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PRACTICAL LABORATORY INFORMATION 11.73 TABLE 11.26 HeatingTemperatures, Composition of WeighingForms, and Gravimetric Factors (Continued) Element Thermal stability range, C Final heating temperature, C Composition of weighing form Gravimetric factors Co 285–946 750–850 Co 3 O 4 Co: 0.7342 130 Co(C 10 H 6 NO 2 ) 3 ·2H 2 O Co: 0.09639; CoO: 0.1226 450–500 CoSO 4 Co: 0.3802 Cr 120 PbCrO 4 Cr: 0.1609 Cu 105–120 CuSCN Cu: 0.5225; CuO: 0.6540 115 100–105 Cu(C 7 H 5 NO 2 ) 2 Cu: 0.1891 105–115 Cu(C 13 H 11 NO 2 ) Cu: 0.2201 110–115 Cu(C 10 H 6 NO 2 )·H 2 O Cu: 0.1494 105 Cu(C 12 H 10 NOS) 2 ·H 2 O Cu: 0.1237 F 66–538 130–140 PbClF F: 0.07261 Fe 470–946 900 Fe 2 O 3 Fe: 0.6994 Ga 408–946 900 Ga 2 O 3 Ga: 0.7439 Hg105 Hg(C 12 H 10 NOS) 2 Hg: 0.3169 I 60–900 130–150 AgI I: 0.5405 In 345–1200 1200 In 2 O 3 In: 0.8271 Ir IrO 2 Ir: 0.8573 K 73–653 653 KClO 4 K: 0.2822; K 2 O: 0.3399 270 K 2 PtCl 6 K: 0.1609; K 2 O: 0.1938 KIO 4 K: 0.1700 120 KB(C 6 H 5 ) 4 K: 0.1091 Li 200 Li 2 SO 4 Li: 0.1263; Li 2 O: 0.2718 Mg1050–1100 2 P 2 O 7 Mg: 0.2184; MgO: 0.3622 88–300 155–160 Mg(C 9 H 6 NO) 2 Mg: 0.07775; MgO: 0.1289 Mn 946 1000 Mn 3 O 4 Mn: 0.7203 1000 Mn 2 P 2 O 7 Mn: 0.3871; MnO: 0.4998 Mo 505 PbMoO 4 Mo: 0.2613; MoO 3 : 0.3291 500–525 MoO 3 Mo: 0.6666 N (as NO ) 3 20–242 105 Nitron nitrate N: 0.3732; NO 3 : 0.1652 Na 360–674 125 NaMg(UO 2 ) 3 (C 2 H 3 O 2 ) 9 · 6.5 H 2 O Na: 0.01527; Na 2 O: 0.02058 Nb 650–950 900 Nb 2 O 3 Nb: 0.6990 Ni 79–172 110–120 Ni(C 4 H 7 N 2 O 2 ) 2 Ni: 0.2032; NiO: 0.2586 Os 800 (in H 2 ) Os metal P 477 Mg 2 P 2 O 7 P: 0.2783; PO 4 : 0.8536 160–415 110 (NH 4 ) 3 [P(Mo 3 O 10 ) 4 ] P: 0.0165; P 2 O 5 : 0.0378 Pb 271–959 500–600 PbSO 4 Pb: 0.6832; PbO: 0.7359 600 PbMoO 4 Pb: 0.5643; PbO: 0.6078 120 PbCrO 4 Pb: 0.6411 271–959 600–800 PbSO 4 Pb: 0.6832; PbO: 0.7359 105 Pb(C 12 H 10 NOS) 2 Pb: 0.3240 Pd 45–171 110 Pd(C 4 H 7 N 2 O 2 ) 2 Pd: 0.3162 Rb 70–674 674 Rb 2 PtCl 6 Rb: 0.2954; Rb 2 O: 0.3230 Re 130 (C 6 H 5 ) 4 AsReO 4 Re: 0.2939 110 Nitron perrhenate Re: 0.3306 S 780 BaSO 4 S: 0.1374; SO 3 : 0.3430; SO 4 : 0.4116 Sb 100 Sb(C 12 H 10 NOS) 3 Sb: 0.1581 SCN 130 AgSCN SCN: 0.3500 110–120 CuSCN SCN: 0.4775 Se 120–130 Se metal SeO 2 : 1.4052 Si 358–946 358 SiO 2 Si: 0.4675
11.74 SECTION 11 TABLE 11.26 HeatingTemperatures, Composition of WeighingForms, and Gravimetric Factors (Continued) Element Thermal stability range, C Final heating temperature, C Composition of weighing form Gravimetric factors Sn 834 900 SnO 2 Sn: 0.7877 Sr 130–140 Sr(NO 3 ) 2 Sr: 0.4140 100–300 100–300 SrSO 4 Sr: 0.4770; SrO: 0.5641 Te 105 Te metal Th 610–946 700–800 ThO 2 Th: 0.8788 900 ThP 2 O 7 Th: 0.5863 Ti 350–946 900 TiO 2 Ti: 0.5992 Tl(III) 100 Tl(C 12 H 10 NOS) Tl: 0.4860 U 1000 U 3 O 8 U: 0.8480; UO 2 : 0.9620 V 581–946 700–800 V 2 O 5 V: 0.5602 W 674 800–900 WO 3 W: 0.7930 Zn 1000 950–1000 ZnO Zn: 0.8034 1000 Zn 2 P 2 O 7 Zn: 0.4292; ZnO: 0.5342 125 Zn(C 10 H 6 NO 2 ) 2 ·H 2 O Zn: 0.1529 Zr 850 ZrP 2 O 7 Zr: 0.3440; ZrO 2 : 0.4647 1200 ZrO 2 Zr: 0.7403 Source: J. A. Dean, ed., Analytical Chemistry Handbook, McGraw-Hill, New York, 1995. 