Сталл Д. Вестрам Э. Зинке Г. Химическая термодинамика органических соединений

г

1

Formula

Name Slate

C7H7NO2 O-NlTMOTOLUENt

CD

C7H7N02 P-NITHOTOLUENE

CS)

C7H7NO2 SALICYLALOEHYUE OXIME

. . . CS)

C7H7N3O1 N-MtTHYL-2»4-UINITR0ANILINF

CS)

C7H7N5 -i-PHENYLAMINUTETRAZULt

. . . CS)

C7H7N5 1-PHENYL-5-AMIN0TETRAZULF

. CS)

С7И8 1t3.5-CrCLOHLPTATRIENt

. . . CL)

С7И8 1,3.5-CYCLOHEPTATRIENL

. . . CG)

C7H8 2t5-N0RH0RNAUIENE

CD

C7H8 TOLUENE

CD

C7H8 TOLUENt

CG)

C7H8N20 PHENYLUREA

<S)

C7H8N202 N-MFTHYL-P-NITROANILINE

. . CS)

C7H8N202 3-NITRO-P-TULUIDINE

. . . . CS)

C7H8N2Q2 5-NITR0-0-TULUI0INE

. . . . CS)

C7H8N4O2 THEOBRUMINE

CS)

C7H8O ANISOLE

CD

C7H80 BENZYL ALCOHUL

CD

C7H80 M-CRESOL

CD

C7H8O M-CRESOL

CG)

C7H80 O-CRESOL

CS)

С7И80 O-CRESOL

CG)

C7H8O P-CRESOL,

CS)

C7H8O P-CRESOL

CG)

C7H802 0-HYDROXYBENZYL ALCOHUL

. . CS)

C7H802 METHYLHYOROOUINQNE

CS)

C7H8O2 5-METHYLRESOKCINOL

CS)

C7H802S METHYL PHENYL SULFONE

. . . CD

C7H8O2S METHYL PHENYL SULFONE

. . . CG)

C7H8O3S P-TOLUENESULfUNIC ACID

. . . CS)

C7H803S P-TOLUENESULFUNIC ACID

. . . CG)

C7H8S METHYL PHENYL SULFIDE

. . . CL)

C7H8S METHYL PHENYL SULFIDt

. . . CG)

C7H8S ALPHft-TOLUENfcTHIOL

. . . . • CD

С7И85

UL

PH

'-TULUENt IHIOL

. . . • . CG)

........CD

Mol

Wt

137.134

197.150

161.166

92.131

136.150

152.150

180.

166

108.131

108.134

108.131

108.134

124.134

121.131

156.200

(kcal/mole)

-0.4

-8.9

-43.9

-22.6

72.9

74.3

34.22

43.47

-48.0

2.87

11.95

-51.4

-7.4

-17.2

-21.8

-85.8

-28.6

-38.49

-46.19

-31.63

-48.84

-30.74

-47.61

-29.97

-86.2

-95.9

-106.7

-82.5

156.206—

-62.6

172.200

121.200

124.200

121.158

-298.4

11.5

23.6

10.5

22

.8

?.

0

Source

CC

ВС

ее

AC

ТС

ВС

АС

ТС

ее

ВС

ее

ВС

АС

ТС

АС

ТС

АС

ТС

СС

сс

СС

ВС

сс

ВС

сс

744)

744

)

1610)

981)

1616)

124)

470)

94)

1248)

397)

744)

741)

1440)

744)

56)

1112)

285)

566)

285)

567)

285)

568)

744

)

744)

744

)

V05)

905)

1125)

898)

901

)

V01

)

1 на i

(cal/mole°K) Source (kcal/mole)

51

.30 MC 424)

75.44

TC 470)

52.81 МС13Ц)

76.64

TC 397)

51.8 MC1118)

85.27

TC 566)

85.47

TC 567)

83.09

TC 568)

91.87

EC 69)

58.99

61.01

27.19

29.16

-«3.237

-14.711

"19.928

-21

.376

-6.57

-9.69

-8,86

-7.38

4.813

7.099

6.491

5.406

Formula Name State

C7H9N

2-ETHYLPYH10INE CD

C7H9N

2.3-LUTIOINE

CD

C7H9N 2»3-LUTIDINE

... ^-. ... (G)

C7H9N ?>4-LUTI0INE

CD

C7H9N 2.1-LUTIDINE

CG)

C7H9N

2.5-LUTIOINE

CD

C7H9N 2»5-LUTI0INE

CG)

C7H9N

2,6-LUTIDINE

CD

C7H9N 2»6-LUTI0INE

CG)

C7H9N 3»«-LUTIDINE

CL)

C7H9N 3>4-LUTIDINE

CG)

C7H9N

3.5-LUTIOINE

CD

C7H9N 3»5-LUTIDINE

. CG)

C7H9N N-METHYLANILINE

CL)

C7H9N N-METHYLANILINE

CG)

C7H9N

M-TOLUIDINE

CD

C7H9N 0-TOLUIOINE

CL)

C7H9N P-TOLUIDINE

CS)

C7H9N0 P-ANISIDINE

CS)

C7H9N02 ETHYLMETHYLMALEIMIOE

. . . . CS)

C7H9N03 ETHYL 2-CYAN0ACET0ACETATE

. CS)

C7H10 1>3-CYCLOHEPTAOIENE

. . . . CG)

C7H10N2 1-METHYL-l-PHENYLHYDRAZINE

. CS)

C7H10N203 BENZYLAMINE NITRATE

. . . . CS)

C7H100 3-METHYL-2-CYCL0HEXEN-1-0NE

CD

C7H100 2-NDRB0RNAN0NE

CS)

C7H1002 1-CYCLOHExENE-l-CARBOxYUIC

C7H1002

•

ACID

CS)

C7H1002 2-CYCL0HEXENE-1-CARB0XYLIC

C7H1002 ACID

CS)

C7H1002 ETHYL-2»4-PENTAOIENEOATE

. , CD

С7НЮ03 TRIMETHYLSUCCINIC ANHYDRIDE

CS)

C7H1004 1.2-CYCLOPENTANEDICARBOXYLIC

C7H1004 ACID» TRANS

CS)

C7H1004 DIMETHYLMETHYLENESUCCINIC

C7H1004 ACID

CS)

MolWl

107.1=50

107.150

107.

15-0

107.150

107.1-50

107.150

123.150

139.150

155.150

94.150

122.166

170.166

110.150

ДН/1

Ю

(kcal/mole)

0.69

1.61

16.31

3.81

15.26

1.44

15.87

3.01

14.02

4.35

16.73

b.35

17.39

7.7

20.4

-0.3

-1.3

-7.2

-41.1

-110.5

-128.6

22.3

-39.0

-57.2

-57.0

-53.8

Source

AC

CC

C(

CC

AC

CC

8C

67)

269)

284)

289)

284)

289)

284)

289)

284)

289)

284)

289)

284)

714)

1547)

744)

1414)

7««)

261)

744)

277)

7««)

90)

(cal/mole

53.6

81.6

ДС/1,

8

°K) Source (kcal/mole)

EC1547) 43.26

EC1547)

«7.61

Log Kp

-31.707

-34.897

126.150 -142.4

CC 744)

126.150 -112.7

CC 744)

126.150

-80.1

BC1288)

142.150 -163.8 BC1538)

158.150 -218.4

CC 714)

158.150 -203.3

CC M4)

Formula

Name

State

C7H1004 DIMETHYL TRIMETHYLENE-APLHA,

C7H1OO4

'

ALPHA-DICAKBOXYLATE

,

(U»L)

C7H1004 Cl-HYDROXY-1-METHYLETHYL)

C7H1004 SUCCINIC ACID GAMMA LACTONE

CD

C7H1005 DIMETHYL ACETONYLMALONATE

. CD

С7Н100

10

3-HYDR0XY-4-0X0-4H-PYKAN-

С7НЮ010 OICARROXYLIC ACID TRIHYDHATE

СS

)

C7H11CL302 ISOPENTYL

TK

ICHLOROACETATE

CD

C7H11N5 l-ALLYL-5-CALLYLAMINQ)TETRAZ0LECS)

•5-CDIALLYLAMINOHETRAZOLE

. CS)

CYCLOHEPTENE

CD

CYCLOHEPTENE

CG)

C7H11N5

C7H1Z

C7H12

C7H1Z

C7H12

2-CYCL0PR0PYL-1-BUTENE

. .' . CL)

2-CYCLOPR0PYL-2-BUTENE

... CD

1#2-OIMETHYLCYCLOPENTLNE

. . CG)

1»3-DIMETHYLCYCLOPENTENE

. . CG)

1,4-DIMETHYLCYCLOPENTLNE

. . CG)

l»5"0IMETHYLCYCL0PENTENE

. . CG)

3.3-DIMETHYLCYCLOPENTENE

. . CG)

3»4-0IMETHYLCYCL0PENTtNE» CISCG)

3>4-0IMETHYLCYCL0PENTENE,TWANSCG)

3»5-DIMETHYLCYLCOPENTENE» CISCG)

3»b-DIMETHYLCYCLOPENTENE»TrtANSCG)

1-ETHYLCVCLOPENTENE

.... CD

FTHYLIDENECYCLOPENTANE

... CD

1-HEPTYNE

CD

1-HEPTYNE

CG)

1-METHYLCYCLUHEXENE

.... CD

4-METHYLCYCLOHEXENE

.... CD

METHYLENECYCLUHEXANE

.... CD

NORBORNANE

CS)

VINYLCYCLUPENTANE

CD

C7H12CL2O2 ISOPENTYL

0

I

CHLOROАСЕТА

ТЕ

. CL)

C7H12Q CYCLOHEPTANONE

CD

C7H12Q ?,5-01METHYLCYCL0PENTAN0NE

. 'LI

•C7H12Q FNDQ-?-METHYL-

MolWt

(kcal/mole) Source (cal/mole

°K)

Source (kcal/mole)

15?.150 -171.7

CC 744)

158.150

174.150

•221.7

•247.2

254.

