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12 Cards in this Set
- Front
- Back
Acid Catalyzed Hydration |
Group header |
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Alkene |
H2SO4, H2O - More subst. Addition of OH group - Carbocation rearrangement - Dilute forms more alcohol, conc. More alkene |
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Alkyne |
Enol-Ketone tautomerization -- forms ketone |
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E1 rxn |
Conc. H2SO4 and heat Works on primary and secondary alcohols
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Primary Alcohol |
Creates symmetrical ether |
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Epoxide |
Sn2 ring opening R-OH attacks more substituted side |
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Halogenation |
Group header |
|
Alkene |
X on more subst. side Carbocation created |
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Alkyne |
X on more subst. Side Excess creates geminal dihalide |
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Alcohols |
Become alkyl halides |
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Ethers |
Primary R group = 2 mol alkyl halide Tertiary R group = sn1, carbocation, alkene second product |
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Epoxides |
Sn2 ring opening |