Primary amine reacts in presence of chloroform gives isonitrile which is toxic in nature which further reacts in presence of HCl/H3O+ to give primary amine and acid.
Hence, A-primary amine, B-isonitrile compound and C-conc.
HCl.
Primary amine reacts in presence of chloroform gives isonitrile which is toxic in nature which further reacts in presence of HCl/H3O+ to give primary amine and acid.
Hence, A-primary amine, B-isonitrile compound and C-conc.
HCl.
Gabriel phthalimide synthesis
Explanation : aniline is more basic than acetamide because in acetamide, lone pair of nitrogen is delocalized to more electronegative element oxygen.
In Aniline lone pair of nitrogen delocalized over benzene ring.
The intermolecular association is more prominent in case of primary amines as compared to secondary, due to the availability of two hydrogen atom.
Hofmann bromamide degradation In this degradation, the migration of the alkyl/aryl group occurs to the electron-deficient nitrogen (nitrene).
Statement (I) is not absolutely correct as it mentions only the alkyl group, whereas migration of aryl groups may also occur depending on migratory aptitude.
Statement (II) is correct as the migration occurs to the electron-deficient atom.
Aniline does not undergo Friedel Craft reaction because the reagent AlCl3 being electron deficient acts as a Lewis acid.
Propanamide
Ethylamine
Hydrazine
doesn't contain any carbon atom and hence doesn't give Lassaigne test.
The correct answer is Option B: C6H5SO2Cl.
Hinsberg's reagent is benzenesulfonyl chloride (C6H5SO2Cl).
It is used to differentiate primary, secondary, and tertiary amines.
Here's why the other options are incorrect : Option A: C6H5COCl is benzoyl chloride, a reagent used in Friedel-Crafts acylation reactions.
Option C: SOCl2 is thionyl chloride, a reagent used to convert alcohols into alkyl chlorides.
Option D: (COCl)2 is oxalyl chloride, a reagent used for the conversion of carboxylic acids into acid chlorides.
Match with . .tg .tg
| List - I | List - II | ||
|---|---|---|---|
| (A) | Benzenesulphonyl chloride | (I) | Test for primary amines |
| (B) | Hoffmann bromamide reaction | (II) | Anti Saytzeff |
| (C) | Carbylamine reaction | (III) | Hinsberg reagent |
| (D) | Hoffmann orientation | (IV) | Known reaction of Isocyanates. |
(A) Benzene sulphonyl chloride is also known as Hinsberg reagent.
(B) Hoffmann bromamide reaction involves conversion of amide to amine having one atom less.
This reaction involves isocyanate as intermediate.
(C) Carbylamine reaction is a test given by all primary amines.
(D) Hoffmann orientation refers to the addition of molecules to unsymmetrical alkenes according to anti Saytzeff's rule.
Correct match is A-III, B-IV, C-I, D-II