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- #REDIRECT [[Organic chemistry]]31 bytes (3 words) - 03:42, 15 July 2008
- ...d F. and Sally J. Daley, ''Organic Chemistry'', www.ochem4free.com, Online organic chemistry textbook.</ref>. The original definition of organic chemistry came from the misperception that these compounds were always related to [[l21 KB (3,107 words) - 09:16, 6 March 2024
- 253 bytes (35 words) - 17:12, 13 May 2008
- 12 bytes (1 word) - 09:41, 12 November 2007
- ...://www.cem.msu.edu/~reusch/VirtualText/intro1.htm#info Virtual Textbook of Organic Chemistry] ...://library.thinkquest.org/3659/orgchem/functionalgroups.html The Nature of Organic Chemistry] ]393 bytes (53 words) - 13:27, 2 October 2010
- {{r|IUPAC nomenclature of organic chemistry}}403 bytes (52 words) - 14:09, 2 October 2010
- ...<ref>{{cite book|author=Dieter Hellwinkle|title=Systematic Nomenclature of Organic Chemistry|edition=1st Edition|publisher=Springer-Verlag|year=2001|id=ISBN 3-540-4113825 KB (3,880 words) - 09:42, 28 September 2013
- 195 bytes (26 words) - 22:32, 23 March 2009
- 12 bytes (1 word) - 21:26, 23 October 2007
- {{r|Organic chemistry}}273 bytes (31 words) - 23:18, 23 March 2009
- *[http://www.acdlabs.com/iupac/nomenclature/ IUPAC Nomenclature of Organic Chemistry] (online version of the IUPAC "Blue Book")462 bytes (60 words) - 23:22, 23 March 2009
Page text matches
- ...://www.cem.msu.edu/~reusch/VirtualText/intro1.htm#info Virtual Textbook of Organic Chemistry] ...://library.thinkquest.org/3659/orgchem/functionalgroups.html The Nature of Organic Chemistry] ]393 bytes (53 words) - 13:27, 2 October 2010
- {{r|IUPAC nomenclature of organic chemistry}}403 bytes (52 words) - 14:09, 2 October 2010
- {{r|Organic chemistry}}394 bytes (47 words) - 19:49, 11 April 2010
- ...contributions to physical chemistry, thermodynamics, electromagnetism and organic chemistry.165 bytes (17 words) - 06:09, 22 October 2008
- {{r|Organic chemistry}} {{r|IUPAC nomenclature of organic chemistry}}614 bytes (83 words) - 23:20, 9 May 2010
- *[http://www.acdlabs.com/iupac/nomenclature/ IUPAC Nomenclature of Organic Chemistry] (online version of the IUPAC "Blue Book")462 bytes (60 words) - 23:22, 23 March 2009
- {{r|Organic chemistry}}826 bytes (105 words) - 05:45, 6 March 2024
- ...mixture of [[hydrocarbon]]s of various [[molecular weight]]s plus other [[Organic chemistry|organic compound]]s.297 bytes (37 words) - 14:24, 6 October 2009
- #REDIRECT[[Organic chemistry]]30 bytes (3 words) - 22:30, 20 February 2009
- #REDIRECT [[Organic chemistry]]31 bytes (3 words) - 03:42, 15 July 2008
- {{r|Organic chemistry}}550 bytes (67 words) - 05:42, 6 March 2024
- {{R|Organic chemistry}}363 bytes (44 words) - 12:21, 18 March 2012
- ...nclude>{{Subpages}}</noinclude>A pungent chlorination agent widely used in organic chemistry96 bytes (12 words) - 12:58, 28 November 2010
- * Clayden, Greeves, Warren, Wothers. ''Organic Chemistry.'' Oxford University Press (2001), ISBN 0-19-850346-6.606 bytes (83 words) - 03:42, 5 December 2007
- {{r|Organic chemistry}}365 bytes (44 words) - 12:30, 18 March 2012
- {{r|Organic chemistry}}273 bytes (31 words) - 23:18, 23 March 2009
- (1852 – 1919) is one of the founders of classic organic chemistry; 1902 Nobelist.119 bytes (13 words) - 09:06, 14 January 2010
- {{r|Organic chemistry}} {{r|Organic chemistry}}2 KB (246 words) - 16:13, 1 April 2011
- {{r|IUPAC nomenclature of organic chemistry}}297 bytes (34 words) - 22:36, 6 August 2009
- {{r|IUPAC nomenclature of organic chemistry}}566 bytes (73 words) - 16:24, 11 January 2010
- 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
- {{r|IUPAC nomenclature of organic chemistry}}881 bytes (116 words) - 10:53, 11 January 2010
- ...neogenesis]] - <i>de novo</i> synthesis of glucose molecules from simple [[organic chemistry|organic]] compounds977 bytes (128 words) - 02:04, 2 June 2009
- * Clayden J, Greeves N, Warren S, Wothers P (2000) ''Organic Chemistry'' (Oxford University Press) ISBN 0-19-850346-61 KB (165 words) - 03:03, 28 September 2007
