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Solve the structure of this compound by looking at the 1H, 13C NMR data provided.  You must fill all of the parts to this question in the given spaces.  Molecular formula:  C6H14N2O2

Solve the structure of this compound by looking at the 1H, 13C NMR data provided.  You must fill all of the parts to this question in the given spaces.  Molecular formula:  C6H14N2O2

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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Solve the structure of this compound by looking at the 1H, 13C NMR data provided.  You must fill all of the parts to this question in the given spaces.  Molecular formula:  C6H14N2O2

**NMR Spectrum Analysis** **1H NMR Spectrum:** - **Solvent:** D2O - **Field Strength:** 500 MHz (^1H); 125 MHz (^13C) - The spectrum displays several peaks with chemical shifts noted in parts per million (ppm). These peaks indicate the presence of different hydrogen environments in the compound. **DEPT 135 Spectrum:** - This graph identifies carbon types in the compound. It shows positive peaks for CH and CH3 groups and negative peaks for CH2 groups. **13C NMR Spectrum:** - The spectrum covers a range from 0 to 170 ppm, indicating distinct carbon environments within the molecule. --- **Solution to Problem #3:** **Degree of Unsaturation:** - (Not provided in the text; typically calculated based on the molecular formula.) **13C NMR Interpretation:** - (Not provided in the text; typically involves identifying carbon signals and their respective chemical environments.) **DEPT Interpretation:** - (Not provided in the text; involves using DEPT to distinguish between CH, CH2, and CH3 groups.) **1H NMR Interpretation:** - Identify fragments based on the chemical shift and splitting pattern for each peak: - **Peak A:** 3.75 ppm - **Peak B:** 3.01 ppm - **Peak C:** 1.90 ppm - **Peak D:** 1.72 ppm - **Peak E:** 1.56 ppm **Structure of Unknown Compound:** - A placeholder for the structural determination based on the combined data from the NMR spectra. This setup guides the analysis of hydrogens and carbons in the unknown compound through its NMR spectra, essential for identifying the molecular structure.
Transcribed Image Text:**NMR Spectrum Analysis** **1H NMR Spectrum:** - **Solvent:** D2O - **Field Strength:** 500 MHz (^1H); 125 MHz (^13C) - The spectrum displays several peaks with chemical shifts noted in parts per million (ppm). These peaks indicate the presence of different hydrogen environments in the compound. **DEPT 135 Spectrum:** - This graph identifies carbon types in the compound. It shows positive peaks for CH and CH3 groups and negative peaks for CH2 groups. **13C NMR Spectrum:** - The spectrum covers a range from 0 to 170 ppm, indicating distinct carbon environments within the molecule. --- **Solution to Problem #3:** **Degree of Unsaturation:** - (Not provided in the text; typically calculated based on the molecular formula.) **13C NMR Interpretation:** - (Not provided in the text; typically involves identifying carbon signals and their respective chemical environments.) **DEPT Interpretation:** - (Not provided in the text; involves using DEPT to distinguish between CH, CH2, and CH3 groups.) **1H NMR Interpretation:** - Identify fragments based on the chemical shift and splitting pattern for each peak: - **Peak A:** 3.75 ppm - **Peak B:** 3.01 ppm - **Peak C:** 1.90 ppm - **Peak D:** 1.72 ppm - **Peak E:** 1.56 ppm **Structure of Unknown Compound:** - A placeholder for the structural determination based on the combined data from the NMR spectra. This setup guides the analysis of hydrogens and carbons in the unknown compound through its NMR spectra, essential for identifying the molecular structure.
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C6H14N2O2

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