In electrophilic aromatic substitution reaction, the nitro group is meta directing because it

Question

In electrophilic aromatic substitution reaction, the nitro group is meta directing because it, decreases electron density at ortho and para positions, decreases electron density at meta position, increases electron density at meta position, increases electron density at ortho and para positions

MARKS App · Accepted Answer

When nitro group is present in the benzene nucleus, it withdraws electrons from o and p -positions. Thus, the electron density at the o and p -positions decreases. m-positions become positions of comparatively higher electron density and therefore, electrophilic attack occurs at m-positions.

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