Cyclohexene
- Formula: C6H10
- Molecular weight: 82.1436
- IUPAC Standard InChIKey: HGCIXCUEYOPUTN-UHFFFAOYSA-N
- CAS Registry Number: 110-83-8
- 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. - Other names: Benzene tetrahydride; Benzene, tetrahydro-; Cyclohex-1-ene; Tetrahydrobenzene; 1,2,3,4-Tetrahydrobenzene; Cykloheksen; Hexanaphthylene; UN 2256; 1-Cyclohexene; NSC 24835
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Condensed phase thermochemistry data
Go To: Top, Phase change data, Gas phase ion energetics data, Mass spectrum (electron ionization), 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
DH - Eugene S. Domalski and Elizabeth D. Hearing
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔfH°liquid | -37.8 ± 8.2 | kJ/mol | Ccr | Steele, Chirico, et al., 1996 | ALS |
ΔfH°liquid | -38.2 ± 0.59 | kJ/mol | Ccb | Good and Smith, 1969 | ALS |
ΔfH°liquid | -38.8 ± 0.59 | kJ/mol | Ccb | Labbauf and Rossini, 1961 | ALS |
ΔfH°liquid | -40.6 ± 0.79 | kJ/mol | Ccb | Epstein, Pitzer, et al., 1949 | Unpublished results; ALS |
Quantity | Value | Units | Method | Reference | Comment |
ΔcH°liquid | -3752.39 ± 0.49 | kJ/mol | Ccr | Steele, Chirico, et al., 1996 | Corresponding ΔfHºliquid = -37.82 kJ/mol (simple calculation by NIST; no Washburn corrections); ALS |
ΔcH°liquid | -3752.0 ± 0.50 | kJ/mol | Ccb | Good and Smith, 1969 | Corresponding ΔfHºliquid = -38.2 kJ/mol (simple calculation by NIST; no Washburn corrections); ALS |
ΔcH°liquid | -3751.5 ± 0.50 | kJ/mol | Ccb | Labbauf and Rossini, 1961 | Corresponding ΔfHºliquid = -38.7 kJ/mol (simple calculation by NIST; no Washburn corrections); ALS |
ΔcH°liquid | -3761. | kJ/mol | Ccb | Konovalon, 1926 | Heat of combustion at 15°C; Corresponding ΔfHºliquid = -30. kJ/mol (simple calculation by NIST; no Washburn corrections); ALS |
Quantity | Value | Units | Method | Reference | Comment |
S°liquid | 214.60 | J/mol*K | N/A | Haida, Suga, et al., 1977 | DH |
S°liquid | 216.19 | J/mol*K | N/A | Huffman, Eaton, et al., 1948 | DH |
S°liquid | 216.7 | J/mol*K | N/A | Parks and Huffman, 1930 | Extrapolation below 90 K, 49.20 J/mol*K.; DH |
Constant pressure heat capacity of liquid
Cp,liquid (J/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
148.8 | 298.15 | Steele, Chirico, et al., 1993 | DH |
152.90 | 298.12 | Kalinowska and Woycicki, 1988 | T = 183 to 298 K. Unsmoothed experimental datum.; DH |
148.35 | 298.15 | Haida, Suga, et al., 1977 | T = 15 to 293 K.; DH |
149.16 | 298.15 | Huffman, Eaton, et al., 1948 | T = 12 to 300 K.; DH |
145.6 | 293.2 | Parks and Huffman, 1930 | T = 92 to 293 K. Value is unsmoothed experimental datum.; DH |
Phase change data
Go To: Top, Condensed phase thermochemistry data, Gas phase ion energetics data, Mass spectrum (electron ionization), 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:
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
BS - Robert L. Brown and Stephen E. Stein
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DRB - Donald R. Burgess, Jr.
