preface to fifteenth edition

6.80 SECTION 6
TABLE 6.2
Heats of Fusion, Vaporization, and Sublimation and Specific Heat at Various Temperatures of
Organic Compounds (Continued)
C p
Substance Hm Hv Hs 400 K 600 K 800 K 1000 K
1,2,3-Trimethylbenzene 8.37 40.0 49.1 196.2 267.8 320.9 359.4
Ht 0.7 54.5
Ht 1.3 42.9
1,2,4-Trimethylbenzene 39.3 47.9 196.5 269.0 321.9 360.2
1,3,5-Trimethylbenzene 9.51 39.0 47.5 194.2 268.1 321.5 360.1
2,6,6-Trimethylbicyclo[3.1.1]-2-heptene 44.8
Trimethylbismuthine 34.7
Trimethylborane 20.2
2,2,3-Trimethylbutane 2.20 28.9 32.0 212.7 291.3 346.1 386.3
Ht 2.5 151.8
2,3,3-Trimethyl-1-butene 32.2
cis,cis-1,3,5-Trimethylcyclohexane 242.9 351.2 427.6 482.0
Trimethylene oxide 28.7 29.9
Trimethylene sulfide 8.3 32.3 36.0 91.6 127.4 152.3 170.2
Ht 0.7 96.5
Trimethylgallium 38.1
2,2,5-Trimethylhexane 6.2 33.7 40.2
2,3,5-Trimethylhexane 10.00 34.4 41.4
Trimethylindium 48.5
2,4,7-Trimethyloctane 38.2 49.9
2,2,3-Trimethylpentane 8.62 31.9 36.9
2,2,4-Trimethylpentane 9.04 30.8 35.1
2,3,3-Trimethylpentane 0.86 32.1 37.3
Ht 7.7 109.0
2,3,4-Trimethylpentane 9.27 32.4 37.7
2,2,4-Trimethyl-1,3-pentanediol 8.6 55.7
2,2,4-Trimethyl-3-pentanone 35.6 43.3
2,4,4-Trimethyl-1-pentene 31.4 35.8
2,4,4-Trimethyl-2-pentene 32.6 37.5
Trimethylphosphine 28.0
Trimethylphosphine oxide 50.2
Trimethyl phosphate 36.8
2,3,6-Trimethylpyridine 40.0 50.6
2,4,6-Trimethylpyridine 9.53 39.9 50.3
Trimethylsilanol 45.6
Trimethylstibine 31.4
Trimethylsuccinic anhydride 74.1
Trimethylthiacyclopropane 39.3
Trimethyltin bromide 47.3
2,4,6-Trinitroanisole 133.1
1,3,5-Trinitrobenzene 16.7 99.6
Trinitromethane 32.6 46.7
2,4,6-Trinitrophenetole 120.5
2,4,6-Trinitrotoluene 104.7
1,3,6-Trioxacycloactane 48.8
1,3,5-Trioxane 15.11 56.6
Triphenylarsine 99.3
Triphenylbismuthine 110.9
Triphenylborane 81.6
Triphenylene 118.0