A Levels Chemistry (9701)•9701/12/M/J/24

Explanation
Iodoform test for methyl ketones from alcohol oxidation
Steps:
- Yellow precipitate with alkaline I2(aq) indicates iodoform test, positive for methyl ketones (RCOCH3) or acetaldehyde.
- Compound X is an alcohol oxidized to Y, a carbonyl compound; for Y to be a methyl ketone, X must be a secondary alcohol of form RCH(OH)CH3.
- Primary alcohols oxidize to aldehydes (then carboxylic acids), and tertiary do not oxidize to carbonyls.
- Among options, only butan-2-ol (CH3CH(OH)CH2CH3) yields butan-2-one (CH3COCH2CH3), a methyl ketone.
Why B is correct:
- Butan-2-ol oxidizes to butan-2-one, which has the CH3CO- group required for iodoform reaction.
Why the others are wrong:
- A: Butan-1-ol oxidizes to butanal (CH3CH2CH2CHO), which lacks CH3CO- or CH3CH(OH)- and fails iodoform test.
- C: Methylpropan-1-ol (2-methylpropan-1-ol) oxidizes to 2-methylpropanal ((CH3)2CHCHO), not a methyl ketone.
- D: Methylpropan-2-ol (2-methylpropan-2-ol) is tertiary and resists oxidation to any carbonyl compound.
Final answer: B
Topic: Hydroxy compounds
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