences to form a vast variety of proteins. An example of a segment of a
protein is shown below.
O H H
O H H O
N
C C N C
C C N
(CH2)2
CH2
COOH
OH
(i)
In the space provided below, draw the structural formulae of the amino acids
formed from the hydrolysis of the above protein with aqueous sodium
hydroxide.
O H H
-
(ii)
O
-
O C C N H
O H H
O C
O C C N H
CH2
(CH2)2
OH
COO-
Amino acids from can be separated using electrophoresis. With reference to

the isoelectric point of the amino acids provided, indicate the positions of the
amino acid on the gel at a pH of 5.96.
Amino acid
Structure
Isoelectric point
O H
Aspartic acid
2.77
HO C C NH2
H C
COOH
Proline
O
HO C
Valine
H
H 2N C C
CH3
C H
O
OH
CH3
Analysis :Species at 5.96 for respective amino acids:

O H
-
O C C
For aspartic acid:

O
HO C
NH2
COO-
shift towards anode
N+
For proline:
shift towards cathode
O H
-
O C C NH3+
CH3
For valine:
C H
CH3
remains in the middle
6.30
5.96
Aspartic acid
Anode
valine
(iii)
Cathode
proline
A common secondary structure of proteins is the alpha helix. With the aid of a
diagram and your knowledge in chemical bonding, describe the alpha helix
structure.
[7]
On diagram:
1) 2 lone pair of electrons on O atom
2) dipoles (+ and -) and
3) hydrogen bond (IIIIIIII) must be
shown
Hydrogen bonds formed between O atom of (-C=O -) group for C1 and the H
atom of (-N-H+) group of the fourth peptide bond for C4 down the same
protein chain which stabilises the structure.
(b)
(i)
Methamphetamine, C10H15N, is a psychostimulant. It has high potential for

abuse and addiction. In high doses, it can induce euphoria and anxiety. Under
the Misuse of Drugs Act in Singapore, a person who carries 500 grams of
methamphetamine will be sentenced to the Mandatory Death Penalty. Its
structure is as shown:
H
N
A 25.0 cm3 sample of 0.500 mol dm-3 methamphetamine was titrated with
aqueous hydrochloric acid of the same concentration.
Would you expect the equivalence point to be above 7 or below 7? Explain
your answer.
Due to salt hydrolysis pH of equivalence point should be below 7.
(ii)
State the formula of the organic product formed when methamphetamine was
reacted with sulfuric acid instead of hydrochloric acid.
[3]
H
N+
H
SO422
Total 10 marks
Elements L to S are consecutive Period 3 elements with proton number less than 20.
The following graph shows the third ionisation energies of these elements.
[L to S are not specific elements from the Periodic Table].
-1
lg 9000
3rd I.E.
3rd Ionisation Energy / kJ mol
8000
7000
6000
5000
4000
3000
2000
1000
0
A
(a)
B
M
C
N
D
P
E
Q
Elements
F
R
G
S
Identify the group that element P belongs to.

[1]
Group V
(b)
Sketch a graph to show the successive ionisation energies of element P when the
first eight electrons are removed from it.
[1]
lg I.E.
No of
Electrons
removed
(c)
Explain the drop in the third ionisation energy from element N to P.

[2]
N2+: 1s22s22p63s2
P2+: 1s22s22p63s23p1
The 3p electron to be removed from P2+ is further away from the nucleus than
the 3s electron to be removed from N2+.
The 3p electron experiences weaker electrostatic forces of attraction than the
3s electron and requires less energy to remove. Thus there is a drop in third
ionisation energy from element N to P.
(d)
Write down the equations for the reaction of the oxide of M with aqueous
hydrochloric acid and aqueous sodium hydroxide.
[2]
M2O3(s) + 6 HCl (aq) 2 MCl3(aq) + 3 H2O (l)
M2O3(s) + 2 NaOH(aq) + 3 H2O(l) 2 Na[M(OH)4] (aq)
(e)
Describe the reactions, if any, of the chlorides of element M and P with water,
suggesting the pH of the resulting solutions and writing equations, where
appropriate.
[6]
M undergoes hydrolysis as it has high charge density, able to polarise and
weaken O-H bond in H2O of [B(H2O)6]3+ (aq) to release acidic H+ and give an
acidic solution.
MCl3 (s) + 6 H2O (l) [M(H2O)6]3+ (aq) + 3 Cl (aq)
[M(H2O)6]3+(aq) [M(H2O)5(OH)]2+ (aq) + H+ (aq)
pH of solution = 3
PCl3 (l) + 3 H2O (l) H3PO3 (aq) + 3 HCl (aq)
Or
PCl5 (l) + 4 H2O (l) H3PO4 (aq) + 5 HCl (aq)
pH of solution = 2
[L to S are not specific elements from the Periodic Table]

Total 12 marks
(a)
Nitrogen monoxide in the air can be converted to nitric acid, which results in acid
rain. Both nitrogen monoxide and nitrogen dioxide participate in ozone layer
depletion. One way of forming nitrogen monoxide is through the dissociation of
nitrogen dioxide.
2NO2 (g)
2NO (g) + O2 (g)
At 494 oC, the value of Kp for the above reaction is 36.9 kPa.
When a certain partial pressure of nitrogen dioxide is put into an empty vessel at
494 oC, equilibrium is reached when 45% of the original nitrogen dioxide has
decomposed.
(i)
Write an expression for the equilibrium constant, Kp, for the reaction.
PNO PO2
2
Kp =
(ii)
PNO2
What is the original partial pressure of nitrogen dioxide before any

dissociation occurred?
[3]
Let the initial pressure of NO2 be x mol.

2 NO2 (g)
Initial pressure (kPa)
Change in Presure
-0.45x
Equilibrium pressure (kPa)
0.55x
(0.225x)(0.45 x )2
Kp =
= 36.9
(0.55 x )2
x = 244 kPa
Hence, initial pressure of NO2 = 244 kPa
2 NO (g) + O2 (g)
0
+0.45x +0.225x
0.45x
0.225x
(b) Draw the structural formula of the organic products formed when compound T
reacts with the following reagents.
OH
OH
O
C
NH2
C CH2
CH3
OH
NH2
Compound T
(i)
Alkaline aqueous KMnO4, heat
O-
O
O
O-
O
C O
COO- O
(ii)
O
O-
NH2 O-
Br2 in CCl4, absence of UV light

[5]
OH
Br
Br
OH O
Br
C
Br
CH3
OH
NH2
CH CH2
Br
NH2 Br Br
(c)
Compound U has the molecular formula C9H12O.

It reacts with chlorine gas in the presence of light to form compound V, C9H11OCl,
which is optically active.
On addition of bromine water at room temperature, U forms a white precipitate W,
C9H10OBr2.
When treated with acidified potassium manganate(VII) under reflux, U forms
compound X, C8H6O5. 1 mole of X reacts with 2 mole of thionyl chloride.
Draw the structures for compounds U to X.
[4]
U:
V:
OH
OH
CH3
CH3
CH2
CHCl
CH3
CH3
W:
X:
OH
Br
Br
OH
CH3
CH2
COOH
COOH
CH3
Total 12 marks
END

Higher 2
CANDIDATE NAME
CLASS
CHEMISTRY
9647/03
22 August 2012
2 hours

Writing Papers

You may use a soft pencil for any diagrams, graphs or rough work.
You are reminded of the need for good English and clear presentation in your answers
The number of marks is given in the brackets [ ] at the end of each question or part
question.
At the end of the examination, fasten all your work securely together with the cover page
provided.
2012 JC2 PRELIM 9647 P3
Turn Over]
2
1
(a)
Aqueous sodium hydroxide is an important reagent in many organic reactions

where the hydroxide ion can act as both a base and a nucleophile.
In the Reimer-Tiemann reaction, phenol is heated with chloroform in the presence
of aqueous sodium hydroxide to give 2-hydroxybenzaldehyde, compound B. The
reaction involves the formation of a reactive intermediate, CCl2, through an acidbase reaction.
CHCl3 + OH- CCl2 + H2O + Cl
chloroform
OH
OH
OH
CHCl2
+ CCl2
CHO
NaOH (aq)
heat
II
(i)
State the type of reaction that occurred in reaction I.
(ii)
Suggest a chemical test to differentiate compounds B and A under room

conditions.
(iii) Compound B can undergo further reaction to form the product below.
OH
CHO
OH
OH
C
CN
B
Name and describe the mechanism involved, using curly arrows to show the
movement of electrons and indicating all charges.
(iv) Comment on the relative acidity of phenol and compound B.

