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In STEREOCHEMISTRY OF BROMINE ADDITION experiment, we got the product 1) only the syn enantiomers, 2)...

In STEREOCHEMISTRY OF BROMINE ADDITION experiment, we got the product 1) only the syn enantiomers, 2) only the anti enantiomers, or 3) a mixture of diastereomers bycotton. Then we weigh the product and take the melting point. Determine which stereoisomers of 2,3-dibromo-3-phenylpropanoic acid were formed and propose a mechanism for the reaction.

we don’t crystallize the final product. This means that your final product might be slightly impure. Why will this not affect your mechanistic analysis?

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