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Question
Which alkyl halide from the given options will undergo SN1 reaction faster?
Options
\[\ce{(CH3)3C - Br}\]
\[\ce{(CH3)2CH - Br}\]
\[\ce{CH3 - CH2 - Br}\]
\[\ce{(CH3)3C - CH2 - Br}\]
MCQ
Solution
\[\ce{(CH3)3C - Br}\]
Explanation:
Tertiary carbon compounds undergo SN1 is a tertiary carbon halide.
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