- Page 1 and 2: THE CHEMICAL ELEMENTS AND THEIR COM
- Page 3 and 4: PREFACE THIS book is an attempt to
- Page 5 and 6: CONTENTS VOLUME I Abbreviations . .
- Page 7 and 8: CONTENTS IX Phosphorus . . . . . .
- Page 9 and 10: ABBREVIATIONS Journals Ann. Liebig'
- Page 11: PHYSICAL CONSTANTS XHl Einstein's E
- Page 14 and 15: xvi INTRODUCTION form a gas half as
- Page 16 and 17: XVlJl INTRODUCTION conditions its a
- Page 18 and 19: xx INTRODUCTION unshared electrons
- Page 20 and 21: xxii INTRODUCTION other modifying i
- Page 22 and 23: Group SvJbgp. 37Rb 38Sr 39 Y 40Zr 4
- Page 24 and 25: xxvi INTRODUCTION Group Subgp, 73Ta
- Page 26 and 27: H He Ne A Kr Xe Li Na K Rb Cs Cu Ag
- Page 28 and 29: xxx INTRODUCTION Atomic Se= 1-07 Te
- Page 30 and 31: C-C C=C C=C N-N N=N N=E=N o—o 0=0
- Page 32 and 33: 2 Group O. Helium . Helium is produ
- Page 36 and 37: 6 Group O. Helium proportional to (
- Page 38 and 39: 8 Oroup O. Inert Oases ceptible eve
- Page 40 and 41: JO Group 0. Inert Gases gaseous pha
- Page 42 and 43: 12 Group /. Hydrogen II. Elementary
- Page 44 and 45: 14 Group I. Hydrogen The physical p
- Page 46 and 47: 16 Group I. Hydrogen H2 and emittin
- Page 48 and 49: 18 Group I. Hydrogen grpup untouche
- Page 50 and 51: 20 Group I. Hydrogen present; in th
- Page 52 and 53: 22 Group /• Hydrogen NaCl (6:1) l
- Page 54 and 55: 24 Group I. Hydrogen work 69 showed
- Page 56 and 57: 26 Group L Hydrogen The experimenta
- Page 58 and 59: 28 Group I. Hydrogen The correspond
- Page 60 and 61: 30 Group I. Hydrogen The N—H-"N i
- Page 62 and 63: 32 Group / CHCl2F > CHClF2; thus wi
- Page 64 and 65: 34 Group I. Deuterium difference wa
- Page 66 and 67: 36 Group I. Deuterium It is probabl
- Page 68 and 69: 38 Group I. Deuterium deuterium or
- Page 70 and 71: 40 Group I. Deuterium at these temp
- Page 72 and 73: 42 Group I. Deuterium importance, b
- Page 74 and 75: 44 Group I. Deuterium Baits 2548 ha
- Page 76 and 77: 46 Group J, Deuterium The mixed com
- Page 78 and 79: 48 Group I. Deuterium CH3-COCH3 is
- Page 80 and 81: 50 Group I. Deuterium sium chromium
- Page 82 and 83: 62 Group L Deuterium ethane at 110
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U Group L Deuterium paraffins, are
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56 Group I. Deuterium Kharasch 351
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58 Group L Tritium have shown that
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60 Group 1(2). Alkali Metals GROUP
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62 Group 1(2). Alkali Metals amalga
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64 Group 1(2). Alkali Metals cent,
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66 Group 1(2). Alkali Metals Compou
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68 Group 1(2). Alkali Metals increa
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70 Group 1(2). Alkali Metals Gilman
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72 Group 1(2). Alkali Metals Caroth
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74 Group 1(2). Alkali Metals Ziegle
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76 Group 1(2). Alkali Metals Di-met
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78 Group 1(2). Alkali Metals In all
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80 Group 1(2). Alkali Metals are de
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82 Group 1(2). Alkali Metals This l
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84 Group I(2). Alkali-Metals of dou
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86 Group 1(2). Alkali Metals of met
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88 Group 1(2). Alkali Metals potass
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90 Group 1(2). Alkali Metals They h
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92 Group 1(2). Alkali Metals SULPHI
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LiF 204 LiCl 2-57 LiBr 2-75 LiI 303
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Complex Compounds 97 covalency are
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Complex Compounds 99 The ammonia in
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Peculiarities of Lithium 101 the de
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GROUP 1(3) COPPER, SILVER, GOLD T H
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The Elements 105 reaction with chlo
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Limitations of Univalent State 107
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Ionization of Compounds 109 silver
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Copper Hydride 111 We can therefore
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Acetylides 113 It regenerates acety
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Alhyls and Aryls by treating silver
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Nitrides, Phosphides, Oxides 117 wi
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Sulphides, Halides 119 what amphote
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Cuprous Halides: Argentous Halides
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Argentous Halides 123 Solid silver
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Derivatives of Oxy-acids 125 There
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Oxalates, Nitrates 127 The crystal
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Univalent Complexes / 129 Silver pe
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Ethylene Complexes 131 (cy = cycloh
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Cyanide Complexes 133 chloride at 9
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Nitrile Complexes 135 The isonitril
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Ammines 137 Other amino-derivatives
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Phosphine and Arsine Complexes 139
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Oxygen Complexes 141 The aurous com
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Sulphur Complexes 143 2 mono-, 2 di
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Chelate Complexes 145 ammonia, we m
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Complex Halides 147 The correspondi
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Cupric Compounds 149 They should al
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Cupric Oxide and Sulphide 151 loss
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Cupric Halides 153 the crystal stru
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Cupric Salts of Oxy-acids 155 This
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Cupric Ammines 157 cupric ion at 25
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Complex Cupric Azides and Nitrites
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Sulphur and Halide Complexes 161 a
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Chelate Complexes 163 it is, howeve
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Chelate Nitrogen-oxygen Complexes 1
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Chelate Nitrogen-oxygen Complexes 1
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Chelate Oxygen Complexes 169 Oxalat
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Neutral Chelate Oxygen Complexes 17
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Hexol Complexes 173 (c) .ff&roZ Com
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Argentic Ions and Fluoride 175 Arge
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Auric Compounds 177 It will be obse
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Auric Oxide and Sulphide 179 owing
