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»ù´¡»¯Ñ§³£ÓÃÓ¢Óï´Ê»ã »ù´¡»¯Ñ§¡¢»¯¹¤³£ÓÃÓ¢Óï´Ê»ã 1. The Ideal-Gas Equation ÀíÏëÆøÌå״̬·½³Ì 2. Partial Pressures ·Öѹ 3. Real Gases: Deviation from Ideal Behavior ÕæÊµÆøÌ壺¶ÔÀíÏëÆøÌåÐÐΪµÄÆ«Àë 4. The van der Waals Equation ·¶µÂ»ª·½³Ì 5. System and Surroundings ϵͳÓë»·¾³ 6. State and State Functions ״̬Óë״̬º¯Êý 7. Process ¹ý³Ì 8. Phase Ïà 9. The First Law of Thermodynamics ÈÈÁ¦Ñ§µÚÒ»¶¨ÂÉ 10. Heat and Work ÈÈÓ빦 11. Endothermic and Exothermic Processes ÎüÈÈÓë·¢Èȹý³Ì 12. Enthalpies of Reactions ·´Ó¦ÈÈ 13. Hess¡¯s Law ¸Ç˹¶¨ÂÉ 14. Enthalpies of Formation Éú³ÉìÊ 15. Reaction Rates ·´Ó¦ËÙÂÊ 16. Reaction Order ·´Ó¦¼¶Êý 17. Rate Constants ËÙÂʳ£Êý 18. Activation Energy »î»¯ÄÜ 19. The Arrhenius Equation °¢ÀÛÄáÎÚ˹·½³Ì 20. Reaction Mechanisms ·´Ó¦»úÀí 21. Homogeneous Catalysis ¾ùÏà´ß»¯¼Á 22. Heterogeneous Catalysis ·Ç¾ùÏà´ß»¯¼Á 23. Enzymes ø 24. The Equilibrium Constant ƽºâ³£Êý 25. the Direction of Reaction ·´Ó¦·½Ïò 26. Le Chatelier¡¯s Principle ÁÐ?É³ÌØÁÐÔÀí 27. Effects of Volume, Pressure, Temperature Changes and Catalysts i. Ìå»ý£¬Ñ¹Á¦£¬Î¶ȱ仯ÒÔ¼°´ß»¯¼ÁµÄÓ°Ïì 28. Spontaneous Processes ×Ô·¢¹ý³Ì 29. Entropy (Standard Entropy) ìØ£¨±ê×¼ìØ£© 30. The Second Law of Thermodynamics ÈÈÁ¦Ñ§µÚ¶þ¶¨ÂÉ 31. Entropy Changes ìØ±ä 32. Standard Free-Energy Changes ±ê×¼×ÔÓÉÄܱä 33. Acid-Bases Ëá¼î 34. The Dissociation of Water Ë®Àë½â 35. The Proton in Water Ë®ºÏÖÊ×Ó 36. The pH Scales pHÖµ 37. Bronsted-Lowry Acids and Bases Bronsted-Lowry ËáºÍ¼î 38. Proton-Transfer Reactions ÖÊ×Ó×ªÒÆ·´Ó¦ 39. Conjugate Acid-Base Pairs ¹²éîËá¼î¶Ô 40. Relative Strength of Acids and Bases Ëá¼îµÄÏà¶ÔÇ¿¶È 41. Lewis Acids and Bases ·Ò×˹Ëá¼î 42. Hydrolysis of Metal Ions ½ðÊôÀë×ÓµÄË®½â 43. Buffer Solutions »º³åÈÜÒº 44. The Common-Ion Effects ͬÀë×ÓЧӦ 45. Buffer Capacity »º³åÈÝÁ¿ 46. Formation of Complex Ions ÅäÀë×ÓµÄÐÎ³É 47. Solubility Èܽâ¶È 48. The Solubility-Product Constant Ksp ÈܶȻý³£Êý 49. Precipitation and separation of Ions Àë×ӵijÁµíÓë·ÖÀë 50. Selective Precipitation of Ions Àë×ÓµÄÑ¡Ôñ³Áµí 51. Oxidation-Reduction Reactions Ñõ»¯»¹Ô·´Ó¦ 52. Oxidation Number Ñõ»¯Êý 53. Balancing Oxidation-Reduction Equations Ñõ»¯»¹Ô·´Ó¦·½³ÌµÄÅ䯽 54. Half-Reaction °ë·´Ó¦ 55. Galvani Cell Ôµç³Ø 56. Voltaic Cell ·üÌØµç³Ø 57. Cell EMF µç³Øµç¶¯ÊÆ 58. Standard Electrode Potentials ±ê×¼µç¼«µçÊÆ 59. Oxidizing and Reducing Agents Ñõ»¯¼ÁºÍ»¹Ô¼Á 60. The Nernst Equation ÄÜË¹ÌØ·½³Ì 61. Electrolysis µç½â 