SN1, SN2,

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SN1, SN2, E1, E2, NR
Most Reactive Nucleophile
Most Reactive Alkyl Halide
Epoxides
Synthesis
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(No Transcript)
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What is SN2?
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What is NR?
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What is E2?
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What is SN1?
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What is SN2?
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• Of these nucleophilesCH3O-, CH3OH, CH3CO2-

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What is CH3O-?
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• In water, CH3Se-, CH3O-, CH3S-

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What is CH3Se-?
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In DMF, I-, Br-, Cl-, F-
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What is F-?
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• (CH3)2NH, CH3NH2, CH3OH, (CH3)3N

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What is CH3NH2?
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What is A?
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• For SN2, HCCI, CH2CHI, CH3CH2I, FCH2CH2I

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What is CH3CH2I?
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Daily Double

• For SN1, (CH3)3CBr, Cl3C(CH3)2CBr, CH3O(CH3)2CBr

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What is CH3O(CH3)2CBr?
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• For E1, C6H5CH2Cl, (C6H5)3CCl, (C6H5)CHClCH3,
  (C6H5)CH2CH2Cl

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What is (C6H5)CHClCH3?
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• For SN2,
• BrCCCH2Br, HCCCHBr2, HCCCBr3, HCCCH2Br

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What is HCCCH2Br?
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For E2
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What is D?
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The major organic product
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What is 2-methyl-2-butanol?
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The major organic product
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What is 2-bromo-2-methyl-1-propanol?
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The correct mechanism
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What is B?
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A reaction NOT forming epoxide
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What is A?
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The size of the ring formed
Daily Double
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What is a 6-sided ring?
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A synthetic route
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What is react compound A with BH3, then alkaline
H2O2, next PBr3, and finally cyanide?
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Retrosynthetic analysis
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What is
?
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Retrosynthetic analysis
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What is
?
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Retrosynthetic analysis
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What is
?
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Retrosynthetic analysis
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What is
?