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Auric Alkyls 181 auric chloride is
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Auric Alky I Cyanides 183 cryoscopi
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Dialkyhgold Compounds 185 Ewens and
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Aryl Compounds 187 into potassium b
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Phosphorus and Oxygen Complexes 189
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Complex Halides 191 A curious serie
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GROUP II THE difference in properti
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GBOTJP II A BERYLLIUM, MAGNESIUM, C
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BERYLLIUM THE chemistry of berylliu
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Beryllium and Carbon 199 ntronger a
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Beryllium and Oxygen 201 Beryllium
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Beryllium Halides 203 fluoride, or
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Salts of Oxy~acids 205 viscous solu
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Salts of Oxy-acids indefinite basic
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Ammines 209 lluoride only gives a m
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Beryllated Beryllium Tons 211 There
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Chelate Oxygen Complexes 213 dissol
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Chelate Oxygen Complexes 215 become
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Chelate Complexes 217 The existence
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MAGNESIUM, CALCIUM, STRONTIUM, BARI
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Alkaline Earth Salts 221 TABLE II,
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Metal: Carbides 223 Magnesium is of
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Grignard Reagents 225 In this solut
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Grignard Reagents 227 The percentag
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Grignard Reagents 229 The relative
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Grignard Reagents 231 It is evident
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Dialkyls and Diaryls 233 The questi
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Oxygen Compounds 235 It reacts with
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Halides Magnesium Chloride, MgCl2 T
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Oxy-salts 239 dilution. This behavi
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Complex Compounds 241 it decomposes
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Alkaline Earth Metals 243 The Eleme
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Hydrides radium chloride, with a me
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Nitrides: Oxides 247 re-examined by
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Peroxides 249 Peroxides MO2 and MO2
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Halides 251 solution rapidly turns
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Halides: Carbonates 253 Bromides Ca
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Salts of Oxy-acids 255 Oxalates Cal
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Oxy-halide Salts 257 A saturated so
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Complexes 259 explosively at 300°
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Complexes 261 given, and for compar
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ZINC AND CADMIUM THESE elements giv
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Zinc Alhyls and Aryls 265 Zinc Alhy
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Cadmium Alhyls and Aryls 267 which
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Oxides: Hydroxides 269 Cadmium amid
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Halides 271 Cadmium sulphide, CdS,
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Halides 273 Zinc Iodide This salt m
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275 OXY-SALTS OF ZINC AND CADMIUM 0
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Oxy~halogen Salts 277 The conductiv
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Cyanides, Ammines 279 a lead anode
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Oxygen-complexes 281 This is tetrah
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Oxygen-complexes Acetylacetone Deri
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Mercury 285 cadmium; this differenc
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Metallic Mercury 287 and thus mercu
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Mercurous Compounds 289 TABIIB Li 0
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Mercurous Ion 291 (4) The X-ray ana
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Mercurous Halides 293 to a mercurou
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Mercurous Compounds 295 but there i
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Mercuric Salts 297 The mercuric sal
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Mercury-Carbon Compounds 299 format
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Mercury-Carbon Compounds 301 (2) Bu
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Mercury-Carbon Compounds 303 The on
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Mercury-Carbon Compounds 305 the de
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Mercury-Carbon Compounds 307 thiona
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Mercury "Carbon Compounds 309 Physi
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Mercury "Carbon Compounds 311 The w
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Mercury-Carbon Compounds 313 into a
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Mercury-Carbon Compounds 315 Acetyl
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Mercury-Nitrogen Compounds 317 low
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Mercury-Nitrogen Compounds 319 The
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Sulphur Compounds 321 On heating th
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Halides presence of potassium fluor
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Oxy-Salts 325 nitric sulphuric and
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Complexes 327 Oxy-salts of Sulphur
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Complexes 329 p. 322) form covalent
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Complexes 331 Complex Sulphides 8 *
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Complexes These sulphonium salts (R
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Group III 335 The change is most cl
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Boron 337 which is thus reached by
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Boron Hydrides 339 derivatives. A f
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Boron Hydrides 341 determined. The
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Boron Hydrides 343 Diborane melts a
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Boron Hydrides 345 By electron diff
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Boron Hydrides 347 It is insoluble
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Alkyl Derivatives 349 450° leaves
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Nitrogen Derivatives 351 is at 100
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Ammonia Derivatives 353 - + - being