[9]
2012 JC2 PRELIM 9647 P3
Turn Over]
3
(b) Besides its extensive use in organic chemistry, aqueous sodium hydroxide is also
used in photographic development.
The black-and-white photography process involves four steps:
Step 1
Photo-taking: Interaction of light with silver halides (AgX) on film.
Step 2
Developing: Redox reactions to develop the actual image.
Step 3
Fixing: Changing the solubility of chemical compounds with different

conditions to preserve the image on the film.
Step 4
Printing: Shining light through the film onto photosensitive paper,

producing the final photograph using the same chemistry as step 1 to 3.
When light is shone on the film during the phototaking process, a very small
number of X- ions in AgX are oxidised.
(i)
A small amount of silver is produced as a result of the oxidation reaction of

X-. The silver produced catalyses the reduction of the surrounding AgX to
black silver metal in the presence of a reducing agent, D, during the
developing process.
2AgX + D + 2OH- 2Ag + E + 2H2O + 2XState and explain why the rate of reaction changes as the developing
process proceeds.
(ii)
Under appropriate conditions, chloride can be oxidised to chlorine gas. With

the aid of an equation, suggest how Cl2 will react with hydroxide ions under
room conditions.
(iii) E, formed from the oxidation of D, has the molecular formula C6H4O2.
E forms an orange precipitate when warmed with 2,4-dinitrophenylhydrazine.
One mole of E decolourises two mole of bromine dissolved in
tetrachloromethane. Heating E with acidified potassium manganate(VII)
produces only one product.
D has the molecular formula C6H6O2. It is insoluble in water but can dissolve
in aqueous sodium hydroxide. Addition of sodium carbonate to D does not
result in effervescence but addition of sodium metal to D gives mild
effervescence.
Suggest the structures of D and E, explaining your reasoning.
(You are not required to explain the oxidation process of E from D)
[11]
Total 20 marks
2012 JC2 PRELIM 9647 P3
Turn Over]
4
2
Halogens are highly reactive and they are the only group in the Periodic Table which
contains elements in all three familiar states of matter at 25 oC and 1 atm.
The halogens form hydrogen halides with hydrogen, all of which are strong acids with
the exception of HF.
(a)
Discuss the thermal stability trend of the hydrogen halides, HCl, HBr and HI and
variation in volatility of the halogens from fluorine to iodine.
[5]
(b) Concentrated sulfuric acid will react with solid sodium halides NaX.
(X = Cl -, Br - or I-).
Using relevant data from the Data Booklet, describe and explain why hydrogen
chloride can be prepared by the reaction between sodium chloride and
concentrated sulfuric acid while hydrogen iodide cannot be synthesised using a
similar method with sodium iodide and concentrated sulfuric acid. You are to
include relevant chemical equation(s) in your discussion.
[5]
(c)
Halogens form many compounds with metals. These compounds range from ionic
compounds such as lithium chloride, monomeric covalent compounds such as
uranium hexafluoride, and polymeric covalent compounds like palladium chloride.
The Corey-Posner, Whitesides-House reaction is an organic reaction that involves
the reaction of a lithium dialkyl cuprate with an alkyl halide to form a new alkane,
an organocopper compound and a lithium halide.
The formation of propane from a halogeno compound using the Corey-Posner,
Whitesides-House reaction is as shown.
(CH3)2CuLi + CH3CH2X CH3CH2CH3 + CH3Cu + LiX
(X = Cl -, Br - or I-)
(i)
Draw the structural formulae of the three alkanes produced when (C3H7)2CuLi
and C3H7Br undergo the CoreyPosner, WhitesidesHouse reaction.
(ii)
Suggest with reasoning which of the alkanes in (c)(i) has the lowest boiling
point.
[6]
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5
(d) Chlorine and fluorine react exothermically to form an interhalogen compound, ClF3.
(i)
With the help of a Lewis structure, state the shape of the ClF3 molecule.
(ii)
The interhalogen compounds are very strong oxidising agents.

When gaseous ClF3 is added to water, a vigorous reaction occurs, giving
three gases as the only products. The gaseous product mixture appears as
white fumes which forms a weak acid. The gaseous mixture not only turns
moist blue litmus paper red but also bleaches it. In addition, it relights a
glowing splint.
State the three gases in the gaseous mixture.
Hence, construct a balanced equation, including state symbols, for the
reaction.
[4]
Total 20 marks
2012 JC2 PRELIM 9647 P3
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6
3
(a)
Nitrous acid, HNO2, is an unstable, weakly acidic compound. It can easily be

prepared by acidifying a solution of a nitrite.
Barium nitrite, Ba(NO2)2 is often used since the insoluble barium sulfate can be
easily filtered off.
Ba(NO2)2 (aq) + H2SO4 (aq) 2HNO2 (aq) + BaSO4 (s)
Nitrite ions can be oxidised by potassium manganate(VII) to form nitrate ions:
5NO2- (aq) + 2MnO4- (aq) + 6H+ (aq) 5NO3- (aq) + 2Mn2+ (aq) + 3H2O (l)
The following are some thermochemistry data.
enthalpy change of atomisation of barium
enthalpy change of Ba (s) Ba2+ (aq) +2e
enthalpy change of hydration of NO3lattice energy of barium nitrate
DHq / kJ mol-1
+175
+286
-325
-1395
(i)
Using the data above, and relevant data from the Data Booklet, construct an
energy cycle to calculate the enthalpy change of hydration of the barium ion.
(ii)
The DSqhydration of barium ion is -188 J mol-1 K-1. Explain why the sign of
DSqhydration is negative.
(iii) Hence, calculate DGqhydration of barium ion at 298K.

(iv) Predict the effect of high temperature on the spontaneity of the above
reaction.
(v)
Using your answer in (a)(i), and relevant data from the table, calculate the
enthalpy change of solution of barium nitrate.
(b) (i)
When barium nitrate is heated, it decomposes. Write an equation to

represent the thermal decomposition of barium nitrate.
(ii)
Group II iodates decomposed according to the following equation.

2Mg(IO3)2 (s) 2MgO (s) + 2I2 (g) + 5O2 (g)
Describe and explain how the thermal stabilities of Group II iodates vary
down the group.
[10]
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7
(c)
Nitrous acid is useful in converting amines into diazonium compounds:

Reaction 1
NH2
N N
HNO2
HSO4-
H2SO4
2H2O
diazonium salt
+
In a process named the Sandmeyer reaction, the NN is replaced by Cl or Br
using the corresponding cuprous halide, CuX, together with concentrated HCl.
Reaction 2
N N
CuX
conc HCl
Outline how you could convert nitrobenzene into 1,3-dichlorobenzene in a four

steps synthesis, using both reactions 1 and 2 in your synthesis. In your answer,
you are to clearly state the reagents and conditions used and the intermediates
formed.
[5]
2012 JC2 PRELIM 9647 P3
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8
(d) The diazonium salt can undergo a coupling reaction with activated aromatic rings
to obtain brightly coloured azo compounds which can be used as dyes.
The dye, Disperse Yellow, is formed as follows:
OH
NHCOCH3
NH2
NHCOCH3
I
NH2
NH2
NHCOCH3
HNO3
CH3
H2SO4
III
II
N
N
N N Cl-
OH
diazonium salt
CH3
Disperse Yellow
(i)
Identify a reagent which might be used for step I.
(ii)
H 2N
NH2
HO
CH3
Propose a chemical test to differentiate