233.

165.

96.

96

199

1

1?

1

12

150

529

198

166

.166

.

166

.166

.

166

.

166

.166

.

166

.

166

.166-

.

166

.

166

.166

.080

.

166

j.16

6

•304,

•139,

83,

-11,

-2,

19,

14,

CC

744)

CC

744)

CC

744)

ВС

1384)

BC1616)

CCALC)

AC

261)

CC1374)

-13

-13,

16,

24

-19,

-24

-17,

-22

-8

•138

-71

-78

AC

821)

AC

821)

CCALC)

TC

324)

AC

821)

CC

744)

AC1522)

AC

94)

AC

«21

)

8(1364)

АС13П

)

CC

744)

84.0

86.4

87.4

86.4

83.2

86.4

86.8

84.6

EC

622)

97.44

TC 324)

54,24

-39.759

Formula

Name State

C7H12O

7-0XABICYCL0(2.2.1)HEPTANE

CD

C7H120

J-ETHYLCYCLOPENTANONE

... CD

C7H120

EX0-2-METHYL-

C7H12O

7-0X»BICYCL0C2.2.1)HEPTANE CD

C7H120

1.6-HEPTA0IEN-4-0L

CD

C7H120 3-METHYLCYCLUHEXANONE

. . . CL)

C7H1202 ACETYLACETONE-O-ETHYL ETHERClbL)

C7H1202 CYCLOHEXANECARBOXYLIC ACID

, (S)

C7H12O2 ETHYL ANGELATE

CD

C7H12O2 ETHYL 2-PENTENOATE

. . . , . CL)

C7H1202 ETHYL 3-PENTENOATE

..... CD

C7H1202 ETHYL 4-PENTENOATE

CD

C7H1202 ETHYL TIGLATE

CS)

C7H1202 ETHYL TETRAMETHYLENE-

C7H1202 CARBOXYLATE

. CU.D

C7H12O2 ISOPROPYL CROTONATE

.... CD

C7H12Q2 PROPYL CROTONATE

CL)

C7H12O3 ETHYL 2-ETHOXYACRYLATE

. . . CS)

C7H12O3 ETHYL 3-ETHOXYACRYLATE

... CD

C7H1204 BUTYLMALONIC ACID

CS)

C7H1204 DIETHYL MALONATE

CL)

C7H12O4 DIETHYLMALONIC ACID

. . . . CS)

C7H1204 DTMETHYL 6LUTARATE

CD

C7H1204 PIMELIC ACID

CS)

C7H1204 2»4>8»10-TETHA0XASPIR0-

C7H1204 C5.5-UNDECANE)

. CS)

C7H1204 TRIMETHYLSUCCINIC ACID

. . . CS)

C7H1205 DIACETIN

CS)

C7H1207 GLUCOHEPTONIC ACID LACTONE

. CS)

C7H13CLO2 BUTYL 2-CHL0R0PR0PI0NATE

. . CD

C7H13CL02 BUTYL 3-CHLOKQPROP IONATE

. . CD

C7H13CLO2 ISOBUTYL 2-CHLOROPROPIONATE

CL)

C7H13CLO2 ISOBUTYL 3-CHLOROPROPIONATE

CL)

C7H13CLO2 ISOPENTYL CHLOROACETATE

. . CD

C7H13CLO2 ISOPROPYL 2-CHL0R0BUTYRATE

. CD

C7H13CL02 ISOPROPYL 3-CHL0R08UTYRATE

. CD

Mol

Wt

(kcal/mole) Source

112.'166 -59.90

AC 94)

112.166

-77.7 CC 744)

si,,

(cal/mole °K) Source

(kcal/mole)

Log

Kp

Ц2.166

112.V66

112.166

128.166

144.166

160.1*6

160.166

176.166

208.166

164.631

-60.75

-39.9

-73.3

-99.5

134.2

103.3

106.3

104.1

102.8

113.1

103.2

108.75

105.55

141.5

144.2

238,1

207.9

"235.1

20*.5

242.6

-99.5

-238.4

-266.5

-342.1

-136.9

"133.5

-144.3

-137.1

-136.8

"154.8

-145.4

A(

94)

CC

744)

CC

744)

CC

744)

C<

744)

CC

744)

ВС

1287

)

BC1287)

ВС

1287)

CC

744)

CC

744)

BC1286)

B(t286)

Ci

744)

CC

744)

ЭС1535)

CC

744)

CC

744)

CC

744)

AC1354)

AC

431)

BC1538)

BC1472)

CC

744)

BC1384)

6(1384)

8C1384)

BC1384)

I-огпшМ

C7H13CL02

C7H13N

C7H13N0

C7H13N03

С7Н14

1,

С7Н14

f

4

C7H14

1

<

C7H14

1

C7H14

С7И14

C7H14

С7И14

C7H14

С7И14

C7H14

Г7И14

Name

State

TSOPROPYL 4-CHLQR08UTYRATE . (L)

PROPYL 2-CHUUR08UTYRATE . . CL)

PROPYL 3-CHLUR08UTYRATE . . CD

PROPYL «-CHLOROBUTYRATE . . CD

l-AZABICYCL0C2.2,2)0CTANE . (S)

KSI-ENANTOIACTAM (g)

FORMYL LEUCINE» OL (S)

CYCLOHEPTANE .CD

CYCLOHEPTANE CG)

2-CYCL0PR0PYLBUTANE

.... CD

1» 1-OIMETHYLCYCLOPENTANE

. . CD

1»1-DIMETHYLCYCLOPENTANE

. . (G)

1-DIMETHYL-2-ETHYLCYCL0PH0PANECL)

l»2-0IMETHYUCYeL0PENTANE»

CISCD

1,2-OIMETHYLCYCLOPENTANE» CISCG)

.2-DIMETHYLCYCLOPENTANE.

THANS

CD

»?-OlMETHYLCYCLDPENTANt» THANSCG)

ЬЗ-OIMETHYLCYCLOPENTANEf

CISCL)

1>3-DIMETHYLCYCLQPENTANE»

С IS

С G 3

«3-DIMETHYLCYCLQPENTANE,

TRANSCL)

«3-OIMETHYLCYCLOPFNTANL» TRANSCG)

2.3-DIMETHYL-l-PENTENE

. . . CG)

2»3-DIMETHYU-?-PENTENE

. . . CG)

2»«-OIMET'HYL-l-PENTENE

. . . CL)

2*4-0IMETHYL-1-PENTENE

. . . CG)

2>4-01METHYL-2-PENTENE

... CD

2»4-0IMETHYL-2-PENTENE

. . . CG)

3,3-DIMETHYL-l-PENTENE

. . . CG)

3.4-OIMETHYL-l-PENTENt

. . . CG)

3.4-DIMETHYL-2-PENTENE»

CIS. CG)

3»4-DIMETHYL"2-PENTENE»

THANSCG)

4,4-OIMETHYL-l-PENTFNE

... CD

4.4-0IMETHYL-1-PENTENE

. . . CG)

4.4-DIMETHYL-2-PENTENL»

CIS. CL)

4.«-DIMEThYL-2-PFNTENE»

CIS CG)

4,4-0!METHYL-2-PENTENt>

THANSCL)

Mol

Wt

164.Л31

164.631

111

.182

127.182

159.182

98.182

98.

182

98.182

9Й.182

98.182

9Я.

182

98.

182

98.182

9

8^.18

2

98.162

ДНЯ,,

(kcal/mole)

-145.3

-151

.0

-141.3

-141.6

-183.6

-37.78

-28.52

-17.9

-41.14

-33.05

-21.6

-39.52

-30.96

-40.94

-32.67

-40.68

-32.47

-40.19

-31.93

-19.5

-21

.1

-28.18

-20.27

-29.64

-21.44

-18.2

_ -17.6

-?0.9

-26.65

-19.20

-25.39

-17.60

-?9.31

Source

ВС1Э84)

BC1384)

ВС 1384)

CC

744)

AC

707)

TC

342)

CC1375)

AC

694)

TC

349)

AC

710)

AC

694)

TC

350)

AC

694)

TC

351)

AC

694)

TC

352)

AC

694)

TC

353)

EC1248)

EC 1248

)

ДС1236)

AC 1236)

AC1236)

EC1248)

EC 1248)

AC 1236)

ДС1236)

AC 1236)

Sm

(cal/mole

°K)

Source

49.47

45.4

57.97

81.82

63.34

85.87

64.33

87.51

64.86

87.67

64.97

87.67

66.90

87.67

MC

TC

MC

TC

MC

TC

MC

TC

EC

TC

MC

TC

1624)

794)

424)

342)

544)

349)

544)

350)

655)

351)

1248)

352)

544)

353)

до;,,»

(kcal/mole)

12.

15.

7.

9.

10.

7.

9.

7.

9.

7.

9.

92

06

95

33

28

93

70

17

93

37

84

91

LoRKp

-9.467

-11

.04?

-5.831

-6.837

-6.802

-8,010

-5.645

-6.722

-5.812

-6.868

-5.749

-7.264

r

1

Formula

Name State

C7H14

4,4-0IMETHYl-2-PENTENE»

TRANSCG)

C7H14

FTHYLCYCLOPENTANE

CL)

C7H14

ETHYLCYCLOPENTANE

.'....

