COMEDK2025ChemistryAlcohols Phenols and EthersActual
What are the intermediates formed during the reactions A and B ? A. Reimer-Tiemann reaction. B. Dehydration of alcohols in the slow rate determining step.
Correct answer
3
Step-by-step solution
A. Reimer-Tiemann Reaction: Phenol is treated with CHCl₃ and NaOH . The base generates dichlorocarbene (:CCl₂) , which attacks the ortho position of the phenoxide ion. The intermediate is sodium 2-(dichloromethyl)phenolate — a phenoxide ring with an ortho -CHCl₂ group (option 4, structure A). B. Dehydration of Alcohols (slow step): In acid-catalyzed E1 dehydration, the slow rate-determining step is the breaking of the C - O bond after protonation of -OH , forming a carbocation R^+ . The intermediate is the carbocat