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Baeyer-Villiger Oxidation

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Sections
Naming Aldehydes	8 mins	0 completed	Learn
Naming Ketones	8 mins	0 completed	Learn
Oxidizing and Reducing Agents	9 mins	0 completed	Learn
Oxidation of Alcohols	40 mins	0 completed	Learn
Ozonolysis	8 mins	0 completed	Learn
DIBAL	6 mins	0 completed	Learn
Alkyne Hydration	9 mins	0 completed	Learn
Nucleophilic Addition	8 mins	0 completed	Learn
Cyanohydrin	11 mins	0 completed	Learn Summary
Organometallics on Ketones	18 mins	0 completed	Learn
Overview of Nucleophilic Addition of Solvents	13 mins	0 completed	Learn
Hydrates	6 mins	0 completed	Learn
Hemiacetal	10 mins	0 completed	Learn Summary
Acetal	12 mins	0 completed	Learn Summary
Acetal Protecting Group	16 mins	0 completed	Learn Summary
Thioacetal	7 mins	0 completed	Learn Summary
Imine vs Enamine	15 mins	0 completed	Learn Summary
Addition of Amine Derivatives	5 mins	0 completed	Learn Summary
Wolff Kishner Reduction	7 mins	0 completed	Learn Summary
Baeyer-Villiger Oxidation	28 mins	0 completed	Learn Summary
Acid Chloride to Ketone	7 mins	0 completed	Learn
Nitrile to Ketone	9 mins	0 completed	Learn Summary
Wittig Reaction	19 mins	0 completed	Learn Summary
Ketone and Aldehyde Synthesis Reactions	14 mins	0 completed	Learn

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Acetal and Hemiacetal

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Next SectionAcid Chloride to Ketone

Now we're going to learn about a really unique oxidation reaction called the Baeyer-Villiger Oxidation. This reaction uses peroxy acids to convert ketones and aldehydes into esters and carboxylic acids.

Concept #1: General Reaction: