Inorganic 2 Labwork Manual
Inorganic 2 Labwork Manual
Inorganic 2 Labwork Manual
Laboratory manual
Of
PRACTICAL INORGANIC II
CHEMISTRY
HCP
CCP
By:
M. Pranjoto Utomo
PREFACE
M. Pranjoto Utomo
LABORATORY PRECAUTIONS
A. Inside the Laboratory
1.
Do not eat, drink beverages or chew gum in the laboratory. Do not use laboratory
glassware as containers for food or beverages
2.
3.
4.
5.
B. Handling Chemicals
1.
All chemicals in the laboratory are to be considered dangerous. Do not touch, taste
or smell any chemical unless specifically instructed to do so
2.
Check the label on chemical bottles twice before removing any of the contents.
3.
4.
Acid must be handled with extreme care. ALWAYS ADD ACID SLOWLY TO
WATER.
5.
Handle flammable hazardous liquids over a pan to contain spills. Never dispense
flammable liquids anywhere near an open flame or source of heat.
2.
When removing an electrical plug from its socket, grasp the plug, not the electrical
cord. Keep your hands dry when working with electricity.
3.
4.
D. Heating Substances
1.
2.
Never leave a lit burner unattended. Never leave anything that is being heated or is
visibly reacting unattended.
3.
LABORATORY EQUIPMENTS
Gas collecting
tube
Measuring pipette
Stirring rod
Thermometer
Glass-stoppered
burette
Volumetric flask
funnel
Graduated
cylinder
Test tube
Spot plate
s-shaped test
tube rack
Forceps
Dropper pipette
spatula
Triangular file
Erlenmeyer flask
Beaker
Gas-collecting
bottle
Pinch clamp
Watch glass
Evaporating dish
Rubber stoppers
Pneumatic
trough
Safety goggles
Crucible tongs
Clay triangle
Wire gauze
Utility clamp
Iron ring
Burette clamp
Wing tip
Burner
Ring stand
CONTENTS
Page
PREFACE
............................................................................................
...............................................
i
ii
iii
LABORATORY EQUIPMENTS
......................................................
iv
CONTENTS ............................................................................................
10
12
15
18
....
20
23
24
26
28
30
32
REFERENCES
34
7
EXPERIMENT 1
CLOSE PACKING GEOMETRY IN SOLID
Purpose
The main purpose of this activity is to study close packing geometry i.e. to illustrate
the structure of ionic solid.
Introduction
Ionic solid can be viewed as a close packing of metal atoms. The arrangement of
atoms, molecules, or ions in a regularly and repeatedly pattern is known as a lattice space.
The arrangements nature is determined by three factors:
1) relative shape and size of atom, molecule or ion
2) nature and relative strength of chemical bonding
3) thermal energy of the system
Two applied models of the arrangement are hole filling model (balls represent atoms
or ions that are packed close one to others) and ball and stick expanding model, where the
balls are separated by the stick connectors. In ball and stick crystal structure model, stick
connectors represent covalent bonds (such as bonds in diamond) or ionic bonds (such as
bonds in NaCl). On the other hand, stick connector illustrate crystal lattice of a solid.
In this activity, you have to arrange the balls, observe and fill the observation data on
your work sheet to understand close packing geometry in solid.
Materials
ping-pong balls (at least contain of two colors)
marbles
buckshot
A
A
(b)
(a)
(c)
(d)
10
Answer:
Is the coordination number of this pattern still the same with the previous one?
Answer: (Yes / No)*
(a)
(b)
(c)
(d)
(e)
11
Determine the maximum balls that touch the centered-ball in the fcc pattern.
Answer: balls, consists of .. balls in the same layer and
.. balls in above and under those layer. This numeric called as
coordination number.
Analogically, arrange the fcc pattern with three layers of 7-ballshexagon layer
(Figure 2e).
Determine the coordination number of this pattern.
Answer:
Is the coordination number of this pattern still the same with the previous one?
Answer: (Yes / No)*
Hold this fcc packing pattern and direct it to the light source. Pay attention to the
route of the light on the fcc packing. What do you get?
Answer: .
Alternatively, put the fcc packing on the desk and put the wire through the fcc
packing via the holes among the balls. Pay attention to the route of the wire in the hole of
fcc packing. What do you get?
Answer: .
The terminology of closest packing of face centered cubic (fcc) in the previous
activity is often confusing, because the fcc geometry is invisible. To overcome that
problem, see Figure 3. The structure is represented by 14 balls consisted of 8 balls at the
corner of cubic and 6 balls at the center of cubic face. Investigate the 14 balls carefully.
12
Radius ratio
r
= ..............................
r+
H
Figure 1.4.
B
F
D
A
C
B
13
Imagine, ball M that fit the tetrahedron hole touch 4 ball of ABCD. Determine the
radius ratio of ping-pong ball (A=B=C=D) with hole ball (M).
Hint: 3 = 1.732 and 2 = 1.414
i) State the ball radius in the term of r+ or r- and the length in a.
ii) State the face diagonal, CD, and body diagonal, ED, (and then MD) in the term of r+ or
r- and a.
iii) Obtain the value of r+ and r- in the term of a, then calculate its ratio
Answer: ..
..
Therefore the radius ratio:
r+
r
= ..................., OR
r
=
r+
.................
r+
= .., or
r
r
= ..............................
r+
14
= ..................., OR
r
=
r+
.................
15
r+
= .., or
r
r
= ..............................
r+
= ..................., OR
r
=
r+
.................
