5. Given the spectral data below, provide a structure. Note you must assign all of the...
5. 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 or MS that assisted you in deriving your answer. (6 pts.) 6H, d 3H, d 2H, d 1H, sextet 1Hm Relative Intensity M+ = 164 50 75 125 150 100 m/z 2000 Wavnumber icm-1)
5 Given the spectral data below, provide a structure. Note you must assign all of the signals in the spectrum below receive full credit. Also assign any key sionals in the IR OMS that assisted you in deriving your answer. (6 pts.) 6H. d 3H, d 2H. 1H, sextet PPM Relative Intensity M+s 164 m /z wavenumber im-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
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
DIRECTIONS: You must complete the entire assignment. 1. Given the 'H NMR spectrum below and a molecular formula of CH, 0, provide a structure. Note you must assign all of the signals in the spectrum below to receive full credit. IR: 1600-1650 cm (multiple peaks) (5 pts.) 3H, 3H,t 2H, d 2H, d 2H,9 PPM 2. Given the 'H NMR spectrum below and a molecular formula of C.H.O. provide a structure. Note you must assign all of the signals in...
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...
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...
%O'S CHE 310 Homework #9 Due WED NOV 20 5. Given the spectral data below, provide a structure. Nove you must assign all of the signals in the spectrum below to receive full credit. Ale asin any key signals in the IR or MS that assisted you in deriving your answer. (6 pts.) TH, sextet Rotive Welly M+ - 164
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...