8) CH3 CH3 CH3 CH3 A Bo H Н 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).
8) CH3 CH3 CH3 CH3 A Bo H Н 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).
Chapter14: Conjugated Compounds And Ultraviolet Spectroscopy
Section14.SE: Something Extra
Problem 53AP: Treatment of 3,4-dibromohexane with strong base leads to loss of 2 equivalents of HBr and formation...
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