Question
The product was 2,3-dibromo-3-phenylpropanoic acid, with a melting point of 198-200 °C . So a racemic mixture of (2R,3S) and (2S,3R).
Based on your knowledge of the bromination of alkenes, did this alkene behave like other alkenes, or was the mechanism differ
ОН NHBrz acetic acid NHBr Br 0 OH Br 2,3-dibromo-3- phenylpropanoic acid pyridinium bromide trans cinnamic acid pyridinium br
0 0
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