Sketch the expected proton NMR for each of the compounds (include relative integration of each signal)
Can you please explain how to solve NMR H1 for these, including how to do ratios/integration. Very confusing I can't get past these. Thank you so much, the more info the better!
Problem 17.1 Sketch the expedted proton NMR for each of the compounds listed below. You should give the approximate chemical shift for each type of hydrogen in each sample (see Table 17.2), as well as the relative integration of each signal in the spectrum. (a) chloromethyl methyl ether (b) 1,2,4,5-tetramethylbenzene (c) 1,4-dihydroxybenzene (d) 1,4-dimethoxybenzene (e) di(2,2-dichloropropyl) ether (answer) The Phenomenon of Spin-Spin Splitting First Order Coupling Interactions - Consider yet another proton NMR spectrum of a relatively simple molecule, wherein a complication is introduced to the types of observations we have made thus far. To this point we have developed an understanding of chemical shift as well as integration of spectra. Fortunately, for structural analysis purposes, there is more to NMR than this. Ethyl cyanoacetate - The 400 MHz proton NMR spectrum for ethyl cyanoacetate (17.5) neeted since there are three different tynes of hydrogen