and
.
In your answer, state clearly the reagents and conditions required and any
observations made.
(iii) Another azo dye, H, can be obtained from an amine and a phenol under
suitable conditions.
CH3
CH3
N N
OH
CH3
azo dye, H
Draw the structural formulae of the amine and of the phenol used to make H.
[5]
Total 20 marks
2012 JC2 PRELIM 9647 P3
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9
4
The pickling of steel is the process of removing rust, or iron(III) oxide, from steel by
using excess concentrated hydrochloric acid to react with layers of the oxide and iron
metal. The reaction produces a solution of iron(II) chloride.
A chemist used the set-up shown below to investigate if the resulting solution which
consists of concentrated hydrochloric acid and iron(II) chloride, from the pickling of
steel, can be used to produce iron metal via electrolysis.
Pt (s)
O2 (g)
H+ (aq)
CH3CH2OH (l)
Fe (s)
(a)
concentrated
hydrochloric acid
and iron(II)
chloride
Pt (s)
An organic fuel cell, the direct ethanol fuel cell, is used to drive the electrolysis.
The reaction that takes place at one of the electrodes involves the reduction of
oxygen gas as follows:
O2 + 4H+ + 4e- 2H2O
(i)
Construct the overall equation for the fuel cell reaction, given that carbon
dioxide is produced at the anode.
(ii)
Write the cell diagram for the direct ethanol fuel cell, stating the polarity of the
respective electrodes.
[3]
(b) (i)
Construct a balanced equation for the reaction that takes place during the
pickling of steel, indicating the state symbols clearly.
(ii)
Write half-equations for the reactions taking place at the cathode and anode
of the electrolytic cell and state all observations made within the cell.
(iii) Suggest the observation made at the anode when nitric acid is used in the
pickling of steel instead of hydrochloric acid.
[6]
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10
(c)
Upon addition of cyanide ions, the colour of the electrolyte changes from pale
green to Prussian blue.
Explain why iron complexes are coloured.
[3]
(d) Another chloride of iron, FeCl3, has similar characteristics as aluminium chloride.
Both form dimers at low temperatures, produce acidic solutions when dissolved in
water and are used in the electrophilic substitution reactions of benzene rings.
(e)
(i)
Using suitable data from the Data Booklet, explain the acidic nature of FeCl3
in water.
(ii)
State what role does iron(III) chloride play in the electrophilic substitution
reaction of benzene ring with chlorine.
[4]
(i)
Haemoglobin, which contains iron(II) ions is a protein found in the red blood
cells that carries oxygen. Describe the protein components of haemoglobin.
(ii)
In World War II, the use of cyanide pills were frequently recorded. Pilots of
B-29 Superfortress bombers sent to drop atomic bombs on Japan were
issued with the lethal pills. Fortunately, all aircraft returned safely and none of
the pills were used. These pills contain a concentrated solution of potassium
cyanide and the release of the fast-acting poison causes brain death within
minutes.
Suggest why brain death occurs within minutes after the poison is
administered.
[4]
Total 20 marks
2012 JC2 PRELIM 9647 P3
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11
5
(a)
The Kastle-Meyer test is often used to test for the presence of blood at a crime
scene. It relies on the peroxidase-like activity of haemoglobin in blood to catalyse
the oxidation of colourless phenolphthalein into its bright pink conjugate base.
Phenolphthalein has the following structure:
HO
OH
O
O
Phenolphthalein is a weak acid which dissociates in water according to the

following equation:
HO
OH
HO
+ H 2O
+ H3O+
O
O
colourless (acid)
OO
pink (conjugate base)
The pKa of phenolphthalein is 9.7.

(i)
Draw the structure of the compound formed when phenolphthalein is

heated with aqueous sodium hydroxide.
(ii)
Using Le Chatelier's principle, explain why phenolphthalein appears

colourless in an acidic solution.
(iii) Calculate the ratio of the concentration of the conjugate base to the
concentration of the acid at pH 10.
Using this ratio, predict and explain the colour of phenolphthalein at pH 10.
[6]
(b) Cinnamic acid, commonly found in cinnamon, has a molecular formula of
C9H8O2.
It is known that cinnamic acid can react with liquid bromine in the dark. It also
undergoes oxidation to form benzoic acid and in the process, carbon dioxide gas
was released.
An isomer of cinnamic acid also reacts with liquid bromine in the dark.
Upon oxidation with potassium manganate(VII),1 mole of this isomer reacts with
1 mole of sodium carbonate.
Suggest the displayed formulae of cinnamic acid and its isomer and state the
type of isomerism exhibited by cinnamic acid.
[3]
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12
(c)
Phenolphthalein is usually used as an indicator in a strong base and weak acid

titration.
Aqueous magnesium chloride can act as a weak monobasic acid. In an
experiment, 50.0 cm3 of aqueous magnesium chloride was titrated with
1.00 mol dm-3 sodium hydroxide. The variation of pH of the solution is as shown
in the diagram.
2012 JC2 PRELIM 9647 P3
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13
(i)
Explain what is meant by the term weak acid.
(ii)
Write an equation showing hydrated magnesium ion acting as an acid.
(iii) Using the graph above, calculate the initial concentration of magnesium
ions.
(iv) Calculate the Ka value for aqueous magnesium chloride.
(v)
At the point where 10.0 cm3 of sodium hydroxide has been added to the
solution, a saturated solution of a sparingly soluble salt, magnesium
hydroxide, Mg(OH)2, is formed.
Calculate the solubility product, Ksp of Mg(OH)2.
[7]
(d) Iodine reacts with propanone in acid solution as follows.
I2
H+
CH3COCH3
CH3COCH2I
+ HI
Kinetics studies have shown that the reaction is second order overall, and it has
been suggested that the mechanism involves the following three steps.
CH3COCH3 +
+
CH3C(OH)CH3
H2C
CH3C(OH)CH3
H2C
C(OH)CH3 +
C(OH)CH3 + I2
(fast)
+
(slow)
CH3COCH2I + HI
(fast)
(i) Explain the meaning of order of reaction.

(ii) Construct the rate equation for this reaction.
(iii) An experiment was carried out at 60 C using reagents of the following
concentrations.
Initial concentration / mol dm3

[I2]
[CH3COCH3]
[H+]
0.002
0.050
0.050
The initial rate of reaction was found to be 1.25 106 mol dm3 s1 under
these conditions. Calculate the rate constant for this reaction, stating its
units.
[4]
Total 20 marks
END
2012 JC2 PRELIM 9647 P3
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14
BLANK
BLANK
2012 JC2 PRELIM 9647 P3
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Higher 2
CANDIDATE NAME
CLASS
CHEMISTRY
9647/03
21 August 2012
Suggested Solutions
1
(a)
Aqueous sodium hydroxide is an important reagent in many organic reactions

where the hydroxide ion can act as both a base and a nucleophile.
In the Reimer-Tiemann reaction, phenol is heated with chloroform in the presence
of aqueous sodium hydroxide to give 2-hydroxybenzaldehyde, compound B. The
reaction involves the formation of a reactive intermediate, CCl2, through an acidbase reaction.
CHCl3 + OH- CCl2 + H2O + Cl
chloroform
OH
OH
OH
CHCl2
+ CCl2
CHO
NaOH (aq)
heat
II
A
(i)
State the type of reaction that occurred in reaction I.

(ii)
Suggest a chemical test to differentiate compounds B and A under room

conditions.
Add 2,4-DNPH to B and A separately.
B: Orange precipitate formed
A: No orange precipitate formed
Note: Tollens reagent and aqueous NaOH tests are not allowed, as both
require heating, which is not room conditions
(iii) Compound B can undergo further reaction to form the product below.
OH
OH
CHO
OH
C
CN
B
Name and describe the mechanism involved, using curly arrows to show the
movement of electrons and indicating all charges.
Mechanism: Nucleophilic addition
..
OH
slow
d+
C H
HCN
O-
d-
CN-
OH
fast
OH
C
CN
+ CN-
OH
C H
CN
[9]
(iv) Comment on the relative acidity of phenol and compound B.
Presence of electron withdrawing CHO attached on the benzene ring.
Negative charge of the phenoxide ion of compound B will be further
dispersed. Phenoxide ion of compound B is more stabilised.
Compound B is a stronger acid as compared to phenol.
(b) Besides its extensive use in organic chemistry, aqueous sodium hydroxide is also
used in photographic development.
The black-and-white (B/W) photography process involves four steps:
Step 1
Photo-taking: Interaction of light with silver halides (AgX) on film.
Step 2
Developing: Redox reactions to develop the actual image.
Step 3
Fixing: Changing the solubility of chemical compounds with different

conditions to preserve the image on the film.
Step 4
Printing: Shining light through the film onto photosensitive paper,

producing the final photograph using the same chemistry as step 1 to 3.
When light is shone on the film during the phototaking process, a very small
number of X- ions in AgX are oxidised.
(i)
A small amount of silver is produced as a result of the oxidation reaction of

