preface to fifteenth edition

More documents

Recommendations

Info

THERMODYNAMIC PROPERTIES 6.61 TABLE 6.2 Heats of Fusion, Vaporization, and Sublimation and Specific Heat at Various Temperatures of Organic Compounds (Continued) C p Substance Hm Hv Hs 400 K 600 K 800 K 1000 K Ht 5.4 147.3 Ht 0.3 132.3 2,3-Dimethylbutane 0.80 27.4 29.1 181.2 247.7 314.6 331.0 Ht 6.5 137.1 2,2-Dimethyl-1-butanol 42.6 56.1 2,3-Dimethyl-1-butanol 47.3 3,3-Dimethyl-1-butanol 46.4 2,3-Dimethyl-2-butanol 40.4 51.0 ()-3,3-Dimethyl-2-butanol 43.9 3,3-Dimethyl-2-butanone 33.4 37.9 2,3-Dimethyl-1-butene 27.4 29.2 178.2 231.8 272.0 302.1 3.3-Dimethyl-1-butene 1.1 25.7 27.1 162.8 223.4 266.1 297.1 Ht 4.3 148.3 2,3-Dimethyl-2-butene 5.46 29.6 32.5 156.8 216.7 262.7 297.7 Ht 3.5 76.3 Di(3-methylbutyl) ether 35.2 Dimethylcadmium 38.0 1,1-Dimethylcyclohexane 2.06 32.5 37.9 212.1 310.0 379.5 427.6 Ht 6.0 120.0 cis-1,2-Dimethylcyclohexane 1.64 33.5 39.7 213.8 309.6 377.0 424.3 Ht 8.3 100.6 trans-1,2-Dimethylcyclohexane 10.49 33.0 38.4 217.2 312.1 378.7 425.5 cis-1,3-Dimethylcyclohexane 10.82 32.9 38.3 214.2 310.5 378.7 426.8 trans-1,3-Dimethylcyclohexane 9.86 33.4 39.2 213.8 308.8 375.7 423.0 cis-1,4-Dimethylcyclohexane 9.31 33.3 39.0 213.8 308.8 375.7 423.0 trans-1,4-Dimethylcyclohexane 12.33 32.6 37.9 215.9 312.1 378.9 425.7 1,1-Dimethylcyclopentane 1.1 30.3 33.8 182.2 262.6 318.7 359.1 Ht 6.5 126.4 cis-1,2-Dimethylcyclopentane 1.7 31.7 35.7 182.7 262.4 317.9 358.0 Ht 6.7 131.7 trans-1,2-Dimethylcyclopentane 7.2 30.9 34.6 182.9 262.2 317.3 357.4 cis-1,3-Dimethylcyclopentane 7.4 30.4 34.2 182.9 262.2 317.3 357.4 trans-1,3-Dimethylcyclopentane 7.3 30.8 34.5 182.9 262.2 317.3 357.4 cis-2,4-Dimethyl-1,3-dioxane 39.9 4,5-Dimethyl-1,3-dioxane 42.5 5,5-Dimethyl-1,3-dioxane 41.3 Dimethyl disulfide 9.19 33.8 37.9 110.3 137.4 157.6 172.8 Dimethyl ether 4.94 21.5 18.5 79.6 105.3 125.7 141.4 N,N-Dimethylformamide 16.15 38.4 46.9 Dimethylglyoxime 97.1 2,2-Dimethylheptane 8.90 2,6-Dimethyl-4-heptanone 39.9 50.9 2,2-Dimethylhexane 6.78 32.1 37.3 2,3-Dimethylhexane 33.2 38.8 2,4-Dimethylhexane 32.5 37.8 2,5-Dimethylhexane 12.95 32.5 37.9 3,3-Dimethylhexane 6.98 32.3 37.5 3,4-Dimethylhexane 33.2 39.0 cis-2,2-Dimethyl-3-hexene 37.2
6.62 SECTION 6 TABLE 6.2 Heats of Fusion, Vaporization, and Sublimation and Specific Heat at Various Temperatures of Organic Compounds (Continued) C p Substance Hm Hv Hs 400 K 600 K 800 K 1000 K trans-2,2-Dimethyl-3-hexene 37.3 1,1-Dimethylhydrazine 10.1 32.6 35.0 1,2-Dimethylhydrazine 35.2 39.3 3,5-Dimethylisoxazole 45.2 Dimethyl maleate 14.7 44.3 Dimethylmercury 34.6 6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptane 