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Subjects / Chemistry / Practice exam 9

Practice exam 9 · 28 pages · 120 marks · 15 minutes reading, 2 hours 30 minutes writing

Chemistry – Practice exam 9

Methanol from captured CO2, designing a cell to light an LED, the NOCl equilibrium, a zinc–bromine flow battery, propyl propanoate, isomers of C4H10O, glutamic acid and MSG, and a calcium chloride hand warmer.

Marks by area of study

Unit 3 AOS 1: 39 marksUnit 3 AOS 2: 25 marksUnit 4 AOS 1: 18 marksUnit 4 AOS 2: 28 marksSustainability: 5 marksKey science skills: 6 marks

Section B: short-answer and extended-response questions (90 marks)

QContextMarks
1‘E-methanol’ is made by reacting carbon dioxide captured from the exhaust of a cement factory with hydrogen pr12
2Students were asked to build a single galvanic cell that would light a small LED, which needs a potential diff11
3Nitrosyl chloride, NOCl, is an orange-yellow gas that decomposes when heated.11
4Zinc–bromine flow batteries are used to store energy from solar farms11
5Propyl propanoate, which smells of pears, can be synthesised using propan-1-ol as the only organic starting ma11
6There are four alcohols with the molecular formula C4H10O: butan-1-ol, butan-2-ol, 2-methylpropan-1-ol and 2-m11
7Glutamic acid is a 2-amino acid found in many proteins11
8Students investigated whether anhydrous calcium chloride is suitable for a self-heating hand warmer12

Section A: what each question tests (30 marks)

QKey knowledgeArea of study
1refining crude oilUnit 3 AOS 1
2energy released per mole of CO2Unit 3 AOS 1
3mass–mass stoichiometryUnit 3 AOS 1
4energy and temperature changeUnit 3 AOS 1
5identifying redox reactionsUnit 3 AOS 1
6oxidation half-equations in acidic solutionUnit 3 AOS 1
7predicting reactions from E° valuesUnit 3 AOS 1
8fuel cell half-equations for an unfamiliar electrolyteUnit 3 AOS 1
9rate and amount of productUnit 3 AOS 2
10using Kc to find a concentrationUnit 3 AOS 2
11removing a productUnit 3 AOS 2
12electroplatingUnit 3 AOS 2
13mass changes in a rechargeable cellUnit 3 AOS 2
14Faraday’s laws in industryUnit 3 AOS 2
15presenting dataUnits 3–4 Key science skills
16precisionUnits 3–4 Key science skills
17naming compounds with two functional groupsUnit 4 AOS 1
18semi-structural formulasUnit 4 AOS 1
19solubility and functional groupsUnit 4 AOS 1
20formation of amidesUnit 4 AOS 1
21hydrolysis of amidesUnit 4 AOS 1
22percentage yield with a limiting reactantUnit 4 AOS 1
23green chemistry principlesUnits 3–4 Cross-study
24titration techniqueUnit 4 AOS 2
25concentration unitsUnit 4 AOS 2
26improving separation in HPLCUnit 4 AOS 2
27fragmentation in mass spectraUnit 4 AOS 2
28using IR to detect impuritiesUnit 4 AOS 2
291H NMR chemical shiftsUnit 4 AOS 2
30carbohydrate polymersUnit 4 AOS 2