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The question I want you to answer is: which chiral centers have different chirality in D-glucose as compared to L-gulose. To give you an idea of what I'm asking, compare the chirality at carbon 2, 3, and 4 in D-glucose to the chirality at carbon 2,3, and 4 in D-idose. You'll see that they're opposite at carbon 2; they're the same at carbon 3; and they're the same at carbon 4. So the only difference is at carbon 2. So I'm asking you to perform the same analysis, but this time comparing D-gluocse to L-gulose. You can see D-gulose on the chart; L-gulose has the opposite chirality from it.
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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