62. The Wave Behavior of Electrons µç×ӵIJ¨¶¯ÐÔ 63. Bohr¡¯s Model of The Hydrogen Atom ÇâÔ×ӵIJ¨¶ûÄ£ÐÍ 64. Line Spectra Ïß¹âÆ× 65. Quantum Numbers Á¿×ÓÊý 66. Electron Spin µç×Ó×ÔÐý 67. Atomic Orbital Ô×Ó¹ìµÀ 68. The s (p, d, f) Orbital s£¨p£¬d£¬f£©¹ìµÀ 69. Many-Electron Atoms ¶àµç×ÓÔ×Ó 70. Energies of Orbital ¹ìµÀÄÜÁ¿ 71. The Pauli Exclusion Principle ÅÝÁÖ²»ÏàÈÝÔÀí 72. Electron Configurations µç×Ó¹¹ÐÍ 73. The Periodic Table ÖÜÆÚ±í 74. Row ÐÐ 75. Group ×å 76. Isotopes, Atomic Numbers, and Mass Numbers Í¬Î»ËØ£¬Ô×ÓÊý£¬ ÖÊÁ¿Êý 77. Periodic Properties of the Elements ÔªËØµÄÖÜÆÚÂÉ 78. Radius of Atoms Ô×Ó°ë¾¶ 79. Ionization Energy µçÀëÄÜ 80. Electronegativity µç¸ºÐÔ 81. Effective Nuclear Charge ÓÐЧºËµçºÉ 82. Electron Affinities Ç×µçÐÔ 83. Metals ½ðÊô 84. Nonmetals ·Ç½ðÊô 85. Valence Bond Theory ¼Û¼üÀíÂÛ 86. Covalence Bond ¹²¼Û¼ü 87. Orbital Overlap ¹ìµÀÖØµþ 88. Multiple Bonds ÖØ¼ü 89. Hybrid Orbital ÔÓ»¯¹ìµÀ 90. The VSEPR Model ¼Û²ãµç×Ó¶Ô»¥³âÀíÂÛ 91. Molecular Geometries ·Ö×ӿռ乹ÐÍ 92. Molecular Orbital ·Ö×Ó¹ìµÀ 93. Diatomic Molecules Ë«Ô×Ó·Ö×Ó 94. Bond Length ¼ü³¤ 95. Bond Order ¼ü¼¶ 96. Bond Angles ¼ü½Ç 97. Bond Enthalpies ¼üÄÜ 98. Bond Polarity ¼ü¾Ø 99. Dipole Moments ż¼«¾Ø 100. Polarity Molecules ¼«ÐÔ·Ö×Ó 101. Polyatomic Molecules ¶àÔ×Ó·Ö×Ó 102. Crystal Structure ¾§Ìå½á¹¹ 103. Non-Crystal ·Ç¾§Ìå 104. Close Packing of Spheres ÇòÃܶѻý 105. Metallic Solids ½ðÊô¾§Ìå 106. Metallic Bond ½ðÊô¼ü 107. Alloys ºÏ½ð 108. Ionic Solids Àë×Ó¾§Ìå 109. Ion-Dipole Forces Àë×Óż¼«Á¦ 110. Molecular Forces ·Ö×Ó¼äÁ¦ 111. Intermolecular Forces ·Ö×Ó¼ä×÷ÓÃÁ¦ 112. Hydrogen Bonding Çâ¼ü 113. Covalent-Network Solids Ô×Ó¾§Ìå 114. Compounds »¯ºÏÎï 115. The Nomenclature, Composition and Structure of Complexes ÅäºÏÎïµÄÃüÃû£¬×é³ÉºÍ½á¹¹ 116. Charges, Coordination Numbers, and Geometries µçºÉÊý¡¢ÅäλÊý¡¢¼°¼¸ºÎ¹¹ÐÍ 117. Chelates òüºÏÎï 118. Isomerism Òì¹¹ÏÖÏó 119. Structural Isomerism ½á¹¹Òì¹¹ 120. Stereoisomerism Á¢ÌåÒì¹¹ 121. Magnetism ´ÅÐÔ 122. Electron Configurations in Octahedral Complexes °ËÃæÌå¹¹ÐÍÅäºÏÎïµÄµç×Ó·Ö²¼ 123. Tetrahedral and Square-planar Complexes ËÄÃæÌåºÍÆ½ÃæËıßÐÎÅäºÏÎï 124. General Characteristics ¹²ÐÔ 125. s-Block Elements sÇøÔªËØ 126. Alkali Metals ¼î½ðÊô 127. Alkaline Earth Metals ¼îÍÁ½ðÊô 128. Hydrides Ç⻯Îï 129. Oxides Ñõ»¯Îï 130. Peroxides and Superoxides ¹ýÑõ»¯ÎïºÍ³¬Ñõ»¯Îï 131. Hydroxides ÇâÑõ»¯Îï 132. Salts ÑÎ 133. p-Block Elements pÇøÔªËØ 134. Boron Group (Boron, Aluminium, Gallium, Indium, Thallium) Åð×壨Åð£¬ÂÁ£¬ïØ£¬î÷£¬î裩 135. Borane ÅðÍé 136. Carbon Group (Carbon, Silicon, Germanium, Tin, Lead) ̼×壨̼£¬¹è£¬Õ࣬Îý£¬Ç¦£© 137. Graphite, Carbon Monoxide, Carbon Dioxide ʯī£¬Ò»Ñõ»¯Ì¼£¬¶þÑõ»¯Ì¼ 138. Carbonic Acid, Carbonates and Carbides ̼Ëᣬ̼ËáÑΣ¬Ì¼»¯Îï 139. Occurrence and Preparation of Silicon ¹èµÄ´æÔÚºÍÖÆ±¸ 140. Silicic Acid£¬Silicates ¹èËᣬ¹èËáÑÎ 141. Nitrogen Group (Phosphorus, Arsenic, Antimony, and Bismuth) µª×壨Á×£¬É飬Ì࣬î飩 142. Ammonia, Nitric Acid, Phosphoric Acid °±£¬ÏõËᣬÁ×Ëá 143. Phosphorates, phosphorus Halides Á×ËáÑΣ¬Â±»¯Á× 144. Oxygen Group (Oxygen, Sulfur, Selenium, and Tellurium) Ñõ×åÔªËØ£¨Ñõ£¬Áò£¬Îø£¬íÚ£© 145. Ozone, Hydrogen Peroxide ³ôÑõ£¬¹ýÑõ»¯Çâ 146. Sulfides Áò»¯Îï 147. Halogens (Fluorine, Chlorine, Bromine, Iodine) Â±ËØ£¨·ú£¬ÂÈ£¬ä壬µâ£© 148. Halides, Chloride ±»¯ÎÂÈ»¯Îï 149. The Noble Gases Ï¡ÓÐÆøÌå 150. Noble-Gas Compounds Ï¡ÓÐÆøÌ廯ºÏÎï 151. d-Block elements dÇøÔªËØ 152. Transition Metals ¹ý¶É½ðÊô 153. Potassium Dichromate ÖØ¸õËá¼Ø 154. Potassium Permanganate ¸ßÃÌËá¼Ø 155. Iron Copper Zinc Mercury Ìú£¬Í£¬Ð¿£¬¹¯ 156. f-Block Elements fÇøÔªËØ 157. Lanthanides ïçÏµÔªËØ 158. Radioactivity ·ÅÉäÐÔ 159. Nuclear Chemistry ºË»¯Ñ§ 160. Nuclear Fission ºËÁѱä 161. Nuclear Fusion ºË¾Û±ä 162. analytical chemistry ·ÖÎö»¯Ñ§ 163. qualitative analysis ¶¨ÐÔ·ÖÎö 164. quantitative analysis ¶¨Á¿·ÖÎö 165. chemical analysis »¯Ñ§·ÖÎö 166. instrumental analysis ÒÇÆ÷·ÖÎö 167. titrimetry µÎ¶¨·ÖÎö 168. gravimetric analysis ÖØÁ¿·ÖÎö·¨ 169. regent ÊÔ¼Á 170. chromatographic analysis É«Æ×·ÖÎö 171. product ²úÎï 172. electrochemical analysis µç»¯Ñ§·ÖÎö 173. on-line analysis ÔÚÏß·ÖÎö 174. macro analysis ³£Á¿·ÖÎö 175. characteristic ±íÕ÷ 176. micro analysis ΢Á¿·ÖÎö 177. deformation analysis ÐÎ̬·ÖÎö 178. semimicro analysis °ë΢Á¿·ÖÎö 179. systematical error ϵͳÎó²î 180. routine analysis ³£¹æ·ÖÎö |
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181. random error żȻÎó²î 182. arbitration analysis Öٲ÷ÖÎö 183. gross error ¹ýʧÎó²î 184. normal distribution Õý̬·Ö²¼ 185. accuracy ¡¡×¼È·¶È 186. deviation¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ ¡¡Æ«²î 187. precision ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¾«ÃÜ¶È 188. relative standard deviation ¡¡¡¡¡¡Ïà¶Ô±ê׼ƫ²î£¨RSD£© 189. coefficient variation ¡¡¡¡¡¡¡¡¡¡±äÒìϵÊý£¨CV£© 190. confidence level ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ÖÃÐÅˮƽ 191. confidence interval ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ÖÃÐÅÇø¼ä 192. significant test ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ÏÔÖøÐÔ¼ìÑé 193. significant figure ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ÓÐЧÊý×Ö 194. standard solution ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡±ê×¼ÈÜÒº 195. titration ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡µÎ¶¨ 196. stoichiometric point ¡¡¡¡¡¡¡¡¡¡¡¡¡¡»¯Ñ§¼ÆÁ¿µã 197. end point¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡µÎ¶¨ÖÕµã 198. titration error ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡µÎ¶¨Îó²î 199. primary standard ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡»ù×¼ÎïÖÊ 200. amount of substance ¡¡¡¡¡¡¡¡¡¡¡¡¡¡ÎïÖʵÄÁ¿ 201. standardization ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡±ê¶¨ 202. chemical reaction ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡»¯Ñ§·´Ó¦ 203. concentration¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ ¡¡Å¨¶È 204. chemical equilibrium ¡¡¡¡¡¡¡¡¡¡¡¡¡¡»¯Ñ§Æ½ºâ 205. titer ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡µÎ¶¨¶È 206. general equation for a chemical reaction¡¡»¯Ñ§·´Ó¦µÄͨʽ 207. proton theory of acid-base ¡¡¡¡¡¡¡¡¡¡¡¡Ëá¼îÖÊ×ÓÀíÂÛ 208. acid-base titration ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡Ëá¼îµÎ¶¨·¨ 209. dissociation constant ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡½âÀë³£Êý 210. conjugate acid-base pair ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¹²éîËá¼î¶Ô 211. acetic acid ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ÒÒËá 212. hydronium ion¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ Ë®ºÏÇâÀë×Ó 213. electrolyte ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡µç½âÖÊ 214. ion-product constant of water ¡¡¡¡¡¡¡¡¡¡¡¡Ë®µÄÀë×Ó»ý 215. ionization ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡µçÀë 216. proton condition ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ÖÊ×ÓÆ½ºâ 217. zero level¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ ÁãË®×¼ 218. buffer solution¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ »º³åÈÜÒº 219. methyl orange ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¼×»ù³È 220. acid-base indicator ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡Ëá¼îָʾ¼Á 221. phenolphthalein ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡·Ó̪ 222. coordination compound ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡Åäλ»¯ºÏÎï 223. center ion ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ÖÐÐÄÀë×Ó 224. cumulative stability constant ¡¡¡¡¡¡¡¡¡¡¡¡ÀÛ»ýÎȶ¨³£Êý 225. alpha coefficient ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ËáЧӦϵÊý 226. overall stability constant ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡×ÜÎȶ¨³£Êý 227. ligand ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ÅäλÌå 228. ethylenediamine tetraacetic acid ¡¡¡¡¡¡¡¡ÒÒ¶þ°·ËÄÒÒËá 229. side reaction coefficient ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¸±·´Ó¦ÏµÊý 230. coordination atom ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ÅäλÔ×Ó 231. coordination number ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ÅäλÊý 232. lone pair electron ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¹Â¶Ôµç×Ó 233. chelate compound ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡òüºÏÎï 234. metal indicator ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡½ðÊôָʾ¼Á 235. chelating agent ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡òüºÏ¼Á 236. masking ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ÑڱΠ237. demasking ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡½â±Î 238. electron ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡µç×Ó 239. catalysis ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡´ß»¯ 240. oxidation¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ Ñõ»¯ 241. catalyst ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡´ß»¯¼Á 242. reduction ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡»¹Ô 243. catalytic reaction ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡´ß»¯·´Ó¦ 244. reaction rate ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡·´Ó¦ËÙÂÊ 245. electrode potential ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡µç¼«µçÊÆ 246. activation energy ¡¡¡¡¡¡¡¡ ·´Ó¦µÄ»î»¯ÄÜ¡¡ 247. redox couple ¡¡¡¡¡¡¡¡¡¡¡¡ Ñõ»¯»¹Ôµç¶Ô 248. potassium permanganate ¡¡¡¡ ¸ßÃÌËá¼Ø ¡¡ 249. iodimetry¡¡¡¡¡¡¡¡¡¡¡¡¡¡ µâÁ¿·¨ 250. potassium dichromate ¡¡¡¡ ÖØ¸õËá¼Ø ¡¡¡¡¡¡¡¡ 251. cerimetry ¡¡¡¡¡¡¡¡¡¡¡¡¡¡ ¡¡îæÁ¿·¨ 252. redox indicator ¡¡¡¡¡¡¡¡ Ñõ»¯»¹Ôָʾ 253. oxygen consuming ¡¡¡¡¡¡¡¡ ºÄÑõÁ¿£¨OC£© 254. chemical oxygen demanded »¯Ñ§ÐèÑõÁ¿(COD)¡¡ 255. dissolved oxygen ¡¡¡¡¡¡¡¡ ÈܽâÑõ(DO) 256. precipitation ¡¡¡¡¡¡¡¡¡¡¡¡ ³Áµí·´Ó¦ 257. argentimetry ¡¡¡¡¡¡¡¡¡¡¡¡ ÒøÁ¿·¨ 258. heterogeneous equilibrium of ions ¶àÏàÀë×ÓÆ½ºâ¡¡ 259. aging ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡³Â»¯ 260. postprecipitation ¡¡¡¡¡¡¡¡¼Ì³Áµí 261. coprecipitation ¡¡¡¡¡¡¡¡¡¡¡¡¹²³Áµí 262. ignition ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡×ÆÉÕ 263. fitration ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¹ýÂË 264. decantation ¡¡¡¡¡¡¡¡¡¡¡¡Çãк·¨ ¡¡ 265. chemical factor ¡¡¡¡¡¡¡¡»¯Ñ§ÒòÊý 266. spectrophotometry ¡¡¡¡¡¡¡¡·Ö¹â¹â¶È·¨ ¡¡ 267. colorimetry ¡¡¡¡¡¡¡¡¡¡¡¡±ÈÉ«·ÖÎö 268. transmittance ¡¡¡¡¡¡¡¡¡¡¡¡Í¸¹âÂÊ ¡¡¡¡ 269. absorptivity ¡¡¡¡¡¡¡¡¡¡¡¡Îü¹âÂÊ 270. calibration curve ¡¡¡¡¡¡¡¡Ð£ÕýÇúÏß ¡¡ 271. standard curve ¡¡¡¡¡¡¡¡¡¡¡¡±ê×¼ÇúÏß 272. monochromator ¡¡¡¡¡¡¡¡µ¥É«Æ÷ ¡¡¡¡¡¡ 273. source ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¹âÔ´ 274. wavelength dispersion ¡¡¡¡É«É¢ 275. absorption cell¡¡¡¡¡¡¡¡¡¡¡¡ ÎüÊÕ³Ø 276. detector ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¼ì²âϵͳ ¡¡¡¡ 277. bathochromic shift ¡¡¡¡¡¡¡¡ºìÒÆ 278. Molar absorptivity ¡¡¡¡¡¡¡¡Ä¦¶ûÎü¹âϵÊý ¡¡ 279. hypochromic shift ¡¡¡¡¡¡¡¡×ÏÒÆ 280. acetylene ÒÒȲ 281. ethylene ÒÒÏ© 282. acetylating agent ÒÒõ£»¯¼Á 283. acetic acid ÒÒËá 284. adiethyl ether ÒÒÃÑ 285. ethyl alcohol ÒÒ´¼ 286. acetaldehtde ÒÒÈ© 287. ¦Â-dicarbontl compound ¦Â¨C¶þôÊ»ù»¯ºÏÎï 288. bimolecular elimination Ë«·Ö×ÓÏû³ý·´Ó¦ 289. bimolecular nucleophilic substitution Ë«·Ö×ÓÇ׺ËÈ¡´ú·´Ó¦ 290. open chain compound ¿ªÁ´×廯ºÏÎï 291. molecular orbital theory ·Ö×Ó¹ìµÀÀíÂÛ 292. chiral molecule ÊÖÐÔ·Ö×Ó 293. tautomerism »¥±äÒì¹¹ÏÖÏó 294. reaction mechanism ·´Ó¦Àú³Ì 295. chemical shift »¯Ñ§Î»ÒÆ 296. Walden inversio Íß¶ûµÇ·´×ªn 297. Enantiomorph ¶ÔÓ³Ìå 298. addition rea ction ¼Ó³É·´Ó¦ 299. dextro- ÓÒÐý 300. levo- ×óÐý 301. stereochemistry Á¢Ì廯ѧ 302. stereo isomer Á¢ÌåÒì¹¹Ìå 303. Lucas reagent ¬¿¨Ë¹ÊÔ¼Á 304. covalent bond ¹²¼Û¼ü 305. conjugated diene ¹²éî¶þÏ©Ìþ 306. conjugated double bond ¹²éîË«¼ü 307. conjugated system ¹²éîÌåϵ 308. conjugated effect ¹²éîЧӦ 309. isomer ͬ·ÖÒì¹¹Ìå 310. isomerism ͬ·ÖÒì¹¹ÏÖÏó 311. organic chemistry Óлú»¯Ñ§ 312. hybridization ÔÓ»¯ 313. hybrid orbital ÔÓ»¯¹ìµÀ 314. heterocyclic compound ÔÓ»·»¯ºÏÎï 315. peroxide effect ¹ýÑõ»¯ÎïЧӦt 316. valence bond theory ¼Û¼üÀíÂÛ 317. sequence rule ´ÎÐò¹æÔò 318. electron-attracting grou p Îüµç×Ó»ù 319. Huckel rule Ðݿ˶û¹æÔò 320. Hinsberg test ÐË˹±¤ÊÔÑé 321. infrared spectrum ºìÍâ¹âÆ× 322. Michael reacton Âó¿Ë¶û·´Ó¦ 323. halogenated hydrocarbon ±´úÌþ 324. haloform reaction ±·Â·´Ó¦ 325. systematic