05 19 89

background image

Name

Mol. Form.

Δ

hyd

H

/kJmol

–1

at298.15K

Acenaphthene

C

12

H

10

–52 .1

Acetic acid

C

2

H

4

O

2

–52 .8

Acetone

C

3

H

6

O

–39 .7

Acetonitrile

C

2

H

3

N

–34 .9

Acetophenone

C

8

H

8

O

–53 .3

Ammonia

H

3

N

–35 .4

Aniline

C

6

H

7

N

–56 .5

Anisole

C

7

H

8

O

–41 .4

Argon

Ar

–12 .2

Benzaldehyde

C

7

H

6

O

–42 .1

Benzene

C

6

H

6

–28 .1

Benzonitrile

C

7

H

5

N

–48 .5

Benzyl alcohol

C

7

H

8

O

–66 .9

Biphenyl

C

12

H

10

–47 .2

Bromobenzene

C

6

H

5

Br

–33 .5

Bromodichloromethane

CHBrCl

2

–28 .9

Bromoethane

C

2

H

5

Br

–29 .5

Bromomethane

CH

3

Br

–23 .8

2-Bromo-2-methylpropane

C

4

H

9

Br

–25 .4

1,3-Butadiene

C

4

H

6

–31 .4

Butane

C

4

H

10

–24 .8

1,4-Butanediamine

C

4

H

12

N

2

–91 .6

1,4-Butanediol

C

4

H

10

O

2

–89 .6

Butanenitrile

C

4

H

7

N

–42 .1

1,2,3,4-Butanetetrol

C

4

H

10

O

4

–114

1-Butanethiol

C

4

H

10

S

–36 .3

Butanoic acid

C

4

H

8

O

2

–59 .5

1-Butanol

C

4

H

10

O

–61 .9

2-Butanol

C

4

H

10

O

–62 .7

2-Butanone

C

4

H

8

O

–41 .9

1-Butene

C

4

H

8

–24 .1

2-Butoxyethanol

C

6

H

14

O

2

–73 .6

Butyl acetate

C

6

H

12

O

2

–52 .7

Name

Mol. Form.

