7. Substitution Reactions
SN1 Reaction
10:46 minutes
Problem 6e
Textbook Question
Textbook QuestionPropose a mechanism involving a hydride shift or an alkyl shift for each solvolysis reaction. Explain how each rearrangement forms a more stable intermediate. Hint: Most rearrangements convert 2° (or incipient 1°) carbocations to 3° or resonance-stabilized carbocations. b.
CH3CH2OH heat—> +Verified Solution
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