p-toluenesulphonyl chloride is known as Hinsb | vedclass

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(C) $p$-toluenesulphonyl chloride $(CH_3C_6H_4SO_2Cl)$ is commonly known as Hinsberg's reagent.It is used to distinguish between primary $(1^{\circ})$

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On treatment with a secondary amine,it leads to a product that is soluble in alkali.

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(C) $p$-toluenesulphonyl chloride $(CH_3C_6H_4SO_2Cl)$ is commonly known as Hinsberg's reagent.It is used to distinguish between primary $(1^{\circ})$,secondary $(2^{\circ})$,and tertiary $(3^{\circ})$ amines.$1$. Primary amines react with Hinsberg's reagent to form $N$-alkylbenzenesulphonamide,which contains an acidic hydrogen atom attached to the nitrogen,making it soluble in alkali.$2$. Secondary amines react with Hinsberg's reagent to form $N,N$-dialkylbenzenesulphonamide. This product does not contain any acidic hydrogen atom attached to the nitrogen,so it is insoluble in alkali.$3$. Tertiary amines do not react with Hinsberg's reagent because they lack an acidic hydrogen atom.Therefore,the statement that the product formed with a secondary amine is soluble in alkali is incorrect.

$p$-toluenesulphonyl chloride is known as Hinsberg's reagent. Which of the following statements is $NOT$ correct for it?

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