Hydrogen

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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

Hydrogen + trans-1,2-di-tert-butylethylene = Hexane, 2,2,5,5-tetramethyl-

By formula: H2 + C10H20 = C10H22

Quantity Value Units Method Reference Comment
Δr-118.kJ/molChydDoering, Roth, et al., 1989liquid phase; ALS
Δr-113.kJ/molChydTurner, Nettleton, et al., 1958liquid phase; solvent: Acetic acid; ALS

Mesitylene + 3Hydrogen = Cyclohexane, 1,3,5-trimethyl-

By formula: C9H12 + 3H2 = C9H18

Quantity Value Units Method Reference Comment
Δr-196.1 ± 0.84kJ/molChydDolliver, Gresham, et al., 1937gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -199.2 ± 0.8 kJ/mol; At 355 °K; ALS

3Hydrogen + o-Xylene = Cyclohexane, 1,2-dimethyl-, cis-

By formula: 3H2 + C8H10 = C8H16

Quantity Value Units Method Reference Comment
Δr-194.6 ± 0.84kJ/molChydDolliver, Gresham, et al., 1937gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -197.7 ± 0.84 kJ/mol; At 355 °K; ALS

Ethylbenzene + 3Hydrogen = Cyclohexane, ethyl-

By formula: C8H10 + 3H2 = C8H16

Quantity Value Units Method Reference Comment
Δr-201.6 ± 0.42kJ/molChydDolliver, Gresham, et al., 1937gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -204.7 ± 0.4 kJ/mol; At 355 °K; ALS

Furan + 2Hydrogen = Tetrahydrofuran

By formula: C4H4O + 2H2 = C4H8O

Quantity Value Units Method Reference Comment
Δr-151.1 ± 0.50kJ/molChydDolliver, Gresham, et al., 1938gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -153.3 ± 0.50 kJ/mol; At 355 °K; ALS

2Hydrogen + Acetylene = Ethane

By formula: 2H2 + C2H2 = C2H6

Quantity Value Units Method Reference Comment
Δr-312.0 ± 0.63kJ/molChydConn, Kistiakowsky, et al., 1939gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -314.1 ± 2.8 kJ/mol; At 355 K; ALS

2Hydrogen + Propyne = Propane

By formula: 2H2 + C3H4 = C3H8

Quantity Value Units Method Reference Comment
Δr-289.6 ± 0.63kJ/molChydConn, Kistiakowsky, et al., 1939gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -288.8 ± 0.59 kJ/mol; At 355 K; ALS

2Hydrogen + Allene = Propane

By formula: 2H2 + C3H4 = C3H8

Quantity Value Units Method Reference Comment
Δr-295.1 ± 1.0kJ/molChydKistiakowsky, Ruhoff, et al., 1936gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -298.2 ± 0.84 kJ/mol; At 355 °K; ALS

1,3-Butadiene + 2Hydrogen = Butane

By formula: C4H6 + 2H2 = C4H10

Quantity Value Units Method Reference Comment
Δr-236.7 ± 0.42kJ/molChydKistiakowsky, Ruhoff, et al., 1936gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -238.8 ± 0.4 kJ/mol; At 355 °K; ALS

3Hydrogen + Benzene = Cyclohexane

By formula: 3H2 + C6H6 = C6H12

Quantity Value Units Method Reference Comment
Δr-205.3 ± 0.63kJ/molChydKistiakowsky, Ruhoff, et al., 1936gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -208.4 ± 0.63 kJ/mol; At 355 °K; ALS

1-Propene, 2-methyl- + Hydrogen = Isobutane

By formula: C4H8 + H2 = C4H10

Quantity Value Units Method Reference Comment
Δr-117.8 ± 0.42kJ/molChydKistiakowsky, Ruhoff, et al., 1935gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -118.78 ± 0.75 kJ/mol; At 355 °K; ALS

Hydrogen + 1-Butene, 3-methyl- = Butane, 2-methyl-

By formula: H2 + C5H10 = C5H12

Quantity Value Units Method Reference Comment
Δr-126.3 ± 0.3kJ/molChydDolliver, Gresham, et al., 1937gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -126.9 ± 0.3 kJ/mol; At 355 °K; ALS

2Hydrogen + 1,3-Cyclohexadiene, 1-methyl-4-(1-methylethyl)- = 1-Methyl-4-(1-methylethyl)-cyclohexane

By formula: 2H2 + C10H16 = C10H20

Quantity Value Units Method Reference Comment
Δr-210.1 ± 1.3kJ/molChydDolliver, Gresham, et al., 1937gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -212.2 ± 1.3 kJ/mol; At 355 °K; ALS