AC - William E. Acree, Jr., James S. Chickos
CAL - James S. Chickos, William E. Acree, Jr., Joel F. Liebman, Students of Chem 202 (Introduction to the Literature of Chemistry), University of Missouri -- St. Louis
DH - Eugene S. Domalski and Elizabeth D. Hearing
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
Tboil | 356. ± 2. | K | AVG | N/A | Average of 56 out of 57 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
Tfus | 169. ± 1. | K | AVG | N/A | Average of 9 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
Ttriple | 169.66 | K | N/A | Haida, Suga, et al., 1977, 2 | Crystal phase 1 phase; Uncertainty assigned by TRC = 0.02 K; TRC |
Ttriple | 169.67 | K | N/A | Huffman, Eaton, et al., 1948, 2 | Crystal phase 1 phase; Uncertainty assigned by TRC = 0.05 K; TRC |
Ttriple | 169.0 | K | N/A | Parks and Huffman, 1930, 2 | Crystal phase 1 phase; Uncertainty assigned by TRC = 0.2 K; TRC |
Quantity | Value | Units | Method | Reference | Comment |
Tc | 560.4 ± 0.1 | K | N/A | Tsonopoulos and Ambrose, 1996 | |
Tc | 560.4 | K | N/A | Majer and Svoboda, 1985 | |
Tc | 560.4 | K | N/A | Cheng, McCoubrey, et al., 1962 | Uncertainty assigned by TRC = 0.3 K; Visual (5-cm 2-mm bore tubes) in nitrate-nitrite bath, TE or TH cal. vs NPL thermometer; TRC |
Tc | 560.42 | K | N/A | Ambrose, Cox, et al., 1960 | Uncertainty assigned by TRC = 0.02 K; Visual, PRT, IPTS-48, with decomp.; TRC |
Tc | 553.5 | K | N/A | Ambrose and Grant, 1957 | Uncertainty assigned by TRC = 0.15 K; TRC |
Quantity | Value | Units | Method | Reference | Comment |
ΔvapH° | 33.57 | kJ/mol | N/A | Majer and Svoboda, 1985 | |
ΔvapH° | 33.50 ± 0.53 | kJ/mol | V | Steele, Chirico, et al., 1996 | ALS |
ΔvapH° | 33.5 | kJ/mol | N/A | Steele, Chirico, et al., 1996 | DRB |
ΔvapH° | 33.5 ± 0.5 | kJ/mol | EB | Steele, Chirico, et al., 1996 | Based on data from 285. to 357. K.; AC |
ΔvapH° | 30.5 ± 0.3 | kJ/mol | V | Mathews, 1926 | ALS |
Enthalpy of vaporization
ΔvapH (kJ/mol) | Temperature (K) | Method | Reference | Comment |
---|---|---|---|---|
30.46 | 356.2 | N/A | Majer and Svoboda, 1985 | |
32.8 | 330. | N/A | Marrufo, Aucejo, et al., 2009 | Based on data from 315. to 356. K.; AC |
32.9 | 325. | N/A | Steyer and Sundmacher, 2004 | Based on data from 310. to 356. K.; AC |
32.6 | 327. | N/A | Segura, Lam, et al., 2001 | Based on data from 312. to 356. K.; AC |
32.7 | 324. | A,EB | Stephenson and Malanowski, 1987 | Based on data from 309. to 365. K. See also Meyer and Hotz, 1973.; AC |
33.1 | 308. | MM | Letcher and Marsicano, 1974 | Based on data from 305. to 322. K.; AC |
32.7 ± 0.1 | 313. | C | Svoboda, Veselý, et al., 1973 | AC |
32.2 ± 0.1 | 323. | C | Svoboda, Veselý, et al., 1973 | AC |
31.7 ± 0.1 | 333. | C | Svoboda, Veselý, et al., 1973 | AC |
31.2 ± 0.1 | 343. | C | Svoboda, Veselý, et al., 1973 | AC |
30.7 ± 0.1 | 353. | C | Svoboda, Veselý, et al., 1973 | AC |
33.7 | 300. | MM | Forziati, Camin, et al., 1950 | Based on data from 285. to 357. K.; AC |
