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provide structures for the spectral data provided
Pages 1-5: provide the 5 structures for the spectral...
please help if you can! Thank you! Instructions: This problem set is due to your lecture...
please help if you can! Thank you!
Instructions: This problem set is due to your lecture professor at the start of your lecture section on Friday November 22nd. No extensions will be given. Pages 1-5: provide the 5 structures for the spectral data provided. For full credit, you must be sure to assign/label all the NMR peaks and assign the major IR bands including those readily identifiable in the fingerprint region (use the IR spectral tables handed out in class)....
6. Given the spectral data below, provide a structure. Note you must assign all of the...
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+ 164 (no significant M+2 signal) (6 pts.) 3H, s зн, 2H, d 2H, d 2H, q 8 6 5 PPM 140 120 100 180 160 80 PPM 60 40 0.8 0.6 0.4 3000 2000...
Propose a structure that is consistent with the spectral data below. (The spectra and data provided...
Propose a structure that is consistent with the spectral data below. (The spectra and data provided were obtained from a pure organic molecule. For 'H NMR spectra, the integral is given in number of hydrogens (#H) or as a relative ratio.) Mass Spectrum (not shown): [M] = 162 m/z (100%) IR Spectrum (not shown): 3022, 2980, 1685, 1600, 1510 cm (all listed are strong (s) unless otherwise indicated) 'H NMR Spectrum (300 MHz, DMSO, 25 °C) dd (J= 2 Hz)...
6. Given the spectral data below, provide a structure. Note you must assign all of the...
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+ = 164 (no significant M+2 signal) (6 pts.) 3HS 2H. d 2Hd 2Hg 8 7 6 5 4 3 2 1 0 PPM 180 160 140 120 100 PPM 80 60 40 20 0...
CHE 310 Homework #9 Due WED NOV 20 6. Given the spectral data below, provide a...
CHE 310 Homework #9 Due WED NOV 20 6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and "C NMR spectra that assisted you in deriving your answer. MS: M+= 164 (no significant M+2 signal) (6 pts.) 3H, S 2H, d 2H, a 2H. PPM 180.160. 140 . 120 100 80 60 20 . 20 Relative...
13C NMR 1. Propose a structure for the compound CsH12, with the following 13C NMR spectral...
13C NMR 1. Propose a structure for the compound CsH12, with the following 13C NMR spectral data. 160 140 120 80 60 40 20 0 200 180 CDS-00-748 100 ppm 2. Propose a structure for the compound CaH;Br, with the following C NMR spectral data. 200 180 160 140 120 80 60 40 100 ppm 20 0 3. Propose a structure for the compound C H2O2, with the following "'C NMR spectral data. 200 180 160 140 120 30600 T...
6. Given the spectral data below, provide a structure. Note you must assign all of the...
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+= 164 (no significant M+2 signal) (6 pts.) 3H, S 3H, 2H, 2H, d 2H. PPM 180160140120 100 80 60 40 20 Relative Transmittance 3000 2000 Wave number (cm-11
6. Given the spectral data below, provide a structure. Note you must assign all of the...
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+= 164 (no significant M+2 signal) (6 pts.) 3H, S 3H, 2H, 2H, d 2H. PPM 180160140120 100 80 60 40 20 Relative Transmittance 3000 2000 Wave number (cm-11
6. Given the spectral data below, provide a structure. Note you must assign all of the...
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+= 164 (no significant M+2 signal) (6 pts.) 3H, S 3H, 2H, 2H, d 2H. PPM 180160140120 100 80 60 40 20 Relative Transmittance 3000 2000 Wave number (cm-11
CHE 310 Homework 9 Due WED NOV 20 6. Given the spectral data below, provide a...
CHE 310 Homework 9 Due WED NOV 20 6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer MS: M+-164 (no significant M+2 signal) (6 pts) 2H, 2H, d 2H. per 43 PPM 180 10 10 120 100 80 60 40 20 Relative Transmittance 2000 Wavenumber(cm-1)
please help if you can! Thank you!
Instructions: This problem set is due to your lecture professor at the start of your lecture section on Friday November 22nd. No extensions will be given. Pages 1-5: provide the 5 structures for the spectral data provided. For full credit, you must be sure to assign/label all the NMR peaks and assign the major IR bands including those readily identifiable in the fingerprint region (use the IR spectral tables handed out in class)....
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+ 164 (no significant M+2 signal) (6 pts.) 3H, s зн, 2H, d 2H, d 2H, q 8 6 5 PPM 140 120 100 180 160 80 PPM 60 40 0.8 0.6 0.4 3000 2000...
Propose a structure that is consistent with the spectral data below. (The spectra and data provided were obtained from a pure organic molecule. For 'H NMR spectra, the integral is given in number of hydrogens (#H) or as a relative ratio.) Mass Spectrum (not shown): [M] = 162 m/z (100%) IR Spectrum (not shown): 3022, 2980, 1685, 1600, 1510 cm (all listed are strong (s) unless otherwise indicated) 'H NMR Spectrum (300 MHz, DMSO, 25 °C) dd (J= 2 Hz)...
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+ = 164 (no significant M+2 signal) (6 pts.) 3HS 2H. d 2Hd 2Hg 8 7 6 5 4 3 2 1 0 PPM 180 160 140 120 100 PPM 80 60 40 20 0...
CHE 310 Homework #9 Due WED NOV 20 6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and "C NMR spectra that assisted you in deriving your answer. MS: M+= 164 (no significant M+2 signal) (6 pts.) 3H, S 2H, d 2H, a 2H. PPM 180.160. 140 . 120 100 80 60 20 . 20 Relative...
13C NMR 1. Propose a structure for the compound CsH12, with the following 13C NMR spectral data. 160 140 120 80 60 40 20 0 200 180 CDS-00-748 100 ppm 2. Propose a structure for the compound CaH;Br, with the following C NMR spectral data. 200 180 160 140 120 80 60 40 100 ppm 20 0 3. Propose a structure for the compound C H2O2, with the following "'C NMR spectral data. 200 180 160 140 120 30600 T...
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+= 164 (no significant M+2 signal) (6 pts.) 3H, S 3H, 2H, 2H, d 2H. PPM 180160140120 100 80 60 40 20 Relative Transmittance 3000 2000 Wave number (cm-11
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+= 164 (no significant M+2 signal) (6 pts.) 3H, S 3H, 2H, 2H, d 2H. PPM 180160140120 100 80 60 40 20 Relative Transmittance 3000 2000 Wave number (cm-11
6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer. MS: M+= 164 (no significant M+2 signal) (6 pts.) 3H, S 3H, 2H, 2H, d 2H. PPM 180160140120 100 80 60 40 20 Relative Transmittance 3000 2000 Wave number (cm-11
CHE 310 Homework 9 Due WED NOV 20 6. Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. Also assign any key signals in the IR and C NMR spectra that assisted you in deriving your answer MS: M+-164 (no significant M+2 signal) (6 pts) 2H, 2H, d 2H. per 43 PPM 180 10 10 120 100 80 60 40 20 Relative Transmittance 2000 Wavenumber(cm-1)
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