Friedel-Crafts Alkylation Concepts

Friedel-Crafts Alkylation Concepts

Assessment

Interactive Video

Chemistry

11th - 12th Grade

Hard

Created by

Amelia Wright

FREE Resource

The video tutorial explains the Friedel-Crafts Alkylation reaction, a key process in organic chemistry for forming carbon-carbon bonds by adding alkyl groups to benzene rings. It details the mechanism, starting with the formation of a catalytic intermediate using aluminum trichloride, followed by the generation of a carbocation intermediate. The tutorial highlights the differences from halogenation reactions and concludes with the restoration of aromaticity and the regeneration of the catalyst.

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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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