Δ

hyd

H

/kJmol

–1

at298.15K

sec-Butyl acetate

C

6

H

12

O

2

–51 .9

tert-Butyl acetate

C

6

H

12

O

2

–46 .2

Butylamine

C

4

H

11

N

–59 .2

sec-Butylamine

C

4

H

11

N

–57 .1

tert-Butylamine

C

4

H

11

N

–59 .0

Butylbenzene

C

10

H

14

–38 .5

Butyl butanoate

C

8

H

16

O

2

–63 .5

Butyl ethyl ether

C

6

H

14

O

–48 .4

tert-Butyl ethyl ether

C

6

H

14

O

–53 .4

4-tert-Butylphenol

C

10

H

14

O

–63 .8

Butyl propanoate

C

7

H

14

O

2

–57 .8

1-Butyne

C

4

H

6

–13 .5

Carbon dioxide

CO

2

–17 .9

Carbon monoxide

CO

–11 .1

Chlorine

Cl

2

–23 .4

Chlorine dioxide

ClO

2

–27 .8

Chlorobenzene

C

6

H

5

Cl

–30 .6

2-Chloro-1,1′-biphenyl

C

12

H

9

Cl

–42 .8

1-Chlorobutane

C

4

H

9

Cl

–28 .2

2-Chlorobutane

C

4

H

9

Cl

–34 .6

Chlorodibromomethane

CHBr

2

Cl

–33 .3

Chlorodifluoromethane

CHClF

2

–22 .8

Chloroethane

C

2

H

5

Cl

–22 .0

Chlorofluoromethane

CH

2

ClF

–21 .7

1-Chlorohexane

C

6

H

13

Cl

–34 .5

Chloromethane

CH

3

Cl

–20 .2

1-Chloropentane

C

5

H

11

Cl

–34 .1

3-Chlorophenol

C

6

H

5

ClO

–50 .3

1-Chloropropane

C

3

H

7

Cl

–27 .0

2-Chloropyridine

C

5

H

4

ClN

–42 .6

3-Chloropyridine

C

5

H

4

ClN

–46 .2

2-Chlorotoluene

C

7

H

7

Cl

–38 .3

3-Chlorotoluene

C

7

H

7

Cl

–37 .0

enthalPy of hydration of Gases

The molar enthalpy of hydration Δ

hyd

H

is defined as the en-

thalpy change when one mole of an ideal gas is dissolved in an in-

finite amount of water . Another term for this quantity is enthalpy

(heat) of solvation in water at infinite dilution . The enthalpy of

hydration influences the distribution of a volatile compound be-

tween the aqueous solution phase and air and is thus important in

fields such as environmental science, geochemistry, and chemical

engineering . It is related to the enthalpy of solution of the liquid or

solid phase, Δ

sol

H

, by

Δ

hyd

H

= Δ

sol

H

– Δ

vap

H

0

where Δ

vap

H

0

is the molar enthalpy of vaporization . This table

gives the molar enthalpy of hydration for a number of common

substances .

references

1 . Plyasunov, A . V ., and Shock, E . L ., J. Chem. Eng. Data [Hydrocarbons,

alcohols, and ketones] 46, 1016, 2001 .

2 . Plyasunov, A . V ., Plyasunova, N . V ., and Shock, E . L ., J. Chem. Eng.

Data [Esters] 49, 1152, 2004 .

3 . Plyasunov, A . V ., Plyasunova, N . V ., and Shock, E . L ., J. Chem. Eng.

Data [Ethers, diethers, and polyethers] 51, 276, 2006 .

4 . Plyasunova, N . V ., Plyasunov, A . V ., and Shock, E . L ., J. Chem. Eng.

Data [Thiols, sulfides, and polysulfides] 50, 246 .

5 . Plyasunov, A . V ., Plyasunova, N . V ., and Shock, E . L ., J. Chem. Eng.

Data [Nitriles and dinitriles] 51, 1481, 2006 .

6 . Plyasunov, A . V ., and Shock, E . L ., Geochim. Cosmochim. Acta [Inorganics

and halogen compounds; temperature dependence] 67, 4981, 2003 .

7 . Kühne, R ., Ebert, R-U, and Schüürmann, G ., Environ. Sci. Technol .

[Compilation; temperature dependence] 39, 6705, 2005 .

8 . Mintz, C ., Clark, M ., Acree, W . E ., and Abraham, M . H ., J. Chem. Inf.

Model. [Compilation and modelling] 47, 115, 2007 .

5-88

6679X_S05.indb 88

4/11/08 11:29:50 AM

background image

Name

Mol. Form.

