
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Transcribed Image Text:How many signals would you expect to find in the 13C NMR spectrum of the following
compound?
A.
6
В.
7
C.
D.
Е.
10
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- The MS and 13C NMR spectra for two constitutional isomers with 4 degrees of unsaturation are shown below. Determine the molecular structures of the two constitutional isomers.arrow_forwardHelp needed with analyzing the H-NMR spectra and answering the table below. Thank you in advance!arrow_forwardThe following are all isomers of C10H140. Match the most appropriate structure to the NMR spectra shown below. Make sure to justify your selection using the data. D Он Which of the C1,H¾0 isomers above fits the following NMR spectrum best? 3H. d - - 3H. I 1H. s (disappears in DO) 2H. d 2H. d 2H. pentet 1H, sexlel 0 5. 5.0 4.0 ipan) 4.5 29 w borarrow_forward
- Answer the following questions for compounds L, M, and N drawn below.a.How many signals are expected in the 1H NMR spectrum? b.Into how many peaks is each signal in the 1H NMR spectrum split? c.How many lines are expected in the 13C NMR spectrum?arrow_forwardPlease don't provide handwriting solutionarrow_forward9. Which compound would produce the given ¹H NMR spectrum below? 3 it A. ele 2 i B. ми PPM C. HO D. E.arrow_forward
- Indicate the number of signals and the multiplicity of each signal in the 1H NMR spectrum of each of the following compounds:arrow_forwardIdentify the structure of the molecule most consistent with the molecular formula CgH8O₂ with 13C NMR delta peak values at 41.8, 123.7, 129.2, 132.3, 139.6, 141.5, 144.7, and 190.8. ol ol A. B. HO C. D. of OHarrow_forwardHow many 1H NMR peaks do you expect from the following compounds? (Hint: Distereotopicprotons are not equivalent)arrow_forward
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