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Centre Number

Candidate Number

Name

UNIVERSITY OF CAMBRIDGE INTERNATIONAL EXAMINATIONS
General Certificate of Education
Advanced Subsidiary Level and Advanced Level
CHEMISTRY

9701/04

Paper 4 Structured Questions

For Examination from 2007
SPECIMEN PAPER
1 hour 45 minutes

.
Candidates answer on the Question Paper.
Additional Materials: Data Booklet

READ THESE INSTRUCTIONS FIRST
Write your Centre number, candidate number and name on all the work you hand in.
Write in dark blue or black pen.
You may use a soft pencil for any diagrams, graphs or rough working.
Do not use staples, paper clips, highlighters, glue or correction fluid.
Section A
Answer all questions.
Section B
Answer all questions.
You may lose marks if you do not show your workings or if you do not use appropriate units.
At the end of the examination, fasten all your work securely together.
The number of marks is given in brackets [ ] at the end of each question or part question.

This document consists of 17 printed pages and 1 blank page.
 UCLES 2006

[Turn over
2

For
Examiner's
Use

Section A
Answer all the questions in the spaces provided.
1

Bromine can react with methanoic acid according to the following equation.
Br2(aq) +

HCO2H(aq)

→ 2Br-(aq) + 2H+(aq) + CO2(g)

(a) (i) What maximum volume of gas, measured at r.t.p., would be produced by reacting
3.2 g of bromine?

(ii) Suggest how the rate of the reaction might be followed.

[5]
(b) The graph opposite contains information about this reaction.
(i) What evidence is there to suggest that this reaction is first order with respect to
bromine?

(ii) Write a simple equation relating the rate of reaction to the concentration of bromine
under these conditions.

(iii) Calculate the half-life of this reaction.

[5]
[Total : 10]

SP/QP/9701/04
3

© UCLES 2006

9701/04/SP07

For
Examiner's
Use

[Turn over
4
2

For
Examiner's
Use

(a) Define the standard enthalpy change of formation of a compound.

[2]
The standard enthalpy change of formation of SiCl4(g) is –610 kJ mol-1.
The standard enthalpy changes of atomisation of the elements silicon and chlorine are
+338 and +122 kJ mol-1 of atoms respectively.
(b) Use these values to construct an energy cycle to show the formation of SiCl4(g).

[2]
(c) (i) Hence calculate the average bond energy of the Si-Cl bond from these data.

(ii) Suggest why the calculated value is different from the value given in the Data
Booklet.

[2]

 UCLES 2006

9701/04/SP07
For
Examiner's
Use

5
(d) Pure silicon is made by reducing SiCl3H with hydrogen at a high temperature.
(i) Construct a balanced equation for this reaction.

(ii) The bond energy of the Si-Br bond is 298 kJ mol-1. Use this value, and other bond
energy values given in the Data Booklet to suggest whether the reaction between
SiBr3H and hydrogen would be more or less endothermic than the reaction
between SiCl3H and hydrogen.

(iii) State a use of pure silicon.

[4]
[Total : 10]

© UCLES 2006

9701/04/SP07

[Turn over
6
3

Agricultural lime is manufactured from limestone (calcium carbonate) by first heating the
rock to a high temperature in a lime kiln. The product is allowed to cool and a calculated
amount of water is added. A highly exothermic reaction takes place and a white powder
called ‘slaked lime’ is produced.
(a) Write balanced equations for these two reactions.

[2]
(b) Give two reasons why lime is used in agriculture.

[2]
(c) How does the temperature required to decompose the carbonates of Group II elements
vary down the group, and why is this so?

[3]
(d) The mineral dolomite is a double carbonate of magnesium and calcium, with the
formula CaMg(CO3)2. When 1.000 g of an impure sample of dolomite was completely
dissolved in an excess of hydrochloric acid, 0.450 g of carbon dioxide was given off.
(i) Write a balanced equation for the reaction.

(ii) Calculate the percentage purity of the dolomite.

