$$\text{Benzenesulphonyl chloride} (C_6H_5SO_2Cl) \text{is also known as Hinsberg's reagent.}$$ It reacts with the primary and secondary amine to form sulphonamides.

Hinsberg's reactions are used to differentiate 1,2,3 aniline in which we treat with a benzene sulfonyl chloride in the presence of aqueous potassium dioxide.

Correct option is A. Hofmann bromamide reaction Acetamide changes into methylamine by hoffman bromamide reaction. $$\text{Hoffmann bromamide Reaction}$$; When an amide is …

Hinsberg reaction is a test which involves the reaction of amines with benzene sulphonyl chloride and is used to distinguish between primary, secondary and tertiary amines on the basis of …

Reaction used to convert amide into primary amine with one carbon atom less - Hofmann bromamide reaction; Reaction used to convert primary amines into isocyanides - Crbylamine …

Hinsberg reagent (benzene sulphonyl chloride) is used to distinguish between primary, secondary and tertiary amine. Primary amine, such as methylamine ( a primary amine) will dissolve in an …

An amine 'X' reacts with Hinsberg reagent and the product thus obtained is soluble in KOH. The amine 'X' is.

Hinsberg's method A mixture of primary,secondary.tertiary amines can be separated into individual compounents by fractional distillation since their boiling points are fairly apart. 2 9 0 …

The mixture of amines is treated with benzene sulphonyl chloride (Hinsberg's reagent) and shaken with alkali solution. (1) Primary amine forms alkyl benzenesulphonamide which …

In this reaction, the diazonium group is replaced by chloro group. Sandmeyer reaction is used to replace the diazonium group with chlorine, bromine or cyano group. Option D is correct.