yeah
It s the structure and bonding of Aniline, Phenol, Benzene and Toluene that causes the differences in the boiling points.
Toluene forms from the reaction of bromine with acetophenone.
it,s C7H8+9O2>7CO2+4H2O+HEATapexx
toluene is benzene with CH3 reacting this with KMnO4 in acidic solution will produce a benzene with a carboxylic acid (CH3 will be oxidized)
What is the pH of toluene?
It s the structure and bonding of Aniline, Phenol, Benzene and Toluene that causes the differences in the boiling points.
aniline would go through an electrophilic substitution, it is a weak base
They are highly reactive and form 2,4,6-tribromo Toluene.
Toluene forms from the reaction of bromine with acetophenone.
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
it,s C7H8+9O2>7CO2+4H2O+HEATapexx
toluene is benzene with CH3 reacting this with KMnO4 in acidic solution will produce a benzene with a carboxylic acid (CH3 will be oxidized)
lol huh
Substitutions at 4' and 6' positions of 3-chloro toluene are not normally possible because carbocations are prone to rearrangement.
Burning of any material is an oxidation reaction, a chemical change.
Yes. Two isomers of toluene are known as toluene-2,4-diisocyanate and toluene-2,6-diisocyanate