When toluene reacts with potassium permanganate in the presence of sodium carbonate, the permanganate will oxidize the toluene to form benzoic acid. The sodium carbonate will help neutralize any acidic byproducts formed during the reaction.
Ferrous chloride in presence of hydrochloric acid gives brown precipitates of Ferric chloride with potassium permanganate.
One version would be CH3C6H5.
The reaction between acidified potassium permanganate and toluene results in the oxidation of toluene to benzoic acid. The balanced chemical equation for this reaction is: C7H8 + 2KMnO4 + 8H2SO4 → 2MnSO4 + K2SO4 + 7H2O + 7H2O + C6H5CO2H
When toluene reacts with chlorine in the presence of sunlight, a substitution reaction occurs where one or more hydrogen atoms in the toluene molecule are replaced by chlorine atoms. This reaction can result in the formation of different chlorinated derivatives of toluene, such as benzyl chloride or benzal chloride, depending on the conditions and the position of the substitution on the benzene ring.
Yes, toluene will undergo bromination. When treated with bromine in the presence of a Lewis acid catalysts such as FeBr3 or AlBr3, toluene will undergo electrophilic aromatic substitution to form bromotoluene as the major product.
Acidic conditions promote the oxidation of toluene by potassium permanganate.
Ferrous chloride in presence of hydrochloric acid gives brown precipitates of Ferric chloride with potassium permanganate.
One version would be CH3C6H5.
The reaction between acidified potassium permanganate and toluene results in the oxidation of toluene to benzoic acid. The balanced chemical equation for this reaction is: C7H8 + 2KMnO4 + 8H2SO4 → 2MnSO4 + K2SO4 + 7H2O + 7H2O + C6H5CO2H
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The solution of potassium iodide (if it is not extremely diluted) is more dense.
When toluene reacts with chlorine in the presence of sunlight, a substitution reaction occurs where one or more hydrogen atoms in the toluene molecule are replaced by chlorine atoms. This reaction can result in the formation of different chlorinated derivatives of toluene, such as benzyl chloride or benzal chloride, depending on the conditions and the position of the substitution on the benzene ring.
Yes, toluene will undergo bromination. When treated with bromine in the presence of a Lewis acid catalysts such as FeBr3 or AlBr3, toluene will undergo electrophilic aromatic substitution to form bromotoluene as the major product.
Electrophilic halogenation
yes toluence is more polar than chloroform
Hexane is more nonpolar than toluene because it is an alkane with only C-H bonds, while toluene has a benzene ring which introduces some polarity due to the presence of pi bonds.