O Levels Chemistry (5070)•5070/12/M/J/23

Explanation
Esterification: Alcohol + Carboxylic Acid → Ester
Steps:
- Examine the ester structure to identify the alkyl chain from the alcohol (R-OH) and the acyl chain from the acid (R'-COOH).
- The alkyl part is a three-carbon propyl group (CH3CH2CH2-), matching propan-1-ol.
- The acyl part is a two-carbon acetyl group (CH3CO-), matching ethanoic acid (CH3COOH).
- Confirm the combination forms the ester CH3COOCH2CH2CH3 (propyl ethanoate).
Why C is correct:
- In esterification, propan-1-ol (C3H7OH) reacts with ethanoic acid (CH3COOH) to yield the ester with propyl alkyl and ethanoyl acyl groups, per the general formula RCOOR'.
Why the others are wrong:
- A: Forms butyl methanoate (four-carbon alkyl, one-carbon acyl).
- B: Forms ethyl propanoate (two-carbon alkyl, three-carbon acyl).
- D: Forms propyl methanoate (three-carbon alkyl, one-carbon acyl).
Final answer: C
Topic: Carboxylic acids
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