Δ

hyd

H

/kJmol

–1

at298.15K

4-Chlorotoluene

C

7

H

7

Cl

–33 .3

o-Cresol

C

7

H

8

O

–64 .8

m-Cresol

C

7

H

8

O

–58 .7

p-Cresol

C

7

H

8

O

–61 .3

Cycloheptanol

C

7

H

14

O

–74 .6

Cyclohexane

C

6

H

12

–30 .0

cis-1,2-Cyclohexanediol

C

6

H

12

O

2

–82 .4

Cyclohexanol

C

6

H

12

O

–70 .7

Cyclohexanone

C

6

H

10

O

–49 .8

Cyclohexene

C

6

H

10

–27 .3

Cyclooctane

C

8

H

16

–39 .0

cis-Cyclooctene

C

8

H

14

–45 .5

Cyclopentane

C

5

H

10

–30 .3

Cyclopentanol

C

5

H

10

O

–58 .5

Cyclopentanone

C

5

H

8

O

–44 .3

Cyclopropane

C

3

H

6

–15 .4

Dibromomethane

CH

2

Br

2

–33 .0

Dibutylamine

C

8

H

19

N

–59 .3

Dibutyl ether

C

8

H

18

O

–55 .8

o-Dichlorobenzene

C

6

H

4

Cl

2

–37 .3

m-Dichlorobenzene

C

6

H

4

Cl

2

–35 .3

p-Dichlorobenzene

C

6

H

4

Cl

2

–28 .4

2,3-Dichloro-1,1′-biphenyl

C

12

H

8

Cl

2

–45 .6

2,4-Dichloro-1,1′-biphenyl

C

12

H

8

Cl

2

–43 .0

2,4′-Dichloro-1,1′-biphenyl

C

12

H

8

Cl

2

–44 .2

2,5-Dichlorobiphenyl

C

12

H

8

Cl

2

–45 .6

Dichlorodifluoromethane

CCl

2

F

2

–26 .0

2,2-Dichloro-1,1-difluoro-1-

methoxyethane

C

3

H

4

Cl

2

F

2

O

–30 .4

1,1-Dichloroethane

C

2

H

4

Cl

2

–30 .3

1,2-Dichloroethane

C

2

H

4

Cl

2

–27 .9

1,1-Dichloroethene

C

2

H

2

Cl

2

–28 .5

cis-1,2-Dichloroethene

C

2

H

2

Cl

2

–26 .9

trans-1,2-Dichloroethene

C

2

H

2

Cl

2

–29 .3

Dichloromethane

CH

2

Cl

2

–30 .3

1,2-Dichloropropane

C

3

H

6

Cl

2

–31 .1

1,3-Dichloropropane

C

3

H

6

Cl

2

–29 .7

1,2-Dichloro-1,1,2,2-

tetrafluoroethane

C

2

Cl

2

F

4

–20 .2

1,2-Diethoxyethane

C

6

H

14

O

2

–71 .9

Diethylamine

C

4

H

11

N

–64 .3

N,N-Diethylaniline

C

10

H

15

N

–45 .7

p-Diethylbenzene

C

10

H

14

–46 .4

Diethylene glycol dimethyl ether

C

6

H

14

O

3

–96 .2

Diethyl ether

C

4

H

10

O

–46 .4

Diethyl sulfide

C

4

H

10

S

–40 .2

1,1-Difluoroethane

C

2

H

4

F

2

–20 .7

Difluoromethane

CH

2

F

2

–17 .2

Diiodomethane

CH

2

I

2

–41 .6

Diisopropyl ether

C

6

H

14

O

–51 .7

1,2-Dimethoxyethane

C

4

H

10

O

2

–59 .3

Name

Mol. Form.