16
(a)
(b)
(c)
Figure 1.5 Models of hexagon layer packing (a,b), and layer A, B closest packing (c)
Arrange a 12-balls-hexagon layer, (Figure 5a) and there are 12 holes. Arrange another
12-balls-hexagon layer in opposite direction (Figure 5b). Put layer (b) on layer (a)
according to A, B pattern. Balls of layer (b) fit the holes of layer (a). Identify or mark the
type and the amount of formed holes between two layers (for example, red for tetrahedral
holes and blue for octahedral holes). Identify the tetrahedral and octahedral holes by
directing
the
two
layers
(Figure
TETRAHEDRAL/OCTAHEDRAL*)
5c)
to
holes,
light
source.
but
Light
cannot
can
penetrate
penetrate
17
EXPERIMENT 2
INORGANIC QUALITATIVE REACTION
Purpose
To study the reaction of metal ions with hydroxide ion and ammonia
Introduction
Metal cations react characteristically with base in the term of form and nature of
product solubility, especially in water. Adding of (strong) base excessively often give more
influences, according to the characteristic of cation in the term of amphoterism. Besides,
transition cations often form complex compounds with ammonia. By this, identification of
cation with strong base (NaOH) and weak base (NH3) is an interesting activity in inorganic
qualitative reaction.
Materials
-
2 M NaOH solution
2 M NH3 solution
Dropper bottle
Centrifuge
Dropper pipette
Procedure
1. Put nitrate cations (as mentioned above), 0.5M NaOH solution, 2 M NH3 solution and
NaOH 0.5 M solution in labeled-dropper bottle. Those solutions used as mother liquid.
2. Add drop to drop (about 5 drops) 0.5 NaOH M solution into 0.1M Mg(NO3)2 solution.
Volume of 0.5 M NaOH solution must not exceed of 1 mL.
3. Divide the resulted precipitation into 2 parts, and put each to semi micro test tube.
Centrifuge for 1 minute. Take the supernatant with dropper pipette
a. In tube 1, add 2 M NaOH solution (volume must not exceed of 1 mL) into the
resulted precipitate.
18
b. In tube 2, add 2 M NH3 (solution volume must not exceed of 1 mL) into the resulted
precipitate.
4. Repeat step 2 to 3 for the 0.1 M solution of Ba2+, Al3+, Cr3+, Fe3+, Mn2+, Pb2+, Cu2+,
Ni2+, Ag+ dan Zn2+. Record the observation in the table on the worksheet
5. Identify which cations that form precipitation on the adding of NaOH
6. Identify which cations that form precipitation on the adding of NaOH
a. Dissolves in the adding of excess NaOH
b. Dissolves in the adding of excess ammonia
7. a. Add 0.1 M Al(NO3)3 solution slowly into 1 mL of 2 M NaOH. Record your
observation.
b. Add 0.1 M Fe(NO3)3 solution slowly into 1 mL of 2 M NaOH. Record your
observation.
c. Repeat the activities of (a) and (b) in opposite steps of reactant adding. Record your
observation and explain.
19
EXPERIMENT 3
OXIDATION-REDUCTION REACTION (1)
Purpose
To study oxidation-reduction reaction on several compounds
Introduction
Oxidation is the releasing of electron and reduction is the capturing of electron.
Oxidation and reduction reaction always a pair reaction, that transfer electron occurred.
Oxidizing agent is a species that cause other species oxidized and it self reduced. Reducing
agent is a species that cause other species reduced and it self oxidized.
In this experiment, several general oxidation-reduction reactions studied.
Table 3.1 Several Oxidizing and Reducing Agents
Oxidized
form
MnO4purple
Cr2O72orange
I2
brown
Reduced
form
Mn2+
uncolored
Cr3+
green
Iuncolored
Fe3+
brown
Fe2+
green
Sn4+
Sn2+
SO42-
SO32-
20
*) Generally, sulfite (SO32-) ion is contaminated with sulfate because sulfite easily
oxidized by dissolved oxygen.
Several compounds oxidized and reduced on a reaction. The aims of this activity are
to study oxidation-reduction reaction on several compounds and to test (special test) on it as
seen on Table 2.1.
Each activity is conducted by using two reaction tubes. First tube for test tube,
labeled as T and second one for blank solution tube, labeled as B. Blank solution is a
solution contains all reagents (solvents) except compound that will be tested or studied. Use
water or aquadest to replace the tested compound (in same volume).
Example:
Contents of tube T
Contents of tube B
2+
5 drops of aquadest
The purpose of the blank solution making is to know the condition before and after
reaction. Do the test to both tube T and tube B in order to know every change in the
reaction clearly. In some cases, two blank solutions are needed. First blank solution for
solvent one, and second solution for the other.
Materials
-
Test tube
H2O2 (3%)
H2SO4 (5 M),
(SnCl2) (0.1 M)
KSCN (0.05M)
Dropper pipette
HCl (5 M)
KI (0.1 M)
MnO4 (0.02 M)
H2C2O4 (0.1 M)
K2Cr2O7 (0.02 M)
Procedure
Do the experiments according to the procedure on Table 2.2 in worksheet and refer to Table
2.1.
1. Preparation of fresh solution of Fe2+
21
22
EXPERIMENT 4
OXIDATION-REDUCTION REACTION (2)
THE INFLUENCES OF ACID AND BASE TO METALS
Purpose
To study the influences of acid and base to metals
Introduction
Acid
Acid is species that can donate proton (proton donor). Strong acid donate its entire
proton. Mineral acids such as HCl, HNO3 dan H3PO4 are strong acids. Acid can act as
oxidizing agent. H+ is oxidizing agent (and reduced to H2). Table 4.1 shows the influences
of several acids to metals.
