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(a) Draw what the 'H NMR and 13C NMR spectrum for ONE of the compounds ONE of the boxes below would look like. Be
(a) Draw what the 'H NMR and 13C NMR spectrum for ONE of the compounds ONE of the boxes below would look like. Be sure to clearly label the H's / C's in the compound as well as their signals in the spectrum (see D2L for example if you're not sure). cpd A cpd B cpd M cpd N cpd X cpd Y (b) Now give TWO very specific and easy to spot differences that you would see in the 'H NMR spectrum for the OTHER compound in the box you chose. Please do NOT just give the entire spectrum of the 2nd compound, but state a difference in signals that allows you to tell if you have the compound on the left or the right. Be sure to explain your answer.
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In cpd A due to symmetry all the protons have an equivalent proton from the other half The characterestic peaks are 1 protons on Carbons 9 and 10 at 5...Get Instant Access to Expert-Tailored Solutions
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