С

G)

C7H14

P-ETHYL-1-PENTENE

CG)

C7H14

3-ETHYL-l-PENTENE

CG)

C7H14

3-ETHYL-2-PENTENE

CG)

C7H14

1-HEPTENE

. . CL)

C7H1«

1-HEPTENE

CG)

C7H14

2-HEPTENE»

CIS CG)

CTH14

2-HEPTENE»

TRANS

CG)

C7H1«

3-HEPTENE»

CIS CG)

C7HH

3-HEPTENE»

TRANS

CG)

C7H14

METHYLCYCLOHEXANE

CD

C7H1« METHYLCYCLOHEXANE

CG)

C7H14

3-METHYL-2-ETHYL-1-BUTENE

. CL)

С7Щ4

3-METHYL-2-ETHYL-1-BUTENE

. CG)

C7H14

2-METHYL-l-HEXENE

CG)

C7H14

2-METHYL-2"HtXENE

CG)

C7H14

2-METHYL-3-HEXENE»

CIS . . . CG)

C7H14

2-METHYL-3-HEXENE» THANS

. . CG)

C7H14

3-METHYL-l-HEXENE

CG)

C7HH 3-METHYL-2-HEXF.NE»

CIS ... CG)

C7H14

3-METHYL-2-HEXENE» TRANS

. . CG)

C7H14

3-METHYL-3-HEXENE»

CIS ... CD

C7H14

3-METHYL-3-HEXENE»

CIS . . . CG)

C7H14

3-METHYL-3-HEXENE» TRANS

. . CD

C7H14

3-METHYL-3-HEXENE» TRANS

. . CG)

C7H14

4-METHYL-l-HtXENE

CG)

C7H14

4-METHYL-2-HEXENE/

CIS ... CG)

C7H14

4-METHYL-2-HEXENE» TRANS

. . CG)

C7H14

5-METHYL-l-HEXENE

CD

C7H14 5-METHYL-l-HEXENE

..... CG)

C7H14 5-MfTHYL-2-HtXENE/

CIS ... CG)

С7Ч14 5-METHYL-2-HLXENE» THANS

. . CG)

C7H14 ?»3.3-TRIMETHYL-l-BUTENE

. . CL)

C7H14

7,

3.3-TRIMETHYL-l-BUTENE

. . CG)

Mol

Wt

9

8

.

1

8'2

98.182

98.132

98.182

98,t

82

(kcal/mole)

-?1.46

-39.08

-30.37

-17.9

-15.3

-18.6

-23.41

-14.89

-16.5

-17.5

-16.5

-17.5

-45.45

-36.99

-27.48

-19,25

-18.5

-19.9

-18.2

-19,2

-16.0

"19.3

-19.3

-27.94

-19.22

-27.16

-18,60

-16.0

-17.5

-18.5

-24.36

-16.6

-18.2

-19.2

-28.35

-20.67

Source

AC 1236)

AC1196)

TC

348)

EC1248)

AC1236)

TC

290)

EC1248)

AC1196)

TC

371)

AC 1236)

AC1236)

EC1248)

EC 1248)

EC1248)

AC1236)

EC1248)

ВС

268)

CC

843)

EC1248)

EC 1248)

AC1236)

г»»

(cal/mole

°K)

67

90

7Й

101

59

82

.00

.42

.31

.24

.26

.06

Source

MC

TC

MC

тс

MC

TC

544)

348)

950)

290)

341)

371)

AG/S,

8

(kcal/mole)

8.

10.

21.

22.

4.

6.

92

65

22

90

86

52

Log

Kp

-6

-7

-15

-16

-3

-4

.541

.807

.555

.789

.563

.781

C?H14BJi2

C7H14N2

C7HHN2

C7H14N2Q2

C7H14N2O3

C7H14N2Q3

C7H140

С7НИ0

C7K140

C7H140

CH140

0

7

4

40

С

7, i iO

Г 7

M

4 Q

.

i 4 .

4

0

C7Hi<*0

С ? H

1 •)

0

>-7

Н

;

«о

•;

t н i J

з;.

tfril

'02

СГННИ2

С 7 Н 1

«• ?

; 7

н

14

р

•>

1./И14П

г

Г'

те

Slate

1

,2-OIBROMOHE.PTANE

..... (L)

1,2'OIBROMOHtPTANE

..... CG)

DIISOPROPYLCARBODIIMIOE

. • CS)

01IS0PR0PYLCYANAMI0E

. . , . (S)

DIETHYLMALONAMIOE

...» UbS)

5LYCYLVALINE

..,...>.

CS)

VALINE GLYCINE ANHYDRIDE

, . CS)

CYCLOHEPTANOL .......

CD

CYCLOHEXANEMETHANOI

- . » . CD

1,3-OIMETHYUCYCLOPEU1*NOL

. CD

2*5-DIMETHYLCYCL0PENTAN0l

, CD

2P«-0IMETHYL-3-PENTAN0NE

. . CD

i,3-EPOXY-3-ETHYLPENTANE

=

••

CD

2:

3-EP0XY'3»ETHYLPENTANF.

- - CD

2

•ETHYLOiV.ir'fc.NTANOL

- • CD

HtPTONAL

,

..-...*

CD

4EPT4NAI

r .

.......

CG)

4

.JEPTArti!

•

:.

.......

(L)

1

,flPFNT»L

'.'1

'

.

ETHCR

> CD

?-НЕТ^Щ^

\0htX«hfll

г

v. '

Ь , CD

- .: T.

If CJ

LXANOL

*

T R

Si.

5

CD

j

,L

i"HH

t

rtLO^c

*5N0L*

CIS

, CD

3-METHYLGKLOHEXANOL»

TRANS

CD

3

MFTHYL-5-HEXEN-3*-0L

. . . CD

ft

METHYLCYCLOHEXANOL»

CIS , CD

4-METHYLCYCLUHEXANDl*

TRANS

CD

tiHYL ISOVALEiUTE

, . •> .

С

L)

rlHYL

2~METH>LBUTYRATt

... CD

ETHYL PIVALATE

.......

(L)

ETHYL

VALERATE

.......

CD

2 -ETHYLVAIERIC ACID

. ... CD

HEPTANOIC

ACID

. , .... CD

HLPTANO'C

ACID

* e . • . . . CD

-> . '

•> '.Л

E'<ANEDinL»

CIS

С

<•

1

Mol

w

t

258.

126.

158.

174,

114.

114,

114.

114,

1)4.

-1"

114

130

1J0

130

•

']

014

198

182

,182

,

182

,182

,

182

,182

.

182

,182

.182

,182

182

.182

(kcal/mole)

-37.

-25.

-4.

-11

.

-141.

-199.

-188.

-86.

-88.

-102.

-105.

-90.

-76.

-71.

-97.

-74.

-63.

-85.

-66.

-93.

-99.

-94.

-99.

"86 t

-100.

-103,

-136.

-135.

.162-—

138,

.182

1

82

-132.

-141,

-145,

-146,

-144 ,

6

г

37

70

1

6

5

3

г

5

9

6

1

5

10

9

1

3

6

5

6

4

7

9

.6

,5

,0

,3

,5

.2

Source

nal/molc

I

ВС

АС:

СС

ВС

878)

1275)

744)

1176)

ВС1178)

СС

ВС

СС

АС

тс

СС

ее

СС

ВС

СС

АС

ВС

744)

844)

744)

843)

744)

1065)

83.3

550)

110.34

744)

843)

1366)

744)

1366)

Ь69)

569)

744)

3)

853)

1536)

AC/I»

(kcal/mole)

logKp

МС1109)

-24.05

ТС

550)

-20.71

17.629

15.183

Г

X

< orniula

С7И14О2

C7H14Q2

C7H1406

C7H1407

C7H14S

Name

State

MolVVt

(kcal/mole) Source (cal/mole

°K)

Source

AC/!*,

(kcal/mole)

С7Н15ВЯ

C7H15F

C7H15N

C7H16

С7Н16

C7H16

C7H160

C7H16Q

C7H160

C7H1602

THANS

CS)

130.182

METHYL

HEXANOATE

......

CD

130.182

ALPHA-METHYLGLUC0S10E'

. .

CU.S)

194.182

GLUCOHEPTOSE

........

CS)

210.182

ALLYL

TERT-BUTYL SULFIOE

. , CL)

130.?48

ALLYL

TERT-SUTYL SULFIDE

. , CG)

130.248

1-BROMOHEPTANE

. CL)

179.106

1-BROMOHEPTANE

(G)

179.106

1-FLUOROHEPTANE

CD

118.190

3-METHYLCYCLUHEXYLAMINE

. . CD

113.198

2.2-OIMtTHYLPENTANE

. . . . CL)

100.198

2»2-0IMETHYLPENTANE

. . . . CG)

100.198

2,3-DIMETHYLPENTANE

.... CD

100.198

2.3-DIMETHYLPENTANE

. . . . CG)

100.198

2*4-0IM£THYLPENTANE

. . . . CL)

100.198

2»4-DIMETHYLPENTANE

. . . . CG)

100.198

3«3-DIMETHYLPENTANE

.... CD

100.198

3#3-OIMETHYLPENTANE

. . . , CG)

100.198

3-ETHYLPENTANE

.......

CD

100.198

3-ETHYLPENTANE

.......

CG)

100.198

HEPTANE

..........

CD

100.198

HEPTANE

(G)

100.198

2-METHYLH£XANE

.......

CL)

100.198

2-METHYLHEXANE

. CG)

100.198

3-METHYLHEXANE

.......

CD

100.198

3-METHYLHEXANE

....»,.

CG)

100.198

2>2»3-TRIMETHYLBUTANE

, ,

c

CD

100.198

2»2»3-TRIMETHYL9UTANE

. „ . CG)

100.198

TERT-BUTYL ISOPROPYL tTHER

, CL)

116.198

TERT-BUTYL ISOPROPYL ETHEH

. CG)

116.198

3-ETHYL-3-PENTANOL

. . - , . CD

Ц6.198

HEPTYL ALCOHOL .......

П )

Ц6.198

HEPTYL ALCOHOL с

С.'

