Question
What is Hinsberg reagent?

Answer

Benzenesulphonyl chloride (C6H5SO2Cl), is also known as Hinsberg’s reagent. It reacts with primary and secondary amines to form sulphonamides. Secondary and tertiary amines can be distinguished by allowing them to react with Hinsberg’s reagent (benzenesulphonyl chloride C6H5SO2Cl). Secondary amines react with Hinsberg’s reagent to form a product that is insoluble in an alkali. For example, N, N-diethylamine reacts with Hinsberg’s reagent to form N, N-diethylbenzenesulphonamide, which is insoluble in an alkali. Tertiary amines, however, do not react with Hinsberg’s reagent.

Need a full question paper?

Generate a complete, print-ready paper with questions like this in minutes — across 16+ boards, with answer keys.

Start Generating Free

Similar questions

How the conversion can be carried out :
But-1-ene to n-butyliodide
Name the compound according to IUPAC system of nomenclature :
$\stackrel{5}{ C } H _3 \stackrel{4}{ C } H \left( CH _3\right) \stackrel{3}{ C } H _2 \stackrel{2}{ C } H _2 \stackrel{1}{ C } HO$
Read the given passage and answer the questions number 1 to 5 that follow:
The substitution reaction of alkyl halide mainly occurs by SN1 or SN2 mechanism. Whatever mechanism alkyl halides follow for the substitution reaction to occur, the polarity of the carbon halogen bond is responsible for these substitution reactions. The rate of SN1 reactions are governed by the stability of carbocation whereas for SN2 reactions steric factor is the deciding factor. If the starting material is a chiral compound, we may end up with an inverted product or racemic mixture depending upon the type of mechanism followed by alkyl halide. Cleavage of ethers with HI is also governed by steric factor and stability of carbocation, which indicates that in organic chemistry, these two major factors help us in deciding the kind of product formed.
Predict the stereochemistry of the product formed if an optically active alkyl halide undergoes substitution reaction by SN2 mechanism.
Write the equation of the reaction of hydrogen iodide with :
methoxybenzene
Arrange the following compound in increasing order of their boiling point.

CH3CHO, CH3CH2OH, CH3OCH3, CH3CH2CH3

Write the IUPAC name of the following coordination compound:
[Co(NH3)5Cl]Cl2
Name the following halides according to IUPAC system and classify them as alkyl, allyl, benzyl (primary, secondary, tertiary), vinyl or aryl halides:
CH3CH2C(CH3)2CH2I
Write structure of the compound whose IUPAC names are as follow:

2,3 – Diethylphenol.

Describe the following:

Decarboxylation.

Write the decreasing order of reactivity of following halogen acids :
$HBr , HF , HCl , HI$