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1.56 SECTION 1 TABLE 1.13 Names and Formulas of Organic Radicals (Continued) Name Formula Name Formula cis-9-Octadecenoyl Octadecyl Octanedioyl Octanoyl Octyl Oleoyl Ornithyl Oxalacetyl Oxalaceto Oxalo Oxalyl Oxamoyl Oxido Oxo Oxonio Oxy Palmitoyl (unsubstituted only) Pentafluorothio Pentamethylene Pentanedioyl, see Glutaryl Pentanoyl, see Valeryl Pentenyl (2- shown) Pentyl Pentyloxy Perchloryl Phenacyl Phenacylidene Phenanthryl Phenethyl Phenetidino (o-, m-, or p-) Phenoxy Phenyl Phenylacetyl Phenylazo Phenylazoxy Phenylcarbamoyl Phenylene Phenylenebisazo Phenylimino 2-Phenylpropanoyl 3-Phenylpropenoyl, see Cinnamoyl 3-Phenylpropyl H[CH 2 ] 8 9CH"CH9 [CH 2 ] 7 9CO9 CH 3 9[CH 2 ] 16 9CH 2 9 9CO9[CH 2 ] 6 9CO9 CH 3 9[CH 2 ] 6 9CO9 CH 3 9[CH 2 ] 6 9CH 2 9 H[CH 2 ] 8 9CH"CH9 [CH 2 ] 7 9CO9 H 2 N9[CH 2 ] 3 9 CH(NH 2 )9CO9 9CO9CH 2 9CO9 CO9 HOOC9CO9CH 2 9 CO9 HOOC9CO9 9CO9CO9 H 2 N9CO9CO9 O9 (ion) O" H 2 O9 9O9 CH 3 9[CH 2 ] 14 9CO9 F 5 S9 9CH 2 9CH 2 9CH 2 9 CH 2 9CH 2 9 CH 3 9CH 2 9CH"CH9 CH 2 9 CH 3 9CH 2 9CH 2 9CH 2 9 CH 2 9 CH 3 9[CH 2 ] 4 9O9 O 3 Cl9 C 6 H 5 9CO9CH 2 9 C 6 H 5 9CO9CH" C 14 H 9 9 C 6 H 5 9CH 2 9CH 2 9 C 2 H 5 O9C 6 H 4 9NH9 C 6 H 5 9O9 C 6 H 5 9 C 6 H 5 9CH 2 9CO9 C 6 H 5 9N"N9 C 6 H 5 9N 2 O9 C 6 H 5 9NH9CO 9C 6 H 4 9 9N"N9C 6 H 4 9 N"N9 C 6 H 5 9N" C 6 H 5 9CH(CH 3 )9CO9 C 6 H 5 9CH 2 9CH 2 9 CH 2 9 Phenylsulfamoyl Phenylsulfinyl Phenylsulfonyl Phenylsulfonylamino Phenylthio 3-Phenylureido Phthalamoyl Phthalidyl Phthalimido Phthaloyl Picryl Pimeloyl (unsubstituted only) Piperidino (1- only) Piperidyl (2-, 3-, 4-) Piperonyl Pivaloyl (unsubstituted only) Polythio Propanedioyl, see Malonyl Propanoyl, see Propionyl Propargyl, see 2-Propynyl Propenoyl, see Acryloyl 1-Propenyl 2-Propenyl, see Allyl Propenylene Propioloyl Propionamido Propionyl Propionylamino Propionyloxy Propoxy Propyl Propylene Propylidene Propylidyne Propynoyl, see Propiolyl 1-Propynyl 2-Propynyl Protocatechuoyl 3-Pyridinecarbonyl 4-Pyridinecarbonyl Pyridinio Pyridyl 2-Pyridylcarbonyl Pyridyloxy Pyruvoyl Salicyl Salicylidene Salicyloyl Sarcosyl C 6 H 5 9NH9SO 2 C 6 H 5 9SO9 C 6 H 5 9SO 2 9 C 6 H 5 9SO 2 9NH9 C 6 H 5 9S9 C 6 H 5 9NH9CO9NH9 H 2 N9CO9C 6 H 4 9CO9 (o-) C 6 H 4 9CO9O9CH9 CO9C 6 H 4 9CO9N9 9CO9C 6 H 4 9CO9 (o-) 2,4,6-(NO 2 ) 3 C 6 H 2 9 9CO9[CH 2 ] 5 9CO9 C 5 H 10 N9 NC 5 H 10 9 3,4-CH 2 O 2 :C 6 H 3 9CH 2 9 (CH 3 ) 3 C9CO9 9S 4 9 CH 3 9CH"CH9 9CH 2 9CH"CH9 CH#C9CO9 CH 3 9CH 2 9CO9NH9 CH 3 9CH 2 9CO9 CH 3 9CH 2 9CO9NH9 CH 3 9CH 2 9CO9O9 CH 3 9CH 2 9CH 2 9O CH 3 9CH 2 9CH 2 9 9CH(CH 3 )9CH 2 9 CH 3 9CH 2 9CH" CH 3 9CH 2 9C# CH 3 9C#C9 HC#C9CH 2 9 3,4-(HO) 2 C 6 H 3 9CO9 NC 5 H 4 9CO9 (3-) NC 5 H 4 9CO9 (4-) NC 5 H 5 9 (ion) NC 5 H 4 9 NC 5 H 4 9CO9 (2-) NC 5 H 4 9O9 CH 3 9CO9CO9 o-HO9C 6 H 4 9CH 2 9 o-HO9C 6 H 4 9CH" o-HO9C 6 H 4 9CO9 CH 3 9NH9CH 2 9CO9
