Why does nitrobenzene fail to undergo Friedel-Crafts alkylation with tert-butyl chloride and AlCl₃? A) nitrobenzene reacts with AlCl₃ B) nitrobenzene is a poor nucleophile C) the nitro group is a strong electron donating group D) the tert-butyl cation is a poor electrophile

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Nitrobenzene is a poor nucleophile because the nitro group is a strong electron-withdrawing group, which decreases the electron density on the benzene ring, making it less reactive towards electrophilic aromatic substitution reactions like Friedel-Crafts alkylation.

Why Does Nitrobenzene Fail to Undergo Friedel-Crafts Alkylation with Tert-Butyl