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Icho1986-1994p Technical and Physical
Icho1986-1994p Technical and Physical
OLYMPIADS
1986 - 1994
1993
by Marco Ziegler
This version is free of charge and may be distributed freely. Comments, corrections and other
intersting problems that will be incorprated in a larger problem compilation should be sent to
[email protected]
1. Table of Contents
Problems
1. Analytical chemistry p. 3
2. Inorganic chemistry p. 5
3. Physical chemistry p. 12
4. Technical chemistry p. 19
5. Organic chemistry p. 21
6. Biochemistry p. 29
Solutions
1. Analytical chemistry p. 32
2. Inorganic chemistry p. 34
3. Physical chemistry p. 41
4. Technical chemistry p. 47
5. Organic chemistry p. 53
6. Biochemistry p. 62
Problems
1. Analytical chemistry
a) The end point of the reaction taking place during the ti-
tration are marked with A, B and C. Write the balanced
ionic equation for each reaction.
b) What volume of the titrant is required to reach point B ?
c) Calculate the concentrations of KCl and KCN in the sample solution.
d) Calculate the emf readings at the points A and C in volts.
- -
e) What is the molar ratio Cl /CN in the solution and in the precipitate at point C ?
Data:
o +
E (Ag /Ag): 0.800 V
o
E (Calomel): 0.285 V
-15.8 2 2
Ksp(AgCN): 10 mol /l
-9.75 2 2
Ksp(AgCl): 10 mol /l
[Ag(CN )-2]
2 = = 1021.1 mol-2 l2
[Ag+][CN- ]2
The minimum concentration of chloride ions needed in oyster beds for normal growth is 8 ppm (8 mg/l).
To 50.00 ml a sample of bay water a few drops of a K 2CrO4-solution are added. The sample is then titrated with 16.16
ml of a 0.00164 M AgNO3-solution when a bright red-orange precipitate starts to form.
a) What is the molar concentration of chloride in the sample ? Does the water contain sufficient chloride for the normal
growth of oysters ?
b) Write a balanced equation for the reaction of the analyte with the titrant.
c) Write a balanced net-ionic equation that describes the reaction responsible for the colour change at the endpoint of
the titration. Which compound produces the brick-red colour ?
d) The concentration of chromate at the endpoint is 0.020 M. Calculate the concentration of chloride in the solution
when the red precipitate is formed.
e) For this titration to work most efficiently, the solution being titrated must be neutral or slightly basic. Write a
balanced equation for the competing reaction that would occur in acidic medium influencing the observed endpoint
of this titration.
Typically, a buffer is added to the solution being titrated to control the pH. Suppose the pH of the sample of bay water
was 5.10, thus too acidic to perform the analysis accurately.
f) Select a buffer from the list that would enable you to establish and maintain a pH of 7.20 in aqueous medium. Show
the calculations which leads your choice.
g) Using the selected buffer system, calculate the number of grams of weak acid and of conjugated base you would
need to dissolve in distilled water to prepare 500 ml of a stock solution buffered at a pH of 7.2.
h) The chloride concentration in another 50.00 ml sample was determined by the Vollhard method. In this method an
+
excess of AgNO3 is added to the sample. The excess Ag is titrated with standardized KSCN, forming a precipitate
of AgSCN. The endpoint is signalled by the formation of the reddish-brown
2+ + +
FeSCN complex that forms when Ag is depleted. If the excess Ag from the addition of 50.00 ml of 0.00129 M
-3
AgNO3 to the water sample required 27.46 ml of 1.41 10 M KSCN for titration, calculate the concentration of
chloride in the bay water sample.
-
In natural waters with much higher concentration of Cl , it can be determined gravimetrically by precipitating them as
AgCl. A complicating feature of this method is the fact that AgCl is susceptible to photodecomposition as shown by the
reaction: AgCl (s) Ag (s) + Cl2 (g). Furthermore, if this photodecomposition occurs in the presence of excess
+
Ag , the following additional reaction occurs:
+ - +
3 Cl2 (g) + 3 H2O + 5 Ag 5 AgCl + ClO3 + 6H
i) Will the apparent weight of AgCl be too high or too low ? Explain your answer showing by how many grams the
two values will differ.
-10 -12
data: Ksp for AgCl = 1.78 10 Ksp for Ag2CrO4 = 1.00 10
Column A Column B
t (sec) t (sec) F Area
Unretained compound 120 130
Cholic Acid (CA) 380 350 0.5 2200
Glycocholic Acid (GCA) 399 395 0.2 3520
Internal standard (i.s.) 442 430 2304
Note that:
a) Using R, and K' values, demonstrate which of the two chromatographic columns would be best to use, considering
that an accurate determination requires the best possible (baseline) separation of all compounds (do not take into
account the unretained compound) ?
Lactic acid is formed in the muscles during intense activity (anaerobic metabolism). In the blood, lactic acid is
neutralized by reaction with hydrogen carbonate ions. This will be illustrated by the following calculations:
Lactic acid, written HL, is monoprotic, and the acid dissociation constant is KHL = l.4 x l0-4.
The acid dissociation constants for carbonic acid are: Ka1 = 4.5 x 10-7 and Ka2 = 4.7 x 10-11. All carbon dioxide remains
dissolved during the reactions.
b) Calculate the value of the equilibrium constant for the reaction between lactic acid and hydrogen carbonate ions.
c) 3.00 x 10-3 mol of lactic acid (HL) is added to 1.00 L of 0.024 M solution of NaHCO3 (no change in volume, HL
completely neutralized). Calculate the pH of the solution of NaHCO3 before HL is added. Calculate the pH of the
solution after the addition of HL.
d) The pH of the blood in a person changed from 7.40 to 7.00 due to the lactic acid which formed during physical
activity. Let an aqueous solution having pH = 7.40 and [HCO3-] = 0.022 M represent blood in the following
calculation and in f). Calculate the number of moles of lactic acid which must be added to 1.00 L of this solution so
that the pH becomes7.00.
e) In a saturated aqueous solution of CaCO3(s) the pH is measured as 9.95. Calculate the solubility of calcium
carbonate in water and show that the calculated value for the solubility product constant Ksp is 5 x 10-9.
f) Blood contains calcium ions. Calculate the maximum concentration of "free" calcium ions in the solution given in
d). (pH = 7.40, [HCO3-] =0.022 M)
H2N N or H2N N
2. Inorganic chemistry
dmen pn (racemic)
IChO Leiden 1986
2-
Compounds containing divalent platinum with the general formula PtX2 (amine)2 (X = Cl2, SO4 , malonate, etc.) have
met a lot of scientific interest because of their biological activity, particularly in view of their properties in the
treatment of tumours. The best known compound used clinically is PtCl2(NH3)2. This compound, in which platinum is
coordinated in a planar square, has two geometrical isomers of which only one shows the antitumour activity.
It is possible to replace the amine ligands by one ligand containing two donor atoms (N). Then one obtains a chelating
ligand, such as 1,2-diaminoethane (en).
d) Give spatial structures of all isomers of the following compounds: PtCl2(dmen), PtCl2(pn), PtBrCl(dmen) and
PtBrCl(pn).
These compounds can isomerize in aqueous solution through dissociation of a ligand and transient replacement of the
- -
stronger ligands by the weak ligand water. Cl and Br are replaced relatively easily, but it is more difficult to replace
the amine ligands, which usually requires heating.
e) Considering each of the isomers in the previous questions a-d, indicate which isomers can be converted to another at
room temperature. Give both the original molecule and the products.
