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6
Oxidation of a double bond
1. KMnO![](/pool/data/tex/b49511be6fca00a500dc7cd69ecc6c58.gif)
- mild conditions (vicinal diols)
- extreme conditions (carboxylic acids)
2. Ozonolysis
- mild conditions, reducing Zn/water environment (ketones/aldehydes)
- extreme conditions, oxidizing environment
3. NaBH
or LiAlH![](/pool/data/tex/b49511be6fca00a500dc7cd69ecc6c58.gif)
4. Peroxyacetic acids = CH
CO
H or MCPBA (epoxide formation)
5. Hydroboration (NaBH
, peroxide)
![](/pool/data/tex/b49511be6fca00a500dc7cd69ecc6c58.gif)
- mild conditions (vicinal diols)
- extreme conditions (carboxylic acids)
2. Ozonolysis
- mild conditions, reducing Zn/water environment (ketones/aldehydes)
- extreme conditions, oxidizing environment
3. NaBH
![](/pool/data/tex/b49511be6fca00a500dc7cd69ecc6c58.gif)
![](/pool/data/tex/b49511be6fca00a500dc7cd69ecc6c58.gif)
4. Peroxyacetic acids = CH
![](/pool/data/tex/f806252045a28179caaf0ec8f0b5f298.gif)
![](/pool/data/tex/f806252045a28179caaf0ec8f0b5f298.gif)
5. Hydroboration (NaBH
![](/pool/data/tex/f806252045a28179caaf0ec8f0b5f298.gif)
Tags: rxns
Quelle:
Quelle: