Organic Equations Flashcards
Alcohol to Ester
Carboxylic Acid, conc H2SO4/H3PO4 or
Acyl Chloride or
Acid anhydride

The reaction of an alkane to haloalkane
Free radical substitution
Halogen
The reaction of haloalkane to amine
NH3 and Heat
Nucleophilic Substitution
Aldehyde to Carboxylic acid
K2Cr2O7 heat
Tollen’s reagent
Fehling’s solution
Reflux
Acylation of benzene
Acyl chloride/ acid anhydride
Alkyl hydrogen sulphate to Alcohol
Dilute and warm
Nitration of benzene
conc HNO3
conc H2SO4
50 degrees
2y Alcohol to ketone
Heat acidified potassium dichromate
K2Cr2O7

The reaction of an alkene to haloalkane
HX
X = halogen
Electrophilic addition
Haloalkane to Nitrile
Nucleophilic substitution
KCN dissolved in ethanol with heat
The reaction of Haloalkane to alkene
KOH
ethanol hot
Elimination
The reaction of an alkene to alkyl hydrogen sulphate
Conc H2SO4
Electrophilic Addition
The reaction of Alkene to Alcohol
H3PO4 + Steam/H2O
High temp and pressure
Hydration of alkene

phenylethanoate to phenyl ethanol
NaBH4
The reaction of Alcohol to an alkene
Dehydration
H2SO4
180 degrees

The reaction of Amine to Amide:
Acyl chloride
Dry
Nucleophilic addition to elimination
Nitrile to Amine
LiAlH4 or
H2, Ni 200 degrees
Reduction of nitrile
Alcohol to Aldehyde
Oxidation
[O]
Acidified potassium or sodium dichromate
The product should be syphoned away and cooled as produced
Alkene to alkane
Hydrogenation
H2
Nickel catalyst
200 degrees
Carboxylic acid to ester
Alcohol
conc H2SO4
Nitrobenzene to phenylamine
Sn, conc HCl
then NaOH
Aldehyde to 2-Hydroxynitrile
HCN
Nucleophilic Addition
Aldehyde to Alcohol
Reduction of aldehyde
NaBH4
[H+]

Phenylamine + acyl chloride/acid anhydride
forms N-phenylamide
Benzene to cyclohexane
Hydrogenation
H2/
Nickel Catalyst
Amine to Amide
Acid Anhydride
ACid anhydride
dry
Nucleophilic addition and elimination
The reaction of haloalkane to alcohol
NaOH
Warm
Nucleophilic Substitution
Ketone to 2-hydroxynitrile
HCN
Nucleophilic Addition
Ketone to 2y Alcohol
NaBH4(aq)

Nitrile to Amine
H2, Ni 200C
H2, Ni 200C or
LiAlH4
Reduction of nitrile