IChO 2006

38.
International
Chemistry Olympiad
Korea 2006
National German
competition
and
IChO
Volume 12
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National German competition
and IChO
Volume 12
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Preface
To become a member of the German IChO-team you have to be successful in four

rounds of a national competition.
st
The problems to be solved in the 1 round are sent to all highschools. To solve the
problems the students may use all resources available, e.g. textbooks etc.
All those students who solve about 70% of the tasks correctly will receive the problems
of the 2nd round, which are to be solved in the same way as mentioned above. These
problems are the most difficult ones in the whole competition.
nd rd
The top 60 of the participants of the 2 round are invited to the 3 round, a one-week
chemistry camp. Besides lectures, excursions to chemical plants or universities and
cultural events there are two written theoretical tests of 5 hours each.
rd th
The top 15 of the 3 round are the participants of the 4 round, a one-week practical
training. There are two written five-hour tests - one theoretical and one practical - under
the same conditions as at the IChO. Here the team is selected.
Responsible for organic questions: Dr. Wolfgang Bünder
Responsible for all other questions: Wolfgang Hampe
Responsible for the practical test: Dr. Wolfgang Bünder
Acknowledgements
It is a great pleasure to thank the many people whose help and suggestions were so
valuable in preparing and reviewing all the problems and in helping us to perform the
third and the fourth round.
Michael Hell, PD Dr. Sabine Nick, Alexander Rodenberg, Prof. Dr. Carsten Schmuck, Dr.
Jörg Wagler, made essential contributions to develop the problems. Uwe Amthor, Henry
Bittig, Nicole Fernandez-Biber, PD Dr. Sabine Nick, Alexander Rodenberg, were very
important leading the chemistry camps.
I thank Dr. Angela Koch who reviewed my English translations.
Wolfgang Hampe
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Chemistry Olympiad 2006
Contents
Part 1: The problems of the four rounds
Contact adresses .................................................................. 4

First round (problems solved at home) ............................ 6
Second round (problems solved at home) ............................ 9
Third round, test 1 (time 5 hours) .............................................. 17
Third round, test 2 (time 5 hours) .............................................. 24
Fourth round, theoretical test (time 5 hours) .............................................. 32
Fourth round, practical test (time 5 hours) ........................................................ 42
Part 2: The solutions to the problems of the four rounds
First round .................................................................. 46

Second round .................................................................. 51
Third round, test 1 .................................................................. 64
Third round, test 2 .................................................................. 72
Fourth round, theoretical test .................................................................. 81
Part 3: IChO
Problems .................................................................. 98
Soltions to the theoretical problems............................................................. 115
Practical problems .................................................................. 125
Part 4: Appendix
Tables on the history of the IchO ............................................................... 135
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Chemistry Olympiad 2006
Contact addresses:
IPN, University of Kiel, z.H. Dr. Wolfgang Bünder tel: +431-880-5013 (3168)
Olshausenstraße 62 fax: +431-880-5468
D-24098 Kiel/Germany email: buender@ipn.uni-kiel.de
Wolfgang Hampe tel: +431-79433

Habichtweg 11 email: Hampe@t-online.de
D-24147 Klausdorf/Germany
Association to promote the IChO

(Association of former participants and friends of the IChO)
Christoph Jacob tel. +6101-33100
Erlenweg 4 email: chjacob@web.de
D-61138 Niederdorfelden/Germany
Internet address : www.fcho.de
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Problems
Part 1
The problem set of the four rounds
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Problems Round 1
First Round (homework)

Problem 1-1 Correct Indications in a Catalog?
In catalogs of chemicals you find concentrated sulfuric acid, 95 -98 % solution. On the bottle
shipped to a school is written ”1 L = 1.84 kg”.
To find out the real concentration a student dilutes 5 mL of it to 500 mL. Then he takes five
samples of 10.00 mL each and titrates with standardized sodium-hydroxide solution
(c(NaOH) = 0.1760 mol/L):
sample 1 2 3 4 5
V(NaOH) in mL 20.15 19.65 21.30 20.40 20.35
a) Calculate the concentration (mol/L) in the 500 mL solution.
b) What is the mass percentage of the original sulfuric acid?
c) Calculate the mole fraction of sulfuric acid in the original solution.
Problem 1-2 Production of Aluminium
You cannot imagine modern everyday life without aluminium.

Raw material for the production of aluminium is bauxite which contains aluminium oxide.
a) Name at least three advantages of aluminium as a substance compared to iron. Give

disadvantages too.
Specify the approximate percentage of Al2O 3 in bauxite, name deposits of bauxite which
are actually exploited. Explain the origin of the name “bauxite“.
To produce aluminium aluminium oxide (corundum) has to be seperated from bauxite.

Afterwards a fused salt electrolysis is made of a solution of corundum in cryolite. The
temperature of the melt is about 970 °C, a current of 130 kA is used with an efficiency of 95%
and a voltage of 5 to 7 V.
b) Describe the actually used process of seperation of aluminium oxide. Use reaction
equations.
c) Give the formula of corundum and the reason why it is employed.

Write equations for primary and as the case may be secondary reactions at the anode
and the cathode. Give a total reaction equation which includes the secondary reactions
too.
d) Calculate the energy (in kWh), the mass of bauxite (which contains % of mass of Al2O 3)
and the mass of the anode material graphite to produce 1 t of aluminium.
Assume 5.0 V as voltage of the electrolysis and again a current efficiency of 95%.
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Problems Round 1
The thermodynamical data of the table below are approxomately valid for 970 °C. They shall
be used for the calculations in e).
Al(l) O2(g) Al2O3(s)

ΔfH in kJ/mol at 970 °C 48 38 - 1610
S in J/(K∙
mol) at 970 °C 78 238 98
Using the free enthalpie of the process 2 Al 2O3  4 Al + 3 O 2 you approximately

determine the voltage theoretically necessary for the electrolysis to give aluminium and
oxygen. (As a matter of fact a higher voltage is needed.)
e) Calculate the theoretical voltage of the fused salt electrolysis.
f) Give the reason why aluminium can not be produced from an acidic aqueous solution of
Al3+-ions.
For the given chemical reactions the temperature dependence of ΔG is known:


4 Al + 3 O 2  2 Al2O 3 T/K) kJmol-1
ΔG 1 = (- 3351.4 + 0.6264∙ (T > 933 K)

2 C + O2  2 CO ΔG 2 = (- 221.06 - 0.17872∙
T/K) kJmol -1

C + O2  CO2 T/K) kJmol-1
ΔG 3 = (- 393.51 - 0.00286∙
g) Calculate the minimum temperature above which the reduction of Al2O 3 by carbon is
theoretically possible. (Actually it is not possible because of the formation of Al4C3)
Problem 1-3 An Experiment to Do by Yourself
10 mL of a solution of Fe 3+ and 30 mL of a solution of SCN- are mixed. Both solutions have

equal concentrations otherwise the effect cannot be seen.
Observation 1: A red solution forms.
10 mL of the red solution are filled up with water to 100 mL.

Observation 2: The colour of the solution turns to brown.
To one part of this diluted solution solid iron(III) chloride is added.

Observation 3: The colour changes to red.
To another part of the diluted solution ammonium thiocyanate is added.

Observation 4: The colour changes to red.
a) Interpret the four observations.
b) Why do the explanations of the observations 3 and 4 support the explanation of

observation 2?
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Problems Round 1
Problem 1-4 Substitution with Obstacles
Find an optimal way to synthesize 1-bromo-3-Chlorobenzene. Use only reactions with high
yield.
Starting material for the synthesis is 1-chlorobenzene.
Account for the individuel steps of the synthesis.
Problem 1-5 Aromatic Heterocyclic Compounds
Oxazole is an aromatic heterocyclic compound with a five membered ring:
O Oxazole
N
a) Draw the ring with its p orbitals and the orbitals with free electron pairs.
Explain why oxazole is aromatic.
b) Compare the alkalinity (acceptance of protons) between oxazole and pyrrole.
Pyrrole
N
H
Which of the N atoms in oxazole or in pyrrole is more alkalic?

Justify your decision using orbital images of oxazole and pyrrole.
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Problems round 2
Second Round (homework)
Problem 2-1: Chromium and Chromate
1. The redox couple chromium(III)/dichromate (E°(Cr3+|Cr2O 72–) = +1.380 V) is often used in

analytical chemistry.
a) Write the reaction equation for this redox system and check whether a solution of
chromium(III)/ dichromate (c(Cr3+)=c(Cr2O72-)=1 mol/L) is able to release elemental iodine
from a neutral solution which contains iodide (E(I –|I2) = E°(I–|I2) = +0.54 V).
The intense yellow colour of the chromate ions and the intense orange colour of the
dichromate ions are often used to detect chromium. In an important preliminary test
chromium(III) oxide is molten together with potassium nitrate and soda. In aqueous solutions
reactions with hydrogen peroxide, sodium peroxodisulfate or elemental bromine are common
to identify Cr(III).
b) Write balanced equations of these four reactions. What is the role of potassium nitrate
and sodium carbonate in the melting process?
According to the standard potential of bromide/bromine (E°(Br –|Br2) = + 1.065 V) the reaction
of chromiun(III) ions with bromine should not be suitable as a detection test.
c) Why is it still possible to use bromine as a detecting agent? Refer your answer to the
standard potential E°(Br–|Br2). Show your calculations.
In some detecting reactions the presence of certain compounds cause an interference, e.g. if
you use hydrogen peroxide bromide and iodide ions must not be present, whereas using
bromine there must not be an excess of Mn 2+ ions.
d) Account for these interferences.
Another detection reaction for chromium is the reaction of dichromate with hydrogen
peroxide. If it is positive an intense blue colour appears.
The reaction equation is
Cr2O 72– + 4 H2O 2 + 2 H+  2 CrO 5 + 5 H2O
e) What is reduced during this reaction, what is oxidized? Allocate oxidation numbers.
2. Magnetic measurements are an important method to determine the oxidation states of

metal ions. You can measure the magnetic susceptibility and hence determine the magnetic
moment. On the other hand you can calculate the relative magnetic moment μ
- especially for centres of metals of the first transition series - by μ= n 
(n 2) (n =
number of unpaired electrons). Comparing these two values you may find the formal
oxidations state.
An octahedral cyanide-containing complex of chromium, soluble in water, is able to
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Problems round 2
reduce other compounds. Its magnetic properties are determined by the number of
unpaired electrons which are assumed not to interfere with each other (spin-only complex).
It shows the following susceptibility depending on temperature:
Temperature Susceptibility Temperature Susceptibility
in K in cm3 / g in K in cm3 / g
10 10-4
2.74∙ 140 10-5
1.96∙
20 10-4
1.37∙ 150 10-5
1.83∙
30 10-5
9.15∙ 160 10-5
1.71∙
40 10-5
6.86∙ 170 10-5
1.61∙
50 10-5
5.49∙ 180 10-5
1.52∙
60 10-5
4.57∙ 190 10-5
1.44∙
70 10-5
3.92∙ 200 10-5
1.37∙
80 10-5
3.43∙ 210 10-5
1.31∙
90 10-5
3.05∙ 220 10-5
1.25∙
100 10-5
2.74∙ 230 10-5
1.19∙
110 10-5
2.49∙ 240 10-5
1.14∙
120 10-5
2.29∙ 250 10-5
1.10∙
130 10-5
2.11∙ 260 10-5
1.06∙
f) Plot the magnetic susceptibility as a function of temperature.
C
The magnetic property of this complex follows Curies Law = .
T
g) Determine the Curie constant C of this complex.
The relative magnetic moment in terms of the Bohr magneton is

3
RC
M
μ= 21 
1
NA 
9.274 
10 erg 
Oersted
R = 8.314 · 10 7 erg · K–1 · mol–1

M = 364.49 g · mol –1 NA = 6.022 · 1023 · mol–1
1 erg = 1 g · cm 2 · s –2 1 Oersted = 1 cm–½ · g½ · s–1
h) Calculate the magnetic moment of the complex in Bohr magnetons (BM).
Hint: Magnetic measurements and calculations are conducted in the CGS-unit system with
the basic units centimetre (cm), gram (g) and second (s). It is still used as all values of
magnetic moments given in literature would have to change if you use SI units.
i) What ist the oxidation state of chromium in the complex?
If you replace cyanide ions by ammonium molecules the complex shows paramagnetism.
j) Which magnetic moment (in BM) do you expect after the exchange of ligands for this
complex. Account for your decision.
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Problems round 2
Problem 2-2 Spinels

In a narrower sense spinels are mixed oxides of the type M(II)M´(III) 2O4 (M, M´ = metal
cations), which owe their name to the so called "spinel" MgAl2O 4.
The basis of their crystal lattices forms a cubic face-centred closed packing of oxide ions.
In this packing there are cavities of different sizes, octahedral and tetrahedral holes. The
following figure shows the position of a tetrahedral hole.
Fig.1 Cubic face-centred close packing

with tetrahedral hole
In spinels M2+ ions occupy tetrahedral , M’ 3+ ions octahedral holes.

a) Draw one octahedral hole in a plot like fig. 1. Mark the centres of all the other octahedral
holes.
b) Calculate the percentage of occupied tetrahedral and octahedral holes respectively of the
spinel CoAl2O4.
The unit cell of a spinel lattice consists of eight cubes shown in fig. 1. At a certain
temperature T the edge of the unit cell of CoAl 2O 4 has a length of 912 pm. Thereby directly
neighbouring spheres of oxide ions touch each other.
c) Calculate the density of this compound at the temperature T.
d) Determine the maximal radius which the spherical M2+ ions and the spherical M’ 3+ ions
may have in order to fit in the corresponding holes of this unit cell.
Besides the cubic face-centred packing of the oxide ions it depends on the ratio of cations
and anions whether a compound is assigned to the spinels or not. This ratio has to be 3:4.
These conditions provided even compounds with oxidation numbers of the metal ions
diverging from +II und +III are assigned to spinels.
e) Which oxidation numbers may the metal ions in the spinel SnCo2O 4 exhibit?
It is possible to determine the oxidation states of the metals in SnCo 2O 4 by measuring the
paramagnetism.
f) Give the number of unpaired electrons per formula for all cases mentioned in e).
Take also the possibility into account that not Sn n+- but Com+-ions occupy the tetrahedral
holes.
A spinel X shows a compositon of 43,9% O, 18,5% Al as well as 37,6% of other metal ions
(mass percentage in each case)
g) Determine the other metal ions in the spinel X.
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Problems round 2
In a test the amount of M in MAl 2O4 shall be found by an experimental redox titration. The
students found the results of the preparatory experiment:
mL 0 1 2 3 4 5 6 7 8 9 10 10.5 11 11.5 12
E 0.60 0.71 0.73 0.75 0.76 0.77 0.77 0.78 0.79 0.81 0.83 0.85 1.20 1.47 1.51
Knowing from their lessons that only ions of Sn, Fe, Co, Ti, Mn und Cu have to be
considered they are able to find out which kind of ions they will face in the test. On the sheet
of paper found was not written what the meaning of ‚mL’ and ‚E’ should be but the students
know from former instructions that ‚mL’ means the volume of the added titrant (oxidizing or
reducing agent) and ‚E’ the potential of the solution.
h) Determine M. Find from the data above and by calculation how many electrons per ion M
are released or absorbed.
Aufgabe 2-3 Physical Chemistry
There are 64.4 g of a mixture of NO 2 and N2O 4 in a vessel (V = 15 L). The temperature is
constantly held at 300 K.
a) Calculate the pressure in the vessel when the equilibrium NO 2/N2O 4 has established.
In another vessel there was at the beginning a mixture of NO 2 and N 2O 4 in equilibrium under
a pressure of 3.00 bar. The temperature is constantly 350 K all the time.
A valve of the vessel is defective. This leads to a decline in pressure which is proportional to
the pressure in the vessel and amounts to 0.1 % s-1.
b) Determine the partial pressure of NO 2 as a function of time and plot this function from t=0
h to t=1 h.
c) Determine the mole fraction of NO 2 in the vessel as a function of time and plot this
function in the same time interval as in b).
d) Explain why the graphs proceed with a different trend.
Data of ΔH 0f and S 0f under standard conditions (p = 1 .0000∙

105 Pa (!), T = 298 K)
ΔH 0f in kJ S 0f in JK-1mol-1 Cp in JK -1mol-1
NO 2 33 .20 240 .1 37 .2
N2 O 4 9 .16 304 .3 77 .8
Hints:
Take for granted that NO 2 and N2O 4 are ideal gases.
In a) take the values of 298 K for ΔH0f und S0f at T = 300 K.
In b) and c) the dependence of ΔH0f und S0f on temperature has to be taken into account.
In b) assume for simplification that the gas expands into a vacuum.
Problems round 2
Problem 2-4: Structure and Reaction of an Organic Compound

Compound D naturally occurs in terms of manifold derivates. Essential oils (e.g. camo -mile
oil) which are valued for their anti-inflammatory impact embody some of the deri-vates of D.
D is a blue hydrocarbon, soluble not in water but in strong mineral acids. The dipole moment
amounts to 1.08 Debye, unexpected high for a hydrocarbon. The elementary analysis shows
water and carbon dioxid in the mass fraction of 1 : 6,11.
The following image is the 1H-NMR-spectrum of compound D:

(CHCl3 = contaminant in the solvent CDCl 3 gives rise to the peak at 7,26 ppm)
2 1 1 2 2
Intensitätsverhältnis
Ratio of intensities
a) By means of the spectrum you are able to predict a property of the structure of D without
knowing the exact structure.
Specify this property of the structure.
Calculate the ratio n(C):n(H) and the empirical formula of D.
The exact structure of compound D is to be determined by classical synthesis.

It starts with 2,4-dinitrochlorobenzene and pyridine. These two compounds form in a
nucleophilic substitution a compound A. A does not contain any chlorine.
A reacts with 2 equivalents dimethylamine eliminating 2,4-dinitroaniline to form an open
chain compound B.
Problems round 2
Next B reacts with cyclopentadiene in the presence of sodium methoxide. On basic

conditions an additon takes place at first followed by an elimination of dimethylamine to form
compound C (C12H15N).
In a vacuum at 200°C C eliminates dimethylamine to form the wanted compound D.
b) Give the structures of the compounds A to D.
c) Map out a feasible reaction mechanism of the reaction of B with cyclopentadiene in the
presence of sodium methoxide to form C.
The 1H-NMR- spectrum shows doublets and triplets.

d) Explain how compound D generates a doublet and a triplet in the structure of D. Mark
those carbon atoms that are connected to hydrogen atoms whose signal is a triplet.
Knowing the structure of D you can now understand some of the unusual chemical and
physical properties of D mentioned in the beginning.
e) Account for the following properties: Dipole moment, insolubility in water, solubility in
mineral acids and blue colour.
(Give explanations or models, e.g. resonance structures)
Compound D is able to perform a lot of different reactions, for example:

 D reacts with tert. butanole in a substitution reaction catalysed by acids to form F.
 D reacts with Grignard reagents (addition reaction) to form a salt. Conversion with water
and oxidation with tetrachloro parabenzochinone leads to an alkyl substituted
derivate of compound D.
Two products are imaginable. One of them (G) occurs when using methyllithium, the other
one (H) of the two conceivable isomers forms if triphenylmethyl lithium is used.
f) Draw the structures of F, G and H. What makes the difference when using different
compounds of alkyllithium to form G and H respectively?
Even transition-metal compounds of D are known. If D reacts with lithium aluminium hydride
followed by treatment with iron(II) chloride a red compound I forms, which is a mixture of
several stereoisomers.
Precautious hydrogenation of this mixture of isomers leads to only one orange compound J
(C20H26Fe).
g) Draw the structures of al the isomers of I and of J.
Problems round 3 test 1 + 2
Problems for Round 3
Test 1 Berlin and Köln 29. 03. 2006: Problems 3-01 to 3-10
Test 2 Berlin and Köln 31. 03. 2006: Problems 3-11 to 3-20
time 5 hours,
your name write it on every answer sheet,
relevant calculations write them down in the appropriate boxes,
otherwise you will get no points
atomic masses use only the periodic system given,
constants use only the values given in the table
answers only in the appropriate boxes of the
answer sheets.
nothing else will be marked
draft paper use the back of the pages of the problem booklet,
but everything written there will not be marked,
problem booklet you may keep it.
Good Luck
Problems round 3 test 1 + 2
Useful formulas and data
G = H - T·S G = - E·z·F G = - R·T·ln Kth

S o (T) = So(298) + Cp·ln(T/298)
ΔUreaction = ΔHreaction + W (p,V-work only at constant pressure: W = - p∙
ΔV)
-n -n -1 -1
K th = Kp·po ; Kth = Kc (mol/l) ln (Kp1/Kp2) = -H/R·(T 1 - T2 )
p·V = n·R·T
R
T
Nernst equation : E = E0 + ·ln (cOx/c Red)
z
F
for metals c Red = 1 mol/L
for non-metals c Ox = 1 mol/L
rate laws 0. order c = co - k·t

1. order c = co· e k1 t
2. order c -1 = k2·t + co-1
Arrhenius equation: k = A ∙e-Ea/(R∙T)

A pre-exponential factor,
Ea activation energy
Bragg’s equation: n·= 2a·sin
Law of Lambert and Beer: E=

·c·d
 molar absorption coefficient
d length of the cuvette
c conzentration
Henry’s law for dissolving gases in water (A(g) A(aq))

c(A(aq))
KH = KH Henry constant
p(A(g))
Raoul’s law for perfect solutions (mixtures):

pA = xA ∙p*A
pA vapor pressure of A in the mixture
xA mole fraction of A in the mixture
p*A vapor pressure of the pure liquid A
R = 8,314 JK-1mol-1 F = 96485 Cmol -1 NA = 6,022·1023mol-1

p o = 1,000·105 Pa 1 atm = 1,013·105 Pa 1 bar = 1·105 Pa
A periodic table was provided
Round 3, Test 1
Third Round, Test 1

Problem 3-1 (multiple choice, more than one answer may be correct)
a) Catalysts are substances which

A) change the reaction rate
B) transform a reaction into a spontaneous reaction
C) shift the equilibrium of a reaction towards the products
D) change the activation energy
b) A, B and C are gases which react according to A + B 2 C, K p = 3.6 (5000 K).

In a system it can be observed that pA = 2.3 bar, pB = 4.0 bar and p C = 3.6 bar. Which of
the following statements is correct?
A) the system is at equilibrium

B) the system is not at equilibrium, A and B react to form C
C) the system is not at equilibrium, C reacts to form A and B
D) the system is at equilibrium, nevertheless a part of A and B reacts to form C
E) the system is at equilibrium, nevertheless a part of C reacts to form A and B
c) The two Br isotopes, 79Br and 81Br, have a natural molar abundance of about 50% each.
Which is the expected mass spectrum of the parent cation, Br2+?
abundance
abundance
abundance
relative
relative
relative
158 160 162 157 159 161 158 160 162

A mass B mass C mass
abu nda nce
abu nda nce
abu nda nce

relative
relative
relative
158 160 162 157 159 161 158 160 162
D mass E mass F mass
d) The ions below are isoelectronic. Which of the following sequences is correctly arranged
according to their size?
A) I- < Te2- < Ba2+ < Cs+ B) Ba2+ < Te 2- < Cs+ < I - C) Cs + < Ba2+ < Te2- < I -
D) Te2- < I - < Cs+ < Ba2+ E) Ba2+ < Cs+ < I- < Te 2-
e) A compound has the molecular formula C 4H8. How many isomers may exist maximally?
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A) 2 B) 3 C) 4 D) 5 E) 6
17
Round 3, Test 1
Problem 3-2: Metals
We are studying the following seven metals:

Aluminium, zinc, silver, calcium, potassium, copper and iron.
a) Which of these metals will “dissolve” in water?

b) Which of the remaining “dissolves” in hydrochloric acid?
c) Which of the those left over from a) evolves hydrogen with a solution of sodium
hydroxide?
d) How can you dissolve the metals that have proved to be unreactive previously?
Answer in reaction equations.
There are a solution of lead(II) ions and a solution of copper (II) ions with equal concentra-
tions. Two plates having the same size and mass of an unknown metal Me, which forms
Me 2+ ions, are put into these solutions, one in each.
Copper and lead precipitate on the plates. Later on the plates are removed simulta neously
from the solutions, dried and weighed. During these procedures all the precipitated metal
remains completely on the plates.
The plate taken out of the lead(II) solution shows an increase of mass of 19%, the other one
a decrease of mass of 9,8%, relating to the starting mass of the plates.
Assume that the reaction rate of the precipitation of the metal is the same in both solutions .
e) Determine the unknown metal.
Problem 3-3 Impurities
During a custom control a parcel with heroin (C21H23O 5N) was found, however admixed with
lactose (C 12H22O 11).
1 g of this mixture was dissolved in water, the solution filled up to 100 mL. This solution had
an osmotic pressure of 718 hPa at 25°C.
a) Calculate the composition (mass percentage) of the sample.
Desiccated anhydrous calcium chloride was stored in an improperly closed vessel. Thus it
was partially hydrated again. A 150 g sample of this material was completely dissolved in
80 g of hot water, then the solution was cooled down to 20°C. On cooling 74. 9 g of
CaCl 2∙
6 H2O precipitated.
Solubility of calcium chloride at 20°C is 74.5 g of CaCl 2/100 g of water.
b) Determine the water content of calcium chloride in the 150 g sample (mole of water per 1
mol of CaCl 2)
Round 3, Test 1
Problem 3-4 Acids
The degree of protolysis in an aquous solution of acetic acid is 85% .

10-5), ) and calculate the pH. How
a) Determine the concentration of acetic acid (K a = 1.74∙
many g of acetic acid had to be dissolved to yield 1 L of this solution?
Sodium propionate was dissolved in a solution of sodium hydroxide and the solution was
filled up to 250 mL. It showed a pH value of 12.18. 20 mL of this solution were titrated with
hydrochloric acid of unknown concentration. The image below shows the results graphically.
12
10
pH 6
0
0 5 10 15 20 25 30 35
V(HCl)
b) Calculate the amount of sodium propionate dissolved (in g).
Problem 3-5 Equilibria
103 hPa (= pstandard) the degree of dissociation (homolytic

At T = 1000 K and p = 1.000∙
10-7 and
dissociation into the elements) of water vapor and hydrogen chloride are 2.48∙
10-5 respectively.
1.10∙
Calculate the equilibrium constant and Gibbs free energy change for the reaction

4 HCl + O 2  2 Cl 2 + 2 H2O.
Problem 3-6 Structures
The valence shell electron pair repulsion theory of Gillespie (VSEPR-model) is an

appropriate model to describe the stereochemical structure of molecular compounds.
a) Write down the basic principles of this theory.(One of them shows a relation between the
binding electron pair and the electronegativity of the central ion and the ligand
respectively.)
Round 3, Test 1
b) Using this model draw the possible structures of

CCl 4, TeCl 4 and XeF4
If there exists more than one possible structure, give all of them and indicate, which of
them is most likely. Account for your decision.
c) Anwer the questions in b) also for the following molecules

BeCl2, SnCl2, H 2S und XeF 2.
(Remember, there may be more than one structure for a molecule.)
Estimate the bond angles.
d) Phosphorus forms trihalides PX3 with X = F, Cl, Br, I .