X-. The silver produced catalyses the reduction of the surrounding AgX to
black silver metal in the presence of a reducing agent, D, during the
developing process.
2AgX + D + 2OH- 2Ag + E + 2H2O + 2XState and explain why the rate of reaction changes as the developing
process proceeds.
The reaction is autocatalytic. (Ag produced catalyses the reaction.)
The rate of reaction increases at first due to the formation of the Ag
catalyst, then decreases as the reactants are used up.
(ii)
Under appropriate conditions, chloride can be oxidised to chlorine gas. With

an aid of an equation, suggest how Cl2 will react with hydroxide ions under
room conditions.
2OH- (aq) + Cl2 (aq) Cl- (aq) + ClO- (aq) + H2O (l)
(iii) E, formed from the oxidation of D, has the molecular formula C6H4O2.
E forms an orange precipitate when warmed with 2,4-dinitrophenylhydrazine.
One mole of E decolourises two mole of bromine dissolved in
tetrachloromethane. Heating E with acidified potassium manganate(VII)
produces only one product.
D has the molecular formula C6H6O2. It is insoluble in water but can dissolve
in aqueous sodium hydroxide. Addition of sodium carbonate to D does not
result in effervescence but addition of sodium metal to D gives mild
effervescence.
Suggest the structures of D and E, explaining your reasoning.
(You are not required to explain the oxidation process of E from D)
[11]
E undergoes condensation with 2,4-DNPH
E is a carbonyl compound
1 mol of E undergoes electrophilic addition with 2 mol of Br2
E contains two alkene functional groups
E undergoes oxidation with hot acidified KMnO4 (aq) to give two identical
compounds E is a symmetrical alkene
D is insoluble in water due to large hydrophobic benzene ring but can
undergo neutralisation with NaOH (aq)
D contains phenol or carboxylic acid group
D does not undergo neutralisation with Na2CO3 but undergoes redox
reaction with Na
D is not a carboxylic acid, so D contains phenol group
HO
D:
OH
E:
Total 20 marks
Halogens are highly reactive and they are the only group in the Periodic Table which
contains elements in all three familiar states of matter at 25oC and 1 atm.
The halogens form binary compounds with hydrogen and these compounds are known
as hydrogen halides, all of which are strong acids with the exception of HF.
(a)
Discuss the thermal stability trend of the hydrogen halides, HCl, HBr and HI and
variation in volatility of the halogens from fluorine to iodine.
[5]
Order of thermal stability : HCl > HBr > HI
Down the group,
Covalent bond length of H-X increases
Covalent bond strength decreases
Bond dissociation energy decreases
The number electrons in the halogen molecules increase, thus,
intermolecular van der Waals forces of attraction become more extensive.
This leads to increase in their boiling point.
Volatility of halogens decreases down the group
(b) Concentrated sulfuric acid will react with solid sodium halides NaX.
(X = Cl -, Br - or I-).
Using relevant data from the Data Booklet, describe and explain why hydrogen
chloride can be prepared by the reaction between sodium chloride and
concentrated sulfuric acid while hydrogen iodide cannot be synthesised using a
similar method with sodium iodide and concentrated sulfuric acid. You are to
include relevant chemical equation(s) in your discussion.
[5]
The reducing power of the halides increases down the group as shown by the
stated E values.
Cl2 + 2e 2Cl +1.36 V
Br2 + 2e 2Br +1.07 V
I2 + 2e 2I
+0.54 V
NaCl (s) + H2SO4 (l) HCl (g) + NaHSO4
HCl is produced as Cl - is a weaker reducing agent.
NaI (s) + H2SO4 (l) NaHSO4 (s) + HI (g)
2 HI (g) + H2SO4 (l) I2 (g) + 2H2O (l) + SO2 (g) or
6HI (g) + H2SO4 (l) 3I2 (g) + 4H2O (l) + S (s) or
8HI (g) + H2SO4 (l) 4I2 (g) + H2S (g) + 4H2O
HI is not produced as iodide is a stronger reducing agent and it will reduce the
sulphur to a lower oxidation state.
(c)
Halogens form many compounds with metals. These compounds range from ionic
compounds such as lithium chloride, monomeric covalent compounds such as
uranium hexafluoride, and polymeric covalent compounds like palladium chloride.
The Corey-Posner, Whitesides-House reaction is an organic reaction that involves
the reaction of a lithium dialkyl cuprate with an alkyl halide to form a new alkane,
an organocopper compound and a lithium halide.
The formation of propane from a halogeno compound using the Corey-Posner,
Whitesides-House reaction is as shown.
(CH3)2CuLi + CH3CH2X CH3CH2CH3 + CH3Cu + LiX
(X = Cl -, Br - or I-)
(i)
Draw the structural formulae of the three alkanes produced when (C3H7)2CuLi
and C3H7Br undergo the CoreyPosner, WhitesidesHouse reaction.
CH3
CH3CH2CH2CH2CH2 CH3 :
(ii)
CH3
CH3
CH3
C CH2CH2CH3 CH3
C CH3
Suggest with reasoning which of the alkanes in (c)(i) has the lowest boiling
point.
[6]
CH3
Alkanes has simple molecule structure
CH3
CH3
C CH3
has the lowest

boiling point as the extensiveness of VDW is reduced due to the
branched structure.
Chlorine and fluorine react exothermically to form an interhalogen compound,

ClF3.
(d)
(i)
With the help of a Lewis structure, state the shape of the ClF3 molecule.
F
Cl
F
\ T-shape molecule
(ii)
The interhalogen compounds are very strong oxidising agents.

When gaseous ClF3 is added to water, a vigorous reaction occurs, giving
three gases as the only products. The gaseous product mixture appears as
white fumes which forms a weak acid. The gaseous mixture not only turns
moist blue litmus paper red but also bleaches it. In addition, it relights a
glowing splint.
State the three gases in the gaseous mixture.
Hence, construct a balanced equation, including state symbols, for the
reaction.
[4]
O2, Cl2 and HF
6H2O(l) + 4ClF3(g) 3O2(g) + 2Cl2(g) + 12HF(g)
Total 20 marks
(a)
Nitrous acid is an unstable, weakly acidic compound. It can easily be prepared by

acidifying a solution of a nitrite. Barium nitrite, Ba(NO2)2 is often used since the
insoluble barium sulfate can be easily filtered off.
Ba(NO2)2 (aq) + H2SO4 (aq) 2HNO2 (aq) + BaSO4 (s)
Nitrite ion can be oxidised by KMnO4 to form nitrate ion:
5NO2- (aq) + 2MnO4- (aq) + 6H+ (aq) 5NO3- (aq) + 2Mn2+ (aq) + 3H2O (l)
The following are some thermochemistry data pertaining to the experiment.
DHq / kJ mol-1
enthalpy change of atomisation of barium
+175
2+
+286
enthalpy change of Ba (s) Ba (aq) +2e
enthalpy change of hydration of NO3-325
lattice energy of barium nitrate
-1395
(i)
Using the above data, and relevant data from the Data Booklet, construct an
energy cycle to calculate the enthalpy change of hydration of the barium ion.
DHrxn = +286 kJ mol-1

Ba(s)
Ba2+(aq) +2e
DHa(Ba) = +175 kJ mol-1
DHhyd
1st IE + 2nd IE = +502 +966 = 1468 kJ mol-1
Ba(g)
Ba2+(g) +2e
DHhyd (Ba2+) = -1468-175 +286

= -1360 kJ mol-1
(ii)
The DSqhydration of barium ion is -188 J mol-1 K-1. Explain why the sign of
DSqhydration is negative.
When Ba2+ is hydrated, the ions are surrounded by water molecules.
There is an increase in orderliness of the water molecules. Hence,
DShydration is negative.
(iii) Hence, calculate DGqhydration of barium ion at 298K.

DGqhydration = DHhydration - TDShydration
= -1360 (298)(-188 x 10-3)
= -1300 kJ mol-1
(iv) Predict the effect of high temperature on the spontaneity of the above
reaction.
DH = -ve
DS= -ve
Since DGqhydration = DHhydration - TDShydration
DGqhydration = -ve (-ve)
= -ve + TDS
As temperature increases, DGqhydration will become more positive; reaction will
become less spontaneous at high temperature.
(v)
Using your answer in (a)(i), and relevant data from the table, calculate the
enthalpy change of solution of barium nitrate.
Ba2+(g) + 2NO3-(g)
-1357
-1395
Ba(NO3)2 (s)
-325 2
DHsolution
Ba2+ (aq) + 2NO3- (aq)

DHsolution = DHhyd (Ba2+) + 2DHhyd (NO3-) - LE
= - 1360 + 2(-325) (-1395)
= -615 kJ mol-1
(b) (i)
Write an equation to represent the thermal decomposition of barium nitrate.

