Compound A shows a molecular peak of 56 in Mass Spectrum. When compound A is treated with HBr and peroxides, it produces compound B, which shows twin molecular peaks with weights 136 and 138 in 1:1 ratio. The 'H NMR spectra of both compounds shown below. Identify the structures of A and B in the respective boxes. Compound A 2H 'H NMR of Compound A (integration is listed next to peaks) HBr peroxides 2H PPM 'H NMR of Compound B (integration is listed next to peaks, expansions in above) u М 1H Compound B PPM 6H 6H

Compound A shows a molecular peak of 56 in Mass Spectrum. When compound A is treated with HBr and peroxides, it produces compound B, which shows twin molecular peaks with weights 136 and 138 in 1:1 ratio. The 'H NMR spectra of both compounds shown below. Identify the structures of A and B in the respective boxes. Compound A 2H 'H NMR of Compound A (integration is listed next to peaks) HBr peroxides 2H PPM 'H NMR of Compound B (integration is listed next to peaks, expansions in above) u М 1H Compound B PPM 6H 6H

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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