Chapter 11: Q47cE (page 350)
Question: Predict the product and give the stereochemistry resulting from reaction of each of the following nucleophiles with (R)-2-bromooctane:
(c)
Short Answer
Answer
Chapter 11: Q47cE (page 350)
Question: Predict the product and give the stereochemistry resulting from reaction of each of the following nucleophiles with (R)-2-bromooctane:
(c)
Answer
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Get started for freeThe following Walden cycle has been carried out. Explain the results, and indicate where Walden inversion occurs.
Which compound in each of the following pairs will react faster in an SN2reaction with OH-?
(d)
Which reaction in each of the following pairs would you expect to be faster?
(b) Thedisplacement byon bromoethane or on bromocyclohexane
Which isomer would you expect to undergo E2 elimination faster, trans-1-bromo-4-tert-butylcyclohexane or cis-1-bromo-4-tert-butylcyclohexane? Draw each molecule in its more stable chair conformation, and explain your answer.
What effect would you expect the following changes to have on the rate of thereaction of 1-iodo-2-methylbutane with cyanide ion?
(b) Both theand the 1-iodo-2-methylbutane concentrations are tripled.
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