The following questions apply to the Electrophilic Aromatic Substitution (EAS) Nitration of Methyl Benzoate which yields Methyl m-Nitrobenzoate as the product:1) Draw and name the other possible EAS mono-nitration products that may be formed in addition to the desired methyl m-nitrobenzoate.2) If you perform an EAS nitration reaction with methyl m-nitrobenzoate as the reactant, which isomer is the major product? (At which ring position do you expect substitution to occur?) Draw and name the expected product.3) Suggest two ways to determine if the impure methyl m-nitrobenzoate (before recrystallization) contains other substitution products as impurities.4) Discuss differences you'd expect to see in IR, 1H and 13C NMR spectra of methyl benzoate vs. methyl m-nitrobenzoate that are consistent with the formation of the product in this procedure.