preface to fifteenth edition

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PRACTICAL LABORATORY INFORMATION 11.85 TABLE 11.29 Ba Equations for the Redox Determinations of the Elements with Equivalent Weights (Continued) BaCrO 4 6 KI (excess) 16 HCl 2 BaCl 2 3I 2 6 KCl 2 CrCl 3 8H 2 O I 2 2Na 2 S 2 O 3 2NaI Na 2 S 4 O 6 Ba/3 45.78 BaCrO 4 3Fe 2 (excess) 8H Ba 2 Cr 3 3Fe 3 4H 2 O Titrate excess Fe 2 with permanganate or dichromate; Ba/3 45.78 Br 2 Br 2 2 KI (excess) 2 KBr I 2 I 2 2Na 2 S 2 O 3 : 2NaI Na 2 S 4 O 6 Br 2 /2 79.904 Br Br 3 HClO BrO 3Cl 3H 3 Br/6 13.317 BrO 3 CO BrO 6I (excess) 6H Br 3 3I 2 3H 2 O I 2 2Na 2 S 2 O 3 2NaI Na 2 S 4 O 6 KBrO 3 /6 27.835 5 CO I 2 O 5 5CO 2 I 2 (at 125C; adsorbed and measured colorimetrically) 5/2 CO 70.02 CO 2 2 4 Titrate as for CaC 2 O 4 CO 2 2 6 Acidify and titrate as for HO;CO 2 2 2 6 2 2H H 2 O 2 CO 2 K 2 C 2 O 6 /2 99.11 Ca 5 CaC 2 O 4 2 KMnO 4 8H 2 SO 4 5 CaSO 4 10CO 2 K 2 SO 4 2 MnSO 4 8H 2 O Ca/2 20.039; CaO/2 28.04 Cd Cd(anthranilate) 2 4Br 2 2NH 2 C 6 H 2 Br 2 COOH 4Br Titrate with KBrO 3 9KBr until color of indigo changes to yellow. Add KI and back-titrate iodine liberated with thiosulfate. Cd/8 14.05 Ce Oxidize Ce(III) to Ce(IV) with (NH 4 ) 2 S 2 O 8 plus Ag ; destroy excess by boiling. 2 Ce(SO 4 ) 2 2 FeSO 4 Ce 2 (SO 4 ) 3 Fe 2 (SO 4 ) 3 Ce/1 140.12; Ce 2 O 3 /2 164.12 Cl 2 Same as for Br 2 ;Cl 2 /2 35.453 ClO ClO 2I 2H Cl I 2 H 2 O Titrate liberated I 2 with thiosulfate; HClO/2 26.230 ClO 2 ClO 4I 4H Cl 2 2I 2 2H 2 O Titrate liberated I 2 with thiosulfate; HClO/2 26.230 ClO 3 ClO 6I 6H 2 O Cl 3 3I 2 3H 2 O Titrated liberated I 2 with thiosulfate; HClO 2 /4 17.115 ClO 3H 3 AsO 3 (excess; boil with strong HCl) Cl 3 3H 3 AsO 4 Titrate excess H 3 AsO 3 with bromate; HClO 3 /6 14.077 2 3 3 4 Co Co(NH 3) 6 Fe(CN) 6 [Citrate-NH 3 buffer] Co(NH 3) 6 Fe(CN) 6 Co/1 58.9332 Precipitate Co anthranilate and treat as for cadmium; Co/8 7.3667 Cr Cr O 2 6Fe 2 14H 2Cr 3 6Fe 3 2 7 7H 2 O Cr/3 17.332; Cr 2 O 3 /6 25.337 Cu 2 Cu 2 2I 2SCN 2CuSCN I 2 Titrate the liberated iodine with thiosulfate; Cu/1 63.546 4 CuSCN 7IO 3 14H 7Cl 4Cu 2 2 4SO 4 7ICl 4 HCN 5H 2 O Precipitate and wash CuSCN. Titrate with standard KIO 3 solution with 5 mL CHCl 3 until a definite I 2 color appears in the organic layer. Back-titrate the excess I 2 with standard thiosulfate solution. Cu/7 9.078; KIO 3 /4 53.505 Fe(II) 5 Fe 2 MnO 8H 5Fe 3 Mn 2 4 4H 2 O Fe 2 Ce(IV) Fe 3 Ce(III); use 1,10-phenanthroline iron(II) indicator. 6Fe 2 Cr O 2 14H 6Fe 3 2Cr 3 2 7 7H 2 O; use diphenylamine sulfonate indicator. Fe/1 55.847; Fe 2 O 3 /2 79.845
11.86 SECTION 11 TABLE 11.29 Equations for the Redox Determinations of the Elements with Equivalent Weights (Continued) Fe(III) Fe 3 4SCN Fe(SCN) 4 ; Fe(SCN) 4 Ti(III) Fe 2 Ti(IV) 4SCN Fe/1 55.847; Fe 2 O 3 /2 79.845 2Fe 3 Zn 2Fe 2 Zn 2 ; then proceed by a method under Fe(II). Fe 3 Ag Cl Fe 2 AgCl; then proceed by a method under Fe(II). 2Fe 3 SnCl 2 (slight excess) 4Cl 2Fe 2 2 SnCl 6 2 HgCl 2 SnCl 2 2Cl 2 Hg 2 Cl 2 SnCl 6 Pour above mixture into an H 3 PO 4 plus MnSO 4 solution and titrate with KMnO 4 as under Fe(II). Fe/1 55.847; Fe 2 O 3 /2 79.845 2Fe 3 2I Fe 2 I 2 Titrate liberated iodine with thiosulfate; Fe/1 55.847; Fe 2 O 3 /2 79.845 I 2 I 2 2 2I 2 2SO 2 3 SO 4 6 [titrate solution (pH 7.0) with thiosulfate until color is pale yellow. Add KI and starch and continue titration to disappearance of blue color. I 2 /2 126.9045 I 2 H 3 AsO 3 H 2 O 2I H 3 AsO 4 2H ; use starch and KI as indicator. I 2 /2 126.9045 I 2I Br 2 (excess) I 2 2Br Remove excess Br 2 formic acid and titrate I 2 with thiosulfate. I 2 /2 126.9045 IO 3 5I (excess) 6H 3I 2 3H 2 O; titrate I 2 with thiosulfate. KIO 3 /6 35.67 IO 4 IO 3 IO 4thiosulfate. 