3. Propose an efficient synthesis for the target molecule from the indicated starting material. Assume you have a good selection of other reagents including any inorganic compounds, benzene, and any organic compound containing 3 or fewer carbons. Make sure your synthesis provides a way to control the relative stereochemistry of the target molecule (but not the absolute stereochemistry). Write both a retrosynthetic analysis and the synthesis in the forward direction showing all necessary reagents and reaction conditions for each step. Me Ph OH Ph target Me Me ད starting material
3. Propose an efficient synthesis for the target molecule from the indicated starting material. Assume you have a good selection of other reagents including any inorganic compounds, benzene, and any organic compound containing 3 or fewer carbons. Make sure your synthesis provides a way to control the relative stereochemistry of the target molecule (but not the absolute stereochemistry). Write both a retrosynthetic analysis and the synthesis in the forward direction showing all necessary reagents and reaction conditions for each step. Me Ph OH Ph target Me Me ད starting material
Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter11: Ethers, Epoxides, And Sulfides
Section: Chapter Questions
Problem 11.42P
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![3. Propose an efficient synthesis for the target molecule from the indicated starting material.
Assume you have a good selection of other reagents including any inorganic compounds,
benzene, and any organic compound containing 3 or fewer carbons. Make sure your
synthesis provides a way to control the relative stereochemistry of the target molecule
(but not the absolute stereochemistry). Write both a retrosynthetic analysis and the
synthesis in the forward direction showing all necessary reagents and reaction conditions
for each step.
Me
Ph
OH
Ph
target
Me
Me
도
H
starting material](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F27579ae6-3500-416b-a67a-ebdaba644a69%2F6dd67094-9078-4c40-91fd-e0cfd094e460%2F417uyee_processed.jpeg&w=3840&q=75)
Transcribed Image Text:3. Propose an efficient synthesis for the target molecule from the indicated starting material.
Assume you have a good selection of other reagents including any inorganic compounds,
benzene, and any organic compound containing 3 or fewer carbons. Make sure your
synthesis provides a way to control the relative stereochemistry of the target molecule
(but not the absolute stereochemistry). Write both a retrosynthetic analysis and the
synthesis in the forward direction showing all necessary reagents and reaction conditions
for each step.
Me
Ph
OH
Ph
target
Me
Me
도
H
starting material
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