2Ba(NO3)2 (s) 2BaO (s) + 4NO2 (g) + O2 (g)
or
Ba(NO3)2 (s) BaO (s) + 2NO2 (g) + O2 (g)

(ii)
Group II iodates decomposed according to the following equation.

2Mg(IO3)2 (s) 2MgO (s) + 2I2 (g) + 5O2 (g)
Describe and explain how the thermal stabilities of Group II iodates vary
down the group.
[10]
For Group II cations when going down the group,
Cationic radius of M2+ increases.
Charge density of cation
decreases.
Charge remains constant.
Polarising power of cation decreases and M2+ is less able
to distort the electron cloud of anion
Polarising effect on anion decreases
Higher temperature (more energy) is required to decompose the
compound.
Hence, stability of nitrates increases.
(c)
Nitrous acid is useful in converting amines into diazonium compounds:

Reaction 1
NH2
N N
HNO2
HSO4-
H2SO4
2H2O
diazonium salt
+
In a process named the Sandmeyer reaction, the NN is replaced by Cl or Br
using the corresponding cuprous halide, CuX, together with concentrated HCl.
Reaction 2
N N
CuX
conc HCl
Outline how you could convert nitrobenzene into 1,3-dichlorobenzene in a four

steps synthesis, using both reactions 1 and 2 in your synthesis. In your answer,
you are to clearly state the reagents and conditions used and the intermediates
formed.
[5]
NO2
NO2
conc HNO3
conc H2SO4
o
>55 C
N 2+
NH2
Sn, conc HCl
NO2
heat
HNO2, H2SO4
N 2+
NH2
CuCl, conc HCl
Cl
Cl
(d) The diazonium salt can undergo a coupling reaction with activated aromatic rings
to obtain brightly coloured azo compounds which can be used as dyes.
The dye, Disperse Yellow, is formed as follows:
OH
NHCOCH3
NH2
NHCOCH3
NHCOCH3
HNO3
I
NH2
CH3
N
H2SO4
NH2
II
III
N N Cl-
OH
diazonium salt
(i)
CH3
Disperse Yellow
Identify a reagent which might be used for step I.

CH3COCl
(ii)
H 2N
NH2
HO
CH3
Propose a chemical test to differentiate

and
.
In your answer, state clearly the reagents and conditions required and any
observations made.
Test: Add neutral FeCl3 or
KMnO4 in H2SO4, heat
Observations:
H 2N
NH2
HO
CH3
: No violet complex observed

: Violet complex observed
(Purple solution remains)

(Purple solution decolourised)
(iii) Another azo dye, H, can be obtained from an amine and a phenol under
suitable conditions.
CH3
CH3
N N
OH
CH3
azo dye, H
Draw the structural formulae of the amine and of the phenol used to make H.
[5]
CH3
NH2
CH3
OH
CH3
Total 20 marks
The pickling of steel is the process of removing rust, or iron(III) oxide, from steel by
using excess concentrated hydrochloric acid to react with layers of the oxide and iron
metal. The reaction produces a solution of iron(II) chloride.
A chemist used the set-up shown below to investigate if the resulting solution which
consists of concentrated hydrochloric acid and iron(II) chloride, from the pickling of
steel, can be used to produce iron metal via electrolysis.
Pt (s)
O2 (g)
Salt bridge
CH3CH2OH (l)
H+ (aq)
Fe (s)
Pt (s)
concentrated hydrochloric acid

and iron(II) chloride
(a)
An organic fuel cell, the direct ethanol fuel cell, is used to drive the electrolysis.
The reaction that takes place at one of the electrodes involves the reduction of
oxygen gas as follows:
O2 + 4H+ + 4e- 2H2O
(i)
Construct the overall equation for the fuel cell reaction, given that carbon
dioxide is produced at the anode.
CH3CH2OH + 3O2 2CO2 + 3H2O
(ii)
Write the cell diagram for the direct ethanol fuel cell, stating the polarity of the
respective electrodes.
[3]
Pt (s) | CH3CH2OH (l) | CO2 (g) || O2 (g) | H2O (l) | Pt (s)
Negative
Positive
(b) (i)
Construct a balanced equation for the reaction that takes place during the
pickling of steel, indicating the state symbols clearly.
Fe2O3 (s) + Fe (s) + 6HCl (aq) 3FeCl2 (aq) + 3H2O (l)
(ii)
Write half-equations for the reactions taking place at the cathode and anode
of the electrolytic cell and state all observations made within the cell.
Fe (s) cathode: Fe2+ + 2e- Fe
Observation: Fe (s) cathode increases in mass
or pale green solutions fade off
Anode: 2Cl- Cl2 + 2e- (high concentration of Cl- ions from conc. HCl)
Observation: Effervescence observed.
(iii) Suggest the observation made at the anode when nitric acid is used in the
pickling of steel instead of hydrochloric acid.
[6]
Effervescence observed. Oxygen is evolved instead of chlorine gas.
(c)
Upon addition of cyanide ions, the colour of the electrolyte changes from pale
green to Prussian blue.
Explain why iron complexes are coloured.
[3]
The d orbitals are split into two groups due to the ability of the ligands to
split them into two energy levels.
The d electron undergoes d-d transition and is promoted to a higher
energy d orbital.
The d electron absorbs a certain wavelength of light energy from the
visible region of the electromagnetic spectrum and transmits the
remaining wavelength, which appear as the colour observed.
(d) Another chloride of iron, FeCl3, has similar characteristics as aluminium chloride.
Both form dimers at low temperatures, produce acidic solutions when dissolved in
water and are used in the electrophilic substitution reactions of benzene rings.
(i)
Using suitable data from the Data Booklet, explain the acidic nature of FeCl3
in water.
From the Data Booklet,
Fe3+ has a small cationic radius of 0.064 nm and high charge of +3.
Thus, Fe3+ ion has high charge density and high polarising power.
Hydrolysis of water molecules occurs, thus releasing H+ ions in aqueous
solution.
Or
[Fe(H2O)6]3+
(ii)
[Fe(H2O)5(OH)]2+ + H+
State what role does iron(III) chloride play in the electrophilic substitution
reaction of benzene ring with chlorine.
[4]
FeCl3 acts as a catalyst or halogen carrier or Lewis acid
or form the electrophile Cl+ catalysing the reaction.
(e)
(i)
Haemoglobin, which contains iron(II) ions is a protein found in the red blood
cells that carries oxygen. Describe the protein components of haemoglobin.
Haemoglobin consists of 4 polypeptide chain:
2 -sub-units and 2 -sub-units, with each sub-unit being non-covalently
bonded to a haem (iron) group.
Each heme group consists of a central Fe2+ ion that can bond to one O2
oxygen. Each haemoglobin is able to carry a maximum of four O2 oxygen.
All four components (4 sub-units and 4 haem groups) must be present to
form haemoglobin.
(ii)
In World War II, the use of cyanide pills were frequently recorded. Pilots of
B-29 Superfortress bombers sent to drop atomic bombs on Japan were
issued with the lethal pills. Fortunately, all aircraft returned safely and none of
the pills were used. These pills contain a concentrated solution of potassium
cyanide and the release of the fast-acting poison causes brain death within
minutes.
Suggest why brain death occurs within minutes after the poison is
administered.
[4]
In the presence of cyanide, the CN- bonds irreversibly with haemoglobin to
form a stable complex.
This prevents haemoglobin from transporting oxygen and cells die of
oxygen starvation
Total 20 marks
(a)
The Kastle-Meyer test is often used to test for the presence of blood at a crime
scene. It relies on the peroxidase-like activity of haemoglobin in blood to catalyse
the oxidation of colourless phenolphthalein into its bright pink conjugate base.
Phenolphthalein has the following structure:
OH
HO
O
O
Phenolphthalein is a weak acid which dissociates in water according to the
following equation:
HO
HO
OH
+ H 2O
+ H3O+
O-
colourless (acid)
pink (conjugate base)
The pKa of phenolphthalein is 9.7.

