preface to fifteenth edition

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1.58 SECTION 1 TABLE 1.13 Names and Formulas of Organic Radicals (Continued) Name Formula Name Formula Trityl Tropoyl Tyrosyl Undecanoyl Undecyl Ureido Ureylene Valeryl Valyl (C 6 H 5 ) 3 C9 C 6 H 5 9CH(CH 2 OH)9 CO9 p-HO9C 6 H 4 9CH 2 9 CH(NH 2 )9CO9 CH 3 9[CH 2 ] 9 9CO9 CH 3 9[CH 2 ] 9 9CH 2 9 H 2 N9CO9NH9 9NH9CO9NH9 CH 3 9[CH 2 ] 3 9CO9 (CH 3 ) 2 CH9CH(NH 2 )9 CO9 Vanilloyl Vanillyl Veratroyl Veratryl Vinyl Vinylene Xylidino (all isomers) Xylyl (all isomers) 3,4-CH 3 O(HO)C 6 H 3 9 CO9 3,4-CH 3 O(HO)C 6 H 3 9 CH 2 9 3,4-(CH 3 O) 2 C 6 H 3 9 CO9 3,4-(CH 3 O) 2 C 6 H 2 9 CH 2 9 CH 2 "CH9 9CH"CH9 (CH 3 ) 2 C 6 H 3 9NH9 (CH 3 ) 2 C 6 H 3 9 1.2 PHYSICAL PROPERTIES OF PURE SUBSTANCES TABLE 1.14 Empirical Formula Index of Organic Compounds The alphanumeric designations are keyed <strong>to</strong> Table 1.15. Br 2 OS: t149 ClHO 3 S: c248 ClH 4 NO: h139 Cl 2 OS: t150 Cl 2 H 2 Si: d270a Cl 3 HSi: t249 Cl 3 PS: t158 H 3 NO 3 S: s23 H 4 N 2 : h85 H 6 Si 2 : d791 C 1 CBr 4 : c13 CBrClF 2 : b301 CBrCl 3 : b432 CBrF 3 : b434 CBrN: c325 CBr 2 F 2 : d93 CBr 4 : c13 CClF 3 : c264 CClNO 3 S: c249 CCl 2 F 2 : d218 CCl 3 D: c146 CCl 3 F: t237 CCl 4 : c14 CCl 4 S: t240 CD 2 Cl 2 : d236 CD 4 O: m36 CD 7 O: m40 CFCl 3 : f30 CF 4 : c15 CHBrCl 2 : b316 CHBr 2 Cl: d88 CHBr 2 F: d104a CHBr 3 : t204 CHClF 2 : c101 CHCl 2 F: d233 CHCl 3 : c145 CHF 3 : t307 CHF 3 O 3 S: t308 CHI 3 : i33 CH 2 BrCl: b305 CH 2 Br 2 : d110 CH 2 Cl 2 : d235 CH 2 F 2 : d409 CH 2 I 2 : d452 CH 2 N 2 : c318, d63 CH 2 N 4 : t131 CH 2 O: f32 (CH 2 O) x :p1 CH 2 O 2 : f36 CH 2 O 3 : g29 CH 2 S 3 : t451 CH 3 Br: b354 CH 3 Br 3 Ge: m260 CH 3 Cl: c157 CH 3 ClO 2 S: m36 CH 3 Cl 3 Si: m450, t242 CH 3 DO: m39 CH 3 F: f18 CH 3 I: i37 CH 3 NO: f33 CH 3 NO 2 : m325, n56 CH 3 NO 3 : m324 CH 3 N 5 : a294 CH 4 :m33 CH 4 Cl 2 Si: d240 CH 4 N 2 O: f38, u16 CH 4 N 2 S: t161 CH 4 N 4 O 2 : n54 CH 4 O: m38 13 CH 4 O: m41 CH 4 O 2 : m279 CH 4 O 3 S: m34 CH 4 S: m37 CH 5 AsO 3 : m137 CH 5 N: m127 CH 5 NO 3 S: a201 CH 5 N 3 : g30 CH 5 N 3 S: t160 CH 6 ClN 3 O: s3 CH 6 N 2 : m274 CH 6 N 4 : a180 CH 6 N 4 O: c9 CI 4 : c16 CN 4 O 8 : t123 CS 2 : c10 CO: c11 COS: c12 C 2 C 2 Br 2 ClF 3 : d90 C 2 Br 2 Cl 4 : d129 C 2 Br 2 F 4 : d130 C 2 Br 2 O 2 : o54 C 2 ClF 3 : c263 C 2 Cl 2 F 4 : d270b, d271 C 2 Cl 2 O 2 : o55 C 2 Cl 3 F 3 : t256, t257 C 2 Cl 3 N: t222
