Chapter 21q: Practice Quiz
- Page ID
- 208741
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Nucleophilic Addition
question \(\PageIndex{1}\)
Determine products of the following reactions
Exercise \(\PageIndex{5}\)
Show in multiple steps how the following synthesis could be carried out.
- Answer
-
A Wittig reaction can convert the ketone into the alkene while adding two carbons. Hydroboration oxidation will oxidize the less substituted end of the alkene to an alcohol. Finally chromium oxidation with either chromic acid or pyridinium chlorochromate will oxidize the alcohol to the product ketone.
Contributors
- Layne Morsch (University of Illinois Springfield)