preface to fifteenth edition

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TABLE 11.11 Solvents of Chromatographic Interest Continued Solvent Boiling point, C Solvent strength parameter e (SiO 2 ) e (Al 2 O 3 ) Viscosity, mN · s · m 2 (20C) Refractive index (20C) UV cutoff, nm Diethyl ether 35 0.38 0.38 0.25 1.353 218 Diethyl sulfide 92 0.38 0.45 1.443 290 Chloroform 62 0.26 0.40 0.57 1.443 245 Dichloromethane 41 0.42 0.44 1.425 235 4-Methyl-2-pentanone 116 0.43 0.42 15C 1.396 335 Tetrahydrofuran 66 0.45 0.55 1.407 220 1,2-Dichloroethane 84 0.49 0.80 1.445 228 2-Butanone 80 0.51 0.42 15C 1.379 330 1-Nitropropane 131 0.53 0.80 25C 1.402 380 Acetone 56 0.47 0.56 0.32 1.359 330 1,4-Dioxane 101 0.49 0.56 1.44 15C 1.420 215 Ethyl acetate 77 0.38 0.58 0.45 1.372 255 Methyl acetate 56 0.60 0.48 15C 1.362 260 1-Pentanol 138 0.61 4.1 1.410 210 Dimethyl sulfoxide 189 0.62 2.47 1.478 265 Aniline 184 0.62 4.40 1.586 Diethylamine 56 0.63 0.33 1.386 275 Nitromethane 101 0.64 0.67 1.394 380 Acetonitrile 82 0.50 0.65 0.37 1.344 190 Pyridine 115 0.71 0.97 1.510 330 2-Butoxyethanol 170 0.74 3.15 25C 1.420 220 1-Propanol 97 0.82 2.25 1.386 210 2-Propanol 82 0.82 2.50 1.377 210 Ethanol 78 0.88 1.20 1.361 210 Methanol 65 0.95 0.59 1.328 210 Ethylene glycol 198 1.11 21.8 1.432 210 Acetic acid 118 large 1.23 1.372 260 Water 100 large 1.00 1.333 191 11.17
11.18 SECTION 11 TABLE 11.12 Solvents Having the Same Refractive Index and the Same Density at 25C Solvent 1 Solvent 2 Refractive index 1 2 Density, g/mL 1 2 Acetone Ethanol 1.357 1.359 0.788 0.786 Ethyl formate Methyl acetate 1.358 1.360 0.916 0.935 Ethanol Propionitrile 1.359 1.363 0.786 0.777 2,2-Dimethylbutane 2-Methylpentane 1.366 1.369 0.644 0.649 2-Methylpentane Hexane 1.369 1.372 0.649 0.655 Isopropyl acetate 2-Chloropropane 1.375 1.376 0.868 0.865 3-Butanone Butyraldehyde 1.377 1.378 0.801 0.799 Butyraldehyde Butyronitrile 1.378 1.382 0.799 0.786 Dipropyl ether Butyl ethyl ether 1.379 1.380 0.753 0.746 Propyl acetate Ethyl propionate 1.382 1.382 0.883 0.888 Propyl acetate 1-Chloropropane 1.382 1.386 0.883 0.890 Butyronitrile 2-Methyl-2-propanol 1.382 1.385 0.786 0.781 Ethyl propionate 1-Chloropropane 1.382 1.386 0.888 0.890 1-Propanol 2-Pentanone 1.383 1.387 0.806 0.804 Isobutyl formate 1-Chloropropane 1.383 1.386 0.881 0.890 1-Chloropropane Butyl formate 1.386 1.387 0.890 0.888 Butyl formate Methyl butyrate 1.387 1.391 0.888 0.875 Methyl butyrate 2-Chlorobutane 1.392 1.395 0.875 0.868 Butyl acetate 2-Chlorobutane 1.392 1.395 0.877 0.868 4-Methyl-2-pentanone Pentanonitrile 1.394 1.395 0.797 0.795 4-Methyl-2-pentanone 1-Butanol 1.394 1.397 0.797 0.812 2-Methyl-1-propanol Pentanonitrile 1.394 1.395 0.798 0.795 2-Methyl-1-propanol 2-Hexanone 1.394 1.395 0.798 0.810 2-Butanol 2,4-Dimethyl-3-pentanone 1.395 1.399 0.803 0.805 2-Hexanone 1-Butanol 1.395 1.397 0.810 0.812 Pentanonitrile 2,4-Dimethyl-3-pentanone 1.395 1.399 0.795 0.805 2-Chlorobutane Isobutyl butyrate 1.395 1.399 0.868 0.860 Butyric acid 2-Methoxyethanol 1.396 1.400 0.955 0.960 1-Butanol 3-Methyl-2-pentanone 1.397 1.398 0.812 0.808 1-Chloro-2-methylpropane Isobutyl butyrate 1.397 1.399 0.872 0.860 1-Chloro-2-methylpropane Pentyl acetate 1.397 1.400 0.872 0.871 Methyl methacrylate 3-Methyl-2-pentanone 1.398 1.398 0.795 0.808 Triethylamine 2,2,3-Trimethylpentane 1.399 1.401 0.723 0.712 Butylamine Dodecane 1.399 1.400 0.736 0.746 Isobutyl butyrate 1-Chlorobutane 1.399 1.401 0.860 0.875 1-Nitropropane Propionic anhydride 1.399 1.400 0.995 1.007 Pentyl acetate 1-Chlorobutane 1.400 1.400 0.871 0.881 Pentyl acetate Tetrahydrofuran 1.400 1.404 0.871 0.885 Dodecane Dipropylamine 1.400 1.400 0.746 0.736 1-Chlorobutane Tetrahydrofuran 1.401 1.404 0.871 0.885 Isopentanoic acid 2-Ethoxyethanol 1.402 1.405 0.923 0.926 Dipropylamine Cyclopentane 1.403 1.404 0.736 0.740 2-Pentanol 4-Heptanone 1.404 1.405 0.804 0.813 3-Methyl-1-butanol Hexanonitrile 1.404 1.405 0.805 0.801 3-Methyl-1-butanol 4-Heptanone 1.404 1.405 0.805 0.813 Hexanonitrile 4-Heptanone 1.405 1.405 0.801 0.813 Hexanonitrile 1-Pentanol 1.405 1.408 0.801 0.810 Hexanonitrile 2-Methyl-1-butanol 1.405 1.409 0.801 0.815 4-Heptanone 1-Pentanol 1.405 1.408 0.813 0.810
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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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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
Page 1008 and 1009:
NaIO 3 75.2 72.6 70.9 64.4 60.5 1
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Page 1012 and 1013:
9.2 SECTION 9 9.1 LINEAR FREE ENERG
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9.4 SECTION 9 TABLE 9.1 Hammett and
Page 1016 and 1017:
9.6 SECTION 9 TABLE 9.1 Hammett and
Page 1018 and 1019:
9.8 SECTION 9 TABLE 9.3 pK a and Rh
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10.2 SECTION 10 10.4.6 Polyacrylate
Page 1022 and 1023:
10.4 SECTION 10 10.2 ADDITIVES TO P
Page 1024 and 1025:
10.6 SECTION 10 injection molding.
Page 1026 and 1027:
10.8 SECTION 10 10.3 FORMULAS AND K
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10.10 SECTION 10 Key properties of
Page 1030 and 1031:
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
Page 1040 and 1041:
TABLE 10.2 Properties of Commercial
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Page 1044 and 1045:
Page 1046 and 1047:
Page 1048 and 1049:
Page 1050 and 1051:
Page 1052 and 1053:
Page 1054 and 1055:
Page 1056 and 1057:
Page 1058 and 1059: TABLE 10.2 Properties of Commercial
Page 1076 and 1077: 10.58 SECTION 10 10.4 FORMULAS AND
Page 1078 and 1079: 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
Page 1084 and 1085: 10.6 GAS PERMEABILITY TABLE 10.5 Ga
Page 1086 and 1087: TABLE 10.5 Gas Permeability Constan
Page 1088 and 1089: 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
Page 1095 and 1096: 11.4 SECTION 11 TABLE 11.2 Molecula
Page 1097 and 1098: 11.6 SECTION 11 A saturated aqueous
Page 1099 and 1100: 11.8 SECTION 11 TABLE 11.6 Relative
Page 1101 and 1102: 11.10 SECTION 11 11.3 BOILING POINT
Page 1103 and 1104: 11.12 SECTION 11 TABLE 11.8 Organic
Page 1105 and 1106: 11.14 SECTION 11 TABLE 11.9 Molecul
Page 1107: 11.4 SEPARATION METHODS TABLE 11.11
Page 1111 and 1112: 11.20 SECTION 11 TABLE 11.12 Solven
Page 1113 and 1114: TABLE 11.13 McReynolds’ Constants
Page 1115 and 1116: TABLE 11.13 McReynolds’ Constants
Page 1117 and 1118: 11.26 SECTION 11 11.4.1 McReynolds
Page 1119 and 1120: 11.28 SECTION 11 11.4.2.2 Partition
Page 1121 and 1122: 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
Page 1129 and 1130: 11.38 SECTION 11 TABLE 11.18 Relati
Page 1131 and 1132: 11.40 SECTION 11 distribution coeff
Page 1133 and 1134: 11.42 SECTION 11 TABLE 11.19 Gravim
Page 1159 and 1160:
11.68 SECTION 11 TABLE 11.20 Elemen
Page 1161 and 1162:
11.70 SECTION 11 TABLE 11.22 Common
Page 1163 and 1164:
11.72 SECTION 11 TABLE 11.25 Tolera
Page 1165 and 1166:
11.74 SECTION 11 TABLE 11.26 Heatin
Page 1167 and 1168:
11.76 SECTION 11 TABLE 11.28 Titrim
Page 1169 and 1170:
Page 1171 and 1172:
Page 1173 and 1174:
Page 1175 and 1176:
11.84 SECTION 11 appears becomes le
Page 1177 and 1178:
11.86 SECTION 11 TABLE 11.29 Equati
Page 1179 and 1180:
11.88 SECTION 11 TABLE 11.29 Equati
Page 1181 and 1182:
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
Page 1193 and 1194:
11.102 SECTION 11 TABLE 11.39 Amino
Page 1195 and 1196:
11.104 SECTION 11 TABLE 11.44 Facto
Page 1197 and 1198:
11.106 SECTION 11 11.7 LABORATORY S
Page 1199 and 1200:
11.108 SECTION 11 TABLE 11.48 Stand
Page 1201 and 1202:
11.110 SECTION 11 Alizarin yellow G
Page 1203 and 1204:
11.112 SECTION 11 Bromchlorophenol
Page 1205 and 1206:
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
Page 1213 and 1214:
11.122 SECTION 11 TABLE 11.49 TLV C
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Page 1217 and 1218:
Page 1219 and 1220:
Page 1221 and 1222:
11.130 SECTION 11 TABLE 11.50 Chemi
Page 1223 and 1224:
Page 1225 and 1226:
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
Page 1233 and 1234:
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
Page 1241 and 1242:
11.150 SECTION 11 11.11 CORRECTION
Page 1243 and 1244:
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
Page 1251 and 1252:
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
Page 1261 and 1262:
Index Terms Links 20 Fluorocarbon p
Page 1263 and 1264:
Index Terms Links 22 Halogenated hy
Page 1265 and 1266:
Index Terms Links 24 Impact strengt
Page 1267 and 1268:
Index Terms Links 26 Kα 1 lines, m
Page 1269 and 1270:
Index Terms Links 28 Melmine phenol
Page 1271 and 1272:
Index Terms Links 30 Neon-neon bond
Page 1273 and 1274:
Index Terms Links 32 One-tailed tes
Page 1275 and 1276:
Index Terms Links 34 Physical chemi
Page 1277 and 1278:
Index Terms Links 36 Polyolefin the
Page 1279 and 1280:
Index Terms Links 38 Pyridine: bina
Page 1281 and 1282:
Index Terms Links 40 Rho values: fo
Page 1283 and 1284:
Index Terms Links 42 Single-bond ra
Page 1285 and 1286:
Index Terms Links 44 Stereoisomers
Page 1287 and 1288:
Index Terms Links 46 Tension, aqueo
Page 1289 and 1290:
Index Terms Links 48 Triethylenetet
Page 1291 and 1292:
Index Terms Links 50 Water (Cont.)
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