Chapter 17: 52P (page 847)
Which of the following compounds decarboxylates when heated?
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Chapter 17: 52P (page 847)
Which of the following compounds decarboxylates when heated?
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What product is obtained from the aldol condensation of cyclohexanone?
Propose a mechanism for the formation of fructose-1, 6-bisphosphate from dihydroxyacetone phosphate and glyceraldehyde-3-phosphate, using hydroxide ion as the catalyst.
Problem: starting with bromocyclohexane, how can each of the following compounds be prepared?

The Reformatsky reaction is an addition reaction in which an organozinc reagent is used instead of a Grignard reagent to add to the carbonyl group of an aldehyde or a ketone. Because the organozinc reagent is less reactive than a Grignard reagent, a nucleophilic addition to the ester group does not occur. The organozinc reagent is prepared by treating an ß-bromo ester with zinc.
Describe how each of the following compounds can be prepared, using a Reformatsky reaction:
A ketone undergoes acid-catalyzed bromination, acid-catalyzed chlorination, racemization, and acid-catalyzed deuterium exchange at the -carbon. All of these reactions have similar rate constants. What does this tell you about the mechanisms of these reactions?
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