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] = 177 (100%) m/z IR Spectrum (not shown): 3200 (sh m), 3060, 2981, 1685, 1600, 1495 cm¹ (all listed are strong (s) unless otherwise indicated) ¹H NMR Spectrum (400 MHz, CDCI3, 25 °C) br s 180 10 1H (C) 8 13C NMR Spectrum, proton-decoupled (125 MHz, CDCl3, 25 °C) 160 2H 2H (CH) (C) (C) 140 (CH) PPM 120 100 PPM 80 60 E 2 1H 3H (CH3) (CH) 40 6H (CH3) 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] = 177 (100%) m/z IR Spectrum (not shown): 3200 (sh m), 3060, 2981, 1685, 1600, 1495 cm¹ (all listed are strong (s) unless otherwise indicated) ¹H NMR Spectrum (400 MHz, CDCI3, 25 °C) br s 180 10 1H (C) 8 13C NMR Spectrum, proton-decoupled (125 MHz, CDCl3, 25 °C) 160 2H 2H (CH) (C) (C) 140 (CH) PPM 120 100 PPM 80 60 E 2 1H 3H (CH3) (CH) 40 6H (CH3) 20
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
ChapterL2: Mass Spectrometry
Section: Chapter Questions
Problem 14CTQ
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Oh my gosh, it's been 3 HOURS... PLEASE SOMEONE JUST HELP EXPLAIN THIS... WHY IS IT SO HARD TO FIND ACTUAL HELP ON THIS WEBSITE... CHEGG WOULD HAVE DONE THIS IN 30 MINS!!!
![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] = 177 (100%) m/z
IR Spectrum (not shown): 3200 (sh m), 3060, 2981, 1685, 1600, 1495 cm³¹ (all listed are strong (s) unless otherwise
indicated)
¹H NMR Spectrum (400 MHz, CDCI3, 25 °C)
br s
180
10
1H
(C)
8
160
1³C NMR Spectrum, proton-decoupled (125 MHz, CDCI3, 25 °C)
2H 2H
(CH) (CH)
(C) (C)
140
6
120
PPM
100
PPM
80
60
E
1H 3H
S
2
(CH3)
40
(CH)
6H
(CH3)
20](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F56b89a6c-6ca3-4f25-9a44-1409c69966fc%2Fb3249177-cb97-409e-a823-ef204a39d9ac%2Fibrx4z_processed.png&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] = 177 (100%) m/z
IR Spectrum (not shown): 3200 (sh m), 3060, 2981, 1685, 1600, 1495 cm³¹ (all listed are strong (s) unless otherwise
indicated)
¹H NMR Spectrum (400 MHz, CDCI3, 25 °C)
br s
180
10
1H
(C)
8
160
1³C NMR Spectrum, proton-decoupled (125 MHz, CDCI3, 25 °C)
2H 2H
(CH) (CH)
(C) (C)
140
6
120
PPM
100
PPM
80
60
E
1H 3H
S
2
(CH3)
40
(CH)
6H
(CH3)
20
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