Chapter 22: 48E (page 752)
How might you convert geraniol into either ethyl geranylacetate or geranylacetone?
Short Answer
The geraniol is converted into geranylacetate and geranylacetone.
Chapter 22: 48E (page 752)
How might you convert geraniol into either ethyl geranylacetate or geranylacetone?
The geraniol is converted into geranylacetate and geranylacetone.
All the tools & learning materials you need for study success - in one app.
Get started for freeFill in the reagents aโc that are missing from the following scheme:
Unlike most ฮฒ-diketones, the following ฮฒ-diketone has no detectable enol content and is about as acidic as acetone. Explain.
One way to determine the number of acidic hydrogens in a molecule is to treat the compound with NaOD in D2O, isolate the product, and determine its molecular weight by mass spectrometry. For example, if cyclohexanone is treated with NaOD in D2O, the product has MW =102. Explain how this method works.
How could you use a malonic ester synthesis to prepare the following compound?
Draw structures for all monoenol forms of the following molecule. Which would you expect to be the most stable? Explain.
What do you think about this solution?
We value your feedback to improve our textbook solutions.