I.

Choose the most accurate answer

1. Electrophilic substitution reaction of indole occurs at position:
A. 1 B. 2
C. 3 D. 5

2. o-Formamidotoluene can be used to synthesis:

A. pyrrole B. Indole
C. Furan D. None of the above

3. The reaction between acetone and phenylhydrazine gives:

A. Furan derivative B. Pyrrole derivative
C. Indole derivative D. A or B

4. The catalytic reduction of indole:

A. Trihydro-1H-indole B. Tetrahydro-1H-indole
C. Dihydro-1H-indole D. None of the above

5. The basicity of indole is:

A. Very weak B. Strong
C. Very strong D. None of the above

6. The reaction between indole and bromine gives:

A. 2-Bromoindole B. 3-Bromoindole
C. 4-Bromoindole D. None of the above

7. Oxolane and tetrahydrofuran:

A. Have the same structure B. Have different structures
C. The same chemical properties D. A and C

8. Tryptophane is an amino which contain:

A. Pyrrole B. Indole
C. Furan D. None of the above

9. Oxole and oxirane have?

A. The same number of hydrogens B. The same number of oxygens
C. The same number of carbons D. A and B

10. Oxirane and oxetane are:

A. Heterocyclic compounds B. Folly saturated compounds
C. Aromatic compouds D. A and B
 II. Select (a) for true and (b) for false

11.Indole differs from isoindole in the hybridization of the nitrogen atom.

12.Bromination of indole occur mainly at position 2 due to the effect of N atom.

13.The catalytic reduction of indole gives 2,3-dihydroindole.

14.Vilsmeier reaction of pyrrole gives pyrrole-2-carboxylic acid.

15.The catalytic reduction of pyrrole gives pyrrolidine.

16.Practically furan-2-carboxylic acid cannot react with soda lime.

17.The first step of Paal-Knorr reaction involves keto-enol intermediate.

18.Indole is a very strong base.

19.The catalytic reduction of indole gives an aromatic compound.

20.The partial reduction of indole gives an aromatic compound.