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Experiment: Halogenation: Electrophilic Aromatic Substitution to Yield 4-Bromoacetanilide The experiment we conducted (or tried to conduct!
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Experiment: Halogenation: Electrophilic Aromatic Substitution to Yield 4-Bromoacetanilide

The experiment we conducted (or tried to conduct!) involved the bromination of acetanilide using Br2 (in acetic acid) WITHOUT a catalyst. The reaction equation was : acetanilide + Br2 = p-bromoacetanilide + HBr

We did NOT use an "iron catalyst" (FeBr3) since the substituent group on the benzene is "activating"- that is it releases electron density to the benzene ring system and makes the ring more nucleophilic.

What could be used to make a great theory of this experiment.

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