Which compound might be synthesized by the S_ | vedclass

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(D) The $S_N2$ mechanism involves a concerted nucleophilic substitution where a nucleophile attacks the electrophilic carbon of an alkyl halide,displa

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(D) The $S_N2$ mechanism involves a concerted nucleophilic substitution where a nucleophile attacks the electrophilic carbon of an alkyl halide,displacing the leaving group. $(1)$ The conversion of cyclohexylmethyl chloride to cyclohexylmethanol using $NaOH$ in $DMSO$ is an $S_N2$ reaction. $(2)$ The reaction of cyclohexyl iodide with $NaSEt$ in $DMSO$ to form ethyl cyclohexyl sulfide is an $S_N2$ reaction. $(3)$ The Williamson ether synthesis,where $Me_3C-O^-Na^+$ reacts with $Me-I$ to form $Me_3C-O-CH_3$,is a classic $S_N2$ reaction involving a primary alkyl halide $(Me-I)$. Since all three reactions proceed via the $S_N2$ mechanism,the correct answer is $(D)$.

Which compound might be synthesized by the $S_N2$ displacement of an alkyl-halide?

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