preface to fifteenth edition

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Index Terms Links 7 Benzoylacetone, formation constants with 8.89 Benzyl alcohol, binary azeotropic mixtures 5.71 Berthelot's equation of state 5.170 Beryllium: bond dissociation energies 4.41 gravimetric factors 11.44 Best-fit line 2.133 errors in slope and intercept 2.135 Binary azeotropes 5.58 containing alcohols 5.66 containing ketones 5.74 containing organic acids 5.62 containing water 5.58 Binary compounds between nonmetals 3.2 Biological buffers, pH range 8.110 Biological materials, pH measurement of 8.106 Bis(2-hydroxyethyl) ether, binary azeotropes with 5.76 Bismuth: bond dissociation energies 4.42 gravimetric factors 11.44 Bisphenol epoxy resin, properties of 10.28 Bivalent sulfur, nomenclature of 1.37 Blackbody radiation 7.38 7.39 Blaze wavelength 7.40 Block copolymers 10.3 of styrene, properties of 10.54 Blood, pH measurement of 8.106 Body-centered cubic structure 4.57 Bohr magneton 2.4 Bohr radius 2.4 Boiling point: of chromatographic solvents 11.16 of inorganic compounds 3.14 molecular elevation of 11.13 of organic compounds 1.76 organic solvents arranged by 11.10 of water at various pressures 5.56 Boiling point temperature, calculation of 5.30 Boltzmann constant 2.4 Bond dipole moments 4.53 Bond dissociation energies 4.41 Bond lengths and strengths 4.29 (See also entries for specific elements) Bonds, spatial orientation of 4.56 Borate, reference pH buffer solution at various temperatures 8.105 Boron: bond dissociation energies 4.42 bond lengths with other elements 4.39 gravimetric factors 11.44 Boron compounds: infrared frequencies of 7.61 nomenclature of 1.29
Index Terms Links 8 Boron-11 chemical shifts 7.111 Boyle's law 5.169 Branched polymers 10.3 BR rubber 10.59 Bragg equation 7.40 Bridged hydrocarbons, nomenclature of 1.10 Briggsian system of logarithms 2.102 Brix hydrometer 2.67 2.68 Bromide, formation constants with 8.84 Bromine: bond dissociation energies 4.42 gravimetric factors 11.44 overpotential of 8.140 solubility in water at various temperatures 5.3 Buffer solutions: for control purposes 8.110 standard reference 8.104 Buna N rubber 10.59 Buna S rubber 10.61 Buoyancy effect when weighing in air 2.83 Burets, tolerances for 11.103 Burning rate of polymers 10.22 Butadiene-maleic acid copolymer, properties of 10.42 1-Butanol: binary azeotropes with 5.69 ternary azeotropes with 5.78 2-Butanol, ternary azeotropes with 5.78 2-Butanone, binary azeotropes with 5.74 2-Butoxyethanol, binary azeotropes with 5.72 Butyl rubber 10.60 Butyric acid, binary azeotropes with 5.64 Cadmium: bond dissociation energies 4.42 gravimetric factors 11.44 Calcium: bond dissociation energies 4.42 gravimetric factors 11.45 Calcium chloride solutions, percent humidity of 11.7 Calcium hydroxide reference pH buffer solution at various temperatures 8.105 Calibration of conductivity vessels 8.160 Calmagite, formation constants with 8.90 Calomel reference electrodes, EMF as function of temperature 8.113 Candela, definition of 2.3 Capacity factor (see Partition ratio) Capillarity correction for barometer 2.75 Carbon: attached to double bond, estimation of chemical shifts of 7.103 bond dissociation energies 4.42 gravimetric factors 11.46
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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
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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
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
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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
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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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Page 1137 and 1138:
Page 1139 and 1140:
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Page 1159 and 1160:
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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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
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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
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11.94 SECTION 11 TABLE 11.30 Standa
Page 1187 and 1188:
TABLE 11.32 Properties and Applicat
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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
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
Page 1221 and 1222: 11.130 SECTION 11 TABLE 11.50 Chemi
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: Index Terms Links 6 Aurintricarboxy
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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