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प्रश्न
Arrange the following:
In increasing order of basic strength:
C6H5NH2, C6H5NHCH3, C6H5CH2NH2
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उत्तर
C6H5NHCH3 is more basic than C6H5NH2 due to the presence of an electron-donating −CH3 group in C6H5NHCH3.
Again, in C6H5NHCH3, −C6H5 group is directly attached to the N-atom. However, it is not so in C6H5CH2NH2. Thus, in C6H5NHCH3, the −R effect of −C6H5 group decreases the electron density over the N-atom. Therefore, C6H5CH2NH2 is more basic than C6H5NHCH3.
Hence, the increasing order of the basic strengths of the given compounds is as follows:
C6H5NH2 < C6H5NHCH3 < C6H5CH2NH2
संबंधित प्रश्न
Arrange the following:
Aniline, p-nitroaniline, p-methylaniline - in the increasing order of their basic strength
Write the chemical equations involved when aniline is treated with the following reagents: HCI
Why does NH3 act as a Lewis base?
Write the structures of the main products of the following reactions:

Write the structures of the main products of the following reactions:

Arrange the following in decreasing order of their basic strength:
C6H5NH2, C2H5NH2, (C2H5)2NH2, NH3
The most reactive amine towards dilute hydrochloric acid is:
Explain why \[\ce{MeNH2}\] is stronger base than \[\ce{MeOH}\]?
Account for the following:
Acylation of aniline is carried out in the presence of pyridine.
When methyl iodide is heated with ammonia, what is the product obtained?
Which of the following statement is true about methyl amine?
Which of the following is most basic?
What is the characteristic smell of liquid amines?
Give reasons for the following observation:
pKb of aniline is lower than the m-nitroaniline.
State one reason for the following:
Alkylamine is soluble in water, whereas arylamine is insoluble in water.
The correct order of the increasing basic nature of Ammonia, Methylamine and Aniline is:
