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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
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 101 to 150

1-Dodecene + Hydrogen = Dodecane

By formula: C12H24 + H2 = C12H26

Quantity Value Units Method Reference Comment
Deltar-125.4 ± 1.5kJ/molChydRogers and Skanupong, 1974liquid phase; solvent: Hexane; ALS
Deltar125.7 ± 2.1kJ/molChydBretschneider and Rogers, 1970liquid phase; solvent: glacial acetic acid; ALS

Hydrogen + 1-Methylcycloheptene = Cycloheptane, methyl-

By formula: H2 + C8H14 = C8H16

Quantity Value Units Method Reference Comment
Deltar-100.5 ± 0.4kJ/molChydTurner and Garner, 1958liquid phase; solvent: Acetic acid; ALS
Deltar-100.5 ± 0.4kJ/molChydTurner and Garner, 1957liquid phase; solvent: Acetic acid; ALS

2Hydrogen + Tetracyclo[3.2.0.0(2,7).0(4,6)]heptane = Norbornane

By formula: 2H2 + C7H8 = C7H12

Quantity Value Units Method Reference Comment
Deltar-384.7 ± 1.8kJ/molChydRogers, Choi, et al., 1980liquid phase; solvent: Hexane; ALS
Deltar-385.1 ± 2.1kJ/molChydTurner, Goebel, et al., 1968liquid phase; solvent: Acetic acid; ALS

Hydrogen + Cyclopropane, methylmethylene- = Cyclopropane, 1,2-dimethyl-, cis-

By formula: H2 + C5H8 = C5H10

Quantity Value Units Method Reference Comment
Deltar-160.3 ± 0.50kJ/molChydTurner, Goebel, et al., 1968liquid phase; solvent: Acetic acid; ALS
Deltar-159. ± 4.2kJ/molChydChesick, 1963liquid phase; solvent: Acetic acid; ALS

2-Pentene, 2,3-dimethyl- + Hydrogen = Pentane, 2,3-dimethyl-

By formula: C7H14 + H2 = C7H16

Quantity Value Units Method Reference Comment
Deltar-106.4 ± 1.6kJ/molChydRogers and Dejroongruang, 1989liquid phase; solvent: Cyclohexane; ALS
Deltar-113. ± 4.6kJ/molChydLopes, Nunes, et al., 1975liquid phase; solvent: Acetic acid; ALS

Hydrogen + Bicyclo[2.1.0]pentane = Cyclopentane

By formula: H2 + C5H8 = C5H10

Quantity Value Units Method Reference Comment
Deltar-235. ± 0.4kJ/molChydRoth, Klarner, et al., 1980liquid phase; solvent: Heptane; ALS
Deltar-230.7 ± 1.5kJ/molChydTurner, Goebel, et al., 1968liquid phase; solvent: Acetic acid; ALS

Hydrogen + (Z)-3-Heptene = Heptane

By formula: H2 + C7H14 = C7H16

Quantity Value Units Method Reference Comment
Deltar-118.5 ± 0.3kJ/molChydRogers and Dejroongruang, 1988liquid phase; solvent: Hydrocarbone; ALS
Deltar-117.2 ± 2.8kJ/molChydRogers and Siddiqui, 1975liquid phase; solvent: n-Hexane; ALS

2Hydrogen + Cyclodecyne = Cyclodecane

By formula: 2H2 + C10H16 = C10H20

Quantity Value Units Method Reference Comment
Deltar-236.2 ± 0.96kJ/molChydTurner, Jarrett, et al., 1973liquid phase; solvent: Acetic acid; ALS
Deltar-236.kJ/molChydSicher, Svoboda, et al., 1966liquid phase; solvent: Acetic acid; ALS

Hydrogen + 1-Pentene, 2,4-dimethyl- = Pentane, 2,4-dimethyl-

By formula: H2 + C7H14 = C7H16

Quantity Value Units Method Reference Comment
Deltar-114.6 ± 1.2kJ/molChydRogers and Dejroongruang, 1989liquid phase; solvent: Cyclohexane; ALS
Deltar-112.kJ/molChydTurner, Nettleton, et al., 1958liquid phase; solvent: Acetic acid; ALS

Cyclododecyne + 2Hydrogen = Cyclododecane

By formula: C12H20 + 2H2 = C12H24

Quantity Value Units Method Reference Comment
Deltar-258.4 ± 1.7kJ/molChydTurner, Jarrett, et al., 1973liquid phase; solvent: Acetic acid; ALS
Deltar-258.kJ/molChydSicher, Svoboda, et al., 1968liquid phase; solvent: Acetic acid; ALS

