KnowraElectrophilic aromatic substitutionLinked fromLinked fromThe 52 pages that link to Electrophilic aromatic substitution, each with the reason it gives.All 52Broader topic 4Related 30Narrower topic 12Compared with 6Friedel–Crafts reactionNarrower topic: Friedel–Crafts alkylation and acylation are members of this reaction family.NitrationNarrower topic: This is the usual pathway for nitrating electron-rich aromatic rings.Friedel–Crafts acylationNarrower topic: Acylation follows this general mechanism, including formation and loss of a sigma complex.TolueneNarrower topic: The methyl group directs many ring substitutions toward the ortho and para positions.DiazotizationNarrower topic: Azo coupling, one major use of diazonium salts, proceeds by this reaction family.SulfonationNarrower topic: Aromatic sulfonation proceeds by replacing a ring hydrogen with an electrophilic sulfur-containing group.ThiopheneNarrower topic: Thiophene commonly undergoes substitution rather than addition, retaining aromaticity.ChlorobenzeneNarrower topic: Chlorobenzene undergoes this reaction family, though chlorine slows it relative to benzene.AnisoleNarrower topic: Anisole’s characteristic ring reactions belong to this broader reaction family.NitrobenzeneNarrower topic: The nitro group deactivates the ring and directs incoming electrophiles mainly to the meta position.BenzofuranNarrower topic: It describes common substitution reactions of benzofuran’s electron-rich fused system.Chlorosulfuric acidNarrower topic: Aromatic sulfonation with chlorosulfuric acid proceeds by electrophilic substitution.