Chapter 13: Q13-25E (page 419)
How many absorptions would you expect the following compound tohave in its 1H and 13C NMR spectra?

Short Answer

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Chapter 13: Q13-25E (page 419)
How many absorptions would you expect the following compound tohave in its 1H and 13C NMR spectra?


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How could you use NMR to distinguish between the following pairs of isomers?

Identify the indicated sets of protons as unrelated, homotopic, enantiotopic, or diastereotopic:
a.

b.

c.

Predict the splitting pattern for each kind of hydrogen in isopropyl propanoate,.
Into how many peaks would you expect the 1H NMR signals of the indicated protons to be split? (Green=Cl.)
a)

b)

The compound whose 1H NMR spectrum is shown has the molecular
formula C4H7O2CI and has an infrared absorption peak at 1740cm-1.
Propose a structure.

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