116 198

ACETONE DIETHYL ACETAL

a) 1

5

2 198

ACETONE DIETHYL

ACETAL

, , CG) 132 198

DIPROPOXYMETHANE

. , -

)=-•>(,

-141.8

-129.2

-292.8

-353.2

-21.7

-11.1

-52.24

-40.69

-92.1

-51.9

-57.05

-49.27

-55.81

-47.62

-56.17

-48.28

-56.07

-48.17

-53.77

-45.33

-53.63

-44.88

-54.93

-46.59

-54.35

-45.96

-56.63

-4Й.95

-94.0

-85.60

124.8

-95.31

-80.03

128.2

120.6

118.2

8C1536)

AC

3)

CC

?44)

CC

744)

ВС

900)

ВС

900)

AC

138)

AC

138)

CC

744)

CC

744)

AC 1203)

TC

118)

AC12O3)

TC

119)

AC1203)

TC

120)

AC 1203)

TC

121

)

AC1203)

TC

117)

AC12O3)

TC

114)

AC1203)

TC

115)

AC 1203)

TC

116)

AC 1

203)

TC

122)

BC1390)

TC

509)

eC

744)

AC

215)

TC

527)

AC1416)

CC

744)

71.77

93.90

76.27

98.96

72.46

94.80

73.44

95.53

75.18

98.35

78.53

102.27

77.28

100.38

78.23

101.37

69.85

91.61

M(

654)

TC

118)

EC1248)

TC

119)

MC

654)

TC

120)

EC1248)

TC

121)

MC

654)

TC

117)

MC

654)

TC

114)

MC

654)

TC

115)

EC1248)

TC

116)

MC

654)

TC

122)

77.9

MC1109)

114.83

TC 527)

-1.16

0.02

-1.26

0.16

-0.49

0.74

"0.68

0.63

1.10

2.43

0.24

1.91

-0.69

0.77

-0.39

1.10

-0.17

1.02

99.89

TC 509)

-30.79

•33.95

•29.68

0.853

-0.014

0.927

-0.117

0.358

-0.543

0.499

-0.464

-0.806

"1.929

-0.177

-1.402

0.503

-0.562

0.285

-0.807

0.125

-0.749

22.S70

24,882

21.752

Formula

C7H1604S2

C7H1607

C7H16S

cmes

C7H16S

C7H17N

C8F16

C8H4CL202

C8H4N2

(-1

C8H4N6

V C8H4N6

Я C8H403

C8H5F3O2

C8H5F302

C8H5N0

C8H5N02

C8H6

C8H6BR4

C8H6BH4

C8H6CL2

C8H6CL4

C8H6N20

C8H6N202

C8H6N2O4

'C8H6N2O4

Name Stale

2.2-BISCETHYLSULFONYDPROPANECS)

O-GLYCERO-O-GALACTOHEPTITOL

(S)

BUTYL PROPYL SULFIDE

. . . . (G)

ETHYL PENTYL SULFIOE

. . . . (G)

1-HEPTANETHIOL

(L)

1-HEPTANETHIUL

.......

CG)

HEXYL METHYL SULFIOE

. . . . (G)

HEPTYLAMINE

(L)

Mol

Wt

(kcal/mole)

228.330 -341.6

Source

(cat/mole

°K)

Source

CC1441)

212.198

-368.6

CC 744)

132.264

-34.88

T( 811)

117.90

T( 811)

132.264

-34.85

TC 812)

11',58

T( BlZ)

132.264

-47.85

A( 507)

132.264

-35.76

T( 901)

Ц7.в9

Т( 901)

132.264

-34.27

TC

813)

Ц7.04

TC

813)

115.214

-59.2 CC 744)

(kcal/mole)

9.53

9.65

8.65

10.39

Log Kp

-6.984

-7.076

-6.341

-7.619

UNOECAFLUOROCPENTAFLUORO-

ETHYDCYCLOHEXANE

UNDECAFLUOROCPENTAFLUORO-

ETHYDCYCLOHEXANE

CG)

400.080

PHTHALOYL CHLORIDE

CS)

203.026

PHTHALONITRILE

CS)

128.128

AMMONIUM SALT

OF

bl»2»3»3-PENTACYANOPROPENECS)

184.160

PHTHALIC

ANHYORIOE

CS)

148.112

ALPHA»ALPHA»ALPHA-

TRIFLUORO-M-TOLUIC ACIO

CS)

190.120

PHENYLGLYOXYLONITRILE.

. . . CS)

131.128

IN0OLE-2»3-DI0NE

CS)

147.128

ISATIN

. , CS)

147.128

PHTHALIMIOE

CS)

147.128

ETHYNYL8ENZENE

CD

102.128

ETHYNYLBENZENE

CG)

102.128

TETRABROMO-M-XYLENE

. . . . CS)

421.792

TETRA8R0M0-0-XYLENE

. . . . CS)

421.792

TETRABROMO-P-XYLENE

. . . . (S)

421.792-

2.5-OICHLOROSTYNENE

. . . . CL)

173.042

2»3»5,6-TETRACHL0R0-P-XYLENE

CS)

243.956

PHENYLFURAZAN

CS)

146.144

3-PHENYL0XA0IAZ0L-5-0L

. . . CS)

162.144

5-PHENYL0XADIAZ0L-3-0L

. . . (S)

162.144

M,BETA-DINITHOSTYR£NE.

. . . CS)

194,144

P,BETA-OINITHOSTYRENE.

. . . (S)

194.144

CL)

400.080

-798.2

AC 508) -

•789.0

AC 508)

-97.4

CC 744)

66.35

AC1275)

120.7

•110.1

•254.

17.

-54.

-61.

-73.

67.

78.

7.

6.

1.

8.

-42.

58.

-24.

0.

5.

5

8

7

6

0

72

22

9

4

3

05

5

6

7

о

AC

154)

AC1U6)

A(

512)

CC

744)

CC

744)

CC1414)

CC

744)

AC

432)

TC

471)

CC1180)

AC1359)

AC1387)

С(1012)

CC1012)

CC

744)

C(

744)

42.9

MC1U8)

-79.12

57.992

76.88

TC 471)

86.46

-63.J75

Formula

Name

State

C8H6N402 2-PHENYL-S-TETRAZOLE-

C8H6N402 CAHBOXYLIC ACID

. CS)

C8H6N4010 2»4#6-TRINlTR0PHEN0XY-

C8H6N4010 ETHYL МТЯАТЕ

CS)

C8H602 PHTHALIDE

(S)

C8H603 METHYLENEPROTOCATECHUALDEHYOECS)

C8H604 ISOPHTHALIC ACIO

CS)

C8H604 PHTHALIC ACIO

(S)

C8H604 PIPERONYLIC ACID

(S)

C8H604 TEREPHTHALIC ACID

CS)

C8H6S BENZOTHIOPNENE

. (S)

C8H7CL0 TOLUOYL CHLOHIOE

(S)

C8H7FN203 4'-FLU0H0-3'-NITR0ACETANILIDE(L)

C8H7F2N0 OIFLUOROACETANILIOE

. . .

CU»S)

C8H7I02 METHYL M-IOOUBENZOATE

. . . (S)

С8И7102 METHYL 0-IOOOBENZOATE

. . . (L)

C8H7I02 METHYL P-IODOBENZOATE

. . . (S)

C8H7N BENZYL ISOCYANIOC

(L)

C6H7H INDOLE

CS)

C6H7N PHENYLACETONITRILE

CD

C«H7N 0-TOLUNITWILE

CL)

C8H7N02 INO0LEHY0R0XY-2-IN00LINE

. . CS)

C8H7N02 0ME6A-NITROSTYRENE

CS)

C8H7N30 PHENYLAMINO FURAZAN

. , . . CS)

C8H7N306 l-ETHYL-2»4»6-TRINITR0BENZENECS)

C8H7N306 2>4,6-TRINITR0-M-XYLENE

. . CS)

C8H7N307 2#4,6-TRINlTR0PHENET0LE

. . CS)

C8H7N308 2/4-DINITROPHEN0XYETHYL

C«H7N308 NITRATE

CS)

C8H7N508 METHYLTETRYL

.......

CU»S)

C8H7N508 AR»N-TETRANITROPHENETHYLAMINECS)

C8H8 1#3»5,7-CYCLUOCTATETRAENE

. CD

C8H8 1»3»5»7-CYCLOOCTATETRAENE

. CG)

СвНв STYRENE

, , . . CL)

C8H8 STYRENE

, • . . CG)

C8H8FN0 З'-FLUOROACETANILIOE

. . . . CS)

MolWr

190.160

318.160

134.128

150.128

166.128

166.1'28

166.128

134.194

154.593

198.152

171.144

262.046

117.144

149.144

161.160

241.160

257.160

273.160

301.176

104.144

153.152

(kcal/mole)

-9.9

-66.3

-72.6

-85.9

-191.96

-186.96

-153*3

"195.10

-52.4

-98.1

-131.1

-66.3

-58.1

-68.4

55.9

30.3

32.9

39.7

-75.1

6.1

54.2

-25.1

-24.0

-48.0

-66.4

17.6

-4.8

60.93

71.23

24.83

35.22

-90.4

Source

8C

ВС

CC

AC

CC

AC

CC

ВС

974)

983)

744)

1295)

744)

1295)

744)

1382)

8(1382)

BC1382)

CC

744)

CC1413)

CC

ВС

744)

1640)

CC1012)

ВС

CC

ВС

АС

ТС

АС

тс

ее

984)

55)

57)

983)

744)

981)

1197)

472)

1248)

439)

744)

(cal/mole

°K)

Sourer

(kcal/mole) Log

«A»

49.7

МСЩ8)

-141.39

103.640

42.33

МС 419)

52.65

МС1312)

78.10

ТС 472)

56.78

МС1160)

82.48

ТС 439)

85.70

88.41

48.27

51.10

-62.817

•64.805

-35.454

-37.453

t

4

ДН/'Й«

rormiil»

Nlim

''

Slatc

MnlWt (kail/mole)

C8H8FN0 4'-FLU0R0ACETANILIDE

. . . . CS)

153.152

-89.6

C8H8FNO3 4-FLUORO-3-NITROPHENETOL

. CS)

185.152

-87.2

C8H8N202 PHENYLGLYOXIMECALPHA)

. . . CS)

164.160

-3.2

C8H8N202 PHENYLGLYOXIMECBETA)

. . . . CS)

164.160

11.В

C8H8N203 2'-NITROACETANRIOE

CS)

180.160

-51.1

C8H8N2O3 3'-NITROACETANILIDE.

. . . . CS)

180.160

-56.2

C8HBN203

<•'

-NITROACETANILIDE

CS)

180.160

-56.8

C8H8N20*

BISUCCINIMIOE

CS)

196.160 -169.55

C8H8N204 2»«-DINITR0-H-XYLENE

. . . . CS)

196.160

-19.7

C8H8N204 4,6-OINITRO-M-XYLENE

. . . . CS)

196.160

-23.7

C8H8N204 1-ETHYL-2/4-DINITR0BENZENE

. CD

196.160

-19.6

C8H8N205 2»4-DINITR0PHENET0LE

. . . . CS)

212.160

-53.4

C8H8N4 1-METHYL-5-PHENYLTETRAZ0LE

. CS)

160.176

69.8

C8H8N4 l-PHENYL-5-METHYLTETRAZOLE

. CS)

160.176

69.2

C8H8N4 2-PHENYL-5-METHYLTETRAZ0LL

. CS)

160.176

65.6

C8H8N6 BENZAL-5-HYDRAZIN0TETHAZOLE

CS)

188.192

105.4

C8H8N606 AMMONIUM 5»5"NITRILO-

C8H8N606 OIBARBITURIC ACIO

. CS)

C8H80 ACETOPHENONE

CD

C8H80 ACETOPHENONE

CG)

C8H80S PHENYL THIOLACETATE

.... CD

C8H802 M-ANISALOEHYDE

CD

C8H8Q2 0-ANISALOEHYDE

CS)

C8H802 P-ANISALDEHYOE

CD

C8H802 1,4-BENZODIOXAN-

C8H802 TETRAHYDRONAPHTHALENE

CD

136.144

C8H802 2-HY0R0XYACETOPHEN0NE

. . . CL)

136.144

C8H802 3-HYDROXYACETOPHENONE

. . . CS)

136.144

C8H802 4-HY0R0XYACET0PHEN0NE

. . . CS)

136.144

C8H802 METHYL BENZOATE

CD

136.144

C8H802 PHENYLACETIC ACIO

CS)

136.144

C8H8O2 M-TOLUIC ACIO

CS)

136.144

C8H802 0-TOLUIC ACIO

CS)

136.144

C8H802 P-TOLUIC ACID

CS)

136.144

C8H603 P-ANISIC ACIO

CS)

152.144

C6HR03 ?»3-CRES0TIC ACID

CS)

152.144

Source (cal/mole"

CC

744)

CC

744)

ВСЮ13)

ВС

1013)

CC

744)

247)

55)

ВС

1471 )

ВС

57)

ВС

1616)

ВС

1616)

ВС

974)

ВС

1616)

Source (kcal/mole)

СС

АС

ВС

784.192 -289.4

СС 744 )

120.144 -34.06

АС 251)

-20.76 АС1434)

-32.4 АС1556)

-64.9

СС 928)

-62.6

СС 928)

-63.8

СС 928)

120.144

152.210

136.144

АС

201)

СС

145)

СС

145)

СС

145)

СС

744)

СС

744)

-101.84

АС 250)

-99.55

АС 250)

-102.58

АС 250)

-130.4

СС 744)

-146.3

СС 744)

-61.0

-44

.4

-87.1

-Я6.2

-81.4

-94.7

59.62 МС1354)

89.12 МС1434)

-4.06

0.44

2.977

-0.324

Formula

Name State

С8Н803

2>4-CRES0TIC ACIO

CS)

СвНвОЗ

2.5-CRESOTIC ACID

CS)

СвнвОЗ

2>6-CRES0TIC ACID

CS)

СвНвОЗ 3-HYDROXY-P-ANISALOEHYDE

. . CS)

СвНвОЗ 4-HYDR0XY-M-ANISALDEHYDE

. . CS)

C8H803 MANDELIC ACID»

O.L CS)

СвНвОЗ MANDELIC ACIO»

L CS)

СвНвОЗ METHYL P-HYOHQXYBENZOATE

. . CS)

СвНвОЗ METHYL SALICYLATE

CL)

СвНвОЗ

0-OXYMETHYLBENZOIC ACID

.

CU»S)

СвНвОЭ

PHENOXYACETIC ACIO

CS)

C8H804 CYCLOHEXAOIENE-

C8H804

1.4-OICARBOXYLIC ACID

(S)

C8H804 l»4-CYCL0HEXA0IENE-

C8H804

b«-DICARBOXYLIC ACIO

CS)

СвН80« ?»4-CYCL0HEXADIENE-

C8H804

l»4-0ICAR80XYLIC ACID

CS)

C8H8Q4 2.5-CYCL0HEXA0IENE-

Свн804 l»4-0ICARB0XYLIC ACID CS)

C8H805 METHYL GALLATE CS)

C8H9CL 1-CHL0R0-2-ETHYLBENZENE . . CD

C8H9CL 1-CHL0R0-4-ETHYLBENZENE . . CL)

C8H9F0 M-FLUOROPHENETOLE ..... (L)

C8H9F0 P-FLUOROPHENETOLE CD

C8H9N0 ACETANILIDE CS)

C8H9N0 ACETOPHENONE: OXIME CS)

C8H9NQ2

2-OXYACETOPHENONE OXIME

. . CS)

C8H9N02 «-OXYACETOPHENONE OXIME

. . CS)

C8H9N02 PHENYLGLYCINE CU»S)

C8H9N02

N-PHENYLGLKINE

CS)

C8H9N03

M-NITROPHENETOLE CD

C8H9N03

0-NITROPHENETOLE . CD

C8H9N03

P-NITROPHENETOLE

...... CD

C8H9N30«

DIMETHYL-2»4-DINITR0-

C8H9N304 N»N-ANILINE

CS)

СвнЮ

ETHYLBENZENE

, . CD

MolVVI (kcal/mole) Source (cal/mole

°K)

Source (kcal/mole)

LogAfp

152.144

152,144

152.144

168.144

184.144

140.609

140.152

135.160

151.160

167.160

211.176

106.160

-147.2

-145.5

-142.2

-107.3

-110.9

-138.5

-138.7

-129.6

.-127.1

-137.7

-122.2

-182.5

-189.5

-183.0

-180.2

-223.6

-12.88

-12.33

-79.5

-82.7

-50.3

-5.3

-52.9

-50.9

-103.1

-93.0

-49.9

-38.6

-53.1

"6.9

-2.98

CC

ВС

CC

AC

CC

cc

AC

cc

AC

CC

cc

ВС

AC

744)

928)

744)

1651)

744)

1354)

744)

635)

744)

1558)

744)

843)

744)

204)

1248)

•20.971

С8Н10

СвнЮ

С8Н10

С8НЮ

СвНЮ

свню

СвнЮ

C8H10N20

СвНЮ№0

C8H10N4Q2

свнlONao

t

о

свнюо

сенюо

свнюо

свнюог

СвН1002

свнюог

свнюогя

C8H1002S

СвН1003

свн

юоз

С8Н1003

СвнЮОЗ

C8H1003S

Nairn State

ETHYLBEN2ENE

. . „ CG)

1.7-DCTA0IYNE

CD

M-XYLENE

CD

M-XYLENE

CG)

O-XYLENE

CD

O-XYLENE

CG)

P-XYLENE

. CD

P-XYLENE

CG)

N.N-01HETHYL-P-NITR0SUANILINECS)

N-ETHYL-N-NITHOSOANRINE

. . CS)

CAFFEINE

CS)

ALLOXANTHINE

OIHYDRATE

.

(U»S)

M-ETHYLPHENOL

CD

H-ETHYLPHENOL

CG)

0-ETHYLPHENOL

CD

0-ETHYLPHENOL

CG)

P-ETHYLPHENOL

CS)

P-ETHYLPHE'NOL

C8)

M-METHYLANISULE

CD

PHENETOLE

CD

M-XYLENOL

. CU.S)

O-XYLENQL

CU.S)

P-XYLENOL

CU.S)

9-OIMETHOXYBENZENE

CD

P-DIMETH0XY8ENZENE

..... CS)

P-OIMETHOXYBENZENE

..... CD

P-XYLENE-ALPHA.ALPHA'-OIOL

. CS)

BENZYL METHYL SULFUNE

... CD

BENZYL METHYL SULFONE

. . . CG)

METHYL

P-TOLYL

SULFONt

. . . CL>

METHYL

P-TOLYL

SULFONE

. . . CG)

1»2-CYCLOHEXANEDICARBOXYLIC

ANHYDRIDE»

CIS CS)

1.2-CVCLOHEXANEDICARBOXYLIC

ANHY04IUE» TRANS

CS)

P-ETHYIBENZENESULFONIC ACID

CG)

186,226

Mol

W(

106.160

150.176

194.192

322.192

122.160

122.1*0

122.160

138.160

13Я.160

138.160

170.226

ли/;,»

(kcal/mole)

7.1?

80.0

-6.07

1.12

-5.84

4.54

-5.64

4.29

31.6

25.3

-79.2

•475.9

-51.29

-35.01

-49.99

-34.8?

-53.71

-34.55

-37.6

-38.6

-55.7

-58.0

-57.8

-70.1

-78.5

-70.6

-94.23

-88.7

-67.2

-92.4

-70.8

Source (cal/mole

°K)

Source (kcal/mole)

TC

398)

AC

433)

AC1248)

TC

399)

AC1248)

TC

400)

AC1248)

TC

401)

744)

128)

126)

128)

56)

744)

201)

744)

AC1114)

ВС

905)

ВС

905)

B(

905)

ВС

905)

86.15

ТС 398)

31.21

-22.875

CC

AC

ВС

CC

AC

CC

154.160

-161.3

CC 744)

154.160

-162.0

CC 744)

60,

85,

58,

84,

27

49

80

31

59.20

84.23

MC1248)

TC

399)

MC1166)

TC

400)

MC1166)

TC

401)

25.73

28.41

26.40

29.18

26.28

28.»5

-18.463

-20.821

-19.353

-21.386

-19.265

"21.221

104.04

tC 69)

У.

Formula

C8H1004

С8Н100Я

C8H10S

C8H11N

CBH11N

C8H11N

C8H11N02

C8H11N03

C6H11N03

C8H12

C8H12N203

C8H12N206

C8H12N4

Name

State

1-CYCLOHEXENL-

l»4-0ICARR0XYLIC

ACID

CS)

2-CYCLOHEXENE-

1.4-OICARBOXYLIC

ACID

CS)

DJETHYL

ACETYLENEDICARBOXYLATECD

BENZYL METHYL

SULFIDE

... CD

BENZYL METHYL

SULFIDE

. . . CG)

ETHYL

PHENYL

SULFIOf

.... CD

ETHYL

PHENYL

SULFIDE

. . . . CG)

N,N-OIMETHYLANILINE

.... CD

N,N-OIMETHYLANILINE

. . . . CG)

N-ETHYLANILINE

(L)

N-ETHYLANILINE

CG)

2-NOR90RNANECARBONITRILE»EN00CL5

2-N0P.R0RNANECARB0NITRILE»

EXOCL)

2-0CTY4ii»jTHlLE

CL)

2.4-XY

1

.

:&JNE

CL)

ETHYL

?-»ETHYL-

3-PYRROLECARBUXYLATE

CS)

METHYL

2.4-DIMETHYL-

1-PYRROLECARBQXYLATE

CS)

METHYL

3»5-DIMETHYL-2-

PfRROLECARBOXYLATE

CS)

ETHYL

4-HT0RUXY-5-METHYL-

3-PYRR0LECARB0XYLATE

CS)

8ICYCL0C2*2»2)0CT-2-ENE

. . CS)

1,3-OIMETKrLDIHYDROBENZENE

CU#L)

»4-0IMETHYL-l»3-CYCL0HEXA0IENECD

l-METHYL-3-METHYLENE-

CYCLOHEXENE-1

CD

VINYLCYCLOHEXENE

CG)

5»5-DIETHYLHARBITURIC

ACID

• CS)

1.2-BISC3-CARB0XYPR0PI0NYD-

HYDRAZINE

CS)

2>2'-AZ0BIS-2-METHYL-

PROPIONITRILE

CS)

MolWt

170.160

138.226

121

.176

121.176

153.176

169.176

108.176

184.192

232.192

164,208

ля/;..

(kcal/mole)

-24.1

-212.3

-136.4

6.2

19.0

5.2

.18.4

8.2

20.

10

0.9

13.40

36.3

-19.2

-95.6

-98.3

-143.5

-13.8

-7.9

-10.9

16,8

-178.8

-317.8

54.6

m

Source

CC

ВС

CC

ее

AC

ВС

CC

GC

CC

EC

CC

ВС

744)

B98)

И98)

898)

1547)

744)

1414)

1413)

1414)

744)

356)

744)

1640)

974)

S°

m

(cal/mole

°K)

Source

61.2

87.5

57.2

84.1

53.29

55.11

50.30

96.4

EC1547)

MC1334)

МС13Э4)

MC1624)

EC

356)

\Gf°

n

,

(kcal/mole)

51.20

55.26

45.10

49.58

47.14

-37.531

-40.506

-33.054

-36.338

-34.551

Formula

Name

State

C8H120 BETA-OKYCLOUCTANONE»

CIS

CU»D

C8H120 BFTA-DICYCLOUCTANONE, TRANSCU.D

C8H12O 3.5-DIMETHYL-2-CYCLOHEXEN-

CBH12C

1-ONE

CD

C8H120 ETHYLENECYCLUHEXANONE» ENOOCU.S)

C8H120 3-OXABICYCLOC3»2»2)NUNANE

. CS)

C8H1202 l-CYCLO4EXENt-l-ACETIC ACID

CS)

C8H1202 OELTA-1-ALPHA-CYCLOHEXANE-

C8H1202 ACETIC ACID

CS)

C8H1202 ETHYL SQRBATE

.......

CD

C8H1202 2-OCTYNOIC ACID

......

CD

C8H1203 2.2-DIETHYLSUCCINIC ANHYORIOECD

C8H12Q3 DIETHYLSUCCINIC ANHYORIDE»С IS

CD

C8H12O3 DIETHYLSUCCINIC ANHYOftIUE»THANSCD

C8H1203 TETRAMFTHYLSUCCINIC ANHYONIDECS)

C8H12O4 CYCLOHEXANE-1>2"

C8H12O4 OICARBOXYLIC ACID»

CIS . CS)

C8H120e CYCLOHEXANE-1,2-

C8H1204 DICARBOXYLIC ACID» TRANS

CS)

C8H12Q4 CYCLOHEXANE-1»'4-DICAR«OXYLIC

C8H12O"

ACID»

CIS CS)

C8H1204 CYCL0HEXANE-l»4-0ICARH0XYLIC

C"8Hi?04 ACID» TRANS

(S)

C8H1804 DIMETHYL TETRAMETHYLENE-

C8HJ204 ALPHA»BETA-DICARBOXYLATE CU»L)

C8H1S04 ETHYL 2-ACETYLАСЕ ТО АСЕТА ТЕ

. CD

C8H12S6

1»3»5»7-TETRAMETHYL-2»4»6»8»9.

C8H12S6 10-HExATHIAADAMANTANE

(S)

C8H13NO N-PENTYLPROPIULAMIOE

. . . CS)

C8H14 RrCYCL0C2,2»2)0CTANE

. . . . CS)

C8H14 CYCLOOCTENE

CD

C8H14 CYCLOOCTENE

CG)

C8H14

3-CYCLOPENTYL-l-PROPENE

. . CD

C8H14

2-CYCLOPROPYL-3-METHYL-l-BUTENE(L)

CPM1«

2-CYCLOPROPYL-l-PENTENE

. . (D

CSHV'

?-C V Cl Of

ДНЯ,»

Sn,

MolVVt

(kral/mole) Source (cal/mole °K) Source (kcal/mole)

124.176 «47.8

AC 74)

124.176

-41.0 AC 74)

124.17ft

--59.9

124,176

-45.5

124,176

140,176 -115.7

C(

AC

744)

90)

140.17ft

140.176

156.176

300

139

110

110.

•118.5

-148.5

-79.2

•164.0

•165.1

•166.7

156.176 -169.8

172.176

172.

J76

172,176

-229.8

-232.2

-233.5

-232.6

CC

744)

CC

744)

CC

744)

CC

744)

ВС

1538)

BC1538)

BC153B)

BC1538)

BC1579)

ВС

1579)

CC

744)

CC

744)

172.176 -177.2

CC 744)

172.176 -190.2

С

744)

572

192

-46.0

CC 744)

-16,

-6,

-15,

3,

110.192

7

76

77

0

НС

878)

AC

261)

AC

821

)

CC 1373)

CC

1374)

56,47

MC1624)

76.75

HC 213)

50.18

MC162«)

-2.0

CC

1374

)

X

Formula

Name Slate

C8H14

?»4-DIMETHYLCYCL0HEXENE

. . CD

C8H14 1-ETHYLCYCLOHEXENE

(D

C8H14 ETHYLIDENECYCLOHEXANE

... CD

C8H14

2-METHYLN0HB0RNANE» ENOO

. . CD

C8H1« 2-METHYLN0RBURNANE»

EXO . . CD

C8H14 flCTAHYDROPENTALENE»

CIS . . CD

C8H14 OCTAHYDROPENTALENE» TRANS

. CD

C8H1*

1-OCTYNE

CG)

C8H14 1.2»Э-TRIMETHYLCYCLOPENTENE

CD

C8H14 2»3»3-TRIMETHYLCYCL0PENTENE

CD

C8H1» VINYLCYCLOHEXANE

CD

C8H148RZ

l,2-DIBR0M0CYCL00CTANE

... CD

C8H14BR2

1,2-01BROMOCYCLUOCTANE

. . . CG)

C8H14N4

2»2'-HYDRAZ0BIS-

C8H1«N4

2-METHYLPR0PI0NITRILE

CS)

C8H14N405 TRIGLYCYLGLYCINE

CU.S)

C8H110 CYCLOOCTANONE

CD

C8H140 2»2-DIMETHYLCYCL0HEXAN0NE

. CD

C8HH0 2-ETHYL-2-HEXENAL

(D

C8H140 4-METHYL-l»6-HEPTA0IEN-4-0L

CD

C8H140 2-0CTYNE-1-0L

CD

сенног

BUTYL

CROTONATE

CD

C8H1402 SEC-BUTYL CRUTONATE

.... CD

C8H1402 CYCLOHEPTANECARBOXYLIC ACID

CS)

C8H1402 CYCLOOCTANECARBQXYLIC ACID

C8HH02 CACTIVE)

CS)

C8H1402 2.5-DIMETHYL-3-HEXYNE-2»5-DI0LCD

C8H1102 ISOBUTYL CROTONATE

CD

C8H1402 ISOPROPYL 2-PENTENOATE

... CD

СвНН02

ISOPROPYL 3-PENTENQATE

... CD

C8H1402 ISOPROPYL 4-PENTENOATE

... CD

C8HH02

3-METHYLCYCLOHEXANECARBOXYLIC

C8H1402

ACID

CS)

C8H1«O2

PROPYL 2-PENTENOATE

.... CD

C8HH02 PROPYL 3-PENTENOATE

.... CD

C8HH0Z

PROPYL 4-PENTENOATE

.... CD

Mol

Wt

1

10.

no.

