Hydrohalogenation of Alkynes Quiz

Hydrohalogenation of Alkynes Quiz

Assessment

Interactive Video

Chemistry

11th - 12th Grade

Hard

Created by

Jennifer Brown

FREE Resource

10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is a key difference between the hydrohalogenation of alkynes and alkenes?

Alkynes have one pi bond, while alkenes have two.

Alkynes can undergo hydrohalogenation twice, while alkenes can only do so once.

Alkynes and alkenes have identical hydrohalogenation processes.

Alkenes require more reagent equivalents than alkynes.

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the hydrohalogenation of alkenes, what is formed in the first step?

A peroxide

A free radical

A carbocation

A stable alkene

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the result of Markovnikov addition in alkenes?

No addition occurs.

Bromine adds to the less substituted side.

Hydrogen adds to the more substituted side.

Hydrogen adds to the less substituted side.

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How does the substitution of terminal and internal alkynes affect hydrohalogenation?

Terminal alkynes are more reactive than internal alkynes.

Markovnikov and anti-Markovnikov addition are not applicable to internal alkynes.

Internal alkynes always undergo anti-Markovnikov addition.

Substitution does not affect hydrohalogenation.

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why is the mechanism of hydrohalogenation of alkynes considered uncertain?

It is a well-understood first-order process.

It involves a stable carbocation.

There may be multiple competing mechanisms.

It always follows a single, known pathway.

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is a characteristic of the carbocation formed during alkyne hydrohalogenation?

It is less stable than a primary carbocation.

It is as stable as a secondary carbocation.

It is more stable than a primary carbocation.

It is not formed at all.

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What happens when HBr is used with peroxides in alkyne hydrohalogenation?

It results in anti-Markovnikov addition.

It results in Markovnikov addition.

It prevents any addition from occurring.

It forms a stable alkene.

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