Ok what about this one? I will also put the answer I got in there so you can check if I'm correct or not, or if I need to write it another way.
Ok what about this one? I will also put the answer I got in there so you can check if I'm correct or not, or if I need to write it another way.
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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Ok what about this one? I will also put the answer I got in there so you can check if I'm correct or not, or if I need to write it another way.
![OH
2-phenylethan-2-ol](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fb5f1630e-c465-44f2-a868-b429d99d07e1%2F35fc05f6-0da3-4d10-99e1-a424580a5c56%2F4gx1zk9_processed.png&w=3840&q=75)
Transcribed Image Text:OH
2-phenylethan-2-ol
![4
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 cm³¹
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] = 122 m/z
-1
Infrared Spectroscopy (not shown): 3364, 3030, 2973, 1493, 1451, 1408, 1178 cm*¹
¹H Nuclear Magnetic Resonance.
8
m
160
5H
1³C Nuclear Magnetic Resonance.
140
120
S
1H1H
100
PPM
80
PPM
3
60
40
3H
20](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fb5f1630e-c465-44f2-a868-b429d99d07e1%2F35fc05f6-0da3-4d10-99e1-a424580a5c56%2Fd409hp_processed.png&w=3840&q=75)
Transcribed Image Text:4
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 cm³¹
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] = 122 m/z
-1
Infrared Spectroscopy (not shown): 3364, 3030, 2973, 1493, 1451, 1408, 1178 cm*¹
¹H Nuclear Magnetic Resonance.
8
m
160
5H
1³C Nuclear Magnetic Resonance.
140
120
S
1H1H
100
PPM
80
PPM
3
60
40
3H
20
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Follow-up Question
what about this?
![N
مهلا
Methyl-4,4-dimethyl-3-oxopentanoate](https://content.bartleby.com/qna-images/question/b5f1630e-c465-44f2-a868-b429d99d07e1/3ecac0e9-780a-4877-a585-68b76490082b/cc1j5gf_thumbnail.png)
Transcribed Image Text:N
مهلا
Methyl-4,4-dimethyl-3-oxopentanoate
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