[3]
[Total : 10]

 UCLES 2006

9701/04/SP07

For
Examiner's
Use
For
Examiner's
Use

7
4

(a) State the electronic configurations of
(i)

the Cu atom,

(ii)

the Cu+ ion,

(iii)

the Cu2+ ion.
[2]

(b) Explain the origin of colour in transition metal compounds, and use your explanation to
suggest why copper(I) chloride is white, whereas copper(II) chloride is blue.

[4]
(c) (i) Write equations to show the reactions that occur when dilute ammonia solution is
slowly added to a solution of CuCl2 until the ammonia is in excess.

(ii) What type of chemical reaction is occurring? Explain your answer.

[4]
[Total: 10]

© UCLES 2006

9701/04/SP07

[Turn over
8
5

The elements in Group VII show trends in a number of their physical and chemical
properties.
(a) Explain the trend in boiling points of the elements as shown.
element

boiling point/oC

chlorine

-35

bromine

+59

iodine

+184

[2]
(b) There are also clear trends in both the H-X bond energy and the Eθ values for the cell
½X2(aq)/X -(aq), where X = Cl, Br, I.
Use relevant data from the Data Booklet to describe and explain each of the following.
Give an equation for each reaction that occurs.
(i) The reactions of the halide ions with concentrated sulphuric acid.

 UCLES 2006

9701/04/SP07

For
Examiner's
Use
For
Examiner's
Use

9
(ii) The action of heat on the hydrogen halides.

[8]
[Total : 10]

© UCLES 2006

9701/04/SP07

[Turn over
10
6

For
Examiner's
Use

An organic compound, A, has the composition by mass C, 40.0%; H, 6.65%; O, 53.3%.
(a) Show that the empirical formula of A is CH2O.

[1]
(b) A shows the following properties or reactions. State what can be deduced about A from
each of these.
(i) It is optically active.

(ii) It gives a brisk effervescence with aqueous sodium carbonate.

(iii) It gives a yellow precipitate when warmed with alkaline aqueous iodine.

[3]
(c) Suggest an identity for A and draw its displayed formula.

[1]
(d) Give the displayed formula of the organic product formed when A is warmed with
acidified potassium dichromate(VI).

[1]

 UCLES 2006

9701/04/SP07
For
Examiner's
Use

11
(e) When A is warmed with concentrated sulphuric acid, a cyclic compound of molecular
formula C6H8O4 can be isolated.
Suggest a displayed formula for this cyclic compound, and state what functional group
is present in the molecule.

[2]
(f) A has a non optically active isomer, B. Under the reaction conditions described in (e),
compound B produces compound C, C3H4O2. Suggest a structure for C.

[2]
[Total : 10]

© UCLES 2006

9701/04/SP07

[Turn over
12
7

For
Examiner's
Use

Aspartame is a synthetic sweetening agent that is 180 times as sweet as sugar.
H2N — CH — CO — NH — CH — CO2 — CH3
│
│
CH2
CH2
│
│
CO2H
C6H5
aspartame
(a) (i) Name four different functional groups in the aspartame molecule.
1

2

3

4

(ii) Identify two functional groups in aspartame which contribute to its solubility in
water. Give a reason for your answer.

1

2

Reason

[4]
(b) (i) Suggest conditions and reagents that could be used to hydrolyse aspartame into
its constituent parts.

(ii) Draw the structural formulae of all of the organic molecules obtained by
hydrolysing aspartame.

[5]
(c) Suggest why aspartame is not used as a sweetening agent in baked products.
[1]
[Total : 10]

 UCLES 2006

9701/04/SP07
For
Examiner's
Use

13
Section B – Applications of Chemistry
Answer all the question in the spaces provided.
8

(a) Explain how protein synthesis occurs in cells, including in your answer the role of
ribosomes.

[6]
(b) Explain why the enzyme lysozyme, which consists of 129 amino acid residues, requires
a triplet code of 393 bases.

[2]
(c) (i) Name a disease brought about by a mutation in the DNA of the individual.

(ii)

Give a symptom of the disease.

