Please put your final answer in the box under the 'H NMR. Compound 29 20 40 140 120 100 8060 PPM 180 200
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use both spectra to determine the exact structure of the compound and put your final answer in the box with formula pul youl tmllal answer in the box under the 'H NMR Compound 29 3H 2H 1H 3 P...
our final answer in the box under the ' INMI Please put your final answer in...
our final answer in the box under the ' INMI Please put your final answer in the box under the 'H NMR. Compound 8 6H 1H TH 24 PPM M.F. = CH 100 Please put your final answer in the box under the 'H NMR. Compound 8 200 180 160 140 120 100 PPM 80 60 40 20
254 254 Please put your final answer in the box under the 'H NMR. Compound 36...
254 254 Please put your final answer in the box under the 'H NMR. Compound 36 9H ББИ 30 80 00 50 80 100 S00 6H 2H 1H 2 3 PPM M.F. = CgH180
Compound 2: Use the information provided below and the IR and NMR spectra on the next...
Compound 2: Use the information provided below and the IR and NMR spectra on the next page to answer the following questions. a) An MS was taken of compound 2 and the table is given below. Determine the molecular formula of 2 from the MS given below relative abundance m/z 132 100 133 9.8 b) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule. c) Using the IR spectrum and the 1H- and 13C-NMR spectra given below, determine...
1. Propose structure formulas for each isomer of C7H140 in the boxes below based on the attached ...
1. Propose structure formulas for each isomer of C7H140 in the boxes below based on the attached H-NMR and 18C-NMR spectra. C,H40 Isomer 1 C,Hl40 Isomer 2 CH4 Isomer 3 C,H40 ISOMER 1 1H NMR 9H 2H 3H 3 220 200 180 160 140 120 100 8060 40 0 PPM CjH40 ISOMER 2 1H NMR 6H ЗН 300 2H PPM 13C NMFR 220 20 180 160140 120 1008604020 0) PPM C7H140 ISOMER 3 1H NMR зн зн зн 2H 2H...
The 1H-NMR and 13C-NMR spectra of an unknown compound (formula C8H10) are shown below. Draw the structure of the unknown...
The 1H-NMR and 13C-NMR spectra of an unknown compound (formula
C8H10) are shown below. Draw the structure of the unknown compound.
The total integration of the peaks at around 7 ppm is 4. The
integration of the peak at around 2 ppm is 6.
7 6 5 4 3 ppm TTTTTTTTTTTTTTTT 200 180 160 140 120 100 80 60 40 20 0 pom CH3 Create OscerSketch Answer 8 Incorrect: Answer has an incorrect structure.
Which compound gives the following spectra? For the 1H-NMR assign all signals. interpret mol peak and...
Which compound gives the following spectra?
For the 1H-NMR assign all signals. interpret mol peak and base peak
in the mass spectrum if a mole peak exists. Assign at least two 13C
signals. How does the IR spectrum support your finding?
Check 200 180 160 120 80 60 40 20 0 140 a 100 ppm s, 3H t, 3 H d. 2 a. 2 H d. 2H s, 1 H 1 10 9 8 7 6 4 3 2 1...
Molecule C: Molecule D: Can someone PLEASE EXPLAIN the answers?????? 2. Below are the 'H and...
Molecule C:
Molecule D:
Can someone PLEASE EXPLAIN the answers??????
2. Below are the 'H and 13C NMR spectra for four isomers of C&H:02. Provide the structure that produced each set of spectra. Molecule A: 'H NMR 3H 3H no coupling, so no adjacent carbons with hydrogen atoms 2H 5 3 2 0 PPM 13C NMR aldehyde or ketone no aldehyde in 1H NMR, SO ketone 220 200 180 160 140 120 100 PPM 80 60 40 20 0 Molecule...
28. A compound with the molecular formula of C3H.ON shows 1H NMR and 13C NMR as...
28. A compound with the molecular formula of C3H.ON shows 1H NMR and 13C NMR as below. Give the most plausible structure in the box. 2H, 3 peaks 2H, 3 peaks 1H, 1 peak PPM 180 160 140 120 100 80 60 40 20 PPM
16. Propose a structure for a molecule of formula CaHsCl which gave the following 1H NMR spectrum. PPM 17. Propose a st...
