Published by:
CGP EDU Academic Team
Published on: August 12, 2026
The correct order of increasing acidic strength is:
A
Phenol < ethanol < chloroacetic acid < acetic acid
B
Ethanol < phenol < chloroacetic acid < acetic acid
C
Ethanol < phenol < acetic acid < chloroacetic acid
D
Chloroacetic acid < acetic acid 
phenol 
ethanol
phenol ethanol
Text Solution
Verified by ExpertsThe correct answer is:
C
Due to formation of more stable conjugate base after removal of H from phenol, therefore
phenol is more stable than alcohol. On the other hand, carboxylic acid is more acidic than phenol due to formation of more stable conjugate base after removal of H as compared to phenol. Chloroacetic acid is more acidic than acetic acid due to the presence of electron withdrawing chlorine group attached to a carbon of carboxylic acid.
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
Addition of water to alkynes occurs in acidic medium and in the presence of ions as a
catalyst. Wh…
Which of the following compounds is most reactive towards nucleophilic addition reactions?
Compound can be prepared by the reaction of:
The reagent which does not react with both, acetone and benzaldehyde?
Cannizzaro's reaction is not given by:
Which products is formed when the compound is treated with concentrated
aqueous KOH solution?