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- Q.3. The low resolution mass spectrum of 3-methyl-3-pentanol (see its structure below) shows m/z peaks at 102, 87, 84, and 73. Propose the structures of these peaks. OHG.5 Mass spectra were acquired for 1,4-diethylbenzene and 1-methyl-4- propylbenzene. The base peak of spectrum A is at m/z = 105 and that of spectrum B is at mlz = 119. Match each spectrum to its compound.Draw the structures of the fragments that give rise to the peaks at m/z 43, 57 and 85 in the mass spectrum of 2,4 - dimethylpentane. Thank you!
- 19. Explain the peaks in the following mass spectra: a. 2-pentanone: m/e 86, 71, 57, 43 (100 %) b. 1,2-dichloroethane: m/e 100, 98, 64, 62 (100 %), 51, 49, 27 c. Bromocyclohexane: m/e 163, 161 (both very small), 83 (100 %), 55, 41.The mass spectrum and 13C NMR spectrum of a hydrocarbon are shown. Propose a structure for this hydrocarbon, and explain the spectral data.Which 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.
- Predict the masses and the structures of the most abundant fragments observed in the mass spectra of the followingcompounds.(a) 2-methylpentane (b) 3-methylhex-2-ene (c) 4-methylpentan-2-ol(d) 2-methyl-1-phenylpropaneCalculate the HDI of each FM and propose 2structures for two molecules that are isomers.Specify what the indicated absorption (s) shouldbe to.a.C7H15NO with strong absorptions in 3400, 3270and 1670, 1390, and 1370 cm-1b. C6H10O with absorptions in 2065 (m), 1685 (f),1650 (m) and 970 (f) cm-1c. C9H12O, with absorptions in 1600 and 1500 and1245 cm-1.Q.5. What is the most likely molecular formula of a compound with m/z of 101 for its molecular ion, and m/z of 30 for its base peak in its EI mass spectrum. Write two isomers of this compound (more isomers are possible).
- Following is the mass spectrum of 1-bromobutane. Q.) Propose structural formulas for the cations of m/z 57, 41, and 29.1 (c) 2-Methyl-3-pentanol reacts with PCC to form compound F. (i) Draw the structure of F. (ii) In the mass spectrum, identify the m/z value of the molecular ion peak for compound F. (ii) Fragmentation of radical cation F exhibits two fragment ion peaks at m/z 57 and m/z 71. Propose the structures of these two fragments. (iv) Draw the resonance structure for each of the cation in (iii).Where on the x-axis in the mass spectrum will the M+ be at if themolecule whose structure is attached (C12H16O) is reduced by NaBD4followed by treatment with excess HCl in H2O and isolated?