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15
×
Draw the Sn2 product for (R)-2-bromohexane and NaCN
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boom
Lose 50 points!
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star
Double points!
Okay!
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fairy
Take points!
5
10
15
20
25
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baam
Lose 15 points!
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15
×
Determine whether the following is Sn1/Sn2/E1 or E2 mechanism
E1,E2,E1
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15
×
Arrange the following constitutional isomers of C4H9Br in order of increasing reactivity towards SN2. Hint: Table 7.2
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15
×
Challenge: What would be the product for the following?
SN1
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15
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What would be the E2 product for the following reaction.
No reaction.
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monster
Reset all scores!
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gift
Win 20 points!
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shark
Other team loses 15 points!
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lifesaver
Give 5 points!
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boom
Lose 50 points!
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star
Double points!
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shark
Other team loses 5 points!
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thief
Give points!
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25
15
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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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15
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What are the rate-determining steps in E1 and Sn1 reactions?
Loss of leaving group, carbocation formation
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trap
No points!
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rocket
Go to first place!
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shark
Other team loses 25 points!
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lifesaver
Give 25 points!
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15
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Give an example of a reagent that will favor Hoffman and one that will favor Zaitsev products
Hoffman = Ethoxide Zaitsev = tert-butoxide
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15
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Sn1/E1 rates increase with
Better leaving group, more stable carbocations, polar protic solvents
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15
×
Name the following
5-chloro-1,4dimethylcyclohex-1-ene
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