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- When the 1HNMR spectrum of an alcohol is run in dimethylsulfoxide (DMSO) solvent rather than in chloroform, exchange of the Ο-H proton is slow and spin-spin splitting is seen between the Ο-H proton and C-H protons on the adjacent carbon. What spin multiplicities would you expect for the hydroxyl protons in the following alcohols? (a) 2-Methyl-2-propanol (b) Cyclohexanol (c) Ethanol (d) 2-Propanol (e) Cholesterol (f) 1-MethylcyclohexanolHow could 1H NMR spectroscopy be used to distinguish betweencompounds X and Y?Choose the data that best matches this partial structure; the hydrogens represented by the data are in bold: H H H Od, 2H, 4.0 ppm Os, 2H, 7.1 ppm Od, 2H, 6.8 ppm Ot, 2H, 6.9 ppm H
- ( assign 13C nmr values of each carbon atom do , Do i, ii, iii, iv , v plz with explanation , i will upvote( assign 13C nmr values of each carbon atom do , Do 6, 7 , 8 , 9 , 10 plz with explanation , i will upvoteWhich structure is in agraement with both of thasa R and H NMA data? IR, cm (Intensity)-2965 (strong), 1745 (strong), 1238 (strong) H NMR, ppm (splitting, H): 0.94 (doublet, 6H), 193 (multiplet, 1H), 2.05 (singlet, 3H), 3.8as (doublet, 2H) A. tor B. D. C.
