preface to fifteenth edition

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2.90 SECTION 2 TABLE 2.18 Pressure mm of mercury Molar Equivalent of One Liter of Gas at Various Temperatures and Pressures (Continued) Temperature C 22 24 26 28 30 32 702 0.03816 0.03790 0.03767 0.03740 0.03715 0.03691 704 3827 3801 3777 3750 3726 3701 706 3838 3812 3788 3761 3736 3712 708 3849 3823 3799 3772 3747 3722 710 3860 3834 3810 3783 3758 3733 712 0.03870 0.03844 0.03820 0.03793 0.03768 0.03744 714 3881 3855 3831 3804 3779 3754 716 3892 3866 3842 3815 3789 3765 718 3902 3877 3853 3825 3800 3775 720 3914 3888 3863 3836 3811 3786 722 0.03925 0.03898 0.03874 0.03847 0.03821 0.03796 724 3936 3909 3885 3857 3832 3807 726 3947 3920 3896 3868 3842 3817 728 3957 3931 3906 3878 3853 3828 730 3968 3941 3917 3889 3863 3838 732 0.03979 0.03952 0.03928 0.03900 0.03874 0.03849 734 3990 3963 3938 3910 3885 3859 736 4001 3974 3949 3921 3895 3870 738 4012 3985 3960 3932 3906 3880 740 4023 3995 3971 3942 3916 3891 742 0.04033 0.04006 0.03981 0.03953 0.03927 0.03901 744 4044 4017 3992 3964 3938 3912 746 4055 4028 4003 3974 3948 3922 748 4066 4039 4014 3985 3959 3933 750 4077 4049 4024 3996 3969 3943 752 0.04088 0.04060 0.04035 0.04006 0.03980 0.03954 754 4099 4071 4046 4017 3991 3964 756 4110 4082 4056 4028 4001 3975 758 4121 4093 4067 4038 4012 3985 760 4131 4103 4078 4049 4022 3996 762 0.04142 4114 4089 4060 4033 4006 764 4153 4125 4099 4070 4043 4017 766 4164 4136 4110 4081 4054 4027 768 4175 4147 4121 4092 4065 4038 770 4186 4158 4132 4102 4075 4048 772 0.04197 0.04168 0.04142 0.04113 0.04086 0.04059 774 4207 4179 4153 4124 4096 4070 776 4218 4190 4164 4134 4107 4080 778 4229 4201 4175 4145 4117 4091 780 4240 4211 4185 4155 4128 4101
GENERAL INFORMATION, CONVERSION TABLES, AND MATHEMATICS 2.91 TABLE 2.19 Factors for Reducing Gas Volumes to Normal (Standard) Temperature and Pressure (760 mmHg) Examples: (a) 20 mL of dry gas at 22C and 730 mm 20 0.8888 17.78 mL at 0C and 760 mm. (b) 20 mL of a gas over water at 22 and 730 mm 20 (factor corrected for aqueous tension; i.e., 730 19.8 or 710.2 mm) 20 mL of dry gas at 22 and 710.2 mm 20 0.86475 17.30 mL at 0C and 760 mm. Mass in milligrams of 1 mL of gas at S.T.P.: acetylene, 1.173; carbon dioxide, 1.9769; hydrogen, 0.0899; nitric oxide (NO), 1.3402; nitrogen, 1.25057; oxygen, 1.42904. Pressure mm of mercury Temperature C 10 11 12 13 14 15 16 17 670 0.8504 0.8474 0.8445 0.8415 0.8386 0.8357 0.8328 0.8299 672 0.8530 0.8500 0.8470 0.8440 0.8411 0.8382 0.8353 0.8324 674 0.8555 0.8525 0.8495 0.8465 0.8436 0.8407 0.8377 0.8349 676 0.8580 0.8550 0.8520 0.8490 0.8461 0.8431 0.8402 0.8373 678 0.8606 0.8576 0.8545 0.8516 0.8486 0.8456 0.8427 0.8398 680 0.8631 0.8601 0.8571 0.8541 0.8511 0.8481 0.8452 0.8423 682 0.8657 0.8626 0.8596 0.8566 0.8536 0.8506 0.8477 0.8448 684 0.8682 0.8651 0.8621 0.8591 0.8561 0.8531 0.8502 0.8472 686 0.8707 0.8677 0.8646 0.8616 0.8586 0.8556 0.8527 0.8497 688 0.8733 0.8702 0.8672 0.8641 0.8611 0.8581 0.8551 0.8522 690 0.8758 0.8727 0.8697 0.8666 0.8636 0.8606 0.8576 0.8547 692 0.8784 0.8753 0.8722 0.8691 0.8661 0.8631 0.8601 0.8572 694 0.8809 0.8778 0.8747 0.8717 0.8686 0.8656 0.8626 0.8596 696 0.8834 0.8803 0.8772 0.8742 0.8711 0.8681 0.8651 0.8621 698 0.8860 0.8828 0.8798 0.8767 0.8736 0.8706 0.8676 0.8646 700 0.8885 0.8854 0.8823 0.8792 0.8761 0.8731 0.8700 0.8671 702 0.8910 0.8879 0.8848 0.8817 0.8786 0.8756 0.8725 0.8695 704 0.8936 0.8904 0.8873 0.8842 0.8811 0.8781 0.8750 0.8720 706 0.8961 0.8930 0.8898 0.8867 0.8836 0.8806 0.8775 0.8745 708 0.8987 0.8955 0.8924 0.8892 0.8861 0.8831 0.8800 0.8770 710 0.9012 0.8980 0.8949 0.8917 0.8886 0.8856 0.8825 0.8794 712 0.9037 0.9006 0.8974 0.8943 0.8911 0.8880 0.8850 0.8819 714 0.9063 0.9031 0.8999 0.8968 0.8936 0.8905 0.8875 0.8844 716 0.9088 0.9056 0.9024 0.8993 0.8961 0.8930 0.8899 0.8869 718 0.9114 0.9081 0.9050 0.9018 0.8987 0.8955 0.8924 0.8894 720 0.9139 0.9107 0.9075 0.9043 0.9012 0.8980 0.8949 0.8918 722 0.9164 