Acid and Base Catalysis Concepts

Acid and Base Catalysis Concepts

Assessment

Interactive Video

Chemistry, Science

10th Grade - University

Hard

Created by

Ethan Morris

FREE Resource

This video tutorial explains the mechanisms of ester hydrolysis, focusing on both acid-catalyzed and base-catalyzed reactions. It begins with an introduction to ester hydrolysis, followed by a detailed explanation of the acid-catalyzed mechanism, including protonation and resonance structures. The tutorial then covers the base-catalyzed mechanism, highlighting the role of nucleophiles and the irreversibility of the reaction under basic conditions.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What are the products when methyl acetate reacts with water and HCl under acidic conditions?

Carboxylic acid and methanol

Acetic acid and ethanol

Ethanol and acetic acid

Methanol and ethyl acetate

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the acid-catalyzed ester hydrolysis, which ion is formed when HCl is added to water?

Na+

H3O+

Cl-

OH-

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

During the acid-catalyzed mechanism, which oxygen in the ester is more likely to be protonated?

The oxygen with no charge

The oxygen with a negative formal charge

The oxygen bonded to carbon

The oxygen with a positive formal charge

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the role of water in the acid-catalyzed ester hydrolysis mechanism?

Acts as a weak base

Acts as a strong acid

Acts as a nucleophile

Acts as a catalyst

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the final product of the acid-catalyzed ester hydrolysis?

Ester

Methanol

Deprotonated carboxylic acid

Protonated carboxylic acid

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In the base-catalyzed mechanism, what is the role of hydroxide?

Acts as a catalyst

Acts as an acid

Acts as a solvent

Acts as a nucleophile

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What happens to methoxide in the base-catalyzed ester hydrolysis?

It acts as a nucleophile

It forms a double bond

It attacks the carbonyl carbon

It deprotonates the carboxylic acid

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