Consider the reaction of 1-bromo-1-methylcyclohexane with . The mechanism is primarily . If is added β Reaction Mechanism Chemistry Question
Question
Consider the reaction of 1-bromo-1-methylcyclohexane with $H_2O$. The mechanism is primarily $S_N1$. If $AgNO_3$ is added, the rate of substitution will:
Answer: D
π‘ Solution & Explanation
$Ag^+$ ions strongly precipitate the halide leaving group as solid $AgBr$, acting as a massive driving force to generate the carbocation and accelerating the $S_N1$ rate.
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