By looking at the H1 NMR spectra, draw the structure for the Liquid 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.) 98.0368.0047.926F1: 60.201EX: c:left\HI\ACQ.ppg7.8767.5087.4807.4227.3937.3397.2717654OF1: 360.3NA: 13.161SW1: 1000PW: 14.4 usPD: 3.0 secH1- NMR | Lique'd unknown)3LB: 0.021.3271.2101.088PTS1d: 8192000 0-10 PPMUSER: DATE: 01/25/24 (15:30) 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.

To identify the structure based on the given 1H NMR

Answered: 6 8 7 9 S 3 0 PPM 8.036 8.004 7.926…

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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

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By looking at the H1 NMR spectra, draw the structure for the Liquid 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
8.036
8.004
7.926
F1: 60.201
EX: c:left\HI\ACQ.ppg
7.876
7.508
7.480
7.422
7.393
7.339
7.271
7
6
5
4
OF1: 360.3
NA: 1
3.161
SW1: 1000
PW: 14.4 us
PD: 3.0 sec
H1- NMR | Lique'd unknown)
3
LB: 0.0
2
1.327
1.210
1.088
PTS1d: 8192
000 0-
1
0 PPM
USER: DATE: 01/25/24 (15:30)

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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