7. 8. 9. Proton NMR C₂H₂00 Proton NMR CH100 Proton NMR C₂H₁00 8 10. Proton NMR C6H₁202 5.0 6 6 4.5 4.0 6 Chemical Shift (ppm) 5 5 4 Chemical Shift (ppm) Chemical Shift (ppm) 3 3.5 3.0 2.5 2.0 Chemical Shift (ppm) 3 1.5 2 3 2 1.0 0.5 11. Draw the expected 'H NMR spectrum for the following compound i
7. 8. 9. Proton NMR C₂H₂00 Proton NMR CH100 Proton NMR C₂H₁00 8 10. Proton NMR C6H₁202 5.0 6 6 4.5 4.0 6 Chemical Shift (ppm) 5 5 4 Chemical Shift (ppm) Chemical Shift (ppm) 3 3.5 3.0 2.5 2.0 Chemical Shift (ppm) 3 1.5 2 3 2 1.0 0.5 11. Draw the expected 'H NMR spectrum for the following compound i
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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![### Text and Analysis for Educational Website on Proton NMR Spectra
#### Graphs and their Descriptions
**Graph 7: Proton NMR of C₅H₁₀O**
- **Chemical Shifts (ppm):** Peaks are observed at approximately 0.9, 1.2, 1.4, 2.4, 3.6, and 9.4.
- **Peak Assignments:** Peaks labeled as 1, 5, and 2.
- **Notable Features:** Two peaks labeled as 2 appear as doublets, indicating a coupling pattern commonly seen with certain hydrogen environments.
**Graph 8: Proton NMR of C₈H₁₀O**
- **Chemical Shifts (ppm):** Peaks are observed around 1.3, 2.1, and 7.0.
- **Peak Assignments:** Peaks are labeled as 2 and 3.
- **Notable Features:** Most peaks seem to be singlets or doublets, suggesting a symmetrical hydrogen environment.
**Graph 9: Proton NMR of C₈H₁₀O**
- **Chemical Shifts (ppm):** Peaks are observed at approximately 0.9, 2.0, 4.0, and 7.3.
- **Peak Assignments:** Peaks are labeled as 1, 2, and 5.
- **Notable Features:** The peaks appear as singlets, indicating no coupling with adjacent hydrogen atoms.
**Graph 10: Proton NMR of C₆H₁₂O₂**
- **Chemical Shifts (ppm):** Peaks are observed at approximately 1.1, 2.3, 3.5, and 4.5.
- **Peak Assignments:** Peaks labeled as 1, 2, 3, and 6.
- **Notable Features:** The peaks exhibit various splitting patterns, indicative of coupling between neighboring protons in the molecule.
---
#### Question and Diagram
**Question 11:** Draw the expected ¹H NMR spectrum for the following compound.
- **Compound Structure:** The structure shown is an ether with substituents on either side of the oxygen atom.
- **Expected Features:** The expected NMR spectrum would include peaks corresponding to chemical shifts typical for ether environments, with possible multiplicity due to coupling.
These graphs and descriptions will assist students](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F49425756-a161-4845-94fd-16236bd2737c%2F4d132295-7625-4477-af1e-107502e02e7e%2Flon6uk3_processed.png&w=3840&q=75)
Transcribed Image Text:### Text and Analysis for Educational Website on Proton NMR Spectra
#### Graphs and their Descriptions
**Graph 7: Proton NMR of C₅H₁₀O**
- **Chemical Shifts (ppm):** Peaks are observed at approximately 0.9, 1.2, 1.4, 2.4, 3.6, and 9.4.
- **Peak Assignments:** Peaks labeled as 1, 5, and 2.
- **Notable Features:** Two peaks labeled as 2 appear as doublets, indicating a coupling pattern commonly seen with certain hydrogen environments.
**Graph 8: Proton NMR of C₈H₁₀O**
- **Chemical Shifts (ppm):** Peaks are observed around 1.3, 2.1, and 7.0.
- **Peak Assignments:** Peaks are labeled as 2 and 3.
- **Notable Features:** Most peaks seem to be singlets or doublets, suggesting a symmetrical hydrogen environment.
**Graph 9: Proton NMR of C₈H₁₀O**
- **Chemical Shifts (ppm):** Peaks are observed at approximately 0.9, 2.0, 4.0, and 7.3.
- **Peak Assignments:** Peaks are labeled as 1, 2, and 5.
- **Notable Features:** The peaks appear as singlets, indicating no coupling with adjacent hydrogen atoms.
**Graph 10: Proton NMR of C₆H₁₂O₂**
- **Chemical Shifts (ppm):** Peaks are observed at approximately 1.1, 2.3, 3.5, and 4.5.
- **Peak Assignments:** Peaks labeled as 1, 2, 3, and 6.
- **Notable Features:** The peaks exhibit various splitting patterns, indicative of coupling between neighboring protons in the molecule.
---
#### Question and Diagram
**Question 11:** Draw the expected ¹H NMR spectrum for the following compound.
- **Compound Structure:** The structure shown is an ether with substituents on either side of the oxygen atom.
- **Expected Features:** The expected NMR spectrum would include peaks corresponding to chemical shifts typical for ether environments, with possible multiplicity due to coupling.
These graphs and descriptions will assist students
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