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Organics CHEM5

ReactionConditions
Alkene – Alcohol Electrophilic Addition, H2SO4, warm H20
Alcohol – Alkene Elimination, conc. H2SO4 or H3PO4
Alcohol – Aldehyde Pot. Dich., Heat, distil, partial oxidation
Aldehyde – Alcohol Nucleophilic Addition, Reduction, NaBH4
Aldehyde – Carboxylic Acid Pot. DIch., heat under reflux with excess [O]
Acyl Chloride or Acid Anhydride – Carboxylic Acid Nucleophilic Addition, H2O, room temperature
Carboxylic Acid – Ester Alcohol, H2SO4
Acyl Chloride or Acid Anhydride – Ester Nucleophilic Addition-Elimination, Alcohol, room temp
Alcohol – Ester Carboxylic Acid, H2SO4 (or Acyl Chl. Or Acid Anh.)
Alkene – Haloalkane Electrophilic Addition, HBr, room temp
Haloalkane – Alkene Elimination, KOH (Alcoholic), reflux
Haloalkane – Alcohol Nucleophilic substitution, KOH aqueous, reflux
Alkane – Haloalkane Free Radical Substitution, Cl2, UV light
Haloalkane – Nitrile Nucleophilic substitution, KCN in alcohol, reflux
Haloaklane – Amine Nucleophilic Substitution, Alcoholic NH3, heat + pressure
Nitrile – Amine H2,Ni,200C,LiAlH4
Amine – Amide Acyl Chloride or Acid Anhydride
Acyl Chloride or Acid Anhydride – Amide Nucleophilic Addition-Elimination, NH3, room temp
Alkene – Polyalkene Catalyst, High Pressure
Alcohol – Ketone Pot. Dich., reflux, H2SO4
Ketone – Alcohol Nucleophillic Addition, NaBH4 reduction
Ketone – 2-Hydroxynitrile Nucleophilic addition, aqueous KCN with H2SO4
Created by: joshsnyder
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