Aspirin can be made in the laboratory by reacting acetic anhydride
\(\left(\mathrm{C}_{4} \mathrm{H}_{6} \mathrm{O}_{3}\right)\) with salicylic
acid \(\left(\mathrm{C}_{7} \mathrm{H}_{6} \mathrm{O}_{3}\right)\) to form
aspirin
\(\left(\mathrm{C}_{9} \mathrm{H}_{8} \mathrm{O}_{4}\right)\) and acetic acid
\(\left(\mathrm{C}_{2} \mathrm{H}_{4} \mathrm{O}_{2}\right) .\) The balanced
equation is:
$$
\mathrm{C}_{4} \mathrm{H}_{6} \mathrm{O}_{3}+\mathrm{C}_{7} \mathrm{H}_{6}
\mathrm{O}_{3} \longrightarrow \mathrm{C}_{9} \mathrm{H}_{8}
\mathrm{O}_{4}+\mathrm{C}_{2} \mathrm{H}_{4} \mathrm{O}_{2}
$$
In a laboratory synthesis, a student begins with \(3.00 \mathrm{~mL}\) of acetic
anhydride (density \(=1.08 \mathrm{~g} / \mathrm{mL}\) ) and \(1.25 \mathrm{~g}\)
of salicylic acid. Once the reaction is complete, the student collects \(1.22
\mathrm{~g}\) of aspirin. Determine the limiting reactant, theoretical yield of
aspirin, and percent yield for the reaction.