preface to fifteenth edition

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PHYSICAL PROPERTIES 5.53 TABLE 5.9 Vapor Pressures of Various Organic Compounds (Continued) Substance Eq. Range, C A B C Perfluorocyclobutane 1 32 to 0 6.815 29 862.49 225.19 Perfluorocyclohexane 1 19–65 6.04 597 136 Perfluorocyclopentane 1 17–56 7.039 6 1 069.3 234.6 Perfluoroheptane 1 2 to 106 6.937 72 1 181.14 208.66 Perfluorohexane 1 30–57 6.875 2 1 080.8 213.4 Perfluoromethylcyclohexane 1 33–111 6.824 06 1 133.76 211.22 Perfluorooctane 1 37–105 5.902 5 1 225.93 198.99 Perfluoropentane 1 9–65 7.017 9 1 072.9 230.0 Perfluoropiperidine 1 29–81 6.853 4 1 059.95 217.2 Perfluoropropane 1 79 to 36 6.919 4 825.8 241.2 Perfluoropropene 1 41 to 20 7.355 1 012.1 257 Phenanthrene 1 176–379 7.260 82 2 379.04 203.76 Phenol 1 107–182 7.133 0 1 516.79 174.95 -Phenylethyl acetate 1 149–233 6.834 3 1 555.2 160.8 -Phenylethyl alcohol 1 82–190 1.508 91 263 o-Phenylethylphenol 1 169–250 4.506 0 516.8 32.1 p-Phenylethylphenol 1 174–251 4.304 1 459.3 52.4 Phenylisocyanate 1 10–80 0.708 0 106.4 146.6 4-Phenylphenol 1 177–308 8.657 5 3 022.8 216.1 Phosgene 1 68 to 68 6.842 97 941.25 230 Phthalic anhydride 2 160–285 8.022 2 868.5 -Pinene 1 19–156 6.852 5 1 446.4 208.0 -Pinene 1 19–166 6.898 4 1 511.7 210.2 Piperidine 1 42–144 6.855 69 1 238.80 205.43 Propadiene 1 99 to 16 5.713 7 458.06 196.07 Propane 1 108 to 25 6.803 38 804.00 247.04 1-Propanethiol 1 25 to 91 6.928 46 1 183.307 224.62 2-Propanethiol 1 37 to 75 6.877 34 1 113.895 226.16 1-Propanol 1 2–120 7.847 67 1 499.21 204.64 2-Propanol 1 0–101 8.117 78 1 580.92 219.61 2-Propen-1-ol 1 21–97 11.187 0 4 068.5 392.7 Propionic acid 1 56–139.5 6.403 950.2 130.3 Propionic anhydride 1 67–167 5.819 5 810.3 108.7 Propionitrile 1 84 to 22 5.278 2 665.52 159.10 Propiophenone 1 132–201 7.370 1 894 205 Propyl acetate 1 39–101 7.016 15 1 282.28 208.60 1-Propylamine 1 23–77 6.926 51 1 044.05 210.84 2-Propylamine 1 4–61 6.890 25 985.69 214.07 n-Propylbenzene 1 43–188 6.951 42 1 491.297 207.14 n-Propyl borate 1 85–179 7.399 8 1 741 206 n-Propyl caprate 1 97–186 8.701 22 2 945.99 253.63 n-Propyl caproate 1 43–120 8.667 1 2 556.0 262.9 n-Propyl caprylate 1 70–153 8.516 7 2 599.5 246.2 n-Propyl cellosolve 1 77–149 7.146 4 1 440.6 187.7 n-Propylcyclohexane 1 40–186 6.886 46 1 460.800 207.94 n-Propylcyclopentane 1 21–158 6.903 92 1 384.386 213.16 Propylene 1 112 to 32 6.778 11 770.85 245.51 1,2-Propylene oxide 1 35 to 130 7.064 92 1 113.6 232 n-Propyl formate 1 26–82 6.848 1 127 203 n-Propyl laurate 1 124–205 8.068 9 2 692.4 222.5 n-Propyl myristate 1 147–200 9.216 8 3 744.68 272.87 n-Propyl nitrate 1 0–70 6.954 9 1 294.4 206.7 n-Propyl palmitate 1 166–204 14.129 2 9 759.2 539.7
5.54 SECTION 5 TABLE 5.9 Vapor Pressures of Various Organic Compounds (Continued) Substance Eq. Range, C A B C o-(n-Propyl)phenol 1 104–222 9.215 3 254 292 p-(n-Propyl)phenol 1 0–234 8.329 6 2 661 254 n-Propyl phenyl ether 1 101–190 7.734 3 2 146.2 252.3 Propyne 1 90 to 6 6.784 85 803.73 229.08 Pseudocumenol 1 107–232 6.915 1 547 152 Pyrene 1 200–395 5.618 4 1 122.0 15.2 Pyridine 1 67–153 7.041 15 1 373.80 214.98 Pyrogallol 1 177–309 6.092 1 031 12 Pyrrole 1 66–166 7.294 70 1 501.56 210.42 Quinaldine 1 178–248 7.179 00 1 857.84 184.50 Quinoline 1 164–238 6.817 59 1 668.73 186.26 Spiropentane 1 3–71 6.917 00 1 090.08 231.10 Styrene 1 32–82 7.140 16 1 574.51 224.09 Terpenyl acetate 1 37–150 6.443 46 1 377.27 143.85 -Terpineol 1 84–217 8.141 2 2 479.4 253.7 Terpinolene 1 40–179 7.169 1 706 211 Tetrabutyl tin 1 100–300 6.545 1 649 148 1,1,2,2-Tetrachloro-1,2-difluoroethane 1 10–91.5 10.995 4 437.1 455.2 1,1,1,2-Tetrachloroethane 1 59–130 6.898 75 1 365.88 209.74 1,1,2,2-Tetrachloroethane 1 25–130 6.631 7 1 228.1 179.9 Tetrachloroethylene 1 37–120 6.976 83 1 386.92 217.53 Tetrachloromethane 1 6.879 26 1 212.021 226.41 Tetradecane 1 122–286 7.013 00 1 740.88 167.72 1-Tetradecanethiol 1 7.048 5 1 909.2 151.9 1-Tetradecanol 1 130–264 6.674 1 1 204.5 54.0 1-Tetradecene 1 119–283 7.030 65 1 754.09 171.52 1,2,3,4-Tetrafluorobenzene 1 6–50 7.084 6 1 339.23 223.49 1,2,3,5-Tetrafluorobenzene 1 6–50 6.986 17 1 245.20 218.35 Tetrafluoroethylene 1 131 to 65 6.896 59 683.84 245.93 Tetrafluoromethane 1 6.972 31 540.50 260.10 Tetrahydrofuran 1 23–100 6.995 15 1 202.29 226.25 Tetraiodothiophene 1 65 to 24 5.585 44 871.25 175.59 Tetralin 1 94–206 7.070 55 1 741.30 208.26 1,2,3,4-Tetramethylbenzene 1 80–217 7.059 4 1 690.54 199.48 1,2,3,5-Tetramethylbenzene 1 75–228 7.077 9 1 675.43 201.14 1,2,4,5-Tetramethylbenzene 1 74–227 7.080 0 1 672.43 201.43 2,2,3,3-Tetramethylbutane 1 0–65 6.876 65 1 329.93 226.36 Tetramethyl lead 1 0–60 6.937 7 1 335.3 219.1 2,2,3,3-Tetramethylpentane 1 57–141 6.830 60 1 398.67 213.84 2,2,3,4-Tetramethylpentane 1 52–134 6.834 18 1 375.59 214.94 2,2,4,4-Tetramethylpentane 1 43–123 6.796 20 1 324.59 216.02 Tetramethylsilane 1 64 to 21 6.822 39 1 033.72 235.62 2-Thiabutane 1 26 to 90 6.938 49 1 182.562 224.78 Thiacyclobutane 1 5 to 120 7.016 67 1 321.331 224.51 Thiacyclohexane 1 29–170 6.905 18 1 422.47 211.72 Thiacyclopentane 1 14–148 6.995 40 1 401.939 219.61 Thiacyclopropane 1 35 to 77 7.037 25 1 194.37 232.42 3-Thiaheptane 1 33–172 6.941 02 1 421.32 205.81 4-Thiaheptane 1 32–170 6.935 77 1 413.44 205.73 2-Thiahexane 1 17–150 6.945 83 1 363.808 212.07 3-Thiahexane 1 14–144 6.933 80 1 341.57 212.51
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LANGE'S HANDBOOK OF CHEMISTRY John
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Grateful acknowledgment is hereby m
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PREFACE TO FIFTEENTH EDITION This n
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PREFACE TO FIFTEENTH EDITION ix inv
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xii PREFACE TO FOURTEENTH EDITION l
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PREFACE TO FIRST EDITION This book
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For the detailed contents of any se
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1.2 SECTION 1 is derived from the G
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1.4 SECTION 1 rather than methylide
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1.6 SECTION 1 Styrene Toluene Xylen
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1.8 SECTION 1 TABLE 1.2 Fused Polyc
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1.10 SECTION 1 1.1.1.6 Bridged Hydr
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1.12 SECTION 1 TABLE 1.4 Suffixes f
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1.14 SECTION 1 TABLE 1.5 Trivial Na
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1.16 SECTION 1 TABLE 1.6 Trivial Na
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1.18 SECTION 1 Selection of the pri
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1.20 SECTION 1 attached to one anot
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1.22 SECTION 1 When side chains of
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1.24 SECTION 1 heterocyclic structu
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1.26 SECTION 1 Bivalent radicals of
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1.28 SECTION 1 Complex linear polya
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1.30 SECTION 1 TABLE 1.11 Names of
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1.32 SECTION 1 hydroxyamino- to the
