Question

1. The compound shown below has only two peaks, both singlets, in its 1H NMR spectrum. H3CO OCH3 a. Predict the chemical shift of each peak and show which hydrogen atoms correspond to each peak. b. Explain why this compound with its 12 hydrogen's has such a simple NMR spectrum.

          1. The compound shown below has only two peaks, both singlets, in its 1H NMR spectrum.
H3CO OCH3
a. Predict the chemical shift of each peak and show which hydrogen atoms correspond to each peak.
b. Explain why this compound with its 12 hydrogen's has such a simple NMR spectrum.

1. The compound shown below has only two peaks, both singlets, in its 1H NMR spectrum.
H3CO OCH3
a. Predict the chemical shift of each peak and show which hydrogen atoms correspond to each peak.
b. Explain why this compound with its 12 hydrogen's has such a simple NMR spectrum.

Added by Michael L.

Chemistry: Structure and Properties

Nivaldo Tro 2nd Edition

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Solved by Expert Nicole Krahulik

09/24/2022

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The compound shown below has only two peaks, both singlets, in its 1H NMR spectrum. a. Predict the chemical shift of each peak and show which hydrogen atoms correspond to each peak. b. Explain why this compound with its 12 hydrogen's has such a simple NMR spectrum.