determine the structure of the compound given the mass spec 15434957 १२ १५
Deduce the structure of the mystery compound using the attached Mass Spec, IR Spec, H-NMR, and C-NMR Mass Spectrum 100 41 80 60 28 115 69 40 121 87 123 20 M(194) M+2(96) 1 149 151 0 0 40 120 160 200
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...
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...
Please help identify the organic compound using mass spec, ir spec, CNMR, and HNMR. From looking at the mass spec, I believe the molar mass of the uknown organic compound to be 122 g/mol From looking at CNMR, I believe there are at least 5 carbons for each of the 5 peaks. I recall from class that there can be more due to symmetry, but am not certain how to tell. Above are all of the graphs given to me...
please go into some depth about how you used the mass spec to elucidate the structure (I'm really bad at Mass spec). thanks!! 13. Elucidate each structure below, based on the information provided. (12 pts, 4 pts each) Unknown Compound A Key Mass Spec Peak: Key IR Stretch: NMR Signals triplct (2)-2.0 ppm multiplet (2) 1.4 ppm triplet (3)-0.8 ppm m/z 69 sharp, weak 2245 cm
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
Hi, I need help finding a structure for an IR spec. The Mass spec is 174m/z and the peaks I am given are 2984, 1742, 1464, and 1088cm. I have 14 hydrogens, grouped 4H: 4H: 6H, the first 4 being a singlet, the second 4 being a quartet and the 6 being a triplet. PLEASE HELP!!
Determine the structure of the following compound given the molecular formula, C9H10O2 and the provided spectroscopic data. PROBLEX MW 150 8c 72.0 $H 6.7 [10031-82-01 U DO 0202 2739.27 PORSCT "SITI Mass Spec. Data relative miz abund. 15 10 27 1697.57 - Bot "TIT 1994 ONMEMES 10.0 8.5 9.0 8.5 Proton NMR TITIT 8. 7.5 PPX 140 120 100 200 180 160 Carbon 13 NMR 80 ווווווווות 20 PPM 0
Determine the compound using the Mass Spec, IR, C NMR, and H NMR. H Nmr splitting pattern from left to right: singlet, triplet, septet (7), singlet, doublet Compound 1 Mass Spec: Mpeak : 162 IR: 100 - TRANSMETTANCEI21 DO 4000 2000 2000 1500 1500 - 1000 13C NMR: Broadband in provided below. DEPT data is in the provided table. 200.180.160.140 120 100.80 '60.40.20 PPM DEPT -135 positive DEPT-90 positive -------------- PPM 191 149 138 137 135 128 126 | 34...
Given the proton NMR, carbon NMR, mass spec, and IR, deduce and name the structure, explain each peak in the H NMR, and name functional groups from IR. ot 8 AM ot 6 AM nに !F 4000 3500 2500 1500 S00