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The following IR and NMR were obtained for Alicia’s final product, Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid. Label all hydrogens with the data from 1H NMR. Label all carbons with the provided data from 13C NMR.

The following IR and NMR were obtained for Alicia’s final product, Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid. Label all hydrogens with the data from 1H NMR. Label all carbons with the provided data from 13C NMR.

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
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The following IR and NMR were obtained for Alicia’s final product,
Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid. Label all hydrogens with the data from 1H NMR. Label all carbons with the provided data from 13C NMR.  

### NMR Spectroscopy Analysis #### (a) \( ^1H \) NMR Spectrum (300 MHz) The image displays a proton NMR (nuclear magnetic resonance) spectrum for a specific chemical compound. The horizontal axis indicates the chemical shift in parts per million (ppm). - **Peak at 11.90 ppm**: This peak is likely indicative of a hydrogen atom attached to a carboxylic acid (CO2H) group. - **Peak at 1.34 ppm**: This multiplet is associated with the hydrogen atoms on the cyclohexane ring structure. - Additional peaks are seen in the lower field region, which can correspond to solvent (H2O) and other components such as CD3SOCD2H. A structure is labeled in the diagram, showing the compound's molecular configuration. #### (b) \( ^{13}C \) NMR Data The carbon-13 NMR data for this compound are specified as follows: - Chemical shifts: δ 46.8, 48.7, 49.1, 135.6, 174.4 ppm These values correspond to various carbon environments within the molecule, providing insight into the structural configuration.
Transcribed Image Text:### NMR Spectroscopy Analysis #### (a) \( ^1H \) NMR Spectrum (300 MHz) The image displays a proton NMR (nuclear magnetic resonance) spectrum for a specific chemical compound. The horizontal axis indicates the chemical shift in parts per million (ppm). - **Peak at 11.90 ppm**: This peak is likely indicative of a hydrogen atom attached to a carboxylic acid (CO2H) group. - **Peak at 1.34 ppm**: This multiplet is associated with the hydrogen atoms on the cyclohexane ring structure. - Additional peaks are seen in the lower field region, which can correspond to solvent (H2O) and other components such as CD3SOCD2H. A structure is labeled in the diagram, showing the compound's molecular configuration. #### (b) \( ^{13}C \) NMR Data The carbon-13 NMR data for this compound are specified as follows: - Chemical shifts: δ 46.8, 48.7, 49.1, 135.6, 174.4 ppm These values correspond to various carbon environments within the molecule, providing insight into the structural configuration.
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