Chapter 17: 17-55P (page 847)
Draw the products of the following reactions:
Chapter 17: 17-55P (page 847)
Draw the products of the following reactions:
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Get started for freeDraw the enol tautomer for each of the following compounds. For compounds that have more than one enol tautomer, indicate the one that is more stable.
Draw the product of the reaction of each of the following compounds with a base:
The Reformatsky reaction is an addition reaction in which an organozinc reagent is used instead of a Grignard reagent to add to the carbonyl group of an aldehyde or a ketone. Because the organozinc reagent is less reactive than a Grignard reagent, a nucleophilic addition to the ester group does not occur. The organozinc reagent is prepared by treating an ß-bromo ester with zinc.
Describe how each of the following compounds can be prepared, using a Reformatsky reaction:
What alkyl bromide(s) should be used in the malonic ester synthesis of each of the following carboxylic acids?
a. propanoic acid
b. 2-methylpropanoic acid
c. 3-phenylpropanoic acid
d. 4-methylpentanoic acid
Indicate how the following compounds can be synthesized from cyclohexanone and any other necessary reagents:
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