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- The 1H NMR spectrum of 1,2-dimethoxyethane (CH3OCH32CH2OCH3) recorded on a 300 MHz NMR spectrometer consists of signals at 1017 Hz and 1065 Hz downfield from TMS. (a) Calculate the chemical shift of each absorption. (b) At what frequency would each absorption occur if the spectrum were recorded on a 500 MHz NMR spectrometer?Show that h*c= 1240 eV*nmHow many peaks woudl be observed in the 1H and 13C NMR specutrms of the following compounds?
- Predict the probable structure of a compound with formula Cl,Mn,CgOg, where the mass spectrum included prominent peaks at m/z= 404, 376, 348, 320, 298, 264, 236, 208, 180, 110 and 55 amu.The 1H NMR spectrum of 1,2-dimethoxyethane (CH3OCH2CH2OCH3) recorded on a 300 MHz NMR spectrometer consists of signals at 1017 Hz and 1065 Hz downeld from TMS. (a) Calculate the chemical shift of each absorption. (b) At what frequency would each absorption occur if the spectrum were recorded on a 500 MHz NMR spectrometer?In the electron paramagnetic resonance spectrum ofthe propyl radical, C3H5, the hyperfine splitting constant is1.45 mT for coupl ing to the protons on the terminal carbonatoms and 0.406 mT for coupl ing to the protons attached tothe central carbon atom. Taking 0= 2.25 mT, use the McConnellequation to estimate the unpaired electron density on eachcarbon atom.
- The 'H NMR spectrum of 1,2-dimethoxyethane (CH;OCH,CH2OCH3) recorded on a 300 MHz NMR spectrometer consists of signals at 1017 Hz and 1065 Hz downfield from TMS. (a) Calculate the chemical shift of each absorption. (b) At what frequency would each absorption occur if the spectrum were recorded on a 500 MHz NMR spectrometer?Assign the hydrogens from C9H10O to the spectraAccount for the following observations: (a) The 1H NMR spectrum of cyclohexane shows a single peak at room temperature, but when the temperate is lowered significantly the peak starts to broaden and then separates into two. (b) At room temperature, the 19F NMR spectrum of PF5 shows two lines, and even at the lowest experimentally accessible temperatures the spectrum is substantially unchanged. (c) In the 1H NMR spectrum of a casually prepared sample of ethanol a triplet and a quartet are seen. These multiplets show additional splittings if the sample is prepared with the careful exclusion of water.
- What effect does increasing the operating frequency of a 1H NMRspectrum have on each value: (a) the chemical shift in 5; (b) thefrequency of an absorption in Hz; (c) the magnitude of a couplingconstant J in Hz?For the isomers of C5H10: (a) find # signals, chem shift ranges, integration, splitting (b) match the isomer to the spectrumIndicate two basic differences that exist between the spectra of 1H y 13C in NMR.