Which is the maximum size of the angle XPX according to the VSEPR-model?
Actually the angles of the trihalides are smaller.

Give the reason.
There is a tendency in the size of the angles from I to F.

Specify this tendency and give the reason for it.
e) With the help of the VSEPR model account for the changes of the following bond angles:
NH3 107°  PH 3 93,6°
and
PH3 93,6°  PF3 96,3°
Problem 3-7 A Ceramic Hard Coating
Boron phosphide is a highly esteemed abrasion-resistant hard coating that is produced in the
reaction of boron tribromide and phosphorus tribromide in a hydrogen atmosphere at high
temperatures (>750°C). This ceramic material is used as a thin protecting thin on metal
surfaces.
a) Give the equation for the formation of boron phosphide.
b) Draw 3-D structures of boron tribromide and phosphorus tribromide. What are the
geometrical characteristics?
Boron phosphide crystillises in zinc-blende structure, derived from a cubic-close packed

structure of boron atoms with phosphorus atoms located in tetrahedral holes.
c) Draw the structure of boron phosphide.
d) The lattice parameter of the unit cell ist 4,78 Å.
Calculate the density in kg/m 3.
e)* Calculate the distance between a boron and a phosphorus particle.
Round 3, Test 1
The Born-Landé formula can be used to calculate the lattice energy:

2
Z 
Z M e  1
Ulattice = - f∙  1 
 (U in kJ/mol)
r r  n
e2 amounts to 1390 when r+ and r- are given in Å. The Madelung constant M is
The factor f∙
1.638 and n = 7. The charges of the ions ,Z + and Z- , have to be inserted as absolute values,
as integers.
f) Calculate the lattice energy of boron phosphide.
The rate (r) of formation of boron phosphide depends on the concentration of the reactants
as given in the table.
-1 -1 -1 -1
temperature in °C c(BBr3) in molL c(PBr3 ) in molL c(H2 ) in molL r in mols
-6 -6 -8
800 2.25∙
10 9.00∙
10 0.070 4.60∙
10
-6 -6 -8
800 4.50∙
10 9.00∙
10 0.070 9.20∙
10
-6 -6 -8
800 9.00∙
10 9.00∙
10 0.070 18.4∙
10
-6 -6 -8
800 2.25∙
10 2.25∙
10 0.070 1.15∙
10
-6 -6 -8
800 2.25∙
10 4.50∙
10 0.070 2.30∙
10
-6 -6 -8
800 2.25∙
10 9.00∙
10 0.035 4.60∙
10
-6 -6 -8
880 2.25∙
10 9.00∙
10 0.070 19.6∙
10
g) Determine the rate equation and the order of the reaction.

Calculate the rate constants at 800°C and at 880°C.
h) Calculate the activation energy of the formation of boron phosphide.
* Extract from a formulary concerning a tetrahedron with the edge a:
V = a 3∙2 /12 O = a 2∙3 h = a∙6 /3 rcircumcircle = a∙6 /4 rincircle = a∙6 /12
Problem 3-8 Determination of a Structure

An organic compound X contains 65.2% (m/m) carbon and 8.75% (m/m) hydrogen and no
other element except oxygen.
X is known to be acidic and titration of 43,7 mg of this compound required 23.7 mL of sodium
hydroxide solution (c = 0.0100 mol/L) to reach the equivalent point.
The molecular weight of X was determined to be less then 200 g/mol. There are no rings in
X.
a) What is the molecular formula of X? What functional groups might be responsible for the
acidity of the compound?
Calculate the number of double bonds in X.
2a 2 b
Hint: CaHbO c contains DBE  double bond equivalents.
www.ShimiPedia.ir 2
21
Round 3, Test 1
The following reactions are known:
 X reacts with hydrogen in the presence of finely divided platinum metal to form a new
compound A.
 Further reduction of A with sodium borohydride in ethanol produces substance B.
 Compound B was readily dehydrated upon warming with strong sulfuric acid to form
C. C contains a double bond.
 13
C-NMR of C revealed among other features the presence of a methyl group at-
tached to a double bond.
b) What functional groups are consistent with the above reactions?
Ozonolysis of C followed by an oxidative work up gave only two fragments, acetic acid and
the dicarboxylic acid HOOC-(CH 2)6- COOH.
Similar cleavage of X itself yielded oxalic acid (HOOC-COOH) and a substance E which
contained a carboxylic acid group.
c) Deduce the structures of the compounds A, B, C and of compound X.

There are two isomeric foms of X.
d) Depict the isomers of X. Which kind of isomerism do they show?
Problem 3-9 Synthesis of an Acid

Starting with compound X you get compound Y in high yield performing a multi-step
synthesis.
Suggest how this could be done using structures in the reaction steps shown.
NO2
COOH
CH3 CH3
CH3 CH3
compound X compound Y
Round 3, Test 1
Problem 3-10 Chirality of a Compound
The chirality of1-Bromo–3,4-dichlorocyclopentane shall be analysed.
a) Give the number of stereogenic centres of 1-bromo-3,4-dichlorocyclopentane and the

maximum number of stereoisomers you may expect.
Actually there are less isomers.
b) Depict all structural formulas of the stereoisomers of 1-bromo-3,4-dichlorocyclopentane

and account for the reason that there are less than the maximum number.
Which of them show optical activity?
Hint for the images: In the picture of a three membered ring the thick point indicates an H
atom above the plain of the ring.
If there is not such a point the H atom lies below that plain and therefore the substituent lies
above it.
CH3
CH3
H 1 2
example: 1
= H
H3C
CH3 3
3 2
You may use one of these ways of drawing.
Problems round 3 test 2
Third round, test 2
Problem 3-11
a) Chemical bonding in some species cannot be described by the Lewis model, i.e.
assuming that atoms tend to attain nobel-gas configuration by sharing electron pairs. An
example of such species is
A) NH4+ B) BF 4- C) HF 2- D) SO42- E) S2O 32-
b) Which of the following species has the smallest F - X - F bond angle:

A) BF4- B) CF 2Cl2 C) BF3 D) BeF2
c) Solutions containing H3PO4 and/or NaH 2PO4 are titrated with a strong base. Assign
the contents of these solutions to the titration curves (pH vs. volume of titrant) shown in
the figure (for H 3PO4: pK 1 = 2.1, pK2 = 7.2, pK 3 = 12.0).
pH
Volume of Titrant (in mL)

(i) The solution contains H3PO4 only
(ii) The solution contains H 3PO4 and NaH2PO4 in the mole ratio 2:1
(iii) The solution contains H3PO4 and NaH2PO4 in the mole ratio 1:1.
d) Which of the parallelograms in the figure below are unit cells?
e) To 30 mL of a Ba(OH) 2 solution (0,10 mol/L) 30 mL of a H2SO4 solution are added (0,10

mol/L) . The increase of temperature is ΔT1. The experiment is repeated with 90 mL of
each of the same solutions and the rise in temperature is ΔT2. Which of the following
equation is correct?
1
A) ΔT2 = ΔT1 B) ΔT2 = 3 ∙ΔT1 C) ΔT2 = 6 ∙ΔT1 D) ΔT2 = 3
∙ΔT1
Problem 3-12 Acids
Tea-flavouring tablets are sold in packs of 200. The tablets in 1 pack have the weight of 25 g
altogether. The tablets consist of citric acid (2-Hydroxy-1,2,3-propanetricarboxylic acid) and
other additives.
Tasty tea can be made by dissolving 6 tablets in 1 L of tea. The pH of this solution is 4.2.
(Tea leaves and the additives do not contribute to the change in pH-value)
a) Calculate the mass of citric acid in one tablet.

(Take only the first step of protolysis into consideration)
Actually the second step of protolysis plays a certain role and leads to a deviation of about
16% compared with the result of a).
b) Write all the equations which are necessary to calculate the mass of citric acid in one
tablet if you include the second step.
A person with a stomach content of 2.30 L drinks two cups of the flavoured tea (320mL)-
The original pH of the gastic juice was 2.1 before drinking the tea due to the hydrochloric
10-6 , K a2, citric acid = 7.24∙
acid excreted by the stomach. (Ka1, citric acid = 3.98∙ 10 -11 , Ka3, citric acid =
10-20 )
6.3∙
c) What is the ratio between the protolysis of the citric acid in the tea and in the stomach?
(You may assume that the content of the stomach increases by drinking two cups of tea,
the amount of H 3O + ions, however, remains practically constant.)
d) Assign the pKa values 3.41, 4.01, 4,21, 4.35, 4.46 to the following benzoic acids
R R = H, H, CH3, NO 2, OCH3, Cl
COOH
Explain your decisions.
Problem 3-13
Diluted sulphuric acid was dropping on 1 g of a compound A until no further reaction

occurred. The products of the reaction were a gas B and a nearly colourless solution of C.
After drying the amount of gas was 0.211 L (at 25° and 1.013 hPa) with a weight of 0.38 g.
The solution containing C was diluted to 100 mL. It was treated as follows.
I 50 mL of it were titrated with an acidic solution of potassium permanganate (c = 0.0200
mol/L), consumption 43.15 mL.
II H2O 2 was added to the nearly colourless solution of C. The colour changed to pale
yellow. Further addition of ammonia gives a brown precipitate D.This precipitate was
filtrated off and solved in diluted hydrochloric acid to yield a yellow solution of E. This
solution turned to deep red after addition of potassium thiocyanate.
a) Identify A to E.
Show all your calculations and write balanced equations for all reactions.
b) Prove whether really 1 g of A reacted at the beginning. If not please give reasons.
Problem 3-14 Redox Reaction
A solution containing Sn 2+ ions is titrated potentiometrically with a solution of Fe3+ ions at

25°C.
The standard reaction potentials are

Sn 4+ + 2 e-  Sn 2+ E° = 0.154 V

Fe 3+
+e -
 Fe 2+
E° = 0.771 V
a) Write the overall reaction equation and calculate the standard free energy change (ΔG°)
of it.
b) Determine the equilibrium constant of the reaction.
20 mL of a solution of Sn2+ ions (c = 0.10 mol/L) is titrated with a solution of Fe 3+ ions (c =

0.20 mol/L) . A saturated calomel electrode (E° calomel = 0.242 V) is used as reference
electrode.
Calculate the voltage of the cell
c) when 5 mL of the Fe 3+ solution are added,
d) at the equivalence point (hint: At the equivalence point is E(Sn 4+/Sn 2+) = E(Fe3+/Fe2+)),
e) when 30 mL of the Fe 3+ solution are added.
Problem 3-15 Kinetics
1.00 g of X, a pungent smelling organic liquid, was solved in water and filled up to 100.0 mL.
10.0 mL of this solution were titrated with a solution of potassium hydroxide (c = 0.5000
mol/L). When 43.5 mL of the potassium-hydroxide solution were added the colour of the
solution containing phenolphthalein changed from colourless to pink.
a) Determine X.
Under the influence of a concentrated acid S a portion of X disintegrates to form water and a
gas.
b) Write the reaction equation. Which acid S is likely to be used?
105 Pa:
The following kinetic data of disintegration was obtained at 25°C and p = 1.013∙
t in s 0 50 100 150 200 ∞

V(Gas) in mL 0 11.6 20.2 26.1 30.4 41.5
c) Calculate the amount of X in the beginning. Which reaction order do you expect?
Account for your assumption.
d) Prove your assumption using the given data. Calculate the reaction-rate constant.
The decomposition of nitrosyl chloride between 150°C und 250°C follows a homogeneous

reaction of the second order: 2 NOCl  2 NO + Cl2 .
The following rate constants were found:
Temperature in °C 150 170 190 210 230

mol-1∙
k (in L∙ s -1) /103 3.65 12.9 43.0 123 370
e) Determine the activation energy of the reaction (preferably graphically).
Problem 3-16 UV-Spectroscopy
Using the law of Lambert and Beer you can use UV -spectrometry to determine the
concentration of a substance in a solution. In doing so the absorption A (A = 10log (I o/I) is
measured.
Here the maximal and the minimal concentration of ferroin in a solution will be looked at by
using a spectrometer at λ= 512 nm (ε= 10500 Lmol-1cm-1).
a) Calculate the lowest concentration of ferroin that can be determined in a 1 cm cuvet, if a

2% difference in light intensity still can be measured.
b) Calculate the highest concentration of ferroin that can be determined in a 1cm cuvet, if at
least 2% of the incident light must reach the detector.
The composition of a complex between a metal M and a ligand L can also be determined. In
this method the sum of concentrations of M and L is constant while their ratio is varied (Job’s
methode). The following graph of absorbance vs. mol fraction for a complex is given,
whereby the mol fraction x M = cM/(c M + cL) is varied (measurement at 552 nm).
xM
c) Determine the composition of the complex.
d) Which compound absorbs at xM = 0, which at x M = 1?

Show how you derive your answer.
e) Calculate the ratio of absorption coefficients of M and L.
f) Calculate the percentage of the incident light that has been transmitted through the
solutions at xM = 0 and at x M =1, respectively.
Problem 3-17 An Industrial Process
Methanol is produced in large amounts from synthesis gas, a mixture of carbon monoxide
and hydrogen, whereas synthesis gas is made von methane, a main component of natural
gas, and water vapor.
The continuous process of the methanol synthesis is schematically shown in the figure
below.
In step A synthesis gas is produced, in step B methanol.
 
synthesis gas
unit
 condenser
 methanol  condenser
 step A
unit
step B
 
Stream  consists of methane at a pressure of 250.0 kPa and a temperature of 25.0°C,

stream  consists of water vapor under a pressure of 200.0 kPa and a temperature of
100,0°C.
The flows of stream  and  are 55,0 m3/s and 150,0 m3/s respectively.
Sream  leaving the synthesis gas unit is a mixture of synthesis gas and an excess of one
reactant, which condenses at 25.0°C and is lead off via stream . Methanol is synthesised
in step B.
Stream  contains methanol and the excess of one reactant. In the following unit methanol
condenses at 25°C and is lead off in stream .
mL -1.
ρ(CH3OH) (l) = 0.791 g∙
Assumptions: All gases are perfect, total conversion in steps A and B, complete seperation in
the condensers.
a) Give the reaction equation of step A and of step B.

b) After step A and after step B there is an excess of one reactant. Which and how much of
it is it in each case?
c) Calculate the flows in m3/s (at 25°C and 101.3 kPa) of the following streams
(i)  ii)  iii) 
Actually there is not a complete conversion in step B. The factory is designed in such a way
that 2/3 of the CO is converted to methanol. In stream  the flow of CO is 1500 mol/s
besides the associated amount of hydrogen (these values do not correspond to the data
above).
d) Calculate the flow of CO, H 2 and methanol in stream  in mol/s.
In stream  all species are gases. The total pressure 10 MPa.

e) Calculate the partial pressures in MPa of CO, H 2 and CH3OH in stream .
When the methanol reactor is large enough the reaction goes to equilibrium. The partial
pressures in stream  obey the equation:
p20
p(CH 3 OH) 
Kp = 2
p(CO) 
p (H 2 )
wherein p 0 is a constant (0.1 MPa) and Kp is a function of temperature as is shown in the

figure below (the vertical scale is logarithmic).
100
Kp
10-1
10-2
10-3
10-4
400 500 600 T, K 700
f) Calculate Kp and ascertain the temperature T at which the reaction must be operated to
achieve this equilibrium.
Aufgabe 3-18 Second Substituion

Toluen (Methylbenzene) is treated with a mixture of nitric acid and sulfuric acid.
a) Which compound(s) do you expect to be main product(s) of monosubstitution? Write the

structural formula(s) of the compound(s).
b) Justify your decision by showing all intermediate stages and comparing their energies.
What is the influence of the methyl group?
Phenol (hydroxybenzene) is treated with a mixture of nitric acid and sulfuric acid.
c) Which compound(s) do you expect to be main product(s) of monosubstitution? Write the

structural formula(s) of the compound(s).
d) Justify your decision by showing all intermediate stages and comparing their energies.
What is the influence of the OH group?
The substitution of p-methylphenol leads to 2-brom-4-methylphenol as main product.
e) Give reasons for the formation of this bromo-compound.
Problem 3-19 Bromation of an Allyl Compound

The bromation with N-bromsuccinimide follows a free-radical mechanism.
Is this reaction carried out with a cyclic compound with allylic structure, the C=C -double
bond persists and the appropriate products of bromation form.
The folowing reaction was performed:
H3 C CH3
H
H N -bromosuccinimide Four different products
(I bis IV) of substitution
CCl4, h were found
H
H
H
H
H 3C CH3 H 3C CH 3 H 3C CH 3 H 3C CH3
H H H Br
H H H H
Br H
H H H H
H H H H
Br H
H Br H H
I II III IV
a) Give a mechanism for the formation of these four compounds.

The exlplanation shjould include
 the formation and structure of the radical parent compound
 a reason for the stability of this radical structure
 the formation of the compounds I - IV from this structure.
b) Which kinds of isomerism do you find between the compounds?

Assign to each pair of compounds the approppriate kind of isomerism.
Problem 3-20 Reaction of an Organic Compound

2,3,5 Trimethylhept – 3- ene (compound A) reacts with a diluted solution of permanganate to
form compound B. The reaction of B with periodic acid (HIO 4) leads to two products C and D
with the same molecular formula (C 5H10O).
Compound C shows a positive Tollens’ reaction test. This test is negative when carried out
with D, but D shows a positive iodoform test.
Compound D forms a yellow residue with 2,4-dinitrophenylhydrazine. Both compounds, C
and D, form a pure hydrocarbon E when brought together with zinc amalgm and hydrochloric
acid.
a) Give the structural formulas and the names of the compounds A to E.
Write down the equations of the reactions which lead to the compounds B,C,D and E.
Give also the equations of the reactions with Tollens’ reagent ([Ag(NH 3)2]+) and with 2,4
dinitrophenylhydrazine.
b) Which of the compounds shows optical activity? Mark the stereogenic centres with an
asterix (*).
The compounds C and D can be formed directly from A.

c) Show this reaction with all its intermediates.
Problems round 4 (theoretical)
Fourth round (theoretical problems)
Problem 4-1
Radiotherapy involves the targetting of sites of active cell division by radionuclides to induce
cell death. On the other hand nuclear imaging employs radioisotopes to reveal metabolic
details of an organ. One such technique involves determination of a patient’s blood volume.
Three radiopharmaceutical compounds are available. Thy contain, respectively, the
radioisotopes 71Zn (t1/2 = 2.4 minutes), 67Ga (t 1/2 = 78.25 hours) and 68
Ge (t1/2 = 287 days),
each with an activity of 7.0·107 Bq/mL.
a) Calculate (for each pharmaceutical)
(i) the activity (in Bq/mL) after ¾ of an hour have elapsed and
(ii) the activity after ¾ of an hour and after dilution of 10mL of the pharmaceutical to 25 L
The modes of decay for these three isotopes are β-particle emission ( 71Zn) and electron
capture (67Ga and 68Ge).
b) What are the products of these decay processes?
10.25 mg of Ga, containing 5.0·10-5 % (mol/mol) 67Ga at the moment of synthesis, react
completely to form gallium citrate (GaC 6H5O 6·3H2O). Following syntheses the citrate sample
is dissolved in 100mL of water. Eight hours after syntheses 1 mL of the solution is
administered intravenously to a patient, and one hour later a 1 mL blood sample is taken
from the patient. This blood sample has an activity of 165,6 Bq/mL.
c) Calculate the blood volume of this patient.
(1 Bq (Becquerel) = 1 decay/second)
Problem 4-2
In the construction industry limestone is used in great amounts as raw material. The
technical process of lime burning is known since ancient times.
In this process the partial pressure of CO2 ,p(CO 2), depends on temperature:
T in K 800 900 1000 1100 1200 1300

p(CO2) in hPa 0.50 10.0 112 800 4050 16100
a) Calculate ΔG of the decomposition of calcium carbonate at each of the temperatures

given.
b) Calculate the change of enthalpy ΔH° and the change of entropy ΔS°. Due to the
reaction equation it is possible to predict the algebraic signof ΔS°. State the reason.
c) Above which temperature (in °C) is the reaction spontaneous (be exact upto 10°C)
Standard pressure p0 = 1.000 ∙10 5 Pa

for simplification: ΔH and ΔS independent of temperature
Problem 4-3 Electrochemistry and Solibility Products
L-1
Given a solution A of silver nitrate and lead nitrate in water with c(AgNO 3) = 0.050 mol∙
L-1 .
and c(Pb(NO 3)2) = 0.100 mol∙
a) Calculate the pH of the solution.
L-1) and nitric acid ((c = 0.200 mol∙

10 mL of a solution of potassium iodid (c = 0.250 mol∙ L-1)
are added to 10 mL of solution A to form 20 mL of solution B with a sediment. Together with
a silver electrode half cell 1 is generated.
L-1 silver nitrate and 0.040 mol∙
Solution C is made by dissolving of 0.010 mol∙ L-1 potassium
thiocyanate. Together with a silver electrode half cell 2 is generated.
Both half cells are connected with a salt bridge to form an electrochemical cell.
b) Calculate the voltage of the cell, E cell at 25°C (= 298 K).
c) Write the total cell reaction and calculate the eqilibrium constant of this reaction.
A small amount of sodium hydroxide is added to solution B.
d) How does the voltage change? Discuss two different cases depending on the amount of
sodium hydroxide added.
Iron(III)-nitrate is added to solution C.
e) Explain how the voltage of the cell changes.
Data:
Ag + + H2O AgOH + H+ K 1 = 10-11.70
Pb 2+ + H2O PbOH+ + H+ K 2 = 10-7.80
pK sp(AgI) = 16 pKsp (PbI2) = 7.86 pK sp(AgSCN) =12 E°(Ag+/Ag) = 0.799 V
Many elements e.g. vanadium form ions with different oxidation states. The standdard
potentials are found in tables:
V 3+ + e- V2+ E° = - 0.255 V
2+ + - 3+
VO + 2H + e V + H2O E° = 0.377 V
VO2+ + 2 H+ + e- VO2+ + H2O E° = 1.00 V
+ + - 2+
V(OH) 4 + 2 H + e VO + 3 H2O E° = 1.00 V
V(OH) 4+ + 4 H + + 5 e- V + 4 H2O E° = - 0.25 V
f) Calculate ΔG° for the reactionV2+ + H2 V + 2 H+
Problem 4-4 Michaelis-Menten Mechanism
In some cases steady state approximation is used in the calculation of kinetics. The steady
state approximation assumes that during the major part of the reaction the concentration of
all reactive intermediates are constant and small.
An example are biochemical reactions of the type
k1 k3
S + E ES  P + E
k2
S = substrate (e.g. penicillin) E = enzyme (e.g. β-lactamase)

ES = enzym-substrat-complex P = product.
It is assumed that the pre-equilibrium reaction is installed very quickly, so that the reverse
reaction can be neglected and that the concentration of S is much larger than that of E.
a) Show that these assumptions lead to the equation

[ES] =
 
E total S
with the Michaelis constant KM =
k 2 k 3
K M  S k1
[E] total = total concentration of enzyme ([E] + [ES])
b) Account for the fact that the maximum reaction rate is (d[P]/dt)max = vmax = k3∙
[E] total .

v max 
S
c) Derive from a) and b) the Michaelis-Menten equation v= .
K M 
S
d) Read KM from the plot (v = f([S]) below. Where can you read this value, explain your
decision.

v in 10-6 mol L- 1 s -1
v max = 3.0∙
mol L-1 s -1
-6
2.0∙
10
10-6
1.0∙
1.0∙
10
-4
2.0∙
10
-4
10-4
3.0∙ [S] in mol L-1 
1 1
Often you find the Lineweaver-Burk plot f ( ) .
v [S ]
1 KM 1 1
e) Show that    .
v v max [S ] v max
10-9 mol L-1 the initial rate is

In an experiment with the enzyme concentration Etotal = 1.0∙
measured for several different initial concentrations of S:
[S]0 ∙10 6 in mol L-1 3.0 5.0 10 20

5 -1 -1
v0 ∙10 in mol L min 1.06 1.55 2.37 3.21
f) Draw a Lineweaver-Burk plot and determine the Michaelis constante KM and the reaction
rate constant k3.
10-5 mol∙
In another enuymatic reaction the Michaelis constante is K M = 1.5∙ L-1. The initial
10-5 mol∙
concentration of the substrate is 3∙ L-1.
g) Calculate the fraction (fES ) of enzyme molecules, which bind to the substrate.
The catalytic efficiency of an enzyme is given by the catalytic constant k kat (turnover number).
This number tells you the amount of substrate molecules which form the product per time
unit, if the total amount of enzyme is bound to the substrate.
mol-1) cleaves the peptid bonding of proteins . In 10 mL of
The enzyme pepsin (M = 41977 g∙
a solution 10 -9 g pepsin were dissolved. The maximum reaction rate was measured:
10-11 mol∙
v max = 7.15∙ L -1∙
min-1.
h) Calculate the tunrover number of pepsin in s-1.
Problem 4-5
A solution of potassium permanganate was standardised by titration with a solution of

sodium oxalate. The average of several experiments is: weighed portion 0.1702 g pure
sodium oxalate dissolved in water and 26.70 mL of permanganate solution needed to titrate
up to the equivlance point.
a) Write the reaction equation and determine the concentration of the permanganate
solution.
A sample of 0.2250 g contains a mixure of iron and iron(III)-oxide. This sample is dissoluted
completely and then treated with a saturated solution of SO 2 in water. The excess of SO2 is
removed by adding acid and boiling.
In a following titration with the solution of potassium permanganate (from a)) 37.50 mL are
used.
b) Write the equations of all reactions involved and calculate the mass ratio (%) of iron and
iron(III)-oxide in the sample.
A sample of steel contains 10% nickel and 70% iron. 0.200 g are dissolved completely in
acid and diluted to 200 mL. Iron is precipitated as iron(III)-hydroxide, which is ignited to
constant weight.
c) Calculate the range of pH, in which the precipitation of iron(III)-hydroxide has to be
performed for a quantitative determination of iron without any interference by nickel. After
precipitation a maximum of 0.1% of iron may stay in the solution.
Solubility products Ksp (Fe(OH)3) 10 -38

= 4∙ 10-16
K sp(Ni(OH)2) = 6∙
Problem 4-6
106 molecules/cm3
Mesurements in the exosphere above 700 km show a gas density of 1.0∙
and a temperature of about 1200 K. In this region the mean free path of a molecule exeeds
13000 km, the diameter of the earth.
a) Calculate the medial pressure in the height of 700 km.
In a good vacuum on the earth you can reach a pressure of 10 -9 mm Hg at T = 298 K. This
specification is unusual and not according to SI-units. “Pressure of 1 mm Hg“ is the pressure
of a 1 mm column of mercury on the base area.
b) Convert the pressure in the vacuum to the unit pascal.
c) Calculate the number of gas molecules/cm3 in such a vacuum at 25°C and compare with
the result of a).
Assume that the particles mentioned above are hydrogen atoms.

