The eirzyme aconitase catalyzes a reaction of the Krebs cycle (see Fig. P10.57), an important biochemical pathway. In this equation, *C = 14C, a radioactive isotope of carbon, and each ---CO2- group is the conjugate base of a carfoxylic acid group. Notice that the dehydration occurs toward the branch of citrate that does not contain the radioactive carbon. Imagine carrying out this dehydration in the laboratory using a strong acid such as H3PO4 or H2SO4. How would the product(s) of the reaction be expected to differ, if at all, from those of the enzyme -catalyzed reaction, and why?