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AlcoholsAQA A-Level Chemistry: Topic test

20 questions, 54 marks

AQA A-Level Chemistry

Alcohols topic test

Total 54 marks

Name

Class

Date

  1. 1
    A school science club ferments a solution of glucose using yeast in a sealed flask fitted with an air lock, keeping the flask at 35 °C. After several days the liquid is filtered and then fractionally distilled to collect ethanol.
    (a)
    Why is air kept out of the flask?
    [1 mark]
    • AOxygen would oxidise the ethanol formed to ethanoic acid
    • BOxygen would raise the pH and denature the yeast enzymes
    • COxygen would reduce the glucose to a polymer
    • DOxygen would prevent any carbon dioxide from forming
    (b)
    Which statement describes ethanol used as a biofuel?
    [1 mark]
    • AA fuel obtained only from crude oil
    • BA fuel that does not release carbon dioxide on burning
    • CA fuel made from living or recently living biological material
    • DA fuel made by reacting ethene with steam
    (c)
    Write the equation for the fermentation of glucose and explain why the temperature is kept at 35 °C rather than at 60 °C.
    [2 marks]

    Total for question 1: 4 marks

  2. 2
    Hexan-2-ol, CH₃CH(OH)CH₂CH₂CH₂CH₃, is heated under reflux with an excess of acidified potassium dichromate(VI) solution.
    (a)
    What is the organic product of this reaction?
    [1 mark]
    • AHexanal
    • BHexanoic acid
    • CHex-2-ene
    • DHexan-2-one
    (b)
    What colour change is seen in the reaction mixture?
    [1 mark]
    • AGreen to orange
    • BOrange to green
    • CColourless to orange
    • DPurple to colourless
    (c)
    State the observations when a sample of the organic product is warmed separately with Tollens' reagent and with Fehling's solution.
    [2 marks]

    Total for question 2: 4 marks

  3. 3
    Butan-2-ol, CH₃CH(OH)CH₂CH₃, is heated with concentrated phosphoric acid. A mixture of three alkenes forms and the gases are collected over water.
    (a)
    Outline the mechanism for the formation of but-1-ene from butan-2-ol.
    [3 marks]
    (b)
    Name the three alkenes and explain why a mixture forms rather than a single alkene.
    [4 marks]

    Total for question 3: 7 marks

  4. 4
    Butan-2-ol, CH₃CH(OH)CH₂CH₃, is manufactured by reacting but-1-ene with steam in the presence of a phosphoric acid catalyst. Butan-2-ol is a secondary alcohol that can be oxidised or dehydrated. Its isomer 2-methylpropan-2-ol, (CH₃)₃COH, behaves differently.
    (a)
    State the conditions and outline the mechanism for the formation of butan-2-ol from but-1-ene, explaining why butan-2-ol is the major product.
    [6 marks]
    (b)
    Compare the reactions of butan-2-ol with acidified potassium dichromate(VI) and with concentrated phosphoric acid. Include the organic products, the observation with dichromate(VI), a test that distinguishes the two organic products, and what happens to 2-methylpropan-2-ol with dichromate(VI).
    [6 marks]

    Total for question 4: 12 marks

  5. 5
    Ethanol is made industrially by passing a mixture of ethene and steam over a solid phosphoric acid catalyst. The ethene used is obtained from crude oil.
    (a)
    Which statement about this process is correct?
    [1 mark]
    • AIts atom economy is below 100% because water is a by-product
    • BIts atom economy is 100% because ethanol is the only product
    • CIt is a substitution reaction
    • DThe acid catalyst is used up in the reaction
    (b)
    What is the role of the phosphoric acid?
    [1 mark]
    • AA catalyst that provides H⁺, which is regenerated in the final step
    • BA reactant that is used up forming phosphate by-products
    • CAn oxidising agent for ethene
    • DA dehydrating agent that removes water from ethanol
    (c)
    Explain why ethanol made by this process is not regarded as a renewable or carbon neutral fuel.
    [2 marks]

    Total for question 5: 4 marks

  6. 6
    Four alcohols have the molecular formula C₅H₁₂O. P is 2-methylbutan-1-ol, Q is 3-methylbutan-2-ol, R is 2-methylbutan-2-ol and S is pentan-3-ol. Each is heated separately with acidified potassium dichromate(VI).
    (a)
    Which alcohol is not oxidised by acidified potassium dichromate(VI)?
    [1 mark]
    • AP
    • BQ
    • CR
    • DS
    (b)
    Which pair of alcohols is oxidised to ketones?
    [1 mark]
    • AP and Q
    • BP and R
    • CQ and R
    • DQ and S
    (c)
    State the conditions needed to oxidise P to a carboxylic acid and write an equation for the reaction, using [O] to represent the oxidising agent.
    [2 marks]

    Total for question 6: 4 marks

  7. 7
    Glucose, C₆H₁₂O₆ (Mr = 180.0), is fermented by yeast to form ethanol (Mr = 46.0) and carbon dioxide (Mr = 44.0). A brewer ferments 90.0 g of glucose. The molar gas volume is 24.0 dm³ mol⁻¹ at room temperature and pressure.
    (a)
    Calculate the maximum mass of ethanol that can be formed from 90.0 g of glucose.
    [3 marks]
    (b)
    Calculate the volume of carbon dioxide produced at room temperature and pressure, and the atom economy for the formation of ethanol in this fermentation.
    [4 marks]

    Total for question 7: 7 marks

  8. 8
    Butan-1-ol, CH₃CH₂CH₂CH₂OH (boiling temperature 118 °C), can be oxidised by acidified potassium dichromate(VI) to butanal (boiling temperature 75 °C) or to butanoic acid (boiling temperature 164 °C). It can also be dehydrated by heating with concentrated phosphoric acid to form but-1-ene (boiling temperature −6 °C).
    (a)
    Outline the mechanism for the dehydration of butan-1-ol to but-1-ene and describe how a student can show that the gas collected is an alkene.
    [6 marks]
    (b)
    Explain how the method used determines whether butanal or butanoic acid is obtained from butan-1-ol, and how a student can test the product from the first method to show that it is an aldehyde.
    [6 marks]

    Total for question 8: 12 marks

End of questions

Written by the Exaim team, led by Shaun Daswani (Head of Upper Secondary, Improve ME Institute; MSc Financial Mathematics, Imperial College London; BSc, UCL) and Jason Daswani (operational lead, Improve ME Institute; LSE).