Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For ¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important part of the spectrum. Mass Spectrum (not shown): [M] = 343 (100%), 345 (33%) m/z IR Spectrum (not shown): 3031, 2981, 2250 (m), 1601, 1500, 1246 cm¹ (all listed are strong (s) unless otherwise indicated) 1H NMR Spectrum (400 MHz, CDCl3, 25 °C) 8 7 6 5 4 3 2 4H 4H PPM 4H 2H 2H 6H 13C NMR Spectrum, proton-decoupled (125 MHz, CDCl3, 25 °C) (CH) (CH) Q1 (C) (C) (C) (CH2) (CH3) (C) (CH2) (CH2) 160 140 120 100 80 PPM 60 40 40 20 0 14 1/1

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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What molecule would produce this data?
Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule.
For ¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants
(J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a
"zoom-in" on an important part of the spectrum.
Mass Spectrum (not shown): [M] = 343 (100%), 345 (33%) m/z
IR Spectrum (not shown): 3031, 2981, 2250 (m), 1601, 1500, 1246 cm¹ (all listed are strong (s) unless otherwise
indicated)
1H NMR Spectrum (400 MHz, CDCl3, 25 °C)
8
7
6
5
4
3
2
4H 4H
PPM
4H
2H
2H
6H
13C NMR Spectrum, proton-decoupled (125 MHz, CDCl3, 25 °C)
(CH) (CH)
Q1
(C)
(C)
(C)
(CH2)
(CH3)
(C)
(CH2)
(CH2)
160
140
120
100
80
PPM
60
40
40
20
0
14
1/1
Transcribed Image Text:Spectroscopy Unknown. The spectra and data provided were obtained from a pure organic molecule. For ¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important part of the spectrum. Mass Spectrum (not shown): [M] = 343 (100%), 345 (33%) m/z IR Spectrum (not shown): 3031, 2981, 2250 (m), 1601, 1500, 1246 cm¹ (all listed are strong (s) unless otherwise indicated) 1H NMR Spectrum (400 MHz, CDCl3, 25 °C) 8 7 6 5 4 3 2 4H 4H PPM 4H 2H 2H 6H 13C NMR Spectrum, proton-decoupled (125 MHz, CDCl3, 25 °C) (CH) (CH) Q1 (C) (C) (C) (CH2) (CH3) (C) (CH2) (CH2) 160 140 120 100 80 PPM 60 40 40 20 0 14 1/1
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