Search results
Results from the WOW.Com Content Network
Benzoic acid (C 6 H 5 COOH) can be prepared by oxidation of benzyl chloride in the presence of alkaline KMnO 4: C 6 H 5 CH 2 Cl + 2 KOH + 2 [O] → C 6 H 5 COOK + KCl + H 2 O Benzyl chloride may be used in the synthesis of amphetamine-class drugs, and for this reason, sales of benzyl chloride are monitored as a List II drug precursor chemical ...
The structure of xylylene dichloride is characterized by an benzene ring with two chloromethyl groups and four hydrogen atoms bound to it. [4] The chloromethyl groups can be located on different sites on the ring, leading to a few different possible forms. These forms are: [3] o-xylylene dichloride: 1,2-bis(chloromethyl)benzene
Trichlorobenzene (TCB) may refer to any of three isomeric chlorinated derivatives of benzene with the molecular formula C 6 H 3 Cl 3. They differ by the positions of the chlorine atoms around the ring: 1,2,3-Trichlorobenzene; 1,2,4-Trichlorobenzene; 1,3,5-Trichlorobenzene
Structure of the chloromethyl group. In organic chemistry, the chloromethyl group is a functional group that has the chemical formula −CH 2 −Cl. The naming of this group is derived from the methyl group (which has the formula −CH 3), by replacing one hydrogen atom by a chlorine atom. Compounds with this group are a subclass of the ...
4-Vinylbenzyl chloride is an organic compound with the formula ClCH 2 C 6 H 4 CH=CH 2. It is a bifunctional molecule, featuring both vinyl and a benzylic chloride functional groups . It is a colorless liquid that is typically stored with a stabilizer to suppress polymerization.
All three isomers have the chemical formula C 6 H 6 O 2. Similar to other phenols, the hydroxyl groups on the aromatic ring of a benzenediol are weakly acidic . Each benzenediol can lose an H + from one of the hydroxyls to form a type of phenolate ion.
It hydrolyzes rapidly to benzoic acid and hydrochloric acid with a half life of about 2.4 minutes, thus making the compound unstable in the presence of water. [2] In other chemical reactions, benzotrichloride reacts at the chlorinated α-carbon, for example in substitution reactions. It is used as an intermediate in the synthesis of benzoyl ...
The chemical formula for all the saturated isomers is C 9 H 12. There are three trimethylbenzenes, three ethylmetylbenzenes, and two propylbenzene isomers. 1980s American gasoline contained about 3-4% C 3-benzenes. [1]