Catalytic Hydrogenation Concepts and Challenges

Catalytic Hydrogenation Concepts and Challenges

Assessment

Interactive Video

Chemistry

11th - 12th Grade

Hard

Created by

Lucas Foster

FREE Resource

The video tutorial explores enantioselective hydrogenation, focusing on breakthroughs by Knowles and Noyori. It discusses the outer shell mechanism, catalyst activation, and the reaction cycle. Applications of Noyori's technology, including dynamic kinetic resolution and imine hydrogenation, are highlighted. The tutorial emphasizes the stability and efficiency of these catalysts in synthesizing fine chemicals and pharmaceuticals.

Read more

10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the main advantage of Noyori's catalysts in enantioselective hydrogenation?

They are inexpensive to produce.

They achieve high levels of optical purity.

They require no special conditions.

They are used in all types of reactions.

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the outer shell mechanism, where does the substrate bind?

To a free radical

To the outer shell ligands

To a solvent molecule

Directly to the metal center

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the role of the potassium amide moiety in the catalytic cycle?

It increases the reaction temperature.

It binds the substrate.

It acts as a catalyst poison.

It decomposes the catalyst.

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How is stereoselectivity introduced in the catalytic cycle?

By altering the pressure

Through temperature control

By using a chiral solvent

Via diastereomeric transition states

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the significance of the outer-shell mechanism in catalyst stability?

It reduces the need for ligands.

It prevents substrate binding to the metal center.

It allows for higher reaction temperatures.

It makes the catalyst more reactive.

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is a key feature of dynamic kinetic resolution?

It uses a weak base to equilibrate enantiomers.

It requires high temperatures.

It is only applicable to olefins.

It achieves 100% yield of a pure product.

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is a challenge in the enantioselective hydrogenation of imines?

Imines require high pressure to react.

Imines are not commercially available.

Imines readily hydrolyze.

Imines are too stable to react.

Create a free account and access millions of resources

Create resources
Host any resource
Get auto-graded reports
or continue with
Microsoft
Apple
Others
By signing up, you agree to our Terms of Service & Privacy Policy
Already have an account?