Spectra-given structures consist with the spectra in the following problem. Justify your structure by assigning characteristics of the spectura to the structure.please help I have no idea how to do this. please show all work thank you.
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Spectra-given structures consist with the spectra in
the following problem. Justify your structure by assigning
characteristics...
7. Consider the IR, 'H-NMR and C-NMR spectra of the compound with MFC,1,0, Identify the structure...
7. Consider the IR, 'H-NMR and C-NMR spectra of the compound with MFC,1,0, Identify the structure of the unknown compound MP pls MW 114 *C 73.6 WW 124 Mass Spee, D relativ mix bund, 27 71 74 LESTE WVELDEN Copyright © 1994 래 TTTT 2.0 3.0 Proton NMR 1.5 1.0 PPM MITTIT 200 TTI TITTI 80 60 40 20 PPM 0 180 160 Y 120 140 100 Carbon 13 NMA 8. Consider the IR, 'H-NMR and 13C-NMR spectra of the...
Identify the structure and draw it based on the formula and the spectroscopy. Justify your answer...
Identify the structure and draw it based on the formula and the
spectroscopy. Justify your answer
MF CH40 47 MW 114 C 73.6 SH 12.4 3H 6H Copyright 1994 0.5 2.0 1.0 PPM 3.0 Poton NMR 2.5 1.5 180 160 140 200 80 120 100 20 PPM 0 Carbon 13 NMA ww ab sa ELITSM м М 6е 28 1500 180e 2000 2500 HAVENUMBERS 6H ЗН Copyright 1994 ST'S0T 1289.32 aL L9ET 20 89T 6L 8TLT ALE62 HAVENUMBERS ЗН ©1994...
MF C12H1404 MW 222 *C 64.8 %H 6.4 TRETTANCE cer 144.72 11? 18426 Mass Spec. Data...
MF C12H1404 MW 222 *C 64.8 %H 6.4 TRETTANCE cer 144.72 11? 18426 Mass Spec. Data relative m/z abund. 50 8 65 12 76 14 93 10 104 9 105 11 149 100 150 176 10 177 21 744.62 1967.70 1 3 2500 AVENUMBERS 1000 Copyright © 1994 3H IN Copyright © 1994 3H 2H 1H 1H M 1207077772 Proton NMR 2.0 1.5 PPW 170 166 160 155 136 130 PPM PPW Carbon 13 NMA 18. 1. Provide degrees of...
Spectroscopy Question 1) The following spectra are for a single compound. Determine the chemical formula, degrees...
Spectroscopy Question
1) The following spectra are for a single compound. Determine the chemical formula, degrees of unsaturation and the structure. Clearly correlate your structure's protons, with the proton signals in the 1H NMR, using a Lewis-like structure. MW 136 %C 79.4 %H 8.9 seber Mass Spec. Data relative m/abund. 77 18 79 17 91 12 103 12 105 100 106 28 136 11 w L'esec 14 SCERE she 3H LAVENDERS E 5H D 1H 2H A B с 1H...
identify functional groups and identify the structure of the molecule MF C6H10 MW 82 %C 87.7...
identify functional groups and identify the structure
of the molecule
MF C6H10 MW 82 %C 87.7 %H 12.3 Mass Spec. Data relative abund. m/z 65 27 48 39 40 28 42 48 10 17 53 54 29 67 100 11 81 20- 1008 1500 3200 3508 3H unVENUMNERS Copyright 1994 Note: *Long range coupling. 4H 2H 1.0 0.8 PP,6 1.8 1.6 i.4 1.2 2.2 2.0 2.8 2.6 2.4 Proton NMR TTTTTT 20 30 TTTTTTTIT 40 50 60 70 0 Mdd...
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...
Find the chemical structure using the wave spectrum shown Problem I1.3 40 Exact M.S. (E)- 84.0575 UVAmax-209 (E-16,0...
Find the chemical structure using the wave spectrum
shown
Problem I1.3 40 Exact M.S. (E)- 84.0575 UVAmax-209 (E-16,000) 328 (E-50) FT-IR (NEAT) 20 3000 2000 WAVENUMBERS (CM) 1800 1200 100 Mass Spec. El 70eV 40 20 50 40 44 55 70 m/z T 13C NMR 62.3 MHz COCla D D 192 11 190 CDCI Fwwwwluuluuluulnluulululul luulnluuluuluulun ad 0 ppm 0 HE 150 120 100 120 160 150 140 130 110 50 50 40 20 10 250 10 Ha/dw 250 MHz...
Provide the correct structure for your unknown based on the spectroscopic data provided. Provide the correct...
Provide the correct structure for your unknown based on the
spectroscopic data provided. Provide the correct name for your
compound. Either the IUPAC name, or a commonly accepted name (i.e.,
ethyl acetate in place of ethyl ethanoate) will be accepted.IR
spectrum: Assign as many peaks as possible. In particular, you
should assign peaks that were important in making your structural
interpretation (i.e. functional group peaks such as OH, C=O, N-H,
etc.).
1H-NMR spectrum: Assign all the peaks in the spectrum...
7. Consider the IR, 'H-NMR and C-NMR spectra of the compound with MFC,1,0, Identify the structure of the unknown compound MP pls MW 114 *C 73.6 WW 124 Mass Spee, D relativ mix bund, 27 71 74 LESTE WVELDEN Copyright © 1994 래 TTTT 2.0 3.0 Proton NMR 1.5 1.0 PPM MITTIT 200 TTI TITTI 80 60 40 20 PPM 0 180 160 Y 120 140 100 Carbon 13 NMA 8. Consider the IR, 'H-NMR and 13C-NMR spectra of the...
Identify the structure and draw it based on the formula and the
spectroscopy. Justify your answer
MF CH40 47 MW 114 C 73.6 SH 12.4 3H 6H Copyright 1994 0.5 2.0 1.0 PPM 3.0 Poton NMR 2.5 1.5 180 160 140 200 80 120 100 20 PPM 0 Carbon 13 NMA ww ab sa ELITSM м М 6е 28 1500 180e 2000 2500 HAVENUMBERS 6H ЗН Copyright 1994 ST'S0T 1289.32 aL L9ET 20 89T 6L 8TLT ALE62 HAVENUMBERS ЗН ©1994...
MF C12H1404 MW 222 *C 64.8 %H 6.4 TRETTANCE cer 144.72 11? 18426 Mass Spec. Data relative m/z abund. 50 8 65 12 76 14 93 10 104 9 105 11 149 100 150 176 10 177 21 744.62 1967.70 1 3 2500 AVENUMBERS 1000 Copyright © 1994 3H IN Copyright © 1994 3H 2H 1H 1H M 1207077772 Proton NMR 2.0 1.5 PPW 170 166 160 155 136 130 PPM PPW Carbon 13 NMA 18. 1. Provide degrees of...
Spectroscopy Question
1) The following spectra are for a single compound. Determine the chemical formula, degrees of unsaturation and the structure. Clearly correlate your structure's protons, with the proton signals in the 1H NMR, using a Lewis-like structure. MW 136 %C 79.4 %H 8.9 seber Mass Spec. Data relative m/abund. 77 18 79 17 91 12 103 12 105 100 106 28 136 11 w L'esec 14 SCERE she 3H LAVENDERS E 5H D 1H 2H A B с 1H...
identify functional groups and identify the structure
of the molecule
MF C6H10 MW 82 %C 87.7 %H 12.3 Mass Spec. Data relative abund. m/z 65 27 48 39 40 28 42 48 10 17 53 54 29 67 100 11 81 20- 1008 1500 3200 3508 3H unVENUMNERS Copyright 1994 Note: *Long range coupling. 4H 2H 1.0 0.8 PP,6 1.8 1.6 i.4 1.2 2.2 2.0 2.8 2.6 2.4 Proton NMR TTTTTT 20 30 TTTTTTTIT 40 50 60 70 0 Mdd...
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...
Find the chemical structure using the wave spectrum
shown
Problem I1.3 40 Exact M.S. (E)- 84.0575 UVAmax-209 (E-16,000) 328 (E-50) FT-IR (NEAT) 20 3000 2000 WAVENUMBERS (CM) 1800 1200 100 Mass Spec. El 70eV 40 20 50 40 44 55 70 m/z T 13C NMR 62.3 MHz COCla D D 192 11 190 CDCI Fwwwwluuluuluulnluulululul luulnluuluuluulun ad 0 ppm 0 HE 150 120 100 120 160 150 140 130 110 50 50 40 20 10 250 10 Ha/dw 250 MHz...
Provide the correct structure for your unknown based on the
spectroscopic data provided. Provide the correct name for your
compound. Either the IUPAC name, or a commonly accepted name (i.e.,
ethyl acetate in place of ethyl ethanoate) will be accepted.IR
spectrum: Assign as many peaks as possible. In particular, you
should assign peaks that were important in making your structural
interpretation (i.e. functional group peaks such as OH, C=O, N-H,
etc.).
1H-NMR spectrum: Assign all the peaks in the spectrum...
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