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Magnesium permanganate is an inorganic compound with the chemical formula Mg(MnO 4) 2. It can be used as an oxidant. ... as a catalyst in the air oxidation of toluene ...
Potassium permanganate is an inorganic compound with the chemical formula ... converted into permanganate by electrolytic oxidation in ... toluene to benzoic acid ...
A permanganate (/ p ər ˈ m æ ŋ ɡ ə n eɪ t, p ɜːr-/) [1] is a chemical compound with the manganate(VII) ion, MnO − 4 , the conjugate base of permanganic acid . Because the manganese atom has a +7 oxidation state , the permanganate(VII) ion is a strong oxidising agent .
It is prepared by the oxidation of 2-chlorotoluene. The laboratory scale reaction employs potassium permanganate. [5] Alternatively it arises by the hydrolysis of α,α,α-trichloro-2-toluene. The chloride is readily replaced by ammonia to 2-aminobenzoic acid.
Toluene (/ ˈ t ɒ l. j u iː n /), also known as toluol (/ ˈ t ɒ l. j u. ɒ l , - ɔː l , - oʊ l / ), is a substituted aromatic hydrocarbon [ 15 ] with the chemical formula C 6 H 5 CH 3 , often abbreviated as PhCH 3 , where Ph stands for the phenyl group.
For example, potassium permanganate dissolves in benzene in the presence of 18-crown-6, giving the so-called "purple benzene", which can be used to oxidize diverse organic compounds. [1] Various substitution reactions are also accelerated in the presence of 18-crown-6, which suppresses ion-pairing. [10] The anions thereby become naked nucleophiles.
The oxidation products derived from methyl are hydroxymethyl group −CH 2 OH, formyl group −CHO, and carboxyl group −COOH. For example, permanganate often converts a methyl group to a carboxyl (−COOH) group, e.g. the conversion of toluene to benzoic acid. Ultimately oxidation of methyl groups gives protons and carbon dioxide, as seen in ...
The oxidation of primary alcohols to carboxylic acids normally proceeds via the corresponding aldehyde, which is transformed via an aldehyde hydrate (gem-diol, R-CH(OH) 2) by reaction with water. Thus, the oxidation of a primary alcohol at the aldehyde level without further oxidation to the carboxylic acid is possible by performing the reaction ...