ORGANIC COMPOUNDS 1.57 TABLE 1.13 Names and Formulas of Organic Radicals (Continued) Name Formula Name Formula Sebacoyl (unsubstituted only) Seleneno Selenino Seleninyl Seleno Selenocyanato Selenoformyl Selenonio Selenono Selenonyl Selenoureido Selenoxo Semicarbazido Semicarbazono Seryl Stearoyl (unsubstituted only) Styryl Suberoyl (unsubstituted only) Succinamoyl Succinimido Succinimidoyl Succinyl Sulfamoyl Sulfanilamido Sulfanilyl Sulfenamoyl Sulfeno Sulfido Sulfinamoyl Sulfino Sulfinyl Sulfo Sulfoamino Sulfonato Sulfonio Sulfonyl Sulfonyldioxy Tartaroyl Tartronoyl Tauryl Telluro Terephthaloyl Terphenylyl 9CO9[CH 2 ] 8 9CO9 HOSe9 HO 2 Se9 OSe" 9Se9 NC9Se9 HSeC9 H 2 Se9 (ion) HO 3 Se9 O 2 Se9 H 2 N9CSe9NH9 (C)"Se H 2 N9CO9NH9NH9 H 2 N9CO9NH9N" HO9CH 2 9CH(NH 2 )9 CO9 CH 3 9[CH 2 ] 16 9CO9 C 6 H 5 9CH"CH9 9CO9[CH 2 ] 6 9CO9 H 2 N9CO9CH 2 9CH 2 9 CO9 O CH 2 9C N9 CH 2 9C O 9C("NH)9CH 2 9 CH 2 C("NH)9 9CO9CH 2 9CH 2 9CO9 H 2 N9SO 2 9 p-H 2 N9C 6 H 4 9SO 2 9 NH9 p-H 2 N9C 6 H 4 9SO 2 9 H 2 N9S9 HO9S9 S9 (ion) H 2 N9SO9 HO 2 S9 9SO9 HO9SO 2 9 HO 2 S9NH9 O 3 S9 (ion) H 2 S9 (ion) 9SO 2 9 9O9SO 2 9O9 9CO9CH(OH)9 CH(OH)9CO9 9CO9CH(OH)9CO9 H 2 N9CH 2 9CH 2 9SO 2 9 Te replacing O 9CO9C 6 H 4 9CO9 (p-) C 6 H 5 9C 6 H 4 9C 6 H 4 9 (Terthiophen)yl Tetradecanoyl Tetradecyl Tetramethylene Thenoyl (2- shown) Thenyl Thienyl Thio Thioacetyl Thiobenzoyl Thiocarbamoyl Thiocarbazono Thiocarbodiazono Thiocarbonohydrazido Thiocarbonyl Thiocarboxy Thiocyanato Thioformyl Thiophenecarbonyl, see Thenoyl Thiosemicarbazido Thiosulfino Thiosulfo Thioreido Thioxo Threonyl Toluenesulfonyl (o-, m-) Toluidino (o-, m-, or p-) Toluoyl (o-, m-, or p-) Tolyl (o-, m-, or p-) Tolylsulfonyl Tosyl (p- only) Triazano Triazeno Trichlorothio Tridecanoyl Tridecyl Trifluorothio 3,4,5-Trihydroxybenzoyl Trimethylammonio Trimethylanilino (all isomers) Trimethylene Trimethylenedioxy Triphenylmethyl Trithio Trithiosulfo SC 4 H 3 9SC 4 H 2 9SC 4 H 2 9 CH 3 9[CH 2 ] 12 9CO9 CH 3 9[CH 2 ] 12 9CH 2 9 9CH 2 9CH 2 9CH 2 9 CH 2 9 CO9 CH" C S CH"CH SC 4 H 3 9CH 2 9 SC 4 H 3 9 9S9 CH 3 9CS9 C 6 H 5 9CS9 H 2 N9CS9 HN"N9CS9NH9 NH9 HN"N9CS9N"N9 H 2 N9NH9CS9NH9 NH9 9CS9, SC" HSOC9, HS9CO9 NCS9 SHC9, HCS9 H 2 N9CS9NH9NH9 HOS 2 9 HO 2 S 2 9 H 2 N9CS9NH9 S" CH 3 9CH(OH)9 CH(NH 2 )9CO9 CH 3 9C 6 H 4 9SO 2 9 CH 3 9C 6 H 4 9NH9 CH 3 9C 6 H 4 9CO9 CH 3 9C 6 H 4 9 CH 3 9C 6 H 4 9SO 2 9 p-CH 3 9C 6 H 4 9SO 2 9 H 2 N9NH9NH9 H 2 N9N"N9 Cl 3 S9 CH 3 9[CH 2 ] 11 9CO9 CH 3 9[CH 2 ] 12 9 F 3 S9 3,4,5-(HO) 3 C 6 H 2 9CO9 (CH 3 ) 3 N 9 (ion) (CH 3 ) 3 C 6 H 2 9NH9 9CH 2 9CH 2 9CH 2 9 9O9CH 2 9CH 2 9 CH 2 9O9 (C 6 H 5 ) 3 C9 9S 3 9 HS9S 3 9
