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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] = 346 (51%), 348 (100 % ), 350 (49%) m/z IR Spectrum (not shown): 3018, 2965, 1796, 1610, 1500 cm-1 (all listed are strong (s) unless otherwise indicated) 1H NMR Spectrum (400 MHz, CDCl3, 25 °C) 8 7 2H 2H 6 5 4 3 2 1 0 PPM 4H 4H 13C NMR Spectrum, proton-decoupled (125 MHz, CDCl3, 25 °C) (C) (C) (CHỊCH) (CH2) (CH2) 180 160 140 120 100 80 60 PPM 40 40 20 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] = 346 (51%), 348 (100 % ), 350 (49%) m/z IR Spectrum (not shown): 3018, 2965, 1796, 1610, 1500 cm-1 (all listed are strong (s) unless otherwise indicated) 1H NMR Spectrum (400 MHz, CDCl3, 25 °C) 8 7 2H 2H 6 5 4 3 2 1 0 PPM 4H 4H 13C NMR Spectrum, proton-decoupled (125 MHz, CDCl3, 25 °C) (C) (C) (CHỊCH) (CH2) (CH2) 180 160 140 120 100 80 60 PPM 40 40 20 20

Chemistry
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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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] = 346 (51%), 348 (100 % ), 350 (49%) m/z IR Spectrum (not shown): 3018, 2965, 1796, 1610, 1500 cm-1 (all listed are strong (s) unless otherwise indicated) 1H NMR Spectrum (400 MHz, CDCl3, 25 °C) 8 7 2H 2H 6 5 4 3 2 1 0 PPM 4H 4H 13C NMR Spectrum, proton-decoupled (125 MHz, CDCl3, 25 °C) (C) (C) (CHỊCH) (CH2) (CH2) 180 160 140 120 100 80 60 PPM 40 40 20 20
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] = 346 (51%), 348 (100 % ), 350 (49%) m/z IR Spectrum (not shown): 3018, 2965, 1796, 1610, 1500 cm-1 (all listed are strong (s) unless otherwise indicated) 1H NMR Spectrum (400 MHz, CDCl3, 25 °C) 8 7 2H 2H 6 5 4 3 2 1 0 PPM 4H 4H 13C NMR Spectrum, proton-decoupled (125 MHz, CDCl3, 25 °C) (C) (C) (CHỊCH) (CH2) (CH2) 180 160 140 120 100 80 60 PPM 40 40 20 20
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