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प्रश्न
Give the structures of A, B and C in the following reaction:
उत्तर
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संबंधित प्रश्न
Write short notes on the following Hofmann’s bromamide reaction
Give the structures of A, B and C in the following reaction:
Give the structures of A, B and C in the following reaction.
Write the reactions of aromatic with nitrous acid.
Explain the mechanism of action of hydroiodic acid on 3-methylbutan-2-ol.
Arrange the following in the increasing order of their pKb values:
C6H5NH2, C2H5NH2, C6H5NHCH3
Answer in one sentence.
Predict the product of the following reaction.
\[\ce{Nitrobenzene ->[Sn/conc.HCl]?}\]
Explain Hoffmann’s exhaustive alkylation with suitable reactions.
Identify the product obtained when benzyl chloride undergoes ammonolysis in presence of excess ammonia followed by the reaction with two moles of methyl iodide.
Which nitrogen containing compound amongst the following would undergo Mendius reduction to furnish primary amine \[\ce{(R - NH2)}\]?
Reduction of aromatic nitro compounds using \[\ce{Fe}\] and \[\ce{HCl}\] gives ______.
Best method for preparing primary amines from alkyl halides without changing the number of carbon atoms in the chain is ______.
Which of the following compounds is the weakest Brönsted base?
Which of the following amines can be prepared by Gabriel synthesis.
(i) Isobutyl amine
(ii) 2-Phenylethylamine
(iii) N-methylbenzylamine
(iv) Aniline
The amine 'A' when treated with nitrous acid gives yellow oily substance. The amine A is ______.
Identify the product ‘C’ in the following reaction.
\[\ce{Aniline ->[(CH3CH)2O][Pyridine] A ->[Br2][CH3COOH] B ->[H^+ or OH^-] C}\]
Write short note on the following:
Ammonolysis
Write a short note on the following:
Ammonolysis.