Hydrogen

• Formula: H₂
• Molecular weight: 2.01588
• IUPAC Standard InChI: InChI=1S/H2/h1H Copy

  
• IUPAC Standard InChIKey: UFHFLCQGNIYNRP-UHFFFAOYSA-N Copy
• CAS Registry Number: 1333-74-0
• 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.
• Isotopologues:
  • tritium
  • deuterium hydride
  • Deuterium
• Other names: Dihydrogen; o-Hydrogen; p-Hydrogen; Molecular hydrogen; H2; UN 1049; UN 1966
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• Information on this page:
  • Reaction thermochemistry data (reactions 151 to 200)
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data: reactions 1 to 50, reactions 51 to 100, reactions 101 to 150, reactions 201 to 250, reactions 251 to 300, reactions 301 to 350, reactions 351 to 400, reactions 401 to 450, reactions 451 to 500, reactions 501 to 550, reactions 551 to 600, reactions 601 to 621
  • Henry's Law data
  • Gas phase ion energetics data
  • Ion clustering data
  • Mass spectrum (electron ionization)
  • Constants of diatomic molecules
  • Fluid Properties
• Data at other public NIST sites:
  • Electron-Impact Ionization Cross Sections (on physics web site)
  • Computational Chemistry Comparison and Benchmark Database
  • Gas Phase Kinetics Database
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Reaction thermochemistry data

Go To: Top, References, Notes

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:
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
M - Michael M. Meot-Ner (Mautner) and Sharon G. Lias
MS - José A. Martinho Simões

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.

Reactions 151 to 200

 +  =

By formula: H₂ + C₁₀H₂₀ = C₁₀H₂₂

 + 3 =

By formula: C₉H₁₂ + 3H₂ = C₉H₁₈

3 +  =

By formula: 3H₂ + C₈H₁₀ = C₈H₁₆

 + 3 =

By formula: C₈H₁₀ + 3H₂ = C₈H₁₆

 + 2 =

By formula: C₄H₄O + 2H₂ = C₄H₈O

2 +  =

By formula: 2H₂ + C₂H₂ = C₂H₆

2 +  =

By formula: 2H₂ + C₃H₄ = C₃H₈

2 +  =

By formula: 2H₂ + C₃H₄ = C₃H₈

 + 2 =

By formula: C₄H₆ + 2H₂ = C₄H₁₀

3 +  =

By formula: 3H₂ + C₆H₆ = C₆H₁₂

 +  =

By formula: C₄H₈ + H₂ = C₄H₁₀

 +  =

By formula: H₂ + C₅H₁₀ = C₅H₁₂

2 +  =

By formula: 2H₂ + C₁₀H₁₆ = C₁₀H₂₀

 +  =

By formula: H₂ + C₄H₆O = C₄H₈O

(HO₂⁺ • ) +  = (HO₂⁺ •  • )

By formula: (HO₂⁺ • O₂) + H₂ = (HO₂⁺ • H₂ • O₂)

2 +  =

By formula: 2H₂ + C₁₀H₁₆ = C₁₀H₂₀

 + 2 =

By formula: C₄H₆O + 2H₂ = C₄H₁₀O

(CH₅⁺ • 2) +  = (CH₅⁺ • 3)

By formula: (CH₅⁺ • 2H₂) + H₂ = (CH₅⁺ • 3H₂)

(CH₅⁺ • 3) +  = (CH₅⁺ • 4)

By formula: (CH₅⁺ • 3H₂) + H₂ = (CH₅⁺ • 4H₂)

 +  =

By formula: C₃H₆O + H₂ = C₃H₈O

(CH₅⁺ • ) +  = (CH₅⁺ • 2)

By formula: (CH₅⁺ • H₂) + H₂ = (CH₅⁺ • 2H₂)

 +  =

By formula: C₄H₆O₂ + H₂ = C₄H₈O₂

 +  =

By formula: H₂ + C₅H₈O₂ = C₅H₁₀O₂

(H₃⁺ • 4) +  = (H₃⁺ • 5)

By formula: (H₃⁺ • 4H₂) + H₂ = (H₃⁺ • 5H₂)

(H₃⁺ • 5) +  = (H₃⁺ • 6)

By formula: (H₃⁺ • 5H₂) + H₂ = (H₃⁺ • 6H₂)

