Chemistry, asked by Parthasaha7799, 1 year ago

Why a no2 group is meta directing in benzene ring in nitrobenzene?

Answers

Answered by aayushg1713
6

NO2 has a strong and dominating -M effect. So due to resonance more +ve charge is developed on ortho and para positions. Due to more + charge than meta on ortha and para the electrophilic substitution is preferred at meta position as there is more electron density than other positions.

Answered by jeevankishorbabu9985
0

Answer:

⌬ +be charge

Explanation:

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