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  2. Thionyl chloride - Wikipedia

    en.wikipedia.org/wiki/Thionyl_chloride

    Thionyl chloride is an inorganic compound with the chemical formula SOCl 2.It is a moderately volatile, colourless liquid with an unpleasant acrid odour.Thionyl chloride is primarily used as a chlorinating reagent, with approximately 45,000 tonnes (50,000 short tons) per year being produced during the early 1990s, [5] but is occasionally also used as a solvent.

  3. von Braun amide degradation - Wikipedia

    en.wikipedia.org/wiki/Von_Braun_amide_degradation

    The von Braun amide degradation is the chemical reaction of a monosubstituted amide with phosphorus pentachloride or thionyl chloride to give a nitrile and an organohalide. [1] It is named after Julius Jacob von Braun, who first reported the reaction. [2] [3] The von Braun amide degradation

  4. Oxalyl chloride - Wikipedia

    en.wikipedia.org/wiki/Oxalyl_chloride

    It is also more expensive than thionyl chloride so it tends to be used on a smaller scale. This reaction involves conversion of N,N-dimethylformamide to the imidoyl chloride derivative (chloromethylene(dimethyl)ammonium ion (CH 3) 2 N + =CHCl), akin to the first stage in the Vilsmeier–Haack reaction. The imidoyl chloride is the active ...

  5. Quenching (fluorescence) - Wikipedia

    en.wikipedia.org/wiki/Quenching_(fluorescence)

    The chloride ion is a well known quencher for quinine fluorescence. [2] [3] [4] Quenching poses a problem for non-instant spectroscopic methods, such as laser-induced fluorescence. Quenching is made use of in optode sensors; for instance the quenching effect of oxygen on certain ruthenium complexes allows the measurement of oxygen saturation in

  6. Beckmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Beckmann_rearrangement

    The Beckmann rearrangement is often catalyzed by acid; however, other reagents have been known to promote the rearrangement. These include tosyl chloride, thionyl chloride, phosphorus pentachloride, phosphorus pentoxide, triethylamine, sodium hydroxide, trimethylsilyl iodide among others. [3]

  7. Thiophosgene - Wikipedia

    en.wikipedia.org/wiki/Thiophosgene

    The chlorination must be controlled as excess chlorine converts trichloromethanesulfenyl chloride into carbon tetrachloride. Steam distillation separates the trichloromethanesulfenyl chloride and hydrolyzes the disulfur dichloride. Reduction of trichloromethanesulfenyl chloride with, e.g., tin [2] or dihydroanthracene [3] produces thiophosgene:

  8. House Republicans could raise student loan bills to pay for ...

    www.aol.com/house-republicans-could-raise...

    GOP lawmakers are expected to use the budget reconciliation process to make major cuts to the federal budget. The savings from the student repayment plan overhaul would be $127.3 billion over 10 ...

  9. Thionyl group - Wikipedia

    en.wikipedia.org/wiki/Thionyl_group

    It occurs in compounds such as thionyl fluoride, SOF 2. Thionyl chloride , SOCl 2 , is a common reagent used in organic synthesis to convert carboxylic acids to acyl chlorides . In organic chemistry , the thionyl group is known as a sulfoxide group or sulfinyl group, and has the general structure RS(=O)R'.