Problem # 2 Determine the structure of the compound with the spectra provided and molecular formula C5H₁00. I 200 180 10 9 8 160 140 7 120 6 1100 5 100 80 4 60 3 2000 3H singlet 6H doublet 37 1H septet 40 20 2 1 0 0
Problem # 2 Determine the structure of the compound with the spectra provided and molecular formula C5H₁00. I 200 180 10 9 8 160 140 7 120 6 1100 5 100 80 4 60 3 2000 3H singlet 6H doublet 37 1H septet 40 20 2 1 0 0
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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Step 1: Given
The molecular formula is C5H10O.
The FTIR, 1H, and 13C NMR spectra of the compound are given.
We have to determine the molecular structure of the compound.
The double bond equivalency (DBE) of that compound is
DBE = (No. of carbon atoms + 1) - {(No. of monovalent atoms - No. of trivalent atoms)/2} = (5+1)-(10/2) = 6-5 = 1.
So, the given compound has one degree of unsaturation.
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