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Which among the following is deactivati...

Which among the following is deactivating group ?

A

`-Cl`

B

`-OR`

C

`-NH_(2)`

D

`-NHR`

Text Solution

AI Generated Solution

The correct Answer is:
To determine which among the given options is a deactivating group, let's analyze each option step by step. ### Step 1: Understanding Deactivating Groups A deactivating group is a substituent that reduces the reactivity of the benzene ring towards electrophilic substitution reactions. This typically occurs due to the presence of electron-withdrawing effects, such as the -I (inductive) effect or -M (mesomeric) effect. ### Step 2: Analyzing Option A (Cl) - Chlorine (Cl) exhibits both a -I effect (inductive effect) and a +R effect (resonance effect). - The -I effect means that chlorine pulls electron density away from the benzene ring, which destabilizes the carbocation intermediate formed during electrophilic substitution. - Although it has a +R effect due to resonance, the -I effect is stronger in this case. - **Conclusion**: Cl is a deactivating group. ### Step 3: Analyzing Option B (OR) - The OR group (alkoxy group) has an oxygen atom that is electronegative. - The R group (alkyl) can donate electron density through the +I effect. - Overall, the OR group acts as an electron-donating group due to the +I effect, which enhances the reactivity of the benzene ring. - **Conclusion**: OR is an activating group. ### Step 4: Analyzing Option C (NH2) - The NH2 group (amino group) is a strong electron-donating group. - The nitrogen atom can donate electron density through resonance (+R effect) and has no significant -I effect. - This makes the benzene ring more reactive towards electrophilic substitution. - **Conclusion**: NH2 is an activating group. ### Step 5: Analyzing Option D (NHR) - The NHR group (where R is an alkyl group) also acts as an electron-donating group. - Similar to NH2, the nitrogen atom can donate electron density through resonance (+R effect). - Thus, it does not withdraw electrons significantly. - **Conclusion**: NHR is an activating group. ### Final Conclusion After analyzing all the options, the only deactivating group among the given options is **Option A: Cl**.

To determine which among the given options is a deactivating group, let's analyze each option step by step. ### Step 1: Understanding Deactivating Groups A deactivating group is a substituent that reduces the reactivity of the benzene ring towards electrophilic substitution reactions. This typically occurs due to the presence of electron-withdrawing effects, such as the -I (inductive) effect or -M (mesomeric) effect. ### Step 2: Analyzing Option A (Cl) - Chlorine (Cl) exhibits both a -I effect (inductive effect) and a +R effect (resonance effect). - The -I effect means that chlorine pulls electron density away from the benzene ring, which destabilizes the carbocation intermediate formed during electrophilic substitution. ...
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