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- ...cal Chemistry |year=2009|pages=297–319|issue=1 |volume=2 |title=Forensic Chemistry|pmid=20636064 |author=Bell S |doi=10.1146/annurev-anchem-060908-155251 |url [[Category:Chemistry]]9 KB (1,340 words) - 10:10, 20 September 2010
- ...irst= Kristi| title =Homogeneous| encyclopedia =Acids and Bases, Essential Chemistry. New York: Chelsea House Publishing.| publisher = Online publisher: ''Scien ...ever, it might be possible to see the particles under a [[microscope]]. In Chemistry, another homogeneous substance is [[air]]. It is equally suspended, and the3 KB (486 words) - 10:12, 20 September 2010
- ...ub>4</sub>]]) that are widely used in stoichiometric quantities in organic chemistry, but widely used organic reagents (such as [[oxalyl chloride]]) may belong [[Category:Organic chemistry]]7 members (0 subcategories, 0 files) - 10:16, 20 September 2010
- A '''scavenger''' in [[chemistry]] is a [[chemical substance]] added to a mixture in order to remove or inac ...ost common scavenger is the [[hydroxyl radical]], a short-lived [[radical (chemistry)|radical]] produced [[photolysis|photolytically]] in the atmosphere. It is2 KB (215 words) - 10:17, 20 September 2010
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- | subject = [[physical chemistry]]-related | category = Physical chemistry stubs234 bytes (22 words) - 10:24, 20 September 2010
- ...r [[salts]]) separate or split into smaller particles, ions, or [[Radical (chemistry)|radicals]], usually in a reversible manner. When a [[Bronsted-Lowry]] [[ac [[Fragmentation (chemistry)|Fragmentation]] of a molecule can take place by a process of [[heterolysis7 KB (979 words) - 20:17, 21 September 2010
- ...pplications include [[acid dissociation constant|acid-base]], [[Host-guest chemistry|host-guest]], [[stability constants of complexes|metal-complex]], [[solubil A [[Steady state (chemistry)|steady state]], on the other hand, is not necessarily an equilibrium state42 KB (6,675 words) - 20:17, 21 September 2010
- {{Portal|Chemistry}} {{DEFAULTSORT:Acid-Base Chemistry}}8 members (1 subcategory, 0 files) - 19:26, 27 September 2011
- |name = Organic chemistry |title = Concepts in [[organic chemistry]]717 bytes (65 words) - 22:18, 21 September 2010
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File:Protectionfactorchernobyl30cm.png ...cond edition of 'The radiochemical manual' and 'Radiochemistry and Nuclear Chemistry'(911 × 623 (2 KB)) - 22:10, 10 June 2010File:Protectionfactorchernobyl10cm.png ...cond edition of 'The radiochemical manual' and 'Radiochemistry and Nuclear Chemistry'(911 × 623 (2 KB)) - 19:51, 11 June 2010File:Protectionfactorchernobyl20cm.png ...cond edition of 'The radiochemical manual' and 'Radiochemistry and Nuclear Chemistry'(911 × 623 (2 KB)) - 19:55, 11 June 2010- * For chemistry structures use {{tl|PD-chem}}.1 KB (189 words) - 10:46, 12 June 2010
- Soap consists of sodium or potassium [[salt (chemistry)|salt]]s of fatty acids and is obtained by reacting common oils or fats wit ...p Dispersants, Raymond G. Bistline, Jr., in ''Anionic surfactants: organic chemistry'', Helmut Stache, ed., Volume 56 of Surfactant science series, CRC Press, 120 KB (3,140 words) - 22:41, 17 June 2010
- ..., and sometimes as technical avocation, in conjunction with an interest in chemistry or manufacturing.3 KB (402 words) - 21:24, 16 June 2010
- [[Category:Chemistry]]226 bytes (39 words) - 18:46, 23 June 2010
- [[Category:Chemistry]]2 KB (427 words) - 16:37, 24 June 2010
- ...extensive gas cleaning in order to remove or convert (i.e. to [[Cracking (chemistry)|"crack"]]) tars and particles. The removal of tar is often accomplished by11 KB (1,707 words) - 18:26, 24 June 2010
- | #default = {{#if:{{{IUPAC_name|}}} | [[IUPAC nomenclature of chemistry|Systematic]] (IUPAC) name }} | label4 = [[Chirality (chemistry)|Chirality]]32 KB (3,917 words) - 10:54, 17 June 2016
- ...lation of the alkaloid from natural sources. The first synthetic [[organic chemistry|organic]] [[dye]], [[mauveine]], was discovered by [[William Henry Perkin]] * [http://www.organic-chemistry.org/Highlights/2004/01November.shtm Catalytic Asymmetric Synthesis of Quini27 KB (3,844 words) - 16:41, 27 September 2010
- Mefloquine is a [[Chirality (chemistry)|chiral]] molecule with two [[asymmetric carbon]] centres, which means it h13 KB (1,807 words) - 16:41, 27 September 2010
- ==Chemistry==28 KB (3,682 words) - 16:42, 27 September 2010
- }}</ref> The [[mesylate]] [[salt (chemistry)|salt]] of DFO-B is commercially available.5 KB (714 words) - 20:14, 21 September 2010
- ...e affected enzyme's activity<ref>Goldman M, Dacre JC. (1989) Lewisite: its chemistry, toxicology, and biological effects. Rev Environ Contam Toxicol 110: 75-1155 KB (644 words) - 20:14, 21 September 2010
- ...]] manufacture.<ref name="holleman">Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. ISBN 0-12-352651-5</ref> In the laborato In analytical chemistry, the most important use comes from the fact that the thiosulfate anion reac12 KB (1,720 words) - 16:42, 27 September 2010
- ==Chemistry==16 KB (2,164 words) - 16:42, 27 September 2010
- == Chemistry == ...yces lincolnensis''. It is obtained by 7(''S'')-[[chloro]]-[[substitution (chemistry)|substitution]] of the 7(''R'')-[[hydroxyl]] group of lincomycin.<ref name=25 KB (3,261 words) - 14:17, 11 September 2010
- ...hanism of Action of Chloramphenicol ] July 1963. The Journal of Biological Chemistry)</ref>29 KB (3,876 words) - 16:42, 27 September 2010
- In 1981, Nobel laureate (1965 in chemistry) and Professor of Chemistry at [[Harvard University]] ([[Cambridge, MA]]) [[Robert Burns Woodward|Rober19 KB (2,731 words) - 17:52, 18 September 2010