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identify the unknown from the given spectra
"H-NMR multiplet, 10H triplet, 6H N PPM 13 C-NMR...
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 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...
evaluate if the compound is cyclopentene or cyclihexyl bromide. label each part C IR 100 D...
evaluate if the compound is cyclopentene or cyclihexyl
bromide.
label each part
C IR 100 D j000 530 3000 00 VENUREI- Mass Spec. 100 80- 60 40 20 0 175 100 125 150 75 50 25 m/z Relative Intensity H-NMR quintet, 1H multiplet, 2H multiplet, 6H multiplet, 2H 0 PPM "C-NMR 30 10 40 0 20 PPM 50
Please help me find the unknown structure, Thanks. Unknown 261H-NMR Spectra 3.3 ppm 4-0 4.5 4.0...
Please help me find the unknown structure, Thanks.
Unknown 261H-NMR Spectra 3.3 ppm 4-0 4.5 4.0 3.5 3.4 2.5 2.0 .0 .s a. 3.00 Unknown 26 - 13C-NMR Spectrum 32 34 28 24 20 14 ppm 60 40 200 180 160 140 120 100 20 Unknown 26 IR and Mass Spectra 100 80 40 20 50 75 100 125 m/z 2500 WAVENUMBER [cm-1] 1500 3500 2000 1000 4000 3000 500 TRANSMITTANCE %] Raufive hitensity 06 7 Unknown 26 1H-NMR Spectra...
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...
Please help propose interpretations of the spectra for the two unknowns pictured below. Identification and drawing...
Please help propose interpretations of the spectra for the two
unknowns pictured below. Identification and drawing of the unknowns
would be much appreciated and will get a thumbs up.
Liquid T alcohol MS Relative Intensity 0- r 10 20 30 40 50 70 80 90 100 60 m/z Liquid T "H-NMR broad singlet, IH doublet, 6H quartet, 2H triplet, 2H nonet, IH PPM C-NMR PPM Sold e Carboxylic acid Mass Spec. 100 Relative Intensity optippropri protiletterturmflopperprompt 25 50 75 100...
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...
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
identify what the molecular structure is through its NMR, IR, and MS Unknown 4 CH 40...
identify what the molecular structure is through its NMR, IR, and
MS
Unknown 4 CH 40 Relative Intensity Order 10 20 30 40 50 60 70 80 90 100 110 12965- 2875 1715 6H, triplet 4H, triplet 4H, sextet 10 9 8 7
Identify the unknown compound structure using the spectra information given. Thank you! IR Data 100 Mass...
Identify the unknown compound structure using the
spectra information given. Thank you!
IR Data 100 Mass Spectrometry Data Molecular lon: 104amu Mass Spec. Data relative m/z abund. 9 27 27 8 59 100 TRANSMITTANCE 958.BL 875.79 773.55 SLOTT 2828.27 - SE LLET €6"EITT 10 et te 'TSET 2000 BOG 3000 25.00 HAVENUMBERS 2009 1500 1H NMR Data TTTTTTT "5. 62.5 2.5 1.5 1.6 PM 0.5 3.5 3.0 25 2.0 TTTTT 1.0 PPM 0.5 4.0 3.5 3.0 2.5 2.0 1.0 PPM...
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 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...
evaluate if the compound is cyclopentene or cyclihexyl
bromide.
label each part
C IR 100 D j000 530 3000 00 VENUREI- Mass Spec. 100 80- 60 40 20 0 175 100 125 150 75 50 25 m/z Relative Intensity H-NMR quintet, 1H multiplet, 2H multiplet, 6H multiplet, 2H 0 PPM "C-NMR 30 10 40 0 20 PPM 50
Please help me find the unknown structure, Thanks.
Unknown 261H-NMR Spectra 3.3 ppm 4-0 4.5 4.0 3.5 3.4 2.5 2.0 .0 .s a. 3.00 Unknown 26 - 13C-NMR Spectrum 32 34 28 24 20 14 ppm 60 40 200 180 160 140 120 100 20 Unknown 26 IR and Mass Spectra 100 80 40 20 50 75 100 125 m/z 2500 WAVENUMBER [cm-1] 1500 3500 2000 1000 4000 3000 500 TRANSMITTANCE %] Raufive hitensity 06 7 Unknown 26 1H-NMR Spectra...
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...
Please help propose interpretations of the spectra for the two
unknowns pictured below. Identification and drawing of the unknowns
would be much appreciated and will get a thumbs up.
Liquid T alcohol MS Relative Intensity 0- r 10 20 30 40 50 70 80 90 100 60 m/z Liquid T "H-NMR broad singlet, IH doublet, 6H quartet, 2H triplet, 2H nonet, IH PPM C-NMR PPM Sold e Carboxylic acid Mass Spec. 100 Relative Intensity optippropri protiletterturmflopperprompt 25 50 75 100...
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...
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
identify what the molecular structure is through its NMR, IR, and
MS
Unknown 4 CH 40 Relative Intensity Order 10 20 30 40 50 60 70 80 90 100 110 12965- 2875 1715 6H, triplet 4H, triplet 4H, sextet 10 9 8 7
Identify the unknown compound structure using the
spectra information given. Thank you!
IR Data 100 Mass Spectrometry Data Molecular lon: 104amu Mass Spec. Data relative m/z abund. 9 27 27 8 59 100 TRANSMITTANCE 958.BL 875.79 773.55 SLOTT 2828.27 - SE LLET €6"EITT 10 et te 'TSET 2000 BOG 3000 25.00 HAVENUMBERS 2009 1500 1H NMR Data TTTTTTT "5. 62.5 2.5 1.5 1.6 PM 0.5 3.5 3.0 25 2.0 TTTTT 1.0 PPM 0.5 4.0 3.5 3.0 2.5 2.0 1.0 PPM...
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