ČOEt 1. EtO-Na+ OEt 3. NAOH, H,O, heat EtO 4. HCI, heat 2-Carbethoxy- 4-Butanolactone 4-butanolactone (y-Butyrolactone) Show how the scheme for formation of 4-butanolactone can be used to synthesize lactones (a) and (b), each of which has a peach odor and is used in per- fumery. As sources of carbon atoms for these syntheses, use diethyl malonate, ethylene oxide, 1-bromoheptane, and 1-nonene. (b) (racemic) (racemic)
ČOEt 1. EtO-Na+ OEt 3. NAOH, H,O, heat EtO 4. HCI, heat 2-Carbethoxy- 4-Butanolactone 4-butanolactone (y-Butyrolactone) Show how the scheme for formation of 4-butanolactone can be used to synthesize lactones (a) and (b), each of which has a peach odor and is used in per- fumery. As sources of carbon atoms for these syntheses, use diethyl malonate, ethylene oxide, 1-bromoheptane, and 1-nonene. (b) (racemic) (racemic)
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Transcribed Image Text:ČOEt
1. EtO-Na+
OEt
3. NAOH, H,O, heat
EtO
4. HCI, heat
2-Carbethoxy-
4-Butanolactone
4-butanolactone
(y-Butyrolactone)
Show how the scheme for formation of 4-butanolactone
can be used
to synthesize lactones (a) and (b), each of which has a peach odor and is used in per-
fumery. As sources of carbon atoms for these syntheses, use diethyl malonate, ethylene
oxide, 1-bromoheptane, and 1-nonene.
(b)
(racemic)
(racemic)
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