11. (2) A Diels Alder reaction was performed using compounds (A) and (B). The product was then treated with ozone to produce the di-aldehyde shown below. Propose bond-line structures for compounds (A), (B) and (C). H 200°C 1.03 CH₂Cl2 2. (CH3)2S O H (A) (B) (C) 12. (2) Draw structural formulas for the 1,2- and 1,4-addition products formed by addition of one mole of HBr to one mole of the compound below. Ignore stereochemistry. HBr 1,2-product 1,4-product 13. (5) Starting from a single common alkene, show how you would synthesize the following compounds. Provide the alkene (in the middle) along with the appropriate reagents needed for the transformations. НО OH OH 8 HO OH

11. (2) A Diels Alder reaction was performed using compounds (A) and (B). The product was then treated with ozone to produce the di-aldehyde shown below. Propose bond-line structures for compounds (A), (B) and (C). H 200°C 1.03 CH₂Cl2 2. (CH3)2S O H (A) (B) (C) 12. (2) Draw structural formulas for the 1,2- and 1,4-addition products formed by addition of one mole of HBr to one mole of the compound below. Ignore stereochemistry. HBr 1,2-product 1,4-product 13. (5) Starting from a single common alkene, show how you would synthesize the following compounds. Provide the alkene (in the middle) along with the appropriate reagents needed for the transformations. НО OH OH 8 HO OH

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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