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% Transmittance Relative abundance 80- 60- 40- to 20- 0.0 100- 80- 60- 20- 0.0 4000 3500 3000 2500 2000 11 200 180 19 8 160 140 2H 1500 Wavenumbers (cm) 2H Chemical shift (ppm) 120 100 80 Chemical shift (ppm) 120 2H 60 1000 40 For 1711173 20 500

% Transmittance Relative abundance 80- 60- 40- to 20- 0.0 100- 80- 60- 20- 0.0 4000 3500 3000 2500 2000 11 200 180 19 8 160 140 2H 1500 Wavenumbers (cm) 2H Chemical shift (ppm) 120 100 80 Chemical shift (ppm) 120 2H 60 1000 40 For 1711173 20 500

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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Draw the structure that best fits the below spectra.

### Mass Spectrometry Graph The top graph is a mass spectrometry (MS) spectrum displaying relative abundance against mass-to-charge ratio (m/z). Key peaks occur at m/z values of 171 and 173, indicating these as significant isotopic peaks for analysis. ### Infrared (IR) Spectroscopy Graph The second graph is an infrared (IR) spectroscopy spectrum that shows transmittance (%) versus wavenumbers (cm⁻¹). The spectrum demonstrates peaks at various wavenumbers, with notable absorptions beyond 1500 cm⁻¹, typically indicating functional group vibrations. ### Proton Nuclear Magnetic Resonance (^1H NMR) Spectroscopy Graph The third graph displays a ^1H NMR spectrum. The x-axis is chemical shift (ppm), and peaks are labeled "2H," indicating the protons' integration or quantity. The peaks are distributed between 0 and 10 ppm, suggesting different hydrogen environments in the molecule. ### Carbon-13 Nuclear Magnetic Resonance (^13C NMR) Spectroscopy Graph The bottom graph is a ^13C NMR spectrum. The x-axis is chemical shift (ppm), ranging from 0 to 200 ppm. Multiple peaks across the spectrum demonstrate the different carbon environments within the molecule.
Transcribed Image Text:### Mass Spectrometry Graph The top graph is a mass spectrometry (MS) spectrum displaying relative abundance against mass-to-charge ratio (m/z). Key peaks occur at m/z values of 171 and 173, indicating these as significant isotopic peaks for analysis. ### Infrared (IR) Spectroscopy Graph The second graph is an infrared (IR) spectroscopy spectrum that shows transmittance (%) versus wavenumbers (cm⁻¹). The spectrum demonstrates peaks at various wavenumbers, with notable absorptions beyond 1500 cm⁻¹, typically indicating functional group vibrations. ### Proton Nuclear Magnetic Resonance (^1H NMR) Spectroscopy Graph The third graph displays a ^1H NMR spectrum. The x-axis is chemical shift (ppm), and peaks are labeled "2H," indicating the protons' integration or quantity. The peaks are distributed between 0 and 10 ppm, suggesting different hydrogen environments in the molecule. ### Carbon-13 Nuclear Magnetic Resonance (^13C NMR) Spectroscopy Graph The bottom graph is a ^13C NMR spectrum. The x-axis is chemical shift (ppm), ranging from 0 to 200 ppm. Multiple peaks across the spectrum demonstrate the different carbon environments within the molecule.
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