-
f) PtCl2(en) reacts with Br in a molar proportion of 1:2 at room temperature. Which compound would you expect to
form in what proportion ? You can assume that the Pt-Br and Pt-Cl bonds are equally strong and that there is no
perturbing influence from hydrolysis.
g) Using the equation to express chemical equilibrium, show that hydrolysis hardly ever occurs in blood but that is
2+ - -
does occur in the cells. Note: PtCl2(NH3)2 hydrolyses to Pt(NH3)2(H2O)2 and 2 Cl . In cells the Cl concentration
is low, in blood it is fairly high.
H2O
After hydrolysis in the tumour cell a reactive platinum ion is formed O
H3N
NH3
to which two NH3 groups are still bound, which were found in the Pt
urine of patients treated with this compound. The reactive platinum N
ion appears to be bound to cellular DNA, where the bonding occurs N
via guanine to one of the N-atoms.
N
As a result of the two reactive sites of platinum and the two H2N N
unreactive NH3 ligands, it can form a second bond to DNA in sugar
addition. Research has shown that this happens in particular with a second guanine base from the same strand of DNA.
h) Show by calculation which of the two isomers in question a) can form this bond. (note: Pt-N distance - 210 pm,
DNA base distance = 320 pm).
5- 3-
a) Draw the structure of the ions (P3O10) and (P3O9) assuming that P-P bonds do not occur.
2+ 3-
b) Assuming an octahedral coordination of the Mg ion give a drawing of the Mg(P3O10)(H2O)n) ion also
indicating the value for n.
2+ 2+
The complex ions of Mg and Ca and triphosphate are well soluble in water. They are, among other things,
responsible for the wild growth of algae in surface waters. They could be removed by precipitation as an insoluble
compound.
2+ 2+
c) Give some possibilities (ions) to precipitate the triphosphates bound to Ca or Mg .
d) Calculate the number of grams of Na5P3O10 necessary in a washing machine of 20 liters to reduce the amount of
2+
Ca in city water (0.225 g/l) to an acceptable maximum of 0.02 g/l. Effects of the pH, the precipitation of Ca(OH)2
and possible effects by other positive ions can be neglected. The following data is given:
[H n POn-3
4 ]
Kn =
[ PO4 ][H+ ]n
3-
where pK1 = -11.70; pK2 = -18.6; pK3 = -20.6. Relative atomic masses are: Na = 23.0 and P = 31.0
n-3
a) Calculate the percentage distribution, by moles, of all protonated HnPO4 species at the end point.
b) What is the stoichiometric formula of the salt ?
a) Show where the maxima lie by drawing the contour curves around the maxima, connecting points of equal electron
densities. Label each maximum to show the identities of the atoms in E.
b) When 450.0 mg of C was treated with an excess of mercury, 53.25 ml of A was liberated at a pressure of 101.0 kPa
at a temperature of 25C. Calculate the relative atomic mass of A.
c) Identify A, B, C, D and E.
d) Use the valence-shell electron-pair repulsion theory (VSEPR) to propose electron-pair geometries for B and C.
Using the two electron density maps, sketch the molecular geometry of E.
The original mixture was hydrolysed in water. B reacts to A while liberating oxygen and producing aqueous hydrogen
fluoride. Hydrolysis of C leads to A and oxygen (in molar ratio of 4:3) and yields an aqueous solution of AO3 and
hydrogen fluoride. D hydrolyses to an aqueous solution of AO3 and hydrogen fluoride.
Y-direction
(pm)
600 1 2 2 1 1 2 2 2 1 2 1 2 1 2
1 2 1 2 1 1 2 1 3 1 1 2 1 2
2 2 1 1 2 1 2 4 26 3 1 2 1 2
3 1 2 1 2 2 3 9 32 11 2 2 1 2
500 1 2 1 1 2 2 4 20 58 21 3 1 2 1
2 2 1 1 2 1 3 10 33 11 4 2 2 2
1 1 2 2 1 2 2 8 19 6 3 3 1 1
1 1 2 1 2 2 5 3 6 3 2 1 2 1
400 1 2 2 1 4 17 20 16 3 2 2 3 1 2
1 1 2 4 12 33 76 36 13 4 3 1 2 1
2 1 2 6 36 100 220 101 31 6 1 2 1 2
1 2 4 13 61 149 356 152 62 15 6 1 2 1
300 2 2 1 6 31 105 232 90 26 7 3 1 1 2
1 1 2 6 12 36 65 28 10 4 2 1 1 2
2 2 1 2 7 15 15 13 6 1 2 1 1 2
200 1 1 1 3 5 3 6 2 1 1 1 2 2 1
1 2 2 6 14 6 3 1 1 2 2 2 1 2
2 2 3 11 23 10 3 8 2 1 2 1 2 2
2 2 7 19 32 16 2 1 2 2 1 1 2 2
1 2 3 9 25 12 3 2 2 2 2 1 1 2
100 2 2 1 4 13 5 6 4 2 1 1 1 2 1
1 1 1 2 6 10 33 11 1 2 1 1 1 2
1 2 1 4 11 22 80 23 5 2 1 2 1 2
0 1 2 9 8 30 52 104 49 16 1 2 3 1 2
1 1 2 3 12 21 75 23 6 2 1 2 1 1
1 2 1 2 4 9 36 11 2 2 1 1 2 2
1 1 2 4 15 5 6 4 1 1 2 1 1 2
-100 2 2 3 11 24 18 4 2 1 2 1 2 1 2
1 2 6 17 52 19 6 3 1 2 1 2 2 1
2 1 3 8 23 8 4 1 2 1 2 1 1 2
2 2 1 4 13 5 2 2 1 1 3 2 1 2
-200 1 1 2 1 2 1 1 1 2 1 1 2 2 1
1 2 1 1 2 2 1 2 2 1 1 2 2 1
Z-direction
(pm)
400 1 2 1 1 2 2 2 1 1 1 2 2 2 2
1 2 1 1 2 1 1 2 2 2 1 2 1 1
1 2 2 1 1 1 2 2 1 1 1 2 2 1
1 1 2 2 2 1 2 1 1 1 1 2 1 1
300 1 2 2 2 1 2 1 1 2 1 2 1 1 2
1 1 2 2 2 1 1 2 1 2 1 2 1 1
2 2 2 2 1 1 2 2 1 1 2 2 2 1
1 1 2 1 1 1 2 2 2 1 1 2 2 1
200 2 2 1 1 1 2 3 2 1 1 2 2 1 1
1 2 2 1 1 2 2 1 2 2 2 1 1 1
2 2 2 2 1 1 2 1 1 2 2 3 1 2
1 1 1 2 1 1 2 4 11 3 2 1 1 1
100 1 1 2 2 1 1 1 8 21 9 3 2 1 2
1 2 1 1 2 3 4 10 50 19 3 2 1 2
1 1 2 2 2 5 6 10 23 9 2 1 1 2
1 1 1 2 4 8 33 8 10 3 1 1 2 1
0 1 2 1 3 9 21 74 22 5 1 2 2 2 2
1 2 9 8 20 58 194 49 16 1 2 3 1 2
1 1 3 2 11 23 81 23 13 1 1 1 1 2
1 2 1 3 3 12 37 11 4 2 2 2 1 2
-100 1 1 1 2 1 3 7 5 15 4 2 3 1 1
2 1 2 2 2 2 4 10 24 9 3 1 2 2
1 1 2 1 2 3 8 19 52 18 3 2 2 2
2 2 2 1 1 2 3 9 21 8 3 2 2 1
-200 3 2 1 1 2 1 2 4 12 3 1 1 1 1
2 1 2 2 1 1 2 2 2 1 2 2 2 2
1 2 2 2 1 1 1 2 2 1 2 1 1 2
2 2 1 1 2 2 2 2 1 1 2 2 1 2
-300 1 2 1 1 2 1 1 2 1 1 2 2 2 2
2 1 1 2 2 2 1 3 1 2 2 3 3 1
1 1 1 2 2 2 2 1 3 2 1 1 2 1
2 1 1 2 2 2 1 1 2 1 2 1 1 1
-400 1 2 1 1 2 2 2 2 1 1 2 2 2 1
To determine the solubility product of copper(II) iodate (Cu(IO3)2 by iodometric titration in an acidic solution (T=25
C) 20.00 ml of a saturated aqueous solution 30.00 ml of a 0.10 molar sodium thiosulphate solution are needed.
a) Write the sequence of balanced equations for the above described reactions.
