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प्रश्न
Give one chemical test to distinguish between the following pair of compounds.
Secondary and tertiary amines
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उत्तर
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.

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संबंधित प्रश्न
Which among the following molecular formulae represents urotropine?
(a) C6H12N4
(b) C6H24H4
(c) C6H12N4O2
(d) C6H24N4O2
Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
m−BrC6H4NH2
Give one chemical test to distinguish between the following pair of compounds.
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Give one chemical test to distinguish between the following pair of compounds.
Aniline and benzylamine
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How will you convert methanol to ethanoic acid?
How will you convert ethanoic acid into propanoic acid?
How will you convert methanamine into ethanamine?
Accomplish the following conversion:
Chlorobenzene to p-chloroaniline
An aromatic compound ‘A’ on treatment with aqueous ammonia and heating forms compound ‘B’ which on heating with Br2 and KOH forms a compound ‘C’ of molecular formula C6H7N. Write the structures and IUPAC names of compounds A, B and C.
Complete the following reaction:
\[\ce{C6H5NH2 + H2SO4 (conc.)}\]
Complete the following reaction:
\[\ce{C6H5NH2 + Br2 (aq) ->}\]
Complete the following reaction:
\[\ce{C6H5N2Cl ->[(i) HBF4][(ii) NaNO2/Cu, \Delta]}\]
Give reasons Although –NH2 is o/p directing group, yet aniline on nitration gives a significant amount of m-nitroaniline
Do the following conversions in not more than two steps :
Propanone to Propene
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How are ethylamine and ethyl methyl amine distinguished by using nitrous acid?
Write the IUPAC name of the given compound :

Do the following conversions in not more than two steps:
\[\begin{array}{cc}
\ce{CH3CN to CH3 - C - CH3}\\
\phantom{...........}||\\
\phantom{...........}\ce{O}
\end{array}\]
