

Understanding Substitution and Elimination Reactions
Interactive Video
•
Chemistry
•
11th - 12th Grade
•
Practice Problem
•
Hard
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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