Jump to content

Tetra-tert-butylethylene

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Tom.Reding (talk | contribs) at 11:53, 16 October 2020 (Category:CS1 errors: deprecated parameters (last-author-amp=y/yes → name-list-style=amp; etc.)). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Tetra-tert-butylethylene
Skeletal formula of tetra-tert-butylethylene
Names
IUPAC name
3,4-Di-tert-butyl-2,2,5,5-tetramethylhex-3-ene[1]
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C18H36/c1-15(2,3)13(16(4,5)6)14(17(7,8)9)18(10,11)12/h1-12H3 checkY
    Key: WXTSAYDLWHISDR-UHFFFAOYSA-N checkY
  • CC(C)(C)C(=C(C(C)(C)C)C(C)(C)C)C(C)(C)C
Properties
C18H36
Molar mass 252.486 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Tetra-tert-butylethylene is a hypothetical organic compound, a hydrocarbon with formula C18H36, or ((H3C−)3C−)2C=C(−C(−CH3)3)2. As the name indicates, its molecular structure can be viewed as an ethylene molecule H2C=CH2 with the four hydrogens replaced by tert-butyl −C(−CH3)3 groups.

As of 2006, this compound had not yet been synthesized, in spite of many efforts. It is of interest in chemical research as an alkene whose double bond is strained but protected by steric hindrance. Theoretical studies indicate that the molecule should be stable, with a strain energy of about 93 kcal/mol (390 kJ/mol).[2]

See also

References

  1. ^ CID 13179773 from PubChem
  2. ^ Dieter Lenoir; Carsten Wattenbach & Joel F. Liebman (2006). "Tetra-tert-butylethylene, fantasy, fake, or reality?". Structural Chemistry. 17 (4): 419–422. doi:10.1007/s11224-006-9061-x.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Tetra-tert-butylethylene&oldid=983815129"