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Pearson Edexcel International GCSE (9–1) · CHEMISTRY · Chapter

Esters

68 practice questions

Topics covered

Practice questions

61–68 of 68

  1. Question 61

    5 marks · Easy

    Esters such as propyl methanoate have distinctive smells and are made by reacting an alcohol with a carboxylic acid.

    (a)

    State the name of the alcohol and the carboxylic acid used to form propyl methanoate.

    [2 marks]
    (b)

    Draw the displayed formula of propyl methanoate, showing all atoms and bonds.

    [2 marks]
    (c)

    State one use of esters such as propyl methanoate.

    [1 mark]
    Answer and see the solution →
  2. Question 62

    6 marks · Normal

    Butanol and ethanoic acid are used together in a laboratory to produce an ester. Answer the following questions about this reaction and the practical steps involved.

    (a)

    Name the ester formed in this reaction.

    [1 mark]
    (b)

    Draw the structural formula for the ester you named in part (a).

    [2 marks]
    (c)

    State the name of the catalyst used during this esterification reaction.

    [1 mark]
    (d)

    Describe one step you would take in the laboratory to make the smell of the ester easier to detect after the reaction is complete.

    [2 marks]
    Answer and see the solution →
  3. Question 63

    6 marks · Normal

    A student wants to prepare methyl propanoate in the laboratory using appropriate organic starting materials.

    (a)

    Identify the alcohol and the carboxylic acid required to make methyl propanoate.

    [2 marks]
    (b)

    Draw the structural formula for methyl propanoate.

    [2 marks]
    (c)

    Describe briefly, in two steps, how a small sample of methyl propanoate can be prepared and the smell detected during a school practical.

    [2 marks]
    Answer and see the solution →
  4. Question 64

    6 marks · Normal

    A group of students carried out an experiment to produce an ester from ethanol and propanoic acid. They left the product to stand after completing the practical.

    (a)

    Explain how the students could confirm that an ester had formed, even if the reactants and product are colourless.

    [2 marks]
    (b)

    Ethyl propanoate is an ester. Give the name of the alcohol used to manufacture this ester.

    [1 mark]
    (c)

    The mixture was poured into a beaker containing sodium carbonate solution. Suggest a reason for this step.

    [1 mark]
    (d)

    Explain why small esters are easy to separate from the reaction mixture compared to the carboxylic acid and alcohol used.

    [2 marks]
    Answer and see the solution →
  5. Question 65

    6 marks · Normal

    Propanoic acid reacts with ethanol to form an ester. You are given 1.5 cm³ of propanoic acid (density = 1.00 g/cm³) and an excess of ethanol.

    (a)

    Draw the structural formula of the ester formed in this reaction and name the ester.

    [3 marks]
    (b)

    In a laboratory experiment, you attempt to prepare the ester in part (a). (i) Calculate the maximum mass of the ester that could be formed from 1.5 cm³ of propanoic acid (M_r of propanoic acid = 74, M_r of the ester = 102).

    [2 marks]
    (c)

    Describe how you could separate and identify the smell of the ester after the reaction, referring to the laboratory method and your answer to part (b).

    [1 mark]
    Answer and see the solution →
  6. Question 66

    7 marks · Hard

    Esters are formed from an alcohol and a carboxylic acid in an esterification reaction. Ethanol and butanoic acid react together under suitable conditions.

    (a)

    Draw the full structural formula of the ester formed when ethanol reacts with butanoic acid.

    [3 marks]
    (b)

    Name the ester formed in part (a).

    [1 mark]
    (c)

    State one use of this ester in everyday life.

    [1 mark]
    (d)

    Describe how esters like the one above are prepared in a laboratory. Include any catalyst and any condition needed.

    [2 marks]
    Answer and see the solution →
  7. Question 67

    7 marks · Hard

    A student mixes methanol and propanoic acid in the presence of a few drops of concentrated sulfuric acid and heats the mixture.

    (a)

    Describe the type of reaction taking place and explain what is meant by 'esterification'.

    [2 marks]
    (b)

    Draw the displayed formula of the ester formed in this reaction.

    [3 marks]
    (c)

    State one common use for this ester.

    [1 mark]
    (d)

    Write the balanced chemical equation (using molecular formulae, not names) for the formation of the ester in part (b).

    [1 mark]
    Answer and see the solution →
  8. Question 68

    7 marks · Hard

    Some esters have pleasant smells and are widely used in everyday products.

    (a)

    Give the systematic name of the ester with molecular formula C3H7COOCH3.

    [2 marks]
    (b)

    State the names of the alcohol and the carboxylic acid needed to make this ester.

    [2 marks]
    (c)

    Suggest one use of this ester and explain why esters are suitable for this use.

    [3 marks]
    Answer and see the solution →