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  2. Sulfuryl chloride - Wikipedia

    en.wikipedia.org/wiki/Sulfuryl_chloride

    Sulfuryl chloride is used as a source of Cl 2.Because it is a pourable liquid, it is considered more convenient than Cl 2 to dispense.. Sulfuryl chloride is used in the conversion of C−H to C−Cl adjacent to activating substituents such as carbonyls and sulfoxides: [5] [6]

  3. 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.

  4. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Lewis structure of a water molecule. Lewis structures – also called Lewis dot formulas, Lewis dot structures, electron dot structures, or Lewis electron dot structures (LEDs) – are diagrams that show the bonding between atoms of a molecule, as well as the lone pairs of electrons that may exist in the molecule.

  5. Disulfur dichloride - Wikipedia

    en.wikipedia.org/wiki/Disulfur_dichloride

    Disulfur dichloride is a yellow liquid that fumes in moist air due to reaction with water: 16 S 2 Cl 2 + 16 H 2 O → 8 SO 2 + 32 HCl + 3 S 8. It is produced by partial chlorination of elemental sulfur.

  6. Sulfur dioxide - Wikipedia

    en.wikipedia.org/wiki/Sulfur_dioxide

    A valence bond theory approach considering just s and p orbitals would describe the bonding in terms of resonance between two resonance structures. Two resonance structures of sulfur dioxide. The sulfur–oxygen bond has a bond order of 1.5. There is support for this simple approach that does not invoke d orbital participation. [11]

  7. Sulfur dichloride - Wikipedia

    en.wikipedia.org/wiki/Sulfur_dichloride

    SCl 2 is used in organic synthesis.It adds to alkenes to give chloride-substituted thioethers. Illustrative is its addition to 1,5-cyclooctadiene to give a bicyclic thioether [2] A well tested method for the production of the mustard gas bis(2-chloroethyl)sulfide, is the addition of ethylene to sulfur dichloride: [3]

  8. Sulfuryl chloride fluoride - Wikipedia

    en.wikipedia.org/wiki/Sulfuryl_chloride_fluoride

    The laboratory-scale synthesis begins with the preparation of potassium fluorosulfite: [2]. SO 2 + KF → KSO 2 F. This salt is then chlorinated to give sulfuryl chloride fluoride [3]

  9. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    In chemistry, