A Levels Chemistry (9701)•9701/11/M/J/23

Explanation
Identifying constitutional isomers of secondary alcohols with formula C4H10O Steps:
- Secondary alcohols have OH attached to a carbon bonded to two other carbons.
- Possible skeletons for C4H10O: straight-chain butane and branched 2-methylpropane.
- In butane, OH at position 2 (equivalent to 3) gives CH3CH(OH)CH2CH3, butan-2-ol.
- In 2-methylpropane, the branch carbon is tertiary; OH there gives (CH3)3COH, a tertiary alcohol, not secondary. Why A is correct:
- Only the straight-chain skeleton allows a carbon with exactly two carbon attachments for the OH group, per the definition of secondary alcohols. Why the others are wrong:
- B: Branched skeleton yields no additional secondary alcohol, so not two.
- C: Confuses with total alcohol isomers (four) or larger formulas like C5H12O.
- D: Applies to all alcohol types, not just secondary.
Final answer: A
Topic: Hydroxy compounds
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