32.59 | 300. | V | Lister, 1941 | Heat of bromination at 300 K; ALS |
32.6 | 300. | N/A | Lister, 1941 | Based on data from 229. to 292. K.; AC |
Enthalpy of vaporization
ΔvapH =
A exp(-βTr) (1 − Tr)β
ΔvapH =
Enthalpy of vaporization (at saturation pressure)
(kJ/mol)
Tr = reduced temperature (T / Tc)
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Temperature (K) | A (kJ/mol) | β | Tc (K) | Reference | Comment |
---|---|---|---|---|---|
313. to 353. | 47.19 | 0.2662 | 560.4 | Majer and Svoboda, 1985 |
Antoine Equation Parameters
log10(P) = A − (B / (T + C))
P = vapor pressure (bar)
T = temperature (K)
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Temperature (K) | A | B | C | Reference |
---|---|---|---|---|
310.02 to 364.53 | 3.9973 ± 0.0018 | 1221.9 ± 1.0 | -49.98 ± 0.12 | Meyer and Hotz, 1973 |
Enthalpy of fusion
ΔfusH (kJ/mol) | Temperature (K) | Reference | Comment |
---|---|---|---|
3.28 | 169.7 | Domalski and Hearing, 1996 | AC |
Entropy of fusion
ΔfusS (J/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
30.5 | 138.7 | Domalski and Hearing, 1996 | CAL |
19.35 | 169.7 |
Enthalpy of phase transition
ΔHtrs (kJ/mol) | Temperature (K) | Initial Phase | Final Phase | Reference | Comment |
---|---|---|---|---|---|
1.483 | 112.3 | crystaline, III | crystaline, I | Haida, Suga, et al., 1977 | DH |
4.231 | 138.63 | crystaline, II | crystaline, I | Haida, Suga, et al., 1977 | DH |
3.284 | 169.66 | crystaline, I | liquid | Haida, Suga, et al., 1977 | DH |
4.2505 | 138.7 | crystaline, II | crystaline, I | Huffman, Eaton, et al., 1948 | DH |
3.2932 | 169.67 | crystaline, I | liquid | Huffman, Eaton, et al., 1948 | DH |
4.075 | 138.7 | crystaline, II | crystaline, I | Parks and Huffman, 1930 | DH |
3.289 | 169.0 | crystaline, I | liquid | Parks and Huffman, 1930 | DH |
Entropy of phase transition
ΔStrs (J/mol*K) | Temperature (K) | Initial Phase | Final Phase | Reference | Comment |
---|---|---|---|---|---|
13.2 | 112.3 | crystaline, III | crystaline, I | Haida, Suga, et al., 1977 | DH |
30.52 | 138.63 | crystaline, II | crystaline, I | Haida, Suga, et al., 1977 | DH |
19.36 | 169.66 | crystaline, I | liquid | Haida, Suga, et al., 1977 | DH |
30.65 | 138.7 | crystaline, II | crystaline, I | Huffman, Eaton, et al., 1948 | DH |
19.41 | 169.67 | crystaline, I | liquid | Huffman, Eaton, et al., 1948 | DH |
29.38 | 138.7 | crystaline, II | crystaline, I | Parks and Huffman, 1930 | DH |
19.46 | 169.0 | crystaline, I | liquid | Parks and Huffman, 1930 | DH |
Gas phase ion energetics data
Go To: Top, Condensed phase thermochemistry data, Phase change data, Mass spectrum (electron ionization), References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data evaluated as indicated in comments:
HL - Edward P. Hunter and Sharon G. Lias
L - Sharon G. Lias
Data compiled as indicated in comments:
B - John E. Bartmess
LBLHLM - Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron
View reactions leading to C6H10+ (ion structure unspecified)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
