it is slightly acidic, but usually just considered neutral. The ring pulls some electron density away from the methyl group, so that is where a hydrogen would be removed.
yes it is due to the presence of -OH group in phenol
acid
uric acid
It's anhydrous toluene for nucleic acid synthesis with phosphoramidites
Even though toluene is not soluble in water, it is soluble in sulfuric acid due to its lower pka.
by using kMNo4 and water
Methyl benzene, or toluene, does not have a lone pair of electrons and so cannot act as a base and take the hydrogen ion away from the HCl molecule.
toluene is benzene with CH3 reacting this with KMnO4 in acidic solution will produce a benzene with a carboxylic acid (CH3 will be oxidized)
para-toluene sulfonic acid and ortho toluene sulfonic acid p-CH3-C6H4-SO3H and o-CH3-C6H4-SO3H
It's anhydrous toluene for nucleic acid synthesis with phosphoramidites
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
Toluene reacts with acidic permanganate on heating and forms the Benzoic acid.
Even though toluene is not soluble in water, it is soluble in sulfuric acid due to its lower pka.
by using kMNo4 and water
Methyl benzene, or toluene, does not have a lone pair of electrons and so cannot act as a base and take the hydrogen ion away from the HCl molecule.
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.
toluene is benzene with CH3 reacting this with KMnO4 in acidic solution will produce a benzene with a carboxylic acid (CH3 will be oxidized)
An acid can turn into a base if you mix a much stronger base with it! That way the base acid overpowers the acid and makes the acid a base!
This is a catalysed oxidation reaction at the methyl (CH3-) group of toluene.2C6H5-CH3 + 3O2 --> 2C6H5-COOH + 2H2OI respelled your original question at 3 points! I couldn't find any 'preperation method for bezoic acid from toulene'
Acid + base conjugate base + conjugate acid