Chapter 13: 54P (page 419)
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.

Short Answer

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Chapter 13: 54P (page 419)
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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Identify the different types of protons in the following molecule, and tell
where you would expect each to absorb:
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?
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.


Question: Sketch what you might expect the1H and13C NMR spectra of the following compound to look like (green=Cl):

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.)
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