Which of the following ethers cannot be produ | vedclass

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(D) Williamson ether synthesis involves the $S_N2$ reaction of an alkoxide ion with a primary alkyl halide. It cannot be used to prepare ethers where

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All of these

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(D) Williamson ether synthesis involves the $S_N2$ reaction of an alkoxide ion with a primary alkyl halide. It cannot be used to prepare ethers where the halide is a vinyl halide,aryl halide,or tertiary alkyl halide because these do not undergo $S_N2$ reactions effectively.$1.$ For $(a)$,the reactants would be $(CH_3)_3C-O^-$ and $CH_2=CH-X$ (vinyl halide) or $CH_2=CH-O^-$ and $(CH_3)_3C-X$ (tertiary halide).$2.$ For $(b)$,the reactants would be $Ph-O^-$ and $Ph-X$ (aryl halide).$3.$ For $(c)$,the reactants would be $CH \equiv C-O^-$ and $CH_2=CH-X$ (vinyl halide).Since none of these reactions are feasible via $S_N2$,none of these ethers can be produced.

Which of the following ethers cannot be produced by Williamson ether synthesis?

Similar Questions

Consider the following methods $:$
$I$: Hydration of olefins
$II$: Hydrolysis of alkyl halide
$III$: Reduction of carbonyl compounds
Which of these can be used to prepare alcohols ?

Consider the following reaction:
Which response contains all the correct statements about this process?
$1.$ Dehydration
$2.$ $E_2$ mechanism
$3.$ Carbon skeleton migration
$4.$ Most stable alkene will form
$5.$ Single-step reaction

Match List-$I$ with List-$II$. Choose the correct answer from the options given below:

The correct match about the reaction sequence shown above is:

Which of the following reactions will produce a primary alcohol?

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