1 Information: Each spectra below was obtained from a pure compound. Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm ¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important part of the spectrum. Mass Spectrometry (not shown): [M] = 158 m/z Infrared Spectroscopy (not shown): 2970, 2940, 2880, 1819, 1750, 1039, 1031 cm³ -1 ¹H Nuclear Magnetic Resonance. 3 180 t 13C Nuclear Magnetic Resonance. 160 4H 140 120 m 4HPPM 100 PPM 80 6H 60 40 20
1 Information: Each spectra below was obtained from a pure compound. Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm ¹H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important part of the spectrum. Mass Spectrometry (not shown): [M] = 158 m/z Infrared Spectroscopy (not shown): 2970, 2940, 2880, 1819, 1750, 1039, 1031 cm³ -1 ¹H Nuclear Magnetic Resonance. 3 180 t 13C Nuclear Magnetic Resonance. 160 4H 140 120 m 4HPPM 100 PPM 80 6H 60 40 20
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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please answer with structure and name of chemical compound!
![**Spectroscopic Analysis of a Pure Compound**
**Information:** Each spectrum below was obtained from a pure compound. The Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm⁻¹. For ¹H NMR spectra, the integral is given in the number of hydrogens (H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given, showing a “zoom-in” on an important part of the spectrum.
### Mass Spectrometry (not shown):
- **[M] = 158 m/z**
### Infrared Spectroscopy (not shown):
- **Peaks:** 2970, 2940, 2880, 1819, 1750, 1039, 1031 cm⁻¹
### ¹H Nuclear Magnetic Resonance:
The ¹H NMR spectrum displays several peaks:
- A triplet (t) at approximately 0.9 ppm integrating to 6 hydrogens (6H).
- A multiplet (m) at approximately 1.3 ppm integrating to 4 hydrogens (4H).
- A triplet (t) at approximately 1.7 ppm integrating to 4 hydrogens (4H).
### ¹³C Nuclear Magnetic Resonance:
The ¹³C NMR spectrum shows peaks at various positions:
- A peak near 180 ppm, indicative of a carbonyl group.
- Peaks around 30 ppm, 40 ppm, and 50 ppm, typically associated with various alkyl groups.
This data suggests the presence of different functional groups and carbon-hydrogen environments in the compound.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fa451162e-14ac-4cfd-a2c6-1eae7f4a5f1a%2Fd720bb80-e6c9-41de-bd93-ac9e1adbedf2%2Fgxl0ba_processed.png&w=3840&q=75)
Transcribed Image Text:**Spectroscopic Analysis of a Pure Compound**
**Information:** Each spectrum below was obtained from a pure compound. The Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm⁻¹. For ¹H NMR spectra, the integral is given in the number of hydrogens (H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given, showing a “zoom-in” on an important part of the spectrum.
### Mass Spectrometry (not shown):
- **[M] = 158 m/z**
### Infrared Spectroscopy (not shown):
- **Peaks:** 2970, 2940, 2880, 1819, 1750, 1039, 1031 cm⁻¹
### ¹H Nuclear Magnetic Resonance:
The ¹H NMR spectrum displays several peaks:
- A triplet (t) at approximately 0.9 ppm integrating to 6 hydrogens (6H).
- A multiplet (m) at approximately 1.3 ppm integrating to 4 hydrogens (4H).
- A triplet (t) at approximately 1.7 ppm integrating to 4 hydrogens (4H).
### ¹³C Nuclear Magnetic Resonance:
The ¹³C NMR spectrum shows peaks at various positions:
- A peak near 180 ppm, indicative of a carbonyl group.
- Peaks around 30 ppm, 40 ppm, and 50 ppm, typically associated with various alkyl groups.
This data suggests the presence of different functional groups and carbon-hydrogen environments in the compound.
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