Below are the ¹H NMR spectrum of triphenylmethanol, benzophenone, and bromobenzene. Identify the compound corresponding to each ¹H NMR spectrum and draw the structure next to the ¹H NMR spectrum. Assign ALL peaks in each of the three ¹H NMR spectra. Hint: Conjugated systems (benzophenone) including an electronegative atom will cause a more downfield shift of ring protons in ¹H NMR compared with non-conjugated systems (bromobenzene). 8 8 8 7 7 7 6 6 6 5 5 5 4 PPM 4 PPM 4 PPM 3 3 3 2 2 2 1 1 0 0
Below are the ¹H NMR spectrum of triphenylmethanol, benzophenone, and bromobenzene. Identify the compound corresponding to each ¹H NMR spectrum and draw the structure next to the ¹H NMR spectrum. Assign ALL peaks in each of the three ¹H NMR spectra. Hint: Conjugated systems (benzophenone) including an electronegative atom will cause a more downfield shift of ring protons in ¹H NMR compared with non-conjugated systems (bromobenzene). 8 8 8 7 7 7 6 6 6 5 5 5 4 PPM 4 PPM 4 PPM 3 3 3 2 2 2 1 1 0 0
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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![Below are the ¹H NMR spectrum of triphenylmethanol, benzophenone, and bromobenzene. Identify the
compound corresponding to each ¹H NMR spectrum and draw the structure next to the ¹H NMR spectrum.
Assign ALL peaks in each of the three ¹H NMR spectra. Hint: Conjugated systems (benzophenone)
including an electronegative atom will cause a more downfield shift of ring protons in ¹H NMR compared
with non-conjugated systems (bromobenzene).
8
8
8
7
7
7
6
6
6
5
5
5
4
PPM
4
PPM
4
PPM
3
3
3
2
2
2
1
1
1
0
0
0](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F56312969-557b-4eb4-a541-f59b5e818975%2F82ded69e-7581-4267-bd9c-70038f24d058%2Fzkavvib_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Below are the ¹H NMR spectrum of triphenylmethanol, benzophenone, and bromobenzene. Identify the
compound corresponding to each ¹H NMR spectrum and draw the structure next to the ¹H NMR spectrum.
Assign ALL peaks in each of the three ¹H NMR spectra. Hint: Conjugated systems (benzophenone)
including an electronegative atom will cause a more downfield shift of ring protons in ¹H NMR compared
with non-conjugated systems (bromobenzene).
8
8
8
7
7
7
6
6
6
5
5
5
4
PPM
4
PPM
4
PPM
3
3
3
2
2
2
1
1
1
0
0
0
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