Reaction Conditions Flashcards
Alkene → Alkane (Hydrogenation)
H₂(g), Pt/Ni catalyst, heat
Alkane → Shorter Alkanes + Alkenes (Cracking)
Heat with Al₂O₃
Alkane → CO₂ + H₂O (Complete Combustion)
Excess O₂
Alkane → CO + C (Incomplete Combustion)
Limited O₂
Alkane → Halogenoalkane (Free Radical Substitution)
Cl₂ or Br₂, UV light
Halogenoalkane → Alkene (Elimination)
Ethanolic NaOH, heat
Alcohol → Alkene (Dehydration)
Heated catalyst (Al₂O₃) or conc. H₂SO₄
Alkene → Alkane (Hydrogenation)
H₂(g), Pt/Ni catalyst, heat
Alkene → Alcohol (Hydration)
Steam, H₃PO₄ catalyst, heat
Alkene → Halogenoalkane (Electrophilic Addition)
HX(g), room temperature
Alkene → Dihalogenoalkane (Electrophilic Addition)
X₂ (e.g., Br₂)
Alkene → Diol (Oxidation)
Cold dilute acidified KMnO₄
Alkene → Carbonyl Compounds (Oxidation)
Hot concentrated acidified KMnO₄
Alkene → Polymer (Addition Polymerisation)
Polymerisation conditions
Alcohol → Halogenoalkane (Substitution)
HX(g), KCl + conc. H₂SO₄, or SOCl₂
Alcohol → Aldehyde (Oxidation)
Acidified K₂Cr₂O₇, distillation
Alcohol → Carboxylic Acid (Oxidation)
Acidified K₂Cr₂O₇, reflux
Aldehyde → Primary Alcohol (Reduction)
NaBH₄ or LiAlH₄
Ketone → Secondary Alcohol (Reduction)
NaBH₄ or LiAlH₄
Aldehyde/Ketone → Hydroxynitrile (Nucleophilic Addition)
HCN, KCN catalyst, heat
Carboxylic Acid → Primary Alcohol (Reduction)
LiAlH₄, dry ether
Carboxylic Acid + Alcohol → Ester (Esterification)
Conc. H₂SO₄, heat under reflux
Ester → Carboxylic Acid + Alcohol (Hydrolysis)
Dilute acid or alkali, heat
Halogenoalkane → Alcohol (Nucleophilic Substitution)
NaOH(aq), heat