40.2 46.4 2,4-Dimethyloctane 36.5 47.1 Dimethyl oxalate 21.07 47.4 3,3-Dimethyloxetane 30.9 33.9 2,2-Dimethylpentane 5.86 29.2 32.4 211.0 285.9 340.7 381.6 2,3-Dimethylpentane 30.5 34.3 211.0 285.9 340.7 381.6 2,4-Dimethylpentane 6.69 29.6 32.9 211.0 285.9 340.7 381.6 3,3-Dimethylpentane 7.07 29.6 33.0 211.0 285.9 340.7 381.6 2,2-Dimethyl-3-pentanone 36.1 42.3 2,4-Dimethyl-3-pentanone 11.18 34.6 41.5 2,4-Dimethyl-1-pentene 33.2 4,4-Dimethyl-1-pentene 29.0 2,4-Dimethyl-2-pentene 34.4 cis-4,4-Dimethyl-2-pentene 32.7 trans-4,4-Dimethyl-2-pentene 32.7 2,7-Dimethylphenanthrene 106.7 4,5-Dimethylphenanthrene 104.6 9,10-Dimethylphenanthrene 119.5 2,3-Dimethylphenol 21.02 84.0 2,4-Dimethylphenol 47.1 65.0 2,5-Dimethylphenol 23.38 46.9 85.0 2,6-Dimethylphenol 18.90 44.5 75.3 3,4-Dimethylphenol 18.13 49.7 85.0 3,5-Dimethylphenol 18.00 49.3 82.0 Dimethyl 1,2-phthalate 162.7 2,2-Dimethylpropane 3.10 22.7 21.8 157.1 218.5 254.3 283.7 Ht 2.6 133.1 2,2-Dimethylpropanenitrile 32.4 37.3 2,2-Dimethyl-1-propanol 9.6 2,3-Dimethylpyridine 39.1 47.7 2,4-Dimethylpyridine 38.5 47.5 2,5-Dimethylpyridine 47.8 2,6-Dimethylpyridine 10.04 37.5 45.4 3,4-Dimethylpyridine 40.0 50.5 3,5-Dimethylpyridine 39.5 49.5 Dimethyl sulfate 48.5 Dimethyl sulfide 7.99 27.0 27.7 88.4 113.0 132.2 147.2 Dimethyl sulfite 40.2 Dimethyl sulfone 77.0 Dimethyl sulfoxide 14.37 43.1 52.9 2,2-Dimethylthiacyclopropane 35.8 Dimethylzinc 29.5 Dinitromethane 46.0
Page 2 and 3:
LANGE'S HANDBOOK OF CHEMISTRY John
Page 4 and 5:
Grateful acknowledgment is hereby m
Page 6 and 7:
PREFACE TO FIFTEENTH EDITION This n
Page 8 and 9:
PREFACE TO FIFTEENTH EDITION ix inv
Page 10 and 11:
xii PREFACE TO FOURTEENTH EDITION l
Page 12 and 13:
PREFACE TO FIRST EDITION This book
Page 14 and 15:
For the detailed contents of any se
Page 16 and 17:
1.2 SECTION 1 is derived from the G
Page 18 and 19:
1.4 SECTION 1 rather than methylide
Page 20 and 21:
1.6 SECTION 1 Styrene Toluene Xylen
Page 22 and 23:
1.8 SECTION 1 TABLE 1.2 Fused Polyc
Page 24 and 25:
1.10 SECTION 1 1.1.1.6 Bridged Hydr
Page 26 and 27:
1.12 SECTION 1 TABLE 1.4 Suffixes f
Page 28 and 29:
1.14 SECTION 1 TABLE 1.5 Trivial Na
Page 30 and 31:
1.16 SECTION 1 TABLE 1.6 Trivial Na
Page 32 and 33:
1.18 SECTION 1 Selection of the pri
Page 34 and 35:
1.20 SECTION 1 attached to one anot
Page 36 and 37:
1.22 SECTION 1 When side chains of
Page 38 and 39:
1.24 SECTION 1 heterocyclic structu
Page 40 and 41:
1.26 SECTION 1 Bivalent radicals of
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
Page 48 and 49:
1.34 SECTION 1 may be named (1) by
Page 50 and 51:
1.36 SECTION 1 Examples are methyl
Page 52 and 53:
1.38 SECTION 1 tuted acid, respecti