8RT
d) Calculate the mean speed ( ) of these hydrogen atoms under both conditions and
M
compare.
At low temperatures hydogen atoms meeting each other form molecules. You shall compare
how often hydrogen atoms in intergalactic space ( 1 hydrogen atom/m 3 at T = 2.7 K) and in a
10 15 hydrogen atoms/m3 at a temperature at which their mean speed is
vacuum on earth (40∙
2400 m/s) collide.
Consider for this purpose the so called collision cylinder. This is a cylinder swept out by a
d2∙ 2 ,
hydrogen atom in one second calculated by multiplying the cross sectional area, π∙
10-8 cm).
by its speed (d = diameter of a hydrogen atom = 1∙
The number of particles of this cylinder leads to the number of collisions per second.
e) Calculate under both conditions the collision frequency and and the mean free path i.e.
the average distance a hydrogen atom covers until it meets another one.
Data : ρ(Hg) = 13.55 g/cm 3 g = 9.81 m/s2
Problem 4-7
Gout comprises a number of diseases which are designated by repeated attacks of arthritis
(inflammation of joints) and by formation of kidney stones.
Precondition for the appearance of gout is a concentration of uric acid (HUr) and urate (Ur- )
in blood far to high. Arthritis is created by cristals of sodium urate in the joint fluid.
In this connection the following equilibria play a decisive role:
HUr (aq) + H2O (l) Ur - (aq) + H3O + (aq) pK = 5.4 at 37°C

- +
Ur (aq) + Na (aq) NaUr (s)
At 37°C 8.0 mmol sodium urate are soluble in 1.0 L of water.

a) Calculate the solubility product of sodium urate. Neglect the protolysis of urate.
In blood serum (pH = 7.4; 37°C) is c(Na +) = 130 mmol/L.

b) Calculate the maximum feasable concentration of urate in serum, at which no sodium
urate precipitates.
The solubility product depends on temperature. It is known that pains caused by gout usually
appear at first in toes and fingers.
c) Indicate the dependency of K sp on temperature.
The solubility of uric acid in water at 37°C is 0.5 mmol/L.

d) If there is no precipitation of sodium urate, show by caIculation that uric acid will not
precipitate either i.e. arthristis cannot be caused by sole precipitation of uric acid.
Assume that only HUr and Ur - are responsible for the pH-value.
Often stones consisting of cristals of uric acid are found in kidneys of patients. The reason is
a far too high concentration of (uric acid + urate) in the urine of these patients in connection
with a low (but normal) pH of the urine (pH = 5 to 6).
e) Calculate the pH at which stones of uric acid can form in the urine of a patient
Assume a concentration of (uric acid + urate) of 2.0 mmol/L.
Reason for too much uric acid and urate at gout patients can be both, an increase of
production of uric acid and/or a decrease of excretion of uric acid.
In an experiment 20 mg of radioactive marked uric acid are injected intravenously. It mixes
quickly and evenly with the uric acid in the body, both are excreted in the urine. In the urine
the total amount of excreted uric acid is measured.
The following plot shows the results of an ill patient P and a healthy person N.
2,6

2,4
2,2
mol % marked
uric acid in excreted urinere 2,0
1,8
1,6
1,4
1,2
healthy person N
1,0
0,8
0,6
0,4
ill patient P
0,2
0,0
0 20 40 60 80 100 120
time in hours 
f) Calculate the mass of uric acid in the body of the patient P and in the body of the person
P before the injection of the sample of 20 mg. Use the data of the plot.
g) Derive from the plot that the process of excretion in both cases follows a rate law of first
order. Calculate the rate constants.
Problem 4-8 Aldol Reactions
If two aldehydes or ketones react the products formed are called „aldol“ („-
hydroxyaldehyde“) or „-hydroxyketone“ respectively. The aldol reaction takes place in a
basic surrounding and is reversible.
Example: Two molecules of acetaldehyde are in equilibrium with 3-hydroxybutanal.
(Remark: Don’t bother with stereoisomers when asked for reaction products)
a) Which product forms in an aldol reaction of propanal? Write the reaction mechanism and
give the name of the product.
b) Comment on the reaction mechanism of an aldol reaction of RCH2CHO as an example.
To do this respond to the following questions:
 Which function has the base in the aldol reaction?
 Which is the electrophilic and which the nucleophilic reactant in this aldol
reaction?
 Which precondition of a carbonyl compound is necessary to form the nucleophilic
part in the course of reaction?
Formaldehyde and acetaldehyde react in a simple aldol reaction. Two products form.
c) Give the formulas of these two products. Why do only two but not four products form?
If acetaldehyde (pKs ~17) and 2,4-pentadione (pKs ~9) react in an aldol reaction mainly one
product forms.
d) Give the reaction mechanism of the formation of this favoured product. Account for the
preference of this product.
The compound 2,5-hexadione performs under mild conditions in the presence of a base an
intramolecular aldol reaction. Two products form.
e) Show the course of reactions which lead to these products by giving the respective
intermediate steps.
One of the products is more stable. Account for the reason.
Problem 4-9 Sugars
D-Glucose has the following structure in Fischer projection.
a) Give the structure of L-glucose in Fischer projection.
b) How many stereogenic centres has L-glucose (open chain)?

CHO
Which kind of stereoisormers are D- and L-glucose
H C OH
c) Draw the structure of D-glucose ( -D-glucose, pyranose form) and
L-glucose ( -L-glucose, pyranose form) as Haworth projection HO C H
(ring with oxygen atom at the upper right) H C OH
d) Draw the structures of -D-glucopyranose, -D-glucopyranose H C OH

and -L-glucopyranose) in chair representation. CH2OH
Label the substituents with an a for axial and e for equatorial
position. D-Glucose
Explain which of these compounds is (are) especially stable.
e) -D-glucopyranose reacts with an excess of acetic anhydride (basic surrounding).

Which compound forms?
Draw the Haworth projection of the product.
To which class of compounds does the product belong?
f) -D-glucopyranose react with an excess of alkyl halides (e.g. CH3I) in the presence of
silver oxide.
Which compound forms?
Draw the Haworth projection of the product.
g) After the reaction of -D-glucopyranose with one equivalent of methanol (catalysed by an

acid) a compound forms that does not show mutarotation any longer.
Draw the Haworth projection of this product. Give the reasons why the product does not
show mutarotation.
Problem 4-10 Determination of a structure by Spectroscopic Data
Compound A has the empirical formula (C2H4O)n.

The structure of a is analised by spectroscopic methods.
The following data are acquired:
A) The base peak M+ in the mass spectrum is found at m/z = 88
B) The IR spectrum of A shows a strong band at 1730cm-1 and further bands between
2850cm-1 and 2930cm -1.
C) Spectrum shows the 1H-NMR spectrum of A.
a) Which is the molecular formula of A?
b) Determine possible functional groups of A.
c) Which is the physical base of an IR spectrum? (maximum of 5 sentences)
d) Make a proposal of the structure of A.
Thereto:
 Assign the different peaks or groups of peaks to different protons or groups of protons
in your proposal.
 Determine the respective number of protons for each peak or group of peaks.
 Account for your proposal by interpreting the different couplings.
1H-NMR-Spectrum of A
Problems round 4 (practical)
Fourth round (practical problems)
Problem 4-11
Quantitative Determination of a Solution of Different Salts by Titration
A Problem
You get a solution of magnesium chloride and calcium chloride. The concentrations c of
these salts have to be determined (c in mol/L). To perform this there a differnet possibilities
at your disposal. You have to choose from
Titration of the cations with a solution of EDTA (c = 0.100 mol/L) using Erio T as
indicator.
Seperation of the cations by precipitation of calcium oxalate.
Oxidimetric titration of an oxalate with a solution of potassium permanganate
(c = 0,020 mol/L).
Determination of chloride concentration by Mohr titration.
B Procedures
Titration with EDTA
Fill the volumetric flask up to 250 mL. Take a sample, add 5 mL of buffer solution and a
small amount of water. Before starting the titration add a spaturla-tipfull of indicator (as
trituration NaCl: Erio T = 100 : 1).
Titrate with the solution of EDTA (c = 0.100 ml/L).
Seperation of magnesium ions and calcium ions

Add 6 ml of diluted HCl to a sample and dilute with about 100 mL of water. After adding
solution of NH3 until the sample shows a slightly basic reaction heat it to boiling and add
hot solution of (NH4)2-oxalate slowly in small amounts until there is no more precipitation.
After boiling for 15 minutes the precipitate is filtered off
Then, the precipitate is washed 5x with small amounts of hot solution of (NH4)2 (c=0.01
mol/L) (small!) and then 1x carefully with a small amount of warm water.
The precipitate is dissolved in warm sulfuric acid (3 parts of H2O with 1 part of conc.
H2SO4) and diltuted with 50 mL of water.
Oxidimetric titration of oxalate with a solution of KMnO4 (c = 0.020 mol/L)

The acidic solution of oxalate is heated up to 60 – 80°C and then titrated with the solution
of potassium permanganate. At the equivalence point a weak pink colour can be
observed for several minutes.
Determination of chloride concentration by Mohr titration

The sample has to be neutralised to pH = 7. Add about 2 mL of a solution of potassium
dichromate (w = 5 %).
Titrate with a solution of AgNO3 (c = 0.100 mol/L) until a dark yelllow colour occurs.
C Questions
Choose at least three titrimetric methods to determine the concentrations of both salts.
Therefor
1. Characterise the principle of your titration in keywords.
2. Give the equation of the reaction which you use as basis for your calculation.
3. Write down for each titration
 the volume of the sample (taken from the 250 mL volumetric flask),
 consumption of standard solution in mL,
 consumption taken for calculation (account for your choice),
 calculations of the concentrations of cations and anions in mol/L.
4. Comment about and critical valuation of your results.
Problem 4-12
Preparation of Hydrazones to Identify Aldehydes and Ketones
Hydrazines react with aldehydes and ketones to form hydrazones. Hydrazones form
derivates with different metlting points. These can be used to identify unknown aldehydes
and ketones.
The two test tubes in front of you contain an aldehyde or a ketone each.
Identify the compounds in the test tubes by forming the respective hydrazone and measuring
the melting point.
Chemicals:
2 beakers with 2,4-dinitrophenyl hydrazine dissolved in methanol
2 test tubes (1 and 2), each with an unknown aldehyde or ketone
conc. sulfuric acid, ethanol, dem. water, Tollens reagent,
solution of sodium hydroxide, conc. ammonia, Schiff’s reagent
A: Preparation of the hydrazone

In each of the two given beakers there are 200 mg of 2,4-dinitrophenyl hydrazine dissolved in
5 mL of methanol. (Wear gloves!)
Add dropwise and slowly as much conc. sulfuric acid until all 2,4-dinitrophenyl hydrazine is
dissolved completely (mix accurately).
Take a sample of 5 mL from test tube 1 and test tube 2 with the unknown compounds and
add it to the yellow solution.
If there is no precipitation after 5 minutes add about 10 mL of sulfuric acid (c = 0.5 mol/L).
The crystals formed are filtered off by suction, the product of test tube 2 is recrystallized in
ethanol (heating plate), again fiiltered off by suction, washed with a small amount of water
and dried on the air. The product of test tube 1 is only washed with a small amount of water
and dried on the air.
Question
1. Give the equation of the reaction of 2,4-dinitropheny lhydrazine with acetone as an
example.
B) Identifcation of aldehyde and ketone

While the crystals are drying other reactions are used to idenfy whether in the respective test
tubes are aldehydes or ketones.
The identification is to be performed with Tollens reagent and Schiff’s reagent.
Reaction with Tollens reagent:

5 mL of a solution of silver nitrate are filled in an absolutely clean test tube. Solution of
ammonia is added until the white precipitate is dissolved. Afterwards a pellet of sodium
hydroxide is added.
To this solution two drops of the unknown compound are given. The test tube is heated for a
short time in a water bath up to 60 - 70°C.
Reaction with Schiff’s reagent:

Two drops of the organic compound are added to 2 mL of Schiff’s reagent and shaken well.
Questions
2. Determine the kind of carbonyl compounds in the test tubes.
3. Measure the melting points of the hydrazones.
4. Which aldehyde or which ketone contains test tube 1 and test tube 2 respectively
Table 1
Chosen Aldehydes / Ketones Intervals of melting of the respecive

2,4-dinitrophenyl hydrazones in °C
Crotonaldehyde 190 - 195
Formaldehyde 160 - 166
Propionaldehyde 150 - 155
Chloral 127 - 131
Heptanal 100 - 108
Ethyl methyl ketone 110 - 117

Isopropyl methyl ketone 120 - 123
Methyl propyl ketone 138 - 144
Diethyl ketone 150 - 156
Cyclohexanone 158 - 162
Answers
Part 2
The answers to the problems of the four rounds
The solutions are more detailed than expected from the pupils. That may facilitate
their comprehension in case of mistakes.
Answers Round 1
Answers Round 1
Solution to problem 1-1


a) 2 H3O + + SO 42- + 2 OH-  4 H2O + SO42-
c(NaOH)∙
V(NaOH) = 2∙
c(H2SO4)∙
V(H2SO4)
0.1760 mol/L∙
20.37 mL = 2∙c(H2SO4)∙
10.00 mL
c(H2SO4) = 0.1793 mol/L
b) n = 0.5000 L∙
0.1792 mol/L = 0.0896 mol H 2SO4 , 1 liter contains 17.93 mol H2SO4.
m(H2SO4) = 1759 g, 100% ∙1759/1840 = 95.6%
c) 1 L of sulphuric acid contains 1759 g of H2SO4 (17.93 mol) and 81 g of H2O (4.50 mol)
17.93
x= = 0.799
17. 93 4.00
a) Advantages:
- Low density, alloys have nearly the same stability as steel, suitable for vehicle
construction
- corrosion restistant,
- low melting point, easy deformable, easy to roll out to form plastic films for
wrapping,
- good electrical conductance (2/3 of copper),
- high combustion heat, appropriate to use in explosives and fire crackers.
Disadvantages:
- high consumption of energy at production,
- accurate flue gas cleaning necessary otherwise hydrogen fluoride and dust of
other fluorides will escape during production and damage to the environment.
Percentage of Al 2O 3 in bauxite: 50 - 75 mass %.
Bauxite is exploited in Australia, Guinea, Jamaica, Brasil, France, Hungary, USA,

Guayana, Northern China.
It was called after the first place it was found, Le Baux (southern France).
b) Principally the solubility of amphoteric Al(OH)3 in bases is used to seperate it from

Fe(OH)3, which does not have this property.
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Answers Round 1
Bauxite is mixed with sodium-hydroxide solution (35%) at 170 to 180° C under high
pressure. Under these conditions a soluble aluminium complex and insoluble iron
hydroxide form:
Al2O3 (s) + 3 H2O (l)  2 Al(OH)3 (s)

- -
Al(OH) 3 (s) + OH [Al(OH) 4] (1)
Fe2O3 (s) + 3 H2O (l)  2 Fe(OH)3 (s)
Fe(OH)3 (s) is filtered off. The solution is diluted and seed crystals of Al 2O3 are added. By
dilution the equilibrium (1) moves to the left. Sometimes this effect is supported by
inducing CO2:


- -
( CO2 + OH HCO3 )
 OH + Al(OH)3 (s)
- -
Al(OH) 4]
Al(OH)3 is transformed into Al 2O 3 by heating:
2 Al(OH)3 (s)  Al2O 3 (s) + 3 H2O (g)
c) Cryolyte (Na3AlF 6) has a low melting point (1000° C) compared with aluminium oxide
(2050° C). For practical reasons the electrolysis is performed in a solution of Al2O 3 in
liquid cryolite. In such a solution a melting point of 950° C is achieved.
Reactions: in the melt Al2O3  2 Al3+ + 3 O2-

at the cathode Al3+ + 3 e-  Al
at the anode 2 O  2-
O 2 + 4 e-
O2 + 2 C  2 CO
Total reaction: 2 Al2O3 + 6 C  4 Al + 6 CO
(besides carbon monoxide CO 2, COF2, C2F4 and other gases form in smaller amounts)
Q = I ∙t 10 3 A ∙366 ∙24 ∙3600 s ∙0.95 = 3.905 ∙1012

Q = 130∙
Q = n∙z ∙F Q = m/M ∙3 ∙96485 As/mol M(Al) = 26.98 g/mol
130 
10 
3
366 
24 
3600 
0.95
26 .98
 m= g 364 t
396485
d) W = P ∙t and P = U ∙I
W = U∙
I∙
t W = U ∙Q andQ = n∙
z∙F
W = U∙
n∙z∙
F with U = 5 V n = (106/26,98) molz = 3 F = 96485 As/mol
6
W = 5 ∙10 /26.98 ∙3 ∙96485 As W 14900 kWh
efficiency = 95 %  W (for 1 t Al) = 15700 kWh
10 6/101.96 mol Al 2O3

1 t bauxite contains 600 kg Al 2O3 = 0.6∙
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Answers Round 1
/101,96 ∙26.98 t Al = 0.318 t Al. 

to form 1.2∙ m(for 1 t Al) = 0.318-1 t
m(for 1 t Al) 3 t bauxite.
(In literature you often find 4 t.)
To form 1 mol Al you need 1.5 mol C m(for 1 t Al) 670 kg graphite.
e) 2 Al2O 3  4 Al + 3 O2
ΔRH = [4∙
48 + 3∙
38 - 2∙
(- 1610)] kJ/mol = 3526 kJ/mol
ΔRS = [4∙
78 + 3∙
238 - 2∙
98] kJ/(Kmol) = 830 kJ/(K∙
mol)
ΔRG = ΔR H – T ΔRS ΔRG = (3526 - 1243∙0.830)kJ/mol = 2494.31 kJ/mol
ΔE = - ΔRG / (z∙ 103/(12 ∙96485) V
F) ΔE = 2494.31∙ ΔE = 2.15 V
f) According to the negative standard potential of aluminium [E°(Al 3+/Al) = - 1.66 V]

hydrogen is formed at the cathode.
g) Possible reactions
I 2 Al2O 3 + 6 C  4 Al + 6 CO with ΔGI = 3∙ΔG 2 - ΔG 1
II 2 Al2O 3 + 3 C  4 Al + 3 CO2 with ΔG II = 3∙ΔG 3 - ΔG1
ΔGI < 0: 3 ∙(- 221.06 - 0.17872∙
TI/K) kJ/mol - (- 3351.4 + 0.6264∙
TI/K) kJ/mol < 0
 2688.22 < 1.16256 ∙TI TI > 2313 K
ΔGII < 0: 3∙ TII/K) kJmol-1 - (- 3351.4 + 0.6264∙
(- 393.51 - 0.00286∙ TII/K) kJ/mol < 0
 2170.87 < 0.63498 ∙TII TII > 3419 K , at this temperature CO 2 does not form.
T > 2313 K = 2040°C (Actually it is not possible because of the formation of Al 4C3.)
a) Observation 1:

Fe3+(aq) + 3 SCN-(aq)  Fe(SCN)3 (aq)
(yellow) (coulorless) (red)

or [Fe(H2O)6] 3+
+ 3 SCN-  Fe[(SCN)3(H 2O)3] + 3 H20
Not only Fe(SCN)3 (aq) is reason for the red colour but also complexes like
Fe[(SCN) x(H2O)6-x ]3-x with x ranging from 1 to 6.
Observation 2:
c eq (Fe( SCN) 3 )
K= . Dilution decreases the concentrations from cgl to cgl/10.
c eq ( Fe3 )
c 3eq ( SCN )
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Answers Round 1
c eq ( Fe( SCN) 3 ) / 10
Q= = K∙
1000.
[c eq ( Fe3) /10]
[c 3eq (SCN )]/ 103
To reach equilibrium again, the numerator of Q will decrease and the denominator will
increase by decompositon of Fe(SCN) 3 (aq) to result in showing the brown colour of a
solution of Fe 3+ .
Observations 3 and 4:
By adding the solid material the concentration of a reactant increases and more product
forms. Thus the solution shows again the red colour of a Fe(SCN) 3 solution.
b) Observations 3 and 4 show that observation 2 is not due to an effect of dilution as

someone may use a an explanation.

Substituents like Cl show an ortho and para directing effect. Therefore in the beginning an
additional substituent is inserted in p position.
In this case you choose a strongly activating substituent, e.g. NH 2:
Cl Cl Cl
HNO3/H2SO 4 Red.
NO 2 NH2
Secondly bromine is inserted in ortho-position of the additional substituent (NH 2):

Cl Cl
Br2/FeBr3
Br
NH2 NH2
At last t
the addtional substituent (NH2) is removed
Cl Cl
Cl
NaNO2/HCl H3PO4
< 5°C
Br Br
Br
-
NH2 N N
Cl 1-Bromo-3-chlorobenzene
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Answers Round 1

a)
H H
C C
O N
C
H
Oxazole is aromatic because it

- is cyclic,
- is planar,
- has a conjugated π-elektron system,
- fulfills Hückel’s rule to contain 4n + 2 (with n = 1) electrons.
b) π-elektron system of pyrrole:
H H
C C
H C N H
C
H
In pyrrole the free electron pair of the N Atom is part of the π-elektron system. Adding of
a proton to this free electron pair leads to a loss of aromaticity of pyrrole. On the other
side the N atom of oxazole possesses a free electron pair which is not part of the π-
elektrone system. Therefore the addition of a proton is not accompanied by a loss of
aromaticity.
Thus the N atom of oxazole is more basic.
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Answers Round 2
Answers round 2

1.


2– + – 3+
a) Cr2O 7 + 14 H + 6 e 7 H 2O + 2 Cr
Potential of the given chromium(III)/dichromate solution at pH = 7:
RT c (Cr 2O 72) 
c (H) 14 8,314298
E = 1,38 V + ln E = 1,38 V + ln (10 -7)14
V∙
6F 3 2
c( Cr ) 696485
E = 0,414 V
That does not suffice to set free iodine from a solution which contains iodide.
b) Reaction with potassium nitrate/soda:

Cr 2O 3 + 3 KNO 3 + 2 Na2CO3  2 Na2CrO4 + 2 CO2 + 3 KNO 2
Reaction with hydogenperoxide:

2 Cr3+ + 3 H2O 2 + 10 OH –  2 CrO42– + 8 H2O or
2 Cr3+ + 3 H2O 2 + H 2O  Cr 2O 72– + 8 H+
Reaction with sodium peroxodisulfate:
2 Cr3+ + 3 Na2S2O 8 + 16 OH–  2 CrO42– + 6 SO 42– + 6 Na+ + 8 H2O or
2 Cr 3+
+ 3 Na2S2O 8 + 7 H2O  Cr 2O 7 2–
+ 6 SO4 2– +
+ 6 Na + 14 H +
Reaction with bromine:

2 Cr3+ + 3 Br 2 + 16 OH–  2 CrO42– + 6 Br – + 8 H2O or
2 Cr 3+
+ 3 Br 2 + 7 H2O  Cr 2O 7 2– –
+ 6 Br + 14 H +
Potassium nitrate is used as an oxidizing agent, soda (sodium carbonate) lowers th e

melting point of the mixture.
c) The oxidation of chromium(III) to chromium(VI) depends on the pH-value. Thus you have
to find a pH value with the potential of (Cr3+|Cr 2O72–) being smaller than the standard
potential of the system (Br –|Br2).
8.314 
298
1.065 > 1.38 + ln c(H+)14
∙  - 73.60 > ln c(H+)14
696485
14
e 73.60 10 -3 > c(H+)
= 5.21∙ 2.28 < pH
At pH > 2.28 it is possible to oxidize chromium(III) by using bromine.
d) Hydrogenperoxide oxidizes halides too. Elemental bromine or iodine would form. Both
are coloured and complicate the detection of chromium.
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Answers Round 2
Manganese(II) is oxidized by bromine to form the violet permangante ion, which may
cover the characteristic colouring of the chromate.
e) There is no change of the oxidation state, no reduction and no oxidation takes place.
Hydrogenperoxide becomes attached to the chromium centre as a peroxide dianion.
-II
O
O O -I +VI,-II +I,-I +I +VI,-II,-I +I,-II
Cr Cr 2O 72– + 4 H2O 2 + 2 H+  2 CrO 5 + 5 H2O
O +VI O
f)
0,00025
0,00020
Suszeptibility in cm /g
3
0,00015
0,00010
0,00005
0,00000
0 50 100 150 200 250
Temperature in K
10-3 cm3 K g-1 as mean value.