110.

no..

no.

110.

270.

166.

246.

126.

142.

142

.

142.

192

.192

192

024

224

192

ДНЯ

•98

(kcal/mole)

-35

-25

-24

-30

-24

19

-37

-21

-31

-18

28

-282

-76

-62

-49

-38

-112

-114

-141

-142

-87

-115

-116

-114

-in

.8

.53

.76

.9

,9

.70

.9

.6

.22

.7

.5

.6

.8

.4

.46

.8

.6

.9

.4

.1

.4

.6

.2

.9

л.»

Source (cal/mole

°K)

Source

CC

AC

ВС

ТС

CC

AC

ВС

CC

AC

CC

ВС

CC

ВС

744)

821

)

821

)

56.93

МС1333)

58.85

МС1333)

75)

325)

106.75

ТС 325)

744)

821

)

878)

974)

744)

1272)

744)

1506)

744)

744»

1286)

744)

1286)

BC1287)

ВС

1287)

(kcal/mole)

56.26

-41.236

142.192 -144.4

CC 744)

142.192 -112.2

ВС

1287)

142.192 -109.8 ВС1287)

142.192

-108.3

ВС1287)

Iniimil.i Name State

C8H1403 ETHYL 2-ЕTHOXYCROTONА

ТЕ

. . (L)

C8H1403 ETHYL 2-ЕTHYLАСЕТОАСЕТА

ТЕ

. CD

C8H1403 ISOBUTYRIC ANHYDRIDE

. ... CD

C8H14CJ4 BUTYRYL PEROXIDE

(L)

C8H1404 DIETHYL SUCCINATE

(L)

C8H1404 2#2-DIETHYLSUCCINIC ACID

. . (S)

C8H1404 2»3-DIETHYLSUCCINIC ACID» CISCS)

C8H1404 2»3-OIETHYLSUCCINIC ACID» TKANSCS)

C8H1404 DIMETHYL ADIPATE

CD

C8H1404 DIMETHYLADIPIC ACID

. . . CU.S)

С8НЦ04 ERYTHRITEDIACETAL

.... (U>5)

C8H1404 ETHYLPROPYLMALONIC ACID

. . CS)

C8H1404 PENTYLMALQNIC ACID

CS)

C8H1401 SUBERIC ACID

CS)

C8H1404 TETRAMETHYLSUCCINIC ACID

. . CS)

C8H1106 DIETHYL TARTHATE»

0 .... CD

C8H1106 OIETHYL TARTRATE» MESU

... CD

С8НП06 DIMETHYLOIHYDHQXYADIPIC ACID(U»S)

C8H1406 DIMETHYL DIMETHOXY-

C8H1406 SUCCINATE»

DL CS)

C8H1406 DIMETHYL MESQ-DI METHOXY-

C8H1406 SUCCINATE

CS)

C8HH08 GLUCOOCTONOLACTONE

CS)

C8H15CL02 flUTYL 2-CHLORQBUTYRATE

... CD

C8H15CL02 RUTYL 3"CHLORUBUTYRATE

. . . CD

C8H15CL02 BUTYL 4-CHLORUBUTYHДТЕ

... CD

C8H15CL02 ISOBUTYL 2"CHL0R0BUTYRAТЕ

. CD

C8H15CL02 ISDBUTYL 3-CHLOROBUTYRAТЕ

. CD

C8H15CL02 TSOBUTYL 1-CHLOHOBUTYHAТЕ

. CD

C8H15CL02 ISOPENTYL 2-CHLUROPROPIONAТЕ

CD

C8H15CL02 TSOPENTYL 3-CHLUROPROP I ONATE

CL>

C8H15N 3-AZABICYCL0C3.2.2)N0NANE

. CS)

C8H16 CYCLOOCTANE

CD

C8H16 CYCLOOCTANE

CG)

C8H16

2-CYCLOPRUPYL-3-METH-YLBUTANE

CD

C8H1*

2-CYCLOPRUPYLPENTiNE

. ... CD

Mol Wt

(kcal/mole)

Source

(cal/mole

°K)

Source

(kcal/mole)

I-OR

Kp

158

15R

158

171

174

171

174

192

174.192

206.192

-154.7

-170.9

"181.3

-161.0

-223.4

-216.0

-212.8

-214.5

-210.3

-243.3

-1P0.1

-211.1

-244.0

-246.6

-211.2

299.5

298.9

311.7

AC

CC

AC

CC

996)

258)

679)

744)

BC1538)

ВС

1538)

ВС

1538)

CC

744)

CC

744)

CC

744)

CC

744)

ВС

1535)

CC

741 )

BC1538)

CC

744)

CC

744)

CC

744)

206.192

-265.3

ВС 358)

?06

238

178

125

112

112.208

192

-275

192

-394

657

657-

657

208

-156

-116

-117

-158

-149

-151

-150

-142

-40.

-30.

-14.

,7

,1

,8

2

9

,3

2

,0

1

0

42

06

ВС

358)

CC

744)

RC

1384)

BC1381)

ВС

1381)

RC

1381)

BC1384)

ВС

1384)

BC1384)

ВС

1384)

AC

707)

ТС

343)

CC1373)

CC

1375)

56.11

62.62

87.66

MC

rc

73)

424)

343)

18.60

21

.49

•13.634

•15.755

Formula Name

State

C8H16

1»

1-DIMETHYLCYCLOHEXANE

. . CL)

C8H16 l»l-DIMETHYLCYCLOHEXiNE

. . CG)

C8H16 1»1-OIMETHYL-

C8H16 2-PROPYLCYCLCPHOPANE

CD

C8H16 1,2-DIMETHYLCYCLOHEXANE»

CIS CD

C8H16 1,2-DIMETHYLCYCLOHEXANE»

CIS CG)

C8H16 1,2-DIMETHYLCYCL0HEXANE»THANSCD

C8H16 1,2-OIMETHYLCYCLOHtXANE.TRANSCG)

C8H16

1 »

3-DIMETHYLCYCLt)HtXANE»

CIS CD

СЙН16 1»3-DIMETHYLCYCL0HEXANE.

CIS CG)

C8H16 l»3-DIMETHYLCYCL0HEXANE»TRANSCD

C8H16

1» 3-D

IMETHYLCYCLOHE.XANE» TRANS

CG)

C8H16 1,4-DIMETHYLCYCLOHEXANE»

CIS CL)

C8H16 1«4-DIMETHYLCYCLOHEXANE»

CIS CG)

C8H16 l,4-DIMETHYLCYCL0HEXANE»THANS(L)

C8H16 l,4-DIMETHYLCYCL0HEXANE»THANSCG)

C8H16 2»2-DIMETHYL-3-HEXENE»

CIS . CD

C8H16 2>2-DIMETHYL"3-HEXENE>

CIS . CG)

С8Н1Й 2»2-DIMETHYL-3-HEXENE» TRANS

CD

C8H16 2#2-DIMETHYL-3-HEXENE» TRANS

CG)

C8H16 ETHYLCYCLUHEXANE

CD

C8H16 ETHYLCYCLOHEXANE CG)

C8H16

3-ETHYL-2-METHYL-1-PENTENE

. CD

C8H16

3-ETHYL-2-METHYL-1-PENTENE

. (G)

C8H16

1-OCTENE

CD

C8H16

1-OCTENE

CG)

C8H16 PROPYLCYCLOPENTANE

CL)

C8H16 PROPYLCYCLOPENTANE

CG)

C8H16

l»2»4-TRIMETHYLCYCL0PENTANE. CD

С8Щ6

2»1»4-TRIMETHYL"1-PENTENE . CD

C8H16

?/1»4-TRIMETHYL-l-PENTENE . CG)

C8H16

2»«»4-TRIMETHYL-2-PENTENE . CL)

C8H16

2»1»1"TRIMETHYL-2-PENTENE . (G)

C8H16N203 LEUCYLGLYCINt»

D»L (S)

CflH16N203 VALINE ALANINE ANHYDHIDE

. . (S)

C8H16N201 DIETHYLURETHAN

OF

\Hf°

m

S°

JW

AG/S*.

MolWt

(kial/mole)

Source

(cal/mole

°K)

Source

(kcal/mole)

112.208 -52.31 AC1248) 63.87

MC 6b7) 6.34

112.208 -43.26

TC 373)

87.24

TC 373) 8.42

I

12

112

1

12

112

208

112.208

208

?08

208

224

112.

112,

112.

112,

112.

