1,4-Cyclohexadiene

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1,4-Cyclohexadiene
Skeletal formula with all implicit hydrogen shown, skeletal formula; stereo, skeletal formula with all explicit hydrogens added, all of 1,4-cyclohexadiene
1,4-Cyclohexadiene molecule
1,4-Cyclohexadiene molecule
Names
Systematic IUPAC name
Cyclohexa-1,4-diene[1]
Other names
1,4-Cyclohexadiene[citation needed]
1,4-Dihydrobenzene[citation needed]
Identifiers
628-41-1 YesY
Abbreviations 1,4-CHDN
1900733
ChEBI CHEBI:37611 YesY
ChemSpider 11838 YesY
EC Number 211-043-1
1656
Jmol 3D model Interactive image
MeSH 1,4-cyclohexadiene
PubChem 12343
UN number 3295
  • InChI=1S/C6H8/c1-2-4-6-5-3-1/h1-2,5-6H,3-4H2 YesY
    Key: UVJHQYIOXKWHFD-UHFFFAOYSA-N YesY
  • InChI=1/C6H8/c1-2-4-6-5-3-1/h1-2,5-6H,3-4H2
    Key: UVJHQYIOXKWHFD-UHFFFAOYAM
  • C1C=CCC=C1
Properties
C6H8
Molar mass 80.13 g·mol−1
Appearance Colorless liquid
Density 0.847 g cm−3
Melting point −50 °C; −58 °F; 223 K
Boiling point 82 °C; 179 °F; 355 K
1.472
Thermochemistry
142.2 J K−1 mol−1
189.37 J K−1 mol−1
63.0-69.2 kJ mol−1
-3573.5--3567.5 kJ mol−1
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

1,4-Cyclohexadiene is an organic compound with the formula C6H8. It is a colourless, flammable liquid that is of academic interest as a prototype of a large class of related compounds called terpenoids, an examples being γ-terpinene. An isomer exists of this compound, 1,3-cyclohexadiene.

Synthesis and reactions

In the laboratory, substituted 1,4-cyclohexadienes are synthesized by Birch reduction of related aromatic compounds using an alkali metal and a proton donor such as ammonia. In this way, over reduction to the fully saturated ring is avoided.

1,4-Cyclohexadiene and its derivatives are easily aromatized, the driving force being the formation of an aromatic ring. The conversion to an aromatic system may be performed in the laboratory using an alkene such as styrene, along with a hydrogen transfer agent such as palladium metal supported on charcoal.

References

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External links

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