2. Keeping in mind that a better base is also generally a better nucleophile (I had to get that in one last time!), a compound such as nicotine has two potentially nucleophilic sites. If you react nicotine with one equivalent of methyl iodide, show what the two products could be and explain how you could use spectroscopy to tell which is formed. 3. Two of the key reactions that we considered in this last section of the class both feature catalytik cycles. Pick one of the two following reactions and provide the reaction product as well as the catalytic cycle for the reaction, If you do both, the second will be counted as extra credit. (HO)B. Pd cat NaOH PCy CI Ph PCys HO,

2. Keeping in mind that a better base is also generally a better nucleophile (I had to get that in one last time!), a compound such as nicotine has two potentially nucleophilic sites. If you react nicotine with one equivalent of methyl iodide, show what the two products could be and explain how you could use spectroscopy to tell which is formed. 3. Two of the key reactions that we considered in this last section of the class both feature catalytik cycles. Pick one of the two following reactions and provide the reaction product as well as the catalytic cycle for the reaction, If you do both, the second will be counted as extra credit. (HO)B. Pd cat NaOH PCy CI Ph PCys HO,

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter13: Substitution

Section: Chapter Questions

Problem 4E

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