2+
b) Calculate the initial concentration of Cu and the solubility product of copper(II) iodate. Activity coefficients can
be neglected.
O O Cl O
Cl Cl Cl Cl
+ PCl5 + POCL3 + HCl
P P P
Cl N Cl Cl N Cl
I II III IV
32 +
P labelled phosphorus pentachloride (half-life t1/2 = 14.3 days) is used to study the electrophilic attack of a PCl4
cation on nitrogen or on oxygen. The reaction is carried out in CCl4 and the solvent and product IV distilled off.
Samples of III (remaining in the distillation flask), of IV (in the distillate) and samples of the starting material II are
hydrolyzed by heating with a strong sodium hydroxide solution. The phosphate ions formed are precipitated as
ammonium magnesium phosphate. Purified samples of the three precipitates are then dissolved by known volumes of
water and the radioactivity measured.
a) Write the balanced equations for the reaction of red phosphorus forming PCl5
b) Write the reaction equations for complete hydrolysis of the compounds II and III using sodium hydroxide.
-3
c) How long does it take in order to lower the initial radioactivity to 10 of the initial value?
+
d) Write two alternative mechanisms for the reaction of labelled PCl4 with the anion of I.
e) After hydrolysis the precipitated ammonium magnesium phosphates show the following values for radioactivity:
II. 2380 Bq for 128 mg of Mg(NH4)PO4
III. 28 Bq for 153 mg of Mg(NH4)PO4
IV. 2627 Bq for 142 mg of Mg(NH4)PO4
+
Using these data, what can you say about the nucleophilic centre attacked by PCl4 ?
Data:
f) Calculate the solubility for Mg(NH4)PO4 at pH equal to 10 under idealized conditions (activity coefficients can be
neglected).
A sample of m0 g of this mineral is treated with 50.0 ml of a solution containing 0.500 mol/L phosphoric acid and
0.100 mol/l sulphuric acid. The mixture is completely dehydrated by heating up to 70 C. Toxic gases are emitted
thereby. m1 g of dry residue is obtained. In these conditions, only phosphate Ca(H2PO4)2 is formed, silica and silicate
do not react.
1.00 g of this residue is treated with 50.0 ml of water at 40 C, filtered, dried and m2 g obtained. This new residue is
mainly containing gypsum (CaSO4 2H2O) whose solubility between 20 C and 50 C is equal to 2.3 g/l.
a) Write the balanced equations for all reactions. From what mass of apatite should one start if the reactions are
stoichiometric?
b) Starting with m0 g of apatite, m1 = 5.49 g of residue are obtained. What mass should theoretically have been
obtained? This result is due to the presence of two products that are not expected to be in the residue. Which
product are these?
Traditionally, the yield is expressed as percentage of oxide. The phosphorous content is expressed as if it were P2O5. If
n2 is the amount of soluble product obtained, n1 the amount of substances added as acid, n0 the amount of apatite
added, the yield is:
n2
r exp = 100
n1 + n 0
c) m2 = 0.144 g of residue is obtained on the filter. Calculate rexp.
d) The experimental yield is over 100 %. Calculate a value of r nearer to the real yield.
-2
a) Consider a 1.0010 solution of copper(II) nitrate. The pH of this solution is 4.65. Give the equation for the
2+
formation of the conjugate base of the hydrated Cu ion and calculate the pKa of the corresponding acid-base pair.
-20
The solubility product of copper(II) hydroxide is Ksp = 10 . At what pH would Cu(OH)2 precipitate from the
2+
solution under consideration? Justify your calculation, showing that the conjugate base of this hydrated Cu ion is
present in negligible quantity.
b) Write down the equation for the disproportionation of copper(I) ions and calculate the corresponding equilibrium
0 + 0 2+ +
constant. E1 (Cu /Cu) = 0.52 V, E2 (Cu /Cu ) = 0.16 V. Calculate the composition in mol/l of the solution
-2
obtained on dissolving 1.010 mol of copper(I) in 1.0 l of water. Name two chemical species which also dispro-
portionate in aqueous solution; write down the equations and describe the experimental conditions under which
disproportionation is observed.
-2 2+
c) Consider the stability of copper(I) oxide (Cu2O) in contact with a 1.0010 mol/l solution of Cu ions. The stability
+ - -15
product of copper(I) oxide is Ksp = [Cu ][OH ] = 10
Quote a simple experiment allowing the observation of the precipitation of Cu2O.
+ -11
d) The dissociation constant of the complex ion [Cu(NH3)2] is KD = 10 . Calculate the standard electrode potential
of the couple:
+
Does the disproportionation of the cation [Cu(NH3)2] take place?
a) Show that 0.1 mol of Tl2S dissolves in a 1M solution of any strong monoprotic non-coordinating acid.
b) Show that 0.1 CuS dissolves in a 1M HNO3 but not in a 1M HCl solution.
Information:
Assume that Cu2+ ions don't form stable complexes with chloride ions in aqueous solutions.
Type II electrodes are made of a metal covered with a sparingly soluble salt of the metal that are dipped into a soluble
-
salt solution containing an anion of the sparingly soluble salt. The silver/silverchloride (Ag, AgCl/Cl ) and the calomel
-
electrode (Hg, Hg2Cl2/Cl ) are examples of such electrodes. The standard emf of a cell built of those electrodes (-)
- 0 0
Ag,AgCl/Cl /Hg2Cl2/Hg (+) is E = 0.0455 V. at T = 298 K. The temperature coefficient for this cell is dE /dT =
3.3810-4 V/K.
a) Give the equations of the reactions taking place at both the cell electrodes and the overall cell reaction.
0
b) Calculate the Gibbs free energy change (G ) for the process taking place in the cell. What does its sign imply ?
c) Calculate the enthalpy change for the process taking place at 298 K, given S = n F dE/dT.
+ 0
d) Knowing the standard potential of Ag/Ag electrode is E = 0.799 V and the solubility product of AgCl Ksp =
-10
1.7310 , calculate the standard electrode potential value of the silver/silver chloride electrode. Derive an
0 + 0 -
expression showing the dependence between E (Ag/Ag ) and E (Ag, AgCl/Cl ).
0
e) Calculate the solubility product of Hg2Cl2 knowing that the standard potential of the calomel electrode is E = 0.798
V.
2-
a) Draw the electron dot structure that illustrates the bonding in the S2 -ion, showing all valence electrons.
+
b) Write a balanced chemical equation to show how hydrogen ions (H ) are genrated during the oxidation of pyrite to
form iron(II) ions and sulphate.
c) Write a balanced equation to show how many additional moles of hydrogen are generated when iron(II)ions are
oxidized to form the mineral goethite, FeO(OH).
d) Calculate how many moles of pyrite would be required to bring 1.0 litre of pure water to a pH of 3.0 if the pyrite
+ -
was completely converted into FeO(OH) and H . Neglect the formation of HSO4 .
e) The concentration of iron as Fe(II) in a stream is 0.00835 M. At a very narrow point in the stream it empties into a
large pond, with a flow rate of 20.0 l/min. The water in this stream is sufficiently aerated that 75% of the iron(II) is
oxidized to Fe(III) which immediately precipitates as Fe(OH)3 later aging to became Fe2O3. What mass of Fe2O3
will be deposited on the bottom of the pond in two years ?
