
Electrophilic Aromatic Substitution
Authored by Charles Martinez
Chemistry
University
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8 questions
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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is electrophilic substitution?
A substitution reaction in which an electrophile is substituted for the electrons in the benzene ring
A substitution reaction in which the benzene ring is attacked by a lone pair of electrons from an electrophile
A substitution reaction in which an electrophile is attacked by the electrons in the benzene ring
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which is least reactive in aromatic electrophilic substitution?
Ethyl Benzene
Anisole
Acetophenone
Chlorobenzene
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which gives a meta nitro compound as the main product upon nitration with a nitric acid-sulfuric acid mixture?
Ethyl Benzene
Anisole
Acetophenone
Chlorobenzene
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
With respect to the electrophilic aromatic substitution of benzene which of the following is not true?
A non-aromatic intermediate is formed
Benzene acts as an electrophile
A proton is lost in the final step
Resonance forms are important
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
When considering electrophilic aromatic substitution reactions electron withdrawing substituents (e.g. cyano) are described as...
Ortho/para directing and activating
Ortho/para directing and deactivating
Meta directing and activating
Meta directing and deactivating
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What will be the attacking electrophile in the reaction of halogenation of Benzene?
Halonium ion
carbocation
Benzene
Halogen
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Why does benzene undergo substitution reactions rather than addition reactions
Benzene is a planar, aromatic compound
All the carbon atoms in benzene is sp2 hybridised
All the carbon-carbon bonds in benzene is strong
Benzene has extra stability due to the delocalized π electrons
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