Chapter 11: Q 11-11-33 E (page 350)
Metabolism of S-adenosylhomocysteine (Section 11-6) involves the following sequence. Propose a mechanism for the second step.
Short Answer
The mechanism for the metabolism of S-adenosylhomocysteine is,
Chapter 11: Q 11-11-33 E (page 350)
Metabolism of S-adenosylhomocysteine (Section 11-6) involves the following sequence. Propose a mechanism for the second step.
The mechanism for the metabolism of S-adenosylhomocysteine is,
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Get started for freePredict the product of each reaction below and indicate if the mechanism is likely to be
When primary alcohol is treated with p-toluenesulfonyl chloride at room temperature in the presence of an organic base such as pyridine, a tosylate is formed. When the same reaction is carried out at a higher temperature, an alkyl chloride is often formed. Explain.
Reaction of the following S to sylate with cyanide ion yields a nitrileproduct that also has S stereochemistry. Explain.
Methyl esters () undergo a cleavage reaction to yield carboxylate ions plus iodomethane on heating with LiI in dimethylformamide:
The following evidence has been obtained: (1) The reaction occurs much faster in DMF than in ethanol. (2) The corresponding ethyl ester () cleaves approximately 10 times more slowly than the methyl ester. Propose a mechanism for the reaction. What other kinds of experimental evidence could you gather to support your hypothesis?
Question:What products would you expect from the reaction of 1-bromopropane with each of the following?
(c) NaI
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