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(C) Williamson's synthesis involves the reaction of an alkyl halide with a sodium alkoxide to form an ether. For the reaction to proceed via an $S_N2$

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$ CH_3Br $ and $ (CH_3)_3CONa $

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(C) Williamson's synthesis involves the reaction of an alkyl halide with a sodium alkoxide to form an ether. For the reaction to proceed via an $S_N2$ mechanism,the alkyl halide should be primary $(1^\circ)$ to minimize steric hindrance. If a tertiary alkyl halide is used,elimination (forming an alkene) predominates over substitution. Therefore,to prepare $tert$-butyl methyl ether,we should use a primary alkyl halide $(CH_3Br)$ and a tertiary alkoxide $((CH_3)_3CONa)$. This corresponds to option $C$.

The substances used for the preparation of ether by Williamson's synthesis are:

Similar Questions

Explain the preparation of ethers by dehydration of alcohols and its mechanism with a suitable example.

When a $1^o$ alkyl halide reacts with an alkoxide,what is the product obtained?

$CH_3-Br + NaO-C(CH_3)_3 \to ?$

Write the names of reagents and equations for the preparation of the following ethers by $Williamson$ synthesis:
$(i)$ $1-Propoxypropane$
$(ii)$ $Ethoxybenzene$
$(iii)$ $2-Methoxy-2-methylpropane$
$(iv)$ $1-Methoxyethane$

From Williamson's synthesis,the preparation of which of the following is possible?

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