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1,3-Dichlorobenzene (also known as meta-dichlorobenzene) is an aryl chloride and isomer of dichlorobenzene with the formula C 6 H 4 Cl 2.It is the least common of the three isomers of dichlorobenzene, and it is a colorless liquid that is insoluble in water.
1,2-Dichlorobenzene or ortho-dichlorobenzene; 1,3-Dichlorobenzene or meta-dichlorobenzene; 1,4-Dichlorobenzene or para-dichlorobenzene. All three isomers are colorless chlorobenzenes with the formula C 6 H 4 Cl 2. They differ structurally based on where the two chlorine atoms are attached to the ring.
1,2-Dichlorobenzene, or orthodichlorobenzene (ODCB), is an aryl chloride and isomer of dichlorobenzene with the formula C 6 H 4 Cl 2. This colourless liquid is poorly soluble in water but miscible with most organic solvents. It is a derivative of benzene, consisting of two adjacent chlorine atoms.
Thus, the four remaining hydrogens in meta-dichlorobenzene still fall into three classes, while those of ortho- fall into two, and those of para- are all equivalent again. Still, some of these 3 + 2 + 1 = 6 substitutions end up yielding the same structure, so there are only three structurally distinct trichlorobenzenes : 1,2,3- , 1,2,4- , and 1 ...
1,4-Dichlorobenzene; Dichlorofulvenes; 1,6-Dichloro-2,4-hexadiyne This page was last edited on 28 August 2022, at 12:56 ...
Derived from File:Ortho-dichlorobenzene-3D-vdW.png and File:Meta-dichlorobenzene-3D-vdW.png. Author: Ben Mills and Jynto: Licensing. Public domain Public domain false ...
The nitration of 1,2-dichlorobenzene mainly produces 1,2-dichloro-4-nitrobenzene, together with smaller amounts of the 3-nitro isomer.It can also be prepared by chlorination of 1-chloro-4-nitrobenzene.
Sulfonation of chlorobenzene resulted in addition of methylsulfonyl group at para and ortho positions (with respect to chloride), with a ratio of 2 to 1, respectively; while reaction with Meta-dichlorobenzene gave monosulfonylated product at C4 position. [8] With sulfuric acid, di-aryl sulfones were synthesized. [9]