Reduction of benzene
Reduction of benzene
Birch Reduction (reagents can also be called Birch Conditions)
Sulfonation of benzene
Reverse Sulfonation of benzene
Nitration of benzene
nitro group reduced to an amine
nitrobenzene to aniline
preparing an aniline from benzene
Friedel-Crafts Acylation
Clemmensen Reduction
Friedel-Crafts Alkylation
Strong Activators, Ortho/Para Directors
Moderate Activators, Ortho/Para Directors
Weak activators, Ortho/Para Directors
Weak Deactivators, Ortho/Para Directors
Strong Deactivators, Meta Directors
Benzene Nomenclature
Toluene
Benzene Nomenclature
Phenol
Benzene Nomenclature
Anisole
Benzene Nomenclature
Aniline
Benzene Nomenclature
Benzoic Acid
Benzene Nomenclature
Benzaldehyde
Benzene Nomenclature
Acetophenone
Benzene Nomenclature
Styrene
Benzene Nomenclature
Chlorobenzene
Benzene Nomenclature
Nitrobenzene
Benzene Nomenclature
Ethylbenzene
Alkylbenzenes oxidized by chromic acid to yield benzoic acid AS LONG AS one benzylic hydrogen is present
will work AS LONG AS one benzylic hydrogen is present
Cumulated Diene
Conjugated Diene
Isolated Diene
Halogenation of Benzene
Aryl diazonium salt to fluorine
diazonium salt to hydrogen
aryl diazonium salt to hydroxyl group
aryl diazonium salt to iodine
aryl diazonium salt to nitrile group
aryl diazonium salt to bromine
aryl diazonium salt to chlorine
Leave in group MUST be ortho or para to electron withdrawing group to form the phenol
creates diazonium salt
cyano group hydrolyzed to carboxylic acid