Chapter 22: Q72P-a (page 1205)
Show how you would use the malonic ester synthesis to make the following compounds
Chapter 22: Q72P-a (page 1205)
Show how you would use the malonic ester synthesis to make the following compounds
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Get started for freeIn Solved Problem 22-9, the target molecule was synthesized using a Michael addition to form the bond that is to the upper carbonyl group. Another approach is to use a Michael addition to form the bond that isto the other (lower) carbonyl group. Show how you would accomplish this alternative synthesis.
The Knoevenagel condensation is a special case of the aldol condensation in which an active methylene compound reacts with an aldehyde or ketone, in the presence of a secondary amine as a basic catalyst, to produce a new C=C. Show the starting materials that made each of these by a Knoevenagel condensation.
Propose a mechanism for the acid-catalyzed bromination of pentan-3-one.
Question:Show how you would use the Robinson annulation to synthesize the following compounds
Predict the products of the following reactions.
a. Cyclopentanone +Br2 in acetic acid
b. 1phenylethanol + I2 excess
c.
d)
e)
f)
g)
h)
i)
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