it,s C7H8+9O2>7CO2+4H2O+HEAT
apexx
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
Toluene forms from the reaction of bromine with acetophenone.
No, toluene cannot be directly converted to aniline by the Gabriel synthesis. The Gabriel synthesis involves the reaction of an alkyl halide with potassium phthalimide to form an alkyl phthalimide intermediate, which is then converted to the primary amine through a nucleophilic substitution reaction. Toluene does not contain a suitable leaving group for this type of reaction.
When bromine is added to toluene, bromination of the aromatic ring can occur. This reaction can lead to the formation of mono- or poly-brominated toluene derivatives, depending on reaction conditions. Products may include ortho-, meta-, or para-bromotoluene isomers.
When excess chlorine is passed through boiling toluene, chlorination of the toluene molecule can occur. This reaction can lead to the introduction of chlorine atoms into the benzene ring of toluene, resulting in the formation of chlorinated derivatives of toluene. These derivatives can have different properties and reactivity compared to the original toluene molecule.
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
They are highly reactive and form 2,4,6-tribromo Toluene.
Toluene forms from the reaction of bromine with acetophenone.
No, toluene cannot be directly converted to aniline by the Gabriel synthesis. The Gabriel synthesis involves the reaction of an alkyl halide with potassium phthalimide to form an alkyl phthalimide intermediate, which is then converted to the primary amine through a nucleophilic substitution reaction. Toluene does not contain a suitable leaving group for this type of reaction.
there is no chemical reaction between these two.
para-toluene sulfonic acid and ortho toluene sulfonic acid p-CH3-C6H4-SO3H and o-CH3-C6H4-SO3H
When bromine is added to toluene, bromination of the aromatic ring can occur. This reaction can lead to the formation of mono- or poly-brominated toluene derivatives, depending on reaction conditions. Products may include ortho-, meta-, or para-bromotoluene isomers.
lol huh
Burning of any material is an oxidation reaction, a chemical change.
No, Toluene is considered nonpolar because it has a symmetrical molecular structure with a balanced distribution of charges, which results in a lack of permanent dipole moment.
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.
The products of a toluene-sulfuric acid reaction include toluenesulfonic acid and water. The sulfuric acid protonates the methyl group in toluene, leading to the formation of toluenesulfonic acid as the primary product. Water is also produced as a byproduct of the reaction.