Amines_2
Amines_2
27. Give the chemical tests to distinguish between the following pairs of compounds :
a) Methylamine and Dimethylamine
b) Aniline and N-methylaniline
28. Describe the following giving the relevant chemical equation in each case :
a) Carbylamine reaction
b) Hofmann’s bromamide reaction
29. How would you account for the following :
a) Electrophilic susbstitution in case of aromatic amines takes place more readily than
benzene.
b) Ethanamide is a weaker base than ethanamine.
30. Explain the following reactions :
a) Gabriel Phthalimide reaction
b) Coupling reaction
31. Write the order of solubility of propanaamine, N-methylethanaamine,N,N-
Dimethylmethamine. Give reasons for your answer.
32. Write the order of thermal stability of primary, secondary, and tertiary amines. Andgive
reasons for your answer.
33. Why the melting and boiling point of amines does is less than that of alcohols?
34. Give reasons
A. Pkb of aniline is less than methylamine.
B. Ethylamine is more soluble in water than aniline.
C. P-nitroaniline is less basic than aniline.
35. Convert,
A. n-propylchloride to ethanamine.
B. Hexanenitrile to 1-aminopentane.
C. Propanoic acid to ethanol.
D. Methanamine to ethanamine.
E. Methanol to ethanamide.
F. Ethanol to propanamide.
36. How will you distinguish between primary and secondary amines?
37. Ethylamine is soluble in water whereas aniline is not soluble in water. Why?
38. Primary amines (R-NH2) have higher boiling point than tertiary amines (R3N). why?
39. 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.
40. Acetylation of aniline reduces its activation effect, How would you prepare 4-bromoanilline
using acetylation of aniline?
41. Give one test to distinguish primary, secondary, and tertiary amine.
42. How will you distinguish between ethylamine and aniline?
43. Ethanamide is a weaker base than ethanamine. Why?
44. Write short note on
A. Gabriel-pthalimide synthsis of amine. Explain why it’s a good method to prepare
primary amines.
B. Hoffman-Bromamide synthesis.
C. Diazotization
D. Coupling reaction.
45. Aniline donot give friedel craft alkylation. Why?
46. During preparation of p-nitroaniline , a substancial amount of m- nitroaniline is
formed. Why?
47. Why aniline is acetylated during electrophilic substitution of aromatic amines?
48. Why does amines are less acidic than alcohols?
49. pKb value for aniline is more than that for methylamine.Give reason.
50. Why Gabriel-pthalimide synthesis is avery good way to prepare primary amines?
51. Complete the following conversions.
A. Nitrobenzene to benzoic acid
B. Benzoic acid to aniline
C. Benzamide to toluene
D. Aniline to benzene
E. Ethanoic acid to propanoic acid
F. Ethanoic acid to methanamine
G. Nitromethane to dimethylamine
H. Methanol to ethanoic acid
I. Methylchloride to N-methylethanamine
J. Aniline to nitrobenzene
52. Arrange the following compounds in an increasing order of their solubility in water :
C6H5NH2, (C2H5)2NH, C2H5NH2.
53. Give a chemical test to distinguish between ethylamine and aniline.
54. Arrange the following in increasing order of their basic strength in aqueous solution:
CH3.NH2, (CH3)3N, (CH3)2NH. And give reason for your answer.
55. Identify A and B in each of the following processes:
A.
B.
56. Complete the following reaction equations:
(i) C6H5N2Cl + H3PO2 + H2O →
(ii) C6H5NH2 + Br2 (aq) →
57. How would you account for the following:
A. Aniline is a weaker base than cyclohexyl amine.
B. Methylamine in aqueous medium gives reddish-brown precipitate with FeCl3.
58. What is a coupling reaction, explain by taking example Benzene diazonium chlorideand
phenol?
59.28.
Give the structure of A, B and C in the following reactions:
A.
B.
60. Write the products when aniline reacts with
A. Bromine water
B. HCl
C. Acetic anhydride in presence of pyridine
61. An aromatic compound ‘A’ of molecular formula C7H6O2 undergoes a series of
chemical reactions as follows, complete the following reaction