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4.0⁰ 3.0 2.5 2.0 1.5 PPM 1.0 1H 4H 4H 2 1897.34 2947.81 2851.15 1319 48 1142.00 1452.58 835.28 602.49 2752.77 1862.91 3335.35 1348.41 1248.10 891.23 10: C₂H₂NO

4.0⁰ 3.0 2.5 2.0 1.5 PPM 1.0 1H 4H 4H 2 1897.34 2947.81 2851.15 1319 48 1142.00 1452.58 835.28 602.49 2752.77 1862.91 3335.35 1348.41 1248.10 891.23 10: C₂H₂NO

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
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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10: C₂H,NO 100- 9 2 4000 4.0 4H 3335.35 3.5 2947.61 2851.15 2752.77 4H 3.0 2.5 2.0 1452.58 1588 1H 1348.41 1319 48 1248.10 1142.00 1862.91 1897.34 1.5 PPM 1.0 891.23 602.49 835.28
Transcribed Image Text:10: C₂H,NO 100- 9 2 4000 4.0 4H 3335.35 3.5 2947.61 2851.15 2752.77 4H 3.0 2.5 2.0 1452.58 1588 1H 1348.41 1319 48 1248.10 1142.00 1862.91 1897.34 1.5 PPM 1.0 891.23 602.49 835.28
For each problem, you must: 1) Calculate the degree of unsaturation. -1 2) Assign the principal IR absorption bands above 1500 cm 3) Draw the structure of the compound 4) Label the protons on your structure with letters and assign them to peaks on the NMR spectrum (see the example below). 4.0 C 2H 3.5 3.0 2.5 D 1H 3.0 This peak is a magnified version of this peak A 2.8 2.0 1H B zum 2.6 B 2H Each problem contains the formula of the compound, the IR spectrum (with axes in cm³¹ vs. % transmission), and the ¹H NMR spectrum (with axis in PPM shift). Some NMR spectra show a peak hovering above the baseline. This is a magnified view of one of the actual peaks, to allow you to see splitting more clearly. 1.5 2.4 OHD A 3H 1.0 PPM 0.5
Transcribed Image Text:For each problem, you must: 1) Calculate the degree of unsaturation. -1 2) Assign the principal IR absorption bands above 1500 cm 3) Draw the structure of the compound 4) Label the protons on your structure with letters and assign them to peaks on the NMR spectrum (see the example below). 4.0 C 2H 3.5 3.0 2.5 D 1H 3.0 This peak is a magnified version of this peak A 2.8 2.0 1H B zum 2.6 B 2H Each problem contains the formula of the compound, the IR spectrum (with axes in cm³¹ vs. % transmission), and the ¹H NMR spectrum (with axis in PPM shift). Some NMR spectra show a peak hovering above the baseline. This is a magnified view of one of the actual peaks, to allow you to see splitting more clearly. 1.5 2.4 OHD A 3H 1.0 PPM 0.5
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