112,

11?,

112,

112

168

188.224

-27.8

-50.61

-41.15

-52.19

-43.02

-53.30

-44.16

-51.57

-42.20

-51.55

-42.22

-53.18

-41.12

-30.63

-21.77

-35.05

-26.

lft

-50.72

-41.05

-33.36

-24.10

-29.52

-19.82

-45.21

-35.39

-53.3

-35.21

-26.68

-34.44

-25.50

-205.36

-192.0

AC

710)

AC

1248)

TC

374)

AC

1248)

TC

375)

AC

1248)

TC

376

)

AC

1248)

TC

377)

AC

1248)

TC

378)

AC

1248)

TC

379)

AC

1236)

AC

1236)

AC

1236)

AC

1236)

AC

1196)

TC

372)

AC

1236)

AC

1236)

AC

1236)

TC

291 )

AC1196)

TC

354)

CC

744)

AC

1236)

AC

1236

)

AC

1236)

AC

1236)

AC

643)

ВС

1177)

65.52

MC

89.51

TC

65.30

MC

88.65

TC

65.16

MC

88.54

TC

66.03

MC

89.92

TC

64.80

MC

88.54

TC

61.06

MC

87.19

TC

657)

374)

657)

375)

6b7)

376)

657)

377)

657)

378)

657)

379)

67.14

MC 657)

91.44

TC 372)

86.15

MC 950)

110.55

TC 291)

74.29

MC 993)

99.73

TC 354)

73.2 MC1119)

7<l.5

MC 11 19)

67.2 MC 642)

7.52

9.85

6.03

8.24

«.96

7.13

6.13

8.68

6.82

9.07

5.41

7.58

6.95

9.38

22.19

24.91

10.33

12.57

20.66

21 .04

•112.14

-4.646

-«.172

-5.509

-7.222

-4.421

-6.040

-3.638

-5.228

-4.716

-6.363

-4.999

-6.650

-3.966

-5.552

-5.096

-6.87a

•16.481

•18.259

-7.573

-9.211

•15.H1

•15.421

82.200

Formula

Name

Slate

C8H16N204 ETHYLENEDIAMINE

(S)

C8H16N204 TARTARICOIETHYLAMIDE»

D . (1Ы.)

C8H16N204 TARTAHICDIETHYLAMIDE»

0»L (U»L)

C8H16N2O4 TARTARICDIETHYLAMIDEf MESO

CU.D

C8H160 b2-DIMETHYLCYCL0HEXAN0L

. . (L)

C8H160

1,3-DIMETHYLCYCLOHEXANOL

. . CD

C8H160

2,6-DIMETHYLCYCLOHEXANOL

. . (L)

C8H160

3,5-OIMETHYLCYCLOHEXANOL

C8H160

CIS, CIS; CIS . CS)

C8H160

3.5-DIMETHYLCYCtOHEXANOL

C8H16U

CIS.

CIS» TRANS

. CD

C8H160

3,5-DIMETHYLCYCLOHEXANOL

C8H160

CIS» TRANS,

CIS CD

C8H160

3-ETHVL-5-HEXEN-3-OL

.... CD

C8H16U

4-METHYL-1-HLPTEN-4-0L ... CD

C8H160 OCTANAL CD

C8H160 OCTANAL <G)

C8H160 2-0CTAN0NE ... CD

C8H16D 3-OCTANONE CD

C8H160 4-0CTAN0NE

CD

C8H16O2 SEC-BUTYL BUTYRATE

CD

C8H1602 METHYL HEPTANOATE

CD

C8K1602 OCTANOIC ACID

CD

C8H16O2 OCTANOIC ACID

CD

C8H1602 PROPYL VALERATE

CD

C8H16Q2 2-PROPYLVALENIC

ДС1П .... CD

C8H16O2 TETRAMETHYLBUTENEDIOL

C8H1602 FUMAROID

CU,S)

C8H1602

TETRAMETHYLBUTENEDIOL

C8H16D2

MALE1NOIO

CU,S)

C8H17BR

1-BRClMOUCTANt

CD

C8H17BR

1-BROMOOCTANE

CG)

C8H17F

1-FLUOROOCTANE

CD

C8H17N

CONIINE

CD

C6H17N

N-ISQBUTYLI DENEHUTYLAM

INE

. CL)

C8H17N

N-ISORUTYLIOLNFHUTYLAMINE

. CG)

MolWt

204.?24

20".221

201.221

128.208

12Й.208

(kcal/mole)

-233.1

-231.2

-231.0

-233.0

-100.3

-106.3

-102.8

Source

B(

cc

982)

711)

744

)

741)

744)

711)

744)

(cal/mole

K)

Source

(kcal/mole)

128.208 -102.1 CC 1367)

128.208 -116.9 CC1367)

128.208

111.208

144.208

-126.2

-91.7

-96.9

-80.0

-69.23

-91.9

-91.5

-92.3

-141.5

"135.62

-151.75

-152.2

-141.4

-146.5

CC

C(

CC

ВС

ТС

8(

ВС

AC

ВС

CC

1367)

744)

463)

Ь51

)

1

19.66

T(

551

)

463)

89.35

MC

1084)

463)

1287)

3)

«53)

1287)

744)

-19.91

-33.54

14.594

24.587

144.208

-122.3

CC 744 )

144.208 -125.7

С( 744 )

193.132

-58.61

AC 138)

193.132

-46.26

AC 138)

132.216

-105

127.224

.0

'57.4

31.76

CC

744)

CC

744)

AC

96)

127.224

-21.8 AC 96)

Formula

C8H17N0

C8H18

ceme

C8H18

C6H18

C8H18

Name

State

OCTANAMIOE

(S)

2»2-DIMETHYLHEXANE

CD

2»2-DIMETHYLHEXANE

..... CG)

2#3-DIMETHYLHEXANE

CL)

?#3-DIMETHYLHEXANE

CG)

2»4-DIMETHYLHEXANE

(I)

2.4-DIMETHYLHEXANE

(G)

2,5-DIMETHYLHEXANF

CL)

2»5-DIMETHYLHEXANE

(G)

3.3-01METHYLHEXANE

CL)

3»3-0IMETHYLHEXANE

CG)

3,4-DIMETHYLHEXANE

CD

3»4-0IMETHYLHEXANE

CG)

3-ETHYLHEXANE

. CD

3-ETHYLHEXANE CG)

3-ETHYL-2-METHYLPENTANE . . CL)

3-ETHYL-2-METHYLPENTANE . . CG)

3-ETHYL-3-METHYLPENTANE . . CL)

3-ETHYL-3-METHYLPENTANE . . CG)

2-METHYLHEPTANE CL)

2-METHYLHEPTANE CG)

3-METHYLHEPTANE

......

CD

3-METHYLHEPTANE

......

CG)

4-METHYLHEPTANE

CL)

4-METHYLHEPTANE

CG)

OCTANE

CL)

OCTANE

CG)

2,2»3-TRIMETHYLPENTANE

2,2,3-TRIMETHYLPENTANE

2»2»4-TRIMETHYLPENTANE

Z»2»4-TRIMETHYLPENTANE

2,3.3-TRIMETHYLPENTANE

2»3»3-TRIMETHYLPENTANE

2»3»4-TRIMETHYLPENTANE

2.3,4-TRIMETHYLPENTANE

2#2»3»3-TETRAM ETHYL BUTANE

CD

CG)

CD

CG)

CD

CG)

CL)

CG)

CS)

17

03

14

1.79

AH/1,,

si,,

д(,/;„

Mul

Wl

Ikcal/mole)

Source

(cal/mole

°K)

Source

Ikcal/mole)

143.224 -113.1

ВС

1640)

Ц4.224 -62.63

AC1248)

79.33

EC1248)

0.71

114.224 -53.71

ТС 128)

103.06

ТС 128) 2.56

Ц4.224 -60.40

AC1248)

81.91

EC1248)

2.17

114.224 -51.13

ТС 129)

106.11

ТС 129) 4.23

П4.224

-61.47

АС1248)

82.62

ЕС

1246)

0.89

Ц4.224 -52.44

ТС 130)

106.51

ТС 130) 2.80

Ц4.224 -62.26

АС1248)

80.96

ЕС1248)

0.60

111.224 -53.21

ТС 131)

104.93

ТС 131) Z.50

114.224 -61.58

АС1248)

81.12

ЕС1248)

1.23

114.224 -52.61

ТС 132)

104.70

ТС 132)

114.224 -60.23

А(1248)

82.97

ЕС1248)

Ц4.224 -50.91

ТС 133)

107.15

ТС 133)

114.224 -59.88

АС1248)

84.95

ЕС1248)

114.224 -50.40

ТС 127)

109.51

ТС 127)

114.224 -59.69

АС1248)

81.41

ЕС1248)

114.224 -50.48

ТС 134)

105.43

ТС 134)

114.224 -60.46

АС1248)

79.97

ЕС1248)

114.224 -§1.38

ТС 135)

103.48

ТС 135)

114.224 -60.98

АС1248)

84.16

ЕС1248)

114.224 -51.50

ТС

124),

108.81

ТС 124)

114.224 -60.34

АС1248)

85.66

ЕС

1246)

114.224 -50.82

ТС 125)

110.32

ТС 125)

Ц4.224 -60.17

АС

1248

)

83.72

ЕС1248)

Ц4.224 -50.69

ТС 126)

108.35

ТС 126)

Ц4.224 -59.74

АС1248)

86.23

МС 420)

114.224 -49.82

ТС 123)

111.55

ТС 123)

Ц4.224 -61.44

АС1248)

78.30

ЕС

1248)

Ц4.224 -52.61

ТС 136)

Ю1.62

ТС 136)

114.224 -61.97

АС1248)

78.40

МС 1152)

Ц4.224 -53.57

ТС 137)

101.15

ТС 137)

114.224 -60.63

АС1248)

79.93

ЕС1248)

114.224 -51.73

ТС 138) ЮЗ.И ТС 138)

114.224 -60.94

АС1248)

78.71

МС1165)

Ц4.224 -51.97

ТС 139)

102.31

ТС 139)

Ц4.224 -64.23

АС1248)

65.43

МС1300)

3.95

3.03

5.08

2.49

4.76

0.92

3.05

1.12

3.28

1.»7

4.00

1.55

3.92

2.21

4.09

1.65

3.27

2.54

4.52

2.55

4.52

3.(6

-0.523

1

.876

1.594

-3.100

-0.655

2.053

-0.438

-1.833

-0.902

-2.32*

-1.«87

-3.034

-1

.311

-2.892

-2.224

-3.725

-1.974

-3.492

-0.677

-2.239

-0.819

-2.407

-1.367

-2.933

-Ы34

-2.872

-1.621

-2.997

-1.210

-2.396

-1.858

-3.309

-1.868

-3.315

-2.388

Сталл Д. Вестрам Э. Зинке Г. Химическая термодинамика органических соединений

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