(iii) During the conversion of G into F an undesired, isomeric, cyclopentenone also forms. Draw this compound and explain briefly how it arises. (iv) In a recent publication the conversion of diester H into diketone G was detailed. In this work H was prepared from diethyl malonate I, methyl vinyl ketone J and bromide K. Disconnect H, showing the relevant synthons in order to arrive at the synthetic equivalents (I to K) provided. (v) According to your answer to section (iv), and including curly arrow reaction mechanisms, show how H can be prepared from I, J and K.

(iii) During the conversion of G into F an undesired, isomeric, cyclopentenone also forms. Draw this compound and explain briefly how it arises. (iv) In a recent publication the conversion of diester H into diketone G was detailed. In this work H was prepared from diethyl malonate I, methyl vinyl ketone J and bromide K. Disconnect H, showing the relevant synthons in order to arrive at the synthetic equivalents (I to K) provided. (v) According to your answer to section (iv), and including curly arrow reaction mechanisms, show how H can be prepared from I, J and K.

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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