Page 54 and 55:
1.40 SECTION 1 FIGURE 1.2 Newman pr
Page 56 and 57:
1.42 SECTION 1 from the ring are kn
Page 58 and 59:
1.44 SECTION 1 FIGURE 1.11 Two isom
Page 60 and 61:
1.46 SECTION 1 Chiral Center. The c
Page 62 and 63:
1.48 SECTION 1 FIGURE 1.15 Isomers
Page 64 and 65:
1.50 SECTION 1 entries to bring tog
Page 66 and 67:
1.52 SECTION 1 TABLE 1.13 Names and
Page 68 and 69:
Page 70 and 71:
Page 72 and 73:
Page 74 and 75:
1.60 SECTION 1 TABLE 1.14 Empirical
Page 76 and 77:
Page 78 and 79:
Page 80 and 81:
Page 82 and 83:
Page 84 and 85:
Page 86 and 87:
Page 88 and 89:
Page 90 and 91:
2.2 SECTION 2 2.3.6 Student’s Dis
Page 92 and 93:
2.4 SECTION 2 TABLE 2.1 Fundamental
Page 94 and 95:
2.6 SECTION 2 TABLE 2.1 Fundamental
Page 96 and 97:
2.8 SECTION 2 TABLE 2.2 Physical an
Page 98 and 99:
2.10 SECTION 2 TABLE 2.2 Physical a
Page 100 and 101:
Page 102 and 103:
Page 104 and 105:
Page 106 and 107:
Page 108 and 109:
Page 110 and 111:
Page 112 and 113:
2.24 SECTION 2 TABLE 2.3 Mathematic
Page 114 and 115:
2.26 SECTION 2 TABLE 2.6 Abbreviati
Page 116 and 117:
Page 118 and 119:
Page 120 and 121:
Page 122 and 123:
Page 124 and 125:
2.36 SECTION 2 TABLE 2.7 Conversion
Page 126 and 127:
Page 128 and 129:
Page 130 and 131:
Page 132 and 133:
Page 134 and 135:
Page 136 and 137:
Page 138 and 139:
Page 140 and 141:
Page 142 and 143:
2.54 SECTION 2 TABLE 2.8 Temperatur
Page 144 and 145:
Page 146 and 147:
Page 148 and 149:
Page 150 and 151:
Page 152 and 153:
Page 154 and 155:
2.66 SECTION 2 2.1.1 Conversion of
Page 156 and 157:
2.68 SECTION 2 Oleometer. A hydrome
Page 158 and 159:
2.70 SECTION 2 Example 3. 25 1.2500
Page 160 and 161:
2.72 SECTION 2 TABLE 2.9 Barometer
Page 162 and 163:
2.74 SECTION 2 TABLE 2.9 Barometer
Page 164 and 165:
2.76 SECTION 2 TABLE 2.10 Barometri
Page 166 and 167:
2.78 SECTION 2 TABLE 2.12 Reduction
Page 168 and 169:
2.80 SECTION 2 TABLE 2.12 Reduction
Page 170 and 171:
2.82 SECTION 2 TABLE 2.13 Viscosity
Page 172 and 173:
2.84 SECTION 2 TABLE 2.14 Conversio
Page 174 and 175:
2.86 SECTION 2 TABLE 2.15 Hydromete
Page 176 and 177:
2.88 SECTION 2 TABLE 2.17 Correctio
Page 178 and 179:
2.90 SECTION 2 TABLE 2.18 Pressure
Page 180 and 181:
Page 182 and 183:
Page 184 and 185:
2.96 SECTION 2 TABLE 2.20 Values of
Page 186 and 187:
2.98 SECTION 2 TABLE 2.21 Transmitt
Page 188 and 189:
2.100 SECTION 2 TABLE 2.21 Transmit
Page 190 and 191:
2.102 SECTION 2 2.2 MATHEMATICAL TA
Page 192 and 193:
2.104 SECTION 2 TABLE 2.23 Derivati
Page 194 and 195:
2.106 SECTION 2 TABLE 2.24 Integral
Page 196 and 197:
2.108 SECTION 2 TABLE 2.24 Integral
Page 198 and 199:
2.110 SECTION 2 Regular Polygon of
Page 200 and 201:
