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] = 132 (100%) m/z IR Spectrum (not shown): 3300, 2981, 2850, 2750, 1728 cm-1 (all listed are strong (s) unless otherwise indicated) 1H NMR Spectrum (400 MHz, CDCl 3, 25 °C) m br s 10 8 6 2 PPM 1H 4H 1H 4H2H 13C NMR Spectrum, proton-decoupled (125 MHz, CDCl3, 25 °C) (CH) 220 200 180 160 140 120 PPM 100 80 80 Q1 (CH₂) (CH2) 60 60 (CH) 40 8- 20 20 0 1/1
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] = 132 (100%) m/z IR Spectrum (not shown): 3300, 2981, 2850, 2750, 1728 cm-1 (all listed are strong (s) unless otherwise indicated) 1H NMR Spectrum (400 MHz, CDCl 3, 25 °C) m br s 10 8 6 2 PPM 1H 4H 1H 4H2H 13C NMR Spectrum, proton-decoupled (125 MHz, CDCl3, 25 °C) (CH) 220 200 180 160 140 120 PPM 100 80 80 Q1 (CH₂) (CH2) 60 60 (CH) 40 8- 20 20 0 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] = 132 (100%) m/z
IR Spectrum (not shown): 3300, 2981, 2850, 2750, 1728 cm-1 (all listed are strong (s) unless otherwise indicated)
1H NMR Spectrum (400 MHz, CDCl 3, 25 °C)
m
br s
10
8
6
2
PPM
1H
4H
1H 4H2H
13C NMR Spectrum, proton-decoupled (125 MHz, CDCl3, 25 °C)
(CH)
220
200
180
160
140
120
PPM
100
80
80
Q1
(CH₂)
(CH2)
60
60
(CH)
40
8-
20
20
0
1/1](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F13344a5e-ec4e-46f8-a2ea-c159e4536077%2F2c94660f-a5d3-4253-8475-1e3d03e5f475%2Fob42nk9_processed.jpeg&w=3840&q=75)
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] = 132 (100%) m/z
IR Spectrum (not shown): 3300, 2981, 2850, 2750, 1728 cm-1 (all listed are strong (s) unless otherwise indicated)
1H NMR Spectrum (400 MHz, CDCl 3, 25 °C)
m
br s
10
8
6
2
PPM
1H
4H
1H 4H2H
13C NMR Spectrum, proton-decoupled (125 MHz, CDCl3, 25 °C)
(CH)
220
200
180
160
140
120
PPM
100
80
80
Q1
(CH₂)
(CH2)
60
60
(CH)
40
8-
20
20
0
1/1
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