Question:
Diethyl ether when refluxed with excess of $HI$ gives two molecules of $(i)$. Ethers can be most commonly prepared by reaction of $(ii)$ and $(iii)$. The method is called $(iv)$.
$(i)$, $(ii)$, $(iii)$ and $(iv)$ respectively are
Diethyl ether when refluxed with excess of $HI$ gives two molecules of $(i)$. Ethers can be most commonly prepared by reaction of $(ii)$ and $(iii)$. The method is called $(iv)$.
$(i)$, $(ii)$, $(iii)$ and $(iv)$ respectively are
Updated On: Jul 6, 2022
- ethyl iodide, sodium alkoxide, alkyl halide, Williamson?? synthesis
- ethanol, alcohol, alkyl halide, substitution
- methyl iodide, Grignard?? reagent, alkyl halide, Williamsons synthesis
- ethyl iodide, phenol, ethyl iodide, esterification
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The Correct Option is A
Solution and Explanation
Answer (a) ethyl iodide, sodium alkoxide, alkyl halide, Williamson?? synthesis
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Concepts Used:
Alcohols, Phenols, and Ethers
Alcohol is formed when a saturated carbon atom bonds to a hydroxyl (-OH) group. It is an organic compound that contains a hydroxyl functional group attached to a carbon atom.
Phenol is formed when the -OH group replaces the hydrogen atom in benzene. It is an organic compound in which a hydroxyl group directly attaches to an aromatic hydrocarbon.
Ether is formed when oxygen atom bonds to two alkyl or aryl groups. It is an organic compound that has an oxygen atom that is connected to two aryl and alkyl groups.
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