[2]
[Total : 10]

© UCLES 2006

9701/04/SP07

[Turn over
14
9

For
Examiner's
Use

(a) An aromatic compound D, of Mr 122, is a possible sex attractant for insects. It has the
following composition by mass: C, 78.7%; H, 8.2%; O, 13.1%.
What is the molecular formula of D?

[3]
(b) The NMR spectrum of D is shown below.

Identify the parts of the molecule responsible for each group of peaks. Use your
answer to deduce a structure for D, explaining your reasoning.

[5]

 UCLES 2006

9701/04/SP07
For
Examiner's
Use

15
(c) Explain what effect you would expect the addition of a small amount of D2O to have on
the NMR spectrum of D.

[2]
(d) An isomer of D shows no effect on the NMR spectrum on adding D2O.
Draw the structure of the isomer and suggest how its NMR spectrum would differ from
that of D.

[3]
[Total : 13]

© UCLES 2006

9701/04/SP07

[Turn over
16

For
Examiner's
Use

10 Read the passage about the production of ethanol for fuel, and then answer the questions.
Sugar cane is the world’s largest source of fermentation ethanol. Ethanol can be produced
by converting the starch content of biomass feedstocks, such as sugar cane, into alcohol.
Yeast is used to break down the complex sugars of starch into simpler sugars, which are
fermented to form ethanol. A further advantage is that bagasse, the remains of the cane
after the sugar is extracted, and the tops and leaves of the sugar cane can be used as a
fuel for electricity production. An efficient ethanol distillery using sugar cane by-products
can therefore be self-sufficient and also generate a surplus of electricity.
There is a second process that utilises biomass feedstocks to produce ethanol. The main
carbohydrate constituent of these feedstocks is cellulose, which, like starch, is a sugar
polymer that can be broken down by hydrolysis into simpler sugars. The new process uses
enzymatic hydrolysis or acid hydrolysis of cellulose to produce simple sugars for
fermentation.
The use of bagasse as the cellulose source in the new process could allow off-season
production of ethanol with very little new equipment. This process is relatively new and is
not yet commercially available, but potentially can use a much wider variety of abundant,
inexpensive feedstocks. Alcohol fuels have been developed in a number of African
countries – Kenya, Malawi, South Africa and Zimbabwe – currently producing sugar, with
others, including Mauritius, Swaziland and Zambia also having great potential.
Ethanol has different chemical properties from gasoline. Although one litre of ethanol has
about two-thirds of the energy of a litre of gasoline, tuning the engine for ethanol can make
up as much as half the difference. Furthermore, should there be a spill, ethanol can be
dealt with more quickly and easily than gasoline.
Using ethanol even in low-level blends (e.g. E10 – which is 10% ethanol, 90% gasoline)
can have environmental benefits. Tests show that E10 produces less carbon monoxide,
sulphur dioxide and carbon dioxide than gasoline. Higher blends (E85 – 15% gasoline), or
even neat ethanol burn with less of almost all these pollutants.
(a) Explain two ways in which bagasse can be used to reduce the cost of ethanol
production.
(i)

(ii)

[2]

 UCLES 2006

9701/04/SP07
17
(b) In addition to ethanol, what other product is formed in the fermentation of sugars by
yeast?
[1]
(c) Suggest an equation to show the hydrolysis of cellulose in bagasse to form fermentable
sugars with the molecular formula C6H12O6.

[1]
(d) Using your knowledge of chemical bonding, suggest why a spill of ethanol is more
easily dealt with than a spill of gasoline.

[3]
[Total : 7]

© UCLES 2006

9701/4/SP07

For
Examiner's
Use
18
BLANK PAGE

Copyright Acknowledgements:
Permission to reproduce items where third-party owned material protected by copyright is included has been sought and cleared where possible. Every
reasonable effort has been made by the publisher (UCLES) to trace copyright holders, but if any items requiring clearance have unwittingly been included, the
publisher will be pleased to make amends at the earliest possible opportunity.
University of Cambridge International Examinations is part of the Cambridge Assessment Group. Cambridge Assessment is the brand name of University of
Cambridge Local Examinations Syndicate (UCLES), which is itself a department of the University of Cambridge.