2+ -
CaSiO3 (s) + 2 CO2 + 3 H2O (l) Ca (aq) + 2 HCO3 (aq) + H4SiO4 (aq)
What are the maximum number of grams of CaSiO3 that can be weathered by the carbon dioxide produced from the
decomposition of 1000 blue whales, the number estimated to die annually ?
a) Which species of nitrogen is predominant in a1) O2-rich lakes of pH ~ 6 , a2) O2-depleted lakes of pH ~ 3 b)Which
species of manganese is predominant in b1) O2-rich lakes of pH ~ 6, b2) highly O2-depleted lakes of pH ~ 12 ?
c) People often find that clear, slightly acidic (pH ~ 5) water drawn from wells deposits a black manganese-containing
solid on standing in toilet bowls. What is the chemical formula of the black solid ? What is the corresponding
species of manganese found in well water while it is still underground ?
2+
d) Which of the two species of nitrogen oxidize Mn (s) to Mn (aq) according to the Pourbaix diagrams ? Which one
of this actually (in practice) does not oxidize Mn (s) at room temperature ?
+
e) Which of the following compounds oxidize NH3 (aq) or NH4 (aq) to N2 (g) ?
2+ 2- -
Mn, Mn(OH)2, Mn , Mn3O4, Mn2O3, MnO2, MnO4 , MnO4
We shall discuss the properties of the two salts ammonium permanganate, NH4MnO4, and ammonium manganate,
(NH4)2MnO4, which is a rarely known salt.
IChO Peruggia 93
131I is a radioactive isotope of iodine (e- emitter) used in nuclear medicine for analytical procedures to determine
thyroid endocrine disorders by scintigraphy. The decay rate constant, k, is 9.93 10-7 s-1.
a) Write Lewis structures for the molecules SCl2, SO3, SO2ClF, SF4, and SBrF5. Show all non-bonding electrons.
b) Carefully draw the geometries of the same 5 molecules. (Disregard small deviations from "ideal" angles.)
c) A compound, consisting of sulfur (one atom per molecule), oxygen, and one or more of the elements F, Cl, Br, and
I, was examined. A small amount of the substance was reacted with water. It was completely hydrolyzed without
any oxidation or reduction, and all reaction products dissolved. 0.1M solutions of a series of test reagents were
added to separate, small portions of a diluted solution of the substance.
State which ions were being tested for in the following tests:
iv) Addition of KMnO4 to an acidified solution of the substance followed by addition of Ba(NO3)2
v) Addition of Cu(NO3)2.
i) A yellowish precipitate
ii) No precipitate
iii) No visible reaction
iv) The main features were that the characteristic colour of KMnO4 disappeared, and a white precipitate was
formed upon subsequent addition of Ba(NO3)2
v) No precipitate
Write the formulae of the possible compounds, taking the results of these tests into account.
e) Finally, a simple quantitative analysis was undertaken: 7.190 g of the substance was weighed out and dissolved in
water to give 250.0 mL solution. To 25.00 mL of this solution, nitric acid, and enough AgNO3 to secure complete
precipitation, was added. The precipitate weighed 1.452 g after washing and drying. Determine the formula of the
compound.
f) Write the equation describing the reaction of the compound with water.
If you have not arrived at a formula for the compound, use SOClF for this equation.
b) Calculate the pH of the solution during the titration in a), after 0 mL, 9.65 mL, 19.30 mL and 28.95 mL of sodium
hydroxide have been added. Disregard any volume change during the reaction of ammonia gas with hydrochloric
acid.
d) State the pH range of the indicator which could be used for the back titration.
e) The Kjeldahl method can also be used to determine the molecular weight of amino acids. In a given experiment, the
molecular weight of a naturally occurring amino acid was determined by digesting 0.2345 g of the pure acid, and
distilling the ammonia into 50.00 mL of 0.1010 M hydrochloric acid. A titration volume of 17.50 mL was obtained
for the back titration with 0.1050 M sodium hydroxide. Calculate the molecular weight of the amino acid based on
one and two nitrogen groups in the molecule, respectively.
3. Physical chemistry
hc h
E = where =
p
a) Give a general expression for possible wavelengths of the electron as a function of the length l.
In the 'particle in the box' model, only the variations in the kinetic energy of the electrons are considered.
b) Give an expression for the possible energies that electrons in the molecule can have (as a function of l).
c) Show that for a chain of length l with k electrons, the longest wavelength absorption occurs at:
8 mcl 2
= for even values of k
h(k +1)
d) Derive an expression for the wavelength of the first electronic transition as a function of the number of C-atoms for
even values of n.
e) Calculate the minimum number of C-atoms (conjugated systems) to obtain a visible colour. C-C bond length is 142
pm.
7 11 15
1 9 13 O
2 6 8 10 12 14
59 39
3
4 5
The C-atoms 7 through 12 are planar. The angle between the bonds C5-C6, C7-C8, C11-C12 and C13-C14 is about 39.
According to the 'particle in the box' theory fragment C7 through C12 should absorb at about 213 nm. In reality the
absorption of retinal occurs at 308 nm.
f) Give a reason for the longer wavelength that is observed in praxis using the above mentioned theories.
g) When retinal is bound to opsin to form rhodopsin, the absorption occurs around 600 nm. Which atoms must be
forced into one plane by the protein ? Show by calculation that it's true.
3
a) Calculate the air intake of the engine (m /s). The gasified fuel and air are introduced into the cylinder when its
volume is largest until the pressure is 101.0 kPa. Temperature of both incoming air and fuel are 100 C. Air contains
21.0 % (by volume) of O2 and 79.0 % of N2. It is assumed that 10.0 % of the carbon forms CO upon combustion and
that nitrogen remains inert.
b) The gasified fuel and the air are compressed until the volume in the cylinder is at its smallest and then ignited.
Calculate the composition (% by volume) and the temperature of the exhaust gases immediately after the
combustion (exhaust gases have not yet started to expand). The following data is given:
c) Calculate the final temperature of the leaving gases assuming that the piston has moved to expand the gases to the
maximum volume of the cylinder and that the final gas pressure in the cylinder is 200 kPa.
d) To convert CO(g) into CO2(g) the exhaust gases are led through a bed of catalysts with the following work function:
n(CO) 1 n(CO) T
= k v e- T 0
n(CO2 ) 4 n(CO2 )1
where [n(CO) / n(CO2)]1 is the molar ration before the catalyst, v is the flow rate in mol / s and T the temperature of the
gases entering the catalyst (the same as the temperature of the leaving exhaust gases). T0 is a reference temperature
(373 K) and k is equal to 3.141 s / mol. Calculate the composition (% by volume) of the exhaust gases leaving the
catalyst.
a) Draw the first four periods of the Flatlandian periodic table of the elements. Number them according to their nuclear
charge. Use the atomic numbers (Z) as symbols of the specific element. Write the electron configuration for each
point.
b) Draw the hybrid orbitals of the elements with n = 2. Which element is the basis for the organic chemistry in
Flatlandia? Find the Flatlandian analogous for ethane, ethene and cyclohexane. What kind of aromatic ring
compounds are possible ?
c) Which rules in Flatlandia correspond to the octet and the 18-electron rules in the three dimensional world?
d) Predict graphically the trends in the first ionization energies of the Flatlandian elements with n = 2. Show
graphically how the electronegativities of the elements increase in the Flatlandian periodic table.
e) Draw the molecular orbital energy diagrams of the neutral homonuclear diatomic molecules of the elements with n =
2. Which of these molecules are stable in Flatlandia?
f) Consider simple binary compounds of the elements (n=2) with Z=1. Draw their Lewis structure, predict their
geometries and propose analogs for them in the three dimensional world.
g) Consider elements with n3. Propose an analog and write the chemical symbol from our world for each of these
Flatlandian elements. On the basis of this chemical and physical analog predict which two-dimensional elements are
solid, liquid or gaseous at normal pressure and temperature.
