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(B) Williamson ether synthesis involves the $S_{N}2$ reaction between an alkoxide ion and a primary alkyl halide. The reaction is favored when the lea

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Bicyclo[$2.2$.$2$]octan$-1-$ol and benzyl iodide

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(B) Williamson ether synthesis involves the $S_{N}2$ reaction between an alkoxide ion and a primary alkyl halide. The reaction is favored when the leaving group is good. In this case,the alkoxide is derived from bicyclo[$2.2$.$2$]octan$-1-$ol,and the alkyl halide is benzyl halide. Between benzyl chloride and benzyl iodide,benzyl iodide is preferred because $I^{-}$ is a better leaving group than $Cl^{-}$,making the $S_{N}2$ reaction faster.

The following compound can readily be prepared by Williamson ether synthesis by reaction between:

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