Hexachlorocyclohexane

Hexachlorocyclohexane (HCH), C
₆H
₆Cl
₆, is any of several polyhalogenated organic compounds consisting of a six-carbon ring with one chlorine and one hydrogen attached to each carbon. This structure has nine stereoisomers (eight diastereomers, one of which has two enantiomers), which differ by the stereochemistry of the individual chlorine substituents on the cyclohexane. It is sometimes erroneously called "benzene hexachloride" (BHC). They have been used as models for analyzing the effects of different geometric positions of the large atoms with dipolar bonds on the stability of the cyclohexane conformation.[1] The isomers are poisonous, pesticidal, and persistent organic pollutants, to varying degrees.

Hexachlorocyclohexane was dimerized to produce mirex, a banned pesticide.

Common forms are:

• alpha-hexachlorocyclohexane, α-HCH, or α-BHC (CAS RN: 319-84-6 ), the optically active isomer
• beta-hexachlorocyclohexane, β-HCH, or β-BHC (CAS RN: 319-85-7 )
• gamma-hexachlorocyclohexane, γ-HCH, γ-BHC, or lindane (CAS RN: 58-89-9 ), the most insecticidal isomer
• delta-hexachlorocyclohexane, δ-HCH, or δ-BHC (CAS RN: 319-86-8 )
• technical hexachlorocyclohexane, t-HCH, or t-BHC (CAS RN: 608-73-1 ), a mixture of isomers

• 
  α-Hexachlorocyclohexane, the dextrorotatory enantiomer
• 
  α-Hexachlorocyclohexane, the levorotatory enantiomer
• 
  β-Hexachlorocyclohexane
• 
  γ-Hexachlorocyclohexane, lindane
• 
  δ-Hexachlorocyclohexane
• 
  ε-Hexachlorocyclohexane
• 
  ζ-Hexachlorocyclohexane
• 
  η-Hexachlorocyclohexane
• 
  θ-Hexachlorocyclohexane

Chlorination of benzene under electrophilic aromatic substitution conditions (Cl₂/FeCl₃ or Cl₂/AlCl₃) produces chlorobenzene. Since mono chloro-de-hydrogenation deactivates the molecule against further electrophilic reactions, the reaction can be halted at one chlorine atom substitution.

Electrophilic chlorination: C₆H₆ + Cl₂ → C₆H₅Cl + HCl

In contrast, chlorination of benzene under radical addition conditions (Cl₂, hν (photochlorination) or Cl₂, Δ, high P) yields hexachlorocyclohexane isomers after three successive radical dichlorination steps. Addition rather than substitution takes place, due to the very high C–H bond dissociation energy (112 kcal/mol) that disfavors abstraction of a hydrogen atom. Addition of Cl₂ destroys the aromaticity of the benzene ring, and the addition of two more Cl₂ molecules is rapid compared to the first. Hence, only thrice-dichlorinated product can be isolated from this reaction.

Radical addition: C₆H₆ + 3Cl₂ → C₆H₆Cl₆

Hexachlorocyclohexane isomers with more than one chlorine atom per carbon are:

• 1,1,2,3,4,5-hexachlorocyclohexane
• 1,1,2,3,4,6-hexachlorocyclohexane
• 1,1,2,3,5,6-hexachlorocyclohexane
• 1,1,2,2,3,4-hexachlorocyclohexane
• 1,1,2,2,3,5-hexachlorocyclohexane
• 1,1,2,2,3,6-hexachlorocyclohexane
• 1,1,2,2,4,5-hexachlorocyclohexane
• 1,1,2,3,3,4-hexachlorocyclohexane
• 1,1,2,3,3,5-hexachlorocyclohexane
• 1,1,2,3,4,4-hexachlorocyclohexane
• 1,1,3,3,5,5-hexachlorocyclohexane
• 1,1,2,4,4,5-hexachlorocyclohexane
• 1,1,2,4,4,6-hexachlorocyclohexane
• 1,1,2,4,5,5-hexachlorocyclohexane
• 1,1,2,5,6,6-hexachlorocyclohexane
• 1,1,2,2,3,3-hexachlorocyclohexane
• 1,1,2,2,4,4-hexachlorocyclohexane
• 1,1,3,3,5,5-hexachlorocyclohexane

References

1. Zdravkovski, Zoran (2004). "Theoretical Study of the Stability of Hexachloro- and Hexafluorocyclohexane Isomers" (PDF). Bulletin of the Chemists and Technologists of Macedonia. 23 (2): 131–137. Archived from the original (PDF) on 2005-12-28. Retrieved 2016-04-17.

External links

• Hexachlorocyclohexane (HCH), CDC