11.6 VOLUMETRIC ANALYSIS 11.6.1 Acid-Base Titrations in Aqueous Media TABLE 11.27 Standard Primary Standards for Aqueous Acid-Base Titrations Formula weight Preparation Basic substances for standardizingacidic solutions (HOCH 3 ) 3 CNHH 2 121.137 Tris(hydroxymethyl)aminomethane is available commercially as a primary standard. Dry at 100–103C (110C). In titrations with a strongacid the equivalence point is at about pH 4.5–5. Equivalent weight is the formula weight. [J. H. Fossum, P. C. Markunas, and J. A. Riddick, Anal. Chem., 23:491 (1951).] HgO 216.59 Dissolve 100 g pure HgCl 2 in1LH 2 O, and add with stirringto 650 mL 1.5 M NaOH. Filter and wash with H 2 O until washings are neutral to phenolphthalein. Dry to constant weight at or below 40C, and store in a dark bottle. To 0.4 gHgO ( 40 mL 0.1N acid) add 10–15 gKBr plus 20–25 mL H 2 O. Stir, excluding CO 2 , until solution is complete. Titrate with acid to pH 5–8. Equivalent weight is one-half formula weight. Na 2 B 4 O 7 · 10H 2 O 381.372 Recrystallize reagent-grade salt twice from water at temperatures below 55C. Wash the crystals with H 2 O, twice with ethanol, and twice with diethyl ether. Let stand in a hygrostat oversaturated NaBr · 2H 2 O or saturated NaCl-sucrose solution. Use methyl red indicator. Equivalent weight is one-half the formula weight.
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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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Page 1004 and 1005:
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
Page 1014 and 1015:
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
Page 1020 and 1021:
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
Page 1028 and 1029:
10.10 SECTION 10 Key properties of
Page 1030 and 1031:
10.12 SECTION 10 10.3.8 Fluorocarbo
Page 1032 and 1033:
10.14 SECTION 10 10.3.11 Phenolics
Page 1034 and 1035:
10.16 SECTION 10 The resin has the
Page 1036 and 1037:
10.18 SECTION 10 10.3.19 Polyuretha
Page 1038 and 1039:
10.20 SECTION 10 10.3.22 Sulfones B
Page 1040 and 1041:
TABLE 10.2 Properties of Commercial
Page 1042 and 1043:
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:
Page 1060 and 1061:
Page 1062 and 1063:
Page 1064 and 1065:
Page 1066 and 1067:
Page 1068 and 1069:
Page 1070 and 1071:
Page 1072 and 1073:
Page 1074 and 1075:
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 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
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: 11.72 SECTION 11 TABLE 11.25 Tolera
Page 1167 and 1168: 11.76 SECTION 11 TABLE 11.28 Titrim
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
Page 1215 and 1216:
11.124 SECTION 11 TABLE 11.49 TLV C
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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