In a Baeyer-Villeger reaction, ketones (R_2C = O) ore converted to esters (RCO_2R) by using peroxy acids. With an deformed ketone, brace potential esters can be restraintmed restraint 3, 3-dimethyl-2-butanundivided as starting representative. What are those? How could you reason spectroscopic techniques: 1H NMR, IR and MS to state which ester is restraintmed? Draw and assimilate the structures of ethylene, acetylene, and benzene. Each of these compounds produces solely undivided notable in its 1H NMK spectrum. Arrange these notables in arrange of increasing chemical change. Identify the enumerate of notables expected in the ^13C NMR spectrum of each of the restraintthcoming compounds Redraw and mark it.