Practice Problem: Ozonolysis Reactions

Practice Problem: Ozonolysis Reactions

Assessment

Interactive Video

Engineering, Biology, Chemistry, Science

11th Grade - University

Hard

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The video tutorial explains ozonolysis reactions, focusing on both forward and retro processes. It covers how ozonolysis cleaves double bonds, transforming them into carbonyl groups, and emphasizes the importance of numbering carbons to avoid errors. The tutorial also discusses the transformation of cyclic molecules into linear ones and how to deduce reactants from ozonolysis products.

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5 questions

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1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the primary transformation that occurs during ozonolysis?

Formation of triple bonds from double bonds

Addition of hydrogen atoms to double bonds

Cleavage of double bonds and formation of carbonyl groups

Conversion of single bonds to double bonds

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why is it important to number the carbons during ozonolysis?

To ensure the correct number of carbons are added

To avoid losing or gaining carbons during the reaction

To identify the type of reaction taking place

To determine the molecular weight of the product

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What happens to a cyclic molecule during forward ozonolysis?

It forms a new cyclic structure with more rings

It breaks into two separate cyclic molecules

It transforms into a linear molecule

It remains cyclic but with additional carbonyl groups

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In retro ozonolysis, what is the main goal?

To convert carbonyl groups back to double bonds

To add carbonyl groups to a molecule

To form new carbon-carbon bonds

To deduce the original reactant from carbonyl products

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What common error is highlighted in the retro ozonolysis process?

Adding extra carbonyl groups

Incorrectly identifying the type of reaction

Shifting carbon material incorrectly

Failing to form a cyclic structure