(Solved): The following Green Diels-Alder Reaction was performed and the product below was formed. Use th ...

The following Green Diels-Alder Reaction was performed and the product below was formed. Use the IR of the product obtained and the tables to prove that the reaction was successful. 

\( \longrightarrow \) anthracene-9-methanol \( R=H, M e, E t \) \[ \begin{array}{c} \mathrm{R}=\mathrm{H}, \mathrm{Me}, \mathrm{Et} \\ \mathrm{R}=\mathrm{Me} \\ \mathrm{mp}=237-239^{\circ} \mathrm{C} \end{array} \] \[ \begin{array}{c} \mathrm{R}=\mathrm{Me} \\ \mathrm{N} \text {-methylmaleimide } \end{array} \] Important \( \mathrm{OH}, \mathrm{NH} \) and \( \mathrm{CH} \) Single Bond Stretching Absorptions Important CC and CN Triple Bond Stretching Absorptions Imnnetant Cr CN and Co Dnuklo Rnnd Strotrhing ahcnrntinnc Infrared Absorption Bands Important CO Single Bond Stretching Absorptions