180- 29- 4800 3.0 Proton NMA 2959.18 2908.03 3080 2074 30 2.5 1H 1H pepojamempopesyonpapanpar 230 220 210 200 190 PPM Carbon 13 NMA 2500 HAVENUMBERS 2.0 2000 70 60 1710.00- 1H M 1.5 1400.30 1377.35 1500 2H 1.5H sc cor CC 201 1000 843. 1.5H 1.0 PPM 20 10 PPM 0 MF C8H160 MW 128 %C 74.9 %H 12.6 0.5
180- 29- 4800 3.0 Proton NMA 2959.18 2908.03 3080 2074 30 2.5 1H 1H pepojamempopesyonpapanpar 230 220 210 200 190 PPM Carbon 13 NMA 2500 HAVENUMBERS 2.0 2000 70 60 1710.00- 1H M 1.5 1400.30 1377.35 1500 2H 1.5H sc cor CC 201 1000 843. 1.5H 1.0 PPM 20 10 PPM 0 MF C8H160 MW 128 %C 74.9 %H 12.6 0.5
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...
Related questions
Question
![### Transcription of Spectroscopy Data
#### Molecular Information
- **Molecular Formula (MF):** C₈H₁₆O
- **Molecular Weight (MW):** 128
- **% Carbon (%C):** 74.9
- **% Hydrogen (%H):** 12.6
#### Infrared (IR) Spectroscopy
- The IR spectrum is plotted with % Transmittance on the y-axis and Wavenumbers on the x-axis, ranging from 4000 to 600 cm⁻¹.
- Key Absorption Peaks:
- Around 2954.08 and 2874.26 cm⁻¹: indicative of C-H stretching.
- A sharp peak at 1711.68 cm⁻¹, likely representing C=O stretching.
- Peaks at 1460.23 and 1377.20 cm⁻¹: possibly due to CH₂ and CH₃ bending vibrations.
- Other peaks include 1169.59, 1109.39, and 721.00 cm⁻¹, suggestive of various C-C and C-O stretching or bending modes.
#### Proton Nuclear Magnetic Resonance (¹H NMR)
- The ¹H NMR spectrum shows chemical shifts (ppm) on the x-axis, with peaks indicating the environment of hydrogen atoms:
- Peaks around 2.5 ppm labeled "1H 1H" likely due to protons on carbons adjacent to electronegative groups.
- A peak around 1.5 ppm labeled "2H" indicates protons in a specific chemical environment, possibly adjacent to carbonyl groups.
- Peaks labeled "1.5H" around 1.5 ppm suggest overlapping environments.
#### Carbon-13 Nuclear Magnetic Resonance (¹³C NMR)
- The ¹³C NMR shows peaks with chemical shifts in ppm:
- Peaks range between 10 to 100 ppm, common for sp³ hybridized carbon atoms.
- Specific peaks can indicate particular carbon types such as methyl, methylene, or methine groups.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fcf1e2248-6601-4b3a-9f67-09df2c7ec8de%2Fdfc14c1c-3433-4b0e-8d1a-854840c3edde%2Fhtqtph_processed.jpeg&w=3840&q=75)
Transcribed Image Text:### Transcription of Spectroscopy Data
#### Molecular Information
- **Molecular Formula (MF):** C₈H₁₆O
- **Molecular Weight (MW):** 128
- **% Carbon (%C):** 74.9
- **% Hydrogen (%H):** 12.6
#### Infrared (IR) Spectroscopy
- The IR spectrum is plotted with % Transmittance on the y-axis and Wavenumbers on the x-axis, ranging from 4000 to 600 cm⁻¹.
- Key Absorption Peaks:
- Around 2954.08 and 2874.26 cm⁻¹: indicative of C-H stretching.
- A sharp peak at 1711.68 cm⁻¹, likely representing C=O stretching.
- Peaks at 1460.23 and 1377.20 cm⁻¹: possibly due to CH₂ and CH₃ bending vibrations.
- Other peaks include 1169.59, 1109.39, and 721.00 cm⁻¹, suggestive of various C-C and C-O stretching or bending modes.
#### Proton Nuclear Magnetic Resonance (¹H NMR)
- The ¹H NMR spectrum shows chemical shifts (ppm) on the x-axis, with peaks indicating the environment of hydrogen atoms:
- Peaks around 2.5 ppm labeled "1H 1H" likely due to protons on carbons adjacent to electronegative groups.
- A peak around 1.5 ppm labeled "2H" indicates protons in a specific chemical environment, possibly adjacent to carbonyl groups.
- Peaks labeled "1.5H" around 1.5 ppm suggest overlapping environments.
#### Carbon-13 Nuclear Magnetic Resonance (¹³C NMR)
- The ¹³C NMR shows peaks with chemical shifts in ppm:
- Peaks range between 10 to 100 ppm, common for sp³ hybridized carbon atoms.
- Specific peaks can indicate particular carbon types such as methyl, methylene, or methine groups.
Expert Solution
![](/static/compass_v2/shared-icons/check-mark.png)
This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
Step by step
Solved in 4 steps with 2 images
![Blurred answer](/static/compass_v2/solution-images/blurred-answer.jpg)
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Recommended textbooks for you
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
![Principles of Instrumental Analysis](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
![Principles of Instrumental Analysis](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
![Organic Chemistry](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
![Chemistry: Principles and Reactions](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
![Elementary Principles of Chemical Processes, Bind…](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY