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Nitration ethyl acetanilide

Dinitw4 etbyl l metbyl benzener CH CcH CaHB(NOa)3 mw 210.20, N13.33% yel crysts, mp 48.5° Prepd from 5-ethyl 2 methyl-acetanilide by nitration at -1Q8-mp 177-8°, hydrolysis to the aniline-mp 186° followed by diazotization/removal of the amino group... [Pg.183]

Arrange the following compounds in order of their reactivity towards nitration and give the formulae of the major products of the reactions (a) benzene, benzonitrile, methoxybenzene, tri-fluoromethyObenzene (b) acetanilide, benzoic acid, chlorobenzene, acetophenone (c) phenol, ethyl benzoate, nitrobenzene, bro-mobenzene. [Pg.87]

See other pages where Nitration ethyl acetanilide is mentioned: [Pg.268]    [Pg.85]    [Pg.142]    [Pg.205]    [Pg.205]   
See also in sourсe #XX -- [ Pg.85 ]



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