Difference between revisions 6001545 and 6001546 on simplewiki

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User:Barras/Ferrocene
{{Chembox new
| ImageFileL1 = Ferrocene-2D.png
| ImageSizeL1 = 80 px
| ImageFileR1 = Ferrocene-3D-balls-B.png
| ImageSizeR1 = 120 px
| IUPACName = ferrocene, bis(η<sup>5</sup>-cyclopentadienyl)iron
| OtherNames = ferrocene, iron cyclopentadienyl 
| Section1 = {{Chembox Identifiers
(contracted; show full)

[[Image:Ferrocenelithiation.png|450px|thumb|center|A diagram showing the litiation of ferrocene with BuLi, and then the reactions of the dilithioferrocene with a series of electrophiles]]
⏎
 my name is omar

===Redox chemistry===
Unlike the majority of hydrocarbons, ferrocene undergoes a one-electron oxidation at a low potential, around 0.5 V ''vs''. a [[saturated calomel electrode]] (SCE). Some [[electron]] rich hydrocarbons (e.g., [[aniline]]) also are oxidized at low potentials, but only irreversibly. Oxidation of ferrocene gives a stable cation called ferrocenium. On a preparative scale, the oxidation is conveniently effected with FeCl<sub>3</sub> to give the blue-colored i(contracted; show full)[[pl:Ferrocen]]
[[ru:Ферроцен]]
[[fi:Ferroseeni]]
[[sv:Ferrocen]]
[[th:Ferrocene]]
[[tr:Ferrosen]]
[[ur:Ferrocene]]
[[zh:二茂铁]]