IChO Halle 1989
A mixture of gases containing mainly carbon monoxide and hydrogen is produced by the reaction of alkanes with
steam:
CH 4 + 0.5 O2 CO + 2 H2 H = - 36 kJ mol-1
CH 4 + H 2 O CO + 3 H 2 H = 216 kJ mol-1
a) Using equations (1) and (2) write down an overall reaction (3) so that the net enthalpy change is zero.
b) The synthesis of methanol from carbon monoxide and hydrogen is carried out either
6 6
1. in two steps, where the starting mixture corresponding to equation (3) is compressed from 0.110 Pa to 3 10
Pa, and the mixture of products thereof compressed again from 3 106 Pa to 6 106 Pa
or
2. in one step, where the mixture of products corresponding to equation (3) is compressed from 0.1 106 Pa to 6
6
10 Pa.
Calculate the work of compression, Wa, according to the two step reaction for 100 ml of starting mixture and
calculate the difference in the work of compression between the reactions 1. and 2.
Assume for calculations a complete reaction at constant pressure. Temperature remains constant at 500 K, ideal gas
behaviour is assumed.
To produce hydrogen for the synthesis of ammonia, a mixture of 40.0 mol CO and 40.0 mol of hydrogen, 18.0 mol of
carbon dioxide and 2.0 mol of nitrogen are in contact with 200.0 mol of steam in a reactor where the conversion
equilibrium
CO + H2 O
_
CO2 + H2 is established.
is self-sustaining at 1350 K, i.e that the heat produced is sufficient to bring the reactants from ambient temperature
to the heat temperature.
b) Starting with a stoichiometric mixture of one mole zinc blende only containing ZnS and a necessary quantity of air
at 298 K, calculate the temperature to which the mixture would raise at 1350 K under standard pressure. Is the
reaction self-sustaining? Air is considered to be a mixture of oxygen and nitrogen in a volume ration equal to 1:4.
c) In fact, zinc blende is never pure and always mixed with a gangue consisting of silica SiO2. Assuming that the
gangue does not react, calculate the minimum ZnS content of the mineral so that the reaction would be self-
sustaining. Give the answer is grams of ZnS per hundred grams of zinc blende.
Data:
-1 -1
Standard molar heat capacities (in J K mol ):
ZnS(solid): 58.05 ZnO(solid): 51.64
SO2(gas): 51.10 O2(gas): 34.24
N2(gas): 30.65 SiO2(solid): 72.50
-1
Molar masses (in g mol ): ZnS: 97.5
SiO2: 60.1
mechanism 1:
NO2NH2
k1
N2O + H2O (rate limiting step)
mechanism 2:
/
NO2NH2 + H3O
+
k2 / k2
NO2NH3+ + H2O (rapid equilibrium)
NO2NH3
+
k3
+
N2O + H3O (rate limiting step)
mechanism 3:
/
NO2NH2 + H2O
k4 /k4 - +
NO2NH + H3O (rapid equilibrium)
NO2NH
-
k5
N2O + OH- (rate limiting step)
H3O+ + OH-
k6
2 H2O (very fast reaction)
answer.
c) Show the relationship between the experimentally observed rate constant and the rate constants in the selected me-
chanism.
d) Show that hydroxyl ions catalyze the decomposition of nitramid.
e) The decomposition is studied in a buffered solution of constant volume V at a constant temperature by measuring
the partial pressure of the gas N2O, insoluble in water, in a constant volume of the same value V above the solution.
The following results are obtained:
t(min) 0 5 10 15 20 25
p(Pa) 0 6800 12400 17200 20800 24000
After a sufficiently long time, the pressure stabilises at 40000 Pa. Express the pressure P as a function of time and the
+
constant k` such that k` = k / [H3O ]. Verify graphically that the kinetic law is confirmed by these experimental results.
Calculate k', giving its units.
a) Calculate the energy differences between n = 2 (first excited state) and n = 1 (ground state) and between n = 7 and n
= 1.
b) In what spectral range are the Lyman series lying ?
c) Can a single photon emitted in the first and/or sixth line of the Lyman series ionize
1) another hydrogen atom in its ground state ?
2) a copper atom in the Cu crystal ?
-19
The electron work function of Cu is Cu = 7.44 10 .
d) Calculate the de Broglie wavelength of the electrons emitted from a copper crystal when irradiated by photons from
the first line and the sixth line of the Lyman series.
a) With a diagram, show the bonding present in NO2 (g) using the concept of resonance if necessary. Use dots to
represent electrons.
b) Show, with bonding diagrams, how two molecules of NO2 (g) combine to give a molecule of N2O4 (g).
o
c) At 298 K, the G of formation for N2O4 (g) is 98.28 kJ, whereas for NO2 (g) it is 51.84 kJ. Starting with one mole
of N2O4 (g) at 1.0 atm and 298 K, calculate what fraction will be decomposed if the total pressure is kept constant at
1.0 atm and the temperature is maintained at 298 K.
o
d) If H for the reaction N2O4 (g) 2 NO2 (g) is 53.03 kJ, at what temperature would the fraction of N2O4
decomposed be double the one calculated in part c) ?
4 -1
e) The dissociation of N2O4 (g) to give NO2 (g) is a first order process with a specific rate constant of 5.3 10 s at
298 K. Starting with an initial concentration of 0.10 M, how many seconds would it take for 20 % of the original
N2O4 to decompose ?
6 -
f) The association of NO2 (g) to give N2O4 (g) is a second-order process with a specific rate constant of 9.8 10 L mol
1 -1
s at 298 K. Calculate the concentration equilibrium constant, Kc, at 298 K for the reaction 2 NO2 (g) N2O4 (g)
a) Calculate the concentration, in mol/l, of CO2 dissolved in distilled water equilibrated with the atmosphere in the
year 2020. What is its pH-value ?
Data:
-1 -1
Henry's Law constant for CO2 at 298 K: 0.0343 l mol atm
Thermodynamic values, in kJ/mol at 298 K are:
f f
Go Ho
CO2 (aq) -386.2 -412.9
H2O (l) -237.2 -285.8
-
HCO3 (aq) -587.1 -691.2
+
H (aq) 0.00 0.00
IChO Peruggia 93
Poisoning by carbon monoxide produced by ill-adjusted heating systems is a serious problem. In a methane burner the
following reactions occur:
a) Calculate the equilibrium constants of both reactions at T = 1500 K, assuming that the values of Ho and So are
independant of temperature.
b) Find the relationship between the mole numbers of oxygen and carbon monoxide at equilibrium (T = 1500 K, P =
1 atm) when air is admitted into the burner in such amount that the mole ration CH4/O2 is 2:1. Assume the
following volume composition for air: 80% N2 and 20% O2. Make the approximation that nCH4 = 0 at equilibrium
and justify it on the basis of the answers to question a).
c) Calculate the equilibrium mole fraction (x) of CO in the conditions given in b). Assume that the mole fraction of
CO is very small in comparison with that of CO2 and consequently the total number of moles does not appreciably
vary during the combustion. Justify this assumption.
d) Repeat the calculations of items b) and c) assuming that twice the amount of air (compared to the conditions
of questions b) is admitted into the burner (4 mol O2 / 1 mol CH4).
e) Calculate the concentrations of CO (expressed as ppm by volume) in the fumes after condensation of water
vapour under the conditions of questions b) and d), assuming that the composition does not change during the
cooling from 1500 K to room temperature and neglecting the contributions of water vapour in the composition of
the gas phase.
a) This suggests that the conditions on the Earth, when platinum minerals were formed, were:
b) What are G and Kp for the formation of platinum(IV) oxide at 1 atm oxygen pressure and 650 .C?