 UCLES 2006

9701/04/SP07

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0620 20

  • 1. Centre Number Candidate Number Name UNIVERSITY OF CAMBRIDGE INTERNATIONAL EXAMINATIONS General Certificate of Education Advanced Subsidiary Level and Advanced Level CHEMISTRY 9701/04 Paper 4 Structured Questions For Examination from 2007 SPECIMEN PAPER 1 hour 45 minutes . Candidates answer on the Question Paper. Additional Materials: Data Booklet READ THESE INSTRUCTIONS FIRST Write your Centre number, candidate number and name on all the work you hand in. Write in dark blue or black pen. You may use a soft pencil for any diagrams, graphs or rough working. Do not use staples, paper clips, highlighters, glue or correction fluid. Section A Answer all questions. Section B Answer all questions. You may lose marks if you do not show your workings or if you do not use appropriate units. At the end of the examination, fasten all your work securely together. The number of marks is given in brackets [ ] at the end of each question or part question. This document consists of 17 printed pages and 1 blank page.  UCLES 2006 [Turn over
  • 2. 2 For Examiner's Use Section A Answer all the questions in the spaces provided. 1 Bromine can react with methanoic acid according to the following equation. Br2(aq) + HCO2H(aq) → 2Br-(aq) + 2H+(aq) + CO2(g) (a) (i) What maximum volume of gas, measured at r.t.p., would be produced by reacting 3.2 g of bromine? (ii) Suggest how the rate of the reaction might be followed. [5] (b) The graph opposite contains information about this reaction. (i) What evidence is there to suggest that this reaction is first order with respect to bromine? (ii) Write a simple equation relating the rate of reaction to the concentration of bromine under these conditions. (iii) Calculate the half-life of this reaction. [5] [Total : 10] SP/QP/9701/04
  • 4. 4 2 For Examiner's Use (a) Define the standard enthalpy change of formation of a compound. [2] The standard enthalpy change of formation of SiCl4(g) is –610 kJ mol-1. The standard enthalpy changes of atomisation of the elements silicon and chlorine are +338 and +122 kJ mol-1 of atoms respectively. (b) Use these values to construct an energy cycle to show the formation of SiCl4(g). [2] (c) (i) Hence calculate the average bond energy of the Si-Cl bond from these data. (ii) Suggest why the calculated value is different from the value given in the Data Booklet. [2]  UCLES 2006 9701/04/SP07
  • 5. For Examiner's Use 5 (d) Pure silicon is made by reducing SiCl3H with hydrogen at a high temperature. (i) Construct a balanced equation for this reaction. (ii) The bond energy of the Si-Br bond is 298 kJ mol-1. Use this value, and other bond energy values given in the Data Booklet to suggest whether the reaction between SiBr3H and hydrogen would be more or less endothermic than the reaction between SiCl3H and hydrogen. (iii) State a use of pure silicon. [4] [Total : 10] © UCLES 2006 9701/04/SP07 [Turn over
  • 6. 6 3 Agricultural lime is manufactured from limestone (calcium carbonate) by first heating the rock to a high temperature in a lime kiln. The product is allowed to cool and a calculated amount of water is added. A highly exothermic reaction takes place and a white powder called ‘slaked lime’ is produced. (a) Write balanced equations for these two reactions. [2] (b) Give two reasons why lime is used in agriculture. [2] (c) How does the temperature required to decompose the carbonates of Group II elements vary down the group, and why is this so? [3] (d) The mineral dolomite is a double carbonate of magnesium and calcium, with the formula CaMg(CO3)2. When 1.000 g of an impure sample of dolomite was completely dissolved in an excess of hydrochloric acid, 0.450 g of carbon dioxide was given off. (i) Write a balanced equation for the reaction. (ii) Calculate the percentage purity of the dolomite. [3] [Total : 10]  UCLES 2006 9701/04/SP07 For Examiner's Use
