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21 Cards in this Set

  • Front
  • Back
5 Alkene reactions
(Addition)
Hydrohalogenation
Hydration
Halogenation
Hydroxylation (oxidation)
Hydrogenation (reduction)
Anti addition ( alkenes)
Halogenation
Syn additon ( alkenes)
Hydroxylation (oxidation)
Hydrogenation (reduction)
Oxonium Ion
Hydration (H3O)+
- acid catalysed (H+)
Halonium Ion
Halogenation (Anti)
CO2 ---> CH4 (oxidation number?)
Carbon Reduced +2 to -4
Nucleophilic
Excess of electrons
Wants to give
Electrophilic
Electron deprived (loss of e)
wants to share
Alkene additon reaction
rate of reaction determined by?
Carbocation stability
Carbocation stablity why?
Correct predition of product (% yield)
Rate of reaction per product
Rate determining step (alkene addition rxtn)
1st step (electrophilic attack)
outcome of Alkene addition reaction
if asymmetrical alkenes then possible regioisomers
product stereoselective
Stability of Alkene rxtn determined by
Resonance and Induction
- resonance outweights induction
-SP3 and lone pairs ideal
Halogens stabilize
negative charge (not positive)
note* carbocation is positive, not a good selection
Regioisomers - what kind of isomers
constitutional/structural
* same formula different structure
addition of polar AB to pi bond by common sequence of steps (reaction mechanisms)
Electrophilic addition reaction
-electrophilic= determines rxtn rate
-nucleophilic attacks stable carbocation
Thermodynamics of
Electrophilic (1st step)
Nucleophilic
Endothermic (2 bonds broken 1 made)
Exothermic (2nd step) fast!
Carbocation stablility....what rule?
Markovinov's Rule
carbocation stability (thermodynamically)
In Alkenes, the reactive group is
Double bonds (pi bonds)
Addition over metal (alkenes)
Hydration (reduction) H2
syn addtion
Oxidation of Oxonium tetraoxide (OsO4)
Oxidtion of Potassium permanganate (KMnO4)
Hyroxylation ( oxidation rxtn)
syn addtion of "OH" to both carbons