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identify what the molecular structure is through its NMR, IR, and
MS
Unknown 4 CH 40...
Using the NMR, IR, and MS figure out what the compoud is. ** identify the molecular...
Using the NMR, IR, and MS figure out what the compoud is.
**
identify the molecular structure througu NMR, IR and MS
CHEM 100L Lab 3 NMR Problems Unknown 1 CH 0 M-a 102 Relative Intensity 20 30 40 50 70 80 60 m/z water, not part of sample 1-2975-2877 9H, singlet 2H, 3H, quartet triplet ppm Unknown 2 C,H,O tensity 119 Relative 3200-2600 1680V 3H, singlet 2x 2H, doublet 1H, singlet ppm Unknown 3 C,HO, Relative Intensity 3090 3035...
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
Determine the structure of the compound using the Mass Spec, IR, C NMR, H NMR, and...
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
Compound 3 MS: M* = 81 Relative Intensity 10 20 30 40 70 80 90 50 60 m/z Microsoft Autog LOD TRANSMETTANCE1% 4000 2000 2000 1500 1000 HAVENUHBERI-1 1H NMR + ) PPM | 13C NMR 90 ' 80 ' 70 ' 60 ' 50 ' 40...
Use the IR and MS data to elucidate the structures of the compounds below. Identify the...
Use the IR and MS data to elucidate the structures of the compounds below. Identify the M and other necessary peaks in the mass spectra below. Give the functional group responsible for the IR signals. IR: (1 709) sharp, strong (1607-1653) weak MS: ID 4 peaks 100- Relative Intensity orta pripreme 10 20 30 40 50 60 70 80 90 100 m/z 110 120 IR: (1753) strong (1602 - 1658) weak MS: ID 4 peaks 100 MS-NU-18 Relative Intensity 10...
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,...
What is the molecular formula and structure? Use the mass, infrared, proton NMR, and carbon NMR....
What is the molecular formula and structure? Use the mass,
infrared, proton NMR, and carbon NMR. I have a structure and
formula completed, but I wanted to confirm.
TRANSMETTANCE 41 50 4000 3000 2000 DOST 1000 HAVENUHBERI-1 Mass of molecular ion: 116 100 80- Relative Intensity 40 20- TI Other 10 20 ITHTHIS 30 40 fittihristutt tartott 50 60 70 80 m/z T 110 TITT 120 90 100 200 180 160 140 TTTTTT 120 100 80 60 40 20 ppm...
Please identify the structure of the compound with explanation MS IR H-NMR 13C NMR. The molecular...
please identify the structure of the compound with explanation MS
IR H-NMR 13C NMR. The molecular formula is not available just try
to get us as close as possible you can
Even though the molecular formula is not given get us close as
possible as you can
Electron ionization (El-MS) 167 75 50 25 139 84 63 113 7074 87 28 39 50 e 98 20 30 40 50 60 70 80 90 100 110 120 130 140 150 160...
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
What is the structure of this compound? 1. Molecular Formula: CHCI 'H NMR 6 3.42 ppm,...
What is the structure of this compound?
1. Molecular Formula: CHCI 'H NMR 6 3.42 ppm, 1H, pentet 61.80 ppm, 2H, quartet 6 1.73 ppm, 2H, doublet 6 1.56 ppm, 2H, triplet 6 1.53 ppm, 2H, pentet 60.99 ppm, 6H, singlet PC NMR 8 57.2 ppm, 10 6 49.3 ppm, 1C 6 38.4 ppm, 1C 6 37.7 ppm, 1C 6 33.3 ppm, 10 6 30.9 ppm, 2C 8 22.4 ppm, 1C 60 50 40 10 IR: 2964 cm(s) 713 cm...
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...
Using the NMR, IR, and MS figure out what the compoud is.
**
identify the molecular structure througu NMR, IR and MS
CHEM 100L Lab 3 NMR Problems Unknown 1 CH 0 M-a 102 Relative Intensity 20 30 40 50 70 80 60 m/z water, not part of sample 1-2975-2877 9H, singlet 2H, 3H, quartet triplet ppm Unknown 2 C,H,O tensity 119 Relative 3200-2600 1680V 3H, singlet 2x 2H, doublet 1H, singlet ppm Unknown 3 C,HO, Relative Intensity 3090 3035...
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
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
Compound 3 MS: M* = 81 Relative Intensity 10 20 30 40 70 80 90 50 60 m/z Microsoft Autog LOD TRANSMETTANCE1% 4000 2000 2000 1500 1000 HAVENUHBERI-1 1H NMR + ) PPM | 13C NMR 90 ' 80 ' 70 ' 60 ' 50 ' 40...
Use the IR and MS data to elucidate the structures of the compounds below. Identify the M and other necessary peaks in the mass spectra below. Give the functional group responsible for the IR signals. IR: (1 709) sharp, strong (1607-1653) weak MS: ID 4 peaks 100- Relative Intensity orta pripreme 10 20 30 40 50 60 70 80 90 100 m/z 110 120 IR: (1753) strong (1602 - 1658) weak MS: ID 4 peaks 100 MS-NU-18 Relative Intensity 10...
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,...
What is the molecular formula and structure? Use the mass,
infrared, proton NMR, and carbon NMR. I have a structure and
formula completed, but I wanted to confirm.
TRANSMETTANCE 41 50 4000 3000 2000 DOST 1000 HAVENUHBERI-1 Mass of molecular ion: 116 100 80- Relative Intensity 40 20- TI Other 10 20 ITHTHIS 30 40 fittihristutt tartott 50 60 70 80 m/z T 110 TITT 120 90 100 200 180 160 140 TTTTTT 120 100 80 60 40 20 ppm...
please identify the structure of the compound with explanation MS
IR H-NMR 13C NMR. The molecular formula is not available just try
to get us as close as possible you can
Even though the molecular formula is not given get us close as
possible as you can
Electron ionization (El-MS) 167 75 50 25 139 84 63 113 7074 87 28 39 50 e 98 20 30 40 50 60 70 80 90 100 110 120 130 140 150 160...
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
What is the structure of this compound?
1. Molecular Formula: CHCI 'H NMR 6 3.42 ppm, 1H, pentet 61.80 ppm, 2H, quartet 6 1.73 ppm, 2H, doublet 6 1.56 ppm, 2H, triplet 6 1.53 ppm, 2H, pentet 60.99 ppm, 6H, singlet PC NMR 8 57.2 ppm, 10 6 49.3 ppm, 1C 6 38.4 ppm, 1C 6 37.7 ppm, 1C 6 33.3 ppm, 10 6 30.9 ppm, 2C 8 22.4 ppm, 1C 60 50 40 10 IR: 2964 cm(s) 713 cm...
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...
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