Inserting different pairs leads to C = 2,74∙
g) C = T∙
7 1 
1 3 
1 
1
3
8. 314 
10 erg 
K 
mol 
0 .00274cm 
Kg 
364. 49g 
mol
h) μ= 23 1 21 1
6 .022 
10 mol 
9. 274 
10 erg 
Oersted
μ= 2.83
The magnetic moment equals 2.83 BM.
i) Comparing μ= 2,83 with the value from μ = n

(n 2) (n = number of unpaired
electrons)you get n = 2.
2 unpaired electrons may occur for Cr(IV) (d2-system) or for Cr(II) (d4-system) in a low-
spin complex.
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Answers Round 2
Cr(IV) is not existent in this case as it has no reducing properties, furthermore it is not
stable in an aquous solution.
Chromium is existent in the (formal) oxidation state+2.
j) With ammonium as ligands instead of cyanide the complex changes from low-spin to
high-spin. Thus there are four unpaired electrons and the expected relative magnetic
moment is μ= 4  ( 4 2) , μ= 4.90.
a) x = centres of octahedral holes
x x
x
x x
x x
x
x x
b) 8∙
1/8 + 6∙
½ = 4 oxide ions per cube  1 formula unit CoAl 2O 4 per cube
1/4 + 1 = 4 octahedral holes for 2 Al 3+ ions
12∙ 50%
8 tetrahedral holes for 1 Co 2+ ion 12.5%
c) Length of the edge of the unit cell = 912 pm  length of the cube = 456 pm
1010m)3
Vcube = (4.56∙
mass of particles (Co + 2 Al + 4 O) in that cube
m = [(58.93 + 2∙
26.98 + 4∙ 16.00)/NA] g
176 .89 g mol1
= m/V = 1 10
= 3097904 g/m 3
6.022
10 mol 
23
(4.56·10 m) 3
ρ= 3.1 g/cm3
d) r(M 2+) = radius of the circumcircle of the tetrahedron - radius of the oxide ion
r(O2- ) = length of a diagonal of the plane = 456∙2 pm
4∙
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Answers Round 2
r(O2-) = 114∙2 pm = 161.22 pm

2-
length of the edge of the tetrahedron a = 2∙r(O ) = 322.44 pm
radius of the circumcircle of the tetrahedron r = a∙6 /4 = 197.45 pm
r(M 2+) = r - r(O2- ) r(M2+) = 36.23 pm
3+ 2-
r(M’ ) = [edge length of the cube - 2 ∙r(O )] / 2
r(M’ 3+) = [456 pm - 322.44 pm] / 2 r(M’ 3+) = 66.78 pm
e) Sn(II)Co(III)2O 4 und Sn(IV)Co(II)2O 4

(Sn(0)Co(IV) 2O4 shows a very unfavourable oxidation state of Co, so this is an unlikely
possibility)
f) Sn(II)Co(III)2O 4: Sn: 0 unpaired electrons

Co: 0 unpaired electrons in case of low-spin octahedron,
4 unpaired electrons in case of high-spin octahedron,
2 unpaired electrons in case of low-spin tetrahedron,
4 unpaired electrons in case of high-spin tetrahedron,
thus: 0, (6,) 8 possible
(6 drops out as for the same ligand the octahedron splitting is
far larger than the tetrahedron splitting and thus the
coexistence of high-spin octahedron and low-spin tetrahedron
is impossible)
Sn(IV)Co(II)2O 4: Sn: 0 unpaired electrons

Co: 1 unpaired electron in case of low-spin octahedron,
3 unpaired electrons in case of high-spin octahedron,
3 unpaired electrons in case of tetrahedron (you cannot
distinguish between high- and low-spin because the number of
unpaired electrons is equal)
thus: 2, 4, 6 possible
g) 43.9 % O: 43.9 / 16 = 2.74375

18.5 % Al: 18.5 / 26.98 = 0.68569 37.6 % remainder
 n(Al) : n(O) = 1 : 4 compound MM´AlO4
37.6 % (M + M’)
for the sum x of the atom masses of M and M’ you find
mol-1 / x
18.5 / 26.98 = 37.6 g∙ mol-1
x = 54.84 g∙
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Answers Round 2
M M’ 
M (27.41) = M’ (27.41) 54.84 no solution for M = M’
Li (6.94) Ti (47.88) 54.82 possible
Be (9.01) Sc (44.96) 53.97 deviation to large, no solution
Na (22.99) S (32.07) 55.06 sulphur is not a metal, no solution
Mg (24.31) P (30.97) 55.28 phosphorus is not a metal, no solution
Al (26.98) Si (28.09) 55.07 the percentage of Al would
not be correct, no solution
X = LiTiAlO4
R
T c Ox
h) E = E° + 
ln .
n
F c Red
1,4
1,2
E 1,0
0,8
0,6
0 2 4 6 8 10 12
V
From the image: equivalence point at 11

at V = 5.5 is cOx = cRed and thus E = E°  E° = 0.77 V = E°(Fe2+/Fe3+)
As the function is rising, c Ox is rising during the titration, so in the original solution you
find Fe2+.
If ln(cOx/c Red) =1 then cOx/cRed = e and you can calculate n:

c Ox/cRed = V / (11 mL - V) V = e∙
(11 mL - V) V = 8.04 mL 8 mL
E(V=8 mL) = 0.79 V
298 Jmol-1)/(n∙
0.79 V = 0.77V + (8.314∙ mol-1) n = 1.28
96485 C∙
n has to be an integer n=1
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Answers Round 2
a) The total pressure depends on the equilibrium, so you have to calculate the equilibrium
constant first.

2 NO2  N2O 4 ΔH = (9160 - 2∙33200) Jmol -1 = - 57240 Jmol-1
ΔS = (304.3 - 2∙240.1) JK-1mol-1 = - 175.9 JK-1mol-1
175.9) Jmol-1
ΔG = (- 57240 + 300∙ = - 4470 kJmol-1
lnK = - ΔG/RT ln K = 4470/8.314∙
300 K = 6.00
This K is dimensionless and stands for the term
p( N2O 4 ) / p s tan dard
K=
p2 (NO 2 ) / p 2stan dard
 Kp = K/pstandard 10 -5 Pa-1
Kp = 6.00∙
105 Pa set by IUPAC)
(Standard pressure p0 = 1,0000∙
You may start your calculation of the equilibrium with any composition of the mixture of NO 2
and N2O4, e.g. you can assume that only NO 2 exists in the beginning: n(NO2) = 64 .4g/46 .0
gmol-1 = 1 .40 mol

2 NO2  N2O4
Amount of substance in equilibrium: (1.40 - 2x)mol x mol
total amount of substance in equilibrium: ntotal = (1.40 - x)mol
partial pressures in equilibrium: p(NO2) = (n(NO 2)/ntotal)∙ptotal
p(N2O 4) = (n(N2O 4)/ntotal )∙ptotal
p( N O )
Kp = 2 2 4
p (NO 2 )
n( N2O 4 )
n total
10-5 Pa-1 =
6 .00∙ and ptotal = ntotal∙
R∙T/V
n (NO 2 ) 
2
p total
x(1. 40 x ) 15 10 3
10-5 =
6 .00∙ 
(1 .40 2x ) 2 ( 1.40 x ) 
8 .314
300
 x 2 + x∙
¼∙(-5 .6 - 15/(18∙ 1.42 = 0
8 .314)) + ¼∙
 x 1 = 0 .846 (not relevant because of 1 .40 - 2x < 0) x2 = 0 .579
 n(N2O4) = 0 .579 mol n(NO 2) = 0 .241 mol ntotal = 0 .821 mol
ptotal = (0 .821 ∙8 .314 ∙300 / 15∙ -3
10 ) Pa = 136.516 Pa ptotal 1 .37 bar
b) As the pressure decreases the position of the equivalence changes. Thus the partial
pressure does not decrease in the same way as the total pressure. The equilibrium
composition has to be taken into account.
The decline of the total pressure follows the same law as the radioactive decay:
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Answers Round 2
-kt -1
p gesamt = p0, total∙
e with k = 0.001 s
Determination of the equilibrium constant:

ΔH = ΔHproducts - ΔHreactants + (Cpproducts - Cpreactants)∙ΔT
-1 -1 -1
ΔH = - 57240 Jmol + (77 .8 - 2∙
37 .2)∙
52 Jmol = -57063 Jmol
ΔS = ΔS products - ΔS reactants + (Cpproducts - Cpreactants)∙

ln(T2/T1)
-1 -1 -1 -1 -1 -1
ΔS = - 175 .9 JK mol + (77 .8 - 2∙
37 .2) JK mol ∙ln(350/298) = -175 .35JK mol
-1 -1 -1 -1
ΔG = -57063 Jmol - 350 K ∙(-175 .35 JK mol ) = 4310 Jmol
-6 -1
ln K = -4310/(8 .314∙
350) K = 0 .227 Kp = 2 .27∙
10 Pa
p( N2 O 4 )
Kp = and p(N2O 4) + p(NO2) = p total e-0 .001/s ∙t
with p total = p0, total ∙
p 2 (NO 2 )
-0 .001/s ∙
t
p(N2O 4) + p(NO2) = p0 , gesamt ∙
e
s 1
105 Pa 
3. 00 e 0 .001 t
p(NO 2 )
Kp = 2
p (NO 2 )
p 2(NO 2) + p(NO 2)∙

Kp-1 - (3 .00∙ e- 0 .001/s ∙t)∙
105 Pa∙ Kp-1 = 0
s 1
1 1 105 Pa 
3.00  e0 .001 t
p(NO2) =    or
2
Kp Kp 2
4 Kp
1
10 11 0. 001 s 
t
10 3 + 4 .85 
p(NO2) = [- 220∙ 10 1. 32 
10  e ] Pa (0)
2,0
1,5
NO 2 pressure in bar
1,0
0,5
0,0
0 600 1200 1800 2400 3000 3600
time in s
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Answers Round 2
c) Molar fraction x = p(NO2) / p total
s 1 
1 1 3.00 e 0.001
10 5 Pa t
(1) x = (    e-0 .001/s ∙t)
10 5 Pa ∙
) /(3 .00∙
2
Kp 4
Kp 2 Kp
10-6 Pa -1 inserted and rounded with three significant figures:

or Kp = 2 .27∙
1
e 0.001 s
0.734  0.539 1.47  
t
(2) x =
s 1 
e 0.001 t
(Function (1) reacts very sensitive on rounding. The graphs of (1) and (2) hardly differ in the
time interval asked for but already at t > 4000 s the graph of (2) exceeds the value 1, what
cannot apply to a mole fraction.
If you use equation (0) to determine the function of the molar fraction you get an equation
similar to (2):
s 1 
e 0.001
0 .733  0.539 1.47 t
(3) x =
s 1 
e 0.001 t
The course of the plot (3) shows even in the time interval asked for that the molar fraction
becomes > 1.)
(3)
1,0
(2)
(1)
0,9
molar fraction of NO2
0,8
0,7
0 600 1200 1800 2400 3000 3600

time in s
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Answers Round 2
d) Decrease of total pressure leads to decrease of partial pressure of NO 2 as shown in the

plot b).
But if the total pressure decreases the composition of the equivalent changes to the side
of a higher number of particles (principle of Le Chatelier), thus the formation of NO2 is
favoured and the mole fraction of NO 2 increases according to plot in c).
a) As there are signals only in the range from 7 ppm to 8,5 ppm in the 1H-NMR spectrum D
is an aromatic compound.
n ( C ) : n ( H ) = 5:4
b) Due to the NMR spectrum five different kinds of protons exist. Thus the empirical
formula of D is likely to be C10H8.
Two compounds come into consideration, naphthaline and azulene. Naphthaline is
dropped out because of the spectrum and the given properties (dipole moment, blue
colour). So D should be azulene.
The classical Hafner syntheses confirms this assumption:
NO 2
NO2
S nAr +2 (CH3 ) 2NH

+ NO2
N+ N
+ -
N NO2 N Cl -
Cl
Cl
B
+ , NaOCH3
N T
- (CH3) 2NH
C D
Azulene
Azulen
Comment; Pyridine is used as C5 module which can be condensed
with cyclopentadiene to form azulene. In a first step pyridine is transferred into a reactive
pyridinium salt by reaction with 2,4-dinitrochlorobenzene (nucleophilic substitution).
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Answers Round 2
Through this the pyridine system is activated to undergo a nucleophilic process to open the
ring by dimethylamine. At first base B arises.
B condenses in a basic surrounding with cyclopentadiene to yield fulvene C.
On heating C eliminates dimethylamine and cyclises to form azulen D.
c)
N+ N
H H
- H+
H H
N N N N
H H + -O-Me H
H
- Me-OH
N N N N
(Thermodynamisch stabileres Produkt,

für Weiterreaktion aber unerheblich)
N
-Me-O -
- (CH3 )2 NH
Comment: The reaction of B with cyclopentadiene can be described analogous to a kind

of Mannich reaction as an addition of the iminium salt to the double bond of cyclopentadiene.
Under the influence of sodium methoxide the intermediate formed expels dimthylamine
(E1cb-reaction) to give fulvene C.
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Answers Round 2
The reaction can also be described as an attack of the deprotonated cyclopentadienide

anion on the iminium ion (= analogon of a carbonyl compound). Another deprotonation of
cyclopentadiene in the product of the addition reaction leads in an E1cb-elimination to
fulvene C as shown above.
d) 8
1 7
2 6
3 5
4
Doublet is due to the coupling of an 1H nucleus to only one proton at a neighbouring C

atom.
Triplet is due to the coupling of an 1H nucleus to exactly two protons at neighbouring C
atoms.
H atoms at the C atoms 2, 5, 6 and 7 can be considered to give rise to triplets.
e)
These resonance structures account for the blue colour, the aromatic character and the
dipole moment, which is unusually high for a hydrocarbon.
Obviously the dipole moment of D is small compared with other compounds soluble in
water. Thus azulene in insoluble in water but soluble in strong acids because the
molecule can be protonated relative easily. In this case not the whole aromatic system is
destroyed and the positive charge is well delocalised. This protonated form solves well
in water (see image next page).
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Answers Round 2
+ H+
H
H
f) Structure of F, G and H:
F G H
Comment
Compound F forms in an elctrophilic substitution. The tert. butylcation which forms from
acid and tert. butanole attacks azulene in position 1 and 3 respectively (see the last two
resonance structures in e)).
The overall reaction to G und H is a nucleophilic substitution. The process can be looked
at as an addition-elimination process:
At first an addition of the nucleophilic alkyl group takes place resulting in the formation of
a salt. To restore the aromatic system a hydride ion should be eliminated which is done
on detour by oxidation (= elimination of a proton and two electrons instead of elimination
of a hydride ion).
The nucleophilic attack should take place at position 4 (8) and 6 respectively, the attack
in position 4 (8) is more likely. With small substituents to insert the product substituted in
position 4 will occur.
Having a greater volume as e.g. the triphenylmethyl group the substitution will take place
at position 6 due to sterical intramolecular interaction especially to the H atom at C3.
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Answers Round 2
g) Structure of I
Fe2+ Fe 2+ Fe 2+
Pair of Enantiomers
Enantiomerenpaar Meso Compound
meso-Form
Comment
Again the nucleophile (in this case hydride) attacks in position 4 (8) as shown above. (An
attack in position 6 would not lead to a mixture of stereoisomers.)
A cyclopentadienide salt is formed which reacts to the ferrocen derivate I.
There exist three stereoisomers of I according to the position of the remaining two
double bonds: a pair of enantiomers and a meso compound.
Structure of J
Fe
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Answers Round 3 test 1
Answers Round 3 Test 1

a) A and D b) B c) C d) E e) E
a) Ca + 2 H2O  Ca2+ + 2 OH- + H2

2 K + 2 H 2O  2K +
+ 2 OH -
+ H2
b) 2 Al + 6 H3O +  2 Al3+ + 6 H2O + 3 H2
Zn + 2 H3O+  Zn2+ + 2 H 2O + H2
Fe + 2 H3O +
 Fe 2+
+ 2 H 2O + H2
c) 2 Al + 6 H 2O + 2 OH-  2 [Al(OH)4] - + 3 H2
Zn + 2 H2O + 2 OH -
 [Zn(OH)4] 2-
+ H2
d) 3 Ag + HNO3 + 3 H3O+  3 Ag+ + NO + 5 H2O
3 Cu + 2 HNO 3 + 6 H3O +  3 Cu2+ + 2 NO + 10 H2O
e) n(Me) = n(Cu) = n(Pb) M(Me) = x
Me + Pb 2+
 Me 2+
+ Pb 100 g  119g
Me + Cu 2+
 Me 2+
+ Cu 100 g  90,2 g
100 g - n∙
x + n∙
207.2 g/mol = 119 g
100 g - n∙
x + n∙
63.55 g/mol = 90.2 g
9.8 g + n∙
63.55 g/mol = - 19 g + n∙
207.2 g/mol n = 0.2 mol
x = M(Me) = 112.4 g/mol Me = Cadmium
a) ntotal = p∙
V/R∙
T ntotal = 71800∙ 10 -6/((8.314∙
100∙ 298) 10-3 mol
ntotal = 2.90∙
M1 = M(C21H23O 5N) = 369.45 g/mol M2 = M(C 12H22O 11) = 342.34 g/mol
n = m/M n1 + n 2 = n total m 1 + m2 = 1 g
-3
 (1-m 2)/M1 + m 2/M2 = 2.90∙
10 mol m2 = 0.902 g (90.2 %)
m1 = 0.098 g ( 9.8 %)
b) Together with the sample water is brought into the solution. Cristallisation takes water
out of the solution.
M(CaCl2) = 110.98 g/mol M(CaCl2∙
6 H2O) = 219.1 g/mol
In 74.9 g CaCl 2∙
6 H2O (residue) are
74.9 g∙
110.98/219.1 = 37.94 g CaCl2
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total mass - mass of residue = mass of the saturated solution

230.00 g - 74.90 g = 155.10 g
x = mass of CaCl2 y = mass of H2O in the saturated solution in each case
x + y = 155.10 g 74.5/100 = x/y  y = 88.88 g x = 66.22 g
In 150 g are 66.22 g + 37.94 g = 104.16 g CaCl2 (0.939 mol) and
150 g - 104.16 g = 45.84 g H2O (2.54 mol)  2.7 mol H2O per 1 mol CaCl 2

2
(c 0 
)
a) c(Ac- ) = c0(HAc)∙
α. c(Ac-) = c(H3O +) Ka =
c 0 (1 ) 
mol / L
2
c0 0,1
10-5 =
1.74∙ 10-3 mol/L
c0 = 1.566∙
0,9 
mol / L
c(Ac- ) = c(H3O+ ) = 1.566∙

10-4 mol/L pH = 3.8
M(HAc) = 60.04 g/mol m(HAc) = 0.094 g
b) At pH 12 the propionate anion (Pr -) is the only species of propionic acid i.e. all OH --
ions derive from sodium hydroxide  log(c(NaOH)) = - 14 + pH = -1. 82
c(NaOH) = 0.015 mol/L.
Until you reach the first equivalent point (15 mL HCl) exactly these OH --ions are
neutralised  c(NaOH)∙
V(NaOH) = c(HCl)∙
V(HCl)
c(HCl) = (20∙
0.015 mol/L)/15 = 0.02 mol/L
consumption for the titration of Pr - = 15 mL HCl
 c(NaPr in the parent solution) = 0.015 mol/L
M(NaC2H5COO) = 96.09 g/mol m(NaPr) = 0.25∙ 0.015 g = 0.360 g
96.09∙

p 2 (H 2 ) 
p(O2 ) ( p
1) 2 
0. 5
p1
a) 2 H2O 2 H2 + O2 Kp’ = 2
=
p (H2 O) p2
(11 ) 2
10-21 ∙
K p’ = 7.63∙ p
(0 .5
2 ) 2
2 HCl H2 + Cl2 Kp’’ = 10-11
= 3.03∙
(12 ) 2
p2 (H 2 O) 
p 2 (Cl 2 )
4 HCl + O2 2 Cl2 + 2 H2O Kp = 4
p(O2 ) 
p (HCl)
p 2 (H2 O) p 2 (H 2 ) 
p2 (Cl 2 )
Kp =  = Kp’’2/Kp’ p-1
K p = 0.12 ∙
2 4
p(O2 ) 
p (H2 ) p (HCl)
K = K p∙
p0 K = 0.12 (as p = p0)
ΔG = - R∙
T∙lnK ΔG = - 8.314 JK mol ∙ -1
1000 K∙
ln0.12 -1
ΔG = 17.6 kJmol -1
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a) (i) The electron pairs are situated in a way that their distance is at a maximum.
(ii) A non-binding electron pair requires more space than a binding one.
(iii) The size of a binding electron
declines with increasing electronegativity of the ligands
declines with declining electronegativity of the central atom
(iv) The two pairs of a double bond require more space than the pair of an single bond.
b)
Cl
Cl
Cl Cl
Te or Cl Te
C Cl
Cl Cl Cl
Cl
Cl Cl
CCl 4 (more stable) TeCl4
F F F F
Xe or
Xe
F F F
F
(more stable) XeF4
c) BeCl2 Cl  Be  Cl angle = 180°
Cl Cl
SnCl2 angle 120°
Sn
Cl Cl
H2 S angle 109.5°
S H
H
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XeF2 or oder or
F Xe F Xe Xe
F
F F
favoured
angle 180°
d) Maximal angle according to VSEPR: 109.5°.

Actually the angle is smaller. The free electron pair needs
P more space and pushes the binding electron pairs down-
X wards so the angles between the substituents become
X X smaller.
Trend I F: The angle becomes smaller (102°, 101.5°, 100.3°, 97.9°).
Reason: Increasing electronegativity of the substituents.
The space at the central atom occupied by the binding electron pairs decreases the
more they are attracted to the substituents. Thus it is easier for the free electron pair to
enforce its claim of space.
e) NH3/PH3 (107°/93.6°)
As the electronegativity decreases from N to P the binding pairs need less space an the
central atom and are easier to push away by the free pair.
PH3/PF3 (93.6°/96.3°)
The angle increases though the EN of F is larger than that of H. Phosphorus possesses
empty orbitals which can undergo resonance with the free electron pairs of the fluorine.
Thus all bonds are partial double bonds. As double bonds need more space than single
bonds (in PH3), the binding electrons at P can not be pushed away as easily.

a) BBr 3 + PBr 3 + 3 H2  BP + 6 HBr
b)
Br Br
B
P
Br Br
Br Br
trigonal planar trigonal pyramidal

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c)
outside: boron
inside: phosphorus
(the thick lines do not

represent bonds but
clarify the tetrahedral
holes)
d) One unit cell contains 4 BP units

ρ= m/V m = 4∙M(BP)/NA V = (4.78 Å)3
4 10 3 kg / mol
41,78 
ρ= ρ= 2541 kg/m3
 
6,022 
10 23
mol 
1
( 4,78
10 10
m) 3
e) The distance B-P is equal to a quarter of space diagonal

distance B-P = 4.78 Å ∙3 /4 = 2.070 Å
or
Distance B-P is equal to the radius of circumcircle r circumcircle of the tetrahedron, the basic
edge of the tetrahedron is equal to half of the plane diagonal of the elementara unit.
a/2 = 4.78 Å ∙2 /2 distance B-P = 4.78 Å ∙3 /4 distance B-P = 2.070 Å
3
31.638 
1390  1 
f) Ulattice = - 1 J/mol
 Ulattice = - 8485 kJ/mol
2.070  7
c(BBr 3)n∙
g) r = k∙ c(PBr 3)m∙
c(H2)p
From the data given : n = 1. m = 1. p = 0 r = k∙
c(BBr3)∙
c(PBr3)
overall order = 2
k 800 = 4.60∙ -8
10 ∙9∙
10 /(2.25∙ 10 ) -6 -6
k 800 = 2272 (mol/L)-1s-1
k 880 = 9679 (mol/L)-1s-1
h) k = A ∙e-Ea/(R∙T) ln(k800/k 880 ) = - Ea/(R∙
1073 K) + Ea/(R∙
1153 K)
E a = R∙ln(k 800/k 880 )/(1/1153 - 1/1073) E a = 186 kJ/mol
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a) n (C) : n (H) : n (O) = (65.2/12.01) : (8.75/1.007) : (26.05/16)
n (C) : n (H) : n (O) = 5.43 : 8.69 : 1.63 = 3.33 : 5.33 : 1 = 10 : 16 : 3
M (C10H16O3) = 184.13 g/mol  X = C10H16O3.
Assumption: one COOH-group is responsible for the acidity.

Titration shows: amount of acid groups n = 0.237 mmol
 M = 184 g/mol. Just 1 COOH-group in X.
2a 2 b
DBE  =3
2
X contains 3 double bonds, one of them in the COOH-group.
b) B is a secondary alcohol with a OH-group.

A is a ketone with a carbonyl group (-C=O).
c)
O O
ozonolysis
C CH3 COOH + (CH 2)6
oxidation OH
HO
Compound C: CH3 - CH = CH - (CH2)6 - COOH
OH
OH
H3C
H3C (CH2)7
(CH2)7
O O HO
O
A B
If you get oxalic acid from the ozonolysis of X then X must have the structure
R1 - HC = CH - COOH .

OH
OH
H2 (Pt)
H3C (CH2)5 C C H3C (CH2)7
H H
O O O O
X A
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d) Z,E- isomerism
CH3 H3C
O
O H
(H2C)5 (H2C)5
COOH
H COOH
H H
Z-compound E-compound
(cis) (trans)

N
NO2 NH 2 Cl N
reduction
NaNO2 / HCl
i.e.. Zn/HCl
T < 5°C
CH 3 CH 3 CH 3
CH 3 CH 3 CH 3
C COO H
Cu(CN) H+ / H2O
-N2
CH3 CH 3
CH3 CH 3
Another possibility:
CuBr Mg CO2 H
RN2 RBr RMgBr RCOOMgBr RCOOH
-N2
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a) 23 = 8
b) Stereoisomers
Br Br Br Br
= =
Cl Cl Cl Cl Cl Cl Cl Cl
meso-compound (optically inactive) meso-compound (optically inactive)
Br Br Br Br
Cl Cl Cl Cl Cl Cl Cl Cl
enantiomers enatiomers
(optically active) (optically active)
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Answers round 3 test 2
Answers Round 3 Test 2

a) C b) C c) (i) A (ii) B (iii) D d) A, D und E e) A

a) m = m(H 3Cit in 6 tablets)/6 = n0 (H3Cit in 6 tablets)∙
M(H3Cit)/6
c 0(H3Cit) = n0 (H3Cit in 6 tablets)/L M(H3Cit) = 192.14 g/mol
c(H2 Cit ) 
c(H3 O)
K a1. citirc acid = with c(H 2Cit -) = c(H 3O +)
c(H3 Cit)
-
and c(H 3Cit) = c 0(H3Cit) - c(H2Cit )
10 8.4 mol / L
 7.1∙
10 -4 = 4.2
 c0(H3Cit) = 6.87∙
10-5 mol/L
c 0 (H3 Cit ) 10 mol /L
10-5 ∙
m = 6.87∙ 192.12 g /6 10-3 g citric acid/tablet
m = 2.2∙
b) m = c 0(H3Cit)∙M(H3Cit)/6 m = c 0(H3Cit)∙
(192.14 g/mol)/6
c 0(H3Cit) = c(H3Cit) + c(H2Cit ) + c(HCit2-)-

c(H2 Cit ) c(H3 O )

-4 c (H2 Cit ) 
10 4.2
K a1. citric acid = 7.1∙
10 =
c(H3 Cit) c( H3 Cit )
c(HCit
2
)
c(H 3O )

c (HCit 2) 
10 4.2
K a2. citric acid = 10-5
1.68∙ =
c(H 2 Cit ) c (H2 Cit )
+ - 2- -4.2 - 2-
c(H3O ) = c(H2Cit ) + 2∙c(HCit ) 10 mol/L = c(H2Cit ) + 2∙c(HCit )
10-3 g citric acid/tablet

c) m = 3∙
10 -3 g = c0(H3Cit in tea)∙
3∙ 1 L∙
(192.14 g/mol)/6 10 -5 mol/L
c 0(H3Cit in tea) = 9.37∙
degree of protolysis in tea α1 = c(H2Cit -)/ c0(H3Cit) = 10-4.1/9.37∙
10-5 = 0.85
degree of protolysis in the stomach
V 1. before drinking = 2.30 L n1(H3O+) = 2.3 L ∙
10-2.1 mol/L
V 2. after drinking = 2.62 L n2(H3O+) = n 1(H3O +)
2.310 2.1 mol
c 2(H3O +) = 10-3 mol/L
= 6.97∙
2.62 L
This is the concentration of H3O+-ions, the degree of protolysis of citric acid has to be
determined:
9.37·10 -5 mol/L
0.32 L
c 0(H3Cit in the stomach) = 10 -5 mol/L
= 1.14∙
2.62 L
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 
c(H2 Cit ) 
c(H3 O )
K a1. citric acid =
c(H3 Cit)
c (H 2Cit ) 10 3
6.97
10-4 =
7.1∙  c(H2Cit-) = 1.05∙
10-6 mol/L
5 
1 .14
10 mol / L c( H2 Cit )
10-6 /1.14∙
α2 = = 1.05∙ 10-5 10-2
α2 = 9.21∙
1 0.85
 9.2 α1/α2 9.2
2 9. 21
10 2
d) Electron donators as R diminish, electron acceptors increase the acidity.