Hydrogen + 2-Pentene, 4,4-dimethyl-, (E)- = Pentane, 2,2-dimethyl-

By formula: H2 + C7H14 = C7H16

Quantity Value Units Method Reference Comment
Deltar-114.2 ± 0.4kJ/molChydRogers and Dejroongruang, 1989liquid phase; solvent: Cyclohexane; ALS
Deltar-111.kJ/molChydTurner, Nettleton, et al., 1958liquid phase; solvent: Acetic acid; ALS

Hydrogen + 2-Pentene, 4,4-dimethyl-, (Z)- = Pentane, 2,2-dimethyl-

By formula: H2 + C7H14 = C7H16

Quantity Value Units Method Reference Comment
Deltar-130.4 ± 0.4kJ/molChydRogers and Dejroongruang, 1989liquid phase; solvent: Cyclohexane; ALS
Deltar-129.kJ/molChydTurner, Nettleton, et al., 1958liquid phase; solvent: Acetic acid; ALS

Hydrogen + 2-Pentene, 2,4-dimethyl- = Pentane, 2,4-dimethyl-

By formula: H2 + C7H14 = C7H16

Quantity Value Units Method Reference Comment
Deltar-109.4 ± 1.2kJ/molChydRogers and Dejroongruang, 1989liquid phase; solvent: Cyclohexane; ALS
Deltar-105.kJ/molChydTurner, Nettleton, et al., 1958liquid phase; solvent: Acetic acid; ALS

2Hydrogen + 1-Octyne = Octane

By formula: 2H2 + C8H14 = C8H18

Quantity Value Units Method Reference Comment
Deltar-291.0 ± 2.0kJ/molChydMolnar, Rachford, et al., 1984liquid phase; solvent: Dioxane; ALS
Deltar-289.3 ± 2.7kJ/molChydRogers, Dagdagan, et al., 1979liquid phase; solvent: Hexane; ALS

2Hydrogen + Cyclooctyne = Cyclooctane

By formula: 2H2 + C8H12 = C8H16

Quantity Value Units Method Reference Comment
Deltar-291. ± 0.8kJ/molChydRoth, Hopf, et al., 1994liquid phase; solvent: Isooctane; ALS
Deltar-289.kJ/molChydTurner, Jarrett, et al., 1973liquid phase; solvent: Acetic acid; ALS

(E)-Stilbene + Hydrogen = Bibenzyl

By formula: C14H12 + H2 = C14H14

Quantity Value Units Method Reference Comment
Deltar-77.78 ± 0.84kJ/molChydWilliams, 1942liquid phase; solvent: Acetic acid; Reanalyzed by Cox and Pilcher, 1970, Original value = -84.2 ± 1.5 kJ/mol; At 302 K; ALS

Hydrogen + cis-Stilbene = Bibenzyl

By formula: H2 + C14H12 = C14H14

Quantity Value Units Method Reference Comment
Deltar-131.5 ± 0.84kJ/molChydWilliams, 1942liquid phase; solvent: Acetic acid; Reanalyzed by Cox and Pilcher, 1970, Original value = -108.0 ± 8.5 kJ/mol; At 302 K; ALS

1,5-Cyclooctadiene + 2Hydrogen = Cyclooctane

By formula: C8H12 + 2H2 = C8H16

Quantity Value Units Method Reference Comment
Deltar-230. ± 0.4kJ/molChydRoth, Adamczak, et al., 1991liquid phase; ALS
Deltar-224.6 ± 0.08kJ/molChydTurner, Mallon, et al., 1973liquid phase; solvent: Glacial acetic acid; ALS

2Hydrogen + 1,3-Cyclooctadiene, (Z,Z)- = Cyclooctane

By formula: 2H2 + C8H12 = C8H16

Quantity Value Units Method Reference Comment
Deltar-208.kJ/molChydRoth, Adamczak, et al., 1991liquid phase; ALS
Deltar-204.8 ± 0.3kJ/molChydTurner, Mallon, et al., 1973liquid phase; solvent: Glacial acetic acid; ALS

2Hydrogen + 1,4-Cyclohexadiene = Cyclohexane

By formula: 2H2 + C6H8 = C6H12

Quantity Value Units Method Reference Comment
Deltar-233.kJ/molChydRoth, Adamczak, et al., 1991liquid phase; ALS
Deltar-225.5 ± 1.4kJ/molChydTurner, Mallon, et al., 1973liquid phase; solvent: Glacial acetic acid; ALS