Metal
Metal tends to form cation (positive ion) whether in solution or compound. Solid
Mn+ (aq)
ne
The released electron is captured by oxidizing agent (H+, NO3-, SO42-) and gas
released. The series of metals listed in Table 4.1 known as activity series. Left (above)
series elements will reduce right (below) elements. Therefore, potassium (K) is the
strongest reducer that can replace all right (below) metals in activity series, according to
the reaction:
n K (s) + Mn+ (aq)
n K+ (aq) + M (s)
Vice versa, all left (above) metal of hydrogen, can replace acid (for example replace
with H+) and all right (below) metals of hydrogen will react with oxidizing acids.
Alkali
Alkali refers to strong base with the formula of M(OH)n, where M is alkali metals
(such as Na, K) or alkaline earth metals (such as Ca, Mg) and the value of n is 1 (for alkali)
or 2 (for alkaline earth). Several metals react with alkali solution. The alkali reaction shows
the semi metal nature of the elements. Semi metal nature is a combination of metal and
non-metal nature. In some cases, metal oxide found react with acid and base. Those metal
23
oxides called as amphoteric oxides. Elements that have amphoteric oxides are also able to
react with alkali and acid to produce H2 gas.
Zinc also reacts with acid and base in the same way, but slow and relatively difficult
to observe the occurrence of H2 gas. To prove that zinc has already dissolved, add sulfide
ion to form white precipitate of zinc sulfide.
Table 4.1 The Influence of Acids to Metals
Acid replacement
Metals
K
Na
Ba
Sr
Ca
Mg1)
Al2)
Zn
Cd
Fe
Co
Ni
Sn
Pb
H
Cu3)
Hg
Ag
Pt
Au
Notes:
Oxidizing acids
HCl dilute /
concentrated
(up to 10 M)
H2SO4
dilute
H2SO4
concentrated
( 18 M)
Dissolve to
form
chloride
with lower
oxidation
state and
hydrogen.
Dissolve to
form sulfate
with lower
oxidation
state and
hydrogen.
Dissolve to
form sulfate
with higher
oxidation
state and
sulfur
dioxide
(SO2)
Dissolve to
form nitrate
with lower
oxidation
state and
nitrogen(II)
oxide (NO)
1)
2)
3)
Dissolve to
form nitrate
with higher
oxidation
state and
nitrogen(IV)
oxide (NO2)
2)
No
influence
No
influence
No
influence
No
influence
HNO3 dilute
HNO3
concentrated
( 15 M)
No
influence
24
Materials
-
Test tube
NaOH (2 M)
Iron nail
HNO3 (5 M)
Dropper pipette
Na2S solution
HCl (5 M)
Procedure
1. Prepare small pieces of Zn, Fe, Cu, Al and Pb metals. Clean those metals by using steel
fiber (sandpaper) and place the samples to test tube rack separately.
2. Add 3 mL of 5 M HCl solution to test tube and record the resulted-observation in Table
4.2 in worksheet. Write the reaction equation.
3. If the reaction does not occur, heat the test tube gently and record the resultedobservation.
4. Repeat steps 2 to 3 for other metals.
5. Replace HCl 5 M with 5 M HNO3 solution, and repeat step 1 to 4. Record the resultedobservation in Table 4.2. Write the reaction equation.
6. Replace 5 M HCl with 5 M NaOH solution, and repeat step 1 to 4. If there is no
resulted-observation after heating, pour the solution to another test tube. Record the
resulted-observation in Table 4.3. Write the reaction equation.
7. Add 2 mL of Na2S solution into the test tube. Record the resulted-observation in Table
4.3. Write the reaction equation.
Attention.
1. Acid and alkali are corrosive substances. Use goggles during the experiment.
2. If the solution spilled out to clothes or skin, wash it with water immediately.
3. Poisonous gas may be resulted during the experiment. Do the experiment separately and
use reagents in small amount to avoid or to minimize the produced-poisonous gas. If
excess reagents are used, move rack and test tube to the fume hood.
4. Clean the residue with flowing water. Take the metal residue from washing vessel and
throw to rubbish bin.
5. Sulfide solution is dangerous and poisonous compound. Store the solution in the fume
hood. Throw residual solution into the washing vessel in fume hood.
25
EXPERIMENT 5
ELECTROCHEMISTRY CELL AND ELECTRODE POTENTIAL
Purpose
To study electrode potential of several metals in electrochemistry cell
Introduction
Electrode potential of a metal illustrates the reduction-oxidation tendency of
particular metal relatively to standard electrode, usually H2 system (100 kPa)H+ (1 M)
where the value of E0 = 0.00 V. The measurement of electrode potential carried out simpler
by using standard electrode Cu2+ (1 M) Cu. Of course, converting relative to hydrogen
electrode, the value of standard electrode of Cu2+ Cu (E0 = 0.34 V) must be subtracted.
Standard Electrode of Cu2+ (1M) | Cu and salt bridge
Standard electrode contains narrow glass
tube and hollowed-bottom.
The mixture
Copper wire
Glass
2+
1 M Cu (aq)
Gel + NaNO3
| Cu
2+
immersed in another half-cell cation standard solution, such as Zn | Zn and both terminal
(Cu and Zn) are connected to Voltmeter, electromotive force cell value is obtained. Gel
electrolyte is used to keep charge balance during redox process occurred and gel for prevent
the mixing of ions from the two half-cell areas.
