Q7-Synthesis question. Show how the starting material can be converted to the product through any of the reactions you have learned in OChem 1 and OChem 2. Show all the reagents you need and indicate the stereochemistry when appropriate. You do not need to show arrow pushing like in a mechanism question, only the reactions. If a chiral molecule is formed mark the chiral center with an asterisk (*) and write "racemic" below the structure unless the chiral center has unambiguous stereochemistry. All carbon atoms in the product should come from the same starting material. Use as many molecules of the starting material as you might need to get to the product. You can use carbon containing reagents for temporary protection of functional groups, if needed. A) B) OH CO₂ OCH3 racemic

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Chapter1: Chemical Foundations
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Q7-Synthesis question. Show how the starting material can be converted to the product through any of
the reactions you have learned in OChem 1 and OChem 2. Show all the reagents you need and indicate
the stereochemistry when appropriate. You do not need to show arrow pushing like in a mechanism
question, only the reactions. If a chiral molecule is formed mark the chiral center with an asterisk (*) and
write "racemic" below the structure unless the chiral center has unambiguous stereochemistry. All
carbon atoms in the product should come from the same starting material. Use as many molecules of the
starting material as you might need to get to the product. You can use carbon containing reagents for
temporary protection of functional groups, if needed.
A)
B)
OH
CO₂
OCH3
racemic
Transcribed Image Text:Q7-Synthesis question. Show how the starting material can be converted to the product through any of the reactions you have learned in OChem 1 and OChem 2. Show all the reagents you need and indicate the stereochemistry when appropriate. You do not need to show arrow pushing like in a mechanism question, only the reactions. If a chiral molecule is formed mark the chiral center with an asterisk (*) and write "racemic" below the structure unless the chiral center has unambiguous stereochemistry. All carbon atoms in the product should come from the same starting material. Use as many molecules of the starting material as you might need to get to the product. You can use carbon containing reagents for temporary protection of functional groups, if needed. A) B) OH CO₂ OCH3 racemic
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