4Hydrogen + 1,5-Hexadiyne = n-Hexane

By formula: 4H2 + C6H6 = C6H14

Quantity Value Units Method Reference Comment
Deltar-582.8 ± 4.2kJ/molChydSkinner and Snelson, 1959liquid phase; solvent: Acetic acid; Reanalyzed by Cox and Pilcher, 1970, Original value = -583.2 ± 4.2 kJ/mol; ALS

2Hydrogen + Bicyclo[3.2.1]octa-2,6-diene = Bicyclo[3.2.1]octane

By formula: 2H2 + C8H10 = C8H14

Quantity Value Units Method Reference Comment
Deltar-254. ± 0.8kJ/molChydRoth, Adamczak, et al., 1991liquid phase; ALS
Deltar-242.1 ± 1.1kJ/molChydTurner, Jarrett, et al., 1973liquid phase; solvent: Acetic acid; ALS

C12H34P4Ru (solution) + Carbon monoxide (solution) = C13H32OP4Ru (solution) + Hydrogen (solution)

By formula: C12H34P4Ru (solution) + CO (solution) = C13H32OP4Ru (solution) + H2 (solution)

Quantity Value Units Method Reference Comment
Deltar-84.9kJ/molPACBelt, Scaiano, et al., 1993solvent: Cyclohexane; The reaction enthalpy relies on 0.85 for the quantum yield of H2 dissociation.; MS

C12H34P4Ru (solution) + Nitrogen (solution) = C12H32N2P4Ru (solution) + Hydrogen (solution)

By formula: C12H34P4Ru (solution) + N2 (solution) = C12H32N2P4Ru (solution) + H2 (solution)

Quantity Value Units Method Reference Comment
Deltar16.3kJ/molPACBelt, Scaiano, et al., 1993solvent: Cyclohexane; The reaction enthalpy relies on 0.85 for the quantum yield of H2 dissociation.; MS

C39H68O3P2W (solution) + 1,3-Diazine (solution) = C44H71NO3P2W (solution) + Hydrogen (g)

By formula: C39H68O3P2W (solution) + C4H4N2 (solution) = C44H71NO3P2W (solution) + H2 (g)

Quantity Value Units Method Reference Comment
Deltar-39.7 ± 2.1kJ/molRSCGonzalez, Zhang, et al., 1988solvent: Toluene; MS
Deltar-41.8 ± 2.1kJ/molRSCGonzalez, Zhang, et al., 1988solvent: Tetrahydrofuran; MS

C39H68O3P2W (solution) + Carbon monoxide (solution) = C40H66O4P2W (solution) + Hydrogen (g)

By formula: C39H68O3P2W (solution) + CO (solution) = C40H66O4P2W (solution) + H2 (g)

Quantity Value Units Method Reference Comment
Deltar-85.8 ± 2.9kJ/molRSCGonzalez, Zhang, et al., 1988solvent: Toluene; MS
Deltar-95.4 ± 4.2kJ/molRSCGonzalez, Zhang, et al., 1988solvent: Tetrahydrofuran; MS

8Hydrogen + 2Indene = 1H-Indene, octahydro-, trans- + 1H-Indene, octahydro-, cis-

By formula: 8H2 + 2C9H8 = C9H16 + C9H16

Quantity Value Units Method Reference Comment
Deltar-585.2 ± 4.2kJ/molChydDolliver, Gresham, et al., 1937gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -587.4 ± 4.2 kJ/mol; At 355 °K; ALS

Ethane, 1,2-dichloro- + 2Hydrogen = Ethane + 2Hydrogen chloride

By formula: C2H4Cl2 + 2H2 = C2H6 + 2HCl

Quantity Value Units Method Reference Comment
Deltar-143.0 ± 0.96kJ/molChydLacher, Amador, et al., 1967gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -147.77 ± 0.50 kJ/mol; At 250 C; ALS

2Hydrogen + Propane, 1,2-dichloro- = Propane + 2Hydrogen chloride

By formula: 2H2 + C3H6Cl2 = C3H8 + 2HCl

Quantity Value Units Method Reference Comment
Deltar-126.5 ± 1.1kJ/molChydLacher, Amador, et al., 1967gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -130.60 ± 0.54 kJ/mol; At 250 C; ALS

