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- An aprotic colorless solvent widely used in organic chemistry reactions and the main ingredient in many fingernail polish removers.167 bytes (22 words) - 08:58, 15 June 2008
- {{r|Organic chemistry}}549 bytes (72 words) - 19:15, 11 January 2010
- '''Oxazolidinone''' is a cyclopentane-like molecule frequently used in organic chemistry reactions and is a central part of many medications, particularly some card786 bytes (108 words) - 14:35, 26 November 2010
- {{r|IUPAC nomenclature of organic chemistry}} {{r|Organic chemistry}}1 KB (162 words) - 16:24, 11 January 2010
- {{r|Organic chemistry}}528 bytes (64 words) - 17:46, 11 July 2010
- {{r|IUPAC nomenclature of organic chemistry}}681 bytes (92 words) - 11:40, 11 January 2010
- {{r|Organic chemistry}}275 bytes (35 words) - 05:42, 6 March 2024
- {{r|Organic chemistry}}178 bytes (23 words) - 16:09, 4 November 2010
- {{r|organic chemistry}}337 bytes (50 words) - 13:09, 6 February 2010
- {{r|Organic chemistry}}409 bytes (48 words) - 12:33, 18 March 2012
- ...] — a [[chemical compound|compound]] important in many branches of [[organic chemistry]] — from the [[chemical element|elements]] [[nitrogen]] and [[hydroge258 bytes (31 words) - 08:37, 4 March 2010
- {{r|Organic chemistry}}1,019 bytes (130 words) - 18:38, 11 January 2010
- {{r|IUPAC nomenclature of organic chemistry}}506 bytes (65 words) - 07:42, 8 January 2010
- ...chwarzenbach, Philip M. Gschwend and Dieter M. Imboden|title=Environmental Organic Chemistry|edition=2nd Edition|publisher= Wiley-Interscience|year=2003|id=ISBN 0-471-3576 bytes (79 words) - 17:57, 1 October 2010
- {{r|Organic chemistry}}592 bytes (79 words) - 15:49, 11 January 2010
- {{r|Organic chemistry}}796 bytes (103 words) - 11:57, 31 December 2022
- {{r|Organic chemistry}}572 bytes (71 words) - 10:59, 24 March 2011
- {{r|IUPAC nomenclature of organic chemistry}}673 bytes (86 words) - 07:42, 8 January 2010
- {{r|Organic chemistry}}581 bytes (74 words) - 18:06, 22 February 2010
- {{r|Organic chemistry}}1 KB (156 words) - 08:01, 16 April 2010