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H C 3. (5S,7R)-7-bromo-3,9-diethyl-6,6-dimethylundec-3,8-dien-5-ol HC Н.С. OH by CH₂ Br -CH₂ "CH₂ I b. number of peaks = С.

H C 3. (5S,7R)-7-bromo-3,9-diethyl-6,6-dimethylundec-3,8-dien-5-ol HC Н.С. OH by CH₂ Br -CH₂ "CH₂ I b. number of peaks = С.

Chemistry
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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Нас 3. (5S,7R) -7-bromo-3,9-diethyl-6,6-dimethylundec-3,8-dien-5-ol H C Н.С Ay statuvos OH CH3 Ay si Br Н CH3 CH3 I b. number of peaks = С.
Transcribed Image Text:Нас 3. (5S,7R) -7-bromo-3,9-diethyl-6,6-dimethylundec-3,8-dien-5-ol H C Н.С Ay statuvos OH CH3 Ay si Br Н CH3 CH3 I b. number of peaks = С.
For each of the molecules below: (a) Provide the bond line structures (b) Indicate the number of peaks that would be seen in their ¹H-NMR spectra by numbering each unique type of hydrogen peaks as shown in the example on the right. (c) Label the diasterotopic and enantiotopic atoms and/or groups. 1. (1R, 4S) 4-secbutyl-2,3-diethyl-6,6-dimethylcyclohex-2-enol H₂C. Br H₂C CH3 OH OH 2. (2R,6S) 2,6-dibromo-4,4-dimethylcyclohexanol Br H₂C CH₂ -CH₂ CH3 CH3 -CH3 CH3 b. number of peaks: C. b. number of peaks = C. Example: ¹H 2 U 2 1
Transcribed Image Text:For each of the molecules below: (a) Provide the bond line structures (b) Indicate the number of peaks that would be seen in their ¹H-NMR spectra by numbering each unique type of hydrogen peaks as shown in the example on the right. (c) Label the diasterotopic and enantiotopic atoms and/or groups. 1. (1R, 4S) 4-secbutyl-2,3-diethyl-6,6-dimethylcyclohex-2-enol H₂C. Br H₂C CH3 OH OH 2. (2R,6S) 2,6-dibromo-4,4-dimethylcyclohexanol Br H₂C CH₂ -CH₂ CH3 CH3 -CH3 CH3 b. number of peaks: C. b. number of peaks = C. Example: ¹H 2 U 2 1
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