If you use $6\mathrm{.}0g$ of maleic anhydride in this experiment, approximately how many moles

of maleic anhydride will you be using?

a$.0\mathrm{.}061$mol

b$.0\mathrm{.}074$mol

c$.0\mathrm{.}089$mol

d$.0\mathrm{.}17$mol

If you use $6\mathrm{.}0mL$ of cyclopentadiene, approximately how many moles of

cyclopentadiene will you be using?

a$.0\mathrm{.}061$mol

b$.0\mathrm{.}074$mol

c$.0\mathrm{.}089$mol

d$.0\mathrm{.}17$mol

Which reagent is the limiting reagent in the first reaction, maleic anhydride or

cyclopentadiene?

a$.$ maleic anhydride

b$.$ cyclopentadiene

c$.$ there are the same number of moles of both reagents

Based on your answers to the previous three questions, what is the theoretical yield of

the Diels$-$Alder product $($anhydride$)$ if you follow the procedure as written?

a$.4\mathrm{.}4g$

b$.9\mathrm{.}0g$

c$.10\mathrm{.}0g$

d$.12\mathrm{.}2g$

If you use $4\mathrm{.}0g$ of the Diels$-$Alder product $($anhydride$)$ for the hydrolysis reaction, what is

the theoretical yield of dicarboxylic acid?

a$.4\mathrm{.}4g$

b$.9\mathrm{.}0g$

c$.10\mathrm{.}0g$

d$.12\mathrm{.}2g$