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Chemistry
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ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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10
NMR: 8 9.8 (1 H, s) , 8 1.1 (9 H, s)
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Transcribed Image Text:Deduce the structure of an unknown compound using the data. C, HO:
10
NMR: 8 9.8 (1 H, s) , 8 1.1 (9 H, s)
Deduce the structure of the unknown compound.
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- 8) CH3 CH3 O 36 Hu H CH3 CH3 Fo H H Answer the following questions, which refer to the two acetonide diastereomers shown above. a) Would you expect any difference in the number of peaks in the ¹H NMR spectra of each acetonide? (Y or N). b) Would you expect any difference in the number of peaks in the 13C NMR spectra of each acetonide? (Y or N) c) Would you expect any difference in the integral values for the peaks in the ¹H NMR spectra of each acetonide? (Y or N) d) Would you expect any difference in the multiplicities for the peaks in the ¹H NMR spectra of each acetonide? (Y or N). e) Would you expect any difference in the chemical shifts for the peaks in the ¹H NMR spectra of each acetonide? (Y or N)arrow_forward4. Deduce the structure of a compound with the molecular formular C8H10O that exhibits the following ¹H NMR and ¹³℃ NMR spectra. (6 pts) Proton NMR 22 7 Carbon NMR There are two. 160 unresolved lines at 130 ppm 140 120 5 Chemical Shift (ppm) 100 80 60 Chemical Shift (ppm) 40 3 20 2V 0arrow_forwardLoudon | Parise SEVENTH EDITION presented by Macmillan Learning Propose a structure for an amine of formula C,H,N, which liberates a gas when treated with NaNO, and HCl. The 13C NMR spectrum is given, with attached protons in parentheses. 13C NMR: 8 14 (2), 8 34.3 (2), 8 50.0 (1)arrow_forward
- Deduce the structure of an unknown compound using the data. C,H,O: 10 NMR: 8 9.8 (1 H, s), 8 1.1 (9 H, s)arrow_forward7arrow_forward14. Propose structure for a compound, C9H₁1Br that fits the following ¹H NMR data: 2.15 8 (2H, quintet) 2.75 8 (2H, triplet) 3.38 8 (2H, triplet) 7.22 8 (5H, singlet)arrow_forward
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