Elimination Reactions and Alkene Stability

Elimination Reactions and Alkene Stability

Assessment

Interactive Video

Chemistry

11th - 12th Grade

Hard

Created by

Amelia Wright

FREE Resource

Professor Dave explains Zaitsev and Hoffman elimination products, focusing on how different beta protons can lead to different products. He discusses the concepts of alkene substitution and stability, highlighting the differences between thermodynamic and kinetic products. The video includes examples of elimination reactions, demonstrating how steric hindrance affects the outcome. The Zaitsev product is more stable and thermodynamically favored, while the Hoffman product is kinetically favored when the base is sterically hindered.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What determines the formation of different elimination products in a reaction?

The concentration of the reactants

The type of solvent used

The temperature of the reaction

Which beta proton is extracted by the base

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How is the Zaitsev product defined in terms of alkene substitution?

It is always the least substituted alkene

It is the alkene with the least carbon atoms

It is the more highly substituted alkene

It is the alkene with the most hydrogen atoms

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which alkene is considered more stable?

Unsubstituted alkene

Monosubstituted alkene

Tetrasubstituted alkene

Disubstituted alkene

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the thermodynamically favored product in an elimination reaction?

The more stable, highly substituted alkene

The product with the highest energy

The product formed fastest

The product with the least steric hindrance

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which base would likely lead to a higher proportion of the Hoffman product?

Ethoxide

Tert-butoxide

Methoxide

Hydroxide

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why might a sterically hindered base favor the Hoffman product?

It reacts with the solvent

It forms the most stable product

It has a lower activation energy for certain protons

It can easily access all protons

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which product is formed when the base is sterically unhindered?

The most substituted alkene

The least stable product

The least substituted alkene

The fastest forming product

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