- most powerful acceptor in this row with a -M and -I effect is NO 2  pKa = 3.41
- following Cl with a -I and a smaller +M effect  pKa = 4.01
- most powerfull donator is OCH 3 with a -I and a strong +M effect  pKa = 4.46
- following CH3 with a +I effect  pKa = 4.35
- without effects is H  pKa = 4.21

101300Pa  10 3 m 3
0. 211
a) p∙
V = n∙
R∙T n(B) = 10-3 mol
n(B) = 8.63∙
8 .314JK 1mol1 
298K
M = m/n 10 -3 mol M(B) 44 g/mol
M(B) = 0.38 g / 8.63∙
 B = CO2
A = FeCO3 B = CO2 C = FeSO4 D = Fe(OH)3 E = FeCl3
Reactions:
2 H3O + + SO42- + FeCO3  Fe2+ + SO42- + 3 H2O + CO 2
5 Fe2+ + MnO 4- + 8 H 3O+  5 Fe3+ + Mn2+ + 12 H2O
2 Fe2+ + H 2O2 + 2 H3O+  2 Fe3+ + 4 H2O
Fe3+ + 3 OH -  Fe(OH)3
Fe(OH)3 + 3 H3O+ + 4 Cl-  FeCl4- + 6 H2O
FeCl4- + 3 SCN-  Fe(SCN)3 + 4 Cl-
(instead of FeCl4- and Fe(SCN)3 there are other possibilities)
b) weighed portion: n(FeCO3) = 1g / 115.86 gmol -1 = 8.631∙

10 -3 mol
titration: ½ ∙n(Fe 2+) n(MnO 4-)
= 5∙
n(Fe2+) 10-3 L = 8.631∙
= 2 ∙5 ∙0.02 mol/L ∙43.15∙ 10-3 mol
the total amount reacted
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a) Sn 2+ + 2 Fe3+  Sn4+ + 2 Fe 2+ mit ΔG°

ΔG° = -E°∙
z∙F Sn 4+
+2e -
 Sn 2+
ΔG1 = - 2∙
F∙0.154 V

Fe 3+
+ e -
 Fe 2+
ΔG2 = - 1∙
F∙0.771 V
ΔG° = 2∙
ΔG2 - ΔG 1 ΔG° = - 1.234∙
96485 J/mol ΔG° - 119 kJ/mol
b) ΔG = - R∙
T∙ln K ln K = - (-119 kJ/mol) / (8.314 JK-1mol-1 ∙298 K)
ln K = 48.03 1020
K = 7.23∙
c) The cell consitsts of the calomel electrode (positive potential) and the half cell with the
solution to be titrated.  voltage of the cell = E°Kalomel - E Lösung
In the solution c(Sn4+)/c(Sn2+) = 1/3
8,314 
298
E solution = 0.154 V + V∙
ln(1/ 3) E solution = 0.140 V
296485
voltage of the cell = 0.242 V - 0.140 V = 0.102 V
d) Voltage of the cell = E°calomel - E(Fe3+/Fe2+)

3
R T c(F )
= 0.242 V - (0.771 V + ∙
ln ) (1)
F c(Fe2 )
4 2 2
c(Sn )
c (Fe )
K=
c(Sn2 ) 
c 2 (Fe3 )
at the equivalence point c(Sn4+) = 0.5 ∙c(Fe2+) therefore 0.5 ∙c(Fe3+) = c(Sn2+)
3 2 3

c (Fe ) c(F ) 1
 K=  = 3 inserted in (1)
3
c (Fe 3
) c(Fe 2
) K
R T 1
voltage of the cell = 0.242 V - (0.771 V + ∙
ln 3 ) = - 0.118 V
F 10 20
7,23 
3+ 2+
e) Beyond the equivalence point you use c(Fe )/c(Fe ) to calculate Esolution
8,314 
298
c(Fe3+)/c(Fe2+) = ½ Esolution = 0.771 V + V∙
ln 0.5 = 0.753 V
96485
voltage of the cell = 0.242 V - 0.753 V = - 0.511 V
a) 43.5 mL OH - solution  2.175 mmol OH- for 0.1 g X  M(X) = 46 g/mol

 X = HCOOH, formic acid
b) HCOOH  H2O + CO S = sulfuric acid, H2SO4
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6
p
V 101300 
41,5 
10
c) n∞(CO) = n0(HCOOH) =  10-3 mol
mol = 1.70∙
RT 8,314 
298
supposably of 1. order due to the reaction equation
d) Proving wether the reaction is of 1. order:

1 c0 c 0 n 0 (HCOOH) 10 3
1,70 
k=  ln with  
t c 10 3 n(CO )
c n t (HCOOH) 1,70 
t (in s) 0 50 100 150 200 ∞

nt (in mol)∙ 103 1.70 1.23 0.874 0.633 0.457 0
ln(c0/c) 0 0.324 0.665 0.988 1.31 -
k (in s -1)∙
103 - 6.48 6.65 6.59 6.55 -
k is almost constant, q.e.d. 10 -3 s-1

k = 6.57∙
E
 a Ea 1
e) Arrhenius equation e
k = A∙ RT  ln k = lnA - 
R T
plotting ln k as a function of 1/T results in a straight line with the slope -E a/R
1/T (in K -1) ∙103 2.36 2.26 2.16 2.07 1.99
ln k 8.20 9.46 10.7 11.7 12.8
14
13
reading off two points

12
(1.97/13) und (2.3/9)
m = - E a/R
ln k
11
13 9
- Ea= ∙R
10 3 K 1
( 1.97 2.30 )
10
9 Ea = 101 kJ/mol
8
2,0 2,1 2,2 2,3 2,4
3
1/T x 10
Solution problem 3-16
a) I/I0 = 98/100
A = 10log (100/98) = 0.00877 A=ε
∙c∙
d
0.00877 = 10500 Lmol cm ∙
c min∙
1 cm -1 -1
10 -7 mol/L
cmin = 8.352∙
b) I/I0 = 2/100  A = 10log (100/2) A = 1.6990
1.6990 = 10500 Lmol cm ∙
c max∙
1 cm -1 -1
10-4 mol/L
cmax = 1.618∙
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c) A(x M = 0.33) = 0 (the complex does not absorb)  0.33 = cM/(cM + c L)

c L = 2 cM ML2
d) x M = 0  c M/(c M + cL) = 0  cM = 0 only L absorbs

x M = 1  c M/(c M + cL) = 1  cL = 0 only M absorbs
e) At xM = 0 and A = 0.5 L has the same concentration as M at xM = 1 and A = 1

ε
L/ε
M = AL/AM = 0.5/1 εM = 2∙
εL
f) x M = 0 0.5 = 10log(I 0/I) I/I0 = 0.32 transmission 32 %

10
x M = 1 1 = log(I 0/I) I/I0 = 0.10 transmission 10 %

a) CH4 + H 2O  CO + 3 H2
CO + 2 H 2  CH3OH
250 
10 3 Pa 
55 m 3
b) 55.0 m 3/s methane: 10 3 Pa. T = 298 K
p = 250∙ n=
8.314JK 1mol1 
298K
103 mol/s
flow of methane 5.55∙
200 
10 3 Pa 
150m 3
150.0 m3/s water vapor: 10 3 Pa. T = 423 K
p = 200∙ n=
8.314JK 1mol 1 
423K
103 mol/s
flow of water vapor 8.53∙
 excess in stream : (8.53 - 5.55)∙
103 mol/s = 103 mol/s water vapor
2.98∙
103 mol/s CO and 3∙
in step A 5.55∙ 103 mol/s H2 form
5.55∙
103 mol/s CO and 2∙
in step B 5.55∙ 103 mol/s H2 are consumed
5.55∙
 excess in step  103 mol/s hydrogen (H2)
5.55∙
c) i) stream  water: 103 mol/s  53.70 kg/s

2.98∙  53.70 L/s
ii) stream  methanol: 5.55∙ 3
10 mol/s CH4  5.55∙ 3
10 mol/s CH3OH
 177.9 kg/s CH3OH  225 L/s
iii) stream  hydrogen: 5.55∙ 3
10 mol/s H2 at 25°C and 101.3 kPa
 135.7 m /s H2 3
103 L/s
 135.7∙
d) 1500 mol/s CH4 and 4500 mol/s H2 flow in

 after step 2 in stream : 1000 mol/s CH3OH. 500 mol/s CO and 2500 mol/s H2
e) p = ptotal∙
ni /ntotal p total = 10 MPa ntotal = 4000 mol
p(CH3OH) = 10 MPa ∙(1000/4000) = 2.50 MPa
p(CO) = 10 MPa ∙(500/4000) = 1.25 MPa
p(H2) = 10 MPa ∙(2500/4000) = 6.25 MPa
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2 2 -4
f) K = 2.50∙
(0.1) / (1.25∙
6.25 ) K = 5.12∙
10
read from the diagram T 630 K (360°C)

a) Main products:
CH3 CH3
NO2
ortho: para:
NO2
b) see textbooks
c) ortho- and para- nitrophenol
d) see textbooks
e) OH The OH group as well as the methyl group of the compound are

ortho directing. As the +M-effect of the OH group overrules the +I-
effect of the methyl group the OH group is ortho directing the
bromine to form 2-Brom-4-methylphenol as main product.
CH3
a) H3C CH3
H (1)
(6) H The hydrogen atoms H(3) or H(4) of the
starting compound can be split off leading to
the following radical:
(5) H
H (2)
H
(4) H
(3)
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H3C CH3
H Due to the adjacent double bound an allyl
H radical forms stabilised by resonance:
H
H
H
H3C CH3 H3C CH3

H H
H H
H H
H H
H H
This radical may react at both ends of the allyl system, at each end from „upside“ and
„downside“, to form the different compounds I – IV .
b) (I / II) as well as (III / IV) pairs of enantiomers

(I / III), (I / IV), (II / III), (II / IV) pairs of structural isomers

a)
KMnO4
OH OH
(compound A) (compound B)
2.3.5 - Trimethylheptane – 3.4 – diol
HIO4 +
O
OH OH O
(compound B) (compound C) (compound D)
2-Methylbutanal 3–Methylbutane-2-on
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Zn-Hg / HCl
O
(compound E) 2-Methylbutane
Zn-Hg / HCl
reaction with Tollens reagent (detection of aldehydes)

O
H
+ 2 [Ag(NH 3)2] 2 Ag + O
O + 3 OH- 2 NH3 + 2 H 2O
(compound C)
reaction mit 2,4 Dinitrophenylhydrazine (detection of ketons)
H2N-NHR´ NO2
-H2O
R´ =
O
N NHR´
(compound D)
NO2
b) optical active compounds

H
 
    
O
OH OH
compound A compound B compound C
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c)
O3
T< 0°C
O
O
O
primary ozonide
O
+
O
O
O
O
compound C compound D secondary ozonide
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Answers round 4
Answers round 4
a) It = Io· e t
ln 2/ t1/ 2
.
nuclide It It after dilution

-1
in Bq mL in Bq mL-1
71
Zn 1.59·102 0.064
67 7
Ga 6.95·10 2.78·104
68
Ge 7.00·107 2.80·104
b) 71
30 Zn  71
31 Ga + 0
1 e (+
)
67
31 Ga + 0
1 e  67
30 Zn (+
)
68
32 Ge + 0
1 e  68
31 Ga (+
)
c) n(Ga) = 10.25·10-3 g / 69.72 gmol-1 = 1.47·10-4 mol Ga.

n(67Ga) = 1.47·10-4 mol·5.0·10-7 = 7.35·10-11 mol 67Ga.
z(67Ga) = 4.43·1013 atoms
for radioactive decay of 1. order kinetics the rate of disintegration is
It = k·z t(67Ga). It = activity in Bq at time t.
z t = amount of atoms at time t
k = ln 2 /t1/2 = 2.461·10-6 s -1
t = 0 s: I0 = 2.461·10 -6 · 4.43·1013 Bq/100 mL = 1.090·10 6 Bq/mL
t = 9 h: I9 = I 0· e 9ln 2/78,25 I9 = 1.006·106 Bq/mL
Iblood = 165.6 Bq/mL
factor of dilution I9 / Iblood = 1.006·10 / 165.6 = 6075. 6
 V blood = 6.1 L
a) CaCO 3 CaO + CO 2 K p = p(CO2)

ΔG = - R∙
T∙ln K mit K = Kp/p 0
T in K 800 900 1000 1100 1200 1300

Kp in Pa 50 1,000 11,200 80,000 405,000 1,610,000
-4
K 5∙
10 0.01 0.112 0.8 4.050 16.1
-1
ΔG in kJ∙
mol 50.6 34.5 18.2 2.04 - 14.0 - 30.0
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Answers round 4
b) If the pairs (T, ΔG) found in a) form a straight line and if you assume that ΔH and ΔS are
independent of temperature, you find ΔH° and ΔS° as intersection and negative slope
respectively of the straight line ΔG = ΔH° - T∙
ΔS°.
Whether a straight line is formed you can prove by a plot or by calculation of the slopes:
T in K 800 900 1000 1100 1200 1300

-1
ΔG in J∙
mol 50,600 34,500 18,200 2,040 - 14,000 - 30,000
m with (800/50,600) - - 161.0 - 162.0 -161.9 - 161.5 -161.2
oder
ΔG in J∙
-1
mol ΔG = (- 0.162 K-1 ∙T + 180) kJ∙
mol-1
K-1 ∙
ΔS° = 162 J∙ mol -1
40000
mol-1
ΔH° = 180 kJ∙
prediction: ΔS° is positive because a gas
20000 forms and the number of particles increases,
saying the disorder, i.e. entropy, increases.
0 T in K 
800 900 1000 1100
c) reaction spontaneous  ΔG < 0 kJ∙

mol-1 - 0.162 K-1 ∙T + 180 < 0
T > 180 K / 0.162 = 1111 K or 1110 K to be read from the plot
as of 840°C the reaction is spontaneous.

a) Ag + + H2O AgOH + H+ K1 = 10-11.70
Pb 2+ + H2O PbOH+ + H+ K2 = 10-7.80
Only the second equilibrium determines the value of pH as K 2 >> K1 ist.
Pb2+ + H 2O PbOH+ + H+
L-1:
equilibrium conc. in mol∙ 0.10 - x x x
x2
= 10-7.80  10 -5
x = 3.98∙  pH = 4.40
0.10 x
b) The concentration of Ag + has to be determined in both half cells.
Half cell 1: After unifying both solutions it would be
c(Ag +) = 0.025 mol∙
L-1. c(Pb 2+) = 0.050 mol∙
L-1. c(I-) = 0.125 mol∙
L-1 . c(H +) = 0.10 mol∙
L-1
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Answers round 4
The amount of I - is equivalent to the amount of Ag+ and Pb2+, thus AgI and PbI2 will
precipitate completely.
AgI Ag + + I- K sp(AgI) = 10 -16
1∙
PbI 2 Pb2+ + 2 I- K sp(PbI2) = 10 -7.86
1∙
[The formation of PbOH+ can be neglected because of c(H+) = 0.10 mol∙-1
L :
2+ + +
Pb + H2 O PbOH + H
c( PbOH ) 10 7.8
2
 = 10
-6.8
 c(PbOH ) << c(Pb ) ]
+ 2+
c (Pb ) 0 .1
As K sp(AgI) << Ksp(PbI 2), only Ksp(PbI2) determines the iodine concentration and thus the
concentration of the silver ions.
(2x)2 = 1∙
x∙ 10-7.86  x = 1.51∙
10-3 c(I -) 10-3 mol∙
= 3.02∙ L-1
c(Ag +)∙ 10-3 mol∙
3.02∙ L-1 = 10-16 (mol∙
L-1)2 c(Ag +) = 3.31∙
10-14 mol∙
L-1
Potential of half cell 1 for Ag+ + e- Ag :

+ +
T/F ∙ln c(Ag )
E 1 = E°(Ag /Ag) + R∙ 10 -3 V
E 1 = 2∙
Half cell 2: AgSCN precipitates:

Ag + + SCN- AgSCN K sp(AgSCN) = 10-12
x ∙(0.03 + x) = 10 -12 10-11
x = 3.33∙ c(Ag +) = 3.33∙
10-11 mol∙
L-1
E 2 = 0.179 V
 ΔE = E cell = E2 -E1 E cell = 0.177 V
c) Total cell reaction: Ag + I- AgI + e-

AgSCN + e - Ag + SCN-
AgSCN + I - AgI + SCN-
c ( SCN ) c( SCN ) c ( Ag ) K sp (AgSCN) 10 12
K=  K=  16 K = 104
c( I) c (I ) 
c ( Ag ) K sp (AgI) 10
d) Case 1: The amount of NaOH is so small that the acid is not neutralised.
Then the formation of Pb(OH)+ doesn’t play a role further on, the concentrations of lead,
iodine and silver stay constant, the voltage does not change.
Case 2: The amount of NaOH added is sufficient to neutralise the acid.

Then Pb(OH) + is formed in a remarkable amount, c(Pb2+) decreases , c(I- ) increases and
c(Ag +) decreades. Thus E1 decreases and the voltage increases
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Answers round 4
e) Fe3+ + SCN-  FeSCN2+ …  Fe(SCN)2+ …

- +
c(SCN ) decreases, c(Ag ) increase and for this reason E2 also. The voltage increases.
f) You have to calculate the standard potential E° of V2+ + 2 e- V

because standard potentials refer to a standad hydrogen cell with E° = 0 V.
ΔG° = - n∙
F∙E° n=2 E° = ?
1.00 0.337 -0.255 x

V(OH) 4  VO  V  V  V
+ 2+ 3+ 2+
-0.25
1.00 + 0.337 - 0.255 + 2∙

x = 5∙
(- 0.25) x = - 1.17 E°(V2+/V) = - 1.17 V
ΔG° = - 2 ∙96485 ∙(- 1.17) J ΔG° = 226 kJ
Solution to 4-4
d([ES ])
a) Steady state: =0
dt
k1∙ [S] - k2∙[ES] - k3∙[ES]
[E]∙ =0 [E] = [E] total- [ES]
k1∙
([E] total - [ES])∙
[S] = (k2 + k3)∙[ES]
k1∙
[E] total ∙
[S] = (k2 + k3 + k1∙
[S]) ∙[ES]
k   
E total S  
E total S
[ES] = 1  [ES] =

k 2 k 3 k 1 S K M  S
d([P])
b) = k3 ∙
[ES] [ES]max = [E] total  vmax = k3∙
[E] total
dt
c)
d([P])
= k3∙
[ES] with a): [ES] =
 
E total S


E 
v = k3∙ ttal

S
dt K M  S K M 
S
with b): k 3∙
[E] total = vmax  v=

v max S
K M 
S
d) With c) v = ½ ∙vmax  K M = [S],

10 -6 mol L-1 s -1
read the value of [S] at v = 1.5∙
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Answers round 4
-6 -1 -1
vmax = 3.0∙
10 mol L s

v in
mol L-1 s-1
-6
2.0∙
10
10-4 mol L -1
KM = 0,5∙
10- 6
1.0∙
10- 4
1.0∙ 10-4
2.0∙ 10-4
3.0∙ [S] in mol L-1 
e) with c): v=

v max S

1 K M 

S

1 KM
 
1

1
K M 
S 
v v max 
S v v max 
S v max
f)
106 in mol L-1
[S] 0∙ [S]0-1 in mol -1 L 105 in mol L -1 min-1
v0∙ v0-1 in mol -1 L min
3 105
3,33∙ 1,06 104
9,43∙
5 105
2,00∙ 1,55 104
6,45∙
10 105
1,00∙ 2,37 104
4,22∙
20 105
0,50∙ 3,21 104
3,12∙
1/v in
mol-1 L min

4
8∙
10
104
6∙
1 KM 1 1
  
4∙
10
4 v v max 
S v max
(1)
 1/[S] in mol-1 L
105
1∙ 105
2∙ 105
3∙
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Answers round 4
1
intersection 1/[S] = 0  104 mol-1 L min
= 2∙
v max
10-9 mol L-1
mit [E] total = 1,0∙  [with b)] 104 min-1
k3 = 5∙
with equation (1) for the straight line 10-5 mol/L

KM = 1.1∙
g) fES =
v0
=

S0
v max K M 
S0
10 5 mol
3 L1
fES = fES = 0.67
10 5 mol
1 .5 L1 3 
10 5 mol 
L1
h) kkat = k3 from the equation given in b) vmax = k3∙

[E]total
10 9 g
[E]total = 10-12 mol∙
= 2.38∙ L-1
0.01 L 
41977 g·mol -1
min 1
7.15·10 -11 mol·L-1 
kkat = -12 -1
= 30 min -1 kkat = 0.5 s-1
2.38·10 mol·L
a) 2 MnO4- + 5 C2O 42- + 16 H3O +  2 Mn 2+ + 10 CO2 + 24 H 2O

0.1702 g 01702 g
n(C2O 42- ) = = n(C2O42-) = 1.27∙
10-3 mol
M(Na 2C 2O 4 ) 134,02 g/mol
n(C2O 42-) = n(MnO4-)
0.4∙ = c(MnO 4- )∙V(MnO4- )
c(MnO4- ) = 0.4∙ 10-3 mol / 26.70∙
1.27∙ 10-3 L c(MnO 4-) = 0.019 mol/L
b) Fe + 2 H3O +  Fe2+ + H2 + 2 H 2O
Fe2O 3 + 6 H3O +
 2 Fe 3+
+ 9 H 2O
2 Fe 3+
+ SO3 2-
+ 3 H2O  2 Fe 2+
+ SO 42- + 2 H 3O +
SO32- + 2 H3O +  SO2 + 3 H 2O
MnO4 -
+ 5 Fe 2+
+ 8 H 3O +
 Mn 2+
+ 5 Fe 3+ + 12 H2O
n(Fetotal) = 5∙n(MnO 4- ) 0.019 mol/L ∙
= 5∙ 37.5∙
10 L = 3.56∙ -3
10-3 mol
n(Fetotal) = n(Fe) + 2∙
n(Fe 2O 3) n(Fe) 10-3 mol - 2∙
= 3.56∙ n(Fe 2O 3)
m total = n(Fe)∙M(Fe) + n(Fe2O3)∙
M(Fe 2O 3)
0.225 g 10 -3 mol - 2∙
= [3.56∙ n(Fe2O 3)]∙
55.85 g/mol + n(Fe 2O3)∙
159.7 g/mol
n(Fe2O 3) 10 -4 mol
= 5.45∙ m(Fe2O 3) = 0.087 g  38.7 % Fe2O 3
61.3 % Fe
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Answers round 4
10-3 mol/L
c) c(Ni) = 1.70∙
6
10 16
no precipitate of Ni(OH) 2: c(OH)  3
10-7 mol/L
mol/L = 5.94∙
1,7 
10
pH 7.7 (at 7.8 Ni(OH) 2 precipitates)
-2
c(Fe)before precipitation = 1.25∙
10 mol/L
c(Fe)after precipitation 1.25∙
10-5 mol/L
10 -5 mol/L:
maximum concentration of the solution 1.25∙
10 38
4
c(OH) 3 5
10-11 mol/L
mol/L = 1.47∙
1 .25
10
pH 3.2 (at 3.1 error > 0.1%)
precipitation in the range 3.2 pH 7.7
a) 1.0∙106 molecules/cm3 = 1.0∙

1012 molecules /m3
1,0
1012 
8,314 1200
p∙V = n∙R∙
T  p= Pa 10-8 Pa
p = 1.66∙
6,022 
10 23
b) p = F/A F = m∙
g ρ
m = V∙(Hg)  p = A∙
h∙ρ(Hg)∙
g
e.g. A = 1 m2  p = (1 m2 ∙
10-12 m ∙ 10 3 kg/m3 ∙
13.55∙ 9.81 m/s 2) / 1 m 2
10-7 N/m2
p = 1.33∙ 10-7 Pa
p = 1.33∙
105/760 Pa ect.)
(or 1 mm Hg equals 1 Torr equals 1.013∙
10 7 
1.33  .,02210 23
c) Analogous to a) molecules /m3 = 3.23∙
1013 molecules /m3
8 .314 298
107 molecules/cm3 , 32 times more than in the oxosphere.
= 3.23∙
8RT 8.314 JK 1mol 1 

8 1200K
d) v v 1200  v 1200 5000 m/s
M  10 kgmol 1
1. 008 3
v 298 2500 m/s v 1200 : v 298 = 2 : 1
e)
Mean speed v
v 1 = 2400 m/s 88.314 JK 1mol 1 
2.7K
v2  = 238 m/s
 10 kgmol 1
1 .008 3
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Answers round 4
Volume of collision cylinder = π∙ 10-10 m)2∙ 2 ∙

(1∙ v
V1 = π∙ 10-10 m)2∙ 2 ∙
(1∙ 2400 m/s
-16 3 -17 3
V1 = 1.066∙
10 m /s V2 = 1.057∙
10 m /s
Density of particles
15 3
40∙
10 /m 1/m 3
Number of collisions/s = (volume ofcollision cylinder) ∙(density of particles)
10 -16 m3/s ∙40∙
z1 = 1.066∙ 1015/m3
z1 = 4.264 /s 10 -17/s
z2 = 1.057∙
mean time until first collision = 1/z
t 1 = 0.235 s 1016 s
t 2 = 9.46∙ 3∙
10 9 years
free path = t ∙v
free path1 = 564 m 1019 m
free path2 = 2.25∙
2400 light years
Solution to 4-7
10-5 (mol/L) 2
10-3 mol/L) 2 = 6.4∙
a) Ksp = (8∙
b) c(Na+) = 0.130 mol/L  c(Ur -) = 6.4∙ 10-4 mol/L
10-5 /0.130 mol/L = 4.9∙
c) The lower the temperature the smaller Ksp .
 
c (Ur ) c( Ur )
d) pH = pK + lg pH = 7.4  7.4 = 5.4 + lg (1)
c (HUr ) c (HUr )
If NaUr does not precipitate then c(Ur -) 4.9∙

10-4 mol/L (see b) and with (1)
10-6 mol/L < solubiulity of HUr in water.

c(HUr) 4.9∙

c( Ur )
e) pH = 5.4 + lg c(HUr) + c(Ur -) = 2∙
10-3 mol/L c(HUr) 0.5∙
10 -3 mol/L
c (HUr )
10 3
1,5 
 pH 5.4 + lg pH 5.9
10 3
0,5 
f) t = 0 h corresponds to 2.5% of the injected 20 mg. Thus there are 800 mg of uric acid
totally in the body of N, before injection 780 mg
analogous calculation for P 1980 mg
g) The plot shows that the half life in constant in both cases, characteristic for processes of
1. order only
N: half life t1/2 = 40 hours k = ln2/t1/2 10 -2 h-1
k = 1.73∙
P: half life t1/2 = 40 hours k = ln2/t1/2 10 -2 h-1
k = 1.73∙
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Answers round 4
Solution to Problem 4-8
a) O
O - _ O C2H 5C H
OH
CH3CH2C CH3CHC + H2O
H H
O
H 3C CHC CH3
H H+
C2H5CHCHCH
C2H5 C O
OH O
H
3-Hydroxy-2-methylpentanal
b) The base abstracts the hydroxyl proton to yield a -keto alkoxide ion which fragments to
give one molecule of enolate ion
_
OH -
RCH2CHO RCHCHO + H2O
_
RCH – CHO RCH = CH – O -
electrophilic reactant: nucleophilic reactant: _


-
O RCHCHO
: RCH2C

+
H
The enolate ion (nucleophil) reacts with the C-atom of the carbonyl group (electrophil)
H
_ O R C CHO
R CHCHO + R CH2C
H HC O
CH2R
Precondition ketones or aldehydes with an -hydrogen atom
OH - _
c) 1. HCHO + CH3CHO HCHO + CH2CHO
OH O
O H+ O
CH2 CH2 C CH2 CH2C
H H
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Answers round 4
O
-
_ CH3 C H
OH
2. CH3CHO CH2CHO
CH2CHO
OH O
H+
HC O CH 3CHCH2CH
CH3
Formaldehyde contains no -H atom and thus cannot form an enolate ion to condense
with itself.
d) Aldol reaction of acetaldehyde and 2,4-pentadione,

favoured reaction:
O O O O
H2 base O H
CH3C H + H3C C _C
CH3CHO + H 3C C C C CH3 C CH3
O O O O
H H
H3 C C C C CH3 H3 C C C C CH3
H+
H3C CH H3C CH
OH O
If one of the carbonyl components (diketone) is unusually acidic and easily transformed into
its enolate ion, then a mixed aldol reaction is likely to be successful.
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Answers round 4
e) Aldol reaction of 2,5-hexadione
O O
H2 H2 H3C H+ H3 C
H 3C C C C C _ 2
CH
O O HO O
base
O O
CH3 CCH 2 CH2 CCH 3
2,5-hexandione
base
O O O
H2 H H3 C H+
H3C C _C C product
C CH3 C CH3 unstable
O
The 5-membered ring is more stable than the 3-membered ring according to the great ring
strain of the 3-membered ring.

a)
O H
H O C
C
C OH HO C
HO C C OH
C OH HO C
C OH HO C
CH2 OH CH2OH
D-Glucose mirror L-Glucose
b) There are 4 stereogenic centres in L-glucose. D- and L-glucose are enantiomers.
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Answers round 4
c)
CH2OH O
OH
O CH2OH
OH
OH
OH
OH OH OH
OH -L-Glucopyranose
-D-Glucopyranose
d)
e O
HO HOH2C e
-D-Glucopyranose
HO e
e OH a
OH
e HOH2C
HO e O
-D-glucopyranose
HO e OH
e OH e
OH e
a e OH
O HOH2 C
Turning the chair O
a OH
CH 2OH a e OH
HO e HO e
a a
OH OH
-L-Glucopyranose
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Answers round 4
In -D-glucopyranose and in -L-Glucopyranose all substituents of the ring are equatorial.

