9701_s12_4_2_qp
9701_s12_4_2_qp
9701_s12_4_2_qp
CHEMISTRY 9701/42
Paper 4 Structured Questions May/June 2012
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.
Total
IB12 06_9701_42/5RP
© UCLES 2012 [Turn over
2
For
Section A Examiner’s
Use
Answer all the questions in the spaces provided.
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(iii) Suggest a reason why of the Mg2+ ion is greater than of the Ca2+ ion.
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(iv) Suggest why it is impossible to determine the enthalpy change of hydration of the
oxide ion, O2–.
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[5]
(b) The enthalpy change of solution for MgCl 2, (MgCl 2(s)), is represented by the
following equation.
Describe the simple apparatus you could use, and the measurements you would make,
in order to determine a value for (MgCl 2(s)) in the laboratory.
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By constructing relevant thermochemical cycles, use the above data to calculate a value for
= ....................................... kJ mol–1
= ....................................... kJ mol–1
[3]
(d) Describe and explain how the solubility of magnesium sulfate compares to that of barium
sulfate.
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[Total: 16]
(ii) Suggest one reason why CO is produced in addition to CO2 in some internal
combustion engines.
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(iii) Carbon monoxide can be removed from the exhaust gases by a catalytic converter.
Write an equation for a reaction that occurs in a catalytic converter that removes CO.
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[3]
(b) The standard enthalpy change of formation, , of CO is –111 kJ mol–1, and that of CO2 is
–1
–394 kJ mol .
Calculate the standard enthalpy change of the following reaction.
∆H o = ....................................... kJ mol–1
[2]
(c) Carbon monoxide reacts with a ruthenium(II) chloride complex according to the equation
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(ii) During the reaction, the colour of the solution changes from deep blue to green.
Explain the origin of colour in transition element complexes, and why different
complexes often have different colours.
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[[Ru(H2O)2Cl 4]2–] / mol dm–3 [CO] / mol dm–3 rate / mol dm–3 s–1
(iii) Use these data to determine the order of reaction with respect to each reagent, and
write the rate equation for the reaction.
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There are three possible mechanisms for this reaction, which are described below.
slow
mechanism 1 [Ru(H2O)2Cl 4]2– + CO [Ru(H2O)(CO)Cl 4]2– + H2O
slow
mechanism 2 [Ru(H2O)2Cl 4]2– [Ru(H2O)Cl 4]2– + H2O
fast
[Ru(H2O)Cl 4]2– + CO [Ru(H2O)(CO)Cl 4]2–
slow
mechanism 3 [Ru(H2O)2Cl 4]2– + CO [Ru(H2O)2(CO)Cl 4]2–
fast
[Ru(H2O)2(CO)Cl 4]2– [Ru(H2O)(CO)Cl 4]2– + H2O
(iv) Deduce which of these three mechanisms is consistent with the rate equation you
suggested in part (iii). Explain your answer.
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[10]
[Total: 15]
O OH
OH OH
+ 2H+ + 2e– E o = +0.36 V
O OH
lawsone 1,2,4-trihydroxynaphthalene, A
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(ii) Describe a reaction (reagent with conditions) that you could use to distinguish
lawsone from compound A.
Describe the observations you would make with both compounds.
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(iii) Suggest a reagent that could be used to convert lawsone into compound A in the
laboratory.
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(iv) Draw the structural formula of the compound formed when lawsone is reacted with
Br2(aq).
[6]
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(ii) Construct an equation for this reaction. Use the molecular formulae of lawsone,
C10H6O3, and compound A, C10H8O3, in your equation.
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(iii) When 20.0 cm3 of a solution of compound A was acidified and titrated with
0.0500 mol dm–3 K2Cr2O7, 7.50 cm3 of the K2Cr2O7 solution was needed to reach the
end-point.
Calculate [A] in the solution.
O
O– Na+
NaOH
lawsone
O
C
B
Reacting B with ethanoyl chloride, CH3COCl, produces compound C, with the molecular
formula C12H8O4.
(i) Suggest the identity of compound C, and draw its structure in the box above.
(iii) Suggest a mechanism for the formation of D from B and ethanoyl chloride by drawing
relevant structures and curly arrows in the following scheme.
O
Na+
O–
B + O Cl D
C
CH3
[3]
[Total: 14]
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(b) For each of the following pairs of compounds, predict which compound has the higher
boiling point, and explain the reasons behind your choice.
Use diagrams in your answers where appropriate.
[4]
(c) Briefly explain the shape of the SF6 molecule, drawing a diagram to illustrate your answer.
