13C-NMR, Sample #1


Analysis: C4H10O2
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C4H10O2

From the molecular formula, the compound has "0 degrees of unsaturation" (no double bonds or rings).

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The 13C NMR has two peaks, a quartet at 54 (a CH3) and a triplet at 80 (a CH2). Since the molecule has four carbons and only two 13C NMR peaks, there must be symmetry. Both peaks are in the regions where carbons next to electronegative atoms occur (oxygen).

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Structure: structure

IUPAC Name: 1,2-dimethoxymethane

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Copyright 1996, Paul R. Young, University of Illinois at Chicago, All Rights Reserved