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Nitrohalobenzenes, nucleophilic displacement

The greater activation produced by a substituent when it is in the para-position than when it is in the ortrifluoromethyl groups are relatively inert to nucleophilic displacement but they approach acetoxy and trimethyl-ammonium groups in activating power. ... [Pg.232]

See other pages where Nitrohalobenzenes, nucleophilic displacement is mentioned: [Pg.232]    [Pg.125]    [Pg.157]    [Pg.241]    [Pg.244]    [Pg.244]    [Pg.157]    [Pg.244]    [Pg.157]    [Pg.325]    [Pg.367]   


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Nucleophilic displacement

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