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A certain aldose is added to an aqueous sodium hydroxide solution. After equilibrium is reached it is found that there are 3 open chain sugars in the solution. It is believed that the original aldose tautomerizes to the enediol which then tautomerizes back to a carbonyl containing open chain sugar. One of the three is L-xylulose.
Draw the enediol that is believed to be the intermediate.
Show all the steps in the mechanism for the following reaction, When benzene is mixed with deuterated sulfuric acid, deuterium is slowly incorporated onto the ring. Show the mechanism for this reaction and explain how this relates the sulfonation of ..
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