Since the compound that you would have the longest wavelength absorption in its UV spectrum. Explain....
Which of the following compounds would show the Imax of longest wavelength in its UV-Vis spectrum?
5. Identify the base peak in your mass spectrum. 6. Are there other significant isotope patterns in your mass spectrum? If so, what do they indicate? 7. Provide at least one fragment (not the parent ion) that was useful in determining (or confirming) the structure of the unknown and briefly explain how it was useful. Compound 14 is a liquid (b.p. 85") which finds its greatest application as an aprotic solvent UV-transparent; IR-liquid fim. MASS SPECTRAL DATA 99 100 Mass...
8. Give several pieces of data you gathered from the IR spectrum that aided in determining (or confirming) the structure of your unknown. For example, you might mention the presence (or absence) of certain definitive peaks (include wavenumbers). Do NOT use anything from the fingerprint region. 9. Fill in the table below with the information on each unique 1H-NMR signal. You may treat all aromatic protons as a single signal if that helps. Peak Chemical Shift (8) # of *10...
Deduce the ester compound structure with M/Z=136 on this mass spectrum; significant peaks at 51, 77, 105, 136. Relative Abundance M(136) 25 30 35 40 45 50 55 60 65 70 75 80 85 90 95 100 105 110 115 120 125 130 135 140 mz
determine the compound structure based on the spectrums. V (em) 100 Mass Spectrum No significant UV absorption above 210 nm 40E 8 C3H6 O2 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (500 Mrz. Coci, solution) protion coupled proton decoupled 200 80 40 0 δ(ppm) 160 120 H NMR Spectrum (100 MHz, CDC, soluton) TMS expansion 4x 10 9 8 6 5 4 3 2 1 0 6 (ppm) V (em) 100 Mass Spectrum No significant UV...
1. Show all your work calculating the # of Cs based on the Mand (M+1]' peaks. 2. Based on the mass spectrum, do you think your compound has a nitrogen atom? Explain. 3. Propose at least two molecular formulas based on the mass spectrum and calculate the exact mass of the parention. Is one of your formula more likely than the other? If so, explain. Compound 14 is a liquid (b.p. 85") which finds its greatest application as an aprotic...
LThe structure of a compound and its IR spectrum are given below List all the bond types in this molecule that you would expect to observe in the IR spectrum-include both stretches and bends. [6 pts Clearly label on the spectrum which peak corresponds to cach bond type. [6 pts 2 Circle the compound that best fits the IR spectrum for cach part. [3 pts each b) fracr CHe 1. The structure of a compound and its IR spectrum are...
Compound 2 IR Spectrum Chri) 4000 3000 2000 18001200 vom",000 1200000 100 Mass Spectrum UV Spectrum M 220 (1) 2. max 253 nm 0091626) 2. max 250 nm (09, 2.7) 2. max 264 nm (09,06 2.5) PS.... CH2O3 solvent thanol 40 80 120 160 200 240 280 13C NMR Spectrum (100 MHE COCI, solution) DEPT CH CH CH proton decoupled 30 128 ppm 200 - 160 120 80 40 08 (ppm) 'H NMR Spectrum (400MHE. COCI, solution Exchanges wie Do...
Use the data below from an electron impact mass spectrum of a pure compound to deduce its structure. Draw your structure. PART 1: m/z relative intensity 52 31 50 100 15 2 PART 2: m/z Relative intensity 17 1.6 16 100 15 89 14 20 13 11
Use the data below from an electron impact mass spectrum of a pure compound to deduce its structure. Draw your structure in the drawing window. Data selected from the NIST WebBook, https://webbook.nist.gov/chemistry/ m/z Relative intensity 96 94 94 100 15 47