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Unformatted text preview: o ), or tertiary (3 o ). Structure IUPAC Name Classification 3. By assuming that the heat of combustion of the cis- isomer was larger than the trans, structural assignments were made many years ago for the steroisomeric 2-, 3-, and 4-methylcyclohexanols. This assumption is valid for two of the steroisomeric pairs, but not for the other. For which pair of steroisomers is the assumption incorrect? Why? 4. Different reagents and conditions are used to convert secondary alcohols or tertiary alcohols to alkyl halides. Specify appropriate reagents for the following conversions and explain, in mechanistic terms, why different reagents and conditions are required. OH Cl OH Cl (a) (b)...
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This note was uploaded on 03/07/2012 for the course CHEM 341 taught by Professor Oh during the Fall '10 term at IUPUI.
- Fall '10
- Organic chemistry