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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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Page 46 and 47: 1.32 SECTION 1 hydroxyamino- to the
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Page 50 and 51: 1.36 SECTION 1 Examples are methyl
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Page 112 and 113: 2.24 SECTION 2 TABLE 2.3 Mathematic
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2.32 SECTION 2 TABLE 2.6 Abbreviati
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2.34 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
Page 918 and 919:
4-Hydroxyproline (1) 1.900 1C 1.850
Page 920 and 921:
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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Page 964 and 965:
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
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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
Page 1078 and 1079:
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
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
Page 1105 and 1106:
11.14 SECTION 11 TABLE 11.9 Molecul
Page 1107 and 1108:
11.4 SEPARATION METHODS TABLE 11.11
Page 1109 and 1110:
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
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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
Page 1129 and 1130:
11.38 SECTION 11 TABLE 11.18 Relati
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11.40 SECTION 11 distribution coeff
Page 1133 and 1134:
11.42 SECTION 11 TABLE 11.19 Gravim
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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
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
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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
Page 1191 and 1192:
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
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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
Page 1213 and 1214:
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
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
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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
Page 1265 and 1266:
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
Page 1289 and 1290:
Index Terms Links 48 Triethylenetet
Page 1291 and 1292:
Index Terms Links 50 Water (Cont.)
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