Hydrogen + 2-Butenal = Butanal

By formula: H2 + C4H6O = C4H8O

Quantity Value Units Method Reference Comment
Δr-104.2 ± 0.42kJ/molChydDolliver, Gresham, et al., 1938gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -105.3 ± 0.4 kJ/mol; At 355°K; ALS

(HO2+ • Oxygen) + Hydrogen = (HO2+ • Hydrogen • Oxygen)

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

Quantity Value Units Method Reference Comment
Δr17.kJ/molPHPMSHiraoka, Saluja, et al., 1979gas phase; M
Quantity Value Units Method Reference Comment
Δr71.J/mol*KPHPMSHiraoka, Saluja, et al., 1979gas phase; M

2Hydrogen + α-Phellandrene = 1-Methyl-4-(1-methylethyl)-cyclohexane

By formula: 2H2 + C10H16 = C10H20

Quantity Value Units Method Reference Comment
Δr-221.4 ± 1.3kJ/molChydDolliver, Gresham, et al., 1937gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -223. ± 1. kJ/mol; At 355 °K; ALS

Vinyl ether + 2Hydrogen = Ethyl ether

By formula: C4H6O + 2H2 = C4H10O

Quantity Value Units Method Reference Comment
Δr-237.4 ± 0.42kJ/molChydDolliver, Gresham, et al., 1938gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -239.5 ± 0.4 kJ/mol; At 355°K; ALS

(CH5+ • 2Hydrogen) + Hydrogen = (CH5+ • 3Hydrogen)

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

Quantity Value Units Method Reference Comment
Δr6.74 ± 0.42kJ/molPHPMSHiraoka, Kudaka, et al., 1991gas phase; M
Quantity Value Units Method Reference Comment
Δr94.6J/mol*KPHPMSHiraoka, Kudaka, et al., 1991gas phase; M

(CH5+ • 3Hydrogen) + Hydrogen = (CH5+ • 4Hydrogen)

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

Quantity Value Units Method Reference Comment
Δr6.57 ± 0.42kJ/molPHPMSHiraoka, Kudaka, et al., 1991gas phase; M
Quantity Value Units Method Reference Comment
Δr108.J/mol*KPHPMSHiraoka, Kudaka, et al., 1991gas phase; M

2-Propen-1-ol + Hydrogen = 1-Propanol

By formula: C3H6O + H2 = C3H8O

Quantity Value Units Method Reference Comment
Δr-130.6 ± 1.8kJ/molChydDolliver, Gresham, et al., 1938gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -132. ± 1. kJ/mol; At 355°K; ALS

(CH5+ • Hydrogen) + Hydrogen = (CH5+ • 2Hydrogen)

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

Quantity Value Units Method Reference Comment
Δr7.45 ± 0.42kJ/molPHPMSHiraoka, Kudaka, et al., 1991gas phase; M
Quantity Value Units Method Reference Comment
Δr67.8J/mol*KPHPMSHiraoka, Kudaka, et al., 1991gas phase; M

Acetic acid ethenyl ester + Hydrogen = Ethyl Acetate

By formula: C4H6O2 + H2 = C4H8O2

Quantity Value Units Method Reference Comment
Δr-129. ± 4.6kJ/molChydVilcu and Perisanu, 1980liquid phase; ALS
Δr-130.2 ± 0.3kJ/molChydDolliver, Gresham, et al., 1938gas phase; At 355 °K; ALS

Hydrogen + Methyl methacrylate = Methyl isobutyrate

By formula: H2 + C5H8O2 = C5H10O2

Quantity Value Units Method Reference Comment
Δr-108. ± 5.0kJ/molChydVilcu and Perisanu, 1980liquid phase; ALS
Δr-119.8 ± 0.2kJ/molChydDolliver, Gresham, et al., 1938gas phase; At 355 K; ALS

(H3+ • 4Hydrogen) + Hydrogen = (H3+ • 5Hydrogen)

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

Quantity Value Units Method Reference Comment
Δr6.9 ± 0.4kJ/molPHPMSHiraoka, 1987gas phase; M
Quantity Value Units Method Reference Comment
Δr79.1J/mol*KPHPMSHiraoka, 1987gas phase; M

(H3+ • 5Hydrogen) + Hydrogen = (H3+ • 6Hydrogen)

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

Quantity Value Units Method Reference Comment
Δr6.4 ± 0.4kJ/molPHPMSHiraoka, 1987gas phase; M
Quantity Value Units Method Reference Comment
Δr83.7J/mol*KPHPMSHiraoka, 1987gas phase; M

(H3+ • 6Hydrogen) + Hydrogen = (H3+ • 7Hydrogen)

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

Quantity Value Units Method Reference Comment
Δr3.7 ± 0.4kJ/molPHPMSHiraoka, 1987gas phase; M
Quantity Value Units Method Reference Comment
Δr69.0J/mol*KPHPMSHiraoka, 1987gas phase; M

