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  2. 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]

  3. Sulfonyl halide - Wikipedia

    en.wikipedia.org/wiki/Sulfonyl_halide

    Sulfonyl chlorides react with water to give the corresponding sulfonic acid: . RSO 2 Cl + H 2 O → RSO 3 H + HCl. These compounds react readily with many other nucleophiles as well, most notably alcohols and amines (see Hinsberg reaction).

  4. Nafion - Wikipedia

    en.wikipedia.org/wiki/Nafion

    The combination of fluorinated backbone, sulfonic acid groups, and the stabilizing effect of the polymer matrix make Nafion a very strong acid, with pK a ~ -6. [8] In this respect Nafion resembles the trifluoromethanesulfonic acid, CF 3 SO 3 H, although Nafion is a weaker acid by at least three orders of magnitude.

  5. Camphorsulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Camphorsulfonic_acid

    Camphorsulfonic acid, sometimes abbreviated CSA or 10-CSA is an organosulfur compound. Like typical sulfonic acids , it is a relatively strong acid that is a colorless solid at room temperature and is soluble in water and a wide variety of organic substances.

  6. Sulfamic acid - Wikipedia

    en.wikipedia.org/wiki/Sulfamic_acid

    Without the presence of any catalysts, sulfamic acid will not react with ethanol at temperatures below 100 °C. ROH + H 2 NSO 3 H → ROS(O) 2 O − + NH + 4. An example of this reaction is the production 2-ethylhexyl sulfate, a wetting agent used in the mercerisation of cotton, by combining sulfamic acid with 2-ethylhexanol.

  7. Benzenesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Benzenesulfonic_acid

    Benzenesulfonic acid (conjugate base benzenesulfonate) is an organosulfur compound with the formula C 6 H 6 O 3 S.It is the simplest aromatic sulfonic acid.It forms white deliquescent sheet crystals or a white waxy solid that is soluble in water and ethanol, slightly soluble in benzene and insoluble in nonpolar solvents like diethyl ether.

  8. 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.

  9. Methanesulfonic acid - Wikipedia

    en.wikipedia.org/wiki/Methanesulfonic_acid

    Methanesulfonic acid (MsOH, MSA) or methanesulphonic acid (in British English) is an organosulfuric, colorless liquid with the molecular formula CH 3 SO 3 H and structure H 3 C−S(=O) 2 −OH. It is the simplest of the alkylsulfonic acids ( R−S(=O) 2 −OH ).