Why a no2 group is meta directing in benzene ring in nitrobenzene?
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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.
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Answer:
⌬ +be charge
Explanation:
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