(H3+ • 7Hydrogen) + Hydrogen = (H3+ • 8Hydrogen)

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

Quantity Value Units Method Reference Comment
Δr3.3 ± 0.4kJ/molPHPMSHiraoka, 1987gas phase; M
Quantity Value Units Method Reference Comment
Δr74.9J/mol*KPHPMSHiraoka, 1987gas phase; M

(H3+ • 8Hydrogen) + Hydrogen = (H3+ • 9Hydrogen)

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

Quantity Value Units Method Reference Comment
Δr2.6 ± 0.4kJ/molPHPMSHiraoka, 1987gas phase; M
Quantity Value Units Method Reference Comment
Δr79.9J/mol*KPHPMSHiraoka, 1987gas phase; M

Hydrogen + Propane, 2-bromo- = Hydrogen bromide + Propane

By formula: H2 + C3H7Br = HBr + C3H8

Quantity Value Units Method Reference Comment
Δr-45.40 ± 0.92kJ/molChydDavies, Lacher, et al., 1965gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -45.06 kJ/mol; ALS

Cyclobutanone + Hydrogen = Cyclobutanol

By formula: C4H6O + H2 = C4H8O

Quantity Value Units Method Reference Comment
Δr-67.91 ± 0.75kJ/molChydWiberg, Crocker, et al., 1991liquid phase; ALS
Δr-53. ± 1.kJ/molChydWiberg, Crocker, et al., 1991gas phase; ALS

(HN2+ • Hydrogen) + Hydrogen = (HN2+ • 2Hydrogen)

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

Quantity Value Units Method Reference Comment
Δr7.5kJ/molPHPMSHiraoka, Saluja, et al., 1979gas phase; M
Quantity Value Units Method Reference Comment
Δr71.J/mol*KPHPMSHiraoka, Saluja, et al., 1979gas phase; M

Hydrogen + Cycloheptanone = Cycloheptanol

By formula: H2 + C7H12O = C7H14O

Quantity Value Units Method Reference Comment
Δr-62.5 ± 0.4kJ/molChydWiberg, Crocker, et al., 1991liquid phase; ALS
Δr-46. ± 1.kJ/molChydWiberg, Crocker, et al., 1991gas phase; ALS

2Hydrogen + 3-Butynoic acid = Butanoic acid

By formula: 2H2 + C4H4O2 = C4H8O2

Quantity Value Units Method Reference Comment
Δr-292.0 ± 0.84kJ/molChydFlitcroft and Skinner, 1958solid phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -303. ± 4.6 kJ/mol; ALS

Butanal + Hydrogen = 1-Butanol

By formula: C4H8O + H2 = C4H10O

Quantity Value Units Method Reference Comment
Δr-81.88 ± 0.75kJ/molCmWiberg, Crocker, et al., 1991liquid phase; ALS
Δr-70.5 ± 1.3kJ/molChydBuckley and Cox, 1967gas phase; ALS

CH5+ + Hydrogen = (CH5+ • Hydrogen)

By formula: CH5+ + H2 = (CH5+ • H2)

Quantity Value Units Method Reference Comment
Δr7.87 ± 0.42kJ/molPHPMSHiraoka, Kudaka, et al., 1991gas phase; M
Quantity Value Units Method Reference Comment
Δr50.6J/mol*KPHPMSHiraoka, Kudaka, et al., 1991gas phase; M

Hydrogen + 1-Butene, 2,3-dimethyl- = Butane, 2,3-dimethyl-

By formula: H2 + C6H12 = C6H14

Quantity Value Units Method Reference Comment
Δr-116.3 ± 0.58kJ/molChydRogers, Crooks, et al., 1987liquid phase; ALS
Δr-116.1 ± 0.4kJ/molChydKistiakowsky, Ruhoff, et al., 1936, 2gas phase; ALS

HN2+ + Hydrogen = (HN2+ • Hydrogen)

By formula: HN2+ + H2 = (HN2+ • H2)

Quantity Value Units Method Reference Comment
Δr30.kJ/molPHPMSHiraoka, Saluja, et al., 1979gas phase; M
Quantity Value Units Method Reference Comment
Δr94.6J/mol*KPHPMSHiraoka, Saluja, et al., 1979gas phase; M

Formyl cation + Hydrogen = (Formyl cation • Hydrogen)

By formula: CHO+ + H2 = (CHO+ • H2)

Quantity Value Units Method Reference Comment
Δr16.kJ/molPHPMSHiraoka and Kebarle, 1975gas phase; M
Quantity Value Units Method Reference Comment
Δr85.8J/mol*KPHPMSHiraoka and Kebarle, 1975gas phase; M