(H₃⁺ • 6) +  = (H₃⁺ • 7)

By formula: (H₃⁺ • 6H₂) + H₂ = (H₃⁺ • 7H₂)

(H₃⁺ • 7) +  = (H₃⁺ • 8)

By formula: (H₃⁺ • 7H₂) + H₂ = (H₃⁺ • 8H₂)

(H₃⁺ • 8) +  = (H₃⁺ • 9)

By formula: (H₃⁺ • 8H₂) + H₂ = (H₃⁺ • 9H₂)

 +  =  + 

By formula: H₂ + C₃H₇Br = HBr + C₃H₈

 +  =

By formula: C₄H₆O + H₂ = C₄H₈O

(HN₂⁺ • ) +  = (HN₂⁺ • 2)

By formula: (HN₂⁺ • H₂) + H₂ = (HN₂⁺ • 2H₂)

 +  =

By formula: H₂ + C₇H₁₂O = C₇H₁₄O

2 +  =

By formula: 2H₂ + C₄H₄O₂ = C₄H₈O₂

 +  =

By formula: C₄H₈O + H₂ = C₄H₁₀O

CH₅⁺ +  = (CH₅⁺ • )

By formula: CH₅⁺ + H₂ = (CH₅⁺ • H₂)

 +  =

By formula: H₂ + C₆H₁₂ = C₆H₁₄

HN₂⁺ +  = (HN₂⁺ • )

By formula: HN₂⁺ + H₂ = (HN₂⁺ • H₂)

 +  = ( • )

By formula: CHO⁺ + H₂ = (CHO⁺ • H₂)

HO₂⁺ +  = (HO₂⁺ • )

By formula: HO₂⁺ + H₂ = (HO₂⁺ • H₂)

 +  =

By formula: H₂ + C₂H₄ = C₂H₆

=  + 

By formula: C₅H₁₀O = C₅H₈O + H₂

=  + 

By formula: C₄H₁₀O₂S₂ = H₂ + C₈H₁₈O₄S₄

=  + 

By formula: C₄H₁₀O = H₂ + C₄H₈O

=  + 

By formula: C₃H₈O = H₂ + C₃H₆O

3 +  =

By formula: 3H₂ + C₉H₁₂ = C₉H₁₈

2 (l) +  (cr) =  (cr) +  (g)

By formula: 2C₅H₆ (l) + Mg (cr) = C₁₀H₁₀Mg (cr) + H₂ (g)

Ar⁺ +  = (Ar⁺ • )

By formula: Ar⁺ + H₂ = (Ar⁺ • H₂)

2 +  =

By formula: 2H₂ + C₆H₈ = C₆H₁₂

3 +  =

By formula: 3H₂ + C₆H₆ = C₆H₁₂

2 +  =

By formula: 2H₂ + C₈H₁₀ = C₈H₁₄

References

Go To: Top, Reaction thermochemistry data, Notes

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

Doering, Roth, et al., 1989
Doering, W.E.; Roth, W.R.; Bauer, F.; Breuckmann, R.; Ebbrecht, T.; Herbold, M.; Schmidt, R.; Lennartz, H-W.; Lenoir, D.; Boese, R., Rotational barriers of strained olefines, Chem. Ber., 1989, 122, 1263-1266. [all data]

Turner, Nettleton, et al., 1958
Turner, R.B.; Nettleton, J.E.; Perelman, Heats of Hydrogenation. VI. Heats of hydrogenation of some substituted ethylenes, J. Am. Chem. Soc., 1958, 80, 1430-1433. [all data]

Dolliver, Gresham, et al., 1937
Dolliver, M.a.; Gresham, T.L.; Kistiakowsky, G.B.; Vaughan, W.E., Heats of organic reactions. V. Heats of hydrogenation of various hydrocarbons, J. Am. Chem. Soc., 1937, 59, 831-841. [all data]

Cox and Pilcher, 1970
Cox, J.D.; Pilcher, G., Thermochemistry of Organic and Organometallic Compounds, Academic Press, New York, 1970, 1-636. [all data]

Dolliver, Gresham, et al., 1938
Dolliver, M.A.; Gresham, T.L.; Kistiakowsky, G.B.; Smith, E.A.; Vaughan, W.E., Heats of organic reactions. VI. Heats of hydrogenation of some oxygen-containing compounds, J. Am. Chem. Soc., 1938, 60, 440-450. [all data]

