A student wants to prepare a sample of ethyl ethanoate in the laboratory. Describe how the student would carry out this preparation, including the reagents needed, the conditions required, and how a pure, dry sample of the ester would be obtained.

Eduqas A-Level Chemistry — 4.8 Organic synthesis and analysis · Describe · 5 marks · View as Markdown

Written & reviewed by James Millett — Biology (Imperial College London), PGCE Science (University of Cambridge).

Model answer (5 marks)

1. Mix ethanol and ethanoic acid in a round‑bottom flask.
2. Add a few drops of concentrated sulphuric acid (or HCl) as catalyst.
3. Heat the mixture gently, usually by reflux or in a water bath, for about 30–60 min.
4. Cool the reaction mixture and add a saturated solution of sodium carbonate to neutralise excess acid and any unreacted alcohol.
5. Transfer the mixture to a separating funnel, separate the organic (ester) layer, wash it with water, dry over anhydrous calcium chloride (or sodium sulfate), filter and evaporate the solvent to give a pure, dry ethyl ethanoate.

Examiner tips

  • Use the exact reagent names (ethanol, ethanoic acid) and catalyst (sulphuric acid/HCl).
  • Mention gentle heating or reflux and the use of a water bath if appropriate.
  • Include the neutralisation step with sodium carbonate and the separation/drying steps.

Mark scheme (5 marks)

  1. Names ethanol and ethanoic acid as the reactants (reagents)
  2. States that a (concentrated) acid catalyst is used — sulfuric acid or hydrochloric acid
  3. States that the mixture is heated (gently / under reflux / in a water bath)
  4. States that sodium carbonate (solution) is added to remove excess acid (and alcohol)
  5. States that the ester layer is separated (using a separating funnel) and dried using a drying agent such as anhydrous calcium chloride / anhydrous sodium sulfate

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