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Assertion: p-Chlorobenzoic acid is stron...

Assertion: p-Chlorobenzoic acid is stronger than benzoic acid.
Reason: Chlorine has electron-donating resonance `(+R)`- effect.

A

if both assertion and reson are true, and reason is the true explanation of the assertion.

B

If both assertion and reason are true, but reason is not the true explanation of the assertion.

C

if assertion is true, but reason is false.

D

If both assertion and reason are false.

Text Solution

AI Generated Solution

The correct Answer is:
To solve the question, we need to analyze the assertion and the reason given: ### Step 1: Understand the Assertion The assertion states that p-Chlorobenzoic acid is stronger than benzoic acid. - **Benzoic acid (C6H5COOH)** is a carboxylic acid with a phenyl group attached to the carboxyl group. - **p-Chlorobenzoic acid (C6H4ClCOOH)** has a chlorine atom at the para position relative to the carboxyl group. ### Step 2: Analyze the Acidity The strength of an acid is determined by its ability to donate a proton (H+). The stability of the conjugate base formed after the proton is lost is crucial in determining acidity. - When benzoic acid donates a proton, it forms the benzoate ion (C6H5COO-). - When p-chlorobenzoic acid donates a proton, it forms the p-chlorobenzoate ion (C6H4ClCOO-). ### Step 3: Consider the Effect of Chlorine Chlorine is an electronegative atom and exhibits a -I (inductive) effect, which pulls electron density away from the carboxyl group. However, it also has a +R (resonance) effect due to its ability to donate electron density through resonance. - The -I effect of chlorine stabilizes the conjugate base of p-chlorobenzoic acid more than the +R effect destabilizes it. ### Step 4: Conclusion on Acidity Since the -I effect of chlorine is stronger than its +R effect, the conjugate base of p-chlorobenzoic acid is more stable than that of benzoic acid. Therefore, p-chlorobenzoic acid is indeed a stronger acid than benzoic acid. ### Step 5: Evaluate the Reason The reason states that chlorine has an electron-donating resonance (+R) effect. This statement is misleading because while chlorine does have a +R effect, its -I effect is more significant in this context, making the reasoning incorrect. ### Final Conclusion - **Assertion**: True (p-Chlorobenzoic acid is stronger than benzoic acid). - **Reason**: False (Chlorine's -I effect dominates over its +R effect). ### Answer The correct answer is that the assertion is true, but the reason is false. ---

To solve the question, we need to analyze the assertion and the reason given: ### Step 1: Understand the Assertion The assertion states that p-Chlorobenzoic acid is stronger than benzoic acid. - **Benzoic acid (C6H5COOH)** is a carboxylic acid with a phenyl group attached to the carboxyl group. - **p-Chlorobenzoic acid (C6H4ClCOOH)** has a chlorine atom at the para position relative to the carboxyl group. ### Step 2: Analyze the Acidity ...
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