2.112 SECTION 2 A h[0.4(y y ) 1.
Page 202 and 203:
2.114 SECTION 2 2.2.3.1 Signs of th
Page 204 and 205:
2.116 SECTION 2 x2 x3 x4 x5 ln(1 x
Page 206 and 207:
2.118 SECTION 2 2.3.2 Errors in Qua
Page 208 and 209:
2.120 SECTION 2 The breadth or spre
Page 210 and 211:
2.122 SECTION 2 TABLE 2.26b Areas U
Page 212 and 213:
2.124 SECTION 2 The distribution of
Page 214 and 215:
2.126 SECTION 2 Should there be mor
Page 216 and 217:
2.128 SECTION 2 Example 10 Six samp
Page 218 and 219:
2.130 SECTION 2 2.3.9 The F Statist
Page 220 and 221:
TABLE 2.29 F Distribution (Continue
Page 222 and 223:
2.134 SECTION 2 mathematical treatm
Page 224 and 225:
2.136 SECTION 2 The confidence limi
Page 226 and 227:
2.138 SECTION 2 situation where rel
Page 228 and 229:
3.2 SECTION 3 The alphabetical orde
Page 230 and 231:
3.4 SECTION 3 When it is required t
Page 232 and 233:
3.6 SECTION 3 PO phosphoryl SeO sel
Page 234 and 235:
3.8 SECTION 3 3.1.5 Acids 3.1.5.1 A
Page 236 and 237:
3.10 SECTION 3 3.1.6.6 Multiplicati
Page 238 and 239:
3.12 SECTION 3 3.2 PHYSICAL PROPERT
Page 240 and 241:
TABLE 3.2 Physical Constants of Ino
Page 242 and 243:
Page 244 and 245:
Page 246 and 247:
Page 248 and 249:
Page 250 and 251:
Page 252 and 253:
Page 254 and 255:
Page 256 and 257:
Page 258 and 259:
Page 260 and 261:
Page 262 and 263:
Page 264 and 265:
Page 266 and 267:
Page 268 and 269:
Page 270 and 271:
Page 272 and 273:
Page 274 and 275:
Page 276 and 277:
Page 278 and 279:
Page 280 and 281:
Page 282 and 283:
Page 284 and 285:
Page 286 and 287:
Page 288 and 289:
3.62 SECTION 3 TABLE 3.3 Synonyms a
Page 290 and 291:
SECTION 4 PROPERTIES OF ATOMS, RADI
Page 292 and 293:
4.3 Fermium Fm 100 [Rn] 5f 12 7s 2
Page 294 and 295:
Silver (argentum) Ag 47 [Kr] 4d 10
Page 296 and 297:
PROPERTIES OF ATOMS,RADICALS,AND BO
Page 298 and 299:
Page 300 and 301:
Page 302 and 303:
Page 304 and 305:
Page 306 and 307:
Page 308 and 309:
Page 310 and 311:
PROPERTIES OF ATOMS, RADICALS, AND
Page 312 and 313:
Page 314 and 315:
Page 316 and 317:
Page 318 and 319:
Page 320 and 321:
Page 322 and 323:
Page 324 and 325:
Page 326 and 327:
Page 328 and 329:
Page 330 and 331:
Page 332 and 333:
Page 334 and 335:
Page 336 and 337:
Page 338 and 339:
Page 340 and 341:
Page 342 and 343:
Page 344 and 345:
Page 346 and 347:
Page 348 and 349:
Page 350 and 351:
Page 352 and 353:
Page 354 and 355:
Page 356 and 357:
Page 358 and 359:
Page 360 and 361:
Page 362 and 363:
Page 364 and 365:
Page 366 and 367:
Page 368 and 369:
Page 370 and 371:
Page 372 and 373:
Page 374 and 375:
SECTION 5 PHYSICAL PROPERTIES 5.1 S
Page 376 and 377:
PHYSICAL PROPERTIES 5.3 5.1 SOLUBIL
Page 378 and 379:
TABLE 5.1 Solubility of Gases in Wa
Page 380 and 381:
TABLE 5.1 Solubility of Gases in Wa
