In electrophilic aromatic substitution reaction, the nitro group is meta directing because it
Text Solution
Verified by ExpertsD
: The directive influence of
as an electrophile in electrophilic aromatic substitution is due to the
effect or electron withdrawing effect of
, and can be explained on the basis of the resonating structures obtained by the attack of the group on the benzene ring:

The substituent, i.e.,
withdraws electrons from
and
-positions. Thus,
-position becomes a point of relatively high electron density and further substitution by electrophile occurs at
-position.
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