8)CH3 CH3O36HuHCH3 CH3FoHHAnswer 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)

Answered: Image /qna-images/answer/c8bc9001-ff91-4f51-b55a-bd8206199ef6.jpg

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).

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

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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