For carbylamine reaction, we need hot alcoholic KOH and
any primary amine and chloroform
chloroform and silver powder
a primary amine and an alkyl halide
a mono alkyl amine and trichloromethane
Acetamide and ethyl amine can be distinguished by reacting with
aqueous HCI and heat
aqueous NaOH and heat
acidified KMnO4
bromine water
Amides can be converted into amines by a reaction named after
Perkin
Claisen
Hofmann
Kekule
Phenyl isocyanides are prepared from which of the following reaction ?
Rosenmund's reaction
Carbylamine reaction
Reimer-Tiemann reaction
Wurtz reaction
An organic compound A on reduction with chloroform and potassium hydroxide forms C. The compound C on catalytic reduction gives N-methylaniline. The compound A is
nitrobenzene
nitromethane
methylamine
aniline
In the reaction,
the term Y is
acetone
ethanamine
acetaldehyde
dimethyl amine
Aniline is reacted with bromine water and the resulting product is treated with an aqueous solution of sodium nitrite in presence of dilute hydrochloric acid. The compound so formed is converted into a tetrafluoroborate which is subsequently heated. The final product is
1,3,5-tribromobenzene
p-bromofluorobenzene
p-bromoaniline
2,4,6-tribromofluorobenzene
The decomposition of organic compounds, in the presence of oxygen and without the development of odoriferous substances, is called
decay
N2-fixation
nitrification
denitrification
Which one of the following on reduction with LiAIH4 yields a secondary amine ?
Methyl isocyanide
Acetamide
Methyl cyanide
Nitroethane
The final product C, obtained in this reaction
would be