(i)
Draw the structure of the compound formed when phenolphthalein is

heated with aqueous sodium hydroxide.
+
Na- O
O-Na+
OH
O-Na+
O
(ii)
Using Le Chatelier's principle, explain why phenolphthalein appears

colourless in an acidic solution.
In acidic solution, the concentration of H3O+ is high, hence the above
equilibrium position is shifted to the left and the concentration of the
conjugate base is too low for the pink colour to be observed.
(iii) Calculate the ratio of the concentration of the conjugate base to the
concentration of the acid at pH 10.
Using this ratio, predict and explain the colour of phenolphthalein at pH 10.
[H3O + ] = 10 -10 moldm -3
[H3O + ][conjugate base]

Ka =
[acid ]
[10 -10 ][conjugate base]
=
= 10-9.7
[acid ]
[conjugate base] 10 -9.7

= -10 = 1.995 2.00
[acid ]
10
Since the concentration of the conjugate base is much more than the
acid (2 times), the solution will appear pink (the colour of the conjugate
base).
(b) Cinnamic acid, commonly found in cinnamon, has a molecular formula of
C9H8O2.
It is known that cinnamic acid can react with liquid bromine in the dark. It also
undergoes oxidation to form benzoic acid and in the process, carbon dioxide gas
was released.
An isomer of cinnamic acid also reacts with liquid bromine in the dark.
Upon oxidation with potassium manganate(VII),1 mol of this isomer reacts with 1
mol of sodium carbonate.
Suggest the displayed formulae of cinnamic acid and its isomer.
State the type of isomerism exhibited by cinnamic acid.
O
O H
H O C
[3]
C C
H
H
Cinnamic acid
isomer of cinnamic acid
Both undergo electrophilic addition with liquid bromine.

1 mol of this isomer reacts with 1 mol of sodium carbonate. Indicates there
are 2 carboxylic acid group 2 side chains
Cinnamic acid exhibits geometric isomerism (cis-trans isomerism)
(c)
Phenolphthalein is usually used as an indicator in a strong base and weak acid

titration.
Aqueous magnesium chloride can act as a weak monobasic acid. In an
experiment, 50.0 cm3 of aqueous magnesium chloride was titrated with
1.00 mol dm-3 sodium hydroxide. The variation of pH of the solution is as shown
in the diagram.
(i)
Explain what is meant by the term weak acid.

A weak acid is one which dissociates partially in solution to give protons
(H+)
(ii)
Write an equation showing hydrated magnesium ion acting as an acid.

[Mg(H2O)6]2+
[Mg(H2O)5OH]2+ + H+
(iii) Using the graph above, calculate the initial concentration of magnesium
ions.
VNaOH for equivalence = 20.00 cm3
20.00
1
1000
2+
\ [Mg ] initial =
= 0.4 mol dm-3
50.00
1000
(iv) Calculate the Ka value for aqueous magnesium chloride.
initial pH = 6 [H+] = 1 10-6
Ka =
[Mg (H2O )5 OH ]+ [H + ]
[Mg 2+ ]
(10 -6 ) 2
( 0 .4 )
= 2.5 10-12 mol dm-3
(v)
At the point where 10.0 cm3 of sodium hydroxide has been added to the
solution, a saturated solution of a sparingly soluble salt, magnesium
hydroxide, Mg(OH)2, is formed.
Calculate the solubility product, Ksp of Mg(OH)2.
[7]
At 10 cm3, pH = 9
pOH = 5
[OH-] = 1 10-5
10.00 1
= 0.167
60.00
[Mg2+] =
K sp = [Mg 2+ ] [OH - ] 2 = (0.167) (1 10-5)2 = 1.67 10-11 mol3 dm-9
(d) Iodine reacts with propanone in acid solution as follows.

H+
I2 + CH3COCH3
CH3COCH2I
+ HI
Kinetics studies have shown that the reaction is second order overall, and it has
been suggested that the mechanism involves the following three steps.
CH3COCH3 +
+
CH3C(OH)CH3
H2C
CH3C(OH)CH3
H2C
C(OH)CH3 + I2
C(OH)CH3 +
(fast)
+
CH3COCH2I + HI
(slow)
(fast)
(i) Explain the meaning of order of reaction.

Order of reaction with respect to a reactant is the power to which its
concentration is raised in the rate equation.
.
(ii) Construct the rate equation for this reaction.

Rate = k [CH3COCH3] [H+]
(iii) An experiment was carried out at 60 C using the reagents of the following
concentrations.
[4]
Initial concentration / mol dm3
[I2]
[CH3COCH3]
[H+]
0.002
0.050
0.050
The initial rate of reaction was found to be 1.25 106 mol dm3 s1 under
these conditions. Calculate the rate constant for this reaction, stating its
units.
k=
Rate
[CH3COCH3 ] [H+ ]
1.25 10 -6
= 5.00 104 mol1 dm3 s1
0.05 0.05
Total 20 marks
END
CHEMISTRY
Paper 1
9647/01
Multiple Choice
Wednesday
19th September 2012
1 hour

Additional materials:

Data Booklet

Write your name, Civics Group and index number on the Answer Sheet in the spaces
provided unless this has been done for you.
There are forty questions on this paper. Answer all questions. For each question there are
four possible answers A, B, C and D.
Answer Sheet.
9647/01/TJC Prelim 2012
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2
Section A
1
If a mixture of 0.4 g hydrogen and 9.6 g oxygen is exploded, what will be the volume
of the remaining gas at room temperature and pressure?
A
0.60 dm3
1.20 dm3
2.40 dm3
4.80 dm3
Which of the following contains two isoelectronic species?

A
NH4+ and BH3
NH4+ and CH4
BF3 and NH3
PF5 and BF4-
For a given mass of an ideal gas, which of the following graphs display a different
shape from the rest?
A
PV against V (at constant T)
V/T against T (at constant P)
1/density against T (at constant P)
PV against P (at constant T)
25.0 cm3 of 0.0200 mol dm-3 of yellow FA1 solution reacts with x g of zinc and the
latter is oxidised to Zn2+. The resulting solution required 15.0 cm3 of 0.0200 mol dm-3
of acidified KMnO4 to restore its original colour. Find x.
A
0.0196 g
0.0218 g
0.0327 g
0.0491 g
9647/01/TJC Prelim 2012
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3
5
An aqueous sample containing the following anions is analysed.

Cl
CO32
SO42
In which order should the reagents be added to determine the amount of chloride in
the sample?
[If a precipitate is formed, filtration process is carried out before the addition of the
next reagent to the filtrate.]
Reagent 1
Reagent 2
Reagent 3
AgNO3
HNO3
Ba(NO3)2
HNO3
Pb(NO3)2
AgNO3
HNO3
Ba(NO3)2
AgNO3
Ba(NO3)2
NH3
AgNO3
The successive ionisation energies (IE) of two elements X and Y, are given below:
IE/ kJ mol-1
1st
2nd
3rd
4th
5th
6th
7th
8th
786
1580
3230
4360
16000
20000
23600
29100
1251
2298
3822
5158
6542
9330
11000
33604
The compound formed when X and Y combine is most likely to be

A
ionic, with formula X2Y
ionic, with formula XY2
covalent, with formula XY4
covalent, with formula X2Y5
9647/01/TJC Prelim 2012
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4
7
The reaction between phosphorus and hydrogen can result in the formation of
phosphine as shown:
P4(s) + 6H2(g)
4PH3(g)
The graph shows the change in concentration of hydrogen for this reaction in which
the system was disturbed after four hours.
Concentration of H2(g) / mol dm-3
Time / hours
Which of the following could explain the change in the hydrogen concentration at
time, t = 4 hours?
A
The volume of the reaction vessel was decreased.
A catalyst was added.
The pressure on the reaction mixture was decreased.
More phosphorus was added.
9647/01/TJC Prelim 2012
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5
8
If compound A is heated, it decomposes according to the equation:

B(g) +
2A(g)
C(g)
The following diagram shows the progress of the reaction.
Concentration / mol dm-3

B
A
Time / hours
What is the equilibrium constant for the reaction?
A
0.8
2.0
4.0
10.0
In a blast furnace, carbon or carbon monoxide can be used to reduce iron(III) oxide.
Fe2O3(s) +
3
2
C(s)
2Fe(s) +
3
2
CO2(g)
Fe2O3(s) + 3CO(g) 2Fe(s) + 3CO2(g)
H = +234 kJ mol1
H = 24.8 kJ mol1
Carbon monoxide can be formed by the following reaction.

