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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 card
    786 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}}
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  • {{r|organic chemistry}}
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  • {{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 [[hydroge
    258 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 0-471-3
    576 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}}
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  • {{r|Organic chemistry}}
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  • {{r|IUPAC nomenclature of organic chemistry}}
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  • ...neogenesis]] - <i>de novo</i> synthesis of glucose molecules from simple [[organic chemistry|organic]] compounds
    977 bytes (128 words) - 02:04, 2 June 2009
  • * Clayden J, Greeves N, Warren S, Wothers P (2000) ''Organic Chemistry'' (Oxford University Press) ISBN 0-19-850346-6
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  • *All: An abbreviation in organic chemistry for [[allyl]].
    394 bytes (55 words) - 19:58, 28 November 2013
  • {{r|IUPAC nomenclature of organic chemistry}}
    1 KB (160 words) - 11:58, 31 December 2022
  • ...'' are [[chemical reaction]]s involving [[organic compound]]s. The basic [[organic chemistry]] reaction types are [[addition reaction]]s, [[elimination reaction]]s, [[s ...n]] of organic fuels and [[saponification]] of fats to make soap. Modern [[organic chemistry]] starts with the [[Wöhler synthesis]] in 1828. In the history of the [[No
    9 KB (1,149 words) - 07:52, 2 September 2008
  • ...erocycles play a large role in the biochemistry of living organisms and in organic chemistry. For example, [[DNA]] consists of the heterocyclic [[purine]] bases, [[ade
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  • {{r|Organic chemistry}}
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  • {{r|Organic chemistry}}
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  • {{r|Organic chemistry}}
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  • ...medicinal purposes<ref name=Wilcox1984>Wilcox, C.F. (1984). ''Experimental Organic Chemistry, Theory and Practice.'' Macmillan. p. 332; ch. 24.</ref>. ...xylic acid]] and an [[alcohol]]<ref name=McMurry1996>McMurry, J. (1996). ''Organic Chemistry (4th ed.)''. Scarborough, Ontario: Nelson Canada. pp. 222, 639, 803, 814, 8
    2 KB (299 words) - 07:59, 8 June 2009
  • * Clayden J, Greeves N, Warren S., Wothers,P. ''Organic Chemistry'' 2000 (Oxford University Press) ISBN 0-19-850346-6
    2 KB (245 words) - 15:18, 26 September 2007
  • {{r|IUPAC nomenclature of organic chemistry}}
    2 KB (229 words) - 09:18, 6 March 2024
  • {{r|Organic chemistry}}
    512 bytes (64 words) - 20:52, 11 January 2010
  • ...most commonly-used tests are the undergraduate-level tests for general and organic chemistry. Each of these tests consists of 75 multiple-choice questions, and gives st *[[Journal of Organic Chemistry]]
    5 KB (759 words) - 15:19, 8 April 2023
  • ...ity of organic semiconductor devices, combined with the power of synthetic organic chemistry, may open up the way to completely new device configuration, fabrication pr
    3 KB (425 words) - 08:02, 12 November 2007
  • ...ry]], [[thermodynamics]], [[electromagnetic force|electromagnetism]] and [[organic chemistry]]. His work on the size of molecules was sufficiently important that in Ger
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  • {{r|Organic chemistry}}
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  • {{r|Organic chemistry}}
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  • {{r|Organic chemistry}}
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  • ...s">A central goal of chemical biology is to harness the power of synthetic organic chemistry to discover and to elucidate molecular pathways fundamental in cellular, de
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  • {{r|Organic chemistry}}
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  • ...]] &ndash; [[Berlin]], 15 July 1919) is one of the founders of classic [[organic chemistry]]. He received the 1902 [[Nobel Prize Chemistry|Nobel Prize]] in chemistry ...esearches into the sugar group, begun in 1883, were of great importance to organic chemistry. In 1875 he had published his discovery of the compound [[phenylhydrazine]]
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  • ...ller monomers. In most cases, polymers are prepared using principles of [[organic chemistry]]. Polymer chemists are especially interested in techniques that allow the ...hemists are also investigating polymerization methods outside the scope of organic chemistry. One area of interest involves preparing polymers by imitating the biologi
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  • ...b>, is a pungent toxic chemical widely used as a chlorination reagent in [[organic chemistry]]. It has many synonyms, including thionyl dichloride, sulfurous oxychlorid
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  • ...ll organic matter. [[Diamond]], [[graphite]], and [[fullerene]]s are non-[[Organic chemistry|organic]] compounds consisting of carbon only; these are known as [[allotro
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  • {{r|Organic chemistry}}
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  • 2 KB (217 words) - 19:18, 10 November 2007
  • ...om/books?id=ZOm8L9oCwLMC&pg=PA633}} and {{cite book |title=Modern physical organic chemistry |author=Eric V. Anslyn, Dennis A. Dougherty |pages=pp. 68 ''ff'' |chapter=� ...VirtTxtJml/react2.htm Examples of Organic Reactions] ''Virtual Textbook of Organic Chemistry'', William Reusch, Emeritus Professor, Department of Chemistry, [[Michigan
    11 KB (1,592 words) - 09:15, 28 September 2013
  • ...Inorganic chemistry|inorganic compounds]]. With the massive expansion of [[organic chemistry]] in the mid-nineteenth century and the greater understanding of the struct
    11 KB (1,596 words) - 09:29, 2 August 2023
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