A Levels Chemistry (9701)•9701/13/M/J/19

Explanation
Naming Esters Correctly
Steps:
- Identify the alcohol part: "ethyl" indicates ethanol (C2H5OH), so the alkyl group is ethyl.
- Identify the acid part: "propanoate" comes from propanoic acid (CH3CH2COOH), so the chain is three carbons with the carbonyl.
- Combine: The ester is CH3CH2COOCH2CH3, where the acid chain is numbered starting from the carbonyl carbon as 1.
- Verify IUPAC name: It's ethyl propanoate, not "1 ethyl propanoate," which is non-standard.
Why D is correct:
- D matches the standard IUPAC structure for ethyl propanoate (CH3CH2C(O)OCH2CH3).
Why the others are wrong:
- A shows propyl ethanoate, swapping alkyl and acyl groups.
- B depicts methyl butanoate, with wrong chain lengths.
- C is ethyl acetate, using acetic acid instead of propanoic.
Not enough information on exact choice labels, but D is the valid ester.
Final answer: D
Topic: Carboxylic acids and derivatives
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