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2.86 SECTION 2 TABLE 2.15 Hydrometer Conversion Table (Continued) Density Degrees Baumé (NIST* scale) Degrees Twaddell Density Degrees Baumé (NIST* scale) Degrees Twaddell 1.03 4.22 6 1.04 5.58 8 1.05 6.91 10 1.06 8.21 12 1.07 9.49 14 1.08 10.78 16 1.09 11.97 18 1.10 13.18 20 1.11 14.37 22 1.12 15.54 24 1.13 16.68 26 1.14 17.81 28 1.15 18.91 30 1.16 20.00 32 1.17 21.07 34 1.18 22.12 36 1.19 23.15 38 1.20 24.17 40 1.21 25.16 42 1.22 26.15 44 1.23 27.11 46 1.24 28.06 48 1.25 29.00 50 1.26 29.92 52 1.27 30.83 54 1.28 31.72 56 1.29 32.60 58 1.30 33.46 60 1.31 34.31 62 1.32 35.15 64 1.33 35.98 66 1.34 36.79 68 1.35 37.59 70 1.36 38.38 72 1.37 39.16 74 1.38 39.93 76 1.39 40.68 78 1.40 41.43 80 1.41 42.16 82 1.42 42.89 84 1.43 43.60 86 1.44 44.31 88 1.45 45.00 90 1.46 45.68 92 1.47 46.36 94 1.48 47.03 96 1.49 47.68 98 1.50 48.33 100 1.51 48.97 102 1.52 49.60 104 1.53 50.23 106 1.54 50.84 108 1.55 51.45 110 1.56 52.05 112 1.57 52.64 114 1.58 53.23 116 1.59 53.80 118 1.60 54.38 120 1.61 54.94 122 1.62 55.49 124 1.63 56.04 126 1.64 56.58 128 1.65 57.12 130 1.66 57.65 132 1.67 58.17 134 1.68 58.69 136 1.69 59.20 138 1.70 59.71 140 1.71 60.20 142 1.72 60.70 144 1.73 61.18 146 1.74 61.67 148 1.75 62.14 150 1.76 62.61 152 1.77 63.08 154 1.78 63.54 156 1.79 63.99 158 1.80 64.44 160 1.81 64.89 162 1.82 65.31 164 1.83 65.77 166 1.84 66.20 168 1.85 66.62 170 1.86 67.04 172 1.87 67.46 174 1.88 67.87 176 1.89 68.28 178 1.90 68.68 180 1.91 69.08 182 1.92 69.48 184 1.93 69.87 186 1.94 70.26 188 1.95 70.64 190 1.96 71.02 192 1.97 71.40 194 1.98 71.77 196 1.99 72.14 198 2.00 72.50 200 * NIST, National Institute for Science and Technology (formerly the National Bureau of Standards, U.S.).
GENERAL INFORMATION, CONVERSION TABLES, AND MATHEMATICS 2.87 TABLE 2.16 Pressure Conversion Chart psi Inches H 2 O at 4C Inches Hg at 0C mmH 2 O at 4C mmHg at 0C atm Pascals (N · m 2 ) 0.01 0.2768 0.0204 7.031 0.517 0.0007 68.95 0.02 0.5536 0.0407 14.06 1.034 0.0014 137.90 0.03 0.8304 0.0611 21.09 1.551 0.0020 206.8 0.04 1.107 0.0814 28.12 2.068 0.0027 275.8 0.05 1.384 0.1018 35.15 2.586 0.0034 344.7 0.06 1.661 0.1222 42.18 3.103 0.0041 413.7 0.07 1.938 0.1425 49.22 3.620 0.0048 482.6 0.08 2.214 0.1629 56.25 4.137 0.0054 551.6 0.09 2.491 0.1832 63.28 4.654 0.0061 620.5 0.10 2.768 0.2036 70.31 5.171 0.0068 689.5 0.20 5.536 0.4072 140.6 10.34 0.0136 1 379.9 0.30 8.304 0.6108 210.9 15.51 0.0204 2 068.5 0.40 11.07 0.8144 281.2 20.68 0.0272 2 758 0.50 13.84 1.018 351.5 25.86 0.0340 3 447 0.60 16.61 1.222 421.8 31.03 0.0408 4 137 0.70 19.38 1.425 492.2 36.20 0.0476 4 826 0.80 22.14 1.629 562.5 41.37 0.0544 5 516 0.90 24.91 1.832 632.8 46.54 0.0612 6 205 1.00 27.68 2.036 703.1 51.71 0.0689 6 895 2.00 55.36 4.072 1 072 103.4 0.1361 13 790 3.00 83.04 6.108 2 109 155.1 0.2041 20 684 4.00 110.7 8.144 2 812 206.8 0.2722 27 579 5.00 138.4 10.18 3 515 258.6 0.3402 34 474 6.00 166.1 12.22 4 218 310.3 0.4083 41 369 7.00 193.8 14.25 4 922 362.0 0.4763 48 263 8.00 221.4 16.29 5 625 413.7 0.5444 55 158 9.00 249.1 18.32 6 328 465.4 0.6124 62 053 10.0 276.8 20.36 7 031 517.1 0.6805 68 948 14.7 406.9 29.93 10 332 760.0 1.000 101 325 15.0 415.2 30.54 10 550 775.7 1.021 103 421 20.0 553.6 40.72 14 060 1 034 1.361 137 895 25.0 692.0 50.90 17 580 1 293 1.701 172 369 30.0 830.4 61.08 21 090 1 551 2.041 206 843 40.0 1 107 81.44 28 120 2 068 2.722 275 790 50.0 1 384 101.8 35 150 2 586 3.402 344 738 60.0 1 661 122.2 42 180 3 103 4.083 413 685 70.0 1 938 142.5 49 220 3 620 4.763 482 633 80.0 2 214 162.9 56 250 4 137 5.444 551 581 90.0 2 491 183.2 63 280 4 654 6.124 620 528 100.0 2 768 203.6 70 307 5 171 6.805 689 476 150.0 4 152 305.4 7 757 10.21 1 034 214 200.0 5 536 407.2 10 343 13.61 1 378 951 250.0 6 920 509.0 17.01 1 723 689 300.0 8 304 610.8 20.41 2 068 427 400.0 27.22 2 757 903 500.0 34.02 3 447 379 1 bar 10 5 pascal.
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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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Page 124 and 125: 2.36 SECTION 2 TABLE 2.7 Conversion
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Page 156 and 157: 2.68 SECTION 2 Oleometer. A hydrome