  • 7. For Examiner's Use 7 4 (a) State the electronic configurations of (i) the Cu atom, (ii) the Cu+ ion, (iii) the Cu2+ ion. [2] (b) Explain the origin of colour in transition metal compounds, and use your explanation to suggest why copper(I) chloride is white, whereas copper(II) chloride is blue. [4] (c) (i) Write equations to show the reactions that occur when dilute ammonia solution is slowly added to a solution of CuCl2 until the ammonia is in excess. (ii) What type of chemical reaction is occurring? Explain your answer. [4] [Total: 10] © UCLES 2006 9701/04/SP07 [Turn over
  • 8. 8 5 The elements in Group VII show trends in a number of their physical and chemical properties. (a) Explain the trend in boiling points of the elements as shown. element boiling point/oC chlorine -35 bromine +59 iodine +184 [2] (b) There are also clear trends in both the H-X bond energy and the Eθ values for the cell ½X2(aq)/X -(aq), where X = Cl, Br, I. Use relevant data from the Data Booklet to describe and explain each of the following. Give an equation for each reaction that occurs. (i) The reactions of the halide ions with concentrated sulphuric acid.  UCLES 2006 9701/04/SP07 For Examiner's Use
  • 9. For Examiner's Use 9 (ii) The action of heat on the hydrogen halides. [8] [Total : 10] © UCLES 2006 9701/04/SP07 [Turn over
  • 10. 10 6 For Examiner's Use An organic compound, A, has the composition by mass C, 40.0%; H, 6.65%; O, 53.3%. (a) Show that the empirical formula of A is CH2O. [1] (b) A shows the following properties or reactions. State what can be deduced about A from each of these. (i) It is optically active. (ii) It gives a brisk effervescence with aqueous sodium carbonate. (iii) It gives a yellow precipitate when warmed with alkaline aqueous iodine. [3] (c) Suggest an identity for A and draw its displayed formula. [1] (d) Give the displayed formula of the organic product formed when A is warmed with acidified potassium dichromate(VI). [1]  UCLES 2006 9701/04/SP07
  • 11. For Examiner's Use 11 (e) When A is warmed with concentrated sulphuric acid, a cyclic compound of molecular formula C6H8O4 can be isolated. Suggest a displayed formula for this cyclic compound, and state what functional group is present in the molecule. [2] (f) A has a non optically active isomer, B. Under the reaction conditions described in (e), compound B produces compound C, C3H4O2. Suggest a structure for C. [2] [Total : 10] © UCLES 2006 9701/04/SP07 [Turn over
  • 12. 12 7 For Examiner's Use Aspartame is a synthetic sweetening agent that is 180 times as sweet as sugar. H2N — CH — CO — NH — CH — CO2 — CH3 │ │ CH2 CH2 │ │ CO2H C6H5 aspartame (a) (i) Name four different functional groups in the aspartame molecule. 1 2 3 4 (ii) Identify two functional groups in aspartame which contribute to its solubility in water. Give a reason for your answer. 1 2 Reason [4] (b) (i) Suggest conditions and reagents that could be used to hydrolyse aspartame into its constituent parts. (ii) Draw the structural formulae of all of the organic molecules obtained by hydrolysing aspartame. [5] (c) Suggest why aspartame is not used as a sweetening agent in baked products. [1] [Total : 10]  UCLES 2006 9701/04/SP07
  • 13. For Examiner's Use 13 Section B – Applications of Chemistry Answer all the question in the spaces provided. 8 (a) Explain how protein synthesis occurs in cells, including in your answer the role of ribosomes. [6] (b) Explain why the enzyme lysozyme, which consists of 129 amino acid residues, requires a triplet code of 393 bases. [2] (c) (i) Name a disease brought about by a mutation in the DNA of the individual. (ii) Give a symptom of the disease. [2] [Total : 10] © UCLES 2006 9701/04/SP07 [Turn over
  • 14. 14 9 For Examiner's Use (a) An aromatic compound D, of Mr 122, is a possible sex attractant for insects. It has the following composition by mass: C, 78.7%; H, 8.2%; O, 13.1%. What is the molecular formula of D? [3] (b) The NMR spectrum of D is shown below. Identify the parts of the molecule responsible for each group of peaks. Use your answer to deduce a structure for D, explaining your reasoning. [5]  UCLES 2006 9701/04/SP07
