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Heterocyclic Compounds Unit III

Total questions: 21

Worksheet time: 16mins

Name
Class
Date
1.

In pyrrole and pyridine the number of electrons that the N atom contributes to n-system is

a)

Pyrrole 2, pyridine 1

b)

Pyrrole 1, pyridine 1

c)

Pyrrole 2, pyridine 2

d)

Pyrrole 1, pyridine 2

2.

What is the correct order of reactivity most reactive first of pyrrole, furan and thiophene towards electrophiles

a)

furan>thiophene>pyrrole

b)

pyrrole>furan>thiophene

c)

furan>pyrrole> Thiophene

d)

None of above

3.

Electrophilic substitution on furan usually occurs at:

a)

C1

b)

C2

c)

C1 & C2

d)

None of above

4.

Nitration of pyrrole is best carried out using

a)

Concentrated nitric acid and sulfuric acid

b)

Acetyl nitrite

c)

Ammonium nitrate

d)

All of above

5.

If you wanted to form 2,3,4,5-tetrabromopyrrole from pyrrole, which of the following conditions would be the best choice

a)

HBr2 at 298K

b)

Br2 with AlBr3 as a Lewis catalyst

c)

Br2 at 273K

d)

Br2 in presence of radical initiation

6.

Which statement below is correct...

a)

Pyrrole is stronger base than triethylamine

b)

Pyrrole readily protonated on the N atom

c)

Pyrrole is a very weak base

d)

None of above

7.

Which statement about thiophene is incorrect

a)

Thiophene is polar

b)

The S atom contributes two electrons to the n-system

c)

Thiophene is less reactive than pyrrole

d)

Thiophene is more reactive than pyrrole

8.

Pyrrole undergoes sulfonation in presence of…..................to produce pyrrole-2-sulfonic acid

a)

Conc H2SO4 + HNO3

b)

Conc H2SO4

c)

Dilute sulphuric acid pyridine

d)

SO3 and ethanol

9.

Pyrrole undergoes iodination in presence of iodine and potassium iodine to produce…

a)

2-iodo pyrrole

b)

3-iodo pyrrole

c)

tetra iodo pyrrole

d)

tri iodo pyrrole

10.

Oxidation of pyrrole in presents of chromium oxide (Cr2O3) and acetic acid produce

a)

Malic acid

b)

Pyrrole-N-oxide

c)

None of above

11.

Pyrrole is reduced by using Zn and acetic acid to yield

a)

2-pyrroline

b)

3-pyrroline

c)

Pyrrolidine

d)

No reaction

12.

Pyrrole is heated with …..........to open the ring and from succinaldehyde dioxime

a)

Concentration sulphuric acid

b)

Strong alkali with pyridine

c)

Hydrogen cyanide with HCl

d)

Ethanolic hydroxylamine hydrocholide

13.

Name the heterocyclic compound present in above structure of Atorvastatin

a)

Furan

b)

Pyrrolidine

c)

Pyrimidine

d)

Pyrrole

14.

How many delocalized pi electrons in .....

a)

6

b)

2

c)

5

d)

4

15.

Pyrrole + CHCl3 + KOH --------> ?

a)
b)
c)
d)
16.

write the IUPAC name of this compound

(a)  

17.

Contains chlorophyll, which hetercyclic compound it contains

a)
b)
c)
d)
18.

what is the correct name of this structure.....

a)

Oxa 2, 4 cyclopentadiene

b)

aza 2, 4 cyclopentadiene

c)

Oxa 2, 4 cyclopantene

d)

aza 2, 4 cyclopantene

19.

Resonance stabilized energy of pyrrole is 22 to 28 Kcal/mole which is less than benzene

a)

True

b)

False

20.

is the structure of antibiotic_______________contain pyrrole

a)

Penicilline

b)

Azithromycine

c)

Erythromycine

d)

Cephalosporine

21.

Write IUPAC name of

(a)