Arrange the following compounds in the order of increasing reactivity toward nucleophilic acyl substitution, with least reactive at the top and most reactive at the bottom. (hint: for carboxylates, think of acid-base chemistry to infer the reactivity).
a. ethyl thioacetate
b. acetyl chloride
c. sodium acetate
d. ethyl acetate
e. acetamide
f. acetic anhydride
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