Chapter 13: Q13-35E (page 419)
The following compounds all show a single line in their NMR spectra. List them in order of expected increasing chemical shift:
,cyclohexane ,,benzene
Short Answer
Increasing order is as follows:
Chapter 13: Q13-35E (page 419)
The following compounds all show a single line in their NMR spectra. List them in order of expected increasing chemical shift:
,cyclohexane ,,benzene
Increasing order is as follows:
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Get started for freeIdentify the indicated sets of protons as unrelated, homotopic, enantiotopic, or diastereotopic:
a.
(b)
(c)
(d)
(e)
(f)
The compound whose 1H NMR spectrum is shown has the molecular
formula C3H6Br2. Propose a structure.
How many peaks would you expect in the 1H NMR spectrum of 1,4-dimethylbenzene(para-xylene, or p-xylene)? What ratio of peak areas would youexpect on integration of the spectrum? Refer to Table 13-3 for approximatechemical shifts, and sketch what the spectrum would look like. (Rememberfrom Section 2-4 that aromatic rings have two resonance forms.)
Question: Identify the indicated protons in the following molecules as unrelated,
homotopic, enantiotopic, or diastereotopic.
a)
b)
Propose structures for compounds that fit the following NMR data:
(a) C5H10O
0.95(6H,double, J = 7Hz)
2.10(3H,singlet)
2.43(1H, mutiplet)
(b) C3H5Br
2.32(3H,singlet)
5.35 (3H,singlet)
5.45(1H, broad signet )
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