Advertisements
Advertisements
प्रश्न
Give reasons Although –NH2 is o/p directing group, yet aniline on nitration gives a significant amount of m-nitroaniline
Advertisements
उत्तर
Nitration is usually carried out with a mixture of concentrated HNO3 and concentrated H2SO4. In the presence of these acids, most of aniline gets protonated to form anilinium ion. Therefore, in presence of acids, the reaction mixture consists of aniline and anilinium ion. Nitration of aniline due to steric hindrance at ortho position, mainly gives para nitroaniline and the nitration of anilinium ion gives m-nitroaniline. In actual practice, approximately 1:1 mixture of p-nitroaniline: m-nitroaniline is obtained.

Thus, nitration of aniline gives a substantial amount of m-nitroaniline due to protonation of the amino group.
APPEARS IN
संबंधित प्रश्न
Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
CH3(CH2)2NH2
Write the IUPAC name of the following compound and classify it as primary, secondary and tertiary amine.
(CH3)3CNH2
Give one chemical test to distinguish between the following pair of compounds.
Secondary and tertiary amines
Give one chemical test to distinguish between the following pair of compounds.
Aniline and N-methylaniline
Account for the following:
Ethylamine is soluble in water, whereas aniline is not.
How will you convert methanamine into ethanamine?
Accomplish the following conversion:
Benzoic acid to aniline
Accomplish the following conversion:
Chlorobenzene to p-chloroaniline
Complete the following reaction:
\[\ce{C6H5NH2 + (CH3CO)2O ->}\]
The following amine is called as:

