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Structural isomer
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==Position isomerism (regioisomerism)<span class="anchor" id="Regioisomer"></span>== <!-- Section linked from more than 60 articles --> {{see also|Arene substitution pattern#Ortho, meta, and para substitution}} '''Position isomers''' (also '''positional isomers''' or '''regioisomers''') are structural isomers that can be viewed as differing only on the position of a [[functional group]], [[substituent]], or some other feature on the same "parent" structure.<ref name=stok2015/> For example, replacing one of the 12 hydrogen atoms βH by a [[Alcohol (chemistry)|hydroxyl]] group βOH on the [[pentane|''n''-pentane]] parent molecule can give any of three different position isomers: {| align="center" class="skin-invert-image" |- | [[File:Pentan-1-ol-pos.png|180px]] | [[File:Pentan-2-ol-pos.png|180px]] | [[File:Pentan-3-ol-pos.png|180px]] |- | style="padding-left:20px;padding-right:20px;text-align:center;" | [[Pentan-1-ol]] | style="padding-left:20px;padding-right:20px;text-align:center;" | [[Pentan-2-ol]] | style="padding-left:20px;padding-right:20px;text-align:center;" | [[Pentan-3-ol]] |} Another example of regioisomers are [[Ξ±-Linolenic acid|Ξ±-linolenic]] and [[Ξ³-linolenic acid]]s, both [[octadecatrienoic acid]]s, each of which has three double bonds, but on different positions along the chain.
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