16. Propose a structure for a molecule of formula CaHsCl which gave the following 1H NMR spectrum. PPM 17. Propose a structure for a molecule whose mass spectrum shows a parent ion at m/z 148, an IR peak at 1680 cm'and gives the following H and 13C NMR spectra 3H зн 2H 2H 2H 3 5 2 7 6 4 PPM 160 140 180 60 220 200 20 0 120 100 80 40 PPM -
Create OscerSkotch Answer 6 Th e 1H-NMR and 13C-NMR spectra of an unknown compound s (formula...
Create OscerSkotch Answer 6 Th e 1H-NMR and 13C-NMR spectra of an unknown compound s (formula CoMzo) are shown below. Draw the structure of B. The total integration of the peaks at around 7 ppm is 4. The integration of the peak at around 2 ppm is 6 ppm 200 180 160 140 120 100 060 4020
our final answer in the box under the ' INMI Please put your final answer in the box under the 'H NMR. Compound 8 6H 1H TH 24 PPM M.F. = CH 100 Please put your final answer in the box under the 'H NMR. Compound 8 200 180 160 140 120 100 PPM 80 60 40 20
254 254 Please put your final answer in the box under the 'H NMR. Compound 36 9H ББИ 30 80 00 50 80 100 S00 6H 2H 1H 2 3 PPM M.F. = CgH180
Compound 2: Use the information provided below and the IR and NMR spectra on the next page to answer the following questions. a) An MS was taken of compound 2 and the table is given below. Determine the molecular formula of 2 from the MS given below relative abundance m/z 132 100 133 9.8 b) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule. c) Using the IR spectrum and the 1H- and 13C-NMR spectra given below, determine...
1. Propose structure formulas for each isomer of C7H140 in the boxes below based on the attached H-NMR and 18C-NMR spectra. C,H40 Isomer 1 C,Hl40 Isomer 2 CH4 Isomer 3 C,H40 ISOMER 1 1H NMR 9H 2H 3H 3 220 200 180 160 140 120 100 8060 40 0 PPM CjH40 ISOMER 2 1H NMR 6H ЗН 300 2H PPM 13C NMFR 220 20 180 160140 120 1008604020 0) PPM C7H140 ISOMER 3 1H NMR зн зн зн 2H 2H...
The 1H-NMR and 13C-NMR spectra of an unknown compound (formula
C8H10) are shown below. Draw the structure of the unknown compound.
The total integration of the peaks at around 7 ppm is 4. The
integration of the peak at around 2 ppm is 6.
7 6 5 4 3 ppm TTTTTTTTTTTTTTTT 200 180 160 140 120 100 80 60 40 20 0 pom CH3 Create OscerSketch Answer 8 Incorrect: Answer has an incorrect structure.
Which compound gives the following spectra?
For the 1H-NMR assign all signals. interpret mol peak and base peak
in the mass spectrum if a mole peak exists. Assign at least two 13C
signals. How does the IR spectrum support your finding?
Check 200 180 160 120 80 60 40 20 0 140 a 100 ppm s, 3H t, 3 H d. 2 a. 2 H d. 2H s, 1 H 1 10 9 8 7 6 4 3 2 1...
Molecule C:
Molecule D:
Can someone PLEASE EXPLAIN the answers??????
2. Below are the 'H and 13C NMR spectra for four isomers of C&H:02. Provide the structure that produced each set of spectra. Molecule A: 'H NMR 3H 3H no coupling, so no adjacent carbons with hydrogen atoms 2H 5 3 2 0 PPM 13C NMR aldehyde or ketone no aldehyde in 1H NMR, SO ketone 220 200 180 160 140 120 100 PPM 80 60 40 20 0 Molecule...
28. A compound with the molecular formula of C3H.ON shows 1H NMR and 13C NMR as below. Give the most plausible structure in the box. 2H, 3 peaks 2H, 3 peaks 1H, 1 peak PPM 180 160 140 120 100 80 60 40 20 PPM
16. Propose a structure for a molecule of formula CaHsCl which gave the following 1H NMR spectrum. PPM 17. Propose a structure for a molecule whose mass spectrum shows a parent ion at m/z 148, an IR peak at 1680 cm'and gives the following H and 13C NMR spectra 3H зн 2H 2H 2H 3 5 2 7 6 4 PPM 160 140 180 60 220 200 20 0 120 100 80 40 PPM -
Create OscerSkotch Answer 6 Th e 1H-NMR and 13C-NMR spectra of an unknown compound s (formula CoMzo) are shown below. Draw the structure of B. The total integration of the peaks at around 7 ppm is 4. The integration of the peak at around 2 ppm is 6 ppm 200 180 160 140 120 100 060 4020
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