For each problem, you must:1) Calculate the degree of unsaturation.-12) Assign the principal IR absorption bands above 1500 cm3) Draw the structure of the compound4) Label the protons on your structure with letters and assign them to peaks on the NMR spectrum(see the example below).OHD4.0C2H3.53.02.5D1H3.0This peakis a magnifiedversion ofthis peakA2.82.01HBzum2.6B2HEach 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 peakhovering above the baseline. This is a magnified view of one of the actual peaks, to allow you to seesplitting more clearly.1.52.4A3H1.0 PPM0.5 7.5 7.0 6.5 6.0 5.5 5.0 PPM.5"чун "2.5 2.6 1.51.62Н2НЗН2НSH-1739.081172.872966.98698.321458.441257.75750.402876.231383.141889.923834.411498.88974.181030100-9: С1Н14Ог

The question is based on the concept of organic spectroscopy. we need to analyse the spectral data…

Answered: 8.0 7.5 7.0 6.5 6.0 5.5 5.0 PPM.5 www…

8.0 7.5 7.0 6.5 6.0 5.5 5.0 PPM.5 www 2.5 2.6 1.5 1.0 PPM 2H 2H al 3H 2H 15H 20 -1739.09 1172.87 2966.98 698.32 1458.44 1257.75 750.40 2876.43 1383.14 1889.92 3034.41 974.18 1498.88 1030 100

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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