Substitution Reactions - SN1 and SN2 Mechanisms - Crash Course Organic Chemistry

Substitution Reactions - SN1 and SN2 Mechanisms - Crash Course Organic Chemistry

Assessment

Interactive Video

Chemistry, Science

11th Grade - University

Hard

Created by

Quizizz Content

FREE Resource

The video tutorial covers the basics of dry cleaning, its environmental impact, and the chemistry behind SN1 and SN2 reactions. It explains the role of substrates, leaving groups, and nucleophiles in substitution reactions, and how factors like substrate structure, nucleophile strength, and solvent type influence the reaction mechanism. The tutorial also provides practical examples and tips for determining the likely reaction pathway.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the primary environmental concern associated with tetrachloroethylene used in dry cleaning?

It can cause water pollution.

It is non-biodegradable.

It is highly flammable.

It is a greenhouse gas.

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following is a characteristic of an SN1 reaction?

Requires strong nucleophiles

Inversion of stereochemistry

Carbocation intermediate

Concerted mechanism

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following is a poor leaving group?

Chloride

Hydroxide

Bromide

Tosylate

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What type of substrate is most likely to undergo an SN2 reaction?

Primary carbon

Secondary carbon

Vinyl carbon

Tertiary carbon

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which substrate structure is least likely to undergo an SN2 reaction?

Allylic carbon

Tertiary carbon

Secondary carbon

Primary carbon

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which nucleophile is considered strong and likely to participate in an SN2 reaction?

Water

Methanol

Acetic acid

Hydroxide ion

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is a common feature of strong nucleophiles?

They are typically neutral molecules.

They are weak bases.

They are large and polarizable.

They are often uncharged.

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