In water, a small amount of acetone is present in a form that is known as an enol: a) Explain why the enol of acetone is not a resonance structure of acetone b) To generate this enol, the first step in the process can be to deprotonate one of the hydrogens from one of acetone's methyl groups: H+ Although this deprotonation is not easy, it is easier to remove one of these hydrogens from acetone than an analogous hydrogen in 2-propanol. Which of the following explains this difference (hint - notice this reaction resembles the relatively facile deprotonation of acetic acid)? [ Select ] The anion is stabilized by a resonance structure with the negative charge on the oxygen The anion is stabilized by hydrogen bonding to the hydroxyl group of 2-propanol Carbon anions are relatively stable species 2-propanol does not have an electronegative oxygen attached to the 2 nd carbon position