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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 |
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