I'm a medical student taking o-chem right now so double checking this might not be a bad idea.
Basically Toluene is oxidized to Benzoic Acid in the presence of Potassium Permanganate. The CH3 group of Toluene become COOH.
Not a lot of info but i hope it's of some help.
What occurs is that a Benzoic acid solution is formed, which soon takes a white solid crystalline structure.
It dissolves in water to give deep purple solutions, evaporation of which gives prismatic purplish-black glistening crystals.
The benzylic carbon becomes oxidized to form a carboxylic acid. The resulting compound is benzoic acid.
Yes. The purple solution of potassium permanganate would technically decolorise but theoretically expected to be pale pink due to formation of Mn2+ . Toluene oxidizes to form benzoic acid.
In water, it forms bright pink or purple solutions. It is used in water treatment because it is highly oxidizing, and has an antiseptic, antibacterial action.
It makes kh20
It dissolves.
the pink colour doesnt discharge
toluene is benzene with CH3 reacting this with KMnO4 in acidic solution will produce a benzene with a carboxylic acid (CH3 will be oxidized)
He dies... :D
Electrophilic halogenation
The hydrogen atom of CH3 group in toluene are substituted by chlorine atom.
Electrophilic halogenation
toluene is benzene with CH3 reacting this with KMnO4 in acidic solution will produce a benzene with a carboxylic acid (CH3 will be oxidized)
Acidic conditions promote the oxidation of toluene by potassium permanganate.
lol huh
The solution of potassium iodide (if it is not extremely diluted) is more dense.
Toluene reacts with acidic permanganate on heating and forms the Benzoic acid.
Yes, but it will depend on what do you want to filter. For example, in metallocenic polymer synthesis, at the end of the polymerization the polymer is precipitated from a toluene solution and then filtrated using a vacuum filter.
He dies... :D
Electrophilic halogenation
The hydrogen atom of CH3 group in toluene are substituted by chlorine atom.
Diethyl Ether, Naphtha, Xylene, Toluene, Petroleum Distillates, etc.
Diethyl Ether, Naphtha, Xylene, Toluene, Petroleum Distillates, etc.
Electrophilic halogenation