- *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 [[No9 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, [[ade1 KB (129 words) - 09:16, 6 March 2024
- {{r|Organic chemistry}}203 bytes (22 words) - 00:08, 29 November 2012
- {{r|Organic chemistry}}983 bytes (126 words) - 18:07, 11 January 2010
- {{r|Organic chemistry}}428 bytes (54 words) - 10:04, 31 July 2009
- ...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, 82 KB (299 words) - 07:59, 8 June 2009
- * Clayden J, Greeves N, Warren S., Wothers,P. ''Organic Chemistry'' 2000 (Oxford University Press) ISBN 0-19-850346-62 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 pr3 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 Ger1 KB (180 words) - 08:13, 14 September 2013
- {{r|Organic chemistry}}2 KB (256 words) - 09:18, 6 March 2024
- {{r|Organic chemistry}}856 bytes (107 words) - 16:19, 11 January 2010
- {{r|Organic chemistry}}992 bytes (122 words) - 11:06, 11 January 2010
- ...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, de7 KB (909 words) - 21:51, 2 July 2010
- {{r|Organic chemistry}}2 KB (230 words) - 07:42, 30 July 2009
- ...]] – [[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]]4 KB (622 words) - 10:24, 2 March 2010
- ...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 biologi8 KB (1,157 words) - 09:16, 6 March 2024
- ...b>, is a pungent toxic chemical widely used as a chlorination reagent in [[organic chemistry]]. It has many synonyms, including thionyl dichloride, sulfurous oxychlorid1 KB (135 words) - 13:39, 28 November 2010
- ...ll organic matter. [[Diamond]], [[graphite]], and [[fullerene]]s are non-[[Organic chemistry|organic]] compounds consisting of carbon only; these are known as [[allotro5 KB (806 words) - 17:16, 1 January 2021
- {{r|Organic chemistry}}3 KB (457 words) - 12:49, 15 March 2024
- 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, [[Michigan11 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 struct11 KB (1,596 words) - 09:29, 2 August 2023
- {{r|Organic chemistry}}2 KB (265 words) - 10:53, 11 January 2010
- ==Distinctions between inorganic and organic chemistry== The distinction or boundary between inorganic chemistry and [[organic chemistry]] is not very well defined. In general, the above definition of inorganic c13 KB (1,921 words) - 09:37, 6 March 2024
- ...d F. and Sally J. Daley, ''Organic Chemistry'', www.ochem4free.com, Online organic chemistry textbook.</ref>. The original definition of organic chemistry came from the misperception that these compounds were always related to [[l21 KB (3,107 words) - 09:16, 6 March 2024
- The term ''Volatile organic compound (VOC)'' refers to [[Organic chemistry|organic]] chemical compounds having significant vapor pressures and which c14 KB (2,165 words) - 15:39, 25 February 2012
- In [[biochemistry]], an <math>\alpha</math>-'''amino acid''' is an [[organic chemistry|organic]] [[monomer]] consisting of an [[amino group]], a [[carboxyl group]3 KB (443 words) - 21:24, 16 February 2010
- ...udolph Pariser]], (born 1923), [[theoretical chemistry|theoretical]] and [[organic chemistry|organic chemist]] *Richard Taylor, (1965-), Professor of Organic Chemistry, University of York.14 KB (1,549 words) - 05:42, 6 March 2024
- {{r|Organic chemistry}}4 KB (486 words) - 19:46, 11 January 2010
- ...]s and [[sewer]]s as a result of the [[bacteria|bacterial]] breakdown of [[Organic chemistry|organic matter]] in the absence of [[oxygen]], which is known as [[anaerobi6 KB (862 words) - 09:35, 6 March 2024
- ...mistry.'' Oxford University Press (2001), ISBN 0-19-850346-6.</ref> <ref>''Organic chemistry'' John McMurry 2nd Ed. ISBN 0534079687</ref>. The hybridisation theory finds its use mainly in organic chemistry, and mostly concerns C, N and O (and to a lesser extent P and S). Its expla14 KB (2,154 words) - 09:32, 12 November 2007
- ...r <b>dimethyl ketal</b>), is an aprotic colorless solvent widely used in organic chemistry reactions and the main ingredient in many fingernail polish removers. Beca5 KB (834 words) - 08:12, 15 March 2024
