Chapter 13: Q13-12P (page 404)
Identify the indicated sets of protons as unrelated, homotopic, enantiotopic, or diastereotopic:
a.
(b)
(c)
(d)
(e)
(f)
Short Answer
- Homotopic
- Enantiotopic
- Homotopic
- Diastereotopic
- Homotopic
- homotopic
Chapter 13: Q13-12P (page 404)
Identify the indicated sets of protons as unrelated, homotopic, enantiotopic, or diastereotopic:
a.
(b)
(c)
(d)
(e)
(f)
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Get started for freeThe compound whose 1H NMR spectrum is shown has the molecular
formula C4H7O2CI and has an infrared absorption peak at 1740cm-1.
Propose a structure.
How could you use and1H 13C NMR to help distinguish the following
isomeric compounds of the formula C4H8?
Propose structures for compounds that fit the following descriptions:
(a) A hydrocarbon with seven lines in its 13C NMR spectrum
(b) A six-carbon compound with only five lines in its 13C NMR spectrum
(c) A four-carbon compound with three lines in its 13C NMR spectrum
A NMR spectrum of commercially available 2,4-pentanediol, shows five peaks at 23.3, 23.9, 46.5, 64.8, and 68.1 d. Explain.
Long-range coupling between protons more than two carbon atoms apart is sometimes observed when p bonds intervene. An example is found in 1-methoxy-1-buten-3-yne. Not only does the acetylenic proton, , couple with the vinylic proton , it also couples with the vinylic proton , four carbon atoms away. The data are:
Construct tree diagrams that account for the observed splitting patterns of ,, and .
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