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1.34 SECTION 1 may be named (1) by
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1.36 SECTION 1 Examples are methyl
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1.38 SECTION 1 tuted acid, respecti
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1.40 SECTION 1 FIGURE 1.2 Newman pr
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1.42 SECTION 1 from the ring are kn
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1.44 SECTION 1 FIGURE 1.11 Two isom
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1.46 SECTION 1 Chiral Center. The c
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1.48 SECTION 1 FIGURE 1.15 Isomers
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1.50 SECTION 1 entries to bring tog
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1.52 SECTION 1 TABLE 1.13 Names and
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1.60 SECTION 1 TABLE 1.14 Empirical
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2.2 SECTION 2 2.3.6 Student’s Dis
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2.4 SECTION 2 TABLE 2.1 Fundamental
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2.6 SECTION 2 TABLE 2.1 Fundamental
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2.8 SECTION 2 TABLE 2.2 Physical an
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2.10 SECTION 2 TABLE 2.2 Physical a
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2.24 SECTION 2 TABLE 2.3 Mathematic
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2.26 SECTION 2 TABLE 2.6 Abbreviati
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2.36 SECTION 2 TABLE 2.7 Conversion
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2.54 SECTION 2 TABLE 2.8 Temperatur
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2.66 SECTION 2 2.1.1 Conversion of
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2.68 SECTION 2 Oleometer. A hydrome
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2.70 SECTION 2 Example 3. 25 1.2500
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2.72 SECTION 2 TABLE 2.9 Barometer
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2.74 SECTION 2 TABLE 2.9 Barometer
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2.76 SECTION 2 TABLE 2.10 Barometri
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2.78 SECTION 2 TABLE 2.12 Reduction
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2.80 SECTION 2 TABLE 2.12 Reduction
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2.82 SECTION 2 TABLE 2.13 Viscosity
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2.84 SECTION 2 TABLE 2.14 Conversio
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2.86 SECTION 2 TABLE 2.15 Hydromete
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2.88 SECTION 2 TABLE 2.17 Correctio
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2.90 SECTION 2 TABLE 2.18 Pressure
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2.96 SECTION 2 TABLE 2.20 Values of
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2.98 SECTION 2 TABLE 2.21 Transmitt
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2.100 SECTION 2 TABLE 2.21 Transmit
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2.102 SECTION 2 2.2 MATHEMATICAL TA
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2.104 SECTION 2 TABLE 2.23 Derivati
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2.106 SECTION 2 TABLE 2.24 Integral
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2.108 SECTION 2 TABLE 2.24 Integral
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2.110 SECTION 2 Regular Polygon of
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2.112 SECTION 2 A h[0.4(y y ) 1.