Conn, Kistiakowsky, et al., 1939
Conn, J.B.; Kistiakowsky, G.B.; Smith, E.A., Heats of organic reactions. VIII. Some further hydrogenations, including those of some acetylenes, J. Am. Chem. Soc., 1939, 61, 1868-1876. [all data]

Kistiakowsky, Ruhoff, et al., 1936
Kistiakowsky, G.B.; Ruhoff, J.R.; Smith, H.A.; Vaughan, W.E., Heats of organic reactions. IV. Hydrogenation of some dienes and of benzene, J. Am. Chem. Soc., 1936, 58, 146-153. [all data]

Kistiakowsky, Ruhoff, et al., 1935
Kistiakowsky, G.B.; Ruhoff, J.R.; Smith, H.A.; Vaughan, W.E., Heats of organic reactions. II. Hydrogenation of some simpler olefinic hydrocarbons, J. Am. Chem. Soc., 1935, 57, 876-882. [all data]

Hiraoka, Saluja, et al., 1979
Hiraoka, K.; Saluja, P.P.S.; Kebarle, P., Stabilities of Complexes (N2)nH+, (CO)nH+ and (O2)nH+ for n = 1 to 7 Based on Gas Phase Ion Equilibrium Measurements, Can. J. Chem., 1979, 57, 16, 2159, https://doi.org/10.1139/v79-346 . [all data]

Hiraoka, Kudaka, et al., 1991
Hiraoka, K.; Kudaka, I.; Yamabe, S., Gas-Phase Solvation of CH5+ with H2, Chem. Phys. Lett., 1991, 184, 4, 271, https://doi.org/10.1016/0009-2614(91)85122-D . [all data]

Vilcu and Perisanu, 1980
Vilcu, R.; Perisanu, S., The ideal gas state enthalpies of formation of some monomers, Rev. Roum. Chim., 1980, 25, 619-624. [all data]

Hiraoka, 1987
Hiraoka, K., A Determination of the Stabilities of H3+(H2)n with n=1-9 from Measurements of the gas-Phase Ion Equilibria H3+(H2)n-1 + H2 = H3+(H2)n, J. Chem. Phys., 1987, 87, 7, 4048, https://doi.org/10.1063/1.452909 . [all data]

Davies, Lacher, et al., 1965
Davies, J.; Lacher, J.R.; Park, J.D., Reaction heats of organic compounds. Part 4.-Heats of hydrogenation of n- and iso-Propyl bromides and chlorides, Trans. Faraday Soc., 1965, 61, 2413-2416. [all data]

Wiberg, Crocker, et al., 1991
Wiberg, K.B.; Crocker, L.S.; Morgan, K.M., Thermochemical studies of carbonyl compounds. 5. Enthalpies of reduction of carbonyl groups, J. Am. Chem. Soc., 1991, 113, 3447-3450. [all data]

Flitcroft and Skinner, 1958
Flitcroft, T.L.; Skinner, H.A., Heats of hydrogenation Part 2.-Acetylene derivatives, Trans. Faraday Soc., 1958, 54, 47-53. [all data]

Buckley and Cox, 1967
Buckley, E.; Cox, J.D., Chemical equilibria. Part 2.-Dehydrogenation of propanol and butanol, Trans. Faraday Soc., 1967, 63, 895-901. [all data]

Rogers, Crooks, et al., 1987
Rogers, D.W.; Crooks, E.; Dejroongruang, K., Enthalpies of hydrogenation of the hexenes, J. Chem. Thermodyn., 1987, 19, 1209-1215. [all data]

Kistiakowsky, Ruhoff, et al., 1936, 2
Kistiakowsky, G.B.; Ruhoff, J.R.; Smith, H.A.; Vaughan, W.E., Heats of organic reactions. III. Hydrogenation of some higher olefins, J. Am. Chem. Soc., 1936, 58, 137-145. [all data]

Hiraoka and Kebarle, 1975
Hiraoka, K.; Kebarle, P., Stability and Structure of H3CO+ Formed from COH+ + H2 at Low Temperature, J. Chem. Phys., 1975, 63, 4, 1688, https://doi.org/10.1063/1.431499 . [all data]

