MISTRY 2400 EXPERIMENT 7: BROMINATION OF CINNAMIC ACID WINTER 2022 For the trans isomer of cinnamic acid: Draw the structure of the trans isomer of cinnamic acid and the structure of the intermediate bromonium ion. Note that the bromonium ion can exist as two enantiomeric forms. You should draw both of these isomeric forms. Draw the structures of the two dibrominated products which can form when a bromide ion adds to the bromonium ion intermediate. These must be drawn to show the correct stereochemistry. Assign the chiral carbons as R or S. L. 20 Based on the information in the introduction, what is the expected melting point of these + enantiomeric products? yONng pont, which set of stereoisomers

MISTRY 2400 EXPERIMENT 7: BROMINATION OF CINNAMIC ACID WINTER 2022 For the trans isomer of cinnamic acid: Draw the structure of the trans isomer of cinnamic acid and the structure of the intermediate bromonium ion. Note that the bromonium ion can exist as two enantiomeric forms. You should draw both of these isomeric forms. Draw the structures of the two dibrominated products which can form when a bromide ion adds to the bromonium ion intermediate. These must be drawn to show the correct stereochemistry. Assign the chiral carbons as R or S. L. 20 Based on the information in the introduction, what is the expected melting point of these + enantiomeric products? yONng pont, which set of stereoisomers

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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