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Starting with an aqueous solution of fully deprotonated isoleucine (draw the structure of this form of isoleucine!), would you need to add strong acid or strong base to fully protonate the amino acid (draw the structure of this form of isoleucine!)? How many equivalents of strong acid/base would you need until half of isoleucine's a-carboxyl groups have been protonated? Explain and draw the structure of this form of isoleucine! What is the protonation state of the a-amino group at this point?
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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