26
Materials
-
Half cell system of Fe2+ | Fe, Mg2+ | Mg, Zn2+ | Zn, Sn2+ | Sn, Pb2+ | Pb, Al3+ | Al
Voltmeter
Procedure
1. Immerse the standard electrode into the solution of half-cell system.
2. Connect each terminal with voltmeter wire; turn the voltmeter button to DC position,
read, and record the value of emf.
3. Lift the standard electrode; wash it with flowing water on glass part, use again for other
half-cell systems.
27
EXPERIMENT 6
CORROSION OF METALS (1)
Purpose
To study the nature of corrosion of several metals in gel medium
Introduction
Spontaneously redox reaction in electrochemistry cell is the sum of two half reaction
cell with positive value of total electromotive force cell, emf. The level of corrosion of
metal is studied by comparing oxidation level relative to O2 in water. In base condition,
reduction of oxygen in water yield to OH- ion, which forms pink-red color with
phenolphthalein (pp) indicator.
ferricyanide ion. If such redox reactions take place in gel medium, the resulted-color
localized in oxidation or reduction area. Due to the slow spreading of ions, it is possible to
identify anode and cathode side. The active site of iron stick (such as iron nail), found at the
end of nail. The electrons flow trough the stick and then captured by oxygen. Therefore,
oxidation occurred at the end of nail, and reduction at the center.
Iron
nail
Tin
Zink
Aluminum
Copper
28
Materials
-
Test tube
K3[Fe(CN)6] solution *)
Gel
Phenolphthalein (pp)
Iron nail
Zink sheet
Aluminum sheet
Tin sheet
Copper sheet
Procedure
A. Seaweed gel making
1. Boil 80 mL of aquadest in beaker glass 250 mL.
2. Pour 0.5 g seaweed into aquadest and stir it until the gel dissolved.
3. Add 5 g of NaCl into the solution and stir continuously
4.
29
9. Place those pairs of metals in the test tube 2 5. Pour gel indicator (that has made)
gently into test tube 1 5. Attention: there must no bubble.
10. Place the test tubes on a shelf tube. After a while, observe the color changing around
gel. According to the observation, color the area around nail and metal sheet on Figure
6.1
Note:
If the color changing unobserved, move the test tubes to beaker glass and observe it next
day.
30
EXPERIMENT 7
CORROSION OF METALS (2)
Purpose
To study the corrosion character of metals (iron and copper)
Introduction
The amount of electron transferred during corrosion process measured by using
multimeter. The function of electrodes (anode species and cathode species) confirmed by
knowing the direction of electron flowing or potential gap. Sodium chloride acts as
electrolyte to keep ions mobility.
Materials
-
Iron sheet 8 cm x 2 cm
Copper sheet 8 cm x 2 cm
Phenolphthalein (pp)
Sandpaper
3% NaCl solution
Multimeter or milliammeter
Acetone
Procedure
1. Clean the iron and copper sheets with sandpaper and acetone soaked-cotton to clean the
fat.
2. Mix the solutions of 40 mL of 3 % NaCl solution and 20 mL of 0.1 M K3[Fe(CN)6
solution in beaker glass 250 mL to make feroxyl indicator. Add phenolphthalein
indicator gently into the mixture and stir it. In this experiment, feroxyl indicator
produces blue color with Fe2+ ion and pp produce pink color with OH- ion.
3. Place an iron sheet and a cooper sheet into white paper based-beaker glass 250 mL. By
using alligator clips, connect the two metals with milliammeter. Pour the feroxyl
solution into the beaker glass until the electrode ends immersed. (Note: keep the
alligator clip dry and two metals do not connect directly).
31
32
EXPERIMENT 8
CORROSION OF METALS (3)
Purpose
To study the corrosion characters of metals (iron, magnesium and copper)
Introduction
The protection of corrosion of metals on machineries is an important effort. Beside
painting and platting, there is a method to prevent corrosion based on the characteristic of
metals. In many cases, metal is becoming less reactive due to the protection of strong oxide
layer from more reactive metal. By this, metal is protected from the corrosion process by
sacrificed-electrode. The method is known as sacrificial anode.
Sacrificial anode means that anode is sacrificed to protect the anode from further
corrosion. The process based on the chemistry nature of the metals. The more oxidized
metals will protect the lower oxidized metals from the corrosion.
Materials
-
Iron sheet 8 cm x 2 cm
3% NaCl solution
Copper sheet 8 cm x 2 cm
Acetone
Magnesium ribbon
Sandpaper
Multimeter or milliammeter
Procedure
1. Clean the iron and copper sheets with sandpaper and acetone soaked-cotton to clean the
fat.
2. Prepare 50 mL of 3% NaCl solution in beaker glass 250 mL.
3. Immerse an iron sheet and a copper sheet into the beaker glass and then use alligator
clips to connect the two metals to milliammeter. (Note: keep the alligator clips dry and
two metals do not connect directly).
4. Observe the electricity current indicator on milliammeter to investigate the amount
electrons flow through the two metals.
33
5. Change copper electrode with magnesium ribbon and then observe the electricity
current indicator on milliammeter to investigate the amount electrons flow through the
two metals.
6. Record the result of the observation on worksheet paper and compare the results with
the rate of iron metals corrosion.
34
EXPERIMENT 9
PREPARATION OF POTASSIUM-CHROMIUM ALUM, KCr(SO4)212H2O
Purpose
To study the preparation of potassium-chromium alum
Introduction
Alum is a double salt of MIMII(SO4)2nH2O, where MI is alkali metas (Na, K); MII is
metals with oxidation state +3, such as Al, Cr and Fe. Alum of K/Na Al sulfate and
K/Na Cr sulfate are good example of alum, which its crystallization is easy to be
studied.