nomenclatur ϵͳÃüÃû·¨e 326. Newman projection ŦÂüͶӰʽ 327. aromatic compound ·¼Ïã×廯ºÏÎï 328. aromatic character ·¼ÏãÐÔr 329. Claisen condensation reaction¿ËÀ³Éõ¥ËõºÏ·´Ó¦ 330. Claisen rearrangement ¿ËÀ³ÉÖØÅÅ 331. Diels-Alder reation µÒ¶û˹-°¢¶ûµÃ·´Ó¦ 332. Clemmensen reduction ¿ËÀ³ÃÅÉ»¹Ô 333. Cannizzaro reaction ¿²ÄáÔúÂÞ·´Ó¦ 334. positional isomers λÖÃÒì¹¹Ìå 335. unimolecular elimination reaction µ¥·Ö×ÓÏû³ý·´Ó¦ 336. unimolecular nucleophilic substitution µ¥·Ö×ÓÇ׺ËÈ¡´ú·´Ó¦ 337. benzene ±½ 338. functional grou ¹ÙÄÜÍÅp 339. configuration ¹¹ÐÍ 340. conformation ¹¹Ïó 341. confomational isome ¹¹ÏóÒì¹¹Ìå 342. electrophilic addition Ç×µç¼Ó³É 343. electrophilic reagent Ç×µçÊÔ¼Á 344. nucleophilic addition Ç×ºË¼Ó³É 345. nucleophilic reagent Ç׺ËÊÔ¼Á 346. nucleophilic substitution reactionÇ׺ËÈ¡´ú·´Ó¦ 347. active intermediate »îÐÔÖмäÌå 348. Saytzeff rule ²éÒÀ²É·ò¹æÔò 349. cis-trans isomerism ˳·´Òì¹¹ 350. inductive effect ÓÕµ¼Ð§Ó¦ t 351. Fehling¡¯s reagent ·ÑÁÖÊÔ¼Á 352. phase transfer catalysis Ïà×ªÒÆ´ß»¯×÷Óà 353. aliphatic compound Ö¬·¾×廯ºÏÎï 354. elimination reaction Ïû³ý·´Ó¦ 355. Grignard reagent ¸ñÀûÑÅÊÔ¼Á¡¡¡¡¡¡¡¡¡¡¡¡¡¡ 356. nuclear magnetic resonance ºË´Å¹²Õñ 357. alkene Ï©Ìþ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ 358. allyl cation Ï©±û»ùÕýÀë×Ó 359. leaving group ÀëÈ¥»ùÍÅ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ 360. optical activity Ðý¹âÐÔ 361. boat confomation ´¬Ð͹¹Ïó¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ 362. silver mirror reaction Òø¾µ·´Ó¦ 363. Fischer projection ·ÆÉá¶ûͶӰʽ¡¡¡¡¡¡¡¡¡¡¡¡¡¡ 364. Kekule structure ¿¿âÀսṹʽ 365. Friedel-Crafts reaction ¸µÁе¶û-¿ËÀ·ò´Ä·´Ó¦¡¡ 366. Ketone ͪ 367. carboxylic acid ôÈËá¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ 368. carboxylic acid derivative ôÈËáÑÜÉúÎï 369. hydroboration ÅðÇ⻯·´Ó¦¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ 370. bond oength ¼ü³¤ 371. bond energy ¼üÄÜ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ 372. bond angle ¼ü½Ç 373. carbohydrate ̼ˮ»¯ºÏÎï ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ 374. carbocation ̼ÕýÀë×Ó 375. carbanion ̼¸ºÀë×Ó¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ 376. alcohol ´¼ 377. Gofmann rule »ô·òÂü¹æÔò¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ 378. Aldehyde È© 379. Ether ÃÑ 380. Polymer ¾ÛºÏÎï |
2Â¥2007-01-13 13:24:52
6Â¥2007-01-24 17:14:54
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