¤pM¥Í 2010-7-27 12:25 PM
OrgChem-organic synthsis ÃD¥Ø2±ø(SOLVED)
OrgChem-organic synethsis ÃD¥Ø2±ø
¦]¬°ÉNµª®×,,©Ò¥H§Ú³£øª¾¾Ç¥ª¥¼(§Ú¾Ç¨ìalkene,aromatic hydrocarbon¦Phalo-compound)
¢÷¢ý¢ü¢ô¢ñ¢ö¢í¡@¢ü¢ð¢í¡@¢î¢÷¢ô¢ô¢÷£@¢ñ¢ö¢ï¡@¢û£B¢ö¢ü¢ð¢í¢û¢í¢û
²Ä¤@±ø:KO
²Ä2±ø: ko
[[i] ¥»©«³Ì«á¥Ñ ¤pM¥Í ©ó 2010-7-27 11:02 PM ½s¿è [/i]]
ivannww 2010-7-27 02:47 PM
²Ä¤@±ø§A¥¼¾Ç...nSn2+oxidation...
²Ä¤G±ø«Yø«Y¥i¥Helimination+hydrogenation
ps§Úı±o²Ä¤G±ø«Ychem-is-try...±oÊ\·|ø¨£咗benzene¤J±d嘢
[[i] ¥»©«³Ì«á¥Ñ ivannww ©ó 2010-7-27 02:48 PM ½s¿è [/i]]
Simon 2010-7-27 03:15 PM
Halogeno-compound¤@½ÒÀ³¸Ó·|±ÐSn1 / Sn2
kctsui75 2010-7-27 03:28 PM
²Ä¤G±ø¡G
(a). Heated under reflux with a concentrated solution of sodium or potassium
hydroxide in ethanol.
C6H5 CHBrCH3 ¡÷ C6H5 CH = CH2
(b) Reacts with hydrogen in the presence of a finely divided nickel catalyst at
a temperature of about 150¢XC.
C6H5 CH = CH2 + 4H2 ¡÷ C6H11 CH2 CH3
¤pM¥Í 2010-7-27 03:39 PM
¦^ÂÐ #4 kctsui75 ªº©«¤l
²Ä2±ø©ú¥Õ
ì¨Ó«Yhydrogenation«{©Ò¦³c=c double bond
²Ä¤@±ønremove 1C
·|ø·|«Y¾Ç§¹carboxylic acid and their derivativesªG½Ò¥ýÃѰµ?
[[i] ¥»©«³Ì«á¥Ñ ¤pM¥Í ©ó 2010-7-27 03:40 PM ½s¿è [/i]]
¤pM¥Í 2010-7-27 03:41 PM
[quote]ì©«¥Ñ [i]ivannww[/i] ©ó 2010-7-27 02:47 PM µoªí [url=http://lsforum.net/board/redirect.php?goto=findpost&pid=2265158&ptid=145707][img]http://lsforum.net/board/images/common/back.gif[/img][/url]
²Ä¤@±ø§A¥¼¾Ç...nSn2+oxidation...
²Ä¤G±ø«Yø«Y¥i¥Helimination+hydrogenation
ps§Úı±o²Ä¤G±ø«Ychem-is-try...±oÊ\·|ø¨£ Wbenzene¤J±d O [/quote]
ø«Ychem-is-try«Y k.kwong notes¬Jexercise
¤õ®ã 2010-7-27 03:44 PM
remove 1C ¦n¦ü«Yn¥ÎHofman degradation, øª¾¦³¨Sout-syl...
Simon 2010-7-27 03:46 PM
¦^ÂÐ #7 ¤õ®ã ªº©«¤l
¨ä¹êbenzene¬J³¥
¦³¤@Óoxidation¥i¥H¥O¨ì¥»¨¤@±øcarbon chain
oxidize ¤§«á´N±oªð -COOH
biggertommy 2010-7-27 03:52 PM
hofmann....out syl
Ans is dehydrohalogenation,hydration,iodoform formation,reduction,(mild)oxidation.....
biggertommy 2010-7-27 03:54 PM
¦^ÂÐ #8 ³ÇSimon ªº©«¤l
your method is better =)
¤õ®ã 2010-7-27 04:33 PM
[quote]ì©«¥Ñ [i]³ÇSimon[/i] ©ó 2010-7-27 03:46 PM µoªí [url=http://lsforum.net/board/redirect.php?goto=findpost&pid=2265222&ptid=145707][img]http://lsforum.net/board/images/common/back.gif[/img][/url]
¨ä¹êbenzene¬J³¥
¦³¤@Óoxidation¥i¥H¥O¨ì¥»¨¤@±øcarbon chain
oxidize ¤§«á´N±oªð -COOH [/quote]
em32 ©OÓ³£«Y¨ä¤¤¤@Ó¤èªk
Simon 2010-7-27 06:53 PM
¦^ÂÐ #10 biggertommy ªº©«¤l
³Ìª½±µ¤F·í
ø¨Ï³vÓcarbonËݩ
¤pM¥Í 2010-7-27 07:21 PM
[quote]ì©«¥Ñ [i]³ÇSimon[/i] ©ó 2010-7-27 03:46 PM µoªí [url=http://lsforum.net/board/redirect.php?goto=findpost&pid=2265222&ptid=145707][img]http://lsforum.net/board/images/common/back.gif[/img][/url]
¨ä¹êbenzene¬J³¥
¦³¤@Óoxidation¥i¥H¥O¨ì¥»¨¤@±øcarbon chain
oxidize ¤§«á´N±oªð -COOH [/quote]
©O¼Ë§Úª¾¹D
ËÝÅܧ¹-COOH ¤§«áÂI?
Simon 2010-7-27 07:23 PM
¦^ÂÐ #13 ¤pM¥Í ªº©«¤l
°µreduction
¤pM¥Í 2010-7-27 07:24 PM
¦^ÂÐ #14 ³ÇSimon ªº©«¤l
OK
Ú»¾¤§Ú¥¼Ú»¨ì©Opart
-COOH --> COH
kctsui75 2010-7-27 08:36 PM
²Ä¤@±ø¡G
(a). Heated under reflux with a concentrated solution of sodium or potassium hydroxide in
ethanol.
C6H5 CH2CH2 Cl ¡÷ C6H5 CH = CH2
(b) Ozonolysis
C6H5 CH = CH2 ¡÷ C6H5 CHO
Reagents : ozone, O3, followed by a reducing work-up, usually Zn in acetic acid.
µù¡G¥t¤@²£«~¬Omethanal HCHO¡A¥i¥Îfractional distillation ±N¨ä¤ÀÂ÷¡C
biggertommy 2010-7-27 08:57 PM
¦^ÂÐ #16 kctsui75 ªº©«¤l
«Ywo....¨ÌÓ§ó¦n....step¤Ö,yield³£À³¸Ó°ª..:)
§Úø»{¼o³£ø±o°Õem35
Simon 2010-7-27 09:02 PM
§Ú¦n¤Ö·|çÜozonolysis
Eternal_Tale 2010-7-27 09:06 PM
¨ä¹ê- carbon¬J¸Üozonolysis«Y¤@Ó¦n¦n¬J¤èªk....
¯S§O«Y¦n©ö¾ã¨ìdouble dond¥X¾¤Ó°}
¦n¹Lhoffman degradation,¥»¨out c,¦P®IµLËÝ©ö¾ã¨ìdegrade¤§«eÓ¼Ë
Propane 2010-7-27 09:11 PM
Reduction of an acid to an aldehyde is not that simple.