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Ammonia Derivatives 355 can be heat
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Triborine Triamine 357 conclusive,
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Triborine Triamine 359 triborine tr
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Oxygen Derivatives 361 L Addition C
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Oxygen Derivatives 363 This has bee
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Borohydrides 365 followed. Recently
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Borohydrides 367 Na and BH4 ions. T
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THalkyls and Triaryls 369 carbide c
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Trialkyls and Triaryls 371 Oxygen*
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Alkyl and Aryl Compounds 373 wein a
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Alkyl and Aryl Compounds 375 Branch
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Allcyl and Aryl Compounds 377 near
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Alkyl and Aryl Compounds 379 The al
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Ammonia Derivatives 381 by the acti
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Oxygen Derivatives joined to three
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Oxygen Derivatives 385 Borotungstat
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Oxygen Derivatives 387 can be isola
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Oxygen Derivatives 389 alcohols whi
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Sulphur and Halogen Derivatives 391
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Trihalides 393 As Meerwein has poin
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Halides 395 the atomic weight of bo
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Halide Derivatives 397 and the chlo
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Nitrogen Complexes 399 upper (ether
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Ammines 401 Boron tricyclohexyl and
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Phosphorus Complexes 403 Methyl bor
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Oxygen Complexes 405 The trihalides
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Oxygen Complexes 407 Li[B(OCH3)J, 2
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Complex Halides 409 by Boeseken and
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Complex Halides 411 agree in not be
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Aluminium Hydride and Carbide 413 c
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Alkyls 415 Brockway and Davidson 39
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Alhyl Compounds 417 ture, 405 while
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Oxide and Hydroxide 419 A kind of i
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Aluminates 421 them. The alkaline s
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Halides 423 with aldehydes) by usin
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Halides 425 The Al—X distance is
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Salts of Oxy-acids 427 the acetate
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Complexes 429 ALUMINIUM COMPLEXES A
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Complexes 431 its benzene solution
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Oxygen Complexes 433 points (especi
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Halide Complexes 435 The 8-hydroxy-
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Friedel-Crafts Reaction 437 tially
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GROUP IIIA THIS subgroup consists o
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Scandium 441 The metal is dimorphic
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Lanthanides 443 ionic moments known
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Lanthanides 445 Relative Abundance
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Metals 447 order of basicities, fal
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Lanihanide Salts 449 curves, the fi
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Ceric Compounds 451 hydrochloric ac
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Abnormal Valencies 453 Tetravalent
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Divalent Compounds 455 Divalent Ytt
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Actinium 457 reduction, samarium, y
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Metals: Hydrides 459 The divalent c
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Alkyls and Aryls 461 Oallium Trialk
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Thallium Alkyls and Aryls Thallium
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Alhyl Thallium Compounds 465 go ove
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Oxides, Calcides 467 Gallium hydrox
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Trihalides 469 (like aluminium and
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Oxy-acid Salts 471 of crystallizati
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Nitrogen and Oxygen Complexes 473 t
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Oxygen Complexes 475 methoxide, m.p
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Divalent Gallium 477 Divalent Galli
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Divalent Indium 479 Aiken, Haley, a
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Monovalent Indium 481 ride, for the
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Thallous Compounds 483 following ta
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Thallous Compounds 485 highly polym
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Thallous Complexes 487 Several oxy-
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Group IV 489 the normal group valen
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Elementary Carbon 491 There are two
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Graphite 493 The positions of the d
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Graphite oxidized, especially by po
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Hydrocarbons 497 established experi
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Free and Restricted Rotation 499 wh
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Ethane Barrier 501 seemed to be sup
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Paraffins 503 It will be seen that
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Olefines 505 Solid hydrates are for
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Ethylene Derivatives 507 in oxygen
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Aromatic Compotmds 509 hydrogenatio
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'Mills-Nixon' Effect 511 5-ring pre
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' Mills-Nixon' Effect 513 It is obv
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Organic Reactivity 515 Bates of Rea
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Organic Reactivity 517 the next. Su
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Metallic Carbides 519 Metallic and
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Binary Carbides 521 the carbon; and
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Organic Oxygen Compounds 523 stable
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Carboxylic Acids 525 The structure
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Co-ordination Compounds 527 Esters.
