Short Answer Type

Advertisement

An organic compound (A) with IMF C4H11N, capable of being resolved into optical isomers gives a base soluble product with benzene sulphonyl chloride. What is the structure and IUPAC name of (A)? What happens when this compound (A) is treated with ethanoyl chloride?


As the compound (A) is giving a base soluble product with Hinsberg’s reagent, it means the compound is a primary amine with —NH2 group. As the compound is capable of being resolved into optical isomers, it indicates the presence of chiral carbon. Therefore, the structure of compound (A) is:



With ethanoyl chloride, compound (A) forms an amide.

155 Views

Advertisement

Long Answer Type

Draw all possible isomers of a benzene containing compound with molecular formula C7H9N. Write their IUPAC names. Explain their reaction towards nitrous acid.
161 Views

Short Answer Type

How would you protect the amino group during the nitration of an aromatic amino compound? Give chemical equations.
132 Views

How is benzene diazonium chloride obtained?

110 Views

Show by means of equations how an amide may be converted into an amine containing one carbon atom less than the amide.

109 Views

Advertisement
Why are aryl diazonium ions more stable than alkyl diazonium ions?
149 Views

Write the structure of the products of the following reactions:


100 Views

Explain what is meant by the 'protection of the amino group'.?

112 Views

Show by means of equations how an amide may be converted into an amine containing the same number of carbon atoms.

101 Views

Advertisement
<

Why does bromination of aniline, even under very mild conditions give 2, 4, 6- tribromo aniline instantaneously?

255 Views

Advertisement