I'm a medical student taking o-chem right now so double checking this might not be a bad idea.
Basically Toluene is oxidized to Benzoic Acid in the presence of Potassium Permanganate. The CH3 group of Toluene become COOH.
Not a lot of info but i hope it's of some help.
Ferrous chloride in presence of hydrochloric acid gives brown precipitates of Ferric chloride with potassium permanganate.
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 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.
Toluene can be oxidized to benzoic acid using a strong oxidizing agent, such as potassium permanganate (KMnO4) or chromic acid (H2CrO4). The reaction typically occurs under acidic conditions. The methyl group of toluene is oxidized to a carboxylic acid group, resulting in the formation of benzoic acid.
When toluene is treated with alkaline KMnO4, it undergoes oxidation. Toluene is converted to benzyl alcohol, and further oxidation can convert benzyl alcohol to benzoic acid. The purple color of the KMnO4 solution will fade as the reaction proceeds.
Ferrous chloride in presence of hydrochloric acid gives brown precipitates of Ferric chloride with potassium permanganate.
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
Acidic conditions promote the oxidation of toluene by potassium permanganate.
lol huh
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.
The solution of potassium iodide (if it is not extremely diluted) is more dense.
Toluene reacts with acidic permanganate on heating and forms the Benzoic acid.
Toluene can be oxidized to benzoic acid using a strong oxidizing agent, such as potassium permanganate (KMnO4) or chromic acid (H2CrO4). The reaction typically occurs under acidic conditions. The methyl group of toluene is oxidized to a carboxylic acid group, resulting in the formation of benzoic acid.
When toluene is treated with alkaline KMnO4, it undergoes oxidation. Toluene is converted to benzyl alcohol, and further oxidation can convert benzyl alcohol to benzoic acid. The purple color of the KMnO4 solution will fade as the reaction proceeds.
Yes, but it will depend on what do you want to filter. For example, in metallocenic polymer synthesis, at the end of the polymerization the polymer is precipitated from a toluene solution and then filtrated using a vacuum filter.
Sodium hydroxide is not soluble in toluene. Toluene is a nonpolar solvent, while sodium hydroxide is an ionic compound that is highly soluble in water but not in nonpolar solvents like toluene.
Toluene is soluble in ligroin. Both are hydrocarbons and have similar chemical properties, allowing them to mix and form a solution.