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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×ÓµÄÐγÉ
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 ˫ԭ×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«ÃܶÈ
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 ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡Åäλԭ×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 ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡ÑÚ±Î
237. 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»¯»¹Ô­Ö¸Ê¾
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׺˼ӳÉ
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»¯×÷ÓÃ
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
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

lotusliu

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¡ï¡ï¡ï¡ï¡ï ÎåÐǼ¶,ÓÅÐãÍÆ¼ö

very good!
thanks!
6Â¥2007-01-24 17:14:54
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

syccxy

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лл£¡ ºÃºÃѧϰһÏ£¡
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