1. Using the starting material molecule(s) provided, propose a synthesis of the target molecule using as many steps and/or reagents as necessary. 2. Write out your synthesis and include all reagents and/or reaction conditions. 3. Explained how you arrived at your answer. You may wish to address the following issues in your response, if they are pertinent to the reaction(s) you propose to employ: 1. Chemoselectivity (why this functional group and not another?) 2. Regioselectivity (why here and not there?) 3. Stereoselectivity (why this stereisomer?) 4. Changes in oxidation state. OH но MeO Мео

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
Chapter16: Aldehydes And Ketones
Section: Chapter Questions
Problem 16.63P
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Design a Synthesis
1. Using the starting material molecule(s) provided,
propose a synthesis of the target molecule using as many
steps and/or reagents as necessary.
2. Write out your synthesis and include all reagents
and/or reaction conditions.
3. Explained how you arrived at your answer.
You may wish to address the following issues in your
response, if they are pertinent to the reaction(s) you
propose to employ:
1. Chemoselectivity (why this functional group and not
another?)
2. Regioselectivity (why here and not there?)
3. Stereoselectivity (why this stereisomer?)
4. Changes in oxidation state.
он
HO
MeO
МеO
"I
Transcribed Image Text:Design a Synthesis 1. Using the starting material molecule(s) provided, propose a synthesis of the target molecule using as many steps and/or reagents as necessary. 2. Write out your synthesis and include all reagents and/or reaction conditions. 3. Explained how you arrived at your answer. You may wish to address the following issues in your response, if they are pertinent to the reaction(s) you propose to employ: 1. Chemoselectivity (why this functional group and not another?) 2. Regioselectivity (why here and not there?) 3. Stereoselectivity (why this stereisomer?) 4. Changes in oxidation state. он HO MeO МеO "I
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