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  2. Chlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Chlorobenzene

    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. [6]

  3. Benzoyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzoyl_chloride

    Benzoyl chloride, also known as benzenecarbonyl chloride, is an organochlorine compound with the formula C 7 H 5 ClO.It is a colourless, fuming liquid with an irritating odour, and consists of a benzene ring (C 6 H 6) with an acyl chloride (−C(=O)Cl) substituent.

  4. Benzyl chloride - Wikipedia

    en.wikipedia.org/wiki/Benzyl_chloride

    Indicative of its high reactivity (relative to alkyl chlorides), benzyl chloride slowly reacts with water in a hydrolysis reaction to form benzyl alcohol and hydrochloric acid. In contact with mucous membranes, hydrolysis produces hydrochloric acid. Thus, benzyl chloride is a lachrymator and has been used in chemical warfare. It is also very ...

  5. Water chlorination - Wikipedia

    en.wikipedia.org/wiki/Water_chlorination

    Water chlorination is the process of adding chlorine or chlorine compounds such as sodium hypochlorite to water. This method is used to kill bacteria, viruses and other microbes in water. This method is used to kill bacteria, viruses and other microbes in water.

  6. Phenyl group - Wikipedia

    en.wikipedia.org/wiki/Phenyl_group

    The phenyl group is closely related to benzene and can be viewed as a benzene ring, minus a hydrogen, which may be replaced by some other element or compound to serve as a functional group. A phenyl group has six carbon atoms bonded together in a hexagonal planar ring, five of which are bonded to individual hydrogen atoms, with the remaining ...

  7. Halogen addition reaction - Wikipedia

    en.wikipedia.org/wiki/Halogen_addition_reaction

    In this way the two halogens add in an anti addition fashion, and when the alkene is part of a cycle the dibromide adopts the trans configuration. For maximum overlap of the C–Br σ* antibonding molecular orbital (the LUMO , shown to the right in red) and the nucleophile (X − ) lone pair (the HOMO , shown to the right below in green), X − ...

  8. Freezing-point depression - Wikipedia

    en.wikipedia.org/wiki/Freezing-point_depression

    In the above equation, T F is the normal freezing point of the pure solvent (273 K for water, for example); a liq is the activity of the solvent in the solution (water activity for aqueous solution); ΔH fus T F is the enthalpy change of fusion of the pure solvent at T F, which is 333.6 J/g for water at 273 K; ΔC fus p is the difference ...

  9. Hexachlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Hexachlorobenzene

    In 1867, Henry Bassett proved that the compound produced from benzene and antimony was the same as Julian's carbon chloride and named it "hexachlorobenzene". [ 10 ] [ 9 ] Leopold Gmelin named it "dichloride of carbon" and claimed that the carbon was derived from cast iron and the chlorine was from crude saltpetre .