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Assertion : The presence of nitro group...

Assertion : The presence of nitro group facilitates nucleophilic substiution reactions in aryl halides. Reason : The intermediate carbanion is stabilised due to the presence of nitro group.

A

a. if both Assertion and Reason are true and reason is the correct explanation of the assertion.

B

b. if both assertion and reason are true but reason is not the correct expalanation of the assertion

C

c. if assertion is true, reason is false

D

d. both assertion and reason are false statements.

Text Solution

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The correct Answer is:
To solve the question, we need to analyze both the assertion and the reason provided. ### Step 1: Understand the Assertion The assertion states that "The presence of nitro group facilitates nucleophilic substitution reactions in aryl halides." - Aryl halides are compounds where a halogen atom is bonded to an aromatic ring. - The nitro group (-NO2) is an electron-withdrawing group that increases the electrophilicity of the aromatic ring. This means that it makes the ring more susceptible to nucleophilic attack. **Hint:** Consider how electron-withdrawing groups affect the reactivity of aromatic compounds. ### Step 2: Understand the Reason The reason states that "The intermediate carbanion is stabilized due to the presence of nitro group." - In nucleophilic aromatic substitution (SNAr), a nucleophile attacks the aromatic ring, forming a negatively charged intermediate (carbanion). - The nitro group can stabilize this carbanion through resonance. When the carbanion forms, the negative charge can be delocalized onto the nitro group, which stabilizes the intermediate. **Hint:** Think about how resonance structures can distribute charge and stabilize intermediates. ### Step 3: Analyze the Relationship Now, we need to determine if the reason correctly explains the assertion. - Since the nitro group does facilitate nucleophilic substitution by stabilizing the carbanion intermediate, the reason does indeed provide a correct explanation for the assertion. **Hint:** Reflect on whether the stabilization of the intermediate is crucial for the reaction to proceed. ### Conclusion Both the assertion and the reason are true, and the reason is the correct explanation of the assertion. ### Final Answer The correct option is: **A** - Both assertion and reason are true, and reason is the correct explanation of the assertion.

To solve the question, we need to analyze both the assertion and the reason provided. ### Step 1: Understand the Assertion The assertion states that "The presence of nitro group facilitates nucleophilic substitution reactions in aryl halides." - Aryl halides are compounds where a halogen atom is bonded to an aromatic ring. - The nitro group (-NO2) is an electron-withdrawing group that increases the electrophilicity of the aromatic ring. This means that it makes the ring more susceptible to nucleophilic attack. **Hint:** Consider how electron-withdrawing groups affect the reactivity of aromatic compounds. ...
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