Nitric acid acts as a base by accepting a proton.
Organic Compounds Containing Nitrogen
Reduction of alkyl isocyanides in presence of LiAlH 4 yields secondary amines containing methyl as one of the alkyl group.
Benzylamine is more basic than aniline.
The reason is that in aniline, the lone pair of nitrogen is conjugated with benzene ring so it is not available readily for others.
On the other hand in Benzylamine, nitrogen is not directly attached with ring so lone pairs are not conjugated with ring.
The Hofmann bromamide reaction is as : RCONH 2 + Br 2 + KOH RNH 2 The mechanism is as follows :
Ethyl isocyanide on hydrolysis form primary amines. Therefore it gives only one mono chloroalkane.
Gabriel phthalimide synthesis is used to prepare 1o aliphatic amine.
Basic strength availability of lone pair. In this case lone pair of
is highly participating in resonance.
Carbonyl carbon is lost as
.
In Dumas method nitrogen present in organic compound is converted into gas whose volumetric analysis gives the percentage of nitrogen atom in the organic compound.
Wurtz reaction is for the preparation of hydrocarbons from alkyl halide