3Hydrogen + 3-Penten-1-yne, (Z)- = Pentane

By formula: 3H2 + C5H6 = C5H12

Quantity Value Units Method Reference Comment
Deltar-405. ± 0.4kJ/molChydRoth, Adamczak, et al., 1991liquid phase; ALS
Deltar-400. ± 4.6kJ/molChydSkinner and Snelson, 1959liquid phase; solvent: Acetic acid; ALS

3Hydrogen + 3-Penten-1-yne, (E)- = Pentane

By formula: 3H2 + C5H6 = C5H12

Quantity Value Units Method Reference Comment
Deltar-406. ± 1.kJ/molChydRoth, Adamczak, et al., 1991liquid phase; ALS
Deltar-402. ± 2.kJ/molChydSkinner and Snelson, 1959liquid phase; solvent: Acetic acid; ALS

6Hydrogen + 2Indane = 1H-Indene, octahydro-, trans- + 1H-Indene, octahydro-, cis-

By formula: 6H2 + 2C9H10 = C9H16 + C9H16

Quantity Value Units Method Reference Comment
Deltar-377.1 ± 2.1kJ/molChydDolliver, Gresham, et al., 1937gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -383. ± 2. kJ/mol; At 355 °K; ALS

2Hydrogen + Methylene chloride = Methane + 2Hydrogen chloride

By formula: 2H2 + CH2Cl2 = CH4 + 2HCl

Quantity Value Units Method Reference Comment
Deltar-163.4 ± 1.3kJ/molChydLacher, Amador, et al., 1967gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -167.7 ± 1.3 kJ/mol; At 250 C; ALS

2Hydrogen + Ethane, 1,1-dichloro- = Ethane + 2Hydrogen chloride

By formula: 2H2 + C2H4Cl2 = C2H6 + 2HCl

Quantity Value Units Method Reference Comment
Deltar-140.8 ± 1.0kJ/molChydLacher, Amador, et al., 1967gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -145.0 ± 0.50 kJ/mol; At 250C; ALS

Vanadium, tetracarbonyl(η5-2,4-cyclopentadien-1-yl)- (solution) + Hydrogen (solution) = C8H7O3V (solution) + Carbon monoxide (solution)

By formula: C9H5O4V (solution) + H2 (solution) = C8H7O3V (solution) + CO (solution)

Quantity Value Units Method Reference Comment
Deltar56. ± 5.kJ/molPACJohnson, Popov, et al., 1991solvent: Heptane; The reaction enthalpy relies on 0.80 for the quantum yield of CO dissociation.; MS

Hydrogen + 1-Pentene, 2-methyl- = Pentane, 2-methyl-

By formula: H2 + C6H12 = C6H14

Quantity Value Units Method Reference Comment
Deltar-116.3 ± 0.43kJ/molChydRogers, Crooks, et al., 1987liquid phase; ALS
Deltar-115.6 ± 2.2kJ/molChydMolnar, Rachford, et al., 1984liquid phase; solvent: Dioxane; ALS

2-Pentene, 2,4,4-trimethyl- + Hydrogen = Pentane, 2,2,4-trimethyl-

By formula: C8H16 + H2 = C8H18

Quantity Value Units Method Reference Comment
Deltar-112.kJ/molChydTurner, Nettleton, et al., 1958liquid phase; solvent: Acetic acid; ALS
Deltar-118.8kJ/molChydDolliver, Gresham, et al., 1937gas phase; At 355 °K; ALS

Hydrogen + Benzene, 1,1',1'',1''',1'''',1'''''-(1,2-ethanediylidyne)hexakis- = 2Triphenylmethane

By formula: H2 + C38H30 = 2C19H16

Quantity Value Units Method Reference Comment
Deltar-169. ± 3.kJ/molChydBent and Cuthbertson, 1936liquid phase; ALS
Deltar-146.kJ/molChydBent and Cuthbertson, 1936liquid phase; solvent: Ethylacetate; ALS

Hydrogen + 2-Pentene, 4-methyl-, (Z)- = Pentane, 2-methyl-

By formula: H2 + C6H12 = C6H14

Quantity Value Units Method Reference Comment
Deltar-116.9 ± 0.38kJ/molChydRogers, Crooks, et al., 1987liquid phase; ALS
Deltar-114.kJ/molChydTurner, Nettleton, et al., 1958liquid phase; solvent: Acetic acid; ALS

