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20- 30- 50- 10- 20 4000 3.0 2.8 3500 2.6 6H 2.4 2959 2934 3000 2874 2.2 2799 2.0 2500 1.8 1.6 2000 6H Ми 1.4 1466 1500 1.2 1379 1290 1.0 2611 1076 9Н 1000 O.B 0.6 PPM

20- 30- 50- 10- 20 4000 3.0 2.8 3500 2.6 6H 2.4 2959 2934 3000 2874 2.2 2799 2.0 2500 1.8 1.6 2000 6H Ми 1.4 1466 1500 1.2 1379 1290 1.0 2611 1076 9Н 1000 O.B 0.6 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
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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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). OHD 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 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). OHD 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 A 3H 1.0 PPM 0.5
4A: C₂H₂1N 100 80- 60 40- 20 0 4000 TTTTTTTTTT 3.0 2.8 3500 2.6 6H 2.4 2959 2934 3000 2874- 2.2 2799 2.0 2500 1.8 T T T 1.6 2000 6H 1.4 T 1.2 1466 1500 1379 1290 1.0 26TT 1076 9H 1000 0.8 0.6 PPM
Transcribed Image Text:4A: C₂H₂1N 100 80- 60 40- 20 0 4000 TTTTTTTTTT 3.0 2.8 3500 2.6 6H 2.4 2959 2934 3000 2874- 2.2 2799 2.0 2500 1.8 T T T 1.6 2000 6H 1.4 T 1.2 1466 1500 1379 1290 1.0 26TT 1076 9H 1000 0.8 0.6 PPM
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