Δ

hyd

H

/kJmol

–1

at298.15K

Dimethylamine

C

2

H

7

N

–53 .1

2,4-Dimethylaniline

C

8

H

11

N

–58 .7

2,5-Dimethylaniline

C

8

H

11

N

–61 .5

2,6-Dimethylaniline

C

8

H

11

N

–60 .5

N,N-Dimethylaniline

C

8

H

11

N

–49 .6

2,3-Dimethylbutane

C

6

H

14

–32 .4

3,3-Dimethyl-2-butanone

C

6

H

12

O

–47 .5

cis-1,2-Dimethylcyclohexane

C

8

H

16

–38 .3

trans-1,2-Dimethylcyclohexane

C

8

H

16

–36 .1

Dimethyl ether

C

2

H

6

O

–34 .0

N,N-Dimethylformamide

C

3

H

7

NO

–62 .9

2,4-Dimethyl-3-pentanone

C

7

H

14

O

–54 .0

2,3-Dimethylpyridine

C

7

H

9

N

–57 .7

2,4-Dimethylpyridine

C

7

H

9

N

–60 .7

2,5-Dimethylpyridine

C

7

H

9

N

–54 .9

2,6-Dimethylpyridine

C

7

H

9

N

–52 .3

3,4-Dimethylpyridine

C

7

H

9

N

–50 .5

3,5-Dimethylpyridine

C

7

H

9

N

–51 .3

Dimethyl sulfide

C

2

H

6

S

–31 .5

Dimethyl sulfoxide

C

2

H

6

OS

–71 .9

2,5-Dimethyltetrahydrofuran

C

6

H

12

O

–56 .3

1,4-Dioxane

C

4

H

8

O

2

–48 .4

1,2-Dipropoxyethane

C

8

H

18

O

2

–76 .8

Dipropylamine

C

6

H

15

N

–65 .2

Dipropyl ether

C

6

H

14

O

–49 .9

Dipropyl sulfide

C

6

H

14

S

–47 .7

1-Dodecanol

C

12

H

26

O

–81 .9

Ethane

C

2

H

6

–17 .9

1,2-Ethanediamine

C

2

H

8

N

2

–76 .1

1,2-Ethanediol

C

2

H

6

O

2

–77 .3

Ethanethiol

C

2

H

6

S

–28 .9

Ethanol

C

2

H

6

O

–50 .6

2-Ethoxyethanol

C

4

H

10

O

2

–66 .4

1-Ethoxy-2-methoxyethane

C

5

H

12

O

2

–66 .1

Ethyl acetate

C

4

H

8

O

2

–45 .3

Ethylamine

C

2

H

7

N

–53 .7

2-Ethylaniline

C

8

H

11

N

–59 .7

4-Ethylaniline

C

8

H

11

N

–65 .0

Ethylbenzene

C

8

H

10

–39 .4

Ethyl butanoate

C

6

H

12

O

2

–52 .7

Ethylcyclohexane

C

8

H

16

–36 .8

Ethyl 2,2-dimethylpropanoate

C

7

H

14

O

2

–50 .3

Ethylene

C

2

H

4

–13 .7

Ethyl formate

C

3

H

6

O

2

–38 .1

Ethyl hexanoate

C

8

H

16

O

2

–60 .2

Ethyl 3-methylbutanoate

C

7

H

14

O

2

–56 .0

Ethyl 2-methylbutanoate

C

7

H

14

O

2

–55 .4

Ethyl 2-methylpropanoate

C

6

H

12

O

2

–51 .3

Ethyl pentanoate

C

7

H

14

O

2

–56 .5

Ethyl propanoate

C

5

H

10

O

2

–49 .5

2-Ethylpyridine

C

7

H

9

N

–55 .7

EnthalpyofHydrationofGases

5-89

6679X_S05.indb 89

4/11/08 11:29:51 AM

background image

Name

Mol. Form.