Hydrogen + 2-Pentene, 4-methyl-, (E)- = Pentane, 2-methyl-

By formula: H2 + C6H12 = C6H14

Quantity Value Units Method Reference Comment
Deltar-114.2 ± 0.57kJ/molChydRogers, Crooks, et al., 1987liquid phase; ALS
Deltar-110.kJ/molChydTurner, Nettleton, et al., 1958liquid phase; solvent: Acetic acid; ALS

2Sodium hydroxide + Dioxybismethanol = Hydrogen + 2sodium formate + 2Water

By formula: 2HNaO + C2H6O4 = H2 + 2CHNaO2 + 2H2O

Quantity Value Units Method Reference Comment
Deltar-293.3 ± 5.0kJ/molCmJenkins and Style, 1953solid phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -292. kJ/mol; ALS

Hydrogen + Propanal, 2-methyl- = 1-Propanol, 2-methyl-

By formula: H2 + C4H8O = C4H10O

Quantity Value Units Method Reference Comment
Deltar-87.4 ± 0.3kJ/molCmWiberg, Crocker, et al., 1991liquid phase; ALS
Deltar-68.1 ± 0.9kJ/molEqkConnett, 1975gas phase; Heat of dehydrogenation; ALS

2Hydrogen + Ethene, chlorotrifluoro- = 1,1,2-Trifluoroethane + Hydrogen chloride

By formula: 2H2 + C2ClF3 = C2H3F3 + HCl

Quantity Value Units Method Reference Comment
Deltar-267.7 ± 2.1kJ/molChydLacher, Kianpour, et al., 1956gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -271.6 kJ/mol; At 410 K; ALS

2Hydrogen + 2-Butyne = Butane

By formula: 2H2 + C4H6 = C4H10

Quantity Value Units Method Reference Comment
Deltar-272.4 ± 1.3kJ/molChydConn, Kistiakowsky, et al., 1939gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -274.4 ± 0.54 kJ/mol; At 355 K; ALS

Hydrogen + 2-Butene, (E)- = Butane

By formula: H2 + C4H8 = C4H10

Quantity Value Units Method Reference Comment
Deltar-114.6 ± 0.42kJ/molChydKistiakowsky, Ruhoff, et al., 1935gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -115.57 ± 0.088 kJ/mol; At 355 °K; ALS

Hydrogen + 2-Butene, (Z)- = Butane

By formula: H2 + C4H8 = C4H10

Quantity Value Units Method Reference Comment
Deltar-118.5 ± 0.42kJ/molChydKistiakowsky, Ruhoff, et al., 1935gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -119.54 ± 0.079 kJ/mol; At 355 °K; ALS

Styrene + 4Hydrogen = Cyclohexane, ethyl-

By formula: C8H8 + 4H2 = C8H16

Quantity Value Units Method Reference Comment
Deltar-320.1 ± 1.0kJ/molChydDolliver, Gresham, et al., 1937gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -324.2 ± 0.84 kJ/mol; At 355 °K; ALS

2Hydrogen + 1,4-Pentadiene = Pentane

By formula: 2H2 + C5H8 = C5H12

Quantity Value Units Method Reference Comment
Deltar-252.0 ± 0.63kJ/molChydKistiakowsky, Ruhoff, et al., 1936gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -254.3 ± 0.63 kJ/mol; At 355 °K; ALS

2Hydrogen + 1,3-Cyclopentadiene = Cyclopentane

By formula: 2H2 + C5H6 = C5H10

Quantity Value Units Method Reference Comment
Deltar-210.8 ± 0.84kJ/molChydKistiakowsky, Ruhoff, et al., 1936gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -212.8 ± 0.84 kJ/mol; At 355 °K; ALS

Hydrogen + 3-Hexene, 2,2,5,5-tetramethyl-, (Z)- = Hexane, 2,2,5,5-tetramethyl-

By formula: H2 + C10H20 = C10H22

Quantity Value Units Method Reference Comment
Deltar-158.kJ/molChydDoering, Roth, et al., 1989liquid phase; ALS
Deltar-151.kJ/molChydTurner, Nettleton, et al., 1958liquid phase; solvent: Acetic acid; 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.

