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प्रश्न
Account for the following:
Aniline cannot be prepared by the ammonolysis of chlorobenzene under normal conditions.
उत्तर
In case of chlorobenzene, the C – Cl bond is quite difficult to break as it acquires a partial double bond character due to conjugation. So Under the normal conditions, ammonolysis of chlorobenzene does not yield aniline.
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संबंधित प्रश्न
Write the reactions of aromatic with nitrous acid.
Explain Hoffmann’s exhaustive alkylation with suitable reactions.
Identify compound 'B' in following series of reactions?
\[\ce{Acetonitrile ->[Na/alcohol] A ->[NaNO2/dil.HCI] B}\]
Which of the following amines cannot be prepared by Gabriel phthalimide synthesis?
Identify product B in the following reaction.
\[\ce{Aniline ->[NaNO2][HCl] A ->[KI] B}\]
Which of the following amines can be prepared by Gabriel synthesis.
(i) Isobutyl amine
(ii) 2-Phenylethylamine
(iii) N-methylbenzylamine
(iv) Aniline
Identify A and B in the following reaction.
Assertion: Hoffmann’s bromamide reaction is given by primary amines.
Reason: Primary amines are more basic than secondary amines.
Assertion: Aromatic 1° amines can be prepared by Gabriel Phthalimide Synthesis.
Reason: Aryl halides undergo nucleophilic substitution with anion formed by phthalimide.
Identify the compo ds A and B in the following reactions:
\[\ce{A ->[Nitrating mixture] B ->[(i) Sn/cone. HCI][(ii) NaOH] Aniline}\]
