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Question 80 is about the substitution of acid derivatives, but I'm very confused because I thought that you needed an acid or base catalyst for all of the substitutions for acid derivatives except for the substitution of acyl chlorides which are highly reactive on their own. Also, I was under the impression that unless you heated the reaction, you wouldn't get a good yield by going from a less reactive acyl substitution to a more reactive acyl substitution. Especially with a reaction between acetic acid and an alcohol because the formation of an ester from a carboxylic acid would be an endothermic reaction? Yet the problem here says that all of the choices presented are correct? I'm just confused. My textbook says one thing and the solution says another! Is there something that I'm missing? Any further explanation would be greatly appreciated.