Thus these compounds are the least sterically crowded and most stable.
e) H3COCOH2C
O ester
H3COCO
H3COCO OCOCH3
OCOCH3
f) H3COH2C
O
H 3CO
ether
H 3CO OCH 3
OCH 3
g)
HOH 2C
O
HO
acetal
HO OCH 3
OH
Mutarotation is to the following equilibrium

open form
CH 2OH CH2OH CH 2OH

OH O O
OH
H OH + OH
OH O OH OH OH
OH
OH OH
D-Glucose OH -D-Glucopyranose -D-Glucopyranose
As the OH-group in - or -position reacted to form the acetal the equilibrium shown
above cannot establish via open form.
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Answers round 4
a) C4H8O 2.
b) Band at 1730cm -1 according to carbonyl compound or ester

-1 -1
Band at ~2850cm – 2930cm according to alkyl group
c) All molecules have a certain amount of energy distributed throughout their structure
causing bonds to stretch and bend, atoms to wag and rock, and other molecular
vibrations to occur.
The amount of energy is quantised that is a molecule dan stretch, bend,or vibrate only at
specific frequencies corresponding to specific energy levels.
When a molecule absorbs infrared radiation the vibrating bond will absorb energy only if
the frequency of the light and the vibration are the same.
Since each light frequency absorbed corresponds to a precific molecular motion, we can
see what kind of molecular motions a sample has by measuring its infrared spectrum.
d) Proposal for a structure:

O
CH 3COCH2
Assingments:
There are three different peaks and peak groups respectively. That is there are three
protons or proton groups with different surroundings:
 The singulet at = 2.1 ppm leads to an acetyl group (2.1 ppm – 2.4 ppm).
 The triplet at = 1.3 ppm indicates a CH3 group adjacent to a CH2 group.
 The quartet bei = 4.1 ppm is difficult to interprete.
( X C H ? X = O etc.)
Number of protons:
The total number of H atoms is 8. These 8 protons may be divided in the ratio 2 : 3 : 3.
Thus the singulet is a CH3 group, the triplet another CH3 group and the quartet a CH2
group.
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Answers round 4
Couplings:
.
 The CH3 group at the carbonyl hydrogen has no further hydrogen to couple
with. That results to a singulet.
 The triplet at = 1,3 ppm is caused by a terminal CH 3 group which couple
with an adjacent CH 2 group.
 The quartet at = 4,1ppm arises from the coupling with the three H atoms of
the CH 3-Gr..
O
The structure of A is (ethylacetate)
CH3COCH 2
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Answers round 4
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Problems of the IChO
Chemistry for Life,

Chemistry for better Life
Theoretical Test
2006. 7. 7
Gyeongsan, Korea
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Problems of the IChO
Constants and useful formulas
Gas constant R = 8.314 J K-1 mol -1

Faraday constant F = 96485 C mol-1
Use as standard pressure: p = 1.013∙ 105 Pa
Use as standard temperature: T = 25°C = 298.15 K
Avogadro’s number NA = 6.022∙1023 mol-1
Planck constant h = 6.626∙10-34 J s
Speed of light c = 3.00∙108 m s -1
G = H - TS G = - nFE
product of c( products)
G0 = - RT∙
lnK G = G0 + RT∙
lnQ with Q =
product of c( reactands)
H(T1) = H0 + (T1 - 298.15 K)∙
Cp (Cp = constant)
E
 a
Arrhenius equation k=A∙
e RT
Ideal gas law pV = nRT

RT c
Nernst equation E = E0 + ln ox

nF c red
P0
Beer- Lambert Law A = log = ∙
c∙
d
P
V(cylinder) = r2h
A(sphere) = 4r 2
4
V(sphere) = r 3
3
1J=1Nm 1 N = 1 kg m s-2 1 Pa = 1 N m-2

1 W = 1 A V = 1 J s-1 1C=1As
Theoretical Problems of the IChO
1. Avogadro's number
Spherical water droplets are dispersed in argon gas. At 27oC, each droplet is 1.0 micrometer
in diameter and undergoes collisions with argon. Assume that inter-droplet collisions do not
occur. The root-mean-square speed of these droplets was determined to be 0.50 cm/s at
27oC. The density of a water droplet is 1.0 g/cm3.
1-1. Calculate the average kinetic energy (mv2/2) of this droplet at 27oC. The volume of a
sphere is given by (4/3) πr3 where r is the radius.
If the temperature is changed, then droplet size and speed of the droplet will also change.
The average kinetic energy of a droplet between 0 oC and 100oC as a function of temperature
is found to be linear. Assume that it remains linear below 0 oC.
At thermal equlibrium, the average kinetic energy is the same irrespective of particle masses
(equipartition theorem).
The specific heat capacity, at constant volume, of argon (atomic weight, 40) gas is 0.31 J g -1
K-1.
1-2. Calculate Avogadro's number without using the ideal gas law, the gas constant,
Boltzmann’s constant).
2. Detection of Hydrogen
Hydrogen is prevalent in the universe. Life in the universe is ultimately based on hydrogen.
2-1. There are about 1023 stars in the universe. Assume that they are like our sun (radius,
700,000 km; density, 1.4 g/cm 3; 3/4 hydrogen and 1/4 helium by mass). Estimate the
number of stellar protons in the universe to one significant figure.
In the 1920s, Cecilia Payne discovered, by spectral analysis of starlight, that hydrogen is the
most abundant element in most stars.
2-2. The electronic transition of a hydrogen atom is governed by ∆E(ni→nf) = -C(1/n f2 - 1/ni2),
where m and n are principle quantum numbers, and C is a constant. For detection of the
∆E(3→2) transition (656.3 nm in the Balmer series), the electron in the ground state of
the hydrogen atom needs to be excited first to the n = 2 state. Calculate the wavelength
(in nm) of the absorption line in the starlight corresponding to the ∆E(1→2) transition.
2-3. According to Wien's law, the wavelength (λ

) corresponding to the maximum light
intensity emitted from a blackbody at temperature T is given by λT = 2.9×10-3 m K.
Calculate the surface temperature of a star whose blackbody radiation has a peak
intensity corresponding to the n = 1 → n = 2 excitation of hydrogen.
The ground state of hydrogen is split into two hyperfine levels due to the interaction between
the magnetic moment of the proton and that of the electron. In 1951, Purcell discovered a
spectral line at 1420 MHz due to the hyperfine transition of hydrogen in interstellar space.
2-4. Hydrogen in interstellar space cannot be excited electronically by starlight. However, the
cosmic background radiation, equivalent to 2.7K, can cause the hyperfine transition.
Calculate the temperature of a blackbody whose peak intensity corresponds to the 1420
MHz transition.
2-5. Wien generated hydrogen ions by discharge of hydrogen gas at a very low pressure and
determined the e/m value, which turned out to be the highest among different gases
tested. In 1919, Rutherford bombarded nitrogen with alpha-particles and observed
emission of a positively charged particle which turned out to be the hydrogen ion
observed by Wien. Rutherford named this particle the “proton”.
Fill in the blank.
3. Interstellar Chemistry
Early interstellar chemistry is thought to have been a prelude to life on Earth. Molecules can
be formed in space via heterogeneous reactions at the surface of dust particles, often called
the interstellar ice grains (IIGs). Imagine the reaction between H and C atoms on the IIG
surface that forms CH. The CH product can either desorb from the surface or further react,
through surface migration, with adsorbed H atoms to form CH2, CH3, etc.
Depending on how energetically a molecule “jumps” from its anchored site, it either leaves
the surface permanently (desorption) or returns to a new position at the surface (migration).
The rates of desorption and migratory jump follow the Arrhenius formula, k = A exp(-E/RT),
where k is the rate constant for desorption or migratory jump, A the jumping frequency, and
E the activation energy for the respective event.
3-1. Desorption of CH from the IIG surface follows first-order kinetics. Calculate the average
residence time of CH on the surface at 20 K. Assume that A = 1 x 1012 s -1 and Edes = 12
kJ mol-1.
3-2. Consider the shortest time it would take for one CH unit to move from its initial position
to the opposite side of an IIG by successive migratory jumps. Assume that the activation
energy for migration (Emig) is 6 kJ mol-1, and the IIG is a sphere with a 0.1 μm radius.
Each migratory jump laterally advances the molecule by 0.3 nm. Show work and choose
your answer from (a)-(e) below.
(a) t ≤1 day (b) 10 day ≤t ≤102 yr (c) 10 3 yr ≤t ≤106 yr
(d) 107 yr ≤t ≤1010 yr (e) t ≥10 11 yr
3-3. Consider the reaction of CO with H 2 to form H2CO. The activation energy on a metal
catalyst is 20 kJ mol -1, which produces formaldehyde at a rate of 1 molecule/s per site at
300 K. Esitmate the rate of formaldehyde formation per site if the reaction takes place at
20 K.
3-4. Which is a set of all true statements? Circle one.
(a) Most CH species desorb from the IIG surface before encountering other reactants by
surface migration.
(b) IIGs can assist transformation of simple molecules to more complex ones in
interstellar space.
(c) For a reaction on the IIG to occur at an appreciable speed during the age of the
Universe (1 x 1010 yr), the reaction energy barrier must be absent or negligible.
(a) (b) (c) (a, b) (a, c) (b, c) (a, b, c)
4. The Chemistry of DNA

4-1. In 1944 Oswald Avery isolated a genetic material and showed, by elemental analysis,
that it was a sodium salt of deoxyribonucleic acid. A segment of DNA with formula mass
of 1323.72 is shown.
Assuming that equimolar amounts of the four bases are present in DNA, write the
number of H atoms per P atom. Calculate, to 3 significant figures, the theoretical weight
percentage of H expected upon elemental analysis of DNA.
4-2. Chargaff extracted the separated bases and determined their concentrations by
measuring UV absorbance. The Beer-Lambert law was used to obtain the molar
concentration. Chargaff discovered the following molar ratio for bases in DNA:
adenine to guanine = 1.43 thymine to cytosine = 1.43
adenine to thymine = 1.02 guanine to cytosine = 1.02
Chargaff’s discovery suggested that the bases might exist as pairs in DNA. Watson and
Crick mentioned in their celebrated 1953 paper in Nature: "It has not escaped our notice
that the specific pairing we have postulated immediately suggests a possible copying
mechanism for the genetic material."
Draw structures of the specific pairing found in DNA. Indicate hydrogen bonds. Omit the
sugar-phosphate backbone.
4-3. Mutation can occur through base pairings different from the above.
Draw structures of any three alternative base pairs.
4-4. The plausibility of the formation of purine and pyrimidine bases in the prebiotic
atmosphere of the Earth from HCN, NH 3, and H2O has been demonstrated in the
laboratory.
Write the minimum number of HCN and H2O molecules required for formation of the
following compounds.
NH2 O O NH2
N N N NH NH N
N N N N NH2 N O N O
H H H H
adenine guanine Uracil cytosine
5. Acid-Base Chemistry
5-1. Calculate [H+], [OH-], [HSO 4-], and [SO42-] in a 1.0 x 10 -7 M solution of sulfuric acid (Kw =
1.0 x 10 -14, K2 = 1.2 x 10-2 at 25 oC). In your work you may use mass- and charge-balance
equations. Answer with two significant figures.
5-2. Calculate the volume of 0.80 M NaOH solution that should be added to a 250 mL
aqueous solution containing 3.48 mL of concentrated phosphoric acid in order to prepare
a pH 7.4 buffer. Answer with three significant figures. (H3PO4 (aq), purity = 85 % wt/wt,
density = 1.69 g/mL, FW = 98.00) (pK1 = 2.15, pK2 = 7.20, pK 3 = 12.44).
5-3. The efficacy of a drug is greatly depende nt on its ability to be absorbed into the blood
stream. Acid-base chemistry plays an important role in drug absorption.
Membrane
Stomach Blood
pH = 2.0 pH = 7.4
+ - + -
H +A HA HA H +A
Assume that the ionic form (A -) of a weakly acidic drug does not penetrate the
membrane, whereas the neutral form (HA) freely crosses the membrane. Also assume
that equilibrium is established so that the concentration of HA is the same on both sides.
Calculate the ratio of the total concentration ([HA] + [A -]) of aspirin (acetylsalicylic acid,
pK = 3.52) in the blood to that in the stomach.
6. Electrochemistry
Water is a very stable molecule, abundant on earth and essential for life. As such, water was
long thought to be a chemical element. However, soon after the invention of a voltaic cell in
1800, Nicholson and Carlyle decomposed water into hydrogen and oxygen by electrolysis.
6-1. Water can be thought of as hydrogen oxidized by oxygen. Thus, hydrogen can be
recovered by reduction of water, using an aqueous solution of sodium sulfate, at a
platinum electrode connected to the negative terminal of a battery. The solution near the
electrode becomes basic.
Write a balanced half-reaction for the reduction of water.
6-2. Water can also be thought of as oxygen reduced by hydrogen. Thus, oxygen can be
recovered by oxidation of water at the Pt electrode connected to the positive terminal.
Write a balanced half-reaction for the oxidation of water.
6-3. When copper is used at both electrodes, gas is generated only at one electrode during
the initial stage of electrolysis.
Write the half-reaction at the electrode that does not generate gas.
Another species in solution that can be reduced is sodium ion. The reduction of sodium ion
to metallic sodium does not occur in aqueous solution, because water is reduced first.
However, as Humphrey Davy discovered in 1807, sodium can be made by electrolysis of
fused sodium chloride.
6-4. Based on these observations, connect the half-reactions with the standard reduction
potential (in volts).
Reduction of copper ion (Cu2+) · -------------------- · +0.340
Reduction of oxygen · · - 2.710
Reduction of water · · - 0.830
Reduction of sodium ion (Na+) · · 0.000
Reduction of hydrogen ion · · +1.230
The electrode potential is affected by other reactions taking place around the electrode.
The potential of the Cu2+/Cu electrode in a 0.100 M Cu2+ solution changes as Cu(OH)2
precipitates. Answer with 3 significant figures for the following problems. The temperature is
25oC. Note that Kw = 1.00 x 10-14 at 25oC.
6-5. Precipitation of Cu(OH)2 begins at pH = 4.84.

Determine the solubility product of Cu(OH) 2.
6-6. Calculate the standard reduction potential for Cu(OH) 2(s) + 2e - → Cu(s) + 2OH- .
6-7. Calculate the electrode potential at pH = 1.00.
Lithium cobalt oxide and specialty carbon are active ingredients for the positive and negative
electrodes, respectively, of a rechargeable lithium battery. During the charge/recharge
cycles, the following reversible half-reactions occur.

LiCoO2  Li1-x CoO2 + x Li+ + x e-

C + x Li+ + x e-  CLi x
The total amount of energy a battery can store is rated in mAh. A battery rated at 1500 mAh
can power a device drawing 100 milliamps for 15 hours.
6-8. Graphite has lithium intercalation sites between its layers. Assuming a maximum 6:1
carbon-to-lithium intercalation stoichiometry, calculate the theoretical charge capacity of
1.00 gram of graphite to intercalate lithium. Answer in mAh/g with 3 significant figures.
7. Hydrogen Economy
Hydrogen is more energy-dense than carbon, by mass. Thus, historically there has been a
move toward fuel with higher hydrogen content: coal → oil → natural gas → hydrogen. Cost-
effective production and safe storage of hydrogen are two major hurdles to the successful
inauguration of a hydrogen economy.
7-1. Consider hydrogen in a cylinder of 80 MPa at 25 oC. Using the ideal gas law, estimate
the density of hydrogen in the cylinder in kg/m 3.
7-2. Calculate the ratio between heat generated when hydrogen is burned and heat
generated when the same weight of carbon is burned. The difference comes to a large
extent from the fact that the most abundant isotope of hydrogen has no neutron and
hydrogen has no inner electron shell. Hfo [H2O(l)] = -286 kJ/mol, Hfo [CO2(g)] = -394
kJ/mol.
7-3. Calculate the theoretical maximum work produced by the combustion of 1 kg hydrogen
(a) from the electric motor using hydrogen fuel cell and (b) from the heat engine working
between 25 oC and 300 oC. The efficiency (work done/heat absorbed) of an ideal heat
engine working between Tcold and Thot is given by [1 – Tcold/Thot ].
So298[H2(g)] = 131 J/(K mol)
So298[O2(g)] = 205 J/(K mol)
So298[H2O(l)] = 70 J/(K mol).
If the fuel cell is working at 1 W and the standard potential difference, how long will the
electric motor run at what current?
8. Chemistry of Iron Oxides

The nucleus of iron is the most stable among all elements and, therefore, iron accumulates
at the core of massive red giant stars where nucleosynthesis of many elements essential for
life (such as C, N, O, P, S, etc.) takes place. As a result, among heavy elements iron is quite
abundant in the universe. Iron is also abundant on Earth.
8-1. Development of a technology for reducing iron oxide to iron was a key step in human
civilization. Key reactions taking place in the blast furnace are summarized below.
C(s) + O2(g) → CO2(g) ΔH◦= -393.51 kJ(/mol) ----- 
◦
CO2(g) + C(s) → 2CO(g) ΔH = 172.46 kJ(/mol) ----- 
Fe2O 3(s) + CO(g) → Fe(s) + CO2(g) ΔH◦= ? ------------------- 
8-1-1. Indicate the reducing agent in each reaction.
8-1-2. Balance reaction  and calculate the equilibrium constant of reaction  at

1200 oC. (ΔHf◦(Fe 2O3(s)) = -824.2 kJ/mol, S°(J/mol/K): Fe(s) = 27.28, Fe2O3(s) = 87.40,
C(s) = 5.74, CO(g) = 197.674, CO 2(g) = 213.74)
8-2. In the manufacture of celadon pottery, Fe2O3 is

partially reduced in a charcoal kiln to mixed oxides of
Fe3O 4 and FeO. The amount of the different oxides
seems to be related to the “mystic” color of celadon
ceramics.
Fe3O 4 (magnetite) itself is a mixed oxide containing Fe2+ and
Fe3+ ions and belongs to a group of compounds with
a general formula of AB2O 4. The oxide ions form a face-centered cubic array. The figure
shows the array of oxygens (gray circles) and representative sites for divalent A and trivalent
B cations. The dark circle represents a tetrahedral site and the white circle an octahedral
site.
8-2-1. How many available octahedral sites for iron ions are there in one AB2O 4 unit? Certain
sites are shared by neighboring units.
AB2O 4 can adopt a normal- or an inverse-spinel structure. In normal-spinel structure, two B

ions occupy two of the octahedral sites and one A occupies one of the tetrahedral sites. In
an inverse-spinel structure, one of the two B ions occupies a tetrahedral site. The other B ion
and the one A ion occupy octahedral sites.
8-2-2. What percentage of available tetrahedral sites is occupied by either Fe2+ or Fe3+ ion in
Fe3O 4?
8-2-3 Fe3O 4 has an inverse-spinel structure. Draw the crystal field splitting pattern of Fe2+
and fill out the electrons. The electron pairing energy is greater than the octahedral field
splitting.
9. Photolithographic process
Photolithography is a process used in semiconductor device fabrication to transfer a pattern

from a photomask to the surface of a substrate. In a typical photolithography process, light is
projected, through a mask that defines a particular circuitry, onto a silicon wafer coated with
a thin layer of photoresist.
9-1. The earliest photoresists were based on the photochemistry that generates a reactive
intermediates from bis(aryl azide). Patterning becomes possible through the cross-linking
reaction of the nitrenes generated from the azides.
SO3- Na+ h reactive intermediate + 2 N

N3 calledas nitrene 2
N3
+Na -O3S
Bis(aryl azide)
9-1-1. Draw two possible Lewis structures of CH3-N3, the simplest compound having the
same active functional group of bis(aryl azide). Assign formal charges.
9-1-2. Draw the Lewis structure of nitrene expected from CH3-N3.
9-1-3. Draw the structures for two possible products, when this nitrene from CH 3-N3 reacts
with ethylene gas (CH 2CH2).
9-2. Photoresists consisting of Novolak polymers, utilizes acid to change their solubility. The
acid component can be produced photochemically from diazonaphthaquinone. In fact,
“Novolaks” have been the representative “positive” photoresists of the modern
microelectronic revolution.
OH
Novolak
n
CH3
When irradiated, diazonaphthaquinone undergoes photochemical decomposition followed by

rearrangement eventually producing a carboxylic acid.
O CO2H
N2
h carbene rearranged
+ N2
intermediate intermediate
+ H2O
O S O O S O
OR OR
Diazonahpthaquinone
derivative
9-2-1. Draw three Lewis structures of diazoacetaldehyde (see below), the simplest
compound having the same active functional group of diazonaphthaquinone. Indicate
formal charges.
H-C-CHN2
diazoacetaldehyde
9-2-2. Draw a Lewis structure of the rearranged intermediate, A (see below), generated from
diazoacetaldehyde after losing N2. A satisfies Lewis’ octet rule and reacts with water to
form acetic acid, CH3CO 2H.
O
carbene A CH3COOH
H CHN2 _
N2 intermediate H2O
9-3. Advanced photoresists were invented in 1982 based on chemical amplification. The
most popular chemical amplification for positive-tone involves the acid catalyzed
deprotection of poly(p-hydroxystyrene) resin protected by various acid-sensitive
protecting groups such as t-butyloxycarbonyl (t-BOC).
O O
The thermal decomposition of carbonate ester itself normally occurs well above 150°C.
9-3-1. Two plausible mechanisms have been suggested for this decomposition reaction
having relatively high activation energy. Draw expected intermediates and products from
this reaction.
+
+
pericyclic
trans. state
O O
CH3 B +
CH3 O O
O CH2 OH
H
+ C
O O OH
O
D B + H+
+
heterolytic
cleavage
E + C
_
O
9-3-2. In the presence of a trace amount of acid, the reaction temperature can be reduced to
below 100°C. Draw expected intermediate F from the following chemical amplification
process based on using t-BOC.
n n
n + C
H+
F O OH
OH
O
O O +
O
D B + H+
10. Natural Products – Structural Analysis
Licorice (Glycyrrhizia. Uralensis) Licorice Root

The flavor extracted from the licorice root is 50 – 150 times sweeter than table sugar.
The most important and abundant compound responsible for the sweetness and medicinal
effects of licorice is glycyrrhizin (C42H62O16).
Glycyrrhizin requires three equivalents of NaOH to effect neutralization.
``When glycyrrhizin was subjected to acid hydrolysis, Glycyrrhizinic acid (A (C30H46O 4)) and
B (C6H10O7) were obtained in a 1:2 molar ratio (figure 1).
Figure 1.
HOOC
O
glycyrrhizin HCl
H + 2 B (C6H 10 O 7)
(C42 H 62 O16) H2 O
H
HO H
A (Glycyrrhizinic acid)
When glycyrrhizin was methylated with methyl iodide (MeI) at every possible site before
hydrolysis, hydrolysis produced A’ (methyl glycyrrhizinate), C and D (figure 2). B, C and D
exist as mixtures of anomers.
Figure 2.
glycyrrhizin i) MeI, Ag2 O
(C42H 62 O16) A' (C31H 48 O 4) + C (C9 H16O7) + D (C10H18 O7 )
ii) HCl / H 2O
Methylation of C and D with MeI produced the same isomeric mixture of compounds, J
(figure 3.)
Figure 3.
MeI, Ag 2O MeI, Ag2 O
C (C9 H16O7 ) J (C11H20 O7) D (C 10 H18O7)
C was reduced with LiAlH4 to give K, and L was produced by the reduction of K. Oxidative
cleavage of vicinal diol of L with NaIO4 produced M and two equivalents of formaldehyde.
Reduction of M produced N. The structure and stereochemistry of N was confirmed by the
synthesis of N from D-(-)-tartaric acid through methylation followed by reduction (figure 4). A
1
H-NMR spectrum of L showed two distinct peaks for methyl groups. (There is no symmetry
in L)
Figure 4.
LiAlH4 H2, Raney-Ni
C (C 9H16O7) K (C8H16O6) L (C8H18O6)
NaIO4
H2, Raney-Ni
N (C 6H14O4) M (C6H10O4)+ 2 HCHO
LiAlH4
OH OMe
COOH COOMe
H OOC MeOOC
OH MeI, Ag2O OM e
10-1. Complete structures for L , M, and N in the answer sheet.
10-2. How many structures for C are possible? Complete possible structures for C.
To determine the correct structure of C, following set of reactions were performed.

