Carbocation Stability and Effects

Carbocation Stability and Effects

Assessment

Interactive Video

Chemistry, Science

10th - 12th Grade

Hard

Created by

Sophia Harris

FREE Resource

The video tutorial explores carbocation stability, explaining that tertiary carbocations are more stable than secondary, primary, and methyl carbocations. It discusses the role of inductive effects and hyperconjugation in stabilizing carbocations. The video also compares the stabilizing effects of methyl and hydroxyl groups, highlighting the importance of resonance structures. Finally, it examines the impact of electron withdrawing groups, like carbonyls, on carbocation stability.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which type of carbocation is the most stable?

Primary carbocation

Secondary carbocation

Tertiary carbocation

Methyl carbocation

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is one way electron donating groups stabilize carbocations?

By resonance

By hyperconjugation

By withdrawing electrons

By forming a double bond

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How does hyperconjugation stabilize a carbocation?

By removing electrons

By breaking a bond

By forming a new bond

By overlapping orbitals

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which group can better stabilize a carbocation, methyl or hydroxyl?

Both equally

Neither

Hydroxyl group

Methyl group

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What effect does the hydroxyl group have on carbocation stability?

It has no effect

It can both donate and withdraw electrons

It only donates electrons

It only withdraws electrons

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which structure is the most stable among the given carbocations?

A simple carbocation

A carbocation allylic to a double bond

A carbocation allylic to two double bonds

A carbocation with a nitrogen in the ring

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why is a carbocation with a nitrogen in the ring more stable?

It has an incomplete octet

It has no resonance structures

It forms a non-aromatic ring

It forms an aromatic ring

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