Kistiakowsky and Nickle, 1951
Kistiakowsky, G.B.; Nickle, A.G., Ethane-ethylene and propane-propylene equilibria, Faraday Discuss. Chem. Soc., 1951, 10, 175-187. [all data]

Kistiakowsky, Romeyn, et al., 1935
Kistiakowsky, G.B.; Romeyn, H., Jr.; Ruhoff, J.R.; Smith, H.A.; Vaughan, W.E., Heats of organic reactions. I. The apparatus and the heat of hydrogenation of ethylene, J. Am. Chem. Soc., 1935, 57, 65-75. [all data]

Fedoseenko, Yursha, et al., 1984
Fedoseenko, V.I.; Yursha, I.A.; Kabo, G.Ya., Equilibrium of cyclopentanol dehydrogenation and hydrogen disproportionation in the cyclopentanol-cyclohexanone system, Dokl. Akad. Nauk BSSR, 1984, 28, 1109-1112. [all data]

Cubberley and Mueller, 1946
Cubberley, A.H.; Mueller, M.B., Equilibrium studies on the dehydrogenation of primary and secondary alcohols. I. 2-Butanol, 2-octanol, cyclopentanol and benzyl alcohol, J. Am. Chem. Soc., 1946, 68, 1149-1151. [all data]

Fukada and Takahashi, 1980
Fukada, H.; Takahashi, K., Calorimetric study of the oxidation of dithiothreitol, J. Biochem., 1980, 87, 1105-1110. [all data]

Kolb and Burwell, 1945
Kolb, H.J.; Burwell, R.L., Jr., Equilibrium in the dehydrogenation of secondary propyl and butyl alcohols, J. Am. Chem. Soc., 1945, 67, 1084-1088. [all data]

Buckley and Herington, 1965
Buckley, E.; Herington, E.F.G., Equilibria in some secondary alcohol + hydrogen + ketone systems, Trans. Faraday Soc., 1965, 61, 1618-1625. [all data]

Doering, Birladeanu, et al., 1996
Doering, W.E.; Birladeanu, L.; Sarma, K.; Shao, L., The cyclohexadienyl radical in the thermal syn-arti isomerization of two crossed pentaenes of the type of bis-homofulvalene, J. Am. Chem. Soc., 1996, 118, 6660-6665. [all data]

Hull, Reid, et al., 1967
Hull, H.S.; Reid, A.F.; Turnbull, A.G., Inorg. Chem., 1967, 6, 805. [all data]

Pedley and Rylance, 1977
Pedley, J.B.; Rylance, J., Computer Analysed Thermochemical Data: Organic and Organometallic Compounds, University of Sussex, Brigton, 1977. [all data]

Cox and Pilcher, 1970, 2
Cox, J.D.; Pilcher, G., Thermochemistry of Organic and Organometallic Compounds in Academic Press, New York, 1970. [all data]

Shul, Passarella, et al., 1987
Shul, R.J.; Passarella, R.; Upshulte, B.L.; Keesee, R.G.; Castleman, A.W., Thermal Energy Reactions Invoving Ar+ Monomer and Dimer with N2, H2, Xe, and Kr, J. Chem. Phys., 1987, 86, 8, 4446, https://doi.org/10.1063/1.452718 . [all data]

Dehmer and Pratt, 1982
Dehmer, P.M.; Pratt, S.T., Photoionization of ArKr, ArXe, and KrXe and bond dissociation energies of the rare gas dimer ions, J. Chem. Phys., 1982, 77, 4804. [all data]

Roth, Lennartz, et al., 1986
Roth, W.E.; Lennartz, H.W.; Vogel, E.; Leiendecker, M.; Masaji, O., Heats of hydrogenation. 6. Resonance energy of fused [4n]annulenes, Chem. Ber., 1986, 119, 837-843. [all data]

Roth, Ruhkamp, et al., 1991
Roth, W.R.; Ruhkamp, J.; Lennartz, H.-W., Bestimmung der Singulett-Triplett-Aufspaltung von Diradikalen mit Hilfe der Sauerstoff-Abfang-Technik, Chem. Ber., 1991, 124, 2047-2051. [all data]

Notes

Go To: Top, Reaction thermochemistry data, References

• Symbols used in this document:
  

  ΔrH°	Enthalpy of reaction at standard conditions
  ΔrS°	Entropy of reaction at standard conditions

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