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  2. p-Toluenesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/P-Toluenesulfonic_acid

    p-Toluenesulfonic acid (PTSA, pTSA, or pTsOH) or tosylic acid (TsOH) is an organic compound with the formula CH 3 C 6 H 4 SO 3 H. It is a white extremely hygroscopic solid that is soluble in water, alcohols, and other polar organic solvents. [6] The CH 3 C 6 H 4 SO 2 group is known as the tosyl group and is often abbreviated as Ts or Tos.

  3. Tosyl group - Wikipedia

    en.wikipedia.org/wiki/Tosyl_group

    This group is usually derived from the compound tosyl chloride, CH 3 C 6 H 4 SO 2 Cl (abbreviated TsCl), which forms esters and amides of toluenesulfonic acid, CH 3 C 6 H 4 SO 2 OH (abbreviated TsOH). The para orientation illustrated (p-toluenesulfonyl) is most common, and by convention tosyl without a prefix refers to the p-toluenesulfonyl group.

  4. Pyridinium p-toluenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_p-toluenesulfonate

    Chemical formula. C 12 H 13 N O 3 S: Molar mass: ... Pyridinium p-toluenesulfonate (PPTS) is a colourless solid salt of pyridine and p-toluenesulfonic acid. Uses

  5. 4-Toluenesulfonyl chloride - Wikipedia

    en.wikipedia.org/wiki/4-Toluenesulfonyl_chloride

    4-Toluenesulfonyl chloride (p-toluenesulfonyl chloride, toluene-p-sulfonyl chloride) is an organic compound with the formula CH 3 C 6 H 4 SO 2 Cl. This white, malodorous solid is a reagent widely used in organic synthesis. [2] Abbreviated TsCl or TosCl, it is a derivative of toluene and contains a sulfonyl chloride (−SO 2 Cl) functional group.

  6. Sodium p-toluenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Sodium_p-toluenesulfonate

    Sodium p-toluenesulfonate is an organic compound with the formula CH 3 C 6 H 4 SO 3 Na. It is white, water-soluble solid. It is produced by the neutralization toluenesulfonic acid with sodium hydroxide. It is also a common product from the reactions of sodium-based reagents with toluenesulfonates. [1]

  7. Sulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Sulfonic_acid

    General structure of a sulfonic acid with the functional group indicated in blue. In organic chemistry, sulfonic acid (or sulphonic acid) refers to a member of the class of organosulfur compounds with the general formula R−S(=O) 2 −OH, where R is an organic alkyl or aryl group and the S(=O) 2 (OH) group a sulfonyl hydroxide. [1]

  8. Acid strength - Wikipedia

    en.wikipedia.org/wiki/Acid_strength

    Acid strength is the tendency of an acid, symbolised by the chemical formula, to dissociate into a proton, +, and an anion, . The dissociation or ionization of a strong acid in solution is effectively complete, except in its most concentrated solutions.

  9. Category:Benzenesulfonic acids - Wikipedia

    en.wikipedia.org/wiki/Category:Benzenesulfonic_acids

    P-Toluenesulfonic acid; 2,4,6-Trinitrobenzenesulfonic acid This page was last edited on 4 July 2017, at 13:28 (UTC). Text is available under the Creative Commons ...