PHASE 1

Oxidation of aromatic carbon atoms (aromatic hydroxylation)

Oxidation of Olefins (C=C BONDS)

Oxidation of Olefins (C=C BONDS)

Oxidation of allylic carbon atoms

Oxidation of carbon atoms alpha to carbonyls and imines

Oxidation of aliphatic carbons atoms (aliphatic hydroxylation)

Oxidation of alicyclic carbon atoms (alicyclic hydroxylation)

N-dealkylation

N-hydroxylation

S-dealkylation

Desulfuration

Desulfuration

S-oxidation

Chloropromazine undergo

O-dealkylation 

O-dealkylation

O-dealkylation

O-dehalogenation

Hepatic microsomal flavin containing monooxygenases  (S-Oxidation)

Alcohol dehydrogenase

Xanthine oxidase

Amine oxidase (N oxidation)

Reductive reaction (-N=N- ——> NH₂ + NH₂)

Reduction of Nitrogroup

Reduction of carbonyls

Reduction of aliphatic aldehydes 

Reduction of aliphatic ketones

Reduction of aliphatic ketones

Reduction of alicyclic ketones

Reduction of aromatic ketones

Reduction of dehalogenation

Ester hydrolysis

Amide hydrolysis (slower)

Carbonate hydrolysis 

Carbamate hydrolysis

Urea hydrolysis

Hydrazide hydrolysis

Hydrolysis of esters (Inorganic acid esters)

Hydrolysis of esters (Hydrolysis of amide (C-N cleavage) - secondary amide with aliphatic substitution

Hydrolysis of esters (Hydrolysis of amide (C-N cleavage) -Secondary amide with aromatic substitution

Hydrolysis of esters (Hydrolysis of amide (C-N cleavage) - tertiary amide