Login processing...

Trial ends in Request Full Access Tell Your Colleague About Jove

13.7: Preparation of Carboxylic Acids: Overview

JoVE Core
Organic Chemistry

A subscription to JoVE is required to view this content. Sign in or start your free trial.

Preparation of Carboxylic Acids: Overview

13.7: Preparation of Carboxylic Acids: Overview

There are various methods for the preparation of carboxylic acids. For example, oxidation of primary alcohols or aldehydes using strong oxidizing agents results in a carboxylic acid.  Aldehydes can also be oxidized in the presence of mild oxidizing agents.


Alkyl benzenes, bearing at least one benzylic hydrogen, can be oxidized using KMnO4 or Na2Cr2O7 to yield benzoic acid exclusively. The reaction is carried out under vigorous conditions such as heat and high oxidant concentration. 


When internal alkynes are treated with concentrated KMnO4 or, upon ozonolysis, undergo oxidative cleavage to yield carboxylic acids. In comparison, terminal alkynes release CO2 along with the generation of the acid.



Preparation Carboxylic Acids Oxidation Primary Alcohols Aldehydes Strong Oxidizing Agents Mild Oxidizing Agents Alkyl Benzenes KMnO4 Na2Cr2O7 Benzoic Acid Vigorous Conditions Heat High Oxidant Concentration Internal Alkynes Concentrated KMnO4 Ozonolysis Oxidative Cleavage Terminal Alkynes CO2

Get cutting-edge science videos from JoVE sent straight to your inbox every month.

Waiting X
Simple Hit Counter