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g Ο 4000 2.8 1Η 3500 2.6 2.4 2937 2972 3000 2.2 3Η 2.0 2500 1.8 T 1.6 2000 1.4 1716 1.2 469 1500 1359 6Η 1.0 1125 1101 956 1000 0.8 π 0.6 PPM

g Ο 4000 2.8 1Η 3500 2.6 2.4 2937 2972 3000 2.2 3Η 2.0 2500 1.8 T 1.6 2000 1.4 1716 1.2 469 1500 1359 6Η 1.0 1125 1101 956 1000 0.8 π 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.
2) Assign the principal IR absorption bands above 1500 cm -1
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)

 

 

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
1A: C5H10O 100- 80 60 40- 20 गुण 3.0 4000 2.8 3500 2.6 2.4 2937 2972 ЗН 1H AI 3000 2.2 2.0 2500 1.8 T 1.6 2000 1.4 1716 1 T 1.2 ॠ 1469 1500 1359 6H 1.0 11455 1101 956 1000 0.8 mmmm 0.6 PPM
Transcribed Image Text:1A: C5H10O 100- 80 60 40- 20 गुण 3.0 4000 2.8 3500 2.6 2.4 2937 2972 ЗН 1H AI 3000 2.2 2.0 2500 1.8 T 1.6 2000 1.4 1716 1 T 1.2 ॠ 1469 1500 1359 6H 1.0 11455 1101 956 1000 0.8 mmmm 0.6 PPM
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