Page 382 and 383:
TABLE 5.2 Solubilities of Inorganic
Page 384 and 385:
formateBa(CHO 2 ) 2 26.2 28.0 29.9
Page 386 and 387:
(III) sulfateCe 2 (SO 4 ) 3 ·9H 2
Page 388 and 389:
iodidePbI 2 0.044 0.056 0.069 0.090
Page 390 and 391:
Nickel sulfateNiSO 4 ·6H 2 O (pale
Page 392 and 393:
Praseodymium bromatePr(BrO 3 ) 3 55
Page 394 and 395:
formate NaCHO 2 43.9 62.5 81.2 102
Page 396 and 397:
Uranyl nitrate UO 2 (NO 3 ) 2 98 10
Page 398 and 399:
PHYSICAL PROPERTIES 5.25 TABLE 5.3
Page 400 and 401:
Page 402 and 403:
Page 404 and 405:
Page 406 and 407:
Page 408 and 409:
Page 410 and 411:
Page 412 and 413:
Page 414 and 415:
Page 416 and 417:
Page 418 and 419:
Page 420 and 421:
Page 422 and 423:
Page 424 and 425:
Page 426 and 427:
Page 428 and 429:
Page 430 and 431:
PHYSICAL PROPERTIES 5.57 5.3 BOILIN
Page 432 and 433:
Page 434 and 435:
Page 436 and 437:
Page 438 and 439:
Page 440 and 441:
Page 442 and 443:
Page 444 and 445:
Page 446 and 447:
Page 448 and 449:
Page 450 and 451:
Page 452 and 453:
TABLE 5.12 Ternary Azeotropic Mixtu
Page 454 and 455:
TABLE 5.12 Ternary Azeotropic Mixtu
Page 456 and 457:
PHYSICAL PROPERTIES 5.83 5.4 FREEZI
Page 458 and 459:
Page 460 and 461:
PHYSICAL PROPERTIES 5.87 5.5 DENSIT
Page 462 and 463:
PHYSICAL PROPERTIES 5.89 dt Dt P
Page 464 and 465:
Page 466 and 467:
Page 468 and 469:
Page 470 and 471:
Page 472 and 473:
Page 474 and 475:
Page 476 and 477:
Page 478 and 479:
Page 480 and 481:
Page 482 and 483:
Page 484 and 485:
Page 486 and 487:
Page 488 and 489:
Page 490 and 491:
Page 492 and 493:
Page 494 and 495:
Page 496 and 497:
Page 498 and 499:
Page 500 and 501:
Page 502 and 503:
Page 504 and 505:
Page 506 and 507:
Page 508 and 509:
PHYSICAL PROPERTIES 5.135 5.6.1 Ref
Page 510 and 511:
PHYSICAL PROPERTIES 5.137 where the
Page 512 and 513:
PHYSICAL PROPERTIES 5.139 5.7 COMBU
Page 514 and 515:
Page 516 and 517:
Page 518 and 519:
Page 520 and 521:
Page 522 and 523:
Temperature, C Substance 40 20 0 20
Page 524 and 525:
Page 526 and 527:
Page 528 and 529:
Page 530 and 531:
Page 532 and 533:
Page 534 and 535:
Page 536 and 537:
Page 538 and 539:
Page 540 and 541:
Page 542 and 543:
Page 544 and 545:
PHYSICAL PROPERTIES 5.171 This equa
Page 546 and 547:
SECTION 6 THERMODYNAMIC PROPERTIES
Page 548 and 549:
THERMODYNAMICPROPERTIES 6.3 6.1.1.2
Page 550 and 551:
THERMODYNAMICPROPERTIES 6.5 A gener
Page 552 and 553:
THERMODYNAMICPROPERTIES 6.7 TABLE 6
Page 554 and 555:
THERMODYNAMICPROPERTIES 6.9 TABLE 6
Page 556 and 557: THERMODYNAMICPROPERTIES 6.11 TABLE
Page 566 and 567: THERMODYNAMIC PROPERTIES 6.21 TABLE
Page 646 and 647: THERMODYNAMIC PROPERTIES 6.101 TABL
Page 656 and 657:
THERMODYNAMIC PROPERTIES 6.111 TABL
Page 658 and 659:
Page 660 and 661:
