Although phenoxide ion has more number o | Class 12 Chemistry Chapter Aldehydes Ketones and Carboxylic Acids, Aldehydes Ketones and Carboxylic Acids NCERT Solutions

Q20.

Although phenoxide ion has more number of resonating structures than carboxylate ion, carboxylic acid is a stronger acid than phenol. Why?

Resonance structures of phenoxide ion are:

It can be observed from the resonance structures of phenoxide ion that in II, III and IV, less electronegative carbon atoms carry a negative charge. Therefore, these three structures contribute negligibly towards the resonance stability of the phenoxide ion. Hence, these structures can be eliminated. Only structures I and V carry a negative charge on the more electronegative oxygen atom.

Resonance structures of carboxylate ion are:

In the case of carboxylate ion, resonating structures I”² and II”² contain a charge carried by a more electronegative oxygen atom.

Further, in resonating structures I”² and II”², the negative charge is delocalized over two oxygen atoms. But in resonating structures I and V of the phexoxide ion, the negative charge is localized on the same oxygen atom. Therefore, the resonating structures of carboxylate ion contribute more towards its stability than those of phenoxide ion. As a result, carboxylate ion is more resonance-stabilized than phenoxide ion. Hence, carboxylic acid is a stronger acid than phenol.

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This question is important because it tests key concepts from the NCERT syllabus and is frequently asked in CBSE exams.

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What is the correct answer to: Although phenoxide ion has more number of resonating structures than carboxylate ion, carboxylic acid is a stronger acid than phenol. Why??

Resonance structures of phenoxide ion are:



It can be observed from the resonance structures of phenoxide ion that in II, III and IV, less electronegative carbon atoms carry a negative charge. Therefore, these thre...

How do you solve Although phenoxide ion has more number of resonating structures than carboxylate ion, carboxylic acid is a stronger acid than phenol. Why? step by step?

Step-by-step explanation:
• Resonance structures of phenoxide ion are:



• It can be observed from the resonance structures of phenoxide ion that in II, III and IV, less electronegative carbon atoms carry a negative charge

What common mistakes should be avoided in this question?

Students often lose marks by skipping steps, writing incomplete explanations, or misunderstanding keywords used in the question.

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