Mechanisms in Organic Chemistry

Mechanisms in Organic Chemistry

Assessment

Interactive Video

Chemistry

11th - 12th Grade

Hard

Created by

Amelia Wright

FREE Resource

The video tutorial presents a mechanism challenge involving a substrate, reaction conditions, and a product. It explains the role of n-butyl lithium as a strong base and nucleophile, its unexpected attack on the iota group, and the subsequent steps involving TMSCl and ammonium chloride. The tutorial details the formation of a five-membered ring and the final product, emphasizing electron-pushing arrows and mechanistic pathways.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the main objective of the mechanism challenge presented in the video?

To identify unknown compounds

To demonstrate the mechanism with electron-pushing arrows

To predict the product of a reaction

To memorize chemical formulas

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the role of n-butyl lithium in the reaction?

It is a strong base and nucleophile

It is a weak acid

It acts as a solvent

It is a catalyst

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which group does n-butyl lithium attack in the first step?

Methyl group

Carbonyl group

Iota group

Hydroxyl group

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is TMSCl commonly used for in reactions?

As a reducing agent

As a protecting group

As a catalyst

As a solvent

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which atom does the carbonyl oxygen attack in the presence of TMSCl?

Chlorine

Silicon

Lithium

Carbon

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is formed as a result of the negative charge attacking the carbonyl?

A linear chain

A double bond

A six-membered ring

A five-membered ring

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the purpose of ammonium chloride in the final step?

To deprotect the silyl ether

To oxidize the compound

To act as a catalyst

To form a new bond

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