Class 12 Chemistry (Part Ii) Chapter 13 Amines Quiz 17 (25 MCQs)

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1. What is the basicity of amines attributed to?
2. In the nitration of benzene using a mixture of conc. H2SO4 and conc. HNO3, the species which initiates the reaction is .....
3. In Hinsberg reaction, after the reaction with benzene sulfonil chloride, tertiary amine will ..... in base solution, than ..... in acid solution.
4. How is a secondary amine indicated in the IUPAC nomenclature?
5. Which reaction produces primary amines from a halogenoalkane?
6. R-cH=N-OH +Na+ C2H5-OH gives
7. In the Hinsberg test, which of the following gives a soluble sulfonamide in alkali?
8. Give correct names for the following amine:CH$_{3}$CH$_{2}$CH$_{2}$NHCH$_{3}$
9. In order to prepare a 1$^\circ$ amine from an alkyl halide with simultaneous addition of one CH2 group in the carbon chain, the reagent used as source of nitrogen is .....
10. Which of the following reagents would not be a good choice for reducing an aryl nitro compound to an amine?
11. The order of reactivity of alkyl halides with amonia is:
12. Have a smell of death / decay or rotting fish
13. The pKb of ethylamine (3.19) is less than that of ammonia (4.75) because of:
14. Describe the continuous monitoring method for measuring rates of reaction and the graphs they produce.
15. One of the the limitation of Gabriel phthalimide synthesis is
16. What is the first step in the Hofmann Elimination process when reacting with amines?
17. Which of the following statements is true regarding the basicity of amines?
18. What type of amines does the Azide Synthesis reaction prepare?
19. Hinsberg's test gives yellow oil to
20. Acid Chlorides and anhydrides only use $\frac{H_2O}{ }$
21. Which of the following compound will not undergo azo coupling reaction with benzene diazonium chloride.
22. LAH reduced carbonyl's
23. What is the product of the reaction between Ethanoic Acid and Sodium Hydroxide?
24. Give correct names for the following amine:CH$_{3}$CH$_{2}$CH(NHCH$_{3}$)CH$_{3}$
25. ..... is shifting negative charge towards this spot in the molecule.