The preparation of platinum(IV) oxide involves boiling a solution which contains hexachloroplatinate(IV) ions with
sodium carbonate. In this process PtO2.nH2O is formed and is subsequently converted by filtration and heat
treatment to platinum(IV) oxide. In the following we assume n=4. PtO2.4H2O (or Pt(OH)4.2H2O) can be dissolved
in acids and strong bases.
c) Write the balanced equations for the preparation of platinum(IV) oxide according to the procedure given above.
d) Write the balanced equations for the dissolution of PtO2.4H2O in both hydrochloric acid and sodium hydroxide.
Platinum is mainly found in nature as the metal (in a mixture or alloyed with other precious metals).
Hexachloroplatinate(IV) ions are formed by dissolving platinum in aqua regia. Aqua regia is a mixture of concentrated
hydrochloric and nitric acids in proportion 3:1. Upon mixing, this forms nitrosyl chloride (NOCl) and atomic chlorine.
The latter is believed to be the active dissolving component.
The hexachloroplatinate(IV) ions can be precipitated as diammonium hexachloroplatinate(IV). By thermal
decomposition of this compound, finely powdered platinum and gaseous products are formed.
e) Write the balanced equations for the formation of aqua regia and its reaction with platinum.
f) Write the balanced equation for the thermal decomposition of diammonium hexachloroplatinate(IV) at elevated
temperature.
From diammonium hexachloroplatinate(IV) we can prepare Pt(NH3)2Cl2 which occurs in the cis (Hfo= -467.4 kJ/mol,
Gfo =-228.7 kJ/mol) and trans Hfo = -480.3 kJ/mol, Gfo = -222.8 kJ/mol) forms.
1. linear ?
2. planar ?
3. tetrahedral ?
4. octahedral ?
h) Indicate whether the cis or trans isomer is thermodynamically more stable. If you choose cis, mark [ 1 ] on the
answer sheet. If you choose trans, mark [ 2 ].
Platinum is used as a catalyst in modern automobiles. In the presence of the catalyst, carbon monoxide Hfo = -110.5
kJ/mol, Gfo = -137.3 kJ/mol) reacts with oxygen to form carbon dioxide Hfo = -393.5 kJ/mol, Gfo = -394.4 kJ/mol).
I) Is the reaction spontaneous at 25 C? [ 1 ] yes or [ 2 ] no. Is the reaction endothermic or exothermic? If you choose
endothermic, mark [ 1 ] on the answer sheet. If you choose exothermic, mark [ 2 ]. Calculate So for the reaction.
Determine whether the entropy of the reaction system [ 1 ] increases or [ 2 ] decreases.
j) Derive an expression for the temperature dependence of the equilibrium constant in this case.
The overall catalytic reaction is simple, whereas the reaction mechanism in the gas phase is very complicated, with a
large number of reaction steps. With platinum as the catalyst the significant reaction steps are:
A one-dimensional energy-diagram for the platinum catalyzed oxidation of carbon monoxide to dioxide can be
represented as:
[Image]
b) Determine how much heat must be added to the gas during the process given under a).
c) The gas will perform less work in an adiabatic expansion than in an isothermal expansion. Is this because the
adiabatic expansion is characterized by (check the square you think is most important).
1. The volume of the gas is constant
2. The expansion is always irreversible
3. No heat is supplied to the gas
d) The cyclic process shown schematically in Figure 1 shows the four steps in a refrigeration system with an ideal gas
as working medium. Identify the isothermal and adiabatic steps in the process. Here, TH and TC represent high and
low temperature, respectively. Specify for each step whether it is adiabatic or isothermal.
4. Technical chemistry
The total heat used at each of the two distillations is 3q J/mol (of the top product). Apart from distillation columns
(each with its own evaporator and condenser) the pieces of apparatus shown of Fig. 5 are available.
cooler/condenser
heater/evaporator
R reactor
a) Draw a flow diagram of the process in which all flows are given (flow sheet) and in which the starting materials are
used as efficiently as possible using as few pieces of apparatus as possible.
b) Express the equilibrium constant in terms of the degree of conversion and of total pressure for the case that the feed
to the reactor is stoichiometric. What is the value of the degree of conversion when total pressure is 0.100 MPa?
c) Number all flows. Calculate the composition of each flow in mol/s for a rate of production of 1 mole of C per
second under the conditions of part b.
d) In what respect can the reaction conditions influence the composition of the mixture that leaves the reactor? (Refer
to question b)
e) The process requires energy. For the conditions of b explain where energy should be supplied in the flow diagram
drawn in part a. Derive an expression for the total energy needed.
a) What is the amount of carbohydrate remaining in the sludge measured in kg per day ?
b) Given the heat of combustion of methane (- 882 kJ / mol), calculate the amount of energy that can be produced by
combustion of the methane formed.
c) Knowing the concentration of the carbohydrate in the waste water to be 250 mg/ l, calculate the daily amount of
3
waste water processed in the plant in m of water per day.
IChO Halle 89
Sulphur dioxide is removed from waste gases of coal power stations by washing with aqueous suspensions of calcium
carbonate or calcium hydroxide. The residue formed is recovered.
Information
The acidity constant Ka is equal to Ka = 10-2.25 mol/l. Assume ideal gases and a constant temperature of 0 C at
standard pressure. M[CaCO3] = 100 g/mol; M[CaSO4] = 172 g/mol
Two different types of reactors are examined: continuous plug flow reactor and continuous stirred reactor (Fig. 6): In
the continuous plug flow reactor, reactants are introduced and mixed in the inlet of the reactant (F1, F2); each slice of
reaction medium (grey shaded zone in the diagram) moves along the inside without mixing with the others and exits
from the reactor (F3). When the flow has stabilized, concentrations and conditions are time-independent but dependent
on the location in the reactor. In the continuous stirred reactor, stirring is perfect and instantaneous. When the flow is
stabilized, concentration and conditions are time-independent and identical at every point of the reactor.
F1 reactor
F3
F2
displacement
F1 stirring
F3
F2
reactor
Fig. 6 Continuous plug flow and continuous stirred reactor
Y = - d([C6H12])/d([C6H6]).
The proportion of benzene already hydrogenated is given by p = [C6H12]/([C6H12]+[C6H6]). The relationship between
p and Y is shown in Fig. 7.
