Problem 1 Spectra 100 89 Relative Intensity 100 FANDALES D 80 CDC13 -0 4000 40 20 0 220 25 2804 66 2736 53 1694 7 3364 77 3076 68 3040 70 2960 17 2936 22 1578 11 2875 27 1510 14 2829 62 1603 4 1474 42 200 3000 100 m/z www 50 1468 41 1428 44 1395 46 1319 23 1258 7 1216 18 1160 9 QE-300 180 160 75 2000 1124 62 1110 50 1057 45 1026 44 1005 44 970 50 877 66 140 HAVENUMBERI 833 20 787 72 780 58 662 47 638 62 619 42 516 56 120 1500 100 rquenftetejuruptajem 80 125 60 150 1000 40 175 20 500
Problem 1 Spectra 100 89 Relative Intensity 100 FANDALES D 80 CDC13 -0 4000 40 20 0 220 25 2804 66 2736 53 1694 7 3364 77 3076 68 3040 70 2960 17 2936 22 1578 11 2875 27 1510 14 2829 62 1603 4 1474 42 200 3000 100 m/z www 50 1468 41 1428 44 1395 46 1319 23 1258 7 1216 18 1160 9 QE-300 180 160 75 2000 1124 62 1110 50 1057 45 1026 44 1005 44 970 50 877 66 140 HAVENUMBERI 833 20 787 72 780 58 662 47 638 62 619 42 516 56 120 1500 100 rquenftetejuruptajem 80 125 60 150 1000 40 175 20 500
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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Question
On spectra 1 are the mass, IR and 13 C and 1 H NMR
spectra of an organic compound.
1) a) From these spectra, determine the structure of the molecule.
Remember to ignore the triad in the 13 C NMR spectrum at 77 ppm that
comes from the NMR solvent.
b) Draw the structure of the molecule and label each hydrogen with a letter
(A, B, C...). Then fill in the peak assignment table below.
hydrogen | chemical shift | integration | splitting pattern | couples to |
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