1). How many signals would you expect to see in 1H-NMR spectrum of each of the following compounds?
2). Assign protons to the peaks in the NMR spectrum of 4,4-dimethyl cyclohex-2-en-1-one in the figure below. Explain the splitting that gives the triplet at 1.8 and 2.4 ppm.
3). Already answered
Due: Fr NAME Chapter 13: NMR HOMEWORK (25 points) (Due on 7/20/2017) 1, How many signals would you expect to see in-H NMR spectrum of each of the following compounds? CH CH CH 2. Assign protons to the peaks in the NMR spectrum of 4,4-dimethyl cyclohex-2-en-1-one in the figure below. Explain the splitting that gives the triplet at 1.8 and 2.4 ppm , CHy δ (ppm) 3. Draw the 'H NMR spectra you would expect for the following compounds and assign the peaks H3 H2 CHy
