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amide → -COOH + NH3 (3)
hydrolysis, dilute acid or alkali, reflux
amide → -COOH + 1o amine (3)
hydrolysis, dilute acid or alkali, reflux
amide → amine + H2O (3)
reduction, LiAlH4, dry ether room temp
acyl chloride → amide (2)
condensation, NH3 or amine
phenylamine → 2,4,6-tribromophenylamine + 3HBr (3)
electrophilic substitution, aq Br2, room temp
phenylamine → diazonium salt + H2O (3)
electrophilic substitution, HNO2 and HCl, below 10C
how is HNO2 formed (1)
NaNO2 and HCl
diazonium salt → azo compound (3)
coupling, phenol, NaOH
nitrobenzene → phenylamine (4)
reduction, hot Sn and conc HCl, reflux, followed by deprotination of product with NaOH
how is phenylamine separated
steam distillation