- ...ractions in living or semiliving (viruses) [[organism]]s. Biochemistry and organic chemistry are closely related, as in [[medicinal chemistry]], [[radiochemistry]] or [ ...ile simultaneously bonding with hydrogen or peripheral functional groups. Organic chemistry is of great commercial importance, providing the underpinnings for the lucr23 KB (3,309 words) - 09:41, 6 March 2024
- ...tion]]s in living or semi-living (viruses) [[organism]]s. Biochemistry and organic chemistry are closely related, as in [[medicinal chemistry]], [[radiochemistry]] or [ * [[Organic chemistry]] is the study of the structure, properties, composition, mechanisms, and r22 KB (3,143 words) - 09:41, 6 March 2024
- ...thin the molecules<ref name=Wilcox1984>Wilcox, C.F. (1984). ''Experimental Organic Chemistry, Theory and Practice''. Macmillan. pp. 81, 92-94, 114-115.</ref>.3 KB (475 words) - 17:57, 29 November 2010
- ...d college or university. Pre-studies required need to be in [[biology]], [[organic chemistry|organic]] and [[inorganic chemistry]], [[psychology]], and [[physics]]. Chi7 KB (978 words) - 07:31, 31 December 2007
- 3 KB (436 words) - 18:19, 24 May 2012
- ...molecules. Orbitals still play this role in introductory texts and also in organic chemistry, where orbitals serve in the explanation of some reaction mechanisms, for i10 KB (1,514 words) - 19:38, 20 November 2009
- In [[organic chemistry]], hydrocarbons may be classified into two categories, ''[[aromatic hydroca8 KB (1,213 words) - 11:30, 2 November 2010
- ...<ref>{{cite book|author=Dieter Hellwinkle|title=Systematic Nomenclature of Organic Chemistry|edition=1st Edition|publisher=Springer-Verlag|year=2001|id=ISBN 3-540-4113825 KB (3,880 words) - 09:42, 28 September 2013
- ...s exhibited ion exchange properties. Their work led them to synthesis of [[Organic chemistry|organic]] ion exchange resins with much better properties than any of the p11 KB (1,647 words) - 11:52, 2 February 2023
- Referring to Figure 3, the process mechanism involves [[adsorption]] of any [[Organic chemistry|organic compounds]] in the sewage or other wastewater by the layer of micro11 KB (1,588 words) - 10:16, 4 July 2023
- ...dium does not preclude translation to other media. Not that the medium of organic chemistry strays far from the underpinnings of its quantum chemical medium.17 KB (2,563 words) - 15:36, 28 June 2012
- ...called simply ether, and [[tetrahydrofuran]] (THF) are common solvents for organic chemistry reactions. Diethyl ether was one of the first anaesthetic agents. Many et4 KB (546 words) - 17:14, 31 October 2010
- ...erials science]] which includes researchers in [[chemistry]] (especially [[organic chemistry]]), [[physics]], and [[engineering]]. The field of polymer science include15 KB (2,117 words) - 16:45, 1 December 2009
- *'''Ascorbic acid''' is an [[organic chemistry|organic]] acid with [[antioxidant]] properties. Its appearance is white cr13 KB (1,893 words) - 10:07, 28 February 2024
- ...own compounds are molecular, a fact that is attributable to the scope of [[organic chemistry]].4 KB (657 words) - 11:36, 22 March 2024
- Organic Chemistry5 KB (781 words) - 13:22, 12 March 2007
- ...f>{{cite book|author=B.S. Furnis et al|title=Vogel's Textbook of Practical Organic Chemistry|edition=5th Edition|publisher=Longman Scientific|year=1989|id=ISBN 0-582-468 KB (1,273 words) - 23:39, 8 February 2010
- ...s — an [[organism]] synthesizes its own constituent, energy-rich ''[[Organic chemistry|organic]]'' compounds from ''[[Inorganic chemistry|inorganic]]'' starting m25 KB (3,545 words) - 17:36, 30 September 2018
- ...onance ([[NMR spectroscopy]]) spectroscopy is commonly used in synthetic [[organic chemistry]] and [[physical chemistry]] and for structural analysis in [[macromolecula ...n isotopic modification of a substrate. This is now a standard method in [[organic chemistry]]. Briefly, replacing normal hydrogen (protons) by deuterium within a chemi31 KB (4,881 words) - 12:55, 15 March 2024
- 5 KB (677 words) - 15:31, 11 December 2010