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Trivalent Carbon Compounds 529 the
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Free Alkyl Radicals 531 which strik
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Triaryl Methyls 533 explained by su
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Triaryl Methyls 535 of a 0-03-molar
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Triaryl Methyls 537 the compounds A
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Triaryl Methyls 539 compound is hig
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Triaryl Methyls 541 difference of e
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Triaryl Methyls 543 The heat of con
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Divalent Carbon 545 With lead the p
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Metallic Garbonyls 547 with the neg
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Metallic Carbonyls 549 Ammines. Car
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GROUP IVB SILICON, GERMANIUM, TIN,
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Hydrides 553 Lead This is more reac
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Hydrides: Carbides 556 n an atmosph
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Organic Compounds 557 increasing at
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Organic Compounds 559 The tin and l
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Silicon Tetra-aryls 561 is 19-3. 49
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Silicon Allcyl Compounds 563 The di
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Silicols acid—dissolves in cold c
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Organic Si—Si Compounds 567 The a
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Germanium Alkyls and Aryls 569 of 0
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Germanium Alhyl Compounds 571 which
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Germanium Alhyl Compounds 573 The a
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Oe—Oe Aryls 575 properties, 597 o
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Stannic Alkyls and Aryls 577 5. By
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Stannic Alhyl Compounds Triphenyl t
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Stannic Alhyl Compounds solvents. A
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Stannic Allcyl Halides These halide
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Distannanes 585 They all dissolve e
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Lead Tetra-alkyls 587 Polystannanes
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Lead aryls 589 ment of alkyls in th
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Lead Alhyl Halides 591 diaryl with
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Lead Aryl Halides 593 through co-or
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Pb—Pb Compounds and PV" Radicals
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Hexa-nryl Diplumbanes 597 get darke
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Silicon Dioxide 599 Tin nitride, Sn
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Silicates: Germanates 601 from Na2O
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Hydroxides: Bisulphides 603 Plumbic
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Tetrahalides Esters of thiostannic
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Silicon Halides 607 compounds gener
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Halides 609 GERMANIUM HYBBIBE-HALID
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Derivatives of Oxy-acids 611 m.pt.
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Oxygen Complexes 613 SnCl4, 2 py ca
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Complex Halides 615 very stable flu
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Divalent Compounds 617 COMPOUNDS OF
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Stannous Compounds 619 would have a
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Stannous Compounds 621 contain stan
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Plumbous Compounds 623 Stannous flu
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Plumbous Compounds 625 of lead. In
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Plumbous Complexes 627 The crystal
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Tetravalent Compounds 629 reflectio
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Metals 631 With hafnium little is k
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Carbides 633 and so it can be got i
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Oxides, Hydroxides 635 Dioxides, AO
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Tetrahalides 637 further proof of t
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Salts of Oxy-acids 639 cent, low at
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Oxygen Complexes 641 Oxygen Complex
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Ato-complexes 643 /°\ Carbonato-co
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Complex Halides 645 Dry hydrogen fl
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Hafnium 647 covered until in 1923 t
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Lower Valencies 649 TRIVALENT AND D
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Divalent Titanium 651 precipitate t
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Divalent Hafnium 053 non-volatile d
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Group V 655 form trivalent cations.