C(s) + CO2(g) 2CO(g)
H1
What is the value of H1?
10
+86.3 kJ mol1
+139.5 kJ mol1
+172.5 kJ mol1
+258.8 kJ mol1
Which of the following reactions shows a positive change in entropy?

[Assume that all measurements are taken at 298 K and 1 atm pressure.]
A
N2O(g) N2(g) + O2(g)
Fe(s) + S(s) FeS(s)
Ca(s) + O2(g) CaO(s)
C3H6(g) + H2(g) C3H8(g)
9647/01/TJC Prelim 2012
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6
11
12
Car manufacturers are developing engines that use H2 as a fuel. Approximately 5%

of industrial hydrogen is produced by electrolysis of water. How many coulombs are
needed to produce 1.02 106 mol of H2 gas?
A
1.02 106 C
9.84 1010 C
1.97 1011 C
1.97 1014 C
Ethyl ethanoate undergoes a slow acid-catalysed hydrolysis in water where the

concentration of acid in the solution remains constant.
H+
CH3CO2CH2CH3 + H2O CH3CO2H + CH3CH2OH
The rate equation is found to be
rate = k[CH3CO2CH2CH3][H+]
When 0.1 mol dm-3 of HCl is reacted with 0.2 mol dm-3 of ethyl ethanoate, the half-life
was found to be 62 min.
Another reaction was carried out with 0.2 mol dm-3 of HCl and 0.2 mol dm-3 of ethyl
ethanoate. How long does it take for the concentration of ethyl ethanoate to fall to
0.025 mol dm-3?
A
13
31 min
62 min
93 min
124 min
25 cm3 of 0.1 mol dm-3 monobasic acid X is titrated with 25 cm3 of 0.2 mol dm-3
NaOH. The end point cannot be detected using screened methyl orange.
Which of the following is not correct?
A
The solution acts as a buffer when 12.50 cm3 of NaOH has been added.
Initial pH of the solution is more than 1.00.
pH of the equivalence point is more than 7.
Acid X is a weak acid.
9647/01/TJC Prelim 2012
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7
14
A 100 cm3 solution consists of 0.20 mol dm-3 MgCl2 and 0.10 mol dm-3 CuCl2. A
solution of sodium hydroxide is added to the mixture. Mg(OH)2 starts precipitating
when 40 cm3 of sodium hydroxide has been added.
The solubility product values of Mg(OH)2 and Cu(OH)2 are 6.3 10-10 and 2.2 10-20
respectively.
What is the concentration, in mol dm-3, of Cu2+ in the solution when Mg(OH)2 just
precipitates?
15
4.99 10-12
6.98 10-12
6.60 10-5
7.14 10-2
Which of the following graphs shows the correct trend in the physical property of the
period 3 elements?
9647/01/TJC Prelim 2012
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8
16
When a white solid W reacts with concentrated H2SO4, the products include pungentsmelling gases and a dark brown solution containing a yellow precipitate. When
aqueous sodium thiosulfate is added, the yellow precipitate remains but the dark
brown colour disappears.
What is W?
17
18
19
NaNO2
KI
MgCl2
Ag2CO3
Which statement is true about the first row transition metals or their compounds?
A
[Ni(C2O4)2(CN)2]4- has a coordination number of 4.
Yellow CrO42- is oxidised to orange Cr2O72- in an acidic medium.
Fe3+ is more stable in acidic than in alkaline medium.
Fe2(CO3)3 cannot be prepared by reacting FeCl3(aq) with Na2CO3(aq).
Transition metals like nickel are used in the manufacture of margarine. Which of the
following statements best explains the role of transition metals in this use?
A
Transition metals have very high melting points because both 3d and 4s
electrons are involved in forming strong metallic bond.
Transition metals have partially filled 3d orbitals for adsorption of reactant

molecules.
Transition metals can exhibit variable oxidation states in their compounds as 3d

and 4s electrons have similar energies.
Transition metals form coloured ions due to absorption of energy in the visible
light region to promote an electron from a lower to a higher energy 3d orbital.
Which row in the table below has the correct number and type of bonds in
CH3
|
H2C = C C CH ?
Number of s - bonds
Number of p - bonds
10
10
9647/01/TJC Prelim 2012
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20
21
Pentane was reacted with limited bromine in the presence of uv light. Assuming that
only monobromination took place and the reaction occurred at the same rate at all
carbon atoms, the ratio of the 3 possible products, 1-bromopentane :
2-bromopentane : 3-bromopentane is
A
3:2:1
1:2:3
1: 3 : 2
3:1:2
Phenylethene undergoes the following reactions to form compound A.

HCl
HCl
BrCll
BrC
Fe 3
FeCl
Phenylethene
styrene
What is the structural formula of A?
Cl
Br
Cl
Br
CH3
Br
Cl
CH3
Br
Cl
9647/01/TJC Prelim 2012
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10
22
The demand for natural shampoos and detergents has led to the development of
more biodegradable detergents such as sorbitan monolaurate, which is made from
plants. Its structure is shown below.
Which statement is correct?
23
There will be no colour change on heating the compound with acidified

potassium dichromate(VI) solution.
It is optically inactive.
It can react with concentrated sulfuric acid on heating.
It is a cyclic ester.
In which pair of molecules is the pKa of molecule I bigger than that of molecule II?
I
II
CH 2CH 3
COCH3
CO2 H
+
NH
NH23
OH
CH3CH2CHClCH2OH
9647/01/TJC Prelim 2012
CO2H
+
NH3
O2N
OH
ClCH2CH2CH2CH2OH
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11
24
The C-H bond lengths of four hydrocarbons are given in the table below.
compound
structural formula
C-H bond length /nm
methane
CH4
0.110
ethane
CH3CH3
0.110
ethene
CH2=CH2
0.108
ethyne
CHCH
0.106
Which of the following helps to explain the shortest C-H bond length observed in
ethyne?
25
Ethyne is a linear molecule.
The carbon orbital used in formation of the C-H bond in ethyne has the greatest
s orbital character.
An sp-sp overlap is observed between the two carbon atoms in ethyne.
The carbon-carbon triple bond in ethyne is the strongest.
A drug containing a carboxyl group can bind to an amino group on a receptor site in
three different ways.
Hydrogen-bond acceptor
C
|
O
H
Hydrogen-bond donor
C
|
O
H
N
Binding site
Ionic interaction
C
|
O-
+ NH3
NH2
Binding site
Binding site
The drug with the following structure

O
CH3
could bind to the same site

A
only by ionic interaction
only as a hydrogen-bond donor
only as a hydrogen-bond acceptor
both as a hydrogen-bond donor and acceptor
9647/01/TJC Prelim 2012
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12
26
The reduction of a nitrile Q produced a compound of the formula CH3CH2NH2. The

same nitrile Q was also hydrolysed separately in acidic medium.
What would be formed if the products from the two reactions are mixed together?
27
(CH3CH2NH3)(CH3CO2)
(CH3CH2NH3)(CH3CH2CO2)
CH3CH2CONHCH2CH3
CH3CONHCH2CH3
The reaction conditions for four different transformations are given.

Which transformation has the correct conditions?
CH3CH2Br
Alcoholic CH3CH2O-Na+
CH2=CH2
Reflux
O
NaBH4, alcohol as solvent

CH3
OH
Room temperature
CH3CH2OH
Anhydrous AlCl3, Cl2(aq)

C
Cl
Room temperature
K2Cr2O7/H+
CH3CH=CH2
CH3
OH + CO2
Heat
9647/01/TJC Prelim 2012
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13
28
Compound X has the following structure.

H
OH
CH2
CH2
CH3
N
H
X
Which of the following statements is true for compound X?
29
It will give white fumes with SOCl2.
It is insoluble in both aqueous acids and alkalis.
The nitrogen containing group in the ring has a higher pKb than the nitrogen
containing group in the side chain.
It contains a total of six sp2 hybridised carbon atoms.
Compound Y is used to treat hypertension.
CH2CH2CHCO2CH2CH3
CO2H
NHCH(CH3)CONH
EnalaprilY
Compound
Which of the following statements about compound Y is true?
30
One mole of compound Y reacts with 3 moles of CH3COCl.
One mole of compound Y reacts with 3 moles of NaOH on heating.
One mole of compound Y liberates 1 mole of hydrogen gas with Na metal.
Compound Y gives an orange precipitate with 2,4-dinitrophenylhydrazine.
Which statement about ammonia, methylamine and phenylamine is not correct?

