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Explain the following with an example.
(i) Kolbes reaction.
(ii) Reimer-Tiemann reaction.
(iii) Williamson ether synthesis.
(iv) Unsymmetrical ether.

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(i) Kolbes reaction.
It is a decarboxylative dimerisation of two carboxylic acids (or carboxylate ions)  to form carbon carbon bond of alkane.

 

(ii) Reimer-Tiemann reaction.
It involves the ortho-formylation of phenols. Phenol is converted to salicylaldehyde.

 

(iii) Williamson ether synthesis.
Sodium alkoxide reacts with alkyl halide to form an ether.

 

(iv) Unsymmetrical ether.
Two different alkyl groups are attached to O atom. The general formula is . An example is ethyl methyl ether .
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Question Text
Explain the following with an example.
(i) Kolbes reaction.
(ii) Reimer-Tiemann reaction.
(iii) Williamson ether synthesis.
(iv) Unsymmetrical ether.
Updated OnFeb 20, 2024
TopicAlcohols, Phenols and Ethers
SubjectChemistry
ClassClass 12
Answer TypeText solution:1 Video solution: 11
Upvotes1089
Avg. Video Duration9 min