(Solved): Hydroboration-oxidation of an internal alkyne using Sia \( _{2} \mathrm{BH} \) followed by \( \math ...

Hydroboration-oxidation of an internal alkyne using Sia \( _{2} \mathrm{BH} \) followed by \( \mathrm{H}_{2} \mathrm{O}_{2} / \mathrm{OH}^{-} \)will lead to the formation of: alkene carboxylic acid aldehyde ketone Question 2 5 pts How will you convert aniline to p-nitroaniline? 1) convert the amine to amide 2) carry out the nitration reaction 3) hydrolyze the amide to amine react aniline with \( \mathrm{H}_{2} \mathrm{SO}_{4} / \mathrm{HNO}_{3} \) use excess \( \mathrm{H} 2 \mathrm{SO} 4 / \mathrm{HNO} 3 \) since the amino group is acidic in nature. use excess \( \mathrm{H}_{2} \mathrm{SO}_{4} / \mathrm{HNO}_{3} \) since the amino group is basic in nature. Hydrolysis of a cyanohydrin using \( \mathrm{H}_{2} \mathrm{O} / \mathrm{H}^{+} \)leads to the formation of: beta-hydroxy acids delta-hydroxy acid gamma-hydroxy acid alpha-hydrox?y acids