Home
Class 12
CHEMISTRY
Assertion (A): Aromatic carboxylic group...

Assertion (A): Aromatic carboxylic groups do not undergo Friedel- Crafts reaction.
Reason (R): Carboxyl group is deactivating and the catalyst aluminium chloride gets bonded to the carboxyl group

A

Both A and Rare true and R is the correct explanation of A

B

Both A and R are true but R is NOT the correct explanation of A

C

A is true but R is false

D

A is false and R is true

Text Solution

AI Generated Solution

The correct Answer is:
To analyze the assertion and reason provided in the question, we can break down the explanation into a step-by-step solution. ### Step-by-Step Solution: 1. **Understanding the Assertion (A)**: - The assertion states that aromatic carboxylic groups do not undergo Friedel-Crafts reactions. - Friedel-Crafts reactions are electrophilic aromatic substitution reactions that typically involve the introduction of alkyl or acyl groups onto an aromatic ring. 2. **Understanding the Reason (R)**: - The reason given is that the carboxyl group (-COOH) is a deactivating group. - Deactivating groups decrease the electron density of the aromatic ring, making it less reactive towards electrophiles. 3. **Role of the Carboxyl Group**: - The carboxyl group is indeed a strong electron-withdrawing group due to its -I (inductive) and -M (mesomeric) effects. - This withdrawal of electron density makes the aromatic ring less nucleophilic and thus less reactive towards electrophilic attack. 4. **Interaction with Aluminium Chloride (AlCl3)**: - Aluminium chloride (AlCl3) is a Lewis acid and acts as a catalyst in Friedel-Crafts reactions. - In the presence of a carboxylic acid, AlCl3 can coordinate with the oxygen of the carboxyl group, further decreasing the electron density of the aromatic ring. 5. **Formation of Carbocation**: - In a typical Friedel-Crafts reaction, a carbocation is generated which then attacks the aromatic ring. - However, due to the strong deactivating nature of the carboxyl group, the generated carbocation cannot effectively attack the aromatic ring. 6. **Conclusion**: - Since the carboxyl group is a strong deactivating group and interacts with AlCl3, it prevents the Friedel-Crafts reaction from occurring. - Therefore, both the assertion and the reason are correct, and the reason correctly explains why the assertion is true. ### Final Answer: Both the assertion (A) and the reason (R) are correct. The carboxylic group is a strong deactivating group, which prevents the Friedel-Crafts reaction from occurring. ---

To analyze the assertion and reason provided in the question, we can break down the explanation into a step-by-step solution. ### Step-by-Step Solution: 1. **Understanding the Assertion (A)**: - The assertion states that aromatic carboxylic groups do not undergo Friedel-Crafts reactions. - Friedel-Crafts reactions are electrophilic aromatic substitution reactions that typically involve the introduction of alkyl or acyl groups onto an aromatic ring. ...
Promotional Banner