Understanding Reaction Mechanisms

Understanding Reaction Mechanisms

Assessment

Interactive Video

Chemistry, Science

10th Grade - University

Hard

Created by

Olivia Brooks

FREE Resource

The video tutorial explores different types of chemical reactions, specifically Sn2, Sn1, E2, and E1. It discusses the role of solvents, particularly protic and aprotic, in determining reaction pathways. The tutorial emphasizes the importance of the leaving group and carbocation stability, focusing on tertiary carbons. Detailed mechanisms for Sn1 and E1 reactions are explained, highlighting the role of methanol as a weak nucleophile and base.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which of the following reactions is least likely to occur in a protic solvent?

E1

Sn2

None of the above

Sn1

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What characteristic of methanol makes it a protic solvent?

Presence of free electrons

Absence of electronegative atoms

Presence of hydrogen bonded to oxygen

Presence of carbon atoms

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why is iodide considered a good leaving group in Sn1 and E1 reactions?

It is a weak base

It is highly electronegative

It is a strong nucleophile

It forms a stable anion

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the first step in both Sn1 and E1 reactions?

Formation of a double bond

Leaving group leaves

Nucleophile attacks

Base removes a hydrogen

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In an Sn1 reaction, what role does methanol play?

Strong nucleophile

Strong base

Weak nucleophile

Weak base

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

During the Sn1 reaction, what happens to the methanol molecule after it donates an electron?

It gains a positive charge

It loses a proton

It forms a double bond

It becomes a strong nucleophile

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In an E1 reaction, what happens to the beta carbon?

It becomes a nucleophile

It loses a hydrogen

It gains a hydrogen

It forms a carbocation

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