The aim is to hydrogenate almost all the benzene, i.e. 0.9 p 1 with the best mean yield
Y = - ([C6H12])/([C6H6]).
a) What is the value of p in a continuous stirred reactor leading to the maximal mean yield of hydrogenation? What is
the maximal value of Y?
b) For a continuous plug flow reactor, give a rough value of Y for 0.9 p 1:
Y = 0.97, 0.98, 0.99 or 1.00 ?
c) Represent by grey shading the quantities of benzene lost in installation P (plug flow reactor) and installation MP
(stirred reactor + plug flow reactor).
d) Give the amount of benzene annually lost in installation P and MP assuming an annual consumption of 100000 tons
of benzene.
y
1.00
0.99
0.98
0.97
0.96
0.0 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.0
[C6H12]/([C6H12]+[C6H6])
Sulphuric acid is produced by catalytic oxidation of SO2 to SO3, absorption of SO3 in concentrated sulphuric acid for-
ming oleum (containing 20% SO3 by mass) and appropriate dilution hereafter. The gas leaving the catalyst chamber
contains nitrogen, oxygen, a trace of SO2 and 10 % (by volume) of SO3.
SO3 is converted into sulphuric acid (98 % by mass) and/or oleum.
3
a) Assuming that oleum is the only product formed, calculate the mass of water which is required for 1000 m of gas
leaving the catalyst chamber (273 K, 101.3 kPa) and determine the mass of oleum produced hereby.
b) Assuming that only 98 % sulphuric acid is produced, calculate the necessary mass of water and the mass of product
produced thereby.
c) In the industry both 98 % sulphuric acid and oleum are produced in a mass ratio of x = m1/m2, where m1 denotes
the mass of oleum, m2 the mass of 98 % sulphuric acid. Find an expression y = f(x) to describe the relation between
3
the mass of water consumed for 1000 m gas. Show that the results of a) and b) are in good agreement with your
mathematical expression.
5. Organic chemistry
O O
O
OH HO
O A O B O C
-2
-3
0 1 2 3 4 5 6 7 pH
Fig. 8 Relation between the rate constant khyd and pH for the hydrolysis of A
The relation between the rate constant khad and pH for the hydrolysis of A at 39 C is shown in figure 8.
Further observations
Addition of water to the iso-imide C gives a rapid reaction, which initially yields A. Subsequently, hydrolysis of A
occurs.
The amid carbonyl group in A is labelled with 13C and the hydrolysis is allowed to take place in H218O at pH = 2 and
39 C. The diacid formed upon hydrolysis is isolated, converted into the di-silver salt and completely decarboxylated
with bromine in a anhydrous reaction medium. The formed carbon dioxide is a mixture of particles of masses 44, 45, 46
and 47 which are formed in equal amounts.
a) Give the spatial structures and Fischer projection of L - (+) - lactic acid and its dilactide
b) Sketch the structure of the polylactide discussed above (at least three units). What is its tacticity (iso-, syndio- or
atactic) ?
c) Draw the isomeric dilactides formed out of racemic lactic acid. Show the configuration of the chiral centres.
L - (+) - lactic acid is used for the preparation of the herbicide Barnon that is used against wild oats. In this case (+) -
lactic acid is esterified with 2 - propanol and then the hydroxyl group is treated with methanesulfonyl chloride. The
product is then submitted to a SN2 - reaction with 3 - fluoro - 4 - chloro - phenylamine, where the methanesulfonate
-
group leaves as CH3SO3 . Finally a benzoyl group is introduced with the help of benzoyl chloride.
O
Mg/abs. ether 1. PBr3 NaCN
A B C D E
2. H2O
H2O/H2SO4 Friedel-Crafts H2
SOCl2
E F G H I
heat AlCl3 cat.
conc. H2SO4
I indene
heat
OH HO HO OH
HO HO OH OH
OH OH HO HO
OH OH HO HO
NH+ N + H+ N + H+
A B C
A common compound A is prepared from phenol and oxidized to compound B. Dehydration of A with H2SO4 leads to
compound C and treatment of A with PBr3 gives D. In the mass spectrum of D there is a very strong peak at m/e = 83
(base peak) and two molecular ion peaks at m/e 162 and 164. The ratio of intensities of the peaks 162 and 164 is 1.02.
Compound D can be converted to an organomagnesium compound E which reacts with a carbonyl compound F in dry
ether to give G after hydrolysis. G is a secundary alcohol with the molecular formula C8H16O.
a) Outline all steps in the synthesis of G and draw the structural formulae of the compounds A- G.
b) Which of the products A - G consist of configurational stereoisomeric pairs ?
c) Identify the three ions in the mass spectrum considering isotopic abundances given in the text.
100
50
M+
0
180 190 200 210 220 230 240 250 260
a) Draw the structural formulae of all isomeric cyclobutanedicarboxylic acids and give the corresponding systematic
names.
b) There are three stereoisomers, I,II and III. Draw perspective stereoformulas of I, II and III indicating the relative
configuration of each molecule.
c) Which pairs of stereoisomers I,II and III are diastereoisomers and which are enantiomers of each other ?
d) Which reaction can be used to determine the relative configuration of diastereoisomers?
e) How may the enantiomers of cyclobutane-1,2-dicarboxylic acid be separated ?
f) Indicate the absolute configuration of each asymmetric centre on the structures of the stereoisomers I, II and III
using the Cahn-Ingold-Prelog rules (R,S system).
g) Draw the structures of Z-octadec-9-enoic acid (oleic acid), octadecanoic acid (stearic acid) and hexadecanoic acid
(palmitic acid). Using the these three fatty acids draw a possible structure of a triacyl glyceride.
h) Write the equations for the hydrolysis reactions of your triacyl glyceride in NaOH(aq). Give the corresponding
mechanism.
i) Which of the following fatty acids, C21H43COOH, C17H35COOH or C5H11COOH is the least soluble in water.
k) Phospholipids are an important class of bio-organic compounds. Draw the structure of the phophatic acid derived
from your triacyl glyceride and mark the hydrophilic and hydrophobic groups.
l) Draw two possibilities for the association of six identical molecules of phopholipids in water.
m) Biomembranes consist of a phospholipid bi-layer. Draw such a structure. What other biomacromolecules are
contained in such biomembranes?
a) Give a simplified equation for the preparation of methyl 4 - chlorobenzoate starting from benzene and all necessary
inorganic substances. Diazomethane must be used in your synthesis.
b) How can -butyrolactone be converted into 4-hydroxybutanoic acid (K)? Convert K into 4-chlorobutanoyl chlorid
(L)!
Methyl 4 - chlorobenzoate is treated with an excess of vinylmagnesiumbromide in anhydrous ether. M is obtained after
hydrolysis. Treating M with an excess of HBr in anhydrous conditions in the presence of benzoyl peroxide, N is
obtained. N reacts with ammonia to form 4-(4-chlorophenyl)-4-hydroxypiperidine (O).
c) Write down the structure of M, N and O and indicate the mechanism of the reaction leading to M.
d) In the presence of moderate amounts of aluminium chloride, L reacts with fluorobenzene to yield mainly a ketone P
(C10H10OFCl). Sketch the structure of P and indicate the mechanism.
e) Give a chemical and physical test method for the determination of the carbonyl group. How can you make sure that
the carbonyl group does not belong to an aldehyde group?
f) P reacts with O on a 1 to 1 mole basis, in basic media, to give H that contains only one chlorine atom on the
aromatic ring. Give the structure of H which is haloperidol.
1
g) State the multiplicity of each resonance in the H NMR spectrum of K. Assume that all coupling constants between
protons and adjacent carbons are identical.
a) Determine the molecular formula and the molar mass of A, B and Y and show its structure.
b) Give an equation for the reaction of Y with bromine.
In the catalytic hydrogenation of 13.6 g of X, 0.2 mole of hydrogen was absorbed. Ozonolysis of X followed by mild
reduction yielded compound Z (80.0% C, 8.0% H).
Compound Z gave a positive reaction with Fehling's solution. Mild oxidation of Z gave an acid C of which a solution
was titrated with aqueous KOH. 0.116 g of C neutralized 0.001 mol KOH.
