Advertisements
Advertisements
प्रश्न
Give the structures of A, B and C in the following reactions :

Advertisements
उत्तर

APPEARS IN
संबंधित प्रश्न
Give a plausible explanation for the following:
Why are amines less acidic than alcohols of comparable molecular masses?
Explain Hoffmann’s exhaustive alkylation with suitable reactions.
The end product C of the following reaction is
\[\ce{C2H5NH2 ->[HNO2] A ->[PCl5] B ->[NH3][Alcohol] C}\]

Identify the major product (B).
Which of the following amines cannot be prepared by Gabriel phthalimide synthesis?
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
Assertion: Aromatic 1° amines can be prepared by Gabriel Phthalimide Synthesis.
Reason: Aryl halides undergo nucleophilic substitution with anion formed by phthalimide.
The compound X is which of the following?
\[\ce{CH3CN ->[Na + C2H5OH] x}\]
Write a short note on the following:
Ammonolysis