A
Basic strength in aqueous solution increases from phenylamine to ammonia to

methylamine.
All of them can act as nucleophiles using the lone pair on the nitrogen atom.
All are trigonal pyramidal in shape with respect to the nitrogen atom.
Only methylamine and phenylamine form white precipitate with aqueous bromine.
9647/01/TJC Prelim 2012
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Section B
3 may be correct.
A
1, 2 and 3 are
correct
1 and 2 only
are correct
2 and 3 only
are correct
1 only is
correct
31
Chromate and dichromate ions form an equilibrium according to the following equation.
2CrO42-(aq) + 2H+(aq)
Cr2O72-(aq) + H2O(l)
Which solution would increase the concentration of the chromate ion, CrO42, when
added to the equilibrium mixture?
32
Sodium ethanoate
Ammonium chloride
Sodium nitrate
When metal A is placed in a solution of a salt of metal B, the surface of metal A

changes colour. When metal B is placed in an acidic solution, gas bubbles forms on
the surface of the metal. When metal A is placed in a solution of a salt of metal C, no
change is observed.
1
When metal B is placed in a solution of silver nitrate, silver deposits can be

formed.
The order of decreasing reducing strength is C > A > B > H2.
H+ is being oxidised to H2 when metal B is placed in acidic solution.
9647/01/TJC Prelim 2012
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15
A
1, 2 and 3 are
correct
1 and 2 only
are correct
2 and 3 only
are correct
1 only is
correct
33
The table below shows the experimental results obtained for the following reaction.
2YO + O2 2YO2
partial pressure of YO
(in arbitrary units)
100
100
50
25
partial pressure of O2
(in arbitrary units)
100
50
50
relative rate
1.00
0.50
0.25
1.00
34
35
The value of D is 400.
The reaction is first order with respect to YO.
Keeping partial pressure of YO constant, increasing partial pressure of O2 does

not change the relative rate.
Which combination of solutions would give a buffer solution?

1
10 cm3 of 0.1 mol dm-3 CH3CO2H and 10 cm3 of 0.1 mol dm-3 CH3CO2Na.
10 cm3 of 0.1 mol dm-3 HCl and 20 cm3 of 0.1 mol dm-3 CH3CO2Na.
20 cm3 of 0.1 mol dm-3 HCl and 10 cm3 of 0.1 mol dm-3 Mg(CH3CO2-)2.
The enthalpy changes involved in the formation of KCl(aq) from K(s) and Cl2(g) are as
follows:
K(s)
H1
+
Cl2(g)
K(g)
+
Cl(g)
H2
K+(g)
+
Cl (g)
H3
KCl(s)
H4
K+(aq)
+
Cl (aq)
Which statements are true?

1
The enthalpy change of solution of potassium chloride is H3 + H4.
The enthalpy change of formation of solid potassium chloride is H1 + H2 + H3.
The lattice energy of potassium chloride is H3.
9647/01/TJC Prelim 2012
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A
1, 2 and 3 are
correct
1 and 2 only
are correct
2 and 3 only
are correct
1 only is
correct
36
Beryllium resembles aluminium in its chemical properties.

Which property of beryllium compounds is not correct?
37
38
Beryllium chloride is an ionic compound.
Beryllium chloride can form the dimer Be2Cl4.
Beryllium chloride dissolves in water to give an acidic solution.
Barium is an element in Group II. Which of the following statements are correct?
1
Barium burns with apple green flame.
Ba(OH)2 has a higher solubility in water than Mg(OH)2.
Barium metal rapidly changes from silvery-white to dark grey colour in presence
of air.
Chemists in the late 1800s knew that cyclic molecules existed, but the limitations on
the ring sizes were unclear. Rings of all sizes from three to thirty and beyond can now
be prepared easily.
Cyclopropane is known to be less stable than cyclohexane.
Cyclopropane
Cyclohexane
Which reasons explain the difference in stability?

1
The sp2-sp2 overlap strengthens the carbon-carbon bonds in cyclohexane.
The C-C-C bond angle of cyclopropane experiences a larger deviation from the
ideal value of 109.5.
The carbon atoms of cyclohexane are not in the same plane, allowing bond
angles to be near the ideal value.
9647/01/TJC Prelim 2012
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A
1, 2 and 3 are
correct
1 and 2 only
are correct
2 and 3 only
are correct
1 only is
correct
39
Polyethene is made by polymerization of ethene molecules via a free radical

mechanism under high temperature and pressure, in the presence of an organic
peroxide.
Chain initiation
O
R
O
O
2R
2CO2 + 2R
organic peroxide
R + CH2=CH2
RCH2CH2
Chain propagation
RCH2CH2 + nCH2=CH2 R(CH2CH2)nCH2CH2
The chain process is eventually ended by combination of two radicals in the
termination step.
Which of the following can be formed in the free radical mechanism?
1
[R(CH2CH2)nCH2CH2]2
O
2
R
40
OCH2CH2
R(CH2CH2)2R
An amino acid has the structural formula HOCH2CH(NH2)CO2H. Which of the following
statements apply to this amino acid?
1
In a buffer solution of pH 9, this amino acid is attracted towards the anode when
a potential difference is applied.
It is an -amino acid which is optically active.
In a polypeptide, the hydroxyl group of this amino acid maintains the secondary
structure by forming ionic bonds with polar R groups of other amino acid
residues.
9647/01/TJC Prelim 2012
[Turn over
18
2012 TJC H2 Chemistry Preliminary Exam Paper 1 Solutions

1
D
11
C
21
B
31
D
2
B
12
C
22
C
32
B
3
C
13
A
23
C
33
B
9647/01/TJC Prelim 2012
4
D
14
A
24
B
34
B
5
C
15
C
25
C
35
C
6
C
16
B
26
A
36
D
7
A
17
D
27
A
37
A
8
C
18
B
28
C
38
C
9
C
19
D
29
B
39
A
[Turn over
10
A
20
A
30
D
40
B

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JC-2 Examination Papers

ANDERSON JUNIOR COLLEGE

Paper 1 Multiple Choice

Multiple Choice Answer Sheet

READ THESE INSTRUCTIONS FIRST

Multiple Choice Answer Sheet

Exam Details: H2 Chem / Paper 1

This document consists of 17 printed pages.

What are the values for a, b, c and d?

The nickelcadmium rechargeable battery is based on the following overall reaction.

AJC Prelim 2012

Americium241 is commonly used in smoke detectors. It works by emitting a constant

What would be the path of the emitted particles in an electric field?

Which of the following is not a feature in the corresponding ion?

All bond angles are 120

AJC Prelim 2012

Solutions of hydrogencarbonates can react with acids as follows.

DHo = +12.7 kJ mol1

Given the following enthalpy changes:

What is the standard enthalpy change of formation of H+(aq)?

Position of equilibrium lies to the left

Some extent of reaction

Reaction goes to completion

AJC Prelim 2012

The electrolysis of a highly concentrated aqueous solution of potassium hydroxide was

pressure/ 103 kPa

pressure/ 103 kPa

AJC Prelim 2012

Water dissociates into H+ and OH as shown.

Aqueous solution of MgCl2

Equal proportions of sodium ethanoate and ethanoic acid

Dilute HCl of concentration 3.0 x 105 mol dm3

Aluminium oxide in aqueous solution

2.25 x 109 years

4.5 x 109 years

9.0 x 109 years

13.5 x 109 years

AJC Prelim 2012

Aluminium, silicon, phosphorus

Magnesium, aluminium, silicon

Silicon, phosphorus, sulfur

Sodium, magnesium, aluminium

Use of the Data Booklet is relevant to this question.

The element is a solid at room temperature and pressure.

Hydrogen astatide is more stable to heat than hydrogen iodide.

Silver astatide is soluble in aqueous ammonia.

Hydrogen astatide is a weak acid.

AJC Prelim 2012

The structures of two complexes are as shown.

Which of the following statements is correct?

Both complexes contain two different ligands.

Co in the complex has four unpaired delectrons.

The oxidation number of Co in the complex is +2.

The electronic configuration of nickel in the complex is [Ar] 3d7.

Platinum(IV) chloride combines with ammonia to form compounds in which the

AJC Prelim 2012

When heated with chlorine, 2,2dimethylbutane undergoes free radical substitution.

How many different forms of X are possible?

A compound has the following structure.

NAME:________________________ PDG: Register No: _