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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 ¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡¡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
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