They are highly reactive and form 2,4,6-tribromo Toluene.
The Étard reaction is a chemical reaction that involves the direct oxidation of an aromatic or heterocyclic bound methyl group to an aldehyde using chromyl chloride. It is named for the French chemist Alexandre Léon Étard (5 January 1852, Alençon - 1 May 1910). For example, toluene can be oxidised to benzaldehyde:
Toluene is not a good conductor of electricity.
KI will crash out completely but KBr and KCl will be partially soluble in THF, particularly KCl. This is due to the THF being polar. For a salt elimination reaction in THF remove the THF and extract with toluene then filter to have the salt completely crash out in the non-polar toluene.
In order for a mixture to conduct electricity ions must be present. HCl dose not ionize in toluene because toluene is nonpolar.
The nitration of phenol is more rapid than that of toluene.
Toluene forms from the reaction of bromine with acetophenone.
HBR
para-toluene sulfonic acid and ortho toluene sulfonic acid p-CH3-C6H4-SO3H and o-CH3-C6H4-SO3H
there is no chemical reaction between these two.
lol huh
yeah
One version would be CH3C6H5.
because e coli will react with toluene to give by-products (I guess?)
it,s C7H8+9O2>7CO2+4H2O+HEATapexx
Bromine in CCl4 is instantly decolorized by 1-octene, because it adds to the double bond, giving 1,2-dibromooctane. Toluene does not give this test because it is aromatic and thus does not add halogens.
toluene is benzene with CH3 reacting this with KMnO4 in acidic solution will produce a benzene with a carboxylic acid (CH3 will be oxidized)
Burning of any material is an oxidation reaction, a chemical change.