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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Predict the splitting patterns you would expect for each proton in the following molecules:
Question: How many electronically non-equivalent kinds of protons and how
many kinds of carbons are present in the following compound? Don’t
forget that cyclohexane rings can ring-flip.

The proton NMR spectrum of a compound with the formula C7H12O2is
shown. The infrared spectrum displays a strong band at 1738 cm-1 and
a weak band at 1689 cm-1 . The normal carbon-13 and the DEPT experimental
results are tabulated. Draw the structure of this compound.


Propose a structure for an aromatic hydrocarbon, C11H16, that has the following 13C NMR spectral data:
Broadband decoupled: 29.5, 31.8, 50.2, 125.5, 127.5, 130.3, 139.8
DEPT-90: 125.5, 127.5, 130.3
DEPT-135: positive peaks at 29.5, 125.5, 127.5, 130.3d;negative peak at
50.2
Question: Propose structures for the three compounds whose NMR spectra are shown.



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