Provided below is the IR and 'H NMR for a compound having the molecular formula of C,H,O, Using this information, determine the degrees of unsaturation for this structure and solve and draw the structure responsible for these spectral data. To validate your answer, you need to assign the type of bond (ie, stretch) responsible for each peak highlighted by a box in the IR. You must also assign each 'H NMR peak (a)-(e) to the correct set of protons in your proposed structure. The integration for each peak has been provided for you. You must label the multiplicity observed for each peak. Is your structure consistent with all of this data? If not, chances are you do not have the correct structure, or the peaks have been assigned incorrectly. In your peer review, offer feedback concerning the accuracy of the submitted structures and spectral assignments. If you believe the answers are incorrect, then you need to provided explanation. In the end, you should all be getting the same correct structure. Please draw the final structure in the box provided underneath the NMR