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Elementary Nitrogen 657 carbon-to-c
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Ammonia 659 electrons, and are to a
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Ammonium Halides 661 and —17-6°
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Binary Nitrides 683 in water; they
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Amines, Amides 665 The alkylamines
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Cyanogen Compounds 667 are similarl
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Hydrogen Cyanide 669 obscure. At th
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Complex Cyanides 671 A—Ns=C. 101
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Cyanic Acid 673 verted into nitrile
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Thiocyanic Acid 675 gives the 'dihy
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Cyanogen Halides 677 Cyanogen Halid
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Cyanurates. Amine Oxides 679 known
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Oxides of Nitrogen 681 like NH3, an
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Nitrous and Nitric Oxides 683 solid
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Metallic Nitrosyls 685 oxides of ni
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Nitrosyls 687 than carbonyls; they
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Nitrogen Peroxide 689 velocity of s
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Nitrogen Pentoxide 691 that this wa
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Oxy-acids of Nitrogen 693 /° struc
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Organic Nitrites 695 these are very
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Nitro-compou nds 697 The nitroparaf
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Nitric Acid 699 spectrum in the nea
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Nitrosyl Halides 701 and both of th
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Fluorine Nitrate 703 have shown tha
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Nitrogen Halides 705 occurs at the
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Nitrogen Halides 707 Nitrogen Bromi
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Hydrazine 709 nitrogen in the prese
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A zo-compounds 711 Di-imide HN=NH,
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Azo-compounds 713 melt at 71-4° (t
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Nitramide 715 The first are strong
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Azides 717 From the electron diffra
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Diaryl Nitrogens B. 3-covalent: val
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Aminium Salts 721 A, 2. Ar2N—N—
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Diaryl Nitrogen Oxides 723 suppose
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PHOSPHORUS THE most fundamental dif
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Elementary Phosphorus 121 atmospher
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Phosphine 729 PH8 is basic, but muc
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Phosphines 731 alcohols, 461 or bet
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Phosphorus-Nitrogen Compounds 733 h
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Phosphorus-Nitrogen Compounds 735 t
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Phosphorus Oxides 737 phorus in air
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Oxy-acids of Phosphorus 739 acid HP
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Hypophosphoric Acid 743 of phosphor
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Phosphates 745 much better (2 to 3
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Organo-acids 747 Organo-acids of Ph
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Phosphorus Sulphides 749 The equili
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Oxyhalides 751 Oxyhalides of Phosph
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Halides 753 The trifluoride PF3 is
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Complex Compounds this acid that do
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Complex Halides 757 The P in [PF6],
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Elementary Antimony ?59 Arsenic vap
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Hydrides 761 highly poisonous. At a
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Arsines oxidized by air, especially
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Oxy-compounds 765 A. 2. Trivalent O
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Oxy-compound$ 765 A. 2. Trivalent O
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Halogen Derivatives 767 The phenyl
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Halides 769 Dimethyl arsenic chlori
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A rseno-Compounds 771 it has a norm
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Stibines 773 still attached to the
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Oxy-stibines 775 Oxy-derivatives of
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Halogen Derivatives 777 halogen. (C
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Bismuth, Organic Compounds 779 on a
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Halide Derivatives 781 Bismuth aryl
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Comparison of Carbon Compounds 783
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Arsenic, Oxy-compounds 785 In the s
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Pentoxides 787 Bismuth Trioxide Bis
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Sulphur Compounds 789 The potassium
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Sulphur Compounds 791 Thioantimonit
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Antimony HaKdes 793 at low temperat
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Sb+++ and Bi+++ Salts 795 shows tha
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797 COMPLEX COMPOUNDS THESE are ver
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Pentavalent Complexes 799 A series
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Chelate Complexes 801 The complex b
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Antimony Tetrachloride Derivatives
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Vanadium 805 has no acidic properti
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Vanadium Compounds 807 Vanadium is
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Vanadium Pentoxide 809 Of the highe
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Vcmadic Acid 811 In its properties
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Vanadic Esters one form to another
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Halides, Oxyhalides extra oxygen, e
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Pentavalent Complexes 817 fades to
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Tetrahalides 819 pentoxide with the
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Tetravalent Vanadyl Salts 821 The p
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Ghelate Complexes 823 a violet trih
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Trivalent Compounds 825 Vanadium Se
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Trivalent Oxyhalides A hexahydrate
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Trivalent Complexes 829 number is n
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Trivalent Chelate Complexes 831 pre
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Vanadium Dihalides 833 in the brown
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Niobium 835 The main characteristic
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Peroxyniobates 837 tantalum pentoxi
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Pentavalent Complexes 839 Niobium P
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Pentavalent Complexes complexes is
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Tantalum 843 MONOVALENT NIOBIFM Thi
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Tantalum Compounds 845 Tantalum and
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Pentahalides 847 It is less reactiv
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Penta- and Tetravalent Tantalum 849
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Protoactinium 851 If the aqueous so
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Protoactinium 853 as the fourth doe