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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.

Figure1

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.

Figure2

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.

Figure3

Tags
Carboxylic Acid PreparationOxidation Of AlcoholsOxidation Of AldehydesOxidation Of Alkyl BenzenesOxidative Cleavage Of AlkynesKMnO4 OxidationNa2Cr2O7 OxidationOzonolysis

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13.7 : Preparation of Carboxylic Acids: Overview

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13.1 : IUPAC Nomenclature of Carboxylic Acids

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13.2 : Physical Properties of Carboxylic Acids

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13.3 : Acidity of Carboxylic Acids

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13.4 : Substituent Effects on Acidity of Carboxylic Acids

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13.5 : IR and UV–Vis Spectroscopy of Carboxylic Acids

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13.6 : NMR and Mass Spectroscopy of Carboxylic Acids

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13.8 : Preparation of Carboxylic Acids: Hydrolysis of Nitriles

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13.9 : Preparation of Carboxylic Acids: Carboxylation of Grignard Reagents

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13.10 : Reactions of Carboxylic Acids: Introduction

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13.11 : Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview

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13.12 : Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism

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13.13 : Carboxylic Acids to Methylesters: Alkylation using Diazomethane

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13.14 : Carboxylic Acids to Acid Chlorides

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13.15 : Carboxylic Acids to Primary Alcohols: Hydride Reduction

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