The compound whose 1H NMR spectrum is shown has the molecular formula C8H9Br. Follow the following questions to predict the unknown structure. 3(a) Degree of the unsaturation of this compound = , 3(b) The two peaks at 3.16 δ and 3.56 δ indicate two triplets Yes or NO = 3(c) The compound has 2 CH2 groups Yes or No = 3(d) Depending on the two triplets' chemical shifts one of the CH2 may have attached to the Br, Yes or No = 3(e) The multiplet at 7.18 δ to 7.29 δ indicate that compound is .........-disubstituted benzene = 3(f) The name of the unknown compound is =
The compound whose 1H NMR spectrum is shown has the molecular formula C8H9Br. Follow the following questions to predict the unknown structure. 3(a) Degree of the unsaturation of this compound = , 3(b) The two peaks at 3.16 δ and 3.56 δ indicate two triplets Yes or NO = 3(c) The compound has 2 CH2 groups Yes or No = 3(d) Depending on the two triplets' chemical shifts one of the CH2 may have attached to the Br, Yes or No = 3(e) The multiplet at 7.18 δ to 7.29 δ indicate that compound is .........-disubstituted benzene = 3(f) The name of the unknown compound is =
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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The compound whose 1H NMR spectrum is shown has the molecular formula C8H9Br. Follow the following questions to predict the unknown structure.
3(a) Degree of the unsaturation of this compound = ,
3(b) The two peaks at 3.16 δ and 3.56 δ indicate two triplets Yes or NO =
3(c) The compound has 2 CH2 groups Yes or No =
3(d) Depending on the two triplets' chemical shifts one of the CH2 may have attached to the Br, Yes or No =
3(e) The multiplet at 7.18 δ to 7.29 δ indicate that compound is .........-disubstituted benzene =
3(f) The name of the unknown compound is =
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