Diazonium Reactions and Azo Compounds

Diazonium Reactions and Azo Compounds

Assessment

Interactive Video

Chemistry, Science

10th Grade - University

Hard

Created by

Ethan Morris

FREE Resource

This video tutorial covers electrophilic aromatic substitution reactions, focusing on nitration, reduction, diazotization, and the Sandmeyer reaction. It explains the mechanisms of these reactions, starting with the nitration of benzene to form nitrobenzene, followed by its reduction to aniline using iron and HCl. The video then describes the conversion of aniline to arene diazonium salt through diazotization. The Sandmeyer reaction is discussed, highlighting the replacement of the diazonium group with various substituents using copper salts. Finally, the video covers diazo coupling reactions, forming azo compounds.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the electrophile in the nitration of benzene?

Nitronium ion

Hydronium ion

Chloride ion

Sulfate ion

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which reagent is used to reduce nitrobenzene to aniline?

Copper chloride

Sulfuric acid

Iron and hydrochloric acid

Sodium nitrite

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the product formed when aniline is treated with sodium nitrite and hydrochloric acid?

Bromobenzene

Arene diazonium salt

Phenol

Nitrobenzene

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the purpose of using sodium nitrite in diazotization?

To act as a solvent

To oxidize the amine group

To form nitrous acid

To reduce the nitro group

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the Sandmeyer reaction, what role does copper play?

Reducing agent

Oxidizing agent

Solvent

Catalyst

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which substituent can replace the diazonium group in the Sandmeyer reaction?

Hydroxyl group

Cyanide group

Methyl group

Ethyl group

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following is a characteristic of the Sandmeyer reaction?

Involves radical intermediates

Uses sulfuric acid

Produces nitro compounds

Occurs at high temperatures

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