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3. Consider the following retrosynthetic analysis of Disparlure, the sex pheromone of the female gypsy moth. Propose the forward synthesis of Disparlure given the names of each step. Please pay close attention to the stereochemical outcomes in each step and number your carbons if you need to keep track of all of the molecular changes. epoxidation A reduction Br C-C bond formation Br D B

3. Consider the following retrosynthetic analysis of Disparlure, the sex pheromone of the female gypsy moth. Propose the forward synthesis of Disparlure given the names of each step. Please pay close attention to the stereochemical outcomes in each step and number your carbons if you need to keep track of all of the molecular changes. epoxidation A reduction Br C-C bond formation Br D B

Chemistry
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
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3. Consider the following retrosynthetic analysis of Disparlure, the sex pheromone of the female gypsy moth. Propose the forward synthesis of Disparlure given the names of each step. Please pay close attention to the stereochemical outcomes in each step and number your carbons if you need to keep track of all of the molecular changes. epoxidation A [2] reduction Br [3] C-C bond formation Br D B
Transcribed Image Text:3. Consider the following retrosynthetic analysis of Disparlure, the sex pheromone of the female gypsy moth. Propose the forward synthesis of Disparlure given the names of each step. Please pay close attention to the stereochemical outcomes in each step and number your carbons if you need to keep track of all of the molecular changes. epoxidation A [2] reduction Br [3] C-C bond formation Br D B
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