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This is a catalysed oxidation reaction at the methyl (CH3-) group of toluene.

2C6H5-CH3 + 3O2 --> 2C6H5-COOH + 2H2O

I respelled your original question at 3 points! I couldn't find any 'preperation method for bezoic acid from toulene'

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Related Questions

Why toluene does not react with acidic or alkaline permanganates?

Toluene reacts with acidic permanganate on heating and forms the Benzoic acid.


Process of preparation of benzoic acid?

Benzoic acid is produced from toluene and oxygen. The toluene is oxidyzed and a water molecule is released, which resuls in benzoic acid source: wikipedia


How do you convert toluene to 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.


How do you separate benzoic acid from a mixture of benzoic acid and toluene using extraction?

Make a solution of Sodium Hydroxide or Sodium Carbonate and do three to four solvent solvent extractions using the aqueous base and the mixture o benzoic acid and toluene. Because benzoic acid reacts with base to form the water soluble carboxylate ion, it will react and the dissolve in the aqueous solution. Upon separation of the two phases acidify the aqueous extract with dilute HCl, a white needle-like precipitate of benzoic acid will form when the solution becomes acidic. Simply filter the crystals, wash with cold water, and then recrystallize using a mixture of 50/50 water and methanol or some other suitable solvent.


How does benzoic acid form dimer in toluene layer?

Benzoic acid can form dimers in a toluene layer due to hydrogen bonding between the carboxylic acid groups of adjacent molecules. The aromatic ring structure of benzoic acid allows for efficient packing in the toluene layer, promoting dimer formation. This dimerization process is driven by the favorable interactions between the molecules, such as hydrogen bonding.


What will happen if toluene react with potassium per magnate in presence of sodium carbonate?

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.


Is benzoic acid react with sodium bicarbonate?

Yes, benzoic acid will react with sodium bicarbonate to produce sodium benzoate, carbon dioxide, and water. This reaction can be used to extract benzoic acid from a mixture as it is relatively insoluble in water but soluble in sodium bicarbonate solution.


Does Benzoic Acid react with Hypochlorous Acid in water and room temperature?

Yes, benzoic acid can react with hypochlorous acid in water at room temperature to form chlorobenzoic acid. This reaction is typically slow and requires higher temperatures or catalysts for efficient conversion.


Where does sodium benzoate come from?

Sodium benzoate is manufactured by reacting benzoic acid with sodium hydroxide. Benzoic acid is produced by partial oxydation of toluene with oxygen. There are half a dozen ways or more ways to make toluene.


What is the balanced chemical equation of the reaction of benzoic acid and sodium bicarbonate?

C6H5COOH + NaHCO3 ===> C6H5COO-Na+ + H2O + CO2


Benzoic acid plus NaOH plus iodine?

C6H5COOH + NaOH + I2 -----------> C6H5COOI + NaI + H2O


Acidified potassium permanganate reaction with toluene equation?

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