Question detail

Write the balanced equation for the reaction of acetic anhydride with ethanol to form an ester and acetic acid.

Try the question, check the answer, then read the explanation to understand the curriculum point.

At a glance

Question

Type

exam_style

Style

Topic

Carboxylic acids and derivatives (A-level only)

Question

Write the balanced equation for the reaction of acetic anhydride with ethanol to form an ester and acetic acid.

Answer

C2H4O2 + C4H6O3 → C6H10O3 + C2H4O2. This answer is anchored to Carboxylic acids, esters and acyl derivatives (A-level only).

Explanation

C2H4O2 + C4H6O3 → C6H10O3 + C2H4O2. is the best answer because it directly supports the AQA A-Level Chemistry objective to explain reactions of acyl chlorides and acid anhydrides. This reasoning is anchored to Carboxylic acids, esters and acyl derivatives (A-level only) in Carboxylic acids and derivatives (A-level only), and it separates acyl chloride from similar A-Level ideas rather than relying on a vague recall statement. Other options are weaker if they use the wrong evidence, calculation, mechanism, observation, unit, or conclusion for this subtopic.

Common mistake

Misunderstanding Reactivity

Students often confuse the reactivity of acyl chlorides with that of carboxylic acids, thinking they react in the same way with nucleophiles.

Remember that acyl chlorides are more reactive than carboxylic acids due to the presence of the chlorine atom, which is a better leaving group. Focus on the mechanism of nucleophilic addition-elimination for acyl chlorides.

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