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Electron-withdrawing groups aromatic substitution, carbanion

Note the differences between electrophilic and nucleophilic aromatic 1 substitutions Electrophilic substitutions are favored by electron-donofi g substituents, which stabilize the carbocation intermediate, while nucleophilic substitutions are favored by d ron-withdrawing substituents, which stabilize a carbanion intermediate. The electron-withdrawing groups that deactivate rings for electrophilic substitution (nitro, carbonyl, cyano, and so on) activate them for nucleophilic substitution. What s more, these groups are meta directors in electrophilic substitution, but are ortho-para directors in nucleophilic substitution. [Pg.620]


See other pages where Electron-withdrawing groups aromatic substitution, carbanion is mentioned: [Pg.241]    [Pg.241]    [Pg.1162]    [Pg.138]    [Pg.1078]    [Pg.199]    [Pg.800]    [Pg.1187]    [Pg.346]    [Pg.594]    [Pg.131]    [Pg.704]    [Pg.174]    [Pg.544]    [Pg.915]    [Pg.591]    [Pg.660]    [Pg.171]    [Pg.376]    [Pg.539]    [Pg.401]   


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Aromatic carbanions

Aromatic groups

Carbanion substitution

Carbanions aromatic substitution

Carbanions substitution

Electron aromatic

Electron withdrawal

Electron withdrawers

Electron withdrawing groups

Electron-withdrawing groups substitution

Electrons substitution

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