Draw the curved arrow mechanism for the reaction between 4-methy1heptan-2-one and (CH_3)_3 O^- in t-butanol to form an enolate. Draw all electrons and charges on both resonance structures. Select all that describe the reaction and/or resonance structures: Did you show all electrons and charges? Did you show the arrows going to the correct product In each box? Is the reaction reversible or irreversible? beta-deprotonation irreversible reaction reversible reaction thermodynamic enolate anion alpha-doprotonation