7I (excess) 8H 4I 2 4H 2 O; use a neutral buffered solution. Titrate I 2 with KIO4 /2 115.00 K K 2 Na[Co(NO 2 ) 6 ]; dissolve in H 2 SO 4 and titrate with either KMnO 4 or Ce(IV). ca. K/5.5 but use an empirical factor. Mg Mg(oxine) 2 ; dissolve precipitate and use procedure for Al(8-hydroxyquinoline) 3 . Mg/8 3.0381 Mn(II) 2 Mn 2 5 14H BiO3 2 MnO4 5Bi 3 7H 2 O 3 2 5 6H 2Mn 2 3 MnO AsO 5 AsO 3H 2 O; Mn/5 10.9876 Mn(IV) 4 3 4 2Mn 2 5 SO 2 2 8 8H 2 O(Ag catalyst) 2 MnO4 10 SO4 2 16H Titrate the permanganate formed with iron(II) as under iron(II); Mn/5 10.9876 2Mn 2 5 IO4 3H 2 O 2 MnO4 5 IO3 6H Slowly precipitate excess KIO 4 with Hg(NO 3 ) 2 . Filter, add excess Fe 2 and titrate excess with standard KMnO 4 solution; Mn/5 10.9876 4Mn 2 2 3 MnO4 15 HPO 2 2 7 [pH range 4 to 7] 5 Mn(HPO) 2 2 7 3 4H 2 O Use Pt9SCE indicator system; Mn/1 54.9380 MnO 2 2Fe 2 (excesss standard) 4H Mn 2 2Fe 3 2H 2 O (use CO 2 atmosphere) MnO 2 H 2 C 2 O 4 (excess standard) 2H Mn 2 2CO 2 2H 2 O (use CO 2 atmosphere) In either of the above, titrate excess with KMnO 4 . Mn/2 27.469; MnO 2 /2 43.47 2 Mn(VI) MnO 2H 2 C 2 O 4 4H Mn 2 4 4CO 2 4H 2 O Add excess oxalate and back-titrate with permanganate. Mn/4 13.7345 Mn(VII) 2 MnO 5H 2 C 2 O 4 6H 2Mn 2 4 10CO 2 3H 2 O; Mn/5 10.9876 Mo Mo(VI) Zn Mo(III) Zn 2 ; catch eluate in excess Fe 2 (SO 4 ) 3 solution Mo(III) 3Fe 3 2 4H 2 O MoO 3Fe 2 8H 4 ; titrate Fe(II) with KMnO 4 Mo/3 31.98 Mo(VI) Ag Cl Mo(V) AgCl; pass through Ag reductor at 60–80C. Mo(V) Ce(IV) Mo(VI) Ce(III); Mo/l 95.94 N 2 H 4 3N 2 H 4 2 BrO (excess) 3N 2 2Br 3 6H 2 O; add excess KI and titrate I 2 with thiosulfate. N 2 H 4 /4 8.01 NH 2 OH NH 2 OH BrO3 NO3 Br H H 2 O; proceed as above for N 2 H 4 .NH 2 OH/6 5.505
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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
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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
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11.32 SECTION 11 11.4.3 Ion-Exchang
Page 1125 and 1126: 11.34 SECTION 11 TABLE 11.16 Guide
Page 1127 and 1128: 11.36 SECTION 11 TABLE 11.16 Guide
Page 1129 and 1130: 11.38 SECTION 11 TABLE 11.18 Relati
Page 1131 and 1132: 11.40 SECTION 11 distribution coeff
Page 1133 and 1134: 11.42 SECTION 11 TABLE 11.19 Gravim
Page 1159 and 1160: 11.68 SECTION 11 TABLE 11.20 Elemen
Page 1161 and 1162: 11.70 SECTION 11 TABLE 11.22 Common
Page 1163 and 1164: 11.72 SECTION 11 TABLE 11.25 Tolera
Page 1165 and 1166: 11.74 SECTION 11 TABLE 11.26 Heatin
Page 1167 and 1168: 11.76 SECTION 11 TABLE 11.28 Titrim
Page 1175: 11.84 SECTION 11 appears becomes le
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 1221 and 1222: 11.130 SECTION 11 TABLE 11.50 Chemi
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11.136 SECTION 11 TABLE 11.51 Chemi
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11.138 SECTION 11 of water which is
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TABLE 11.55 Thermoelectric Values i
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TABLE 11.56 Type B Thermocouples: P
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TABLE 11.58 Type J Thermocouples: I
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TABLE 11.60 Type N Thermocouples: N
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TABLE 11.62 Type S Thermocouples: P
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11.150 SECTION 11 11.11 CORRECTION
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Index Terms Links 2 Acid-base indic
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Index Terms Links 4 Alkynes, nomenc
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Index Terms Links 6 Aurintricarboxy
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Index Terms Links 8 Boron-11 chemic
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Index Terms Links 10 Cellulose acet
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Index Terms Links 12 Collective ino
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Index Terms Links 14 Degree Fahrenh
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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
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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
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Index Terms Links 48 Triethylenetet
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Index Terms Links 50 Water (Cont.)
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