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Page 170 and 171: 2.82 SECTION 2 TABLE 2.13 Viscosity
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Page 178 and 179: 2.90 SECTION 2 TABLE 2.18 Pressure
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Page 186 and 187: 2.98 SECTION 2 TABLE 2.21 Transmitt
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Page 192 and 193: 2.104 SECTION 2 TABLE 2.23 Derivati
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Page 220 and 221: TABLE 2.29 F Distribution (Continue
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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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PHYSICAL PROPERTIES 5.3 5.1 SOLUBIL
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TABLE 5.1 Solubility of Gases in Wa
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TABLE 5.1 Solubility of Gases in Wa
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TABLE 5.2 Solubilities of Inorganic
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formateBa(CHO 2 ) 2 26.2 28.0 29.9
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(III) sulfateCe 2 (SO 4 ) 3 ·9H 2
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iodidePbI 2 0.044 0.056 0.069 0.090
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Nickel sulfateNiSO 4 ·6H 2 O (pale
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Praseodymium bromatePr(BrO 3 ) 3 55
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formate NaCHO 2 43.9 62.5 81.2 102
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Uranyl nitrate UO 2 (NO 3 ) 2 98 10
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PHYSICAL PROPERTIES 5.25 TABLE 5.3
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PHYSICAL PROPERTIES 5.57 5.3 BOILIN
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TABLE 5.12 Ternary Azeotropic Mixtu
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TABLE 5.12 Ternary Azeotropic Mixtu
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PHYSICAL PROPERTIES 5.83 5.4 FREEZI
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PHYSICAL PROPERTIES 5.87 5.5 DENSIT
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PHYSICAL PROPERTIES 5.89 dt Dt P
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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
Page 1080 and 1081:
10.62 SECTION 10 Styrene-butadiene
Page 1082 and 1083:
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
Page 1090 and 1091:
TABLE 10.8 Constants ofWaxes Wax Me
Page 1092:
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
Page 1099 and 1100:
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
Page 1123 and 1124:
11.32 SECTION 11 11.4.3 Ion-Exchang
Page 1125 and 1126:
11.34 SECTION 11 TABLE 11.16 Guide
Page 1127 and 1128:
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
Page 1207 and 1208:
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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Page 1221 and 1222:
11.130 SECTION 11 TABLE 11.50 Chemi
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Page 1227 and 1228:
Page 1229 and 1230:
11.138 SECTION 11 of water which is
Page 1231 and 1232:
TABLE 11.55 Thermoelectric Values i
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TABLE 11.56 Type B Thermocouples: P
Page 1235 and 1236:
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
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Index Terms Links 2 Acid-base indic
Page 1245 and 1246:
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
Page 1253 and 1254:
Index Terms Links 12 Collective ino
Page 1255 and 1256:
Index Terms Links 14 Degree Fahrenh
Page 1257 and 1258:
Index Terms Links 16 Electrical res
Page 1259 and 1260:
Index Terms Links 18 Equivalent wei
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Index Terms Links 20 Fluorocarbon p
Page 1263 and 1264:
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
Page 1277 and 1278:
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
Page 1289 and 1290:
Index Terms Links 48 Triethylenetet
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Index Terms Links 50 Water (Cont.)
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