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Understanding Substitution and Elimination Reactions

Understanding Substitution and Elimination Reactions

Assessment

Interactive Video

Chemistry

11th - 12th Grade

Practice Problem

Hard

Created by

Jennifer Brown

FREE Resource

10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following reactions is impossible with a tertiary substrate?

SN2

E2

SN1

E1

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the main reason SN1 and E1 reactions are unlikely with primary substrates?

Strong nucleophile presence

High steric hindrance

Formation of an unstable carbocation

Formation of a stable carbocation

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which factor makes hydroxide a strong base and good nucleophile?

Its large size

Its stability

Its ability to form hydrogen bonds

Its instability and reactivity

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why is t-butoxide considered a classic E2 promoter?

It forms stable carbocations

It is sterically unhindered

It is too bulky for SN2

It is a weak base

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How does steric hindrance affect the ability of a base to act as a nucleophile?

Enhances carbocation formation

Decreases nucleophilicity

Has no effect

Increases nucleophilicity

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What happens to leaving group ability as you move down the halogen group?

It remains the same

It increases

It decreases

It becomes unpredictable

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In polar protic solvents, which halide ions are better nucleophiles?

Smaller halides

All halides equally

None of the halides

Larger halides

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