Determine the structure of the assigned acyl chloride. Find molecular formula, lable peaks and stuctures. Acyl...
Can you help to figure out the formula and the structure ? 50) 4. Determine the structure of the molecule from these spectra, and draw your answer in the box. 100 80 40 20 4000 2000- 3000 1500 1000 400 100 -[ 196 80 196 40 20 200 20 40 60 80 100 120 140 160 180 200 3H,t 2H,m 2H,t 2H,m 3 2 peaks 20 80 100 120 140 160 180 200 3H,t 2H,d 2H,d 2H,m 2H,t 2H,m 8...
For the following unknown, annotate the corresponding spetras and determine the molecular formula and lewis structure. Anknown IR/HNMR/CNMR MW=122 : 124 AMU 1:1 D 3000 1000 00 RYENUEERI D, 6 M, 1 10 7 4 1 HP-03-172 Ppm N 10 120 60 100 80 40 20 200 180 160 140 ppm CDS-00-26O
Compound Z, C5H160. Deduce its structure. IR: significant peaks at 2962 and 1718 (intense) cm! 13 Mass spectrum: a few of the significant peaks include 128, W, 57 m/z. H-NMR: s, at's 2 H'S 5,34's th's PPM 13 C-NMR 3 signals 220 200 180 160 140 120 PPM 100 80 60 40 20 0
Suggest a composition for the halogen compound whose mass spectrum is shown below and assign the labeled peaks. 127 100 173 160 158 162 25 48 TITTHTT 160 170 91 208 79 35 160 173 30 40 50 60 70 80 90 100 110 120 130 140 150 160 170 180 190 200 210 m/z 127 100 173 160 158 162 25 48 TITTHTT 160 170 91 208 79 35 160 173 30 40 50 60 70 80 90 100...
Draw the structure in the box 40) 7. Based on the spectral data shown, determine the structure of this compound. eo 60 20 1000 1500 200 po00 2000 40 20 140 160 40 120 180 60 100 m/z SH 2H Two 2H triplets Actually 3 peaks 140 160 12o 100
10) Determine the structure of an unknown compound with a molecular formula of CuHz03. IR and NMRS are shown below: (10 points) 100 B0 mm 60 40 20 000 4000 RUM 2000 1500 Wavnumber 1000 3H 3H 2H2H 2H B 3 2 PPM 200 180 160 140 120 100 PPM 20 Draw a structure consistent with the above data and map the proton NMR signals to the structure you have drawn.
need molecular formula, compound name and assign at least 2 13C signals 10 20 30 40 50 60 70 80 90 100 110 120 2 Signals 80 60 40 20 0 200 180 160 140 120 100 ppm m, 5 H t, 3 H CHz t, 2H t, 2H t, 2 H m, 2 H
Compound Z, CaHie0. Deduce its structure. IR: significant peaks at 2962 and 1718 (intense) cm. Mass spectrum: a few of the significant peaks include 128, 103, 57 m/z H-NMR: S,3H's aH's t,2t's PPM 13C-NMR 220 200 180 160 140 120 PPM 100 80 60 40 20
Information: Each spectra below was obtained from a pure compound. Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm 'H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important...
Information: Each spectra below was obtained from a pure compound. Mass Spectrum parent peaks (M) are listed for all examples. IR peaks listed are strong (s) unless otherwise indicated for signals above 1500 cm "H NMR Spectra, the integral is given in number of hydrogens (#H) or as a relative ratio. Important coupling constants (J-values) are listed next to the peaks for some examples. For some spectra, an inset (grey box) is also given showing a "zoom-in" on an important...