Organic reactions and conditions

    Cards (25)

    • Alkene to Alkane:
      • type of reaction: electrophilic addition
      • reagents: H2(g) Ni catalyst
      • conditions: 150ºc and 5 atm
    • Alkene to Haloalkane:
      • type of reaction: electrophilic addition
      • reagents: HBr(aq)
      • conditions: room temp
    • Alkane to Haloalkane:
      • type of reaction: radical substution
      • reagents: halogen
      • conditions: UV light
    • Haloalkane to Amine:
      • type of reaction: nucleophilic substitution
      • reagents: c. NH2 (aq)
      • conditions: heat in a sealed tube
    • Haloalkane to Alcohol:
      • type of reaction: nucleophilic substitution
      • reagents: NaOH (aq)
      • conditions: reflux
    • Alcohol to haloalkane:
      • type of reaction: nucleophilic substitution
      • reagents: c. H2SO4
      • conditions: reflux
    • Haloalkane to Nitrile:
      • type of reaction: nucleophilic substitution
      • reagents: NaCN (aq) in ethanol
      • conditions: reflux
    • Nitrile to Carboxylic Acid:
      • type of reaction: substitution
      • reagents: H2O
      • conditions: reflux
    • Alcohol to Alkene:
      • type of reaction: elimination
      • reagents: Al2O3
      • conditions: 300ºc
    • Alcohol to Aldehyde:
      • type of reaction: oxidation
      • reagents: acidified potassium dichromate and c. H2SO4
    • Aldehyde to Alcohol:
      • type of reaction: reduction
      • reagents: NaBH4
    • Aldehyde to Carboxylic Acid:
      • type of reaction: oxidation
      • reagents: acidified potassium dichromate and c. H2SO4
      • conditions: reflux
    • Carboxylic Acid to Ester:
      • type of reaction: esterification
      • reagents: Alcohol and c. H2SO4
      • conditions: reflux
    • Ester to Carboxylic Acid:
      • type of reaction: hydrolysis
      • reagents: H2O
    • Carboxylic Acid to Acyl Chloride:
      • type of reaction: substitution
      • reagents: SCl2O
      • conditions: reflux
    • Acyl Chloride to Primary Amide:
      • type of reaction: acylation
      • reagents: c. NH2 (aq)
      • conditions: room temp
    • Acyl Chloride to Secondary amide:
      • type of reaction: acylation
      • reagents: amine
      • conditions: room temp
    • Acyl Chloride to Ester:
      • type of reaction: acylation
      • reagents: alcohol
      • conditions: room temo
    • Bromination of Benzene:
      • type of reaction: electrohilic substitution
      • reagents: Br2 (l) Fe catalyst
      • conditions: room temp
    • Chlorination of Benzene:
      • type of reaction: electrophilic substitution
      • reagents: Cl2 (g) AlCl3 catalyst
      • conditions: room temp
    • Sulfination of Benzene:
      • type of reaction: electrophilic substitution
      • reagents: c. H2SO4
      • conditions: reflux
    • Alkylation of Benzene:
      • type of reaction: electrophilic substitution
      • reagents: R-Cl and AlCl3 catalyst
      • conditions: reflux
    • Acylation of Benzene:
      • type of reaction: electrophilic substitution
      • reagents: R-COCl and AlCl3 catalyst
      • conditions: reflux
    • Nitration of Benzene:
      • type of reaction: electrophilic substitution
      • reagents: c. HNO3 and c. H2SO4
      • conditions: greater than 55ºc
    • Amine to Nitrated Benzene:
      • type of reaction: reduction
      • reagents: Sn catalyst c. HCl
      • conditions: reflux
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