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  2. 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 ...

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

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

    The S 2 group is the same as the C i group in the nonaxial groups section. S n groups with an odd value of n are identical to C nh groups of same n and are therefore not considered here (in particular, S 1 is identical to C s). The S 8 table reflects the 2007 discovery of errors in older references. [4] Specifically, (R x, R y) transform not as ...

  4. Periodic table - Wikipedia

    en.wikipedia.org/wiki/Periodic_table

    The periodic table, also known as the periodic table of the elements, is an ordered arrangement of the chemical elements into rows ("periods") and columns ("groups"). It is an icon of chemistry and is widely used in physics and other sciences.

  5. Group (periodic table) - Wikipedia

    en.wikipedia.org/wiki/Group_(periodic_table)

    In the periodic table of the elements, each column is a group. In chemistry, a group (also known as a family) [1] is a column of elements in the periodic table of the chemical elements. There are 18 numbered groups in the periodic table; the 14 f-block columns, between groups 2 and 3, are not numbered.

  6. Sulfonyl group - Wikipedia

    en.wikipedia.org/wiki/Sulfonyl_group

    A sulfone. It consists of a sulfonyl group bonded with two organic substituents. In organosulfur chemistry, a sulfonyl group is either a functional group found primarily in sulfones, or a substituent obtained from a sulfonic acid by the removal of the hydroxyl group, similarly to acyl groups. [1]: 1470–1476

  7. Desulfonylation reactions - Wikipedia

    en.wikipedia.org/wiki/Desulfonylation_reactions

    The modest acidity of carbons adjacent to the sulfonyl group has made sulfones useful for organic synthesis. Upon removal of the sulfonyl group with desulfonylation or reductive elimination, the net result is the formation of a carbon-carbon bond single or double bond between two unfunctionalized carbons, a ubiquitous motif in synthetic targets.

  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. 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 ...