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  2. 4-Toluenesulfonyl chloride - Wikipedia

    en.wikipedia.org/wiki/4-Toluenesulfonyl_chloride

    Being a widely available reagent, TsCl has been heavily examined from the perspective of reactivity. It is used in dehydrations to make nitriles, isocyanides and diimides. [2] In an unusual reaction focusing on the sulfur center, zinc reduces TsCl to the sulfinate, CH 3 C 6 H 4 SO 2 Na. [4]

  3. Tosyl group - Wikipedia

    en.wikipedia.org/wiki/Tosyl_group

    Tosyl group (blue) with a generic "R" group attached Tosylate group with a generic "R" group attached. Note the extra oxygen, compared to plain tosyl. In organic chemistry, a toluenesulfonyl group (tosyl group, abbreviated Ts or Tos [nb 1]) is a univalent functional group with the chemical formula −SO 2 −C 6 H 4 −CH 3.

  4. Trimethylsilyl chloride - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilyl_chloride

    TMSCl is reactive toward nucleophiles, resulting in the replacement of the chloride. In a characteristic reaction of TMSCl, the nucleophile is water, resulting in hydrolysis to give the hexamethyldisiloxane: + + The related reaction of trimethylsilyl chloride with alcohols can be exploited to produce anhydrous solutions of hydrochloric acid in alcohols, which find use in the mild synthesis of ...

  5. Beckmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Beckmann_rearrangement

    Beckmann reaction. The reaction mechanism for this reaction is based on a catalytic cycle with cyanuric chloride activating the hydroxyl group via a nucleophilic aromatic substitution. The reaction product is dislodged and replaced by new reactant via an intermediate Meisenheimer complex. Beckmann cyanuric acid cataly cycle

  6. Neber rearrangement - Wikipedia

    en.wikipedia.org/wiki/Neber_rearrangement

    The oxime is first converted to an O-sulfonate, for example a tosylate by reaction with tosyl chloride. Added base forms a carbanion which displaces the tosylate group in a nucleophilic displacement to an azirine and added water subsequently hydrolyses it to the aminoketone. The Beckmann rearrangement is a side reaction. [4]

  7. Ritter reaction - Wikipedia

    en.wikipedia.org/wiki/Ritter_reaction

    The Ritter reaction (sometimes called the Ritter amidation) is a chemical reaction that transforms a nitrile into an N-alkyl amide using various electrophilic alkylating reagents. The original reaction formed the alkylating agent using an alkene in the presence of a strong acid .

  8. Projected COLA for 2025: September update — how it's ...

    www.aol.com/finance/social-security-cost-of...

    TSCL’s projection decreased from 2.57%, when July's CPI-W came in at 2.9%. According to The Senior Citizens League But remember, this is only an estimate of potential COLA increases for 2025.

  9. Swern oxidation - Wikipedia

    en.wikipedia.org/wiki/Swern_oxidation

    The reaction conditions allow oxidation of acid-sensitive compounds, which might decompose under the acidic oxidation conditions such as Jones oxidation. For example, in Thompson & Heathcock's synthesis of the sesquiterpene isovelleral, [ 15 ] the final step uses the Swern protocol, avoiding rearrangement of the acid-sensitive ...