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proton source needs to be a very strong acid h2so4
problem 1
equilibrium problem
problem 2
adding an excess of alcohol (reagent) to shift the equilibrium towards products
how is the equilibrium problem solved?
water source; using 100% methanol
problem 3
c=o stretch around 1050–1300 cm and small c-h stretch around 2900 cm from the methyl group
what peaks should we see in our final product ir spectra?
it can hydrolyze the newly formed ester to regenerate the starting carboxylic acid
why do we not want water in our reaction?
methyl benzoate ir

benzoic acid ir

two peaks (flat, small) small around 0.9
what should the gc look like for the final product?