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2.114 SECTION 2 2.2.3.1 Signs of th
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2.116 SECTION 2 x2 x3 x4 x5 ln(1 x
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2.118 SECTION 2 2.3.2 Errors in Qua
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2.120 SECTION 2 The breadth or spre
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2.122 SECTION 2 TABLE 2.26b Areas U
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2.124 SECTION 2 The distribution of
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2.126 SECTION 2 Should there be mor
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2.128 SECTION 2 Example 10 Six samp
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2.130 SECTION 2 2.3.9 The F Statist
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TABLE 2.29 F Distribution (Continue
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2.134 SECTION 2 mathematical treatm
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2.136 SECTION 2 The confidence limi
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2.138 SECTION 2 situation where rel
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3.2 SECTION 3 The alphabetical orde
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3.4 SECTION 3 When it is required t
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3.6 SECTION 3 PO phosphoryl SeO sel
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3.8 SECTION 3 3.1.5 Acids 3.1.5.1 A
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3.10 SECTION 3 3.1.6.6 Multiplicati
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3.12 SECTION 3 3.2 PHYSICAL PROPERT
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TABLE 3.2 Physical Constants of Ino
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3.62 SECTION 3 TABLE 3.3 Synonyms a
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SECTION 4 PROPERTIES OF ATOMS, RADI
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4.3 Fermium Fm 100 [Rn] 5f 12 7s 2
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Silver (argentum) Ag 47 [Kr] 4d 10
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PROPERTIES OF ATOMS,RADICALS,AND BO
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PROPERTIES OF ATOMS, RADICALS, AND
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SECTION 5 PHYSICAL PROPERTIES 5.1 S
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Page 384 and 385: formateBa(CHO 2 ) 2 26.2 28.0 29.9
Page 386 and 387: (III) sulfateCe 2 (SO 4 ) 3 ·9H 2
Page 388 and 389: iodidePbI 2 0.044 0.056 0.069 0.090
Page 390 and 391: Nickel sulfateNiSO 4 ·6H 2 O (pale
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PHYSICAL PROPERTIES 5.103 TABLE 5.1
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PHYSICAL PROPERTIES 5.135 5.6.1 Ref
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PHYSICAL PROPERTIES 5.137 where the
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PHYSICAL PROPERTIES 5.139 5.7 COMBU
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Temperature, C Substance 40 20 0 20
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PHYSICAL PROPERTIES 5.171 This equa
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SECTION 6 THERMODYNAMIC PROPERTIES
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THERMODYNAMICPROPERTIES 6.3 6.1.1.2
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THERMODYNAMICPROPERTIES 6.5 A gener
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THERMODYNAMICPROPERTIES 6.7 TABLE 6
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THERMODYNAMICPROPERTIES 6.9 TABLE 6
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THERMODYNAMICPROPERTIES 6.11 TABLE
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THERMODYNAMIC PROPERTIES 6.21 TABLE
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THERMODYNAMIC PROPERTIES 6.101 TABL
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THERMODYNAMIC PROPERTIES 6.143 The
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SECTION 7 SPECTROSCOPY 7.1 X-RAY ME
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SPECTROSCOPY 7.3 TABLE 7.1 Waveleng
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SPECTROSCOPY 7.9 TABLE 7.3 Critical
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SPECTROSCOPY 7.11 TABLE 7.4 X-Ray E
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SPECTROSCOPY 7.13 Emission line K 1
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SPECTROSCOPY 7.15 TABLE 7.7 Analyzi
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SPECTROSCOPY 7.17 TABLE 7.8 Mass Ab
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SPECTROSCOPY 7.19 TABLE 7.9 Electro
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SPECTROSCOPY 7.21 TABLE 7.11 Absorp
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SPECTROSCOPY 7.23 TABLE 7.13 Solven
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SPECTROSCOPY 7.25 7.3 FLUORESCENCE
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SPECTROSCOPY 7.27 TABLE 7.16 Fluore
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SPECTROSCOPY 7.29 TABLE 7.18 Detect
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SPECTROSCOPY 7.35 TABLE 7.19 Sensit
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SPECTROSCOPY 7.37 TABLE 7.19 Sensit
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SPECTROSCOPY 7.39 In terms of m ,
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SPECTROSCOPY 7.41 The ionization co
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SPECTROSCOPY 7.67 TABLE 7.28 Infrar
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7.69
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SPECTROSCOPY 7.71 7.6 RAMAN SPECTRO
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SPECTROSCOPY 7.73 TABLE 7.30 Raman