IE (evaluated) | 8.95 ± 0.01 | eV | N/A | N/A | L |
Quantity | Value | Units | Method | Reference | Comment |
Proton affinity (review) | 784.5 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Quantity | Value | Units | Method | Reference | Comment |
Gas basicity | 752.0 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
8.94 | PE | Kimura, Katsumata, et al., 1981 | LLK |
8.94 ± 0.02 | PE | Bieri, Burger, et al., 1977 | LLK |
8.95 | EI | Lossing and Traeger, 1975 | LLK |
8.94 ± 0.01 | PE | Rang, Paldoia, et al., 1974 | LLK |
9.57 ± 0.05 | EI | Praet, 1970 | RDSH |
8.99 | EI | Lewis and Hamill, 1970 | RDSH |
8.92 | PE | Demeo and Yencha, 1970 | RDSH |
8.95 ± 0.01 | PI | Demeo and El-Sayed, 1970 | RDSH |
8.94 | PE | Bischof and Heilbronner, 1970 | RDSH |
8.92 ± 0.02 | EI | Winters and Collins, 1969 | RDSH |
8.95 ± 0.01 | PI | Watanabe, 1957 | RDSH |
9.09 | PE | Lambert, Xue, et al., 1986 | Vertical value; LBLHLM |
9.12 | PE | Kobayashi, 1978 | Vertical value; LLK |
9.12 | PE | Hentrich, Gunkel, et al., 1974 | Vertical value; LLK |
9.12 | PE | Clary, Lewis, et al., 1974 | Vertical value; LLK |
9.11 | PE | Asmus and Klessinger, 1974 | Vertical value; LLK |
Appearance energy determinations
Ion | AE (eV) | Other Products | Method | Reference | Comment |
---|---|---|---|---|---|
C3H3+ | 13.45 ± 0.18 | ? | EI | Winters and Collins, 1969 | RDSH |
C3H5+ | 13.68 ± 0.05 | ? | EI | Praet, 1970 | RDSH |
C3H5+ | 12.12 ± 0.12 | ? | EI | Winters and Collins, 1969 | RDSH |
C4H5+ | 13.31 ± 0.15 | ? | EI | Winters and Collins, 1969 | RDSH |
C4H6+ | 11.91 ± 0.05 | C2H4 | EI | Praet, 1970 | RDSH |
C4H6+ | 10.67 ± 0.06 | ? | EI | Winters and Collins, 1969 | RDSH |
C5H5+ | 13.57 ± 0.11 | ? | EI | Winters and Collins, 1969 | RDSH |
C5H7+ | 8.95 | CH3 | EI | Lossing and Traeger, 1975, 2 | LLK |
C5H7+ | 10.27 | CH3 | EI | Lossing and Traeger, 1975 | LLK |
C5H7+ | 11.22 ± 0.05 | CH3 | EI | Praet, 1970 | RDSH |
C5H7+ | 10.18 ± 0.12 | CH3 | EI | Winters and Collins, 1969 | RDSH |
C6H7+ | 12.13 ± 0.10 | H2+H | EI | Winters and Collins, 1969 | RDSH |
C6H9+ | 11.8 ± 0.05 | H | EI | Praet, 1970 | RDSH |
C6H9+ | 10.62 ± 0.07 | H | EI | Winters and Collins, 1969 | RDSH |
De-protonation reactions
C6H9- + =
By formula: C6H9- + H+ = C6H10
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1617. ± 21. | kJ/mol | G+TS | Lee and Squires, 1986 | gas phase; Between H2O, MeOH; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 1586. ± 21. | kJ/mol | IMRB | Lee and Squires, 1986 | gas phase; Between H2O, MeOH; B |
Mass spectrum (electron ionization)
Go To: Top, Condensed phase thermochemistry data, Phase change data, Gas phase ion energetics data, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director
Spectrum
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Additional Data
View image of digitized spectrum (can be printed in landscape orientation).
Due to licensing restrictions, this spectrum cannot be downloaded.
