5. "S". Draw the skeletal structures of the products obtained and label all chiral carbon atoms as "R" or 6.) Predict the products that would be formed from the bromination of cis-cinnamic acid. Draw the skeletal structures for the products.

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Could anyone help me out on question 6? The experiment is on the sterochemistry of bromine addition and my question is about the products referenced in the question prompt. Do I need to use the impure 2,3-dibromo-3-phenylpropanoic acid? If so please answer question 6 I'm genuinely confused. Both question 5 and 6 relate to the same reaction I believe. This experiment is titled the stereochemistry of Bromine addition

5.
"S".
Draw the skeletal structures of the products obtained and label all chiral carbon atoms as "R" or
6.5
Predict the products that would be formed from the bromination of cis-cinnamic acid. Draw the
skeletal structures for the products.
Transcribed Image Text:5. "S". Draw the skeletal structures of the products obtained and label all chiral carbon atoms as "R" or 6.5 Predict the products that would be formed from the bromination of cis-cinnamic acid. Draw the skeletal structures for the products.
Starting mass of trans-cinnamic acid
Mass of impure 2,3-dibromo-3-phenylpropanoic
acid
Mass of impure 2,3-dibromo-3-phenylpropanoic
acid used for recrystallization
Mass of recrystallized 2,3-dibromo-3-
phenylpropanoic acid recovered
Melting point range of crude product
Melting point range of recrystallized product
Transcribed Image Text:Starting mass of trans-cinnamic acid Mass of impure 2,3-dibromo-3-phenylpropanoic acid Mass of impure 2,3-dibromo-3-phenylpropanoic acid used for recrystallization Mass of recrystallized 2,3-dibromo-3- phenylpropanoic acid recovered Melting point range of crude product Melting point range of recrystallized product
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