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Electrophilic Aromatic Substitution

Total questions: 8

Worksheet time: 4mins

Name
Class
Date
1.

What is electrophilic substitution?

a)

A substitution reaction in which an electrophile is substituted for the electrons in the benzene ring

b)

A substitution reaction in which the benzene ring is attacked by a lone pair of electrons from an electrophile

c)

A substitution reaction in which an electrophile is attacked by the electrons in the benzene ring

2.

Which is least reactive in aromatic electrophilic substitution?

a)

Ethyl Benzene

b)

Anisole

c)

Acetophenone

d)

Chlorobenzene

3.

Which gives a meta nitro compound as the main product upon nitration with a nitric acid-sulfuric acid mixture?

a)

Ethyl Benzene

b)

Anisole

c)

Acetophenone

d)

Chlorobenzene

4.

With respect to the electrophilic aromatic substitution of benzene which of the following is not true?

a)

A non-aromatic intermediate is formed

b)

Benzene acts as an electrophile

c)

A proton is lost in the final step

d)

Resonance forms are important

5.

When considering electrophilic aromatic substitution reactions electron withdrawing substituents (e.g. cyano) are described as...

a)

Ortho/para directing and activating

b)

Ortho/para directing and deactivating

c)

Meta directing and activating

d)

Meta directing and deactivating

6.

What will be the attacking electrophile in the reaction of halogenation of Benzene?

a)

Halonium ion

b)

carbocation

c)

Benzene

d)

Halogen

7.

Why does benzene undergo substitution reactions rather than addition reactions

a)

Benzene is a planar, aromatic compound

b)

All the carbon atoms in benzene is sp2 hybridised

c)

All the carbon-carbon bonds in benzene is strong

d)

Benzene has extra stability due to the delocalized π electrons

8.

Aromatic compounds usually undergo which type of reaction

a)

Electrophilic substitution reaction

b)

Electrophilic addition reaction

c)

Nucleophilic substitution reaction

d)

Nucleophilic addition reaction