0.9132 0.9100 0.9068 0.9037 0.9005 0.8974 0.8943 724 0.9190 0.9157 0.9125 0.9093 0.9062 0.9030 0.8999 0.8968 726 0.9215 0.9183 0.9151 0.9118 0.9087 0.9055 0.9024 0.8993 728 0.9241 0.9208 0.9176 0.9144 0.9112 0.9080 0.9049 0.9017 730 0.9266 0.9233 0.9201 0.9169 0.9137 0.9105 0.9073 0.9042 732 0.9291 0.9259 0.9226 0.9194 0.9162 0.9130 0.9098 0.9067 734 0.9317 0.9284 0.9251 0.9219 0.9187 0.9155 0.9123 0.9092 736 0.9342 0.9309 0.9277 0.9244 0.9212 0.9180 0.9148 0.9117 738 0.9368 0.9334 0.9302 0.9269 0.9237 0.9205 0.9173 0.9141 740 0.9393 0.9360 0.9327 0.9294 0.9262 0.9230 0.9198 0.9166 742 0.9418 0.9385 0.9352 0.9319 0.9287 0.9255 0.9223 0.9191 744 0.9444 0.9410 0.9377 0.9345 0.9312 0.9280 0.9248 0.9216 746 0.9469 0.9436 0.9403 0.9370 0.9337 0.9305 0.9272 0.9240 748 0.9494 0.9461 0.9428 0.9395 0.9362 0.9329 0.9297 0.9265
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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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2.38 SECTION 2 TABLE 2.7 Conversion
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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
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11.34 SECTION 11 TABLE 11.16 Guide
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11.36 SECTION 11 TABLE 11.16 Guide
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11.38 SECTION 11 TABLE 11.18 Relati
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11.40 SECTION 11 distribution coeff
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11.42 SECTION 11 TABLE 11.19 Gravim
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11.68 SECTION 11 TABLE 11.20 Elemen
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11.70 SECTION 11 TABLE 11.22 Common
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11.72 SECTION 11 TABLE 11.25 Tolera
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11.74 SECTION 11 TABLE 11.26 Heatin
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11.76 SECTION 11 TABLE 11.28 Titrim
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11.84 SECTION 11 appears becomes le
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11.86 SECTION 11 TABLE 11.29 Equati
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11.88 SECTION 11 TABLE 11.29 Equati
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11.90 SECTION 11 The more stable th
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11.92 SECTION 11 11.6.6.2.5 Buffer
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11.94 SECTION 11 TABLE 11.30 Standa
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TABLE 11.32 Properties and Applicat
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11.98 SECTION 11 TABLE 11.36 Maskin
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11.100 SECTION 11 TABLE 11.37 Anion
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11.102 SECTION 11 TABLE 11.39 Amino
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11.104 SECTION 11 TABLE 11.44 Facto
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11.106 SECTION 11 11.7 LABORATORY S
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11.108 SECTION 11 TABLE 11.48 Stand
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11.110 SECTION 11 Alizarin yellow G
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11.112 SECTION 11 Bromchlorophenol
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11.114 SECTION 11 p-Ethoxychrysoidi
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11.116 SECTION 11 Mercurous nitrate
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11.118 SECTION 11 Potassium carbona
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11.120 SECTION 11 until the ammoniu
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11.122 SECTION 11 TABLE 11.49 TLV C
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11.130 SECTION 11 TABLE 11.50 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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