  • 15. For Examiner's Use 15 (c) Explain what effect you would expect the addition of a small amount of D2O to have on the NMR spectrum of D. [2] (d) An isomer of D shows no effect on the NMR spectrum on adding D2O. Draw the structure of the isomer and suggest how its NMR spectrum would differ from that of D. [3] [Total : 13] © UCLES 2006 9701/04/SP07 [Turn over
  • 16. 16 For Examiner's Use 10 Read the passage about the production of ethanol for fuel, and then answer the questions. Sugar cane is the world’s largest source of fermentation ethanol. Ethanol can be produced by converting the starch content of biomass feedstocks, such as sugar cane, into alcohol. Yeast is used to break down the complex sugars of starch into simpler sugars, which are fermented to form ethanol. A further advantage is that bagasse, the remains of the cane after the sugar is extracted, and the tops and leaves of the sugar cane can be used as a fuel for electricity production. An efficient ethanol distillery using sugar cane by-products can therefore be self-sufficient and also generate a surplus of electricity. There is a second process that utilises biomass feedstocks to produce ethanol. The main carbohydrate constituent of these feedstocks is cellulose, which, like starch, is a sugar polymer that can be broken down by hydrolysis into simpler sugars. The new process uses enzymatic hydrolysis or acid hydrolysis of cellulose to produce simple sugars for fermentation. The use of bagasse as the cellulose source in the new process could allow off-season production of ethanol with very little new equipment. This process is relatively new and is not yet commercially available, but potentially can use a much wider variety of abundant, inexpensive feedstocks. Alcohol fuels have been developed in a number of African countries – Kenya, Malawi, South Africa and Zimbabwe – currently producing sugar, with others, including Mauritius, Swaziland and Zambia also having great potential. Ethanol has different chemical properties from gasoline. Although one litre of ethanol has about two-thirds of the energy of a litre of gasoline, tuning the engine for ethanol can make up as much as half the difference. Furthermore, should there be a spill, ethanol can be dealt with more quickly and easily than gasoline. Using ethanol even in low-level blends (e.g. E10 – which is 10% ethanol, 90% gasoline) can have environmental benefits. Tests show that E10 produces less carbon monoxide, sulphur dioxide and carbon dioxide than gasoline. Higher blends (E85 – 15% gasoline), or even neat ethanol burn with less of almost all these pollutants. (a) Explain two ways in which bagasse can be used to reduce the cost of ethanol production. (i) (ii) [2]  UCLES 2006 9701/04/SP07
  • 17. 17 (b) In addition to ethanol, what other product is formed in the fermentation of sugars by yeast? [1] (c) Suggest an equation to show the hydrolysis of cellulose in bagasse to form fermentable sugars with the molecular formula C6H12O6. [1] (d) Using your knowledge of chemical bonding, suggest why a spill of ethanol is more easily dealt with than a spill of gasoline. [3] [Total : 7] © UCLES 2006 9701/4/SP07 For Examiner's Use
  • 18. 18 BLANK PAGE Copyright Acknowledgements: Permission to reproduce items where third-party owned material protected by copyright is included has been sought and cleared where possible. Every reasonable effort has been made by the publisher (UCLES) to trace copyright holders, but if any items requiring clearance have unwittingly been included, the publisher will be pleased to make amends at the earliest possible opportunity. University of Cambridge International Examinations is part of the Cambridge Assessment Group. Cambridge Assessment is the brand name of University of Cambridge Local Examinations Syndicate (UCLES), which is itself a department of the University of Cambridge.  UCLES 2006 9701/04/SP07