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- [[Category:Alkenes]]27 KB (3,844 words) - 16:41, 27 September 2010
- [[Category:Alkenes]]33 KB (4,541 words) - 10:57, 17 June 2016
- [[Category:Alkenes]]40 KB (5,581 words) - 16:45, 27 September 2010
- Processes have been developed to prepare copolymers of alkenes containing carbonyl groups so they will be more susceptible to photolytic c68 KB (9,959 words) - 10:10, 20 September 2010
- ...-Natta catalysts developed for the polymerization of propylene and other 1-alkenes to isotactic polymers usually use TiCl<sub>4</sub> as an active ingredient25 KB (3,657 words) - 10:10, 20 September 2010
- [[Category:Alkenes]]9 KB (1,206 words) - 10:11, 20 September 2010
- *[[Alkenes]] (olefins) which can be manufactured into [[plastics]] or other compounds69 KB (9,885 words) - 10:12, 20 September 2010
- [[Category:Alkenes]]1 KB (142 words) - 13:11, 20 September 2010
- |url = http://www.chemguide.co.uk/organicprops/alkenes/epoxyethane.html |work = Alkenes menu82 KB (11,709 words) - 21:31, 20 September 2010
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45 KB (6,444 words) - 21:33, 20 September 2010
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34 KB (4,726 words) - 21:35, 20 September 2010
- ...philic additions reactions, the most notable one being the chlorination of alkenes and aromatic compounds with a Lewis acid catalyst. Organic chlorine compoun36 KB (5,155 words) - 21:35, 20 September 2010
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5 KB (765 words) - 20:14, 21 September 2010
- ...omogeneous Catalysis. 1. Hydrogenation and Hydroformylation of Alkynes and Alkenes Assisted by Organorhodium Complexes with [{MeC(CH<sub>2</sub>PPh<sub>2</sub4 KB (589 words) - 20:15, 21 September 2010
- ...up>, N<sub>2</sub>², halogen-carbon bond formation,³ polymerization of [[alkenes]]<sup>4,5</sup> and [[alkynes]]<sup>6</sup>, [[alkane dehydrogenation]]<sup5 KB (747 words) - 20:18, 21 September 2010
- The hydroformylation of alkenes to give aldehydes is important : almost 6 million tons of aldehydes are pro12 KB (1,706 words) - 20:18, 21 September 2010
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25 KB (3,607 words) - 20:18, 21 September 2010
- *Organometallic Chemistry: Ligands are organic (alkenes, alkynes, alkyls) as well as "organic-like" ligands such as phosphines, hyd25 KB (3,677 words) - 20:18, 21 September 2010
- [[Category:Alkenes]]2 KB (284 words) - 21:29, 21 September 2010
- [[Category:Alkenes]]12 KB (1,566 words) - 22:09, 21 September 2010
- [[Category:Alkenes]]2 KB (244 words) - 22:17, 21 September 2010
- ====From alkenes====16 KB (2,099 words) - 21:00, 24 September 2010
- {{Alkenes}} [[Category:Alkenes]]32 KB (4,462 words) - 21:01, 24 September 2010
- [[Category:Alkenes]]3 KB (345 words) - 21:01, 24 September 2010
- [[Category:Alkenes]]33 KB (4,639 words) - 21:02, 24 September 2010
- [[Category:Alkenes]]9 KB (1,251 words) - 21:02, 24 September 2010
- ...dition]] chloroform forms the CHCl<sub>2</sub> free radical in addition to alkenes.21 KB (2,827 words) - 21:03, 24 September 2010
- ...e.co.uk/organicprops/alkenes/hydrogenation.html|title=The Hydrogenation of Alkenes:Margarine Manufacture|last=Claek|first=Jim|work=Chemguide:Helping you to un39 KB (5,789 words) - 19:39, 13 October 2010