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Chlorobenzene (abbreviated PhCl) is an aryl chloride and the simplest of the chlorobenzenes, consisting of a benzene ring substituted with one chlorine atom. Its chemical formula is C 6 H 5 Cl. This colorless, flammable liquid is a common solvent and a widely used intermediate in the manufacture of other chemicals.
2,4-Dinitrochlorobenzene (DNCB) is an organic compound with the chemical formula (O 2 N) 2 C 6 H 3 Cl. It is a yellow solid that is soluble in organic solvents.It is an important intermediate for the industrial production of other compounds.
This page was last edited on 3 November 2023, at 19:20 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
This page was last edited on 25 October 2023, at 23:28 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
1,3,5-Trichlorobenzene is an organochlorine compound.It is one of the three isomers of trichlorobenzene.Being more symmetrical than the other isomers, it exists as colourless crystals whereas the other isomers are liquids at room temperature.
Chlorination of benzene under electrophilic aromatic substitution conditions (Cl 2 /FeCl 3 or Cl 2 /AlCl 3) produces chlorobenzene.Since mono chloro-de-hydrogenation deactivates the molecule against further electrophilic reactions, the reaction can be halted at one chlorine atom substitution.
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.
Benzyl bromide is used in organic synthesis for the introduction of the benzyl groups when the less expensive benzyl chloride is insufficiently reactive. [6] [7] Benzylations are often achieved in the presence of catalytic amounts of sodium iodide, which generates the more reactive benzyl iodide in situ. [3]