Subjects
Sections | |||
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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 |
Additional Guides |
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Acetal and Hemiacetal |
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:
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Concept #2: Mechanism:
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Example #1: Predict The product:
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Example #2: Show the mechanism:
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