Which set of conditions most strongly favors the mechanism over for an alkyl halide? — Reaction Mechanism Chemistry Question
Question
Which set of conditions most strongly favors the $S_N1$ mechanism over $S_N2$ for an alkyl halide?
Answer: B
💡 Solution & Explanation
$S_N1$ requires stable carbocations (tertiary halide) and is heavily accelerated by polar protic solvents that solvate the leaving group and intermediate cation.
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