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Calculation of HDI for each compound show work . Label and assign all the functional groups in the diagnostic region of the IR . Label and assign all protons in the NMR on your drawing ( clearly annotate each set of chemically non equivalent protons on your proposed structure and assign their signal on the 1H-NMR spectrum. .what lead to the proposed structure using the HDI,IR AND 1-H-NMR data provided

Calculation of HDI for each compound show work . Label and assign all the functional groups in the diagnostic region of the IR . Label and assign all protons in the NMR on your drawing ( clearly annotate each set of chemically non equivalent protons on your proposed structure and assign their signal on the 1H-NMR spectrum. .what lead to the proposed structure using the HDI,IR AND 1-H-NMR data provided

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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. Calculation of HDI for each compound show work . Label and assign all the functional groups in the diagnostic region of the IR . Label and assign all protons in the NMR on your drawing ( clearly annotate each set of chemically non equivalent protons on your proposed structure and assign their signal on the 1H-NMR spectrum. .what lead to the proposed structure using the HDI,IR AND 1-H-NMR data provided
### Image Transcription for Educational Website #### Chemical Information: - **Molecular Formula (MF):** C₅H₁₀ - **Molecular Weight (MW):** 70 - **Percent Carbon (%C):** 85.6 - **Percent Hydrogen (%H):** 14.4 #### Infrared (IR) Spectrum: The IR spectrum displays key absorption peaks, indicating functional groups. - **Wavenumber Peaks (cm⁻¹):** - 3311 - 2960 - 2940 - 2870 - 1640 - 1465 - 1375 - 1025 - 860 These peaks suggest various characteristic vibrations present in the compound, indicating certain bond types. #### Mass Spectrometry (Mass Spec) Data: - **m/z (mass-to-charge ratio): Relative Abundance** - 15: 10 - 27: 40 - 29: 40 - 30: 100 - 41: 50 - 42: 80 - 43: 15 - 53: 62 - 55: 3 - 69: 2 - 70: 1 This data indicates the presence and abundance of different ions, helping to deduce the molecular structure. #### NMR Spectroscopy: **Proton (¹H) NMR Spectrum:** - Features peaks indicating different hydrogen environments: - Peak at around 0.9 ppm (3H, possibly a methyl group) - Peaks between 1.2 to 1.8 ppm (2H, 2H suggesting methylene groups) - Peak between 5.5 to 6.5 ppm (1H, indicating a possible vinyl hydrogen) **Carbon-13 (¹³C) NMR Spectrum:** - Peaks at approximately: - 140 ppm - 120 ppm - 40 ppm - 20 ppm These peaks reveal the carbon skeleton and different carbon environments in the molecule. #### General Overview: The image contains analytical data from IR, Mass Spectrometry, and NMR spectra, crucial for determining the structure and identifying the compound with a molecular formula of C₅H₁₀. The analysis involves
Transcribed Image Text:### Image Transcription for Educational Website #### Chemical Information: - **Molecular Formula (MF):** C₅H₁₀ - **Molecular Weight (MW):** 70 - **Percent Carbon (%C):** 85.6 - **Percent Hydrogen (%H):** 14.4 #### Infrared (IR) Spectrum: The IR spectrum displays key absorption peaks, indicating functional groups. - **Wavenumber Peaks (cm⁻¹):** - 3311 - 2960 - 2940 - 2870 - 1640 - 1465 - 1375 - 1025 - 860 These peaks suggest various characteristic vibrations present in the compound, indicating certain bond types. #### Mass Spectrometry (Mass Spec) Data: - **m/z (mass-to-charge ratio): Relative Abundance** - 15: 10 - 27: 40 - 29: 40 - 30: 100 - 41: 50 - 42: 80 - 43: 15 - 53: 62 - 55: 3 - 69: 2 - 70: 1 This data indicates the presence and abundance of different ions, helping to deduce the molecular structure. #### NMR Spectroscopy: **Proton (¹H) NMR Spectrum:** - Features peaks indicating different hydrogen environments: - Peak at around 0.9 ppm (3H, possibly a methyl group) - Peaks between 1.2 to 1.8 ppm (2H, 2H suggesting methylene groups) - Peak between 5.5 to 6.5 ppm (1H, indicating a possible vinyl hydrogen) **Carbon-13 (¹³C) NMR Spectrum:** - Peaks at approximately: - 140 ppm - 120 ppm - 40 ppm - 20 ppm These peaks reveal the carbon skeleton and different carbon environments in the molecule. #### General Overview: The image contains analytical data from IR, Mass Spectrometry, and NMR spectra, crucial for determining the structure and identifying the compound with a molecular formula of C₅H₁₀. The analysis involves
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