![PROBLEM 2 MW 122 3C 78.7 AH 8 [104-933] 1994 iH iH Proton NMA 140 Carbon 13 NHA 1.5H There are two lines (unresolvod at 130 ppm. 100 1.5H 20 PPM 0](http://img.homeworklib.com/questions/ee66b750-a12b-11eb-8c69-572cfd9b4c01.png?x-oss-process=image/resize,w_560)
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PROBLEM 2 MW 122 3C 78.7 AH 8 [104-933] 1994 iH iH Proton NMA 140 Carbon...
MF C10H14 MW 134 %C 89.5 %H 10.5 1500 3H 3H Copyright 1994 5H 2H iH...
MF C10H14 MW 134 %C 89.5 %H 10.5 1500 3H 3H Copyright 1994 5H 2H iH PPM Proton NMR 60140 1201008o6*"420 PPN 20 PPM 0 Carbon 13 NMR
PROBLEM 4 MW 150 72.0 SH 6.7 [10031-82 1994 2H 2H 10.09, Proton NMR 00 180...
PROBLEM 4 MW 150 72.0 SH 6.7 [10031-82 1994 2H 2H 10.09, Proton NMR 00 180 160 140 120 100 Carbon 13 NMR 20 PPM
Label each peak on your carbon- and proton-NMR; and label only the principle peaks found in...
Label each peak on your carbon- and proton-NMR; and label only
the principle peaks found in the compound. All peaks are presented
in the 4000-1000 wavenumber range.
Copyright 1994 Proton NMR 60 140 Carbon 13 NMA 120 100 2H 80 MF 8H11 MW 137 %C70.0 EH 8.1 N 10.2 2 PPM 20 PPM
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...
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...
Spectra-given structures consist with the spectra in the following problem. Justify your structure by assigning characteristics...
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.
MFC5H8Oz MW 100 % с 60.0 %H 8.0 108 90 Mass Spec. Data 60 relative m/z abund. 15 16 27 8 29 8 43 100 57 8 58 9 40 28 2580 2008 1500 1880 4000 35 WAVENUMBERS Copyright C 1994 3H 1502...
7. Consider the IR, 'H-NMR and C-NMR spectra of the compound with MF:C,H, 0. 4 pts...
7. Consider the IR, 'H-NMR and C-NMR spectra of the compound with MF:C,H, 0. 4 pts Identify the structure of the unknown compound. MF C7H140 MW 114 $C 73.6 SH 12.4 Mass Spec. D m/ sbund. 27 35 relativ 114 11 Popyright © 1994 1.0 PPM 3.0 Proton NMA TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 200 180 160 140 Carbon 13 NMR T 120 TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 100 80 60 40 20 PPM O en og and 8. Consider the IR, 'H-NMR and C-NMR spectra of the...
DESCRIBE PEAKS OF EACH NMR (Carbon 13 and PROTON 1H) and mass spec on the one page NMR Unknown_18 200 180 160 140 120...
DESCRIBE PEAKS OF EACH NMR (Carbon 13 and PROTON 1H) and mass
spec on the one page
NMR Unknown_18 200 180 160 140 120 80 60 40 20 0 100 pom - 2 2 4 3 11 10 9 8 7 6 4 3 2 1 0 5 ppm - Relative Intensity 25 50 75 100 125 150 m/z
problem 4.05 please 1-3. There are two sets of spectra attached. For each provide a structure...
problem 4.05 please
1-3. There are two sets of spectra attached. For each provide a structure and assign the peaks by labeling the structures and listing the peaks in the tables provided. 208 Label H NMR 6 Label C NMR 6 4.05 Label H NMR 8 Label C NMR 8 Problem 4.05 Given the spectroscopic data below (Proton, Carbon, gHSQC, gCOSY, and gHMBC), provide the structure of the molecule. (HR-MS: 238.1358 amu), {'H, 'H) Nuclear Overhauser effect correlation was observed...
In this problem you have to elucidate the structure of product B. A substrate A (structure...
In this problem you have to elucidate the structure of product B. A substrate A (structure shown in scheme 1) which was subjected to two consecutive reactions as shown in scheme 1 below to give the product B of molecular formula CsH14Br2. Provide the structure for Product B based on the NMR data provided (attachment 2: Problem set 2). (The 1H NMR and 13C NMR of starting substrate A has been provided for reference purpose only) 1. MnO2, CHCI3, rt,...
MF C10H14 MW 134 %C 89.5 %H 10.5 1500 3H 3H Copyright 1994 5H 2H iH PPM Proton NMR 60140 1201008o6*"420 PPN 20 PPM 0 Carbon 13 NMR
PROBLEM 4 MW 150 72.0 SH 6.7 [10031-82 1994 2H 2H 10.09, Proton NMR 00 180 160 140 120 100 Carbon 13 NMR 20 PPM
Label each peak on your carbon- and proton-NMR; and label only
the principle peaks found in the compound. All peaks are presented
in the 4000-1000 wavenumber range.
Copyright 1994 Proton NMR 60 140 Carbon 13 NMA 120 100 2H 80 MF 8H11 MW 137 %C70.0 EH 8.1 N 10.2 2 PPM 20 PPM
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...
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...
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.
MFC5H8Oz MW 100 % с 60.0 %H 8.0 108 90 Mass Spec. Data 60 relative m/z abund. 15 16 27 8 29 8 43 100 57 8 58 9 40 28 2580 2008 1500 1880 4000 35 WAVENUMBERS Copyright C 1994 3H 1502...
7. Consider the IR, 'H-NMR and C-NMR spectra of the compound with MF:C,H, 0. 4 pts Identify the structure of the unknown compound. MF C7H140 MW 114 $C 73.6 SH 12.4 Mass Spec. D m/ sbund. 27 35 relativ 114 11 Popyright © 1994 1.0 PPM 3.0 Proton NMA TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 200 180 160 140 Carbon 13 NMR T 120 TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 100 80 60 40 20 PPM O en og and 8. Consider the IR, 'H-NMR and C-NMR spectra of the...
DESCRIBE PEAKS OF EACH NMR (Carbon 13 and PROTON 1H) and mass
spec on the one page
NMR Unknown_18 200 180 160 140 120 80 60 40 20 0 100 pom - 2 2 4 3 11 10 9 8 7 6 4 3 2 1 0 5 ppm - Relative Intensity 25 50 75 100 125 150 m/z
problem 4.05 please
1-3. There are two sets of spectra attached. For each provide a structure and assign the peaks by labeling the structures and listing the peaks in the tables provided. 208 Label H NMR 6 Label C NMR 6 4.05 Label H NMR 8 Label C NMR 8 Problem 4.05 Given the spectroscopic data below (Proton, Carbon, gHSQC, gCOSY, and gHMBC), provide the structure of the molecule. (HR-MS: 238.1358 amu), {'H, 'H) Nuclear Overhauser effect correlation was observed...
In this problem you have to elucidate the structure of product B. A substrate A (structure shown in scheme 1) which was subjected to two consecutive reactions as shown in scheme 1 below to give the product B of molecular formula CsH14Br2. Provide the structure for Product B based on the NMR data provided (attachment 2: Problem set 2). (The 1H NMR and 13C NMR of starting substrate A has been provided for reference purpose only) 1. MnO2, CHCI3, rt,...
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