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2) What would happen if the product mixture was washed with aqueous sodium bicarbonate before being washed with water? Could the product still be isolated? Explain your answer. Draw the alcohol and carboxylic acid needed to synthesize the ester below. Place an arrow next to the oxygen in the carboxylic acid or alcohol that corresponds to the oxygen indicated by the arrow in the ester below. 3) 4) Given the following reagents, dichloromethane, water, acetone, 10% aqueous HCl, 10% aqueous NaHCO3 and anhydrous sodium sulfate, devise a method to separate 4-methylphenyl acetate from the rest of the reaction mixture for the reaction below. OH H,so
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