3-Hexene, 2,2,5,5-tetramethyl-, (Z)-

• Formula: C₁₀H₂₀
• Molecular weight: 140.2658
• IUPAC Standard InChI: InChI=1S/C10H20/c1-9(2,3)7-8-10(4,5)6/h7-8H,1-6H3/b8-7- Copy

  
• IUPAC Standard InChIKey: UYWLQEPMPVDASH-FPLPWBNLSA-N Copy
• CAS Registry Number: 692-47-7
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
  The 3d structure may be viewed using Java or Javascript.
• Stereoisomers:
  • 3-Hexene, 2,2,5,5-tetramethyl-
  • trans-1,2-di-tert-butylethylene
• Other names: (Z)-2,2,5,5-Tetramethyl-3-hexene; cis-Di-tert-butylethylene; cis-1,2-Di-tert-butylethylene; cis-2,2,5,5-Tetramethyl-3-hexene; (Z)-(t-C4H9)CH=CH(t-C4H9); (Z)-1,2-Di-tert-butylethylene
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• Information on this page:
  • Phase change data
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Reaction thermochemistry data
  • Mass spectrum (electron ionization)
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Phase change data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

Gas phase ion energetics data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled as indicated in comments:
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron

Ionization energy determinations

Appearance energy determinations

References

Go To: Top, Phase change data, Gas phase ion energetics data, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Turner, Nettleton, et al., 1958
Turner, R.B.; Nettleton, D.E.; Perelman, M., Heats of Hydrogenation VI. Heats of Hydr. of SOm Substituted Ethylenes, J. Am. Chem. Soc., 1958, 80, 1430. [all data]

Bader, Buckley, et al., 1957
Bader, A.R.; Buckley, R.P.; Leavitt, F.; Szwarc, M., J. Am. Chem. Soc., 1957, 79, 5621. [all data]

Newman, 1956
Newman, M., Private Communication, Ohio State Univ., 1956. [all data]

Masclet, Grosjean, et al., 1973
Masclet, P.; Grosjean, D.; Mouvier, G., Alkene ionization potentials. Part I. Quantitative determination of alkyl group structural effects, J. Electron Spectrosc. Relat. Phenom., 1973, 2, 225. [all data]

Demeo and El-Sayed, 1970
Demeo, D.A.; El-Sayed, M.A., Ionization potential and structure of olefins, J. Chem. Phys., 1970, 52, 2622. [all data]

Robin, Taylor, et al., 1973
Robin, M.B.; Taylor, G.N.; Kuebler, N.A.; Bach, R.D., Planarity of the carbon skeleton in various alkylated olefins, J. Org. Chem., 1973, 38, 1049. [all data]

Natalis and Franklin, 1966
Natalis, P.; Franklin, J.L., Etude du comportement d'isomeres geometriques sous l'impact electronique. VI. Les cis- et trans-1,2-di-terbutyl-ethylenes, Bull. Soc. Chim. Belges, 1966, 75, 328. [all data]

Notes

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• Symbols used in this document:
  

  AE	Appearance energy
  Tboil	Boiling point

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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