HO2+ + Hydrogen = (HO2+ • Hydrogen)

By formula: HO2+ + H2 = (HO2+ • H2)

Quantity Value Units Method Reference Comment
Δr52.3kJ/molPHPMSHiraoka, Saluja, et al., 1979gas phase; M
Quantity Value Units Method Reference Comment
Δr92.J/mol*KPHPMSHiraoka, Saluja, et al., 1979gas phase; M

Hydrogen + Ethylene = Ethane

By formula: H2 + C2H4 = C2H6

Quantity Value Units Method Reference Comment
Δr-136. ± 2.kJ/molChydKistiakowsky and Nickle, 1951gas phase; ALS
Δr-136.3 ± 0.3kJ/molChydKistiakowsky, Romeyn, et al., 1935gas phase; ALS

Cyclopentanol = Cyclopentanone + Hydrogen

By formula: C5H10O = C5H8O + H2

Quantity Value Units Method Reference Comment
Δr54.9 ± 4.7kJ/molEqkFedoseenko, Yursha, et al., 1984gas phase; ALS
Δr51.30kJ/molEqkCubberley and Mueller, 1946gas phase; ALS

1,4-Dithiothreitol = Hydrogen + 1,2-Dithiane-4,5-diol, trans-

By formula: C4H10O2S2 = H2 + C8H18O4S4

Quantity Value Units Method Reference Comment
Δr-31.5 ± 2.6kJ/molCmFukada and Takahashi, 1980liquid phase; solvent: Buffers pH 6-13; Redox reaction with K3Fe(CN)6; ALS

2-Butanol = Hydrogen + 2-Butanone

By formula: C4H10O = H2 + C4H8O

Quantity Value Units Method Reference Comment
Δr54.22kJ/molEqkCubberley and Mueller, 1946gas phase; ALS
Δr57.170kJ/molEqkKolb and Burwell, 1945gas phase; ALS

Isopropyl Alcohol = Hydrogen + Acetone

By formula: C3H8O = H2 + C3H6O

Quantity Value Units Method Reference Comment
Δr55.23kJ/molEqkBuckley and Herington, 1965gas phase; ALS
Δr56.543kJ/molEqkKolb and Burwell, 1945gas phase; ALS

3Hydrogen + 3,3-Dimethyl-6-methylidene-1,4-cyclohexadiene = 1,1,4-Trimethylcyclohexane

By formula: 3H2 + C9H12 = C9H18

Quantity Value Units Method Reference Comment
Δr-321.kJ/molChydDoering, Birladeanu, et al., 1996liquid phase; solvent: Hydrocarbone; Unpublished results by D. Rogers; ALS

21,3-Cyclopentadiene (l) + magnesium (cr) = Magnesium, bis(η(5)-2,4-cyclopentadien-1-yl)- (cr) + Hydrogen (g)

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

Quantity Value Units Method Reference Comment
Δr-142.5 ± 2.9kJ/molRSCHull, Reid, et al., 1967Please also see Pedley and Rylance, 1977 and Cox and Pilcher, 1970, 2.; MS

Ar+ + Hydrogen = (Ar+ • Hydrogen)

By formula: Ar+ + H2 = (Ar+ • H2)

Quantity Value Units Method Reference Comment
Δr93.7kJ/molFAShul, Passarella, et al., 1987gas phase; switching reaction(Ar+)Ar, ΔrH>; Dehmer and Pratt, 1982; M

2Hydrogen + Cyclobutane, 1,2-bis(methylene)- = cyclobutane, 1,2-dimethyl-, trans-

By formula: 2H2 + C6H8 = C6H12

Quantity Value Units Method Reference Comment
Δr-244. ± 0.8kJ/molChydRoth, Lennartz, et al., 1986liquid phase; solvent: Isooctane; Mixture cis and trans; ALS

3Hydrogen + 3,4-Dimethylenecyclobut-1-ene = cyclobutane, 1,2-dimethyl-, trans-

By formula: 3H2 + C6H6 = C6H12

Quantity Value Units Method Reference Comment
Δr-376. ± 1.kJ/molChydRoth, Lennartz, et al., 1986liquid phase; solvent: Isooctane; Mixture cis and trans; ALS

2Hydrogen + 7-Methylenebicyclo[3.2.0]hept-1-ene = Bicyclo[3.2.0]heptane, 6-methyl-, (1α, 5α, 6α)-

By formula: 2H2 + C8H10 = C8H14

Quantity Value Units Method Reference Comment
Δr-286. ± 0.4kJ/molChydRoth, Ruhkamp, et al., 1991gas phase; The ratio 21.9:78.1 % anti to syn isomers; ALS

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

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