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SPECTROSCOPY 7.89 7.7 NUCLEAR MAGNE
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SPECTROSCOPY 7.91 TABLE 7.41 Nuclea
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SPECTROSCOPY 7.93 TABLE 7.42 Proton
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SPECTROSCOPY 7.95 TABLE 7.44 Estima
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SPECTROSCOPY 7.97 TABLE 7.46 Proton
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SPECTROSCOPY 7.99 TABLE 7.48 Solven
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SPECTROSCOPY 7.101 TABLE 7.49 Carbo
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SPECTROSCOPY 7.103 TABLE 7.51 Effec
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SPECTROSCOPY 7.107 TABLE 7.56 One-B
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SPECTROSCOPY 7.113 TABLE 7.63 Nitro
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SPECTROSCOPY 7.115 TABLE 7.64 Nitro
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SPECTROSCOPY 7.117 TABLE 7.69 Fluor
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SPECTROSCOPY 7.119 TABLE 7.72 Silic
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SPECTROSCOPY 7.121 TABLE 7.73 Phosp
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SPECTROSCOPY 7.123 TABLE 7.74 Phosp
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SPECTROSCOPY 7.125 when z 3 and y
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SPECTROSCOPY 7.127 Masses 19 and 31
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SPECTROSCOPY 7.129 TABLE 7.76 Conde
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SECTION 8 ELECTROLYTES, ELECTROMOTI
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ELECTROLYTES, EMF, AND CHEMICAL EQU
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TABLE 8.7 Proton Transfer Reactions
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TABLE 8.7 Proton Transfer Reactions
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TABLE 8.9 Selected Equilibrium Cons
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8.75 3-tert-Butylbenzoic acid (0) 4
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4-Hydroxyproline (1) 1.900 1C 1.850
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N-Propionylglycine (1) 3.728 3.723
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TABLE 8.14 National Bureau of Stand
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1 part 0.1% neutral red in alc. * V
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3,3-Dimethoxybenzidine dihydrochlor
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TABLE 8.35 Equivalent Conductivitie
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KCl 127.3 124.4 122.4 115.8 112.0 1
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NaIO 3 75.2 72.6 70.9 64.4 60.5 1
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9.2 SECTION 9 9.1 LINEAR FREE ENERG
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9.4 SECTION 9 TABLE 9.1 Hammett and
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9.6 SECTION 9 TABLE 9.1 Hammett and
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9.8 SECTION 9 TABLE 9.3 pK a and Rh
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10.2 SECTION 10 10.4.6 Polyacrylate
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10.4 SECTION 10 10.2 ADDITIVES TO P
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10.6 SECTION 10 injection molding.
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10.8 SECTION 10 10.3 FORMULAS AND K
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10.10 SECTION 10 Key properties of
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10.12 SECTION 10 10.3.8 Fluorocarbo
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10.14 SECTION 10 10.3.11 Phenolics
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10.16 SECTION 10 The resin has the
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10.18 SECTION 10 10.3.19 Polyuretha
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10.20 SECTION 10 10.3.22 Sulfones B
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TABLE 10.2 Properties of Commercial
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10.58 SECTION 10 10.4 FORMULAS AND
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10.60 SECTION 10 10.4.8 Polychlorop
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10.62 SECTION 10 Styrene-butadiene
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10.5 CHEMICAL RESISTANCE TABLE 10.4
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10.6 GAS PERMEABILITY TABLE 10.5 Ga
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TABLE 10.5 Gas Permeability Constan
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TABLE 10.7 Constants ofFats and Oil
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TABLE 10.8 Constants ofWaxes Wax Me
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SECTION 11 PRACTICAL LABORATORY INF
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11.4 SECTION 11 TABLE 11.2 Molecula
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11.6 SECTION 11 A saturated aqueous
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11.8 SECTION 11 TABLE 11.6 Relative
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11.10 SECTION 11 11.3 BOILING POINT
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11.12 SECTION 11 TABLE 11.8 Organic
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11.14 SECTION 11 TABLE 11.9 Molecul
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11.4 SEPARATION METHODS TABLE 11.11
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11.18 SECTION 11 TABLE 11.12 Solven
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11.20 SECTION 11 TABLE 11.12 Solven