J was reduced to E, and acid hydrolysis of E produced F. Reduction of F generated G, and
G was oxidized with NaIO 4 to H with formation of one equivalent of formaldehyde. I was
obtained from H through reduction. Among all compounds from A to I, only I was optically
inactive (figure 5).
Figure 5
LiAlH4 HCl H2, Raney-Ni

J (C11H20 O7 ) E (C 10 H20 O6 ) F (C 9H18 O6) G (C 9 H20 O6)
H2O
NaIO4
H2 , Raney-Ni
I (C 8H18 O5) H (C 8 H16 O5) + HCHO
optically inactive
10-3. Complete structures for G and I.

10-4. Which one is the correct structure for C among ones you have drawn in 10-2?
10-5. Complete structures for B, D, and J.
10-6. Complete the structure for Glycyrrhizin.
11. Enzyme Reaction

Shikimic acid biosynthesis is an important pathway for amino acids, alkaloids and
heterocyclic natural product production. Nature converts shikimic acid to chorismic acid
through a cascade of enzymatic reactions. Then chorismate mutase catalyzes the
conversion of chorismic acid to prephenic acid at the branch point for the biosynthesis of
aromatic amino acids such as tyrosine and phenylalanine.
O
CO2 H COOH
pyruvic acid CO 2H
Chorismate mutase
HO OH Prephenic Acid
O COOH
OH
OH
1 2 3 2H2 O
Chorismic Acid
Shkimic Acid
11-1. During the transformation of shikimic acid to chorismic acid, dehydration is occurring.
Choose the hydroxyl group in shikimic acid that is lost through above dehydration among all
possible reactions.
11-2. Chorismate mutase rearranges chorismic acid into prephenic acid without changing
the molecular formula. Chorismic acid becomes prephenic acid through the Claisen
rearrangement, a concerted pericyclic process like the Cope rearrangement as shown
below:
D D D
D D D
Based on the following spectral data, propose the structure of prephenic acid.
1
H-NMR (D2O, 250 MHz):  6.01 (2H, d, J = 10.4 Hz), 5.92 (2H, dd J = 10.4, 3.1 Hz),
4.50 (1H, t, J = 3.1 Hz), 3.12 (2H, s). Note that there are three protons, which have
been exchanged by D2 O very fast, and two protons at 3.12, which are exchanged
slowly in prephenic acid.
13
C-NMR (D2 O, 75 MHz):  203, 178, 173, 132 (for two identical carbons), 127 (for
two identical carbons), 65, 49, 48.

, chemical shift; H, integrals; d, doublet; dd, doublet of doublet; J, coupling constant; t,
triplet; s, singlet
Chorismate mutase is believed to stabilize the transition state of Claisen rearrangement.

Thus it is an interesting target for inhibitor design. Inhibitors, called transition state analog
(TSA)s that resemble the transition state (TS, e.g., the species in brackets “[ ]” above) of the
reaction are designed to occupy the active site. Several inhibitors were designed and
synthesized, and among them eight turned out to be potent inhibitors of the enzyme. The
lower the IC50 (inhibitor concentration of 50% of the enzymatic activity) value, the better the
inhibitor.
CO2 H CO2H CO2H

CO2H CO 2H
CO2H CO2H CO2H CO2H

HO
OH OH OH OH
1 2 3 4 5
IC 50 = 2.5 mM IC 50 = 1.3 mM IC 50 = 0.78 mM IC 50 = 1.1 mM IC 50 = 5.3 mM
HO2C CO2H Ha
Ha HO2C
O O O
CO2H CO2 H
CO2 H
OH OH OH
6 7 8
IC 50 = 0.017 mM IC 50 =0.0059 mM IC 50 = 0.00015 mM
11-3. Choose all correct statements based on the structures and IC50 values of above
inhibitors. Increase of factor 5 is considered to be important.
(a) Configuration of the hydroxyl group plays an important role in the TS and inhibitor
design.
(b) The presence of both carboxylic groups is important in the TS and inhibitor design.
(c) Transition state of the reaction contains two six-membered rings with one chair and one
twist-boat conformation.
(d) 7 and 8 can be distinguished on the basis of the 1H-NMR of Ha.
11-4. Draw the transition state of the transformation of chorismic acid to prephenic acid
based on the TSA structures and their IC 50 values.
11-5. Compared with the uncatalyzed thermal conversion, chorismate mutase accelerates
conversion of chorismic acid to prephenic acid 1.0 x 106 fold at 25oC by lowering the
activation energy of the reaction. Calculate the decrease in activation energy of chorismate
mutase at 25oC.
ΔH≠uncat is 86,900 J/mol for the thermal conversion of chorismic acid to prephenic acid. At
what temperature will the rate of the uncatalyzed thermal conversion be the same as that of
the enzyme-catalyzed conversion at 25oC, assuming that Ea = ΔH≠.
Solutions to the Theoretical Problems of the IChO
1-1.
The mass of a water droplet:
3 -6 3 3 -16
m = V ρ= [(4/3) πr ] ρ= (4/3) π(0.5x10 m) (1.0 g/cm ) = 5.2x10 kg
o
Average kinetic energy at 27 C:
KE = mv2/2 = (5.2x10-16 kg) (0.51x10-2 m/s)2/2 = 6.9x10-21 kg m2/s2 = 6.9 x10-21 J
1-2.
The average kinetic energy of an argon atom is the same as that of a water droplet.
o
KE becomes zero at –273 C.
From the linear relationship in the figure, KE = aT (absolute temperature)
where a is the increase in kinetic energy of an argon atom per degree.
-21 - 23
a = KE/T = 6.9x10 J/(27+273K) = 2.3x10 J/K
S: specific heat of argon N: number of atoms in 1g of argon S = 0.31 J/g K = a x N
-23 22
N = S/a = (0.31 J/g K) / (2.3x10 J/K) = 1.4x10 Avogadro’s
number (NA) : Number of argon atoms in 40 g of argon
22 23
NA = (40)(1.4x10 ) = 5.6 x10
2.1.
8 3 -6 3 33
mass of a typical star = (4/3)(3.1)(7x10 m) (1.4 g/10 m ) = 2×10 g
33 33
mass of protons of a typical star = (2×10 g)(3/4 + 1/8) = 1.8×10 g
33 23 57
number of protons of a typical star = (1.8×10 g)(6×10 /g) = 1×10
number of stellar protons in the universe = (1×1057)(10 23) = 1×1080
2.2.
∆E(2→3) = C(1/4 - 1/9) = 0.1389 C λ(2→3) = 656.3 nm
∆E(1→2) = C(1/1 - 1/4) = 0.75 C λ(1→2) = (656.3)(0.1389/0.75) = 121.5 nm
2.3.
-3 -7 4
T = (2.9×10 m K)/1.215×10 m = 2.4×10 K
2.4.
λ= 3 × 108 m/1.42 × 109 = 0.21 m T = (2.9 × 10-3 m K)/0.21 m = 0.014 K
2.5.
14
N + 4He → ( 17
O ) + 1H
3-1.
12 -1 -32 - 20 -1
kdes = A exp(-Edes /RT) = (1x10 s )(5x10 ) = 5x10 s at T = 20 K
19 11 19
surface residence time, τ
residence = 1 / kdes = 2x10 s = 6x10 yr = 2x10 s
19 11
(full credit for τ
half-life = ln2 / kdes = 1x10 s = 4x10 yr)
3-2.
The distance to be traveled by a molecule: x = πr = 300 nm.
12 -1 -16 -4 -1
kmig = A exp(-Emig /RT) = (1x10 s )(2x10 ) = 2x10 s at T = 20 K average time
3
between migratory jumps, τ= 1 / kmig = 5x10 s
the time needed to move 300 nm = (300 nm/0.3 nm) jumps x (5x103 s/jump) = 5x106 s = 50 days
(Full credit for the calculation using a random-walk model. In this case:
2 9
t = τ(x/d) = 5 x 10 s = 160 yr. The answer is still (b).)
(a) (b) (c) (d) (e)
3-3.
- 112 -49
k(20 K) / k(300 K) = exp[(E/R) (1/T1 - 1/T2 )] = e = ~ 10 for the given reaction
-49 -42
The rate of formaldehyde production at 20 K = ~ 10 molecule/site/s = ~ 10 molecule/site/ yr
10
(The reaction will not occur at all during the age of the universe (1x10 yr))
-42
rate = 10 molecules/site/yr
3-4. circle one
(a) (b) (c) (a, b) (a, c) (b, c) (a, b, c)
4.1
H P
Number of atoms 11.3 / 1
Theoretical wt % 3.43
4-2.
H
H H O
N O H N N
N N H N
N N H N
N N
N N N
O O
N H
H
guanine cytosine adenine thymine
4.3 Full marks for three of the following structures

O
H H O
N
H N
N H O N O H N N N H O
N H N
N N N H N N
H N O H N
N H N
N N N N N
N H
O O N H O
O
H
cytosine thymine guanine adenine thymine thymine

cytosine cytosine
O
O
H N
N H N H O
N N N
O H
N N
N
N N O H N
N O H N
N H
N H N
N O O
N H
H
guanine thymine cytosine adenine thymine thymine
H
N H N H
N
N O N H N
N N
H N
N
N N N
H N H N N
O N
H N
N
H N
H
guanine guanine adenine adenine
4-4.
NH2 O O NH2
N N N NH NH N
N N N N NH2 N O N O
H H H H
adenine guanine Uracil cytosine
HCN ( 5 ) ( 5 ) ( 4 )( 4 )
H2 O ( 0 ) ( 1 ) ( 2 ) ( 1 )
5-1.
+ -
1st ionization is complete: H2SO 4 → H + HSO4 [H2 SO4 ] = 0
+ 2- - -2
2nd ionization: [H ][SO4 ]/[HSO4 ] = K2 = 1.2 x 10 (1)
- 2- -7
Mass balance: [H2SO 4] + [HSO 4 ] + [SO4 ] = 1.0 x 10 (2)
+ - 2- -
Charge balance: [H ] = [HSO4 ] + 2[SO4 ] + [OH ] (3)
+ -7
Degree of ionization is increased upon dilution. [H2SO 4] = 0 Assume [H ]H2SO4 = 2 x 10
2- - 4 -
From (1), [SO4 ]/[HSO4 ] = 6 x 10 (2nd ionization is almost complete) [HSO4 ] = 0
2- -7
From (2), [SO4 ] = 1.0 x 10
+ -7 - 14 + + -7
From (3), [H ] = (2 x 10 ) + 10 /[H ] [H ] = 2.4 x 10
- -14 -7 -8
[OH ] = 10 /(2.4 x 10 ) = 4.1 x 10
- + 2- -7 -7 -2 -12
From (1), [HSO4 ] = [H ][SO4 ]/K2 = (2.4 x 10 )(1.0 x 10 )/(1.2 x 10 ) = 2.0 x 10
2.4 x 10 (2.0 x 10 ) + 2(1.0 x 10 ) + (4.1 x 10 )

-7 -12 -7 -8
Check charge balance:
+ 1.0 x 10 1.0 x 10
-12 -7 -7
Check mass balance: 0 + 2.0 x 10
Species Concentration
- - 12
HSO4 2.0 x 10
2- -7
SO4 1.0 x 10
+ -7
H 2.4 x 10
- -8
OH 4.1 x 10
5-2.
mmol H3 PO4 = 0.85 3.48 mL 1.69g/mL 1 mol/98.00 g 1000 = 51.0 [5 marks]
The desired pH is above pK 2.
- 2-
A 1:1 mixture of H2PO 4 and HPO4 would have pH = pK2 = 7.20.
2- -
If the pH is to be 7.40, there must be more HPO4 than H 2PO 4 .
- -
We need to add NaOH to convert H3 PO4 to H2 PO4 and to convert to the right amount of H2 PO4 to
2-
HPO4 .
- -
H3PO 4 + OH → H2PO 4 + H2 O
- - 2-
H2PO 4 + OH → HPO4 + H2 O
-
The volume of 0.80 NaOH needed to react with to to convert H3 PO4 to H2 PO4 is:
51.0 mmol / 0.80M = 63.75 mL
To get pH of 7.40 we need:
- - 2-
H2 PO4 + OH → HPO4
Initial mmol 51.0 x 0
Final mmol 51.0-x 0 x
2- -
pH = pK 2 + log [HPO4 ] / [H2 PO4 ] 7.40 = 7.20 + log {x / (51.0-x)}; x = 31.27 mmol
The volume of NaOH needed to convert 31.27 mmol is : 31.27 mmol / 0.80 M = 39.09 mL
The total volume of NaOH = 63.75 + 39.09 = 102.84 mL , 103 mL
5-3.
- - (pH-pKa)
pK = 3.52 pH = pK a + log ([A ]/[HA]) [A ]/[HA] = 10
- (7.40-3.52)
In blood, pH =7.40, [A ]/[HA] = 10 = 7586 Total ASA = 7586 +1 = 7587
- (2.00-3.52) -2 -2
In stomach, pH = 2.00, [A ]/[HA] = 10 = 3.02x10 Total ASA = 1+ 3.02x10 = 1.03
Ratio of total aspirin in blood to that in stomach = 7587/1.03 = 7400
6-1.
- - - -
4 H2 O + 4 e → 2 H2 (g) + 4 OH (or 2 H2 O + 2 e → H2(g) + 2 OH )
6-2.
+ - + -
2 H2 O → O2 + 4 H + 4 e (or H2 O → 1/2 O2 + 2 H + 2 e )
6-3.
2+ -
Cu → Cu + 2e
6-4.
Reduction of sodium ion seldom takes place.
It has a highly negative reduction potential of –2.710 V.
Reduction potential for water to hydrogen is negative (water is very stable).
But, it is not as negative as that for sodium ion. It is –0.830 V.
Reduction of both copper ion and oxygen takes place readily and the reduction potentials for both are
positive.
In the present system, the reverse reaction (oxidation) takes place at the positive terminal. Copper is
oxidized before water.
Reduction potential for hydrogen ion is defined as 0.000 V
6-5.
- -10
pOH = 14.00 – 4.84 = 9.16 [OH ] = 6.92 x 10
2+ - 2 -10 -20
Ksp = [Cu ][OH ] = 0.100 x (6.92 x 10 ) = 4.79 x 10
6-6.
o 2+ 2+
E =E Cu2+/Cu + (0.0592/2) log [Cu ] = +0.340 + (0.0592/2) log [Cu ]
- 2 - 2
= +0.340 + (0.0592/2) log (K sp / [OH ] ) = +0.340 + (0.0592/2) log (Ksp) - (0.0592/2) log [OH ]
-
= +0.340 + (0.0592/2) log (K sp) - 0.0592 log [OH ],
- - -
By definition, the standard potential for Cu(OH)2 (s) + 2e → Cu(s) + 2OH is the potential where [OH ]
= 1.00.
o -20
E =E Cu(OH)2/Cu = +0.340 + (0.0592/2) log (Ksp) = +0.340 + (0.0592/2) log (4.79 x 10 )
= +0.340 - 0.572 = -0.232 V
One may solve this problem as following.
- - o o
Eqn 1: Cu(OH)2 (s) + 2e → Cu + 2OH E+ = E Cu(OH)2/Cu = ?
2+ - o
Eqn 2: Cu(OH)2 (s) → Cu + 2OH E = (0.05916/n) logKsp
-20
= (0.05916/2) log(4.79×10 ) = -0.5715 V
2+ -
Eqn 1 – Eqn 2 : Cu + 2e → Cu
o o o o o o o
E- = E+ - E = E Cu2+/Cu = 0.34 V Therefore, E+ = E- + E = + 0.34 + (-0.5715) = -0.232 V
6-7.
Below pH = 4.84, there is no effect of Cu(OH)2 because of no precipitation.
2+
Therefore, E = ECu2+/Cu = +0.340 + (0.0592/2) log [Cu ] = +0.340 + (0.0592/2) log 0.100
= +0.340 – 0.0296 = +0.310 V
6-8.
1.00 g graphite = 0.0833 mol carbon
6 mol carbon to 1 mol lithium; 1 g graphite can hold 0.0139 mol lithium
To insert 1 mol lithium, 96487 coulombs are needed.
Therefore, 1 g graphite can charge 96487 × 0.0139 = 1340 coulombs
1340 coulombs / g = 1340 A sec / g = 1340 x 1000 mA × (1 / 3600) h = 372 mA h / g
7-1.
6 5
n/V = P/RT = (80 x 10 / 1.013 x 10 atm)/[(0.082 atm L/mol/K)(298K)] = 32 mol/L
3
density = mass/volume = d = 32 x 2 g/L = 64 kg/m
7-2.
H2(g) + 1/2 O2 (g) → H2 O(l); Hrexn- 1 = Hf[H2O(l)] = -286 kJ/mol = -143 kJ/g
C(s) + O2(g) → CO2(g); Hrexn- 2 = Hf[CO2 (g)] = -394 kJ/mol = -33 kJ/g
(-Hrexn-1 ) / (-Hrexn-2 ) = 4.3 or (-Hrexn-2 ) / (-Hrexn- 1) = 0.23
7-3.
H2(g) + 1/2 O2 (g) → H2 O(l)
Hc = -286 kJ/mol = -143 kJ/g = -143 x 10 kJ/kg
3
ΔG = ΔH – TΔS
ΔS c = 70 – 131 – 205/2 = -163.5 J/K/mol
5
ΔGc = -286 kJ/mol + 298K x 163.5 J/K/mol = -237 kJ/mol = -1.2 x 10 kJ/kg
W max = ΔGc 1 kg = - 1.2 x 10 kJ
5
(a) electric motor
(b) heat engine W max = efficiency x Hc
3 4
= (1 – 298/573) x (-143 x 10 kJ) = -6.9 x 10 kJ
3
119 x 10 kJ = 1 W x t(sec)
8 4 3
t = 1.2 x 10 sec = 3.3 x 10 hr = 1.4 x 10 days = 46 month = 3.8 yr
ΔG = -nFE n = # of electrons involved in the reaction
F = 96.5 kC/mol H2 (g) + 1/2 O2(g) → H2 O(l) n=2
E = - ΔG/nF = 237 k J/mol / 2 / 96.5 kC/mol = 1.23 V I = W/E = 0.81 A
8-1-1. ① C ② C ③ CO
8-1-2.
③ Fe 2O3 (s) + 3CO(g) → 2Fe(s) + 3CO2 (g)
◦ ◦
① C(s) + O2 (g) → CO2(g) ΔH① = -393.51 kJ = ΔHf (CO2 (g))
◦
② CO2 (g) + C(s) → 2CO(g) ΔH② = 172.46 kJ
From ① and ②,
◦ ◦
ΔHf (CO(g)) = (1/2){172.46 + (-393.51)} = -110.525 kJ ΔHf (Fe2 O3) = -824.2 kJ
◦ ◦ ◦ ◦
ΔH③ = 3ⅹ ΔHf (CO2 (g)) - ΔHf (Fe2 O3) - 3ⅹΔHf (CO(g))
= 3ⅹ(-393.51) – (-824.2) - 3ⅹ(-110.525) = -24.8 kJ
ΔS ③°=2ⅹ27.28+3ⅹ213.74-87.4-3ⅹ197.674=15.36 J/K
ΔG③°=ΔH°-TΔS°=-24.8kJ-15.36J/Kⅹ1kJ/1000Jⅹ1473.15K=-47.43 kJ
(-ΔG°/RT) (47430J/(8.314J/Kⅹ1473.15K))
K=e =e = 48
8-2-1.
One AB2 O4 unit has available 4 (= 1 + (1/4)ⅹ12) octahedral sites
8-2-2.
Since one face-centered cube in AB2 O4 represents one Fe3 O4 unit in this case, it has 8 available
2+
tetrahedral sites. In one Fe3O4 unit, 1 tetrahedral site should be occupied by either one Fe (normal-
3+
spinel) or one Fe (inverse-spinel). Therefore, in both cases, the calculation gives (1/8) ⅹ100% =
12.5% occupancy in available tetrahedral sites.
8-2-3.
9-1-1.
_ _
+ +
: :
:
:
: :
H3C N N N H3C N N N
9-1-2.
: :
H3C N
9-1-3.
CH2 H
C
:
H3C N
H3C N
CH2 H CH2
9-2-1.
_ _
: :O: N: :
:
: N : + :O: + N
O +
:
N N N
H H :_ H
H
H H
9-2-2.
:
O C CH2
:
9-3-1.
H3C
CH3
H2C CO2 + _
CH3
CH3 O O
H3C
O
B C D E
9-3-2.
O O
OH
+
F
10-1.
N M L
CH2OH
CH2OH CHO
H OH
MeO H MeO H MeO H
H OMe H OMe H OMe
H OH
CH2OH CHO
CH2OH
10-2
Number of possible structures 2
1 2
COOMe H
O H(OH) O H(OH)
H H
H COOMe
H OH
OMe OMe
OMe OH(H) OMe OH(H)
H OH H H
3 4
10-3.
G I
CH2OH
CH2OH
H OMe
H OMe
MeO H
OMe H
H OMe
H OMe
H OH
CH2OH
CH2OH
10-4. Number of the correct structure for C from 10-2: 1
10-5.
B
COOH
O H(OH)
H
H
H
OH
OH OH(H)
H OH
D J
COOMe COOMe
O H(OH) O H(OMe)
H H
H H
H H
OMe OMe
OMe OH(H) OMe OMe(H)
H OMe H OMe
10-6.
HOOC
O
H
COOH H
O
H
O
OH
OH
COOH
O
O
OH
OH
OH
11-1. 3
11-2.
COOH
HOOC
OH
11-3. a, c, d
11-4.
OOC
O
COO
OH
Transition State
11-5.
For the enzyme-catalyzed reaction, Arrehnius equation could be applied.
kcat/kuncat = A exp (-E a, cat / RT) / A exp (-E a, uncat / RT)
= exp [-Ea, cat-uncat / RT]
6
= exp [-Ea, cat-uncat (J/mol) / (2,480 J/mol)] = 10
Therefore, -E a, cat -uncat = 34,300 J/mol
≠ ≠
kuncat, T/kuncat, 298 = exp (- Huncat / RT) / exp (-H uncat / 298R)
≠
= exp [(-H uncat /R)(1/T-1/298)]
ln(kuncat, T /kuncat, 298 ) = 13.8 = [(-86900/8.32)(1/T-1/298)]
o
Therefore, T = 491 K, or 218 C
Practical Problems of the IChO
Chemistry for Life,

Chemistry for better Life
Practical Test
2006. 7. 5
Gyeongsan, Korea
www.ShimiPedia.ir
General Directions
- You have 5 hours to finish the test. Manage your time wisely. You might
spend about one hour for Test 1 (10 points), two hours for Test 2 (15
points), and two hours for Test 3 (15 points).
- Write your name and code number on each page of the Answer Sheet.
- There are 7 pages of Test and 7 pages of Answer Sheet.
- Write answers and calculations within the designated box.
- Use only the pen, ruler, and calculator provided
- An English-language version is available.
- Figures to supplement User’s Instructions for the spectrophotometer, C-
18 cartridge, and pipet filler are provided in a separate sheet.
- Additional samples or supplies will be provided with 1 pt penalty for each
item. (except distilled water)
- You may go to the restroom with permission.
- After finishing the test, place all sheets (Test and Answer Sheets) in the
envelope and seal.
- Remain seated until instructed to leave the room.
- You may take the pencil case, pen, ruler, calculator, and C-18 cartridges
home.
Safety and Disposal
- Wear safety goggles and lab coat.
- No hazardous chemicals are used. All acid, alkali, and dye solutions are
dilute. However, it is better to minimize contact with skin. Wipe off with
wet Kimwipe in case of contact.
- Do not sniff reagents.
- Dispose used chemicals in the plastic bottle labeled “DISPOSABLE”.

