(C) The reaction of a sodium alkoxide with an alkyl halide to form an ether is known as $Williamson$ synthesis. This reaction proceeds via an $S_N2$ m

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(C) The reaction of a sodium alkoxide with an alkyl halide to form an ether is known as $Williamson$ synthesis. This reaction proceeds via an $S_N2$ mechanism where the alkoxide ion acts as a nucleophile and attacks the alkyl halide. The given reaction is: $CH_3-C(CH_3)_2-ONa + CH_3-CH_2-Cl \rightarrow CH_3-C(CH_3)_2-O-CH_2-CH_3 + NaCl$.

Class 12 Chemistry Alcohols, Phenols and Ethers Properties of Ethers

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This reaction,$CH_3-C(CH_3)_2-ONa + CH_3-CH_2-Cl \xrightarrow{-NaCl} CH_3-C(CH_3)_2-O-CH_2-CH_3$ is called:

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A
Etard reaction
B
Gattermann-Koch reaction
C
Williamson synthesis
D
Williamson continuous etherification process

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Alcohols, Phenols and Ethers

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Properties of Ethers

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This reaction,$CH_3-C(CH_3)_2-ONa + CH_3-CH_2-Cl \xrightarrow{-NaCl} CH_3-C(CH_3)_2-O-CH_2-CH_3$ is called:

Similar Questions

Anisole can be prepared by the action of methyl iodide on sodium phenate. The reaction is called:

$C_2H_5I$ and $Ag_2O$ react to produce:

The products formed in the following reaction are $C_6H_5-OCH_3 + HI \xrightarrow{\text{heat}}$

Which of the reactants given below is/are suitable for the preparation of Methoxybenzene?$(x)$ $C_6H_5Br + CH_3ONa$$(y)$ $C_6H_5ONa + CH_3Br$

Which of the following compounds does $NOT$ undergo Williamson's synthesis?

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Which of the reactants given below is/are suitable for the preparation of Methoxybenzene?
$(x)$ $C_6H_5Br + CH_3ONa$
$(y)$ $C_6H_5ONa + CH_3Br$