Page 662 and 663:
Page 664 and 665:
Page 666 and 667:
Page 668 and 669:
Page 670 and 671:
Page 672 and 673:
Page 674 and 675:
Page 676 and 677:
Page 678 and 679:
Page 680 and 681:
Page 682 and 683:
Page 684 and 685:
Page 686 and 687:
Page 688 and 689:
THERMODYNAMIC PROPERTIES 6.143 The
Page 690 and 691:
Page 692 and 693:
Page 694 and 695:
Page 696 and 697:
Page 698 and 699:
Page 700 and 701:
Page 702 and 703:
Page 704 and 705:
SECTION 7 SPECTROSCOPY 7.1 X-RAY ME
Page 706 and 707:
SPECTROSCOPY 7.3 TABLE 7.1 Waveleng
Page 708 and 709:
Page 710 and 711:
Page 712 and 713:
SPECTROSCOPY 7.9 TABLE 7.3 Critical
Page 714 and 715:
SPECTROSCOPY 7.11 TABLE 7.4 X-Ray E
Page 716 and 717:
SPECTROSCOPY 7.13 Emission line K 1
Page 718 and 719:
SPECTROSCOPY 7.15 TABLE 7.7 Analyzi
Page 720 and 721:
SPECTROSCOPY 7.17 TABLE 7.8 Mass Ab
Page 722 and 723:
SPECTROSCOPY 7.19 TABLE 7.9 Electro
Page 724 and 725:
SPECTROSCOPY 7.21 TABLE 7.11 Absorp
Page 726 and 727:
SPECTROSCOPY 7.23 TABLE 7.13 Solven
Page 728 and 729:
SPECTROSCOPY 7.25 7.3 FLUORESCENCE
Page 730 and 731:
SPECTROSCOPY 7.27 TABLE 7.16 Fluore
Page 732 and 733:
SPECTROSCOPY 7.29 TABLE 7.18 Detect
Page 734 and 735:
Page 736 and 737:
Page 738 and 739:
SPECTROSCOPY 7.35 TABLE 7.19 Sensit
Page 740 and 741:
SPECTROSCOPY 7.37 TABLE 7.19 Sensit
Page 742 and 743:
SPECTROSCOPY 7.39 In terms of m ,
Page 744 and 745:
SPECTROSCOPY 7.41 The ionization co
Page 746 and 747:
Page 748 and 749:
Page 750 and 751:
Page 752 and 753:
Page 754 and 755:
Page 756 and 757:
Page 758 and 759:
Page 760 and 761:
Page 762 and 763:
Page 764 and 765:
Page 766 and 767:
Page 768 and 769:
Page 770 and 771:
SPECTROSCOPY 7.67 TABLE 7.28 Infrar
Page 772 and 773:
7.69
Page 774 and 775:
SPECTROSCOPY 7.71 7.6 RAMAN SPECTRO
Page 776 and 777:
SPECTROSCOPY 7.73 TABLE 7.30 Raman
Page 778 and 779:
Page 780 and 781:
Page 782 and 783:
Page 784 and 785:
Page 786 and 787:
Page 788 and 789:
Page 790 and 791:
Page 792 and 793:
SPECTROSCOPY 7.89 7.7 NUCLEAR MAGNE
Page 794 and 795:
SPECTROSCOPY 7.91 TABLE 7.41 Nuclea
Page 796 and 797:
SPECTROSCOPY 7.93 TABLE 7.42 Proton
Page 798 and 799:
SPECTROSCOPY 7.95 TABLE 7.44 Estima
Page 800 and 801:
SPECTROSCOPY 7.97 TABLE 7.46 Proton
Page 802 and 803:
SPECTROSCOPY 7.99 TABLE 7.48 Solven
Page 804 and 805:
SPECTROSCOPY 7.101 TABLE 7.49 Carbo
Page 806 and 807:
SPECTROSCOPY 7.103 TABLE 7.51 Effec
Page 808 and 809:
Page 810 and 811:
SPECTROSCOPY 7.107 TABLE 7.56 One-B
Page 812 and 813:
Page 814 and 815:
Page 816 and 817:
SPECTROSCOPY 7.113 TABLE 7.63 Nitro
Page 818 and 819:
SPECTROSCOPY 7.115 TABLE 7.64 Nitro
Page 820 and 821:
SPECTROSCOPY 7.117 TABLE 7.69 Fluor
Page 822 and 823:
SPECTROSCOPY 7.119 TABLE 7.72 Silic
Page 824 and 825:
