The most reactive site of 2-nitro toluene is its 4th position which is para to methyl group and meta to nitro group.
The reaction between bromine and toluene can result in the substitution of a hydrogen atom on the toluene ring with a bromine atom, forming bromotoluene. Different isomers of bromotoluene can be produced depending on the position of the bromine atom on the toluene ring.
Yes. Two isomers of toluene are known as toluene-2,4-diisocyanate and toluene-2,6-diisocyanate
C6H5CH3 is toluene.
Toluene is not miscible with water; toluene is released by slow evaporation.
Iodination of toluene in the presence of an oxidizing agent, such as iodine monochloride (ICl), helps promote the oxidation of iodide ions to atomic iodine, which is a more reactive species that can then participate in the substitution reaction with toluene. This process allows for the efficient iodination of toluene by enhancing the reactivity of the iodine species.
Toluene is an aromatic compound.
toluene is a common name - The IUPAC name for toluene is methylbenzene.
From what the internet shows, you convert toluene into nitro-toluene, not the other way around. Further, the reagents used to do that are generally things that will allow the toluene to oxidize.
Neither. Toluene is a compound.
No it is not soluble in toluene because toluene is nonpolar and nacl is polar
Toluene is not a good conductor of electricity.
Toluene is non-polar and does not dissolve in water, so it does not have a pH like aqueous solutions.