Abstract
Some six and seven membered saturated hetero cyclic compounds were prepared. 1H NMR spectra were recorded in DMSO - d6. The chemical shifts were compared with those in CDCl3. The COSY, NOESY and 13C‒1H correlation spectra had been recorded to assign the signals unambiguously. The coupling constant of benzylic proton with one of the vicinal proton was found to be zero. The buttressing effect of alkyl groups was also studied. The chemical shift values, area of the signals, multiplicity, COSY and NOESY spectra were used to assign the signals. Further COSY and NOESY and 13C‒1H correlation spectra were also used. The solvent effect, concentration effect, and temperature effect were also studied using DMSO- d6 and CDCl3 α- effect and polar nature of the neighbouring group were also studied.
Highlights
Ever since Barton pointed out the importance of conformational analysis, there has been a rapid development in the conformational analysis of various systems
Nuclear magnetic resonance spectroscopy is a powerful tool for such analysis. 1H, 13C, 15N, 17O and 33S are the nuclei used for analysis
Nowadays 2–D –NMR spectroscopy is used for structural diagnosis
Summary
Ever since Barton pointed out the importance of conformational analysis, there has been a rapid development in the conformational analysis of various systems. Nuclear magnetic resonance spectroscopy is a powerful tool for such analysis. 1H, 13C, 15N, 17O and 33S are the nuclei used for analysis.. Nowadays 2–D –NMR spectroscopy is used for structural diagnosis. The important measurables in the 1H NMR spectra are Chemical Shifts and Constants. Chemical shift of a proton is affected by the electron density around it; the higher the electron density, the higher the field of absorption. The chemical shifts for CH3I, CH3Br, CH3Cl, and CH3F are 2.16, 2.68, 3.05 and 4.26 ppm respectively. The values are in line with the inductive effects of the halogen atoms
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