Which of the following reagents should be used to prepare tert-butyl ethyl ether?

t e r t

-butyl bromide and sodium ethoxide

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t e r t

-butyl alcohol and ethyl bromide

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t e r t

-butyl alcohol and ethanol

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potassium

t e r t

-butoxide and ethyl bromide

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Solution

The correct option is D potassium $t e r t$ -butoxide and ethyl bromide

$t e r t$ -butyl ethyl ether can be prepared by the reaction of potassium $t e r t$ -butoxide with ethyl bromide.

The process is Williamson synthesis.

This reaction follows $S_{N} 2$ mechanism.

Option D is correct.

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Similar questions

When ethyl chloride is added to Sodium tert-butoxide, ethyl tert-butyl ether is obtained as the major product (shown below):

When the concentration of ethyl chloride is doubled, the reaction rate:

When ethyl chloride is added to Sodium tert-butoxide, ethyl tert-butyl ether is obtained as the major product (shown below):

What happens to the rate if the temperature is increased?

To prepare tert-butyl ethyl ether, the reagents required are:

Q. (A) Tert butyl methyl ether is not prepared by the reaction of tert butyl bromide with sodium methoxide.
(R) Sodium methoxide is a strong nucleophile.

Q. Convert Ethyl alcohol to Tert-Butyl alcohol.

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Which of the following reagents should be used to prepare tert-butyl ethyl ether?

The correct option is D potassium tert-butoxide and ethyl bromide tert-butyl ethyl ether can be prepared by the reaction of potassium tert-butoxide with ethyl bromide. The process is Williamson synthesis.This reaction follows SN2 mechanism.Option D is correct.

The correct option is D potassium $t e r t$ -butoxide and ethyl bromide

$t e r t$ -butyl ethyl ether can be prepared by the reaction of potassium $t e r t$ -butoxide with ethyl bromide.

The process is Williamson synthesis.

This reaction follows $S_{N} 2$ mechanism.

Option D is correct.