Owner | NIST Mass Spectrometry Data Center Collection (C) 2014 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. |
---|---|
Origin | NIST Mass Spectrometry Data Center, 1990. |
NIST MS number | 114431 |
References
Go To: Top, Condensed phase thermochemistry data, Phase change data, Gas phase ion energetics data, Mass spectrum (electron ionization), Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Steele, Chirico, et al., 1996
Steele, W.V.; Chirico, R.D.; Knipmeyer, S.E.; Nguyen, A.; Smith, N.K.; Tasker, I.R.,
Thermodynamic properties and ideal-gas enthalpies of formation for cyclohexene, phthalan (2,5-dihydrobenzo-3,4-furan), isoxazole, octylamine, dioctylamine, trioctylamine, phenyl isocyanate, and 1,4,5,6-tetrahydropyrimidine,
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Good and Smith, 1969
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Enthalpies of combustion of toluene, benzene, cyclohexane, cyclohexene, methylcyclopentane, 1-methylcyclopentene, and n-hexane,
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Labbauf and Rossini, 1961
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Heats of combustion, formation, and hydrogenation of 14 selected cyclomonoolefin hydrocarbons,
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Epstein, Pitzer, et al., 1949
Epstein, M.B.; Pitzer, K.S.; Rossini, F.D.,
Heats, equilibrium constants, and free energies of formation of cyclopentene and cyclohexene,
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Konovalon, 1926
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Sur Les Chaleurs de Combustion de Quelques hydrocarbures cycliques,
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Haida, Suga, et al., 1977
Haida, O.; Suga, H.; Seki, S.,
Calorimetric study of the glassy state. XI. Plural glass-transition phenomena of cyclohexene,
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Huffman, Eaton, et al., 1948
Huffman, H.M.; Eaton, M.; Oliver, G.D.,
The heat capacities, heats of transition, heats of fusion and entropies of cyclopentene and cyclohexene,
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Parks and Huffman, 1930
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Thermal data on organic compounds. IX. A study of the effect of unsaturation on the heat capacities, entropies and free energies of some hydrocarbons and other compounds,
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Steele, W.V.; Chirico, R.D.; Knipmeyer, S.E.; Nguyen, A.; Tasker, I.R.,
Determination of ideal gas enthalpies of formation for key compounds the 1991 project results,
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Kalinowska, B.; Woycicki, W.,
Heat capacities and excess heat capacities of (an alkanol + an unsaturated hydrocarbon). II. (Propan-1-ol + cyclohexene),
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Haida, Suga, et al., 1977, 2
Haida, O.; Suga, H.; Seki, S.,
Calorimetric study of the glassy state. XI. Plural glass transition phenomena of cyclohexene,
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Huffman, Eaton, et al., 1948, 2
Huffman, H.M.; Eaton, M.; Oliver, G.D.,
The heat capacities, heats of transition, heats of fusion and entropies of cyclopentene and cyclohexene,
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Thermal data on organic compounds. IX. A study of the effect of unsaturation on the heat capacities, entropies and free energies of some hydrocarbons and other compounds,
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Vapor-Liquid Critical Properties of Elements and Compounds. 6. Unsaturated Aliphatic Hydrocarbons,
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Enthalpies of Vaporization of Organic Compounds: A Critical Review and Data Compilation, Blackwell Scientific Publications, Oxford, 1985, 300. [all data]
Cheng, McCoubrey, et al., 1962
Cheng, D.C.H.; McCoubrey, J.C.; Phillips, D.G.,
Critical Temperatures of Some Organic Cyclic Compounds,
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Ambrose, Cox, et al., 1960
Ambrose, D.; Cox, J.D.; Townsend, R.,
The critical temperatures of forty organic compounds,
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Ambrose and Grant, 1957
Ambrose, D.; Grant, D.G.,
The Critical Temperatures of Some Hydrocarbons and Pyridine Bases,
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Mathews, 1926
Mathews, J.H.,
The accurate measurement of heats of vaporization of liquids,
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Marrufo, Aucejo, et al., 2009
Marrufo, Beatriz; Aucejo, Antonio; Sanchotello, Margarita; Loras, Sonia,
