Chapter 22: 54E (page 752)
Fill in the reagents a–c that are missing from the following scheme:
Short Answer
The reagents are:
(a) NaOC2H5/CH3I
(b) H3O+/Heat ,and
(c) LDA/CH3I.
Chapter 22: 54E (page 752)
Fill in the reagents a–c that are missing from the following scheme:
The reagents are:
(a) NaOC2H5/CH3I
(b) H3O+/Heat ,and
(c) LDA/CH3I.
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Get started for freeThe key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold Helminthosporium sativum, involves the following base treatment of a keto tosylate.
What kind of reaction is occurring? How would you complete the synthesis?
Unlike most β-diketones, the following β-diketone has no detectable enol content and is about as acidic as acetone. Explain.
Show the steps in preparing each of the following substances using either a malonic ester synthesis or an acetoacetic ester synthesis:
.
Draw structures for the enol tautomers of the following compounds:
(a) Cyclopentanone
(b) Methyl thioacetate
(c) Ethyl acetate
(d) Propanal
(e) Acetic acid
(f) Phenylacetone
Write resonance structures for the following anions:
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