Chapter 13: Q10P (page 408)
Draw structures for compounds that meet the following descriptions:
(a) C2H6O ; one singlet
(b) C3H7CI ; one doublet and one septet
(c) C4H8CI2O ; two triplets
(d) C2H8O ; one singlet, one triplet, and one quartet
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Chapter 13: Q10P (page 408)
Draw structures for compounds that meet the following descriptions:
(a) C2H6O ; one singlet
(b) C3H7CI ; one doublet and one septet
(c) C4H8CI2O ; two triplets
(d) C2H8O ; one singlet, one triplet, and one quartet
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Question: The NMR spectra of compound A, , are shown. Propose a structure for A, and assign peaks in the spectra to your structure.


How many kinds of electronically non-equivalent protons are present in each of the following compounds, and thus how many NMR absorptions might you expect in each?
Estimate the chemical shift of each carbon in the following molecule. Predict which carbons will appear in the DEPT-90 spectrum, which will give positive peaks in the DEPT-135 spectrum, and which will give negative peaks in the DEPT-135 spectrum.
How many signals would you expect each of the following molecules to have in its and spectra?
a.
b.
c.
d.
e.
f.
How could you use NMR to distinguish between the following pairs of isomers?

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