ORGANIC COMPOUNDS 1.59 TABLE 1.14 Empirical Formula Index of Organic Compounds (Continued) The alphanumeric designations are keyed <strong>to</strong> Table 1.15. C 2 Cl 4 : t38 C 2 Cl 4 F 2 : d411, d412, t36 C 2 Cl 4 O: t224 C 2 Cl 6 : h27 C 2 D 3 N: a30 C 2 D 4 O 2 : a21 C 2 D 6 OS: d698 C 2 F 4 : t65 C 2 F 6 :h42 C 2 F 6 O 5 S 2 : t309 C 2 HBrClF 3 : b308 C 2 HBr 2 F 3 : d133 C 2 HBr 2 N: d77 C 2 HBr 3 : t203 C 2 HBr 3 O: t199 C 2 HBr 3 O 2 : t200 C 2 HClF 2 : c100a C 2 HClF 2 O 2 : c98 C 2 HCl 3 : t235 C 2 HCl 3 O: d186, t218 C 2 HCl 3 O 2 : t219 C 2 HCl 5 :p7 C 2 HF 3 O 2 : t300 C 2 H 2 :a41 C 2 H 2 BrClO: b255 C 2 H 2 Br 2 : d99, d100 C 2 H 2 Br 2 F 2 : d92 C 2 H 2 Br 2 O: b254 C 2 H 2 Br 2 O 2 : d76 C 2 H 2 Br 4 : t16 C 2 H 2 ClF 3 : c262 C 2 H 2 ClN: c30 C 2 H 2 Cl 2 : d227, d228, d229 C 2 H 2 Cl 2 O: c34 C 2 H 2 Cl 2 O 2 : d182 C 2 H 2 Cl 3 NO: t217 C 2 H 2 Cl 4 : t36a, t37 C 2 H 2 F 2 : d408 C 2 H 2 F 3 NO: t299 C 2 H 2 F 4 : t64 C 2 H 2 N 2 S 3 : d488 C 2 H 2 O: k1 C 2 H 2 O 2 : g28 C 2 H 2 O 3 : g29 C 2 H 2 O 4 : o52, o53 C 2 H 3 Br: b336 C 2 H 3 BrO: a35 C 2 H 3 BrO 2 : b249 C 2 H 3 Br 2 Cl 3 Si: d101 C 2 H 3 Br 3 O: t202 C 2 H 3 Cl: c129 C 2 H 3 ClF 2 : c100 C 2 H 3 ClO: a37, c23a C 2 H 3 ClO 2 : c27, m194 C 2 H 3 Cl 3 : t231, t232 C 2 H 3 Cl 3 O: t233 C 2 H 3 Cl 3 Si: t258 C 2 H 3 DO 2 : a20 C 2 H 3 FO: a43 C 2 H 3 FO 2 :f5 C 2 H 3 F 3 O: t305 C 2 H 3 F 3 O 3 S: m453 C 2 H 3 IO: a48 C 2 H 3 IO 2 : i21 C 2 H 3 N: a29 C 2 H 3 NO: m288 C 2 H 3 NS: m294, m440 C 2 H 3 N 3 : t197 C 2 H 3 N 3 S 2 : a284 C 2 H 4 : e131 C 2 H 4 BrCl: b303 C 2 H 4 BrNO: b247 C 2 H 4 Br 2 : d96, d97 C 2 H 4 ClNO: c24 C 2 H 4 ClO: b165a C 2 H 4 Cl 2 : d225, d226 C 2 H 4 Cl 2 O: d237 C 2 H 4 Cl 6 Si 2 : b227 C 2 H 4 F 2 : d407 C 2 H 4 INO: i20 C 2 H 4 I 2 : d451 C 2 H 4 N 2 : a109 C 2 H 4 N 2 O 2 : o58 C 2 H 4 N 2 S 2 : d795 C 2 H 4 N 4 : a289, d281 C 2 H 4 N 4 O 2 : a314 C 2 H 4 O: e147 C 2 H 4 OS: t147 C 2 H 4 O 2 : a19, h87, m257 C 2 H 4 O 2 S: m16 C 2 H 4 O 3 : h88, p60 C 2 H 4 O 5 S: s26 C 2 H 4 S: e148 C 2 H 5 AlCl 2 : e61 C 2 H 5 Br: b329 C 2 H 5 BrNaO 2 S: b330 C 2 H 5 BrO: b331, b369 C 2 H 5 Cl: c121 C 2 H 5 ClHg: e198 C 2 H 5 ClO: c122, c156, c173 C 2 H 5 ClS: c174 C 2 H 5 Cl 2 OPS: e124 C 2 H 5 Cl 2 O 2 P: e123 C 2 H 5 Cl 3 Si: c171, e269, t236 C 2 H 5 DO: e28 C 2 H 5 F: f17 C 2 H 5 I: i31 C 2 H 5 IO: i32 C 2 H 5 N: e146 C 2 H 5 NO: a5, a6, m255, m291 C 2 H 5 NO 2 : e225, g26, m187, n52 C 2 H 5 NO 3 : e224 C 2 H 5 NS: t138 C 2 H 5 N 3 O 2 : b238, o57 C 2 H 6 : e20 C 2 H 6 AlCl: d533 C 2 H 6 BrN: b333 C 2 H 6 Cd: d578 C 2 H 6 ClN: c126 C 2 H 6 ClNO 2 S: d692 C 2 H 6 ClO 2 PS: d582 C 2 H 6 Cl 2 Si: d222 C 2 H 6 Hg: d631 C 2 H 6 N 2 :a8 C 2 H 6 N 2 O: m460, n78 C 2 H 6 N 2 O 2 : m275 C 2 H 6 N 2 S: m444 C 2 H 6 N 4 O: o56 C 2 H 6 O: d603, e27 C 2 H 6 OS: d697, m20 C 2 H 6 O 2 : e21a, e135 C 2 H 6 O 2 S: d696 C 2 H 6 O 3 S: d695, e25, m301 C 2 H 6 O 4 S: d693 C 2 H 6 O 5 S 2 :m35 C 2 H 6 S: d694, e26a C 2 H 6 S 2 : d600, e24 C 2 H 6 Te: d700 C 2 H 6 Zn: d709 C 2 H 7 AsO 2 : d560 C 2 H 7 ClSi: c111 C 2 H 7 N: d534, e63 C 2 H 7 NO: a162, a163, e29 C 2 H 7 NO 3 S: a160 C 2 H 7 NO 4 S: a169 C 2 H 7 NS: a161 C 2 H 7 N 5 : b137 C 2 H 7 O 3 P: d625 C 2 H 8 N 2 : d623, d624, e21, e133 C 2 H 8 N 2 O: h125 C 2 H 9 BD: b243 C 2 H 10 BN: b242 C 3 C 3 Br 2 F 5 : d105 C 3 Cl 3 N 3 : t255 C 3 Cl 3 N 3 O 3 : t239 C 3 Cl 6 : h30 C 3 Cl 6 O: a27, h2 C 3 F 6 :h44 C 3 HCl 5 O: p5 C 3 H 2 ClN: c35 C 3 H 2 Cl 2 O 2 :m6
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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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Page 42 and 43: 1.28 SECTION 1 Complex linear polya
Page 44 and 45: 1.30 SECTION 1 TABLE 1.11 Names of
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
Page 52 and 53: 1.38 SECTION 1 tuted acid, respecti
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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
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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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Page 950 and 951:
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Page 960 and 961:
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
Page 1006 and 1007:
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
Page 1010 and 1011:
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
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
Page 1101 and 1102:
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
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
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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 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
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:
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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
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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
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Index Terms Links 18 Equivalent wei
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Index Terms Links 20 Fluorocarbon p
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Index Terms Links 22 Halogenated hy
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Index Terms Links 24 Impact strengt
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Index Terms Links 26 Kα 1 lines, m
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Index Terms Links 28 Melmine phenol
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Index Terms Links 30 Neon-neon bond
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Index Terms Links 32 One-tailed tes
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Index Terms Links 34 Physical chemi
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
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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