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...to the removal of a [[sulfonyl]] group from [[organic compound]]s. As the sulfonyl functional group is [[electron]]-withdrawing,<ref>{{Cite book|last1=Kharasc ...presence of certain reducing agents, one of the sulfur-carbon bonds of the sulfonyl group is cleaved, leading to sulfur-free organic products. Depending on the ...

...hereas polychlorostyrene might be a small, multi-substituted molecule. End-groups are described with α- and ω-, e.g., α-chloro-ω-hydroxy-polystyrene.<ref nam ...ake up each of these structures are identified, i.e., the largest divalent groups that can be named using [[IUPAC nomenclature of organic chemistry]]. ...

...-]_\mathit{x}-(R^1_2N)_{3\!-\mathit{x}}P=NR2</chem> with preferably methyl groups as R¹, a [[methyl group]] or [[tert-butyl group|''tert''-butyl g ...]] to its very high [[steric hindrance]] and the involvement of many donor groups in conjugation with the spatially demanding structure of the cation formed ...

...ub>(2''x''−''y''+2)</sub>Cl_''y'' and are categorized into three groups: Low molecular weight chlorinated paraffins are short chain chloroparaffins ...duced into the reaction mixture. The products formed are [[Sulfonyl halide#Sulfonyl chlorides|alkylsulfonyl chlorides]], which are further processed into surfa ...

...[[ChemistryOpen]]|title=Organocatalyzed trifluormethylation of ketones and sulfonyl fluorides by fluoroform under a superbase system|volume=4|pages=581–585|dat ...