Chapter2: Basic Statistical Analysis With Excel
Section: Chapter Questions
Problem 12P
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Question
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)](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fc4436f5f-01e3-4d46-baa5-3f23cf388ae7%2F2f3e1844-fbec-4267-9f54-a228edd9ed91%2Fajk5wck_processed.jpeg&w=3840&q=75)
Transcribed Image Text: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.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fc4436f5f-01e3-4d46-baa5-3f23cf388ae7%2F2f3e1844-fbec-4267-9f54-a228edd9ed91%2Fjagw3sg_processed.png&w=3840&q=75)
Transcribed Image Text: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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