Friedel-Crafts Reactions and Reductions

Friedel-Crafts Reactions and Reductions

Assessment

Interactive Video

Chemistry, Science

10th Grade - University

Hard

Created by

Amelia Wright

FREE Resource

The video tutorial explains the Friedel-Crafts acylation reaction mechanism, using benzene and acetyl chloride with a Lewis acid catalyst. It details the formation of intermediates, the role of water, and the final product, acetophenone. The video also covers the reduction of ketones to alkanes using methods like Clemensen and Wolff-Kishner reductions, and provides practical examples to illustrate these concepts.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the catalyst used in the Friedel-Crafts Acylation reaction?

Potassium permanganate

Aluminum chloride

Sulfuric acid

Sodium hydroxide

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the role of aluminum chloride in the Friedel-Crafts Acylation reaction?

It acts as a base

It acts as a solvent

It acts as a Lewis acid catalyst

It acts as a reducing agent

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the Friedel-Crafts Acylation mechanism, what is the intermediate formed after the reaction of acid chloride with the Lewis acid?

Carbocation

Acylium ion

Carbanion

Radical ion

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the Friedel-Crafts Acylation reaction, what happens to the chlorine atom from the acid chloride?

It forms a chloride ion

It is reduced

It becomes part of the product

It is oxidized

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why is water added in the second step of the Friedel-Crafts Acylation reaction?

To act as a solvent

To increase the reaction temperature

To remove the Lewis acid catalyst

To dissolve the reactants

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following is a method to reduce a ketone to an alkane?

Friedel-Crafts Alkylation

Clemensen Reduction

Grignard Reaction

Diels-Alder Reaction

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the product formed when acetophenone is reduced using the Wolff-Kishner reduction?

Benzene

Ethyl benzene

Toluene

Phenol

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