Rogers and Skanupong, 1974
Rogers, D.W.; Skanupong, S., Heats of hydrogenation of sixteen terminal monoolefins. The alternating effect, J. Phys. Chem., 1974, 78, 2569-2572. [all data]

Bretschneider and Rogers, 1970
Bretschneider, E.; Rogers, D.W., A new microcalorimeter: heats of hydrogenation of four monoolefins, Mikrochim. Acta, 1970, 482-490. [all data]

Turner and Garner, 1958
Turner, R.B.; Garner, R.H., Heats of hydrogenation. V. Relative stabilities in certain exocyclic-endocyclic olefin pairs, J. Am. Chem. Soc., 1958, 80, 1424-1430. [all data]

Turner and Garner, 1957
Turner, R.B.; Garner, R.H., Heats of hydrogenation. V. Relative stabilities in certain exocyclic-endocyclic olefin pairs, J. Am. Chem. Soc., 1957, 80, 1424-1430. [all data]

Rogers, Choi, et al., 1980
Rogers, D.W.; Choi, L.S.; Girellini, R.S., Heats of hydrogenation and formation of quadricyclene, norbornadiene, norbornene, and nortricyclene, J. Phys. Chem., 1980, 84, 1810-1814. [all data]

Turner, Goebel, et al., 1968
Turner, R.B.; Goebel, P.; Mallon, B.J.; Doering, W.E.; Coburn, J.F., Jr.; Pomerantz, M., Heats of hydrogenation. VIII. Compounds with three- and four-membered rings, J. Am. Chem. Soc., 1968, 90, 4315-4322. [all data]

Chesick, 1963
Chesick, J.P., Kinetics of the thermal interconversion of 2-methylmethylenecyclopropane and ethylidenecyclopropane, J. Am. Chem. Soc., 1963, 85, 2720-2723. [all data]

Rogers and Dejroongruang, 1989
Rogers, D.W.; Dejroongruang, K., Enthalpies of hydrogenation of the dimethylpentenes, ethylpentenes, methylbutene, and trimethylbutene, J. Chem. Thermodyn., 1989, 21, 1115-1120. [all data]

Lopes, Nunes, et al., 1975
Lopes, M.T.R.; Nunes, M.F.T.; Florencio, M.H.F.S.; Mota, M.M.G.; Fernandez, M.T.N., Heats of hydrogenation in solution. I. Calorimeter for semimicro determinations, Rev. Port. Quim., 1975, 15, 129-132. [all data]

Roth, Klarner, et al., 1980
Roth, W.R.; Klarner, F.-G.; Lennartz, H.-W., Heats of hydrogenation. II. Heat of hydrogenation of bicyclo[2.1.0]pent-2-ene, an antiaromatic system, Chem. Ber., 1980, 113, 1806-1818. [all data]

Rogers and Dejroongruang, 1988
Rogers, D.W.; Dejroongruang, K., Enthalpies of hydrogenation of the n-heptenes and the methylhexenes, J. Chem. Thermodyn., 1988, 20, 675-680. [all data]

Rogers and Siddiqui, 1975
Rogers, D.W.; Siddiqui, N.A., Heats of hydrogenation of large molecules. I. Esters of unsaturated fatty acids, J. Phys. Chem., 1975, 79, 574-577. [all data]

Turner, Jarrett, et al., 1973
Turner, R.B.; Jarrett, A.D.; Goebel, P.; Mallon, B.J., Heats of hydrogenation. 9. Cyclic acetylenes and some miscellaneous olefins, J. Am. Chem. Soc., 1973, 95, 790-792. [all data]

Sicher, Svoboda, et al., 1966
Sicher, J.; Svoboda, M.; Zavada, J.; Turner, R.B.; Goebel, P., Sterochemical studies - XXXVI. An approach to conformational analysis of medium ring compounds. Unsaturated ten-membered ring derivates, Tetrahedron, 1966, 22, 659-671. [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]

Sicher, Svoboda, et al., 1968
Sicher, J.; Svoboda, M.; Mallon, B.J.; Turner, R.B., Stereochemical studies. Part XLVII. Conformational analysis of many-membered ring compounds. The cyclododecenes, J. Chem. Soc. B, 1968, 441-447. [all data]

Molnar, Rachford, et al., 1984
Molnar, A.; Rachford, R.; Smith, G.V.; Liu, R., Heats of hydrogenation by a simple and rapid flow calorimetric method, Appl. Catal., 1984, 9, 219-223. [all data]

Rogers, Dagdagan, et al., 1979
Rogers, D.W.; Dagdagan, O.A.; Allinger, N.L., Heats of hydrogenation and formation of linear alkynes and a molecular mechanics interpretation, J. Am. Chem. Soc., 1979, 101, 671-676. [all data]

Roth, Hopf, et al., 1994
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Notes

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