In the iodoform probe 2.90 g of C yielded 9.85 g of iodoform. In addition the alkaline filtrate yielded compound E
upon acidification.
d) What is the molar mass of C and what functional groups are present in Z?
When heated, E loses water to form F. Both E and F react with an excess of acidified ethanol to G (C8H14O4).
e) Sketch the structures of C, E, F, G and Z and give an unbalanced reaction scheme for EFG.
X exists in isomeric forms which are stereoregular. Show the structure (containing at least 3 monomer units) for two
possible stereoisomers of X.
Information:
a) Give the structural formulas of A, B, C, D, E, F, G1, G2 and G3. Explain your choice for the halogen.
b) Draw and label stereo-formulas of the rotational isomers of D for = 0, /2, 3/2 where denotes the dihedral
or torsional angle in radians and = 0 describes the configuration with maximal energy.
c) Draw profiles of the energy changes as a function of the angle of rotation around the C-C bond for compounds C and
D.
d) Give G1, G2, G3 in their increasing difficulty of racemization. Explain your answer.
e) Draw stereo-formulas of the enantiomers of G3.
f) Suggest a chemical reaction or a biological method by which compounds like these can be destroyed.
OH
O O O
OH
O
HO
O
a) Give the structure of geraniol (A), B and the two bromides of formula C10H17Br
b) Indicate which of the two bromides is formed in greater proportions.
IChO Pittsburgh 1992
Complete the following reactions and indicate their stereoselctivity (cis/trans) where appropriate.
a) O
+ NaOH
O
isoamyl acetate, bee alarm pheromone
O
b) I2 / NaOH
O
NaBH4
CH3CH2OH
O
CH3CH2MgBr H3O+
c) O3
Zn, H3O+
O3
H2O2, H3O+
d)
H2O / H2SO4
OH
Na2Cr2O7, H2SO4
CH3COOH
e)
Br2/CCl4 HBr
(i) (iv) peroxide
H3O+ H2, Pt
(iii) (vi)
IChO Peruggia 93
Frontalin is a pheromone of the western pine beetle with a composition C 67.58%, H 9.92%, O 22.50%. It is an acetal
that can be prepared starting from sodium diethylmalonate and 3-chloro-2-methylpropene. The resulting product A is
hydrolized by conc. potassium hydroxide and then decarboxylated by treatment with hot acetic acid to give a compound
B. The latter reacts with aq. NaHCO3 (gas evolution is observed) as well as with cold aq. KMnO4 which turns to a
brown color. The compound B is then converted by LiAlH4 into C (C6H12O).
Treatment of C with p-toluenesulfonyl chloride in pyridine and then sodium cyanid in dimethylsulfoxide affords D
(C7H11N). The subsequent reaction of D with methylmagnesium iodide, followed by hydrolisis, yields E (C8H14O). E
shows IR absorption at ca. 1700 cm-1. The epoxidation of E with metachloroperbenzoic acid then affords F
(C8H14O2) which, by treatment with diluted acids is converted to frontalin acetal G.
IChO Peruggia 93
By treatment with a optically active hydroborating agent (R2*BH) and subsequent oxidative work-up, 1-
methylcyclopentene affords a mixture of aclohols that rotates the plane of polarized light. [H.C.Brown, J.Org.Chem.,
47, 5074, 1982]
(CH3)2CHCH(CH2CH3)(CH2CH2CH3)
1. 3-Isopropylhexane
2. 2-Methyl-3-propylpentane
3. Ethyl isopropyl propyl methane
4. 3-Hexylpropane
5. 3-Ethyl-2-methylhexane
b) How many isomers, including stereoisomers, containing only saturated carbon atoms, are there for C5H10?
c) Which one of the following compounds has a dipole moment significantly different from zero?
CN
OH
Br CH3
ClH2C CH2Cl NH
ClH2C CH2Cl HN
H3C Br
HO
NC CN
A B C D E
O
Cl O
Cl
A B C
CH3
H3C
CH3 CH3
H2C H3C
H3C
CH2
D E
e) Which of the following five options is the correct order of relative stabilities of cations a, b and c as written below?
Write the most stable first.
+ +
a b c
1. a > b > c
2. b > c > a
3. c > a > b
4. a > c > b
5. b > a > c
f) What is the correct stereochemical descriptor of the optically active compound drawn below?
Br
H3C
H3C
g) All the molecules drawn below are neutral compounds. Which one does not contain a formal positive charge and a
formal negative charge?
1. (CH3)3N-B(CH3)3
2. (CH3)2N-O-CH3
3. CH2=N=N
4. (CH3)3N-O
5. F3B-O(CH3)2
h) Which one of the IR-spectra shown on the next page corresponds to that of benzaldehyde?
[Image]
a) Based on the above information draw the structural formulae for the compounds A-F and give the overall reaction
scheme, including the 2,4-DNP reaction and the products of the Tollen's and iodoform reactions.
b) Draw C in an R-configuration. Transform this into a Fischer projection and state whether it is a D- or L-
configuration.
6. Biochemistry
a) Give the base sequence of the complementray strand in the 5' - 3' direction and indicate with arrows the location
where the hydrolysis by Cla I would occur.
b) How often on average will this sequence occur in one strand of DNA molecule of 105 base pairs? You can assume
that the four bases occur equally often and that they randomly distribute in the two chains.
100
DNA treated with
ClaI
TaqI
50
0
260 280 300 320 340
T (K)
Fig. 111 Cleavage curve for DNA treated with ClaI and TaqI
Taq I hydrolyses a long double strand DNA molecule into fragments which are on average 256 base pairs long. The 3'
end of these fragments treated by cleavage turns out to be a thymine(T)- and the 5' end a cytosine(C) -end.
The DNA of a phage which occurs as a close circle contains only 5'- pApTpCpGpApT- 3' sequence in each of the two
strands. After treatment with ClaI an equilibrium is established: circular DNA linear DNA
e) Give a schematic drawing of the circular and linear molecules. Indicate the bases adjacent to the cleaning site in
both strands. Indicate also the 3' and 5' ends. In Fig. 11 the percentage of linear DNA is given as a function of
temperature, measured in a solution of 0.15 M NaCl buffered with citrate at pH = 6.5. With Taq I as cleavage
enzyme, the same curve is obtained.
f) Is the reaction as written endothermic or exothermic? Explain your answer.
g) Show, considering the information given, which of the two base sequences of the answer to d) is the correct one.
h) What would look the curve for Taq I like if the recognition pattern had been the other possibility of d) ?
A large DNA molecule is cut into fragments with the aid of Cla I. One fragment is isolated, purified and mixed 1:1 with
phage DNA which was also cleaved with Cla I. Thereby recombinant molecules can be formed through the reaction:
phage-DNA + fragment DNA recombinant-DNA
i) Would the enthalpy of this reaction be positive, negative or about zero ?. Explain your answer.
k) Which combination of temperature, DNA concentration and ionic strength (high or low in each case) will give the
maximum percentage of recombinant molecules ?
a) Write down structures for all the possible stereoisomers obtained by catalytic deuteration of maleic and fumaric
acid. How many isomers are there. Indicate those that are optically active. Establish a stereochemical relationship
between them (compare the isomers two by two). Which is the most stable conformation ? Draw Newman
projections.
b) The proportion of dideuterated fumarate (obtained when each of the 2-3 dideuterated succinates is submitted to the
enzymatic reaction) is 4 % when using fumaric acid as starting molecule, but 48.5 % when using maleic acid.
c) On the basis of the Newman projections of the most stable conformations of each isomere, complete the following
table: