
Friedel-Crafts Alkylation Concepts
Interactive Video
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Chemistry
•
11th - 12th Grade
•
Hard

Amelia Wright
FREE Resource
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10 questions
Show all answers
1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the primary focus of Friedel-Crafts Alkylation in organic chemistry?
Formation of new carbon-sulfur bonds
Formation of new carbon-nitrogen bonds
Formation of new carbon-carbon bonds
Formation of new carbon-oxygen bonds
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which catalyst is used in the Friedel-Crafts Alkylation reaction?
Zinc chloride
Aluminum trichloride
Copper sulfate
Iron trichloride
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
In the Friedel-Crafts Alkylation mechanism, what is the role of the aluminum trichloride?
It acts as a base
It acts as a solvent
It acts as a Lewis acid catalyst
It acts as a reducing agent
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
How does the Friedel-Crafts Alkylation mechanism compare to halogenation?
It does not involve a benzene ring
It does not generate a catalytic intermediate
It involves a different catalyst
It operates in a similar manner with an additional step
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is generated when the carbon-chlorine bond cleaves in the Friedel-Crafts Alkylation?
A radical
A carbocation intermediate
A neutral molecule
An anion
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Why is the carbocation intermediate more reactive with benzene compared to the neutral chloroalkane?
It is less reactive
It is less polar
It is more stable
It has a lower activation energy
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What happens to the aluminum atom during the reaction?
It gains a negative charge
It remains neutral
It loses electrons
It gains a positive charge
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