The given compound CH_3-O-CH_2-Br undergoes w | vedclass

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(C) $CH_3-O-CH_2-Br$ is a primary alkyl halide,which facilitates the $S_N2$ reaction pathway.Additionally,the carbocation intermediate $CH_3-O-CH_2^+$

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$S_N1$ as well as $S_N2$

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(C) $CH_3-O-CH_2-Br$ is a primary alkyl halide,which facilitates the $S_N2$ reaction pathway.Additionally,the carbocation intermediate $CH_3-O-CH_2^+$ is significantly stabilized by the resonance effect of the lone pair on the oxygen atom $(CH_3-O^+=CH_2)$.Due to this stabilization,the compound can also undergo $S_N1$ reactions.Therefore,the compound exhibits both $S_N1$ and $S_N2$ reaction mechanisms.

The given compound $CH_3-O-CH_2-Br$ undergoes which of the following reactions?

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