Isobaric vapor--liquid equilibrium for binary mixtures of 1-hexene+n-hexane and cyclohexane+cyclohexene at 30, 60 and 101.3kPa,
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. [all data]
Steyer and Sundmacher, 2004
Steyer, Frank; Sundmacher, Kai,
VLE and LLE Data for the System Cyclohexane + Cyclohexene + Water + Cyclohexanol,
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Segura, Lam, et al., 2001
Segura, Hugo; Lam, Elizabeth; Reich, Ricardo; Wisniak, Jaime,
Isobaric Phase Equilibria in the Binary Systems Ethyl 1,1-Dimethylethyl Ether + 1-hexene and + Cyclohexene at 94.00 kPa,
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Stephenson and Malanowski, 1987
Stephenson, Richard M.; Malanowski, Stanislaw,
Handbook of the Thermodynamics of Organic Compounds, 1987, https://doi.org/10.1007/978-94-009-3173-2
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Meyer and Hotz, 1973
Meyer, Edwin F.; Hotz, Roger D.,
High-precision vapor-pressure data for eight organic compounds,
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Letcher and Marsicano, 1974
Letcher, T.M.; Marsicano, F.,
Vapour pressures and densities of some unsaturated C6 acyclic and cyclic hydrocarbons between 300 and 320 K,
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Svoboda, Veselý, et al., 1973
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Enthalpy data of liquids. II. The dependence of heats of vaporization of methanol, propanol, butanol, cyclohexane, cyclohexene, and benzene on temperature,
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Forziati, A.F.; Camin, D.L.; Rossini, F.D.,
Density, refractive index, boiling point, and vapor pressure of eight monoolefin (1-alkene), six pentadiene, and two cyclomonoolefin hydrocarbons,
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Lister, 1941
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Heats of organic reactions. X. Heats of bromination of cyclic olefins,
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Domalski and Hearing, 1996
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Heat Capacities and Entropies of Organic Compounds in the Condensed Phase. Volume III,
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Evaluated Gas Phase Basicities and Proton Affinities of Molecules: An Update,
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Kimura, K.; Katsumata, S.; Achiba, Y.; Yamazaki, T.; Iwata, S.,
Ionization energies, Ab initio assignments, and valence electronic structure for 200 molecules
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Bieri, Burger, et al., 1977
Bieri, G.; Burger, F.; Heilbronner, E.; Maier, J.P.,
Valence ionization enrgies of hydrocarbons,
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Lossing and Traeger, 1975
Lossing, F.P.; Traeger, J.C.,
Stabilization in cyclopentadienyl, cyclopentenyl, and cyclopentyl cations,
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Rang, Paldoia, et al., 1974
Rang, S.; Paldoia, P.; Talvari, A.,
Ionization potentials of unsaturated hydrocarbons. 2. Mono-substituted cyclopentenes and cyclohexenes,
Eesti. NSV Tead. Akad. Toim., 1974, 354. [all data]
Praet, 1970
Praet, M.-Th.,
Ionisation et dissociation du 1-methyl-cyclopentene, du methylenecyclopentane et de quelques isomeres par impact d'electrons et de photons,
Org. Mass Spectrom., 1970, 4, 65. [all data]
Lewis and Hamill, 1970
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Excited states of neutral molecular fragments from appearance potentials by electron impact in a mass spectrometer,
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Notes
Go To: Top, Condensed phase thermochemistry data, Phase change data, Gas phase ion energetics data, Mass spectrum (electron ionization), References
- Symbols used in this document:
AE Appearance energy Cp,liquid Constant pressure heat capacity of liquid IE (evaluated) Recommended ionization energy S°liquid Entropy of liquid at standard conditions Tboil Boiling point Tc Critical temperature Tfus Fusion (melting) point Ttriple Triple point temperature ΔHtrs Enthalpy of phase transition ΔStrs Entropy of phase transition ΔcH°liquid Enthalpy of combustion of liquid at standard conditions ΔfH°liquid Enthalpy of formation of liquid at standard conditions ΔfusH Enthalpy of fusion ΔfusS Entropy of fusion ΔrG° Free energy of reaction at standard conditions ΔrH° Enthalpy of reaction at standard conditions ΔvapH Enthalpy of vaporization ΔvapH° Enthalpy of vaporization at standard conditions - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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