Δ

hyd

H

/kJmol

–1

at298.15K

3-Ethylpyridine

C

7

H

9

N

–53 .5

4-Ethylpyridine

C

7

H

9

N

–52 .2

9H-Fluorene

C

13

H

10

–42 .7

Fluorobenzene

C

6

H

5

F

–29 .3

Fluoromethane

CH

3

F

–16 .1

Glycerol

C

3

H

8

O

3

–103 .5

Helium

He

–0 .67

1,1,1,2,3,3,3-Heptafluoropropane

C

3

HF

7

–24 .8

Heptanal

C

7

H

14

O

–56 .6

Heptane

C

7

H

16

–34 .0

1-Heptanol

C

7

H

16

O

–72 .1

2-Heptanol

C

7

H

16

O

–72 .6

4-Heptanol

C

7

H

16

O

–75 .3

2-Heptanone

C

7

H

14

O

–54 .9

4-Heptanone

C

7

H

14

O

–58 .1

1,1,1,3,3,3-Hexafluoro-2-propanol

C

3

H

2

F

6

O

–57 .1

Hexanal

C

6

H

12

O

–55 .2

Hexane

C

6

H

14

–31 .9

Hexanedinitrile

C

6

H

8

N

2

–66 .6

1-Hexanol

C

6

H

14

O

–67 .4

3-Hexanol

C

6

H

14

O

–69 .6

2-Hexanone

C

6

H

12

O

–48 .9

3-Hexanone

C

6

H

12

O

–46 .0

1-Hexene

C

6

H

12

–30 .4

Hexyl acetate

C

8

H

16

O

2

–60 .8

Hexylamine

C

6

H

15

N

–65 .9

Hexylbenzene

C

12

H

18

–52 .7

Hydrogen

H

2

–0 .402

Hydrogen selenide

H

2

Se

–15 .7

Hydrogen sulfide

H

2

S

–18 .0

3-Hydroxybenzaldehyde

C

7

H

6

O

2

–70 .7

3-Hydroxybenzonitrile

C

7

H

5

NO

–70 .7

4-Hydroxybenzonitrile

C

7

H

5

NO

–70 .3

Iodoethane

C

2

H

5

I

–31 .7

Iodomethane

CH

3

I

–28 .2

1-Iodopropane

C

3

H

7

I

–35 .3

2-Iodopropane

C

3

H

7

I

–36 .6

Isobutanal

C

4

H

8

O

–40 .0

Isobutane

C

4

H

10

–21 .7

Isobutene

C

4

H

8

–22 .7

Isobutyl acetate

C

6

H

12

O

2

–51 .8

Isobutyl formate

C

5

H

10

O

2

–43 .0

Isobutyl isobutanoate

C

8

H

16

O

2

–55 .3

Isobutyl propanoate

C

7

H

14

O

2

–54 .7

Isoflurane

C

3

H

2

ClF

5

O

–35 .3

Isopentyl acetate

C

7

H

14

O

2

–53 .8

Isopentyl formate

C

6

H

12

O

2

–47 .7

Isophorone

C

9

H

14

O

–59 .1

Isopropyl acetate

C

5

H

10

O

2

–46 .8

Isopropylamine

C

3

H

9

N

–55 .0

Isopropylbenzene

C

9

H

12

–33 .7

Name

Mol. Form.

Δ

hyd

H

/kJmol

–1

at298.15K

Isopropyl formate

C

4

H

8

O

2

–43 .0

1-Isopropyl-4-methylbenzene

C

10

H

14

–34 .6

Krypton

Kr

–15 .6

Methane

CH

4

–12 .0

Methanethiol

CH

4

S

–24 .4

Methanol

CH

4

O

–52 .0

2-Methoxyethanol

C

3

H

8

O

2

–60 .4

2-Methoxy-2-methylbutane

C

6

H

14

O

–52 .5

2-Methoxyphenol

C

7

H

8

O

2

–62 .6

Methyl acetate

C

3

H

6

O

2

–40 .1

Methylamine

CH

5

N

–45 .3

Methyl benzoate

C

8

H

8

O

2

–50 .3

Methyl butanoate

C

5

H

10

O

2

–47 .5

3-Methyl-1-butanol

C

5

H

12

O

–66 .0

2-Methyl-2-butanol

C

5

H

12

O

–68 .4

3-Methyl-2-butanone

C

5

H

10

O

–57 .6

2-Methyl-2-butene

C

5

H

10

–26 .6

Methyl tert-butyl ether

C

5

H

12

O

–48 .7

Methyl 2,2-dimethylpropanoate

C

6

H

12

O

2

–46 .2

Methyl formate

C

2

H

4

O

2

–32 .0

Methyl hexanoate

C

7

H

14

O

2

–54 .7

Methyl isobutanoate

C

5

H

10

O

2

–46 .0

4-Methylmorpholine

C

5

H

11

NO

–68 .7

1-Methylnaphthalene

C

11

H

10

–45 .0

2-Methylnaphthalene

C

11

H

10

–44 .9

2-Methylpentane

C

6

H

14

–30 .5

3-Methylpentane

C

6

H

14

–36 .8

Methyl pentanoate

C

6

H

12

O

2

–50 .4

4-Methyl-2-pentanol

C

6

H

14

O

–69 .9

4-Methyl-2-pentanone

C

6

H

12

O

–44 .6

1-Methylpiperidine

C

6

H

13

N

–65 .8

2-Methylpropanenitrile

C

4

H

7

N

–40 .0

Methyl propanoate

C

4

H

8

O

2

–44 .5

2-Methyl-1-propanol

C

4

H

10

O

–60 .2

2-Methyl-2-propanol

C

4

H

10

O

–62 .9

Methyl propyl ether

C

4

H

10

O

–38 .0

2-Methylpyridine

C

6

H

7

N

–50 .3

3-Methylpyridine

C

6

H

7

N

–50 .3

4-Methylpyridine

C

6

H

7

N

–51 .8

N-Methylpyrrolidine

C

5

H

11

N

–63 .4

2-Methyltetrahydrofuran

C

5

H

10

O

–51 .4

Morpholine

C

4

H

9

NO

–69 .5

Naphthalene

C

10

H

8

–42 .8

Neon

Ne

–3 .90

Neopentane

C

5

H

12

–23 .4

Nitric oxide

NO

–11 .9

Nitrobenzene

C

6

H

5

NO

2

–43 .8

Nitroethane

C

2

H

5

NO

2

–32 .5

Nitrogen

N

2

–1 .04

Nitromethane

CH

3

NO

2

–35 .7

2-Nitrophenol

C

6

H

5

NO

3

–49 .8

5-90

EnthalpyofHydrationofGases

6679X_S05.indb 90

4/11/08 11:29:52 AM

background image

Name

Mol. Form.

