Published by:
CGP EDU Academic Team
Published on: August 14, 2026
The following steps are given for the mechanism of esterification of carboxylic acids.
(I) The protonated esters loses a proton to give the ester.
(II) Protonation of the carbonyl oxygen activates the carbonyl group towards nucleophilic addition of the alcohol.
(III) Proton transfer in the tetrahedral intermediate occurs.
(IV) Nucleophilic attack of alcohol on protonated carbonyl group.
Arrange the following steps in their correct sequence.
Text Solution
Verified by ExpertsThe correct answer is:
C

Prepare Smarter with CGP Edu
Get practice questions, solutions, and test series in one place.
Write a Review
Share your experience with this question and solution.
Commentary
Send your comment, doubt, correction, or feedback to admin.
Similar Questions
Explore conceptually related problems
Which of the following gives alcohol, when treated with phenyl magnesium bromide?
In the reaction of with carbonyl compounds to form bisulphite product, the nucleophile is
Select the correct dissimilarities between and bond.
Cyanohydrin formation constant will be the highest for
Choose the correct statement from the following with respect to nucleophilic addition
reaction.
Cyanohydrin contains
II
IV
III
IV
III
II
IV
III
I
II
IV
I