Class 12 Chemistry (Part Ii) Chapter 13 Amines Quiz 9 (25 MCQs)

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1. In which of the following reactions, the product formed contains one carbon lessthan that present in the reactant?
2. What is the amino group's structure?
3. Why is the loss of N2 considered advantageous in diazotization reactions?
4. Amides have a Carbonyl group
5. What is the IUPAC name for the compound CH3CH2NH2?
6. The correct increasing order of basic strength for the following compounds is .....
7. Methanamine is stronger base than ethanamine
8. The gas evolved when methylamine reacts with nitrous acid is .....
9. Order of basic strength of ethylamines is
10. Reduction of nitrile compounds is suitable for preparing primary amines.
11. Tretbutylamine, a compound in which a tert-butyl organic group is bound to nitrogen.
12. What is the product of the reaction between a primary amine and hydrochloric acid?
13. What is the base strength of primary aliphatic amines compared to ammonia?
14. Which of the following is an example of a secondary amine?
15. What is the common method for separating a mixture of amines?
16. A suitable reagent Z for the reaction:butanoyl chloride + Z $\rightarrow$ butanamide is
17. Hoffmann Bromamide Degradation reaction is shown by .....
18. What is observed in a clock reaction when a certain amount of product has been made?
19. Aniline does not undergo Friedel-Crafts reaction due to
20. How are secondary amines typically synthesized from primary amines?
21. What is the order of boiling points for amines?
22. Best method for preparing primary amines from alkyl halides without changing the number of carbon atoms in the chain is
23. Which pairing of general formula and compound class is incorrect?
24. Three major part of an amino acid are
25. What is the reagent required to carry out the following conversion?Methylamine $\rightarrow$ N-methylethanamide