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  2. Sulfonyl group - Wikipedia

    en.wikipedia.org/wiki/Sulfonyl_group

    Sulfonyl groups can be written as having the general formula R−S(=O) 2 −R′, where there are two double bonds between the sulfur and oxygen. [1]: 53 [2] Sulfonyl groups can be reduced to the sulfide with diisobutylaluminium hydride (DIBALH). Lithium aluminium hydride (LiAlH 4) reduces some but not all sulfones to sulfides. [1]: 1851

  3. List of character tables for chemically important 3D point groups

    en.wikipedia.org/wiki/List_of_character_tables...

    These groups are characterized by i) an n-fold proper rotation axis C n; ii) n 2-fold proper rotation axes C 2 normal to C n; iii) a mirror plane σ h normal to C n and containing the C 2 s. The D 1h group is the same as the C 2v group in the pyramidal groups section. The D 8h table reflects the 2007 discovery of errors in older references. [4]

  4. Vinyl sulfone dyes - Wikipedia

    en.wikipedia.org/wiki/Vinyl_sulfone_dyes

    The vinylsulfone group reacts with the nucleophilic functional groups of the fibers by Michael addition to form a covalent ether bond: Reaction of vinyl sulfone compounds with hydroxyl groups of cellulose (HO-CELL) An unfavorable side reaction in the dyeing process is the conversion of the vinylsulfone group to the 2-(hydroxy)ethylsulfonyl ...

  5. Category:Sulfonyl groups - Wikipedia

    en.wikipedia.org/wiki/Category:Sulfonyl_groups

    Pages in category "Sulfonyl groups" The following 10 pages are in this category, out of 10 total. This list may not reflect recent changes. * Sulfonyl group; B.

  6. Sulfonyl halide - Wikipedia

    en.wikipedia.org/wiki/Sulfonyl_halide

    In chemistry, a sulfonyl halide consists of a sulfonyl (>S(=O) 2) group singly bonded to a halogen atom. They have the general formula RSO 2 X, where X is a halogen. The stability of sulfonyl halides decreases in the order fluorides > chlorides > bromides > iodides, all four types being well known. The sulfonyl chlorides and fluorides are of ...

  7. Sulfone - Wikipedia

    en.wikipedia.org/wiki/Sulfone

    Sulfone is a relatively inert functional group, typically less oxidizing and 4 bel more acidic than sulfoxides. In the Ramberg–Bäcklund reaction and the Julia olefination, sulfones are converted to alkenes by the elimination of sulfur dioxide. [13] However, sulfones are unstable to bases, eliminating to give an alkene. [14]

  8. Thiol - Wikipedia

    en.wikipedia.org/wiki/Thiol

    The −SH functional group itself is referred to as either a thiol group or a sulfhydryl group, or a sulfanyl group. Thiols are the sulfur analogue of alcohols (that is, sulfur takes the place of oxygen in the hydroxyl ( −OH ) group of an alcohol), and the word is a blend of " thio- " with "alcohol".

  9. IUPAC nomenclature of chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    IUPAC states that, "As one of its major activities, IUPAC develops Recommendations to establish unambiguous, uniform, and consistent nomenclature and terminology for specific scientific fields, usually presented as: glossaries of terms for specific chemical disciplines; definitions of terms relating to a group of properties; nomenclature of chemical compounds and their classes; terminology ...