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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

* Clayden J, Greeves N, Warren S., Wothers,P. ''Organic Chemistry'' 2000 (Oxford University Press) ISBN 0-19-850346-6

{{r|IUPAC nomenclature of organic chemistry}}

{{r|Organic chemistry}}

...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]]

...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

...ry]], [[thermodynamics]], [[electromagnetic force|electromagnetism]] and [[organic chemistry]]. His work on the size of molecules was sufficiently important that in Ger

{{r|Organic chemistry}}

{{r|Organic chemistry}}

{{r|Organic chemistry}}

...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

{{r|Organic chemistry}}

...]] &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]]

...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

...b>, is a pungent toxic chemical widely used as a chlorination reagent in [[organic chemistry]]. It has many synonyms, including thionyl dichloride, sulfurous oxychlorid

...ll organic matter. [[Diamond]], [[graphite]], and [[fullerene]]s are non-[[Organic chemistry|organic]] compounds consisting of carbon only; these are known as [[allotro

{{r|Organic chemistry}}

...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

...Inorganic chemistry|inorganic compounds]]. With the massive expansion of [[organic chemistry]] in the mid-nineteenth century and the greater understanding of the struct