Mechanisms
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Mechanism for acyl chloride to carboxylic acid
Nucleophilic addition elimination H2O
Acyl chloride to amide
Nucleophilic addition elimination NH3
Acyl chloride to N-substituted amide
Nucleophilic addition elimination CH3NH2
Acyl chloride to Ester
Nucleophilic addition elimination CH3OH
Carboxylic acid + alcohol
Esterification Conc H2SO4
Ester to carboxylic acid and alcohol
Acid hydrolysis H2O and conc H2SO4
Ester to sodium salt
Basic hydrolysis NaOH
Benzene to a phenyl ketone
Electrophilic substitution AlCl3 catalyst
Benzene to nitrobenzene
Electrophilic substitution Conc HNO3 Conc H2SO4
Nitrobenzene to amino benzene What is produced
Reduction Sn and H2 Amino benzene and H2O
Anime to quarternary ammonium salt
Nucleophilic substitution Excess haloalkane
Alcohol to ketone
Oxidation Acidified potassium dichromate
Which mechanism uses NaBH4?
Nucleophilic addition Eg reduction of a ketone to an alcohol
Ketone to nitrile
Nucleophilic additon KCN and HCl
Nitrile to amine
Reduction / catalytic hydrogenation H2 and Ni ONLY USE [H] IF THEY SAY otherwise use H2
Ketone to alcohol
Nucleophilic addition Reduction NaBH4
Alkene to haloalkane
Electrophilic addition HBr
Alkene to dibromo-haloalkane
Electrophilic addition Br2
Haloalkane to alkene
Elimination NaoH Hot dissolved in ethanol
Haloalkane to nitrile
Nucleophilic substitution KCN aqueous
Haloalkane to amine
Nucleophilic substitution Excess NH3
Why excess NH3
To prevent further substitution
Haloalkane to alcohol
Nucleophilic substitution NaOH Warm aqueous
Alcohol to aldehyde
Oxidation Acidified potassium dichromate Distillation