Materials
-
Beaker glass
Watch glass
Sodium dichromate
Stirring rod
Water bath
Hydrogen peroxide 3%
Evaporating dish
H2SO4 (5 M)
HNO3(2 M)
Filter paper
Ethanol
NaOH (5 M)
Hirsch funnel
Procedure
1. Pour 25 mL of 5 M H2SO4 solution into a beaker glass and then add 4 g potassium
dichromate. Stir the mixture and heat in a water bath to dissolve dichromate.
2. Cool the solution in ice bath for about 10 minutes and then add 4 mL of ethanol drop to
drop into the mixture. Add ethanol carefully, because the reaction releases heat.
Observe the changing occurred and record on worksheet paper.
3. Cover the beaker glass with watch glass and observe the changing occurred next day.
4. Collect the crystals formed in Hirsch funnel and move the residue from beaker glass by
adding 5 mL of 60 % ethanol solution. If it necessary, repeat the procedure until no
more residue left in Hirsch funnel. Let crystals dry at room temperature (called as airdrying) until next day.
35
5. Weigh the crystal mass and calculate the yield percentage of potassium-chromium alum
based on the amount of dichromate used.
6. Test of the chromium ion presence in alum.
Add drop to drop of 5 M NaOH to sample (0.05 g alum in 2 mL of water) until no more
changing. (Every one drop of NaOH, shake and observe carefully before next adding).
Then add 1 mL of 3% H2O2 solution and heat the mixture until the color change. The
yellow color indicates the presence of chromate ion (CrO42-). Record the observation on
worksheet paper and write the balanced ionic reaction of the oxidation of Cr3+(aq) by
H2O2 in base condition.
Note: the test for Cr3+ must be undertaken in base condition.
7. Test the presence of sulfate ion in alum
In a test tube, dissolve 0.05 g chromium alum in 5 mL of water. Add few drops of 0.1
M Ba(NO3)2 solution and 2 M HNO3 solution. Record the observation on worksheet
paper and write the balanced ionic reaction of the test.
36
EXPERIMENT 10
PREPARATION OF POTASSIUM-ALUMINUM ALUM, KAl(SO4)212H2O
Purpose
To study the preparation of potassium-aluminum alum
Materials
-
Ethanol 60%
Stirring rod
Filter paper
KOH (2 M)
Hirsch funnel
H2SO4 (9 - 10 M)
Graduated cylinder 10 mL
Watch glass
Water bath
Glass wool
Procedure
1. Weigh 0.2 g of small pieces of aluminum on watch glass.
2. Pour 10 mL of 0.2 M KOH solution into beaker glass.
3. Warm the solution on water bath and then add a piece of aluminum (do it in fume
hood).
Note: Do not warm the solution too hot and remove beaker glass from fume hood
until all pieces of aluminum added to the solution. The reaction of aluminum and
KOH releases hydrogen gas.
4. As the reaction occurred, move out the beaker glass from water bath immediately.
Move it back into water bath as the reaction slowed down (no more bubbles produced)
and add other pieces of aluminum.
5. If all pieces of aluminum have been reacted, filter the mixture with a funnel that has
plugged with glass wool. (Ask the assistant how to do it).
6.
Add 20 mL of 9-10 M H2SO4 into filtrate solution carefully and check it with litmus
paper. Ensure that the solution is acid.
Note: Concentrated (10 M) sulfuric acid irritates and burns the skin. If it
happened, wash with flowing water and take medical care.
37
7. Cover the beaker glass with watch glass and let it for about 24 hours. After 24 hours,
the crystal of potassium aluminum alum, KAl(SO4)212H2O, formed. (The growing of
crystal may be speed up by scraping the stirring rod to inner part of solution while
cooling or add 2-3 mL of ethanol).
8. Collect the formed-crystal on Hirsch funnel and move the residue from beaker glass by
adding 5 mL of 60% ethanol. If it necessary, repeat the procedure until no more residue
left in Hirsch funnel.
9. Let the crystal dry until next day.
10. Weigh the crystal mass and calculate the yield percentage based on the amount of
aluminum used.
11. Do the re-crystallization to the impure yield with water as solvent.
12. For students who have synthesized both alum (chromium and aluminum), both alums
have the same structure, therefore possible to grow mixing crystals. Hang up a small
part of aluminum alum with yarn and immerse it into saturated solution of chromium
alum. By this, the alternate layers formed, uncolored of aluminum alum and purple to
reddish of chromium alum.
Re-crystallization technique
The purpose of re-crystallization is to purify resulted-solid. The resulted-solid
dissolved in minimum amount of solvent in an erlenmeyer flask or beaker glass. The solid
must has high solubility in hot solvent, but low in cold one. If undissolved-impurities solid
found in hot solution, filter it with funnel and filter paper in hot condition to avoid early
crystallization. If crystal found on filter paper, wash it with hot solvent. If the filtrate is too
dilute, concentrate it by heating. Pure crystals grow during the cooling process. The
growing of crystal may be speed up by scraping the stirring rod to inner part of glass. The
pure crystal filtered and washed with solvent in minimum amount.
38
EXPERIMENT 11
PREPARATION OF COORDINATION COMPOUND, [Ni(NH3)6]I2
Purpose
To study the preparation of coordination compound of [Ni(NH3)6]I2
Introduction
Complex (coordination) compound is characteristic compound of transition metals
that correspond to the existence of d orbital. The existence of d orbital cause transition
metals not only have various oxidation states but also the capability to interact coordinately
with other atom donor. Complex compound of [Ni(NH3)6]I2 is an example of Ni2+
compound with coordination number 6 where its crystallization is relatively easy to be
studied. The success of the compound preparation is easily tested qualitatively to Ni2+.
