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Zanzabum
4 years ago
15

Draw the mechanism, including the intermediate bromonium ion, generated in the bromination of trans-2-pentene. show each step se

parately and show all electron movement. clearly indicate the stereochemistry of the products and label each chiral center as r or s.

Chemistry
1 answer:
ololo11 [35]4 years ago
6 0
Addition of Bromine to trans-2-pentene give the following product:
Step wise reaction involving a bromonium ion intermediate and the addition is trans- or anti-addition as follow:
Check the attached picture.
also the stereo chemistry of products [Optically active compound]  and R, S is is mentioned

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