Give the names of the reagents and equations for the preparation of the following ethers by Williamson synthesis:
$(i)$ Methoxybenzene $(ii)$ Methoxyethane $(iii)$ Ethoxybenzene $(iv)$ Ethoxyethane

Vedclass pdf generator app on play store
Vedclass iOS app on app store
(N/A) $(i)$ Methoxybenzene: Sodium phenoxide $(C_6H_5ONa)$ + Methyl chloride $(CH_3Cl)$ $\rightarrow$ Methoxybenzene $(C_6H_5OCH_3)$ + $NaCl$
$(ii)$ Methoxyethane: Sodium methoxide $(CH_3ONa)$ + Ethyl chloride $(CH_3CH_2Cl)$ $\rightarrow$ Methoxyethane $(CH_3OCH_2CH_3)$ + $NaCl$
$(iii)$ Ethoxybenzene: Sodium phenoxide $(C_6H_5ONa)$ + Ethyl chloride $(CH_3CH_2Cl)$ $\rightarrow$ Ethoxybenzene $(C_6H_5OCH_2CH_3)$ + $NaCl$
$(iv)$ Ethoxyethane: Sodium ethoxide $(CH_3CH_2ONa)$ + Ethyl chloride $(CH_3CH_2Cl)$ $\rightarrow$ Ethoxyethane $(CH_3CH_2OCH_2CH_3)$ + $NaCl$

Explore More

Similar Questions

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

Difficult
View Solution

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

Ethers can be prepared by Williamson synthesis in which an alkyl halide is reacted with sodium alkoxide. Di-tertiary ether cannot be prepared by this method. Explain.

The compound $(CH_3)_3C-O-CH_3$ is best prepared by which of the following reactions?

Difficult
View Solution

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

Vedclass Products

For Students

Vedclass Test Series

Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.

Start Free Trial
For Teachers

Exam Paper Generator

Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.

Try Free
For Institutes

Online Exam Module

Live online exams with unlimited students, 360° analytics & white-label branding.

See Demo