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Benzamide benzene

Scheme 16 are easily distinguished by the different products obtained, and by the breaks in the LFER plots of the log ko values against mechanism changes.287 The O-protonation mechanism of Scheme 16 is preferred over the more obvious JV-protonation one on the basis of the observed m values.287 The further decomposition of the first-formed benzamide, benzene-sulfonamide and jV-nitroamine reaction products takes place as previously discussed. [Pg.57]

No Name Boiling poinl, X Melting point, C "d Density g/ml Acetamide Benzamide Benzene sulfon- amide P- Toluene sulfon- amide Phenyl thiourea Picrate Miscellaneous... [Pg.295]

No Name Melting point C Boiling point C Acetamide Benzamide Benzene sulfon amide P Toluene sulfon amide Phenyl thiourea Picraie Miscellaneous... [Pg.305]

No Name Mdting point. C Boiling point, C Acetamide Benzamide Benzene suifon amide P- Toluene suifon amide Micnyl thiourea Picrate Miscellaneous... [Pg.308]

See other pages where Benzamide benzene is mentioned: [Pg.1374]    [Pg.1376]   
See also in sourсe #XX -- [ Pg.229 ]



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