(Solved): 1. Draw the ketone that is in equilibrium with the given enol below during tautomerization; draw the ...

1. Draw the ketone that is in equilibrium with the given enol below during tautomerization; draw the enol that is in equilibrium with the given ketone or aldehyde \( (0.25 \mathrm{pt}, 0.125 \mathrm{pt} \) each \( ) \) a. b. 2. Draw the kinetic and thermodynamic enolates formed when 3-methylbutan-2-one (aka methyl isopropyl ketone) is treated with a base ( \( \mathrm{Na} \mathrm{OCH}_{3} \), for example). Please make sure to draw the oxide form. not the carbanion form. \( (0.75 \mathrm{pts}, 0.25 \mathrm{pt} \) each) 3. LDA (aka lithium disopropylamide) is a strong, nonnucleophilic base. It is therefore a very useful base in carbonyl chemistry and it can be freshly prepared by treating diisopropylamine with n-butyllithium. Complete this reaction below. \( (0.75 \mathrm{pts}, 0.25 \mathrm{pt} \) each \( ) \)