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A compound exhibits a peak at 1685 cm1 in its IR spectrum. Describe how 13C NMR can be used to identify the functional group. Amides have a peak around 170 ppm in 13C NMR; conjugated ketones, 200 ppm Ketones and aldehydes are indistinguishable in 13C NMR Esters have a peak around 175 ppm in 13C NMR; conjugated ketones, 200 ppm Amides have a peak around 170 ppm in 1BC NMR; esters, 175 ppm

A compound exhibits a peak at 1685 cm1 in its IR spectrum. Describe how 13C NMR can be used to identify the functional group. Amides have a peak around 170 ppm in 13C NMR; conjugated ketones, 200 ppm Ketones and aldehydes are indistinguishable in 13C NMR Esters have a peak around 175 ppm in 13C NMR; conjugated ketones, 200 ppm Amides have a peak around 170 ppm in 1BC NMR; esters, 175 ppm

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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"A compound exhibits a peak at 1685 cm-1 in its IR spectrum. Describe how 13C NMR can be used to identify the functional group."

A compound exhibits a peak at 1685 cm in its IR spectrum. Describe how 13C NMR can be used to identify the functional group. O Amides have a peak around 170 ppm in 13C NMR; conjugated ketones, 200 ppm O Ketones and aldehydes are indistinguishable in 13C NMR Esters have a peak around 175 ppm in 13C NMR; conjugated ketones, 200 ppm O Amides have a peak around 170 ppm in 13C NMR; esters, 175 ppm
Transcribed Image Text:A compound exhibits a peak at 1685 cm in its IR spectrum. Describe how 13C NMR can be used to identify the functional group. O Amides have a peak around 170 ppm in 13C NMR; conjugated ketones, 200 ppm O Ketones and aldehydes are indistinguishable in 13C NMR Esters have a peak around 175 ppm in 13C NMR; conjugated ketones, 200 ppm O Amides have a peak around 170 ppm in 13C NMR; esters, 175 ppm
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