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Quiz 5 Practice
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Challenge: What would be the product for the following?
SN1
Determine whether the following is Sn1/Sn2/E1 or E2 mechanism
E1,E2,E1
Sn1/E1 rates increase with
Better leaving group, more stable carbocations, polar protic solvents
What are the rate-determining steps in E1 and Sn1 reactions?
Loss of leaving group, carbocation formation
What would be the E2 product for the following reaction.
No reaction.
Give an example of a reagent that will favor Hoffman and one that will favor Zaitsev products
Hoffman = Ethoxide Zaitsev = tert-butoxide
Arrange the following constitutional isomers of C4H9Br in order of increasing reactivity towards SN2. Hint: Table 7.2
Check image
Draw the Sn2 product for (R)-2-bromohexane and NaCN
Check image
Name the following
5-chloro-1,4dimethylcyclohex-1-ene
What does the S, N and the 1/2 stand in Sn1/SN2 reactions?
S for substitution. N for nucleophilic and 1/2 for the order of the rate of reaction.
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