explanation ..........
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When an electron withdrawing group(Like NO2) is present on benzene ring, it withdraws electron from benzene ring due to resonance (Pi- LP conjugation),creating deficiency of electrons on ortho and para positions.Hence Nucleophile easily comes attacks the electron deficient site.
You can try it:Just draw a benzene ring with NO2 on top and draw resonating structures of it.You’ll get to know
that is why the answer is (4)
rithu35:
but the answer is 3
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