SPECTROSCOPY 7.121 TABLE 7.73 Phosp
Page 826 and 827:
SPECTROSCOPY 7.123 TABLE 7.74 Phosp
Page 828 and 829:
SPECTROSCOPY 7.125 when z 3 and y
Page 830 and 831:
SPECTROSCOPY 7.127 Masses 19 and 31
Page 832 and 833:
SPECTROSCOPY 7.129 TABLE 7.76 Conde
Page 834 and 835:
Page 836 and 837:
Page 838 and 839:
Page 840 and 841:
Page 842 and 843:
SECTION 8 ELECTROLYTES, ELECTROMOTI
Page 844 and 845:
ELECTROLYTES, EMF, AND CHEMICAL EQU
Page 846 and 847:
Page 848 and 849:
Page 850 and 851:
Page 852 and 853:
Page 854 and 855:
Page 856 and 857:
Page 858 and 859:
Page 860 and 861:
TABLE 8.7 Proton Transfer Reactions
Page 862 and 863:
TABLE 8.7 Proton Transfer Reactions
Page 864 and 865:
Page 866 and 867:
Page 868 and 869:
Page 870 and 871:
Page 872 and 873:
Page 874 and 875:
Page 876 and 877:
Page 878 and 879:
Page 880 and 881:
Page 882 and 883:
Page 884 and 885:
Page 886 and 887:
Page 888 and 889:
Page 890 and 891:
Page 892 and 893:
Page 894 and 895:
Page 896 and 897:
Page 898 and 899:
Page 900 and 901:
Page 902 and 903:
Page 904 and 905:
Page 906 and 907:
Page 908 and 909:
Page 910 and 911:
Page 912 and 913:
Page 914 and 915:
TABLE 8.9 Selected Equilibrium Cons
Page 916 and 917:
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
Page 922 and 923:
Page 924 and 925:
Page 926 and 927:
Page 928 and 929:
Page 930 and 931:
Page 932 and 933:
Page 934 and 935:
Page 936 and 937:
Page 938 and 939:
Page 940 and 941:
Page 942 and 943:
Page 944 and 945:
Page 946 and 947:
TABLE 8.14 National Bureau of Stand
Page 948 and 949:
Page 950 and 951:
Page 952 and 953:
Page 954 and 955:
Page 956 and 957:
Page 958 and 959:
Page 960 and 961:
1 part 0.1% neutral red in alc. * V
Page 962 and 963:
Page 964 and 965:
3,3-Dimethoxybenzidine dihydrochlor
Page 966 and 967:
Page 968 and 969:
Page 970 and 971:
Page 972 and 973:
Page 974 and 975:
Page 976 and 977:
Page 978 and 979:
Page 980 and 981:
Page 982 and 983:
Page 984 and 985:
Page 986 and 987:
Page 988 and 989:
Page 990 and 991:
Page 992 and 993:
Page 994 and 995:
Page 996 and 997:
Page 998 and 999:
Page 1000 and 1001:
Page 1002 and 1003:
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 1135 and 1136:
Page 1137 and 1138:
Page 1139 and 1140:
Page 1141 and 1142:
Page 1143 and 1144:
Page 1145 and 1146:
Page 1147 and 1148:
Page 1149 and 1150:
Page 1151 and 1152:
Page 1153 and 1154:
Page 1155 and 1156:
Page 1157 and 1158:
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 1169 and 1170:
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
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:
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.)
show all

preface to fifteenth edition

Create successful ePaper yourself

Delete template?

Save as template?