Δ

hyd

H

/kJmol

–1

at298.15K

3-Nitrophenol

C

6

H

5

NO

3

–67 .7

4-Nitrophenol

C

6

H

5

NO

3

–68 .6

1-Nitropropane

C

3

H

7

NO

2

–34 .4

2-Nitropropane

C

3

H

7

NO

2

–34 .1

2-Nitrotoluene

C

7

H

7

NO

2

–46 .4

3-Nitrotoluene

C

7

H

7

NO

2

–38 .5

Nitrous oxide

N

2

O

–19 .8

5-Nonanone

C

9

H

18

O

–62 .8

2-Nonanone

C

9

H

18

O

–65 .3

Octanal

C

8

H

16

O

–48 .8

Octane

C

8

H

18

–36 .0

1-Octanol

C

8

H

18

O

–74 .1

2-Octanone

C

8

H

16

O

–58 .3

1-Octene

C

8

H

16

–39 .2

Octylamine

C

8

H

19

N

–52 .3

Oxygen

O

2

–1 .20

Pentachlorobenzene

C

6

HCl

5

–39 .9

Pentafluoroethane

C

2

HF

5

–21 .5

2,2,3,3,3-Pentafluoro-1-propanol

C

3

H

3

F

5

O

–51 .9

Pentanal

C

5

H

10

O

–42 .9

Pentane

C

5

H

12

–28 .3

1,5-Pentanediamine

C

5

H

14

N

2

–95 .1

Pentanedinitrile

C

5

H

6

N

2

–63 .5

Pentanenitrile

C

5

H

9

N

–45 .6

1-Pentanol

C

5

H

12

O

–61 .9

2-Pentanol

C

5

H

12

O

–63 .3

3-Pentanol

C

5

H

12

O

–59 .6

2-Pentanone

C

5

H

10

O

–45 .3

3-Pentanone

C

5

H

10

O

–49 .6

Pentyl acetate

C

7

H

14

O

2

–55 .3

Pentylamine

C

5

H

13

N

–62 .1

Pentylbenzene

C

11

H

16

–49 .5

Pentyl formate

C

6

H

12

O

2

–48 .1

Perfluoropropene

C

3

F

6

–17 .4

Phenol

C

6

H

6

O

–57 .7

1-Phenyl-1-propanone

C

9

H

10

O

–61 .9

Piperidine

C

5

H

11

N

–65 .4

Propanal

C

3

H

6

O

–39 .4

Propanamide

C

3

H

7

NO

–73 .4

Propane

C

3

H

8

–20 .4

1,3-Propanediamine

C

3

H

10

N

2

–85 .6

1,3-Propanediol

C

3

H

8

O

2

–81 .1

Propanenitrile

C

3

H

5

N

–39 .5

1-Propanethiol

C

3

H

8

S

–30 .2

Propanoic acid

C

3

H

6

O

2

–56 .5

1-Propanol

C

3

H

8

O

–59 .9

2-Propanol

C

3

H

8

O

–58 .2

Propene

C

3

H

6

–21 .6

2-Propoxyethanol

C

5

H

12

O

2

–69 .6

Propyl acetate

C

5

H

10

O

2

–48 .7

Propylamine

C

3

H

9

N

–56 .0

Name

Mol. Form.

