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Reactions between Alkanes & Alkenes
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Alkanes: Free radical substitution - Halogenation
Reagent: Cl2 or Br2 in CCl4
Condition: In UV-light, reaction does not occur in dark
Product: Chloro/Bromoalkanes
Alkanes: Catalytic cracking
Reagent: Al2O3 or Silica
Condition: Heat up to 500 celsius
Product: At least 1 each of alkane & alkene
Alkanes: Combustion
Excess Oxygen → Co2
Limited Oxygen → Co
Very limited Oxgyen → C
Alkenes: Hydrogenation (Addition of hydrogen)
Reagent: H2 (g)
Condition: Heat up with Ni catalyst or RT with Pt catalyst
Product: Alkane
Alkenes: Addition of halogens (halogenation)
Reagent: X2 in CCl4
Condition: Room temp (w/o UV light)
Product: Halogenoalkane
Alkenes: Addition of hydrogen Halides (Markovnikoff’s rule)
Reagent: HX
Condition: Room temp
Product: Halogenoalkane
Rate of reaction matters due to bond length between HX
Major product is following the rule, more stable. Vice versa for minor product.
Alkenes: Hydration (Addition of steam)
Reagent: H20 (g)
Condition: Heat, conc H3Po4 (catalyst), 300 degrees, 70atm
Product: Alcohols
Alkenes: Oxidation by Cold Dilute MnO4-
Reagent: KMnO4 + diluted H2So4
Condition: Cold
Product: Diols
Alkenes: Oxidation by Hot conc MnO4-
Reagent: Hot conc KMnO4 + diluted H2So4
Condition: Heat or heat under reflux
Product:
CO2 + H20 if Primary
Aldehyde → Carboxylic acid if Secondary
Ketone if Tertiary