Chemistry Conditions 0.0 / 5 ? ChemistrySynthesis RoutesA2/A-levelEdexcel Created by: DavidCreated on: 03-02-14 18:46 Alkane to Bromoalkane Br2, U.V. Light 1 of 23 Alkene to Alkane H2(g), 150 Degrees Celsius, Ni Catalyst 2 of 23 Bromoalkane to Alkene NaOH / Ethanol Reflux 3 of 23 Bromoalkane to Primary Amine NH3 / Ethanol Reflux 4 of 23 Alkene to Bromoalkane HBr 20 Degrees Celsius 5 of 23 Alkene to Dibromoalkane Br2 20 Degrees Celsius 6 of 23 Bromoalkane to Alcohol NaOH(aq) Reflux 7 of 23 Alcohol to Bromoalkane NaBr H2SO4 Reflux 8 of 23 Alcohol to Aldehyde / Ketone K2Cr2O7, H2SO4, Heat then Distill 9 of 23 Aldehyde / Ketone to Alcohol LiAlH4 (dry ethyl ether) Heat 10 of 23 Aldehyde / Ketone to Carboxylic Acid K2Cr2O7, H2SO4, Reflux 11 of 23 Aldehyde / Ketone to Hydroxynitrile HCN, Ethanol, Reflux 12 of 23 Carboxylic Acid to Alcohol LiAlH4 (dry ethyl ether) Heat 13 of 23 Carboxylic Acid to Ester Alcohol, H+ Catalyst, Reflux 14 of 23 Ester to Carboxylic Acid H+ (aq), Reflux 15 of 23 Nitrile to Carboxylic Acid HCl (aq), Reflux 16 of 23 Carboxylic Acid to Acyl Chloride PCl5, 20 Degrees Celsius 17 of 23 Acyl Chloride to Carboxylic Acid H2O, 20 Degrees Celsius 18 of 23 Acyl Chloride to Ester Alcohol, 20 Degrees Celsius 19 of 23 Acyl Chloride to N-Substituted Amide Amine, 20 Degrees Celsius 20 of 23 Acyl Chloride to Primary Amide NH3, 20 Degrees Celsius 21 of 23 Phenol to 2,4,6-Tribromophenol Bromine Water, 20 Degrees Celsius 22 of 23 Phenol to 2-Nitrophenol + 4-Nitrophenol Dilute Nitric Acid 23 of 23
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