¬d¬Ý§¹¾ãª©¥»: OrgChem-organic synthsis ÃD¥Ø2±ø(SOLVED)

¤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.
­¶: [1] 2