Understanding SN1 and SN2 Mechanisms

Understanding SN1 and SN2 Mechanisms

Assessment

Interactive Video

Chemistry, Science

10th - 12th Grade

Hard

Created by

Liam Anderson

FREE Resource

This video tutorial explores SN1 and SN2 mechanisms in nucleophilic substitution reactions of halogen alkanes with hydroxide ions. It explains the differences between primary and tertiary halogen alkanes, the role of nucleophiles, and how reaction rates can indicate the mechanism pathway. The video also covers the concepts of transition states and carbocation intermediates, providing a comprehensive understanding of these chemical processes.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is a nucleophile in the context of nucleophilic substitution reactions?

An electron pair acceptor

A molecule that loses electrons

An electron pair donor

A positively charged ion

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In an SN2 reaction, what happens to the carbon-halogen bond?

It remains intact

It breaks as the nucleophile bonds

It forms a double bond

It forms a triple bond

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the role of the hydroxide ion in an SN2 mechanism?

It acts as a catalyst

It acts as an inhibitor

It acts as a nucleophile

It acts as a solvent

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why can't tertiary halogen alkanes undergo SN2 reactions?

Due to lack of nucleophiles

Due to low reactivity

Due to steric hindrance

Due to high electronegativity

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is formed when the carbon-halogen bond breaks in an SN1 mechanism?

A free radical

A carbocation

A neutral molecule

A carbanion

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How does the rate of an SN1 reaction depend on the concentration of reactants?

It depends only on the halogen alkane

It does not depend on concentration

It depends only on the nucleophile

It depends on both nucleophile and halogen alkane

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What does the energy profile of an SN1 reaction show?

Three peaks with multiple intermediates

A flat line with no peaks

Two peaks with a carbocation intermediate

One peak and no intermediate

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