Hi! can you please explain step by step how i would go about proposing a structure for this?
I know that DEPT-90 shows CH groups & DEPT-135 shows CH & CH3 in the positive region and CH2 in the negative region. I also know that the normal graph shows the C's. However, i have answer to this question, but I have no idea how they came up with it. Can you please explain step by step your rationale how to make the structure using the information given? i.e. also how we know how many CH's & CH3's we have. Thank you so much!!
Hi! can you please explain step by step how i would go about proposing a structure for this? I know that DEPT-90 shows...
Please give step by step to figuring this out. Please and thank you. (6 pts) Propose a structure for a compound with the the following spectral data. Parent Peak on Mass Spec: 87 IR: medium single peak at 3350 cm-1 Broadband decoupled 13C-NMR 21, 29, 37, 61 δ DEPT-90: 29 δ DEPT-135: positive peaks at 21, 29, 37 δ negative peaks at 61 δ 1H-NMR: 2.42 δ (3 H, singlet) 2.41 δ (2 H, doublet)...
a) Grignard reagents react with oxirane (ethylene oxide) to form 1° alcohols but can be prepared in tetrahydrofuran (THF) solvent. Why is this difference in behavior observed? Explain clearly b) A compound has the formula CsHio, with the 13C and IH NMR spectral data shown. Propose a structure that fits this data. BC NMR Broadband decoupled 13C NMR: 23.5, 26.7, 68.9 δ DEPT-90: no peaks DEPT-135: no positive peaks negative peaks at 23.5, 267, 689 δ HNMR 1.7 δ, multiplet...
33. Propose a structure for Compound X, which has M -120 and (M+2)-122 of approximately equal intensity in its mass spectrum and has the following "C NMR spectral data: (5 points) Broadband decoupled "C NMR: 32.6, 118.8, 134.3 ppm DEPT-90: 134.3 ppm DEPT-135: positive peaks at 134.3 ppm; negative peaks at 32.6, 118.8 ppm
Please help! Q.4. Determine the correct structure of the compound, which shows following 13C NMR DEPT-135 data is 13C NMR DEPT-135: negative peaks at δ30.2, 31.9, 61.8, 114.7 ppm; positive peak at 130.4 ppm
Please help me figure out this structure. If you can, could you include the justifications for the structure, with how each spectra supports it. Will leave many likes. 1. Use the 'H NMR, "C NMR, mass spectrometry and IR data of a compound to determine its structure. IR Spectrum Mass Spectrometry Data relative m und TH NMR Data 13C NMR Data There are two unresolved lines between 130 and 131 ppm. 0 TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 166 140 120 1000 100 80 0...
can you explain how you do each step. i dont know how to do it. 3. Consider a linear string of five hydrogen atoms. a) Draw the five MOs of this molecule, indicating nodal planes with dashed lines, and give the total number of nodal planes. Indicate positive and negative signs of the wavefunction within the MOs. Give the number of positive and negative overlaps, and the net number of positive overlaps. Give the symmetry label for each MO b)...
Hi, I don’t know how to solve? What would be the explanation? Can you please solve for me using step by step? Thank you!
could someone show me step by step for this such as how to go about/get dy/dx etc. i know the final answer is 4 pi ^2 ab , but I can't seem to get there as no one shows the steps when I attempt it I end up with 2pi instead of the correct 4pi 7. (5 points) A torus is obtained by revolving around the y-axis the circle Determine the surface area of this torus 7. (5 points) A...