By looking at the H1 NMR spectra, draw the structure for the solid organic unknown compound and explain the process you used to determine the identity of your compound. Show all H atoms and label each equivalent set of atoms as A, B, C etc in the structure. Then, calculate the expected chemical shift for each of the equivalent set of H atoms in the structure. Clearly label your calculations Note: (Clearly list the tables used, base shift values and what correction factors were used.) 97.8047.6467.5537 497Fl: 60.201EX: c:left\HI\ACQ.ppg87.4387.3557.2817.2457.1156.4836.326SW1: 1000PW: 14.4 us5PD: 3.0 secH2 NMR (SolidOF1: 360.3NA: 1unknown)3LB: 0.02PTSId: 8192-0.000wwwV/W/HANNABAY0 PPMUSER: DATE: 01/18/24 (1 The list of all the possible organic compounds are as follows:Cumene, 3-Methy-2-butanone, Phenethyl alcohol, Isopropyl Acetate, Ethel benzoate,3-phenylpropionaldehyde, isobutyl cinnamate, cyclamen aldehyde, Styrallyl acetate, Butylbutyrate, propiophenon, phenylacetylene, Cis-Hexenyl-3-Acetate, Benzyl propionate,3-(p-ethyl-phenyl)-2,2-dimethyl propionaldehyde, 2-methoxy-4-ethyl-phenol, P-ethylphenol,diphenyl amine, 4-phenyl-3-buten-2-one, Diethyl Terphthalate, glutaric acid, cinnamic acid, P-ethylbenzoic acid, Coumarin, vanillin, (2,2,2-trichloro-1-phenylethyl)acetate,4-(p-hydroxyphenyl)-2-butanone, 2-ethoxy-5-prop-1-enylphenol, t-butyl-phenol, Thymol,Calone, Syringol, Syringaldehyde. Borderline MP unknowns: Styrallyl alcohol,1,1-dimethyl-2-phenethyl acetate! 1,1-dimethyl-2-phenyl ethanol.

Given:1 spectrumA spectroscopic method used to identify the structure of a molecule is known as NMR…

Answered: 9 7.804 7.646 7.553 F1: 60.201 EX: c:…

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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By looking at the H1 NMR spectra, draw the structure for the solid organic unknown compound and explain the process you used to determine the identity of your compound. Show all H atoms and label each equivalent set of atoms as A, B, C etc in the structure. Then, calculate the expected chemical shift for each of the equivalent set of H atoms in the structure. Clearly label your calculations

Note: (Clearly list the tables used, base shift values and what correction factors were used.)

9
7.804
7.646
7.553
7 497
Fl: 60.201
EX: c:left\HI\ACQ.ppg
8
7.438
7.355
7.281
7.245
7.115
6.483
6.326
SW1: 1000
PW: 14.4 us
5
PD: 3.0 sec
H2 NMR (Solid
OF1: 360.3
NA: 1
unknown)
3
LB: 0.0
2
PTSId: 8192
-0.000
wwwV/W/HANNABAY
0 PPM
USER: DATE: 01/18/24 (1

The list of all the possible organic compounds are as follows:
Cumene, 3-Methy-2-butanone, Phenethyl alcohol, Isopropyl Acetate, Ethel benzoate,
3-phenylpropionaldehyde, isobutyl cinnamate, cyclamen aldehyde, Styrallyl acetate, Butyl
butyrate, propiophenon, phenylacetylene, Cis-Hexenyl-3-Acetate, Benzyl propionate,
3-(p-ethyl-phenyl)-2,2-dimethyl propionaldehyde, 2-methoxy-4-ethyl-phenol, P-ethylphenol,
diphenyl amine, 4-phenyl-3-buten-2-one, Diethyl Terphthalate, glutaric acid, cinnamic acid, P-
ethylbenzoic acid, Coumarin, vanillin, (2,2,2-trichloro-1-phenylethyl)acetate,
4-(p-hydroxyphenyl)-2-butanone, 2-ethoxy-5-prop-1-enylphenol, t-butyl-phenol, Thymol,
Calone, Syringol, Syringaldehyde. Borderline MP unknowns: Styrallyl alcohol,
1,1-dimethyl-2-phenethyl acetate! 1,1-dimethyl-2-phenyl ethanol.

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