b) Product Restrosynthesis Starting materials Forward synthesis Br Synthesis and Retrosynthesis. 3. Propose a retro and forward synthesis of the following compound. No carbons may be introduced from sources other than the given starting materials. If a racemic mixture is formed; draw one enantiomer and write (+/-) next to the structure. a) Restrosynthesis OH Forward synthesis Product Br CO₂ Starting materials

b) Product Restrosynthesis Starting materials Forward synthesis Br Synthesis and Retrosynthesis. 3. Propose a retro and forward synthesis of the following compound. No carbons may be introduced from sources other than the given starting materials. If a racemic mixture is formed; draw one enantiomer and write (+/-) next to the structure. a) Restrosynthesis OH Forward synthesis Product Br CO₂ Starting materials

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter22: Carbonyl Alpha-substitution Reactions

Section22.SE: Something Extra

Problem 25MP

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