Discard used test tubes and broken glasses in the “Waste Basket”.
Apparatus, Chemicals and Supplies
Test-1,2 (white basket) Test-3 (black basket)
spectrophotometer 1 test tube 95

cuvet (1 cm path-length) 1 test tube rack 1
C18 cartridge 4 spatula 2
10 mL syringe 1 1.5 mL graduated pipet 15
1 mL syringe 1 (polyethylene)
pasteur pipet 3 tweezers 1
1 mL pipet 1 pen (for writing on a test 1
5 mL pipet 1 tube)
pipet filler 1 pH test paper 1
10 mL volumetric flask 2 100 mL bottle 3
buret 1
test tube 20 95%
95% ethanol
test tube rack 1 labeled EtOH
50 mL Erlenmeyer flask 1 as CH3CN acetonitrile
100 mL beaker 2 water distilled water
silicone bulb 2
30 mL dropping bottle 6
three-color pen, ruler 1
sqeeze bottle 3 1M HCl 1M HCl solution
Solution E 33% ethanol in 1M
water 1M NaOH solution
labeled NaOH
NaOH less than 5 mM 3% 2,4-
as 2,4-
solution dinitrophenylhydrazine
water distilled water labeled DNPH
solution
100 mL bottle 6 as 20% ceric ammonium
red dye CAN
Solution R nitrate solution
in Solution E 0.5%
blue dye 0.5% KMnO4 solution
Solution B KMnO4
in Solution E
2.5%
mixed dye of B 2.5% FeCl3 solution
Solution MD FeCl3
and R
mixed acids; 10 mL vial 7
labeled acetic acid & Set U-1
Solution MA salcylic acid
as
in water Set U-2
potassium Set U-3
KHP hydrogen labeled
Set U-4
phthalate solution as
Set U-5
phenolphthale
0.05% solution Set U-6
in
Set U-7
How to Use the Spectrophotometer
The spectrophotometer has three compartments, the light source, the detector, and the
cuvet holder. You will find the cover of the cuvet holder open. Leave it open. A cuvet is
placed with the label facing the light source (Fig. A). Use this orientation throughout the
experiment. The spectrophotometer has been stabilized and is ready for use. Follow the
procedure below to take absorbance readings.
a) Fill the cuvet about 3/4-full with Solution E and insert into the cuvet holder. Do not
close the cover of the cuvet holder.
b) Using the mouse of the computer, move the cursor to REFERENCE and click three
times. Then click MEASURE three times and you will get absorbance readings close
to zero at ten wavelengths between 470 and 650 nm at 20 nm intervals (Fig. B).
c) Fill the cuvet with sample solution and click MEASURE three times. You will get
absorbance readings for your sample at the same wavelengths. Record absorbance
values in the Table in the Answer Sheet.
How to Use the C18 Cartridge
a) The cartridge has an inlet and an outlet (Fig. C). The inlet has a larger diameter.
b) To wash or elute, first withdraw the liquid with a proper syringe and connect the
syringe to the inlet of the cartridge. Then push the liquid slowly with a plunger into
the cartridge. (Fig. C & E)
c) To load the sample, attach the 10 mL syringe to the inlet of the cartridge. Using a 1
mL pipet, transfer 1.00 mL aliquot of a sample solution to the syringe (Fig. D). Load
the sample onto the cartridge using the plunger. Make sure that no amount of
sample remains on the syringe. Try to avoid air entering into the cartridge after
sample loading.
d) The cartridge can be reused after washing with Solution E.
e) Separate the syringe from the cartridge when removing the plunger from the syringe.
How to Use the Pipet Filler
Move the dial downward to fill the pipet and upward to release the liquid (see Fig. F).
Practical Test 1
Reverse-phase Chromatography:
Spectrophotometric Analysis
Chromatographic separation followed by spectrophotometric analysis is one of the most

widely practiced analytical techniques in chemical laboratories around the world. For
example, organic compounds in a complex mixture are often analyzed by reverse-phase
liquid chromatography with spectrophotometric detection. In reverse-phase chromatography,
hydrophobic interactions between the stationary phase material (usually octadecyl group)
and the nonpolar moiety of the analyte is utilized. The chromatogram can be simplified and
the compound of interest selectively determined by proper choice of the detector
wavelength. In this part of the Practical Test, spectrophotometric analysis of dyes, with and
without separation, will be performed.
Food Red No. 40 Methyl Violet 2B
1-1. Spectrophotometric Analysis of R and B in a Mixed Solution

a) Measure absorbance of both Solutions R (3.02 x 10-5 M) and B (1.25 x 10 -5 M) (Fig. A &
B). Fill in the Table in the Answer Sheet with your measurements. Draw absorption
spectra for the red dye in red ink and for the blue dye in blue ink (Fig. 1-1).
b) Repeat absorbance measurements for Solution MD. Solution MD is a mixture of Solution

R and B in a certain ratio. Add the spectrum in black ink to Fig. 1-1.
c) Based on the Beer-Lambert law, determine the molar concentration of both dyes in
Solution MD using the data in the Table. Do not determine the fraction of one dye by
subtracting the fraction of another dye from 1.
1-2. Chromatographic Separation Followed by Spectrophotometric Analysis

a) Elute the cartridge with about 10 mL of Solution E using 10 mL syringe (Fig. C).
b) Load 1.00 mL of solution MD onto the cartridge (Fig. D).
c) Using 1 mL syringe, elute with Solution E (Fig. E). Collect the solution eluting through the
outlet in a 10 mL volumetric flask. Repeat until the red compound is completely eluted
and collected.
d) Fill the flask to the 10 mL mark with Solution E and mix. Call this Solution F.
e) Obtain the absorption spectrum of solution F as in Experiment 1-1. Dilution takes place
during elution. Therefore, multiply the measured absorbance by 10 when drawing the
spectrum for Solution F. Draw spectrum with broken line in Fig. 1-1 in red ink.
f) Dilute Solution R as necessary and construct a calibration curve, at a wavelength of your

choice, for analysis of the red dye (R) in Solution F. Draw a calibration curve in the
answer sheet (X-axis, concentration; Y-axis, absorbance, Fig. 1-2). Indicate the
wavelength used. The calibration curve must have three points in addition to the origin.
Mark the position of Solution F on the calibration curve.
g) Report the concentration of R in the original Solution MD.
h) Compare this concentration with the value you obtained in Experiment 1-1 and report the
recovery (amount eluted/amount loaded) associated with chromatography.
Practical Test 2
Reverse-phase Chromatography:
Acid-Base Titration of Acetic Acid and Salicylic Acid
Acetic acid (AA) and salicylic acid (SA) are slightly different in polarity and thus can be
separated on a reverse-phase cartridge using distilled water as eluent. AA is eluted first. The
total amount of AA and SA in a mixed solution will be determined by titration. Then, AA and
SA will be separately determined following chromatographic separation.
2-1. Determination of the Total Amount of AA and SA in a Mixed Acid (MA)

Solution
a) Titrate 10 mL of distilled water with the NaOH (< 5 mM) solution provided. Report blank
acidity in 1 mL of distilled water in terms of the volume of the NaOH solution. Take this
blank acidity into account for all solutions in subsequent data analyses. Show corrections
in the calculation part in the answer sheet.
b) Standardize NaOH solution with 2.00 mL of the standard KHP (potassium hydrogen
phthalate) solution (1.00 x 10-2 M) provided. Repeat and report the concentration of the
NaOH solution. Show how you accounted for the blank acidity .
c) Withdraw 1.00 mL of Solution MA and determine the total acidity. Repeat and report the
total number of moles of AA and SA combined in 1.00 mL of Solution MA.
2-2. Reverse-phase Separation and Titration
a) Elute a new C-18 cartridge with about 10 mL of distilled water using 10 mL syringe.
b) Load 1.00 mL of Solution MA onto the cartridge. Collect the liquid eluting at the outlet in
tube 1 (Fraction 1).
c) Elute with 1 mL of distilled water. Collect the eluent in a test tube (Fraction 2). Repeat until
Fraction 20 is collected. You will have 20 test tubes with about 1 mL liquid in each tube.
d) Titrate acidity in each test tube. Report volume of the NaOH solution consumed and the
amount of acid(s) in each test tube. Make a graph in the answer sheet (Fig. 2-2) showing
the amount of acid(s) in each test tube.
e) Blank acidity and the background (due to leaching out of residual materials from the
column) must be subtracted. In determining the amount of eluted AA, disregard tubes
containing only trace amounts of acids. Tube 2 and 3 contain most AA. Calculate the
total amount of AA eluted by adding the amount of AA in tubes. Similarly calculate the
total amount of SA eluted. Indicate, in Fig. 2-2, which fractions you used to get the
amount of each acid.
f) Calculate the mole percent of AA in solution MA.
Practical Test 3
Qualitative Analysis of Organic Compounds
In this experiment your task is to identify seven solid unknowns from the list of compounds
on page 7 that are common drugs in everyday life and valuable agents in organic chemistry.
To achieve this, perform chemical tests on unknowns according to the following procedures
and analyze your results.
- Unknowns Labeled
SetU-1, SetU-2, SetU-3, SetU-4, SetU-5, SetU-6, SetU-7
Procedure
Helpful Comments
a) The weight of a spatula tip-full of a solid is about 15~20 mg.
b) Wipe spatula cleanly with Kimwipe between uses.
c) After adding any reagent described below to a solution of an unknown sample, mix
the contents thoroughly and observe the resulting mixture carefully.
d) To get full marks, you should perform all the tests and fill out the table.
Test 1: Solubility test

To a test tube, add a spatula tip-full (15~20 mg) of an unknown sample and 1 mL of
CH3CN. Shake the test tube and report the solubility. Repeat the test with 1M HCl,
water, and 1M NaOH.
Test 2: 2,4-DNPH test

Place about 15~20 mg of an unknown sample in a test tube and dissolve with 2 mL of
95% EtOH (For the water soluble unknowns, dissolve about 15~20 mg of an unknown in
1 mL of water). Add five drops of the 2,4-dinitrophenylhydrazine solution in concentrated
sulfuric acid and 95% ethanol (labeled as 2,4-DNPH).
Test 3: CAN test

Mix 3 mL of the cerium(IV) ammonium nitrate solution in dilute HNO 3 (labeled as CAN)
with 3 mL of CH3CN in a test tube. In another test tube add about 15~20 mg of an
unknown sample in 1 mL of the mixed solution. (For the water soluble unknown
samples, dissolve about 15~20 mg of an unknown sample in 1 mL of water first, and
then add 1 mL of CAN.) If there is a color change in the solution, the solution may
contain alcohol, phenol or aldehyde.
Test 4: Baeyer test

In a test tube, dissolve about 15~20 mg of an unknown sample in 2 mL of CH3CN (For
the water soluble unknown samples, dissolve about 15~20 mg of an unknown in 1 mL of
water). To the solution, slowly add five drops of the 0.5% KMnO4 solution, drop by drop
while shaking.
Test 5: pH test
In a test tube, dissolve about 15~20 mg of an unknown sample in 2 mL of 95% EtOH
(For the water soluble unknown samples, dissolve about 15~20 mg of an unknown
sample in 1 mL of water). Measure the pH of the solution with pH paper.
Test 6: Iron(III) chloride test

Take the solution from Test 5 and add five drops of a 2.5% FeCl3 solution.
Results
1. Record your test results in the answer sheet. Write O if soluble and X if insoluble for the
solubility tests. Write (+) for the positive reactions and (–) for the negative reactions for tests
2 ~ 4 and 6. Write a, b and n for acidic, basic or neutral, respectively, for pH test 5.
2. Based on your test results, identify the most plausible structures for the unknown
compounds from the provided list of compounds. Write the compound initial in appropriate
box.
Possible Unknown Compounds
COOH O OH
OH HO
HO HO HO NH 2 HCl
NH 2 OCH3 OCH3 OH
(A) (E) (F) (G)
H
CH 3
O CH3 N
HO
COOH OH HCl
H3 CO
H3 C CH 3
N
(K) (M) (Q)
H CHO OH
N CH 3
O HO OCH 3
HO
OCH 3 O
(T) (V) (W)
About the history of the IChO
About the history of the International Chemistry-Olympiads

The idea of chemistry olympiads was born 1968 during an Czechoslovakian national
olympiad that was attended by observers from Poland and Hungary. These three countries
participated in the first IChO 1968 in Prague. The participating countries of the following
years are shown in the table.
Participating Delegations
(in the alphabetical order of the German names)
(+ = host, + = participant, o = observer)
Country, Year  6 6 7 7 7 7 7 7 7 7 7 8 8 8 8 8 8 8 8 8 8 9 9 9 9 9 9 9 9 9 9 0 0 0 0 0 0 0
 8 9 0 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6
Argentina + + + + ++ + + + + + +
Armenia o o +
Australien o + ++ + + + + + + + + ++ + + + + + +
Austria + + + + ++ + + + + + + + + ++ + + + + + + + + ++ + + + + + +
Azerbaijan o o + + + + + + +
Belarus + + + ++ + + + + + +
Belgium + + + + + + + + + ++ + + + + + + + + ++ + + + + + +
Brasil o o ++ + + + + + +
Bulgaria + + + + + + + + + ++ + + + + + + + + ++ + + + + + + + + ++ + + + + + +
Canada o o + + + ++ + + + + + + + + ++ + + + + + +
China + + ++ + + + + + + + + ++ + + + + +
Chinese Taipei + + + + + + + ++ + + + + + +
Croatia o o + + + + + + +
Cuba + o + + ++ + + + + + + + + + + + + +
Cyprus o + + + + + + + + + ++ + + + + + +
Czech Rep. + + + + + + ++ + + + + + +
Czechoslovakia + + + + + + + + + + ++ + + + + + + + + ++ + +
Denmark + + + + + + + ++ + + + + + + + + ++ + + + + + +
DDR o + + + + + + + + ++ + + + + + + + ++
Egypt o o + + + + +
Estonia + + + + + ++ + + + + + +
Finland o + ++ + + + + + + + + ++ + + + + + + + + ++ + + + + + +
France o + + + + + + + + ++ + + + + + + + + ++ + + + + + +
Germany o + + + + ++ + + + + + + + + ++ + + + + + + + + ++ + + + + + +
Greece + + + + ++ + + + + + + + + ++ + + + + + +
Hungary ++ + + + + + + + + ++ + + + + + + + + ++ + + + + + + + + ++ + + + + + +
Iceland o o + + + + +
India o o ++ + + + + + +
 Year  6 6 7 7 7 7 7 7 7 7 7 8 8 8 8 8 8 8 8 8 8 9 9 9 9 9 9 9 9 9 9 0 0 0 0 0 0 0
Country 8 9 0 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6
Country, Year  6 6 7 7 7 7 7 7 7 7 7 8 8 8 8 8 8 8 8 8 8 9 9 9 9 9 9 9 9 9 9 0 0 0 0 0 0 0
 8 9 0 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6
Indonesia o + + ++ + + + + + +
Iran + + + + + + ++ + + + + + +
Ireland o o + ++ + + + + + +
Israel o o +
Italy + + + + + o o + + ++ + + + + + + + + ++ + + + + + +
Japan o + + + +
Jugoslavia + + + + + + + + + + o
Kazakhstan o o + ++ + + + + + +
Kenia o o
Korea + + + + + + + ++ + + + + + +
Kuwait o o + + + ++ + + + + + ++ + + + + + +
Kyrgyzstan o o + + + + + + + +
Latvia + + + + + + + + ++ + + + + + +
Lithuania + + + + + + + + ++ + + + + + +
Malaysia o o +
Mexico + + + + + + + ++ + + + + + +
Moldova o o
Mongolia o o o +
Netherlands + + + + + + + + + ++ + + + + + + + + ++ + + + + + +
New Zealand + + + + + + + ++ + + + + + +
Norway o + + + + + + + ++ + + + + + + + + ++ + + + + + +
Pakistan o o +
Peru o o + +
Philippines o
Poland ++ + + + + + + + + ++ + + + + + + + + ++ + + + + + + + + ++ + + + + + +
Portugal o o + + + +
Romania + + + + + + + + ++ + + + + + + + + ++ + + + + + + + + ++ + + + + + +
GUS/Russ.Fed. + + + + + + + ++ + + + + + +
Saudi Arabia o o +
Singapore o + + + + + + + + + + ++ + + + + + +
Slovakia + + + + + + ++ + + + + + +
Slovenia + + + + + + + + ++ + + + + + +
Spain o + + + ++ + + + + + +
Sweden + + + + + ++ + + + + + + + + ++ + + + + + + + + ++ + + + + + +
Switzerland o + + ++ + + + + + + + + ++ + + + + + +
Tajikistan o o + + +
Thailand o + + + + + + + + + ++ + + + + + +
 Year  6 6 7 7 7 7 7 7 7 7 7 8 8 8 8 8 8 8 8 8 8 9 9 9 9 9 9 9 9 9 9 0 0 0 0 0 0 0
Country 8 9 0 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6
Country, Year  6 6 7 7 7 7 7 7 7 7 7 8 8 8 8 8 8 8 8 8 8 9 9 9 9 9 9 9 9 9 9 0 0 0 0 0 0 0
 8 9 0 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6
Turkey o + o + + + + + ++ + + + + + +
Turkmenistan o o o + + + +
UdSSR + + + + + + + + + + + + + + + + + + +
Ukraine + + + + + ++ + + + + + +
United
o o + + + + + + ++ + + + + + + + + ++ + + + + + +
Kingdom
United States o o + + + + + ++ + + + + + + + + ++ + + + + + +
Uruguay o o ++ + + + + + +
Venezuela o o + + + + + + ++ + + + + + +
Vietnam + + + ++ + + + + + +
 Year  6 6 7 7 7 7 7 7 7 7 7 8 8 8 8 8 8 8 8 8 8 9 9 9 9 9 9 9 9 9 9 0 0 0 0 0 0 0
Country 8 9 0 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6
Number of 3 4 7 7 7 9 1 1 1 1 1 1 1 1 1 2 2 2 2 2 2 2 3 3 3 4 4 4 4 4 5 5 5 5 5 6 5 6
teams 2 2 2 2 1 3 4 7 8 0 1 2 6 6 6 8 0 3 8 1 2 5 7 7 1 3 4 7 9 1 9 6
Number of teams attending the IChO
70
60
50
Number of teams
40
30
20
10
0
1970 1975 1980 1985 1990 1995 2000 2005 2010
InofficialYear
ranking since 1974
of olympiad
Inofficial ranking since 1974

(set up by adding the points of the teams, up to position 50)
1974 1975 1976 1977 1978 1979 1980 1981 1982 1983 1984 1985 1986 1987 1988
IChO held in RO H DDR CS PL SU A BG S RO D CS NL H FIN
1 SU SU DDR CS SU PL PL H CS RO D SU NL SU RC
. RO H SU SU PL SU D CS D SU CS CS PL RC D
. CS PL H H D RO DDR PL PL D SU D D RO USA
. H BG PL PL DDR CS H BG NL CS H A SU CS PL
5 PL RO A S CS A A A A H A NL A D GB
. DDR DDR RO A H S RO D SU A GB H USA F DDR
. BG S BG D A H BG DDR H F PL DDR H GB N
. YU CS CS DDR RO D CS RO BG DDR USA PL BG PL RO
. S A S RO S BG S SU DDR PL RO USA F H H
10 D* D D BG BG FIN FIN NL S NL DK F RO DDR SU
. YU YU YU TR DDR NL FIN F BG S GB CS NL I
. B B B FIN I S FIN GB NL RO GB USA NL
. B F N N FIN BG S BG BG
. I RO DK F N DDR A CS
15 * hors concours DK FIN BG S CDN S AUS
. YU S N FIN N FIN SGP
. I I I YU DK N F
. YU GR B B DK A
. YU GR FIN I FIN
20 B DK GR GR CDN
. C KWT C DK
. YU B C
. YU S
. CDN B
25 CH CH
. KWT KWT
(List of abbreviations see page 141)
1989 1990 1991 1992 1993 1994 1995 1996 1997 1998 1999 2000
IChO held in DDR F PL USA I N RC RUS CDN AUS T DK
1 DDR RC RC RC RC RC RC IR H SGP USA RC
. D PL RO H TPE GB IR RC D USA ROK RUS
. RC D H PL USA USA RO RUS TR ROK RC USA
. BG USA PL USA I A A A TPE RC IR H
5 SU CS NL A GUS SGP D D IR H RO TPE
. H RO USA GUS H ROK GB USA RUS RA H A
. PL F I D D TPE SK UA ROK RUS TPE SK
. RO A D RO CDN CZ TPE CZ RC AUS UA BY
. CS DDR N F SGP GUS I H SGP D PL VN
10 I H GB I CZ IR CZ RO PL GB AUS TR
. NL GB CS SGP A D RUS GB USA PL VN SGP
. GB I SU CS RO H H TPE UA A D D
. A AUS A AUS P RO AUS BY AUS RO RA ROK
. USA SGP AUS NL NZ DK SGP SGP CDN TPE BY IR
15 S NL DK DK ROK I F RA RO SK T CZ
. F N SGP ROK LV T TR TR A NL F FIN
. N DK CDN GB IR NZ PL F T IR TR T
. AUS T BG CH DK UA USA I EST UA SGP MEX
. CDN FIN F T AUS AUS DK AUS CZ VN IND GB
20 DK CDN S LV NL F RA ROK VN LT GB AUS
. FIN BG T NZ LT PL ROK EST F TR RUS IND
. B C CH S SK NL UA CDN S BY MEX CDN
. C S LV LT F SK LT T BY F A RA
. GR CH LT N C CDN T VN NZ I IRL UA
25 CH B FIN CDN GB LT NL SK LV T NZ PL
. KWT GR C SLO T S CH CH RA FIN I NZ
. KWT GR BG BG N BG NL SLO CZ CDN BG
. CY B TPE B BG S NZ GB CDN LT F
. CY B S FIN NZ DK SK S NL DK
30 SLO FIN FIN EST EST PL LT BG SK NL
. GR SLO LV CDN SLO I N BG B
. CY GR CH MEX MEX DK MEX KZ RO
. MEX MEX MEX N LV NL CH DK KZ
. N SLO SLO N IRL SLO CH LT
35 CH B LV CY N EST CZ CH
. YV CY CY BG MEX CY FIN SLO
. CY GR B S CH LV B EST
. KWT TR GR LT CY DK S S
. YV FIN E E NZ CY YV
40 C YV B FIN GR EST CY
. KWT KWT GR BG KZ LV HR
. C FIN YV E SLO I
. YV GR IRL YV RI
. C B B BR N
45 KWT RI KS E AZ
. KWT YV N IRL
. C RI RI E
. GR LV
. ROU GR
50 C BR
2001 2002 2003 2004 2005 2006 2007 2008 2009 2010 2011 2012
IChO held in IND NL GR D TPE ROK RUS H GB J
1 RC RC RC RC ROK RC
. ROK T IR ROK VN TPE
. USA TPE ROK RUS IR ROK
. RUS ROK T UA RUS RUS
5 IR A BY D AZ VN
. TR UA RUS PL TPE T
. IND USA IND TPE T J
. AUS PL SGP H RA Pl
. TPE IND D TR D IND
10 T D TPE VN IND D
. SGP IR UA IND A SK
. PL H PL IR CZ DK
. RO RUS CDN RO UA SGP
. F CDN CZ LT PL BR
15 SK TR RO CZ AUS CDN
. H AUS KZ USA TR AZ
. VN GB VN SGP H UA
. CZ SGP EST CDN SK USA
. RA E GB AZ USA H
20 BY SK AUS AUS GB CZ
. C BY H KZ RO AUS
. D VN SK GB BY IRL
. GB FIN USA J SGP F
. UA F YV A J IR
25 A LT IND BY RI A
. MEX CZ F SK LV TR
. DK KZ A T BG RI
. CDN LV I RA HR GB
. EST NL TR EST MEX RO
30 RI RO AZ F KZ NL
. HR RA MEX NZ LT HR
. I EST LT SLO F LT
. N HR NL HR EST KZ
. BG BG FIN LV CDN SLO
35 CY NZ HR NL I EST
. KZ I J I DK RA
. B DK DK CH SLO BR
. LT SLO RA FIN FIN TJ
. NZ N GR RI NL LV
40 CH YV LT S IRL MAL
. E MEX E BG GR S
. FIN BR TM KS NZ IRL
. SLO S BR E KS IL
. NL RI BG GR S FIN
45 LV TM CH BR B IS
. BR B NZ TM BR I
. S IRL IS CY CH CY
. YV CH IRL YVA P N
. IRL C CY IRL IS TM
50 GR CY KS IS N CH
List of abbreviations
A Austria KZ Kasakhstan
AUS Australia LV Latvia
AZ Azerbaijan LT Lithuania
B Belgium MAL Malaysia
BG Bulgaria MEX Mexico
BR Brazil MGL Mongolei
BY Belarus N Norway
C Cuba NL Netherlands
CDN Canada NZ New Zealand
CH Switzerland P Portugal
CS Czechoslovacia PE Peru
CY Cyprus Republic PL Polen
CZ Czech Republic RA Argentina
D Germany RI Indonesia
DDR German Democratic Republic RC China
DK Denmark RO Romania
E Spain ROK South Korea
EAK Kenya ROU Uruguay
EST Estonia RUS Russian Federation
ET Egypt S Sweden
F France SGP Singapore
FIN Finland SK Slovakia
GB United Kingdom SLO Slowenia
GR Greece SU Sowjet Union
GUS Commonwealth of Independent States T Thailand
H Hungary TJ Tadschikistan
HR Croatia TM Turkmenistan
I Italy TPE Chinese Taipei
IL Israel TR Turkey
IND India UA Ukraine
IR Iran USA United States of America
IRL Ireland VN Vietnam
IS Iceland WAN Nigeria
J Japan YU Yugoslavia
KS Kyrgistan YV Venezuela
KWT Kuwait

IChO 2006

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38.

To become a member of the German IChO-team you have to be successful in four

Part 1: The problems of the four rounds

Contact adresses .................................................................. 4

Part 2: The solutions to the problems of the four rounds

First round .................................................................. 46

Tables on the history of the IchO ............................................................... 135

Wolfgang Hampe tel: +431-79433

Association to promote the IChO

The problem set of the four rounds

First Round (homework)

Problem 1-2 Production of Aluminium

You cannot imagine modern everyday life without aluminium.

a) Name at least three advantages of aluminium as a substance compared to iron. Give

To produce aluminium aluminium oxide (corundum) has to be seperated from bauxite.

c) Give the formula of corundum and the reason why it is employed.

Al(l) O2(g) Al2O3(s)

Using the free enthalpie of the process 2 Al 2O3  4 Al + 3 O 2 you approximately

e) Calculate the theoretical voltage of the fused salt electrolysis.

For the given chemical reactions the temperature dependence of ΔG is known:

Problem 1-3 An Experiment to Do by Yourself

10 mL of a solution of Fe 3+ and 30 mL of a solution of SCN- are mixed. Both solutions have

10 mL of the red solution are filled up with water to 100 mL.

To one part of this diluted solution solid iron(III) chloride is added.

To another part of the diluted solution ammonium thiocyanate is added.

a) Interpret the four observations.

b) Why do the explanations of the observations 3 and 4 support the explanation of

Problem 1-4 Substitution with Obstacles

Problem 1-5 Aromatic Heterocyclic Compounds

Oxazole is an aromatic heterocyclic compound with a five membered ring:

b) Compare the alkalinity (acceptance of protons) between oxazole and pyrrole.

Which of the N atoms in oxazole or in pyrrole is more alkalic?

Second Round (homework)

Problem 2-1: Chromium and Chromate

1. The redox couple chromium(III)/dichromate (E°(Cr3+|Cr2O 72–) = +1.380 V) is often used in

2. Magnetic measurements are an important method to determine the oxidation states of

f) Plot the magnetic susceptibility as a function of temperature.

The relative magnetic moment in terms of the Bohr magneton is

R = 8.314 · 10 7 erg · K–1 · mol–1

Problem 2-2 Spinels

Fig.1 Cubic face-centred close packing

In spinels M2+ ions occupy tetrahedral , M’ 3+ ions octahedral holes.

Aufgabe 2-3 Physical Chemistry

Data of ΔH 0f and S 0f under standard conditions (p = 1 .0000∙

Problem 2-4: Structure and Reaction of an Organic Compound

The following image is the 1H-NMR-spectrum of compound D:

The exact structure of compound D is to be determined by classical synthesis.

Next B reacts with cyclopentadiene in the presence of sodium methoxide. On basic

The 1H-NMR- spectrum shows doublets and triplets.

Compound D is able to perform a lot of different reactions, for example:

Problems for Round 3

Useful formulas and data

G = H - T·S G = - E·z·F G = - R·T·ln Kth

rate laws 0. order c = co - k·t

Arrhenius equation: k = A ∙e-Ea/(R∙T)

Bragg’s equation: n·= 2a·sin

Law of Lambert and Beer: E=

Henry’s law for dissolving gases in water (A(g) A(aq))

Raoul’s law for perfect solutions (mixtures):