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could you help me identify the molecular weight of this mass spec? and also help me...
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...
6) Use the provided NMR and IR Information to identify a compound with molecular formula CHNO. (20 points) PPM w 3 M EN 180 180 140 120 100 POPIM 80 00 40 220 2 을은 IM 1000 19900 200 not 6) Use the provided NMR and IR information to identify a compound with molecular formula CH19NO2. (20 points) 6 ili 5 PPM لر AA Au لللب H 180 160 140 120 100 PPM 80 60 40 20 26 을은 100...
Identify which of these four mass spectra indicate the presence of sulfur, chlorine, bromine, iondine, nitrogen. suggest a molecular formula for each. 2otten breaks sh ass spec er be mass PROBLEM 12-7 Identify which of these four mass spectra indicate the presence of sulfur, chlorine bromine, iodine, or nitrogen. Suggest a molecular formula for each. AA gIve the lonica 100 77 80 156 158 (a) 60 40 20 Fragn 10 20 30 40 50 60 70 80 100 110 120...
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
Instructions: Write the structure of each molecular formula using the IR and Mass Spec spectra. Important that you justify with at least two arguments in each spectrum for which you present that structure. CH 3500 3000 1500 1000 2500 2000 Wavenumber(cm-1) 20 30 40 50 60 70 80 90 100 110 120 CHBr 100 Transmittance 3500 3000 2500 2000 Wavenumber(cm-1) 1500 1000 119 135 100 110 120 130 140 150 160 170 180 190 10 20 30 40 50 60...
What is the molecular formula and structure? Use the mass, infrared, proton NMR, and carbon NMR. I have a structure and formula completed, but I wanted to confirm. TRANSMETTANCE 41 50 4000 3000 2000 DOST 1000 HAVENUHBERI-1 Mass of molecular ion: 116 100 80- Relative Intensity 40 20- TI Other 10 20 ITHTHIS 30 40 fittihristutt tartott 50 60 70 80 m/z T 110 TITT 120 90 100 200 180 160 140 TTTTTT 120 100 80 60 40 20 ppm...
a) Describe the difference between the base peak and the parent ion (or molecular ion) peak. b) Identify the base peak and the parent ion (or molecular ion) peak (if any) according to the mass spectrum. c) Identify the mass fragments which correspond to m/z = 77, 105, 111, and 139. d) Identify and give explanations for the magnitude (or intensity) of the peaks at m/z = 113, 141, and 218. Mass Spectrum ofp-C hlorobenzophenone 105 100 80 139 CI...
Determine the structure of the assigned acyl chloride. Find molecular formula, lable peaks and stuctures. Acyl Chloride #1 d-1.303 g/mL 100004-025 M+ 160 80 60 40 M+2 162 20 20 40 60 8100 120 140 160 180 200 m/z Hint: aromatic ring is a thiophene 11 10 5 432 ppm All singlets (6 total signals) Three peaks 200 180 160 140 120 100 60 420 CDS-05-174
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
You are provided with the molecular formula for each compound. calculate the unsaturation index for each problem. -u2C+2+N-X-H For IR, determine the functional groups present and annotate the absorbances that confirm the functional group (including finger print region absorbances). 2 . For 1H NMR, label each signal (a, b, c,.... starting from the right (0.0 PPM). Draw the structure of the compound in the spectra and annotate. 13C NMR spectra is provided for information. Annotation of the 13C NMR is...