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TABLE 11.13 McReynolds’ Constants
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TABLE 11.13 McReynolds’ Constants
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11.26 SECTION 11 11.4.1 McReynolds
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11.28 SECTION 11 11.4.2.2 Partition
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11.30 SECTION 11 FIGURE 11.2 Band a
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11.32 SECTION 11 11.4.3 Ion-Exchang
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11.34 SECTION 11 TABLE 11.16 Guide
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11.36 SECTION 11 TABLE 11.16 Guide
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11.38 SECTION 11 TABLE 11.18 Relati
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11.40 SECTION 11 distribution coeff
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11.42 SECTION 11 TABLE 11.19 Gravim
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11.68 SECTION 11 TABLE 11.20 Elemen
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11.70 SECTION 11 TABLE 11.22 Common
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11.72 SECTION 11 TABLE 11.25 Tolera
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11.74 SECTION 11 TABLE 11.26 Heatin
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11.76 SECTION 11 TABLE 11.28 Titrim
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11.84 SECTION 11 appears becomes le
Page 1177 and 1178:
11.86 SECTION 11 TABLE 11.29 Equati
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11.88 SECTION 11 TABLE 11.29 Equati
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11.90 SECTION 11 The more stable th
Page 1183 and 1184:
11.92 SECTION 11 11.6.6.2.5 Buffer
Page 1185 and 1186:
11.94 SECTION 11 TABLE 11.30 Standa
Page 1187 and 1188:
TABLE 11.32 Properties and Applicat
Page 1189 and 1190:
11.98 SECTION 11 TABLE 11.36 Maskin
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11.100 SECTION 11 TABLE 11.37 Anion
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11.102 SECTION 11 TABLE 11.39 Amino
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11.104 SECTION 11 TABLE 11.44 Facto
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11.106 SECTION 11 11.7 LABORATORY S
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11.108 SECTION 11 TABLE 11.48 Stand
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11.110 SECTION 11 Alizarin yellow G
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11.112 SECTION 11 Bromchlorophenol
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11.114 SECTION 11 p-Ethoxychrysoidi
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11.116 SECTION 11 Mercurous nitrate
Page 1209 and 1210:
11.118 SECTION 11 Potassium carbona
Page 1211 and 1212:
11.120 SECTION 11 until the ammoniu
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11.122 SECTION 11 TABLE 11.49 TLV C
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11.130 SECTION 11 TABLE 11.50 Chemi
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Page 1229 and 1230:
11.138 SECTION 11 of water which is
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TABLE 11.55 Thermoelectric Values i
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TABLE 11.56 Type B Thermocouples: P
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TABLE 11.58 Type J Thermocouples: I
Page 1237 and 1238:
TABLE 11.60 Type N Thermocouples: N
Page 1239 and 1240:
TABLE 11.62 Type S Thermocouples: P
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11.150 SECTION 11 11.11 CORRECTION
Page 1243 and 1244:
Index Terms Links 2 Acid-base indic
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Index Terms Links 4 Alkynes, nomenc
Page 1247 and 1248:
Index Terms Links 6 Aurintricarboxy
Page 1249 and 1250:
Index Terms Links 8 Boron-11 chemic
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Index Terms Links 10 Cellulose acet
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Index Terms Links 12 Collective ino
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Index Terms Links 14 Degree Fahrenh
Page 1257 and 1258:
Index Terms Links 16 Electrical res
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Index Terms Links 18 Equivalent wei
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Index Terms Links 20 Fluorocarbon p
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Index Terms Links 22 Halogenated hy
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Index Terms Links 24 Impact strengt
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Index Terms Links 26 Kα 1 lines, m
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Index Terms Links 28 Melmine phenol
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Index Terms Links 30 Neon-neon bond
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Index Terms Links 32 One-tailed tes
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Index Terms Links 34 Physical chemi
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Index Terms Links 36 Polyolefin the
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Index Terms Links 38 Pyridine: bina
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Index Terms Links 40 Rho values: fo
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Index Terms Links 42 Single-bond ra
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Index Terms Links 44 Stereoisomers
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Index Terms Links 46 Tension, aqueo
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Index Terms Links 48 Triethylenetet
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Index Terms Links 50 Water (Cont.)
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