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Which alkyl halide from the given options will undergo SN1 reaction faster? - Chemistry

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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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