CAPE Chemistry Mock Exams U2 2015
CAPE Chemistry Mock Exams U2 2015
CAPE Chemistry Mock Exams U2 2015
CHEMISTRY
UNIT2 - Paper 02
2 hours 30 minutes
2. For Section A, write your answers in the spaces provided in this booklet.
3. For Section B, write your answers in the spaces provided at the end of each question in this
booklet.
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SECTION A Answer ALL questions in this section
MODULE 1
[2 marks]
[ 2 marks]
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(iii) Identify the process which leads to the formation of the products at
a) P___________________________________________________________
b) Q___________________________________________________________
[2 marks]
(iv) State a use of the non-alcoholic product formed at
a) P ________________________________________________________
b) Q ________________________________________________________
[2 marks]
(b) (i) A student was asked to identify the organic compound, Z. Table 1 shows the student’s incomplete
record of tests conducted on Z. Complete the student’s record by writing the correct observation or
inference in the appropriate space.
[14 marks]
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(ii) Draw the LIKELY structure for Compound Z.
[1 mark]
(c) The reaction between carbonyl compounds and HCN occurs via nucleophilic addition.
Outline the mechanism for the reaction, using curved arrows to show the movement of electrons.
[2 marks]
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MODULE 2
2. (a) State TWO characteristics of a molecule which make suitable for analysis by infrared spectroscopy
(IR).
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[2 marks]
(b) Give TWO examples of the use of IR spectroscopy.
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[2 marks]
(c) The IR spectra in Figures 2, 3 and 4 belong to the compounds 2-propanol (CH2CH(OH)CH3), butanoic acid
(CH3CH2CH2COOH) and acetone CH3COCH3). Identify EACH of the compounds A, B and C in Figures 2, 3
and 4 respectively from the IR spectra provided. Justify your choice by indicating which band on the spectra
was used to verify the identity of the compounds-and indicate the functional group responsible for the band
in EACH case.
(i)
Figure 2. Compound A
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a) Identity of Compound A _________________________________________________
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[2 marks]
(ii)
Figure 3. Compound B
a) Identity of Compound B _________________________________________________
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[2 marks]
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(iii)
Figure 4. Compound C
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[2 marks]
(d) A student is asked to prepare a solid sample for analysis using IR spectroscopy.
(i) Describe FOUR steps to be taken by the student in preparing the sample and analysing it.
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[4 marks]
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(ii) Why are the plates used for IR spectroscopy made from NaCl?
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[1 mark]
Total 15 marks
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MODULE 3
3. (a) A stream which flows through an agricultural community is also used for domestic washing.
Samples taken from a site downstream after a heavy rainfall were found to contain a number of pollutants.
(i) State the process that may have resulted in pollutants being present in the stream.
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[1 mark]
(ii) Identify TWO sources of the pollutants (other than fertilizers) that are MOST likely to be present in
the stream.
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[2 marks]
(b) Analysis of the samples revealed excessive quantities of nitrates and phosphates. Describe how the presence
of these pollutants can be identified in a laboratory.
(i) Nitrates
Reagents:
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Observations:
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[2 marks]
(ii) Phosphates
Reagents:
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Observations:
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[2 marks]
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(c) (i) State TWO ways by which oxygen enters waterways.
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[2 marks]
(ii) Dissolved oxygen is essential for maintaining good water quality and the preservation of aquatic life.
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[2 marks]
(iii) Explain why dissolved oxygen must be removed from water before it is used in industrial processes.
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[2 marks]
(d) State TWO steps involved in the treatment of water in order to make it potable.
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[2 marks]
Total 15 marks
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SECTION B
Write your answers in the spaces provided at the end of each question.
MODULE1
4. (a) Table 2 shows some reactions of phenol. Identify the reagents and structures needed to
complete the table correctly. (Write your answers in the space provided on page 13.)
(i)
(ii)
Br2(aq)
(iii)
[3 marks]
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(b) Figure 5 shows the formation of 3-bromoaniline from benzene in three steps labelled I, II and III.
(i) State the reagents and conditions to be used in EACH of the reactions at Steps I, II and III.
[3 marks]
(ii) Outline the reaction mechanism for the reaction in Step !, using curved arrows to show the movement
of electrons. [3 marks]
(iii) State the reaction mechanism outlined in (b) (ii) above. [1 mark]
(iv) For Step II, explain why the bromo substituent occupies its position on the molecule. [1 mark]
(c) Benzene, nitrobenzene and methylbenzene will react with chlorine, in the presence of a catalyst, to form
aromatic substituted compounds. The three reactions take place at different rates.
(i) Arrange the reagents benzene, nitrobenzene and methylbenzene in order of INCREASING ease of
reactivity with chlorine. [1 mark]
(ii) For EACH reaction, draw the MAJOR mono-substituted aromatic product that is formed. [3 marks]
Total 15 marks
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Write the answer to Question 4 here.
(ii) Structure:
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MODULE 2
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ANALYTICAL METHODS AND SEPARATION TECHNIQUES
5. (a) Define the term 'partition coefficient’. [2 marks]
(b) When butanedioic acid was shaken with a mixture of water and ether, 10 cm3 of water was found to contain
0.854 g of the acid while a similar volume of ether contained 0.159 g.
In a separate experiment, 10 cm3 of water and 20 cm3 of ether were shaken together with 1 g of the acid.
Calculate the mass of the acid found in the aqueous layer. [4 marks]
(c) Suggest an appropriate method for separating the components of EACH of the following:
(d)
Use the boiling point-composition curve in Figure 6 to explain the principles of fraction distillation, starting with a
liquid of composition x. [5 mark]
Total 15 marks
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Write the answer to Question 5 here.
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MODULE 3
6. (a) Describe the process of extracting aluminium oxide from its ore. Include TWO relevant equations in
your answer. [7 marks]
(ii) Describe TWO environmental consequences resulting from the named pollutant in (b) (i). [3 marks]
(i) Write equations to show the reactions occurring at the electrodes. [2 marks]
(ii) a) Outline ONE reason for the high cost associated with this method of extraction.
Total 15 marks
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