Halogenation Mechanisms and Concepts

Halogenation Mechanisms and Concepts

Assessment

Interactive Video

Chemistry

11th - 12th Grade

Hard

Created by

Patricia Brown

FREE Resource

This video tutorial by Leia from Leiafirstside.com covers the mechanisms of alkene reactions, focusing on halogenation. It explains the process using examples like cyclohexene and propene, highlighting the formation of bromonium intermediates and anti-addition. The tutorial concludes with information on additional resources and tutoring options.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the primary focus of the video regarding alkene reaction mechanisms?

Polymerization reactions

Halogenation process

Hydrogenation process

Stereochemistry and chirality

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the halogenation mechanism, what role does the pi bond play?

Acts as an electrophile

Acts as a nucleophile

Forms a free radical

Stabilizes the molecule

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the result of the bromonium ion formation in the halogenation mechanism?

Anti-addition of bromine atoms

Formation of a free radical

Creation of a carbocation

Syn-addition of bromine atoms

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How does the bromide ion attack the cyclohexene molecule during halogenation?

From the front of the molecule

From the top of the molecule

From the bottom of the molecule

From the side of the molecule

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What type of product is formed when cyclohexene undergoes halogenation?

Racemic mixture

Trans product

Cis product

Chiral product

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the halogenation of propene, which carbon is more likely to be attacked by the chloride ion?

Tertiary carbon

Primary carbon

Secondary carbon

Quaternary carbon

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why is the secondary carbon in propene more partially positive than the primary carbon?

It is closer to the halogen

It has more electrons

It can form a more stable carbocation

It is less stable

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