C6H5NH2(l) + (CH3CO)2O -?> C6H5NHCOCH3(s)+ CH3COOH(l) Looking at the reaction, you notice that the conjugate base of

C6H5NH2(l) + (CH3CO)2O -?> C6H5NHCOCH3(s)+ CH3COOH(l)

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Looking at the reaction, you notice that the conjugate base of acetic acid is acetate. While acetic acid anhydride is dangerous salting out the acetate with an Arrhenius salt such as sodium bicarbonate yields sodium acetate, which is a harmless salt often added to food products in place of vinegar. Why was this not chosen as our starting material? Looking at the reaction, you notice that the conjugate base of acetic acid is acetate. While acetic acid anhydride is dangerous salting out the acetate with an Arrhenius salt such as sodium bicarbonate yields sodium acetate, which is a harmless salt often added to food products in place of vinegar. Why was this not chosen as our starting material?

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Answer Explanation CH3COOHCH3COOOH On addingCH3COOONadue t... View the full answer