[2]
[Total: 9]
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[3]
(b) For each of the following pairs of compounds, suggest one chemical test (reagents and
conditions) that would distinguish between them.
State the observations you would make with each compound, writing ‘none’ if appropriate.
NH2 NH2
CH3CH2COCl CH3COCH2Cl
CH3CH2CHO CH3COCH3
[7]
O O
O O
E + F O O
O O
polymer G
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E F
(iii) Suggest the conditions needed to make polymer G from E and F in the laboratory.
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(iv) One of the monomers, E or F, could be changed to make a more rigid polymer of a
similar chemical type to G.
Suggest which of your two monomers could be changed, and suggest a structure for
the new monomer.
[6]
[Total: 16]
6 (a) The table shows the structures of four amino acids found in proteins in the human body.
Complete the table by indicating the type of tertiary interaction each side-chain is most
likely to have when its amino acid is present in a protein chain.
alanine H2NCH(CH3)CO2H
cysteine H2NCH(CH2SH)CO2H
lysine H2NCH((CH2)4NH2)CO2H
serine H2NCH(CH2OH)CO2H
[3]
(b) Metal ions play an important role in the biochemistry of the human body. For each of the
following metal ions, outline one of the places in the body it can be found and its main
role there.
iron ....................................................................................................................................
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potassium .........................................................................................................................
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zinc ...................................................................................................................................
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[3]
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[2]
(d) Cystic fibrosis is a genetic disease caused by a mutation in the DNA sequence resulting
in the production of a faulty version of an important protein which acts as an ion pump in
the cell membrane. This pump controls the flow of ions into and out of cells.
People with the faulty protein show two major symptoms.
● water is retained in cells in the lungs resulting in the formation of a thick, sticky mucous
outside the cells;
● their sweat is very salty.
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(ii) suggest and explain what type of bonding might result in thick or sticky mucous.
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[2]
[Total: 10]
(a) Nuclear magnetic resonance, NMR, arises because protons possess spin which
generates a small magnetic moment. When an external magnetic field is applied the
protons can align with or against the external field. If they are given a small amount
of energy in the radio frequency range each can be ‘promoted’ so that their magnetic
moment opposes the external field.
Two factors can influence the energy required for this promotion. What are they?
(i) ....................................................................................................................................
(ii) ....................................................................................................................................
[2]
(b) A compound, J, has the formula C4H10O. The NMR spectrum of J is shown.
10 9 8 7 6 5 4 3 2 1 0
δ / ppm
(i) Indicate the groups responsible for each peak and hence deduce the structure of J.
structure of J
isomer 1 isomer 2
(c) X-ray crystallography can be useful in gathering information about the structure of large
organic molecules, such as nucleic acids.
(i) Which element will show up most strongly in the X-ray crystallography of a nucleic
acid? Explain your answer.
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(ii) X-ray crystallography will not detect hydrogen atoms. Explain why this is so.
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[2]
[Total: 10]
(a) One of the most widespread developments for delivering a range of pharmaceutical
products has been the use of liposomes. These are artificially created spheres made
from phospholipids which have an ionic phosphate ‘head’ and two hydrocarbon ‘tails’.
A B C
phospholipid liposome
Liposomes have also been used to carry pharmaceuticals such as vitamins and
moisturisers used in cosmetic anti-ageing creams. Otherwise these pharmaceuticals
may be oxidised or dehydrated if exposed to air.
(i) State in which area of the liposome, A, B or C, each of the following types of molecule
would be carried.
(ii) For one of the areas, A, B or C, suggest why this would not be an appropriate place
to carry either molecule.
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[3]
(b) When liposomes are used to carry drugs, their main purpose is to prevent the drug
molecules from being broken down on passage through the digestive system.
(i) Name a functional group present in drug molecules that might be broken down by
acid in the stomach.
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(iii) The drug Sirolimus is used to suppress possible rejection by the body after kidney
transplants.
OH
H 3C
O CH3
N O
H H H
O O O
O
H3C
O H 3C
HO
OH
H 3C
H
CH3 O
O O
H 3C H 3C
CH3
CH3
Sirolimus
Circle two bonds, each in a different functional group that could be broken down in
the digestive system.
[4]
(c) Sirolimus is not very soluble in water, greatly reducing its effectiveness when given by
mouth or by injection. To increase its effectiveness when taken by mouth nano-sized
crystals of the drug combined with poly(ethylene glycol) or PEG (shown below) are
produced.
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(ii) Suggest where on the molecule of PEG the drug would be attached.
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(iii) Why would bonding the drug to a PEG molecule improve its solubility in water?
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[3]
[Total: 10]
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