Class 12 Chemistry (Part Ii) Chapter 13 Amines Quiz 4 (60 MCQs)

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1. Which amine is formed from the reduction of benzamide?
2. What happens when Carboxylic Acids are dissolved in water?
3. R-CN + Na+ C2H5-OH gives
4. The breaking of the C-X bond by ammonia molecule is known as
5. Cyonation is what type of reduction?
6. In which of the following reactions, the product formed contains one carbon lessthan that present in the reactant?
7. What is the amino group's structure?
8. Why is the loss of N2 considered advantageous in diazotization reactions?
9. Amides have a Carbonyl group
10. The correct increasing order of basic strength for the following compounds is .....
11. Methanamine is stronger base than ethanamine
12. The gas evolved when methylamine reacts with nitrous acid is .....
13. Reduction of nitrile compounds is suitable for preparing primary amines.
14. Tretbutylamine, a compound in which a tert-butyl organic group is bound to nitrogen.
15. What is the product of the reaction between a primary amine and hydrochloric acid?
16. What is the base strength of primary aliphatic amines compared to ammonia?
17. Which of the following is an example of a secondary amine?
18. What is the common method for separating a mixture of amines?
19. A suitable reagent Z for the reaction:butanoyl chloride + Z $\rightarrow$ butanamide is
20. Hoffmann Bromamide Degradation reaction is shown by .....
21. What is observed in a clock reaction when a certain amount of product has been made?
22. Aniline does not undergo Friedel-Crafts reaction due to
23. How are secondary amines typically synthesized from primary amines?
24. Which pairing of general formula and compound class is incorrect?
25. Three major part of an amino acid are
26. What is the reagent required to carry out the following conversion?Methylamine $\rightarrow$ N-methylethanamide
27. What is the purpose of using hydrazine in the Gabriel Synthesis?
28. Select the Carboxylates in decreasing order from most electrophilic to least
29. Droperidol-is a powerful sleeping pill.
30. Which compound is the strongest base?
31. Ethylenediamine (en) is widely used as:
32. What is varied in a clock reaction to find the order of the reaction?
33. Amides are converted to amines by
34. Which is a suitable amide responsible for preparation of aniline?
35. 3$^{o}$ amines can not form hydrogen bond with water. Therefore they are insoluble in water.
36. Which of the following polymers is biodegradable by acidic/alkaline hydrolysis?
37. Which of the following describes the formation of polyamides?
38. What is the product of the reaction between ammonia and an alkyl halide?
39. Reaction of Amines and Carboxylic acids will produce .....
40. What type of amine has only one hydrogen atom replaced by an carbon group?
41. What type of reaction do amines typically undergo with alkyl halides?
42. Most stable carbo cation?
43. Consider the compounds methylethylamine and trimethylamine. Which of these has the higher boiling point?
44. The most reactive amine towards dilute hydrochloric acid is .....
45. What is the result of the reaction between an amine and an acid?
46. Which of the following substances can be resolved into enantiomers?
47. Catalytic reduction of nitro compounds into amines is:
48. The reaction of an amine with Hinsberg's reagent helps distinguish:
49. Reduction with iron scrap and HCl is preferred because
50. What is a common method for synthesizing primary amines?
51. What is the major product of reaction between methanamine and methylchloride?
52. Cyonation always results in 1ccarbon hologation (an extra CH2 in product)
53. What do the quantities in the rate equation match?
54. What is the reagent required to carry out the following conversion?Hexanamide $\rightarrow$ hexanamine
55. Reduction of primary amide will form ..... amine.
56. Alkylation yields what type of products
57. Estimated pK$_{a }$of aniline
58. What is the final outcome of the Hofmann Elimination process?
59. What is the functional group of Carboxylic Acids?
60. Which of the following is true about the rate determining step?