Cambridge International Advanced Level
Cambridge International Advanced Level
Cambridge International Advanced Level
CHEMISTRY 9701/41
Paper 4 Structured Questions October/November 2014
2 hours
Candidates answer on the Question Paper.
Additional Materials: Data Booklet
Write your Centre number, candidate number and name on all the work you hand in.
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Section A
Answer all questions.
At the end of the examination, fasten all your work securely together. 4
The number of marks is given in brackets [ ] at the end of each question or part
question.
5
Total
IB14 11_9701_41/4RP
© UCLES 2014 [Turn over
2
Section A
The initial rate of this reaction was measured, starting with different concentrations of the two
reactants. The following results were obtained.
(i) Use the data in the table to determine the order with respect to each reactant. Show your
reasoning.
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(ii) Calculate the initial rate in experiment 4. Give your answer to two significant figures.
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(iv) Use the results of experiment 1 to calculate the rate constant, k, for this reaction.
Include the units of k.
● draw two Boltzmann distribution curves, at two different temperatures, T1 and T2 (T2 > T1),
● label the curves and the axes.
(ii) State and explain, using your diagram, the effect of increasing temperature on the rate of
reaction.
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[5]
(c) The compound nitrosyl fluoride, NOF, can be formed by the following reaction.
Suggest equations for the two steps of this mechanism, stating which is the rate determining
slower step.
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[Total: 13]
3d 4s
Ni [Ar]
Ni2+ [Ar]
[2]
(b) The presence of electrons in d orbitals is responsible for the colours of transition element
compounds.
(i) The d orbitals in an isolated transition metal atom or ion are all at the same energy level.
What term is used to describe orbitals that are at the same energy level?
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(ii) Complete the diagram to show the splitting of the d orbital energy levels in an octahedral
complex ion.
energy
(iii) On the axes below, sketch the shapes of one d orbital from the lower energy level and one
d orbital from the higher energy level.
z z
x x
y y
[4]
(c) The octahedral complex [Ni(H2O)6]2+ is green. Explain the origin of the colour of this complex.
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(d) When NH3(aq) is added to the green solution containing [Ni(H2O)6]2+, a grey-green precipitate,
A, is formed. This precipitate dissolves in an excess of NH3(aq) to give a blue-violet solution, B.
Suggest formulae for A and B and write equations for the two reactions producing A and B.
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[Total: 13]
3 (a) Natural phosphorus consists of one isotope, 31P. Chlorine exists naturally as two isotopes, 35Cl
and 37Cl, in the relative abundance ratio of 3 : 1.
(i) The mass spectrum of PCl 3 contains several peaks corresponding to a number of
molecular fragments.
Suggest the isotopic composition of the fragments with the following mass numbers.
101
103
105
(ii) Predict the relative ratios of the peak heights of the three peaks corresponding to these
fragments.
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[4]
(i) Draw a ‘dot-and-cross’ diagram to show the bonding in PCl 5. Show the outer electrons
only.
(ii) Draw diagrams to suggest the shapes of [PCl 4]+ and [PCl 6]–.
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[2]
(d) Phosphate ions in water can be removed by adding a solution containing Ca2+(aq) ions, which
form a precipitate of calcium phosphate, Ca3(PO4)2.
Ksp =
Calculate the solubility product, Ksp, of Ca3(PO4)2 at this temperature. Include the units.
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(ii) Explain why the lattice energy of calcium phosphate is less exothermic than that of
magnesium phosphate.
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[3]
[Total: 16]
(i) Construct an equation for the formation of nitronium ions, NO2+, by this method.
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(ii) Complete the scheme to show the mechanism for this reaction. Use curly arrows to show
the movement of electron pairs.
CH3
NO2+
[4]
(b) (i) Describe and explain the relative acidities of chloroethanoic acid and ethanoic acid.
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(ii) Describe and explain the relative acidities of phenol and ethanol.
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[3]
OH
phenyl 2-hydroxybenzoate
Complete the following table about the reactions of phenyl 2-hydroxybenzoate with the three
reagents.
Na
excess
Br2(aq)
excess hot
NaOH(aq)
[6]
[Total: 13]
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H 2N OH
O
aminolaevulinic acid
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(i) Show the mechanism of the first step of this reaction on the diagram. Include all necessary
curly arrows, lone pairs and relevant dipoles.
O
O
intermediate HN OH
H 2N OH
O
O H 3C
H 3C CH2 Br
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[5]
(d) Three reactions of aminolaevulinic acid are shown. Draw the structures of the products W, X
and Y in the boxes below.
O
NaBH4
H 2N OH
O
aminolaevulinic acid CH3COCl
Y
HCl (aq), warm
W
[3]
Draw the structure of the polymer showing two repeat units. The linkages between the
monomer units should be shown fully displayed.
[2]
[Total: 15]
Section B
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(b) (i) A mixture of amino acids can also be separated by thin-layer chromatography.
Identify the mobile and the stationary phases in this type of chromatography.
(ii) What is the process by which thin-layer chromatography can separate a mixture?
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[3]
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(d) Some diseases are caused by a mutation in the DNA base sequence which results in one
amino acid being replaced by another during protein synthesis.
Suggest what changes in the interactions that form the tertiary structure would result from a
mutation that replaced a valine residue with a serine residue.
O O
NH CH C replaced by NH CH C
HC CH3 CH2
CH3 OH
val ser
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[Total: 11]
7 (a) Oseltamivir is an antiviral drug that slows the spread of the influenza (flu) virus.
O
O
O
HN
NH2
O
oseltamivir
Circle two bonds, each in a different functional group, that could be easily hydrolysed in the
body. [2]
(b) Oseltamivir is a chiral drug. This drug is usually taken as a single optical isomer rather than as
a mixture of isomers.
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Explain the meaning of the term competitive inhibitor and state how its action could be
overcome.
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NH2
N
N O O O
N O CH2O P O P O P O–
N
H H H H O– O– O–
HO OH
ATP
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[Total: 7]
(a) (i) Use the ratio of the heights of the M and M+1 peaks to calculate the number of carbon
atoms in a molecule of T.
(b) The NMR spectrum of T given below shows four absorptions. The absorption at 1.8 ppm is a
multiplet and that at 2.5 ppm is a singlet.
11 10 9 8 7 6 5 4 3 2 1 0
δ / ppm
(i) Use this information and your answer to (a)(ii) to deduce the structure of T.
(ii) Describe and explain which type of proton is responsible for each of the absorptions.
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(iii) The absorption at 1.8 ppm is a multiplet and that at 2.5 is a singlet.
State and explain the splitting patterns of the other absorptions, at 0.9 and 3.4 ppm.
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(iv) Describe and explain how the NMR spectrum of T dissolved in D2O would differ from the
one shown.
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[9]
[Total: 12]
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