Materials
-
Ammonia 1 M
Stirring rod
Ethanol
Filter paper
Hirsch funnel
Potassium iodide
Graduated cylinder 10 mL
Starch indicator
Labeled-test tube
H2O2 (3%)
Procedure
1. Dissolve 1 g of nickel chloride hexahydrate into 5 mL water a beaker glass.
2. Place that beaker glass in the fume hood and add 10 mL of concentrated (15M) NH3
solution.
3. Add 2.6 g of potassium iodide to the mixture. Let the mixture for several minutes.
4. Collect the formed-crystal on Hirsch funnel, wash it twice with 2 mL of ethanol
solution 1:1 and then add 2 mL of ethanol solution.
5. Dry the crystals in windy air for several minutes.
6. Move the dried-crystals to filter paper. Ask the assistant how to move crystals from
Hirsch funnel to filter paper.
39
7. Move out the exceeding solvent by press the crystals between two filter papers.
8. Move the resulted crystal to the weighed and labeled-tube. Weigh the tube mass with
the contents. Calculate mass percentage of the product based on the amount of nickel
chloride hexahydrate.
9. Test the existence of nickel ion in the compound.
Dissolve a small amount of sample (about 0.001 g of compound in 0.5 mL of water),
add 5 M NH3 solution, and then add 5 drops of dimethyl glioxym solution. Red
strawberry solid produced if there is Ni2+ ion.
10. Test the existence of iodide ion in the compound.
Dissolve a small amount of compound (about 0.001 g of compound in 0.5 mL of water),
acidify with 2 drops of 5 M sulfuric acid solution and then add 3% H2O2 solution.
40
EXPERIMENT 12
PURIFICATION OF KITCHEN SALT BY RE-CRYSTALLIZATION METHOD
Purpose
To study the crystallization method on the purification of kitchen salt by evaporation
and precipitation
Introduction
Resulting purity high-level compound is an important thing in chemistry. The usual
method on solid purification is re-crystallization (the forming of repeating crystal). Recrystallization based on the difference of solubility capacity of solid and impurities in
particular solvent. If it possible, use alternate solvent that only dissolve the impurities. Such
purification is widely used in industrial and laboratory to improve the quality of particular
substance.
Requisites of a solvent in re-crystallization process are:
1. Give significant solubility differences between purified-substance and impurities.
2. The solubility of substance in solvent is a temperature function. The solubility usually
decreases with the decreasing of temperature.
3. Easily separate from the crystals.
4. Do not leave the impurities in the purified crystals.
5. Do not react with purified substance.
Kitchen salt contains sodium chloride as major component, and Ca2+, Mg2+, Al3+,
Fe3+, SO42-, I-and Br- as impurities. Those impurities easily dissolved in water. Recrystallization method with water as a solvent is general method to get high-level sodium
chloride from kitchen salt. Particular ions needed to eliminate the existence of impurity
ions. These ions will bind the impurity ions to form low-level solubility compound in
water. By this, the purified and impurities substances easily separated.
Materials
-
Burner
Beaker glass
41
Graduated cylinder
Funnel
Gas adapter
Concentrated H2SO4
Procedure
1. Into a beaker glass, dissolve about 16 g kitchen salt in 50 mL water. Boil and stir the
mixture. Divide the solution into 2 parts in equal amount and called as solution A and
B.
2. Crystallization of solution A
a. Add about 0.2 g of CaO into solution A
b. Add Ba(OH)2 solution drop to drop until no more precipitate formed at the last
drop.
c. Add (NH4)2CO3 solution drop to drop and stir continuously.
d. Filter the mixture into cleaned and weighed beaker glass. Neutralize filtrate by
adding of dilute HCl solution drop to drop. (Test the neutrality of the solution with
litmus paper in every drop).
e. Evaporate the solution until relatively dry.
f.
Weigh the resulted NaCl (which is brighter and whiter than original kitchen salt)
and calculate the percentage.
3.
Crystallization of solution B
a. Saturate the solution B by HCl gas adding. Hydrochloric acid gas obtained from the
reaction of kitchen salt and concentrated sulfuric acid. (Do the reaction in fume
hood). The flowing of HCl stopped when no more NaCl crystal growing in the
solution.
b. Separate the crystal by filtering, dry it and then weigh the product and compare to
method 1 above.
42
REFERENCES
Chia, PSK, Chemistry : Chem 1201, Laboratory Manual, (1995) The School of Chemistry,
UNSW, Australia
Dance, I.G., Chemistry : Chem 1002 - 1101, Laboratory Manual, (1990) The School of
Chemistry, UNSW, Australia
Moeller, T., Bailar, Jr., J.C., Kleinberg, J., Guss, C.O., Castellion, M.E., and Metz, C.,
Chemistry , Third Edition, 1989, San Diego, Harcourt Brace Jovanovich, Publisher.
Petrucci, R.H., and Wismer, R.K., General Chemistry , Second Edition, 1987, New York,
Macmillan Publishing Company.
Rayner-Canham, G., Descriptive Inorganic Chemistry, 1996, New York, W.H. Freeman
and Company.
Department of Inorganic Chemistry, The School of Chemistry, UNSW, Australia (1985)
Inorganic Chemistry, Laboratory Manual
43
WORKSHEET-1
A
A
(a)
(b)
(c)
(d)
Figure 1
Arrange the balls side-by-side in a plane (Figure 1a)
Arrange the balls as closest as possible (Figure 1b)
How many balls that touch center-ball in the same layer for each packing?
Answer: balls for (a) and .. balls for (b)
Which is a closer packing, (a) or (b)?
Answer:
Geometry structure of (a) is not a closest packing, whereas (b) is a closest packing. The
arrangement of layer (b) is known as hexagon.
If we add the second, third layer, etc, to the arrangement model (a) so that the balls of
second and third layer lie above the first layer, we get layer A, A, A (Figure 1c). How
many balls that touch every other ball in layer A, A, A?
Answer: balls
Place one ball into the hole between two layers A, A so that the hole-ball touch all balls.
Layer A, A will expand. The resulted geometry of expanding layer A, A is called
. (Figure 1d), which has coordination number .
Which is the closer packing, (c) or (d)?
Answer:
44
45
4. Determine the amount of balls touch centered-ball in the ccp or fcc geometry
Answer: balls, consisted of .. balls in same layer and
.. balls in layer above and bellow. (The numeric is known as coordination
number).
5. Repeat step 1 to 3 with 3 patterns of 7-balls.
6. Is the coordination number still the same?
Answer: Yes / No, .. balls.
7. Direct this pattern to light source. What do you get?
Answer: ..
...
8. Put the wire through the hole of hcp packing. What do you get?
Answer: : ....
.............
9. Arrange the patterns of 5-balls 4-balls 5-balls (14 balls). Determine the amount of
balls that touch center-ball on every cubic face.
Answer: balls.
10. For every cubic face, is it a closest packing layer?
Answer : ..
11. Is every face of cubic a closest packing layer?
Answer: ....
12. In order to get closest packing layer, from what direction (axis or diagonal) the structure
must be viewed?
Answer: ....
13. Shade the balls in the same layer and label it with layer A, B or C for Figure 1.2
Figure 1.2
46
r+
= .., or
r
r
= ..............................
r+
r- = .
r
=
r+
.................
47
C
B
Figure 1.3 Tetrahedron (a), octahedron (b), and body centered cubic (c) geometries
in cubic perspective
Octahedron geometry (in face centered cubic)
Place 3-balls-triangular pattern (layer 1) on the desk.
Place 3-balls-triangular pattern (layer 2) so that balls of layer 2 lies above layer 1.
Turn 600 clockwise for layer 2 (octahedron hole).
Put a smaller ball and place in the octahedron hole. Ensure that the smaller ball touch six
balls in octahedron geometry precisely.
Measure the diameter or radius of bigger ball (ping-pong ball) and state as r- (anion radius).
Measure the diameter or radius of smaller ball and state as r+ (cation radius).
Note: anion radius is bigger than cation radius
Diameter of small ball
Radius ratio
r
= ..............................
r+
r- = .
48
r
=
r+
.................
Radius ratio
r
= ..............................
r+
r- = .
49
r
=
r+
.................
Which is the bigger hole, tetrahedron, octahedron or body centered cubic hole?
Answer: ....
(a)
(b)
(c)
Figure 1.4 Models of hexagon layer packing (a,b), and layer A, B closest packing (c)
Arrange a 12-balls-hexagon layer (layer 1) as shown in Figure 1.4a. (there are 12 holes)
Arrange another 12-balls-hexagon layer in opposite direction (Figure 1.4b)
Put layer 2 on layer 1 according to AB pattern (balls of layer 2 fit the holes of layer 1). The
holes in layer 1 occupied by layer 2 balls called tetrahedron holes, whereas unoccupied
called octahedron holes)
Identify and mark the type and the amount of holes.
Direct the two layers (Figure 1.5c) to light source. (Light can penetrate octahedron holes,
not tetrahedron holes)
Put the wire through the hole. (Wire may through the octahedron holes, not tetrahedron
hole).
How many tetrahedral and octahedral holes are there?
Answer: .....
Therefore, between two hexagon closest packing, there are tetrahedral holes as twice as
octahedral holes.
Assistants comment
Score: ...................
50
WORKSHEET-2
2+
Observation
Uncolored precipitate formed. The
precipitate does not dissolve in excess
adding of NaOH and NH3.
Ionic Reaction
Mg2+(aq) + 2OH- (aq) Mg(OH)2(s)
Ba2+
Al3+
Cr3+
Fe3+
Mn2+
Pb2+
Cu2+
Ni2+
Ag+
Zn2+
5. Cations that form precipitates on the adding of NaOH are: ......
.
51
6.a. Cations that form precipitates on the adding of NaOH but dissolved in the excess NaOH
are: ..
6b. Cations that form precipitates on the adding of NH3 but dissolved in the excess NH3
are: ....
7a. The observation and equation of ionic reaction in the adding of 0.1 M Al(NO3)3 drop to
drop into 1 mL of 2M NaOH are:
7b. The observation and equation of ionic reaction in the adding of 0.1 M Fe(NO3)3 drop to
drop into 1 mL of 2M NaOH are:
7c. The adding of reactant (between M3+ and NaOH) in reversed order are:
Cation
Observation
Reaction
Al3+
Fe3+
Which cations result different reaction if the reactant adding in reversed order?
Answer: ......
.....
.....
Assistants comment
Score: ..................
52
WORKSHEET-3
Test tube T
5 drops of H2O2 (3%)
Test tube B
5 drops of H2O2 (3%)
5 drops of aquadest
Cold :
Cold : ...
Hot : ...
Hot : ...
Oxidation : .
Reaction
Reduction : ..
Redox : ...
