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] = 138 (100%) m/z IR Spectrum (not shown): 3311, 2962, 2937, 2120, 1685 cm¹ (all listed are strong (s) unless otherwise indicated) ¹H NMR Spectrum (400 MHz, CDCl3, 25 °C) 1H q elle 2 2H 2H 6H 3H PPM 13C NMR Spectrum, proton-decoupled (125 MHz, CDCl 3, 25 °C) (C) (CH3) (C)(CH) (CH2) (CXCH2) (CH3) 200 180 160 140 120 100 80 60 40 8- PPM 20
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] = 138 (100%) m/z IR Spectrum (not shown): 3311, 2962, 2937, 2120, 1685 cm¹ (all listed are strong (s) unless otherwise indicated) ¹H NMR Spectrum (400 MHz, CDCl3, 25 °C) 1H q elle 2 2H 2H 6H 3H PPM 13C NMR Spectrum, proton-decoupled (125 MHz, CDCl 3, 25 °C) (C) (CH3) (C)(CH) (CH2) (CXCH2) (CH3) 200 180 160 140 120 100 80 60 40 8- PPM 20
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] = 138 (100%) m/z
IR Spectrum (not shown): 3311, 2962, 2937, 2120, 1685 cm¹ (all listed are strong (s) unless otherwise indicated)
¹H NMR Spectrum (400 MHz, CDCl3, 25 °C)
1H
q
elle
2
2H
2H
6H 3H
PPM
13C NMR Spectrum, proton-decoupled (125 MHz, CDCl 3, 25 °C)
(C)
(CH3)
(C)(CH)
(CH2)
(CXCH2)
(CH3)
200
180
160
140
120
100
80
60
40
8-
PPM
20](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F13344a5e-ec4e-46f8-a2ea-c159e4536077%2F0a68510e-42b8-4b15-a272-db6873d25244%2F9mfj09b_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] = 138 (100%) m/z
IR Spectrum (not shown): 3311, 2962, 2937, 2120, 1685 cm¹ (all listed are strong (s) unless otherwise indicated)
¹H NMR Spectrum (400 MHz, CDCl3, 25 °C)
1H
q
elle
2
2H
2H
6H 3H
PPM
13C NMR Spectrum, proton-decoupled (125 MHz, CDCl 3, 25 °C)
(C)
(CH3)
(C)(CH)
(CH2)
(CXCH2)
(CH3)
200
180
160
140
120
100
80
60
40
8-
PPM
20
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