Δ

hyd

H

/kJmol

–1

at298.15K

Propylbenzene

C

9

H

12

–36 .4

Propyl butanoate

C

7

H

14

O

2

–54 .9

Propyl formate

C

4

H

8

O

2

–40 .5

Propyl propanoate

C

6

H

12

O

2

–51 .2

Propyne

C

3

H

4

–15 .6

Pyridine

C

5

H

5

N

–42 .1

Quinoline

C

9

H

7

N

–58 .2

Radon

Rn

–24 .0

Styrene

C

8

H

8

–28 .4

Succinonitrile

C

4

H

4

N

2

–58 .2

Sulfur hexafluoride

F

6

S

–20 .7

1,2,3,4-Tetrachlorobenzene

C

6

H

2

Cl

4

–35 .0

1,1,2,2-Tetrachloroethane

C

2

H

2

Cl

4

–34 .8

1,1,1,2-Tetrachloroethane

C

2

H

2

Cl

4

–36 .2

Tetrachloroethene

C

2

Cl

4

–41 .5

Tetrachloromethane

CCl

4

–30 .5

Tetraethylene glycol dimethyl ether C

10

H

22

O

5

–126

1,1,1,2-Tetrafluoroethane

C

2

H

2

F

4

–22 .2

Tetrafluoroethene

C

2

F

4

–15 .1

Tetrafluoromethane

CF

4

–13 .5

2,2,3,3-Tetrafluoro-1-propanol

C

3

H

4

F

4

O

–57 .9

Tetrahydrofuran

C

4

H

8

O

–47 .3

Tetrahydropyran

C

5

H

10

O

–48 .9

Thiophene

C

4

H

4

S

–29 .9

Toluene

C

7

H

8

–32 .4

Tribromomethane

CHBr

3

–35 .8

1,2,3-Trichlorobenzene

C

6

H

3

Cl

3

–32 .6

1,3,5-Trichlorobenzene

C

6

H

3

Cl

3

–34 .2

1,1,1-Trichloroethane

C

2

H

3

Cl

3

–28 .7

1,1,2-Trichloroethane

C

2

H

3

Cl

3

–32 .5

Trichloroethene

C

2

HCl

3

–32 .2

Trichlorofluoromethane

CCl

3

F

–19 .8

Trichloromethane

CHCl

3

–33 .5

1,1,2-Trichloro-1,2,2-

trifluoroethane

C

2

Cl

3

F

3

–28 .8

Triethylamine

C

6

H

15

N

–69 .7

Triethylene glycol dimethyl ether

C

8

H

18

O

4

–102 .4

2,2,2-Trifluoroethanol

C

2

H

3

F

3

O

–50 .2

Trifluoromethane

CHF

3

–22 .6

1,1,1-Trifluoro-2-propanol

C

3

H

5

F

3

O

–53 .5

Trimethylamine

C

3

H

9

N

–52 .7

1,2,3-Trimethylbenzene

C

9

H

12

–37 .4

1,2,4-Trimethylbenzene

C

9

H

12

–36 .6

1,3,5-Trimethylbenzene

C

9

H

12

–39 .1

2,2,4-Trimethylpentane

C

8

H

18

–31 .0

2,3,4-Trimethylpentane

C

8

H

18

–38 .5

Xenon

Xe

–19 .4

o-Xylene

C

8

H

10

–37 .7

m-Xylene

C

8

H

10

–38 .6

p-Xylene

C

8

H

10

–34 .8

EnthalpyofHydrationofGases

5-91

6679X_S05.indb 91

4/11/08 11:29:53 AM


Wyszukiwarka

Podobne podstrony:
05 19 89
!! Wypracowania !!, 05, 19
Kelley Armstrong Complete Timeline of Darkest Powers Stories 2011 05 19
Kolokwium 2015 05 19
pic 2015 05 19 054724
pic 2015 05 19 054638
05 08 89
pic 2015 05 19 053910
2010 11 05(2),19,26 szeregi, geometria analityczna
pic 2015 05 19 054104
Kolokwium 2015 05 19
Prawo wodne Dz U 05#9 19 wersja 10
DGP 2014 05 19 dotacje unijne
Dz U 2006 80 563 wersja 06 05 19
05 (19)
05 1996 89
pic 2015 05 19 054418
2010 05 19 PZPN Egzamin III Liga (2)
Wykłady 2 seria, 05.19.03 W12

więcej podobnych podstron