(b)
Observation
Cold :
Cold : ...
Hot : ...
Hot : ...
Oxidation : ...
Reduction : ..
Redox : ...
(c)
Observation
Cold :
Cold : ...
Hot : ...
Hot : ...
Reduction : ..
Redox : ...
53
Test tube B
5 drops of Fe(NH4)2(SO4)2 (0.1M)
5 drops of aquadest
Observation
Cold : ...
Cold : ...
Hot : .
Hot : ...
Redox
Testt
Oxidation : ...
Reaction
Reduction : ..
Redox : ...
(b)
Observation
Redox
Testt
5 drops KI (0.1M)
Cold : ...
Cold : ...
Hot : .
Hot : ...
Test : .
Observation :
Test :
Observation : ...
..
Oxidation : ...
Reaction
Reduction : ..
Redox : ...
(c)
Observation
Redox
Testt
Cold : ...
Cold : ...
Hot : .
Hot : ...
Test : .
Observation :
Test :
Observation : ...
..
Oxidation : ...
Reaction
Reduction : ..
Redox : ...
54
Test tube B
5 drops of H2O
Cold : ...
Cold : ...
Hot : .
Hot : ...
Test : .
Observation :
Test :
Observation : ...
..
Oxidation : ...
Reaction
Reduction : ..
Redox : ...
(b)
Observation
Redox
Testt
5 drops of KI (0.1M)
Cold : ...
Cold : ...
Hot : .
Hot : ...
Test : .
Observation :
Test :
Observation : ...
..
Oxidation : ...
Reaction
Reduction : ..
Redox : ...
Cold : ...
Cold : ...
Hot : ..
Hot : ...
Oxidation : ...
Reaction
Reduction : ..
Redox : ...
55
Questions:
1. According to the observation no 4 on Table 3.2, explain why sulfuric acid (H2SO4)
solution is used to acidify the solution of KMnO4 and K2Cr2O7, instead of hydrochloric
acid (HCl).
Answer:
2. In the study of permanganate ion as oxidant, redox test is unnecessary. Why? Explain
your argument.
Answer:
Assistants comment
Score: ..................
56
WORKSHEET-4
Metal
Observation
Cold
Hot
Reaction
Zn
Fe
HCl
Cu
Al
Pb
Zn
Fe
HNO3
Cu
Al
Pb
57
Zn
Pb
Fe
Al
Cu
Assistants comment
Score: ..................
58
WORKSHEET-5
anode or cathode
The
measured
E cell
E0 of half-cell
Experiment Literature
Zn2+ Zn
Pb2+ Pb
Sn2+ Sn
Fe2+ Fe
Al3+ Al
Cell notation
E0cell / V
Fe / Zn
Fe / Sn
Fe / Al
Fe / Cu
Assistants comment
Score: ..................
59
WORKSHEET-6
System
Fe
Location of
red color
Along the
nail rod
Location of
blue color
The ends of
nail rod
Ionic Reaction
Anodic
Cathodic
Fe(s)Fe2+(aq) + 2e
O2(aq)+2H2O()+4e 4OH-(aq)
Fe/Sn
Fe/Zn
Fe/Al
Fe/Cu
Iron
nail
Tin
Zink
Aluminum
Copper
60
Write the line notation of the corrosion for each cell and calculate the E0. Remember
that E0 refers to cell of 1M Mn+ solution cell. The value can be used as the reference to
determine the possibility of anodic corrosion if two metals connected.
System
*
Fe/Sn
Fe/Zn
Fe/Al
Fe/Cu
Eo *)
Fe (s)
4 OHSn (s)
Zn (s)
Zn (s)
Cu (s) E0
E0 = - 0,41 V
E0 = + 0,40 V
E0 = - 0,14 V
E0 = - 0,76 V
E0 = - 1,68 V
E0 = +0,34 V
Tin cane made from tin platted-iron sheet. How tin prevent the corrosion of iron?
If the layer scratched, the corrosion rate of tin cane is high, but not for galvanized-iron.
Explain for the differences of decomposition rate between the tin cane and galvanized-iron.
Assistants comment
Score: ..................
61
WORKSHEET-7
Assistants comment
Score: ..................
62
WORKSHEET-8
Assistants comment
Score: ..................
63
WORKSHEET-9
Score: ..................
64
WORKSHEET-10
= ..
= ..
= ..
Write the coefficient of ionic balance (use the method of ion-electron half-reaction balance)
1) Al (s) +
OH- (aq)
2) [Al(OH)4]- (aq) +
H2O ()
H+(aq)
3) K+(aq) + Al3+(aq) +
Al3+(aq)
SO42- (aq) +
Theoretical yield
= .
Percentage yield
= .
H2O ()
H2 (g) +
+
[Al(OH)4]- (aq)
H2O ()
KAl(SO4)2.12H2O
...........
Assistants comment
Score: ..................
65
2. Dimethylglioxim often used as testing agent for the existence of nickel(II) ion. Sketch
the structure of dimethylglioxim.
3. Red strawberry precipitate formed from the reaction of dimethylglioxim and nickel(II)
ion in base condition. Sketch the structure of bis-(dimetilglioksimato)nikel(II) ion.
Assistants comment
Score: ..................
66
WORKSHEET-11
= ..
= ..
Mass of complex
= ..
Theoretical yield
= ..
Percentage yield
= ..
On the iodide ion testing, sulfuric acid solution needs to be added. Why?
Assistants comment
Score: ..................
67
WORKSHEET-12
= .. gram = .. % (weight)
= .. gram = .. % (weight)
68
Score: ..................
69