Problem

Bromomethylcycloheptane has been prepared in 92% yield by the reaction shown. Write a step...

Bromomethylcycloheptane has been prepared in 92% yield by the reaction shown. Write a stepwise mechanism and use curved arrows to show electron flow. The reaction was carried out in water, so use H3O+ as the proton donor in your mechanism. Is the rate-determining step unimolecular (SN1) or bimolecular (SN2)?

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