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Benzene, acylation halogen additions

Benzene s aromaticity causes it to undergo electrophilic aromatic substitution reactions. The electrophilic addition reactions characteristic of alkenes and dienes would lead to much less stable nonaromatic addition products. The most common electrophilic aromatic substitution reactions are halogenation, nitration, sulfonation, and Friedel-Crafts acylation and alkylation. Once the electrophile is generated, all electrophilic aromatic substitution reactions take place by the same two-step mechanism (1) The aromatic compound reacts with an electrophile, forming a carbocation intermediate and (2) a base pulls off a proton from the carbon that... [Pg.617]


See other pages where Benzene, acylation halogen additions is mentioned: [Pg.255]    [Pg.1059]    [Pg.394]    [Pg.394]    [Pg.228]    [Pg.434]    [Pg.98]    [Pg.194]    [Pg.572]    [Pg.715]   
See also in sourсe #XX -- [ Pg.1046 ]




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