Determine the structure of the compound using the Mass Spec, IR, C NMR, H NMR, and Dept experiments .
Splitting pattern from left to right is as follows: triplet, 6,
5, 6, triplet 
Homework Answers
Please see there is some printing mistake in DEPT-135 as there should be 1 quarternary carbon according to 1H and IR datas.
For 1H NMR I have marked H-atoms as a,b,c,d, e for better understanding.
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Determine the structure of the compound using the Mass Spec, IR, C NMR, H NMR, and...
Determine the structure of Compound 2 using the Mass Spec, IR, C NMR, H NMR, and...
Determine the structure of Compound 2 using the Mass Spec, IR, C
NMR, H NMR, and Dept Experiments.
Splitting patterns are as follows from left to right: triplet, 5
peaks (unsure of name), septet (7), 4 peaks (unsure of name),
doublet
Compound 2 Mass Spec MT:M/2 = 164 Relative Intensity 25 50 75 125 150 100 m/z IR LO0 D 4000 3000 2000 1500 1000 500 HAVENUMBERI-i H NMR: ditto as compound 1 6 2 2 4 1 2 PPM...
Using Mass Spec, IR, H-NMR, and C-NMR what would the structure look like? Relative Intensity 10...
Using Mass Spec, IR, H-NMR, and C-NMR what would the structure look
like?
Relative Intensity 10 20 30 40 50 60 70 80 90 TERNSMETTANCEI D 4000 NAVENUMBERI 'H NMR PPM 13C NMR 90 80 70 60 50 40 30 20 10 0 PPM PPM DEPT-90 positive DEPT-135 positive Negative Negative Negative Negative Positive
Determine the compound using the Mass Spec, IR, C NMR, and H NMR. H Nmr splitting...
Determine the compound using the Mass Spec, IR, C NMR, and H
NMR.
H Nmr splitting pattern from left to right: singlet, triplet,
septet (7), singlet, doublet
Compound 1 Mass Spec: Mpeak : 162 IR: 100 - TRANSMETTANCEI21 DO 4000 2000 2000 1500 1500 - 1000 13C NMR: Broadband in provided below. DEPT data is in the provided table. 200.180.160.140 120 100.80 '60.40.20 PPM DEPT -135 positive DEPT-90 positive -------------- PPM 191 149 138 137 135 128 126 | 34...
What would the structure look like using the mass spec with a parent peak of 162, IR, C-NMR and H-NMR? TRETTENCEI...
What would the structure look like using the mass spec with a
parent peak of 162, IR, C-NMR and H-NMR?
TRETTENCEI Singlet doublet Singlet triplet muitplet PPM halides 13C NMR: Broadband in provided below. DEPT data is in the provided table. 200 180 160 140 120 100 PPM 80 60 40 20 0 DEPT-135 positive DEPT-90 positive PPM 191 149 138 137 135 128 126 positive positive positive positive positive positive positive positive positive positive
Propose a reasonable structure for this compound based on the mass spec, IR, and NMR data....
Propose a reasonable structure for this compound based on the mass spec, IR, and NMR data. 100 Relative Intensity M+ 10 20 30 40 60 70 80 90 50 m/z LUU TRINETTRICET 4000 3000 2000 cm1 1500 1000 500 ЗН Зн 2H тттттттттттттттттт 11 10 9 8 7 6 5 4 ppm 200 180 160 140 120 80 60 40 20 100 ppm
1. Use the 'H NMR, 13C NMR, mass spectrometry and IR dat of a compound to...
1. Use the 'H NMR, 13C NMR, mass spectrometry and IR dat of a compound to determine its structure. IR Spectrum Mass Spectrometry Data relative abund 77 105 117 133 147 148 100 1H NMR Data 2H 24 ) H !! 13C NMR Data There are two unresolved lines between 130 and 131 ppa. TTTTTTTT 160 140 120 100 80 60 20 PPM 0 DEPT 135: positive: 18.4, 55.1, 113.9, 123.3, 126.9, 130.5 ppm DEPT 90: 113.9, 123.3, 126.9, 130.5...
identify the unknown from the given spectra "H-NMR multiplet, 10H triplet, 6H N PPM 13 C-NMR...
identify the unknown from the given spectra
"H-NMR multiplet, 10H triplet, 6H N PPM 13 C-NMR 35 30 25 20 15 10 PPM IR LOD TRATTEET 3000 2000 1500 1000 50 BRYNNERE Mass Spec. 100 80 60 Relative Intensity 40 м 20- 0 ti LO 20 30 40 50 60 70 80 90 100 m/z
3. Find the structure of a compound given the MS, IR, and NMR data below. When...
3. Find the structure of a compound given the MS, IR, and NMR data below. When you have the solution, use it to determine the correct multiplicity of the signal at 5.1 ppm and explain the coupling pattern. A correct answer with no explanation will receive no credit. MASS 951 FL 100 128 1107 677 r69 r45 50 557 811 130 120 100 110 90 80 70 60 50 mt IR 100 50 2000 Wavenumber (cm-1) 1000 3000 4000 'H...
6-A compound (C6H4C120) has the following 1H NMR, 13C NMR, and IR spectra. Propose a structure...
6-A compound (C6H4C120) has the following 1H NMR, 13C NMR, and IR spectra. Propose a structure consistent with this data C6H40120 100 Transmittance -1577 SHE 4000 3000 2000 1000 Waven umhers (cm) 121.2 ppm 155 150 145 140 135 130 125 120 115 110 105 100 95 90 85 80 ppm 75 0606067 60 S SO 57
Organic Chemistry - Using the following IR anaylsis identify the major peaks and possible functio...
Organic Chemistry - Using the following IR anaylsis identify the
major peaks and possible functional group identity. Using the two
NMR spectra, discuss the integration of peaks, chemical shifts, and
splitting. Using the mass spectra, identify molecular weight and
important fragments to confirm the structure. Draw the fragments
that correspond to each peak in the mass spectra. Draw the
structure of the unknown that corresponds to all available data.
additional information: Unknown ‘J’ is a alkane.
H-NMR multiplet, 1OH triplet,...
Determine the structure of Compound 2 using the Mass Spec, IR, C
NMR, H NMR, and Dept Experiments.
Splitting patterns are as follows from left to right: triplet, 5
peaks (unsure of name), septet (7), 4 peaks (unsure of name),
doublet
Compound 2 Mass Spec MT:M/2 = 164 Relative Intensity 25 50 75 125 150 100 m/z IR LO0 D 4000 3000 2000 1500 1000 500 HAVENUMBERI-i H NMR: ditto as compound 1 6 2 2 4 1 2 PPM...
Using Mass Spec, IR, H-NMR, and C-NMR what would the structure look
like?
Relative Intensity 10 20 30 40 50 60 70 80 90 TERNSMETTANCEI D 4000 NAVENUMBERI 'H NMR PPM 13C NMR 90 80 70 60 50 40 30 20 10 0 PPM PPM DEPT-90 positive DEPT-135 positive Negative Negative Negative Negative Positive
Determine the compound using the Mass Spec, IR, C NMR, and H
NMR.
H Nmr splitting pattern from left to right: singlet, triplet,
septet (7), singlet, doublet
Compound 1 Mass Spec: Mpeak : 162 IR: 100 - TRANSMETTANCEI21 DO 4000 2000 2000 1500 1500 - 1000 13C NMR: Broadband in provided below. DEPT data is in the provided table. 200.180.160.140 120 100.80 '60.40.20 PPM DEPT -135 positive DEPT-90 positive -------------- PPM 191 149 138 137 135 128 126 | 34...
What would the structure look like using the mass spec with a
parent peak of 162, IR, C-NMR and H-NMR?
TRETTENCEI Singlet doublet Singlet triplet muitplet PPM halides 13C NMR: Broadband in provided below. DEPT data is in the provided table. 200 180 160 140 120 100 PPM 80 60 40 20 0 DEPT-135 positive DEPT-90 positive PPM 191 149 138 137 135 128 126 positive positive positive positive positive positive positive positive positive positive
Propose a reasonable structure for this compound based on the mass spec, IR, and NMR data. 100 Relative Intensity M+ 10 20 30 40 60 70 80 90 50 m/z LUU TRINETTRICET 4000 3000 2000 cm1 1500 1000 500 ЗН Зн 2H тттттттттттттттттт 11 10 9 8 7 6 5 4 ppm 200 180 160 140 120 80 60 40 20 100 ppm
1. Use the 'H NMR, 13C NMR, mass spectrometry and IR dat of a compound to determine its structure. IR Spectrum Mass Spectrometry Data relative abund 77 105 117 133 147 148 100 1H NMR Data 2H 24 ) H !! 13C NMR Data There are two unresolved lines between 130 and 131 ppa. TTTTTTTT 160 140 120 100 80 60 20 PPM 0 DEPT 135: positive: 18.4, 55.1, 113.9, 123.3, 126.9, 130.5 ppm DEPT 90: 113.9, 123.3, 126.9, 130.5...
identify the unknown from the given spectra
"H-NMR multiplet, 10H triplet, 6H N PPM 13 C-NMR 35 30 25 20 15 10 PPM IR LOD TRATTEET 3000 2000 1500 1000 50 BRYNNERE Mass Spec. 100 80 60 Relative Intensity 40 м 20- 0 ti LO 20 30 40 50 60 70 80 90 100 m/z
3. Find the structure of a compound given the MS, IR, and NMR data below. When you have the solution, use it to determine the correct multiplicity of the signal at 5.1 ppm and explain the coupling pattern. A correct answer with no explanation will receive no credit. MASS 951 FL 100 128 1107 677 r69 r45 50 557 811 130 120 100 110 90 80 70 60 50 mt IR 100 50 2000 Wavenumber (cm-1) 1000 3000 4000 'H...
6-A compound (C6H4C120) has the following 1H NMR, 13C NMR, and IR spectra. Propose a structure consistent with this data C6H40120 100 Transmittance -1577 SHE 4000 3000 2000 1000 Waven umhers (cm) 121.2 ppm 155 150 145 140 135 130 125 120 115 110 105 100 95 90 85 80 ppm 75 0606067 60 S SO 57
Organic Chemistry - Using the following IR anaylsis identify the
major peaks and possible functional group identity. Using the two
NMR spectra, discuss the integration of peaks, chemical shifts, and
splitting. Using the mass spectra, identify molecular weight and
important fragments to confirm the structure. Draw the fragments
that correspond to each peak in the mass spectra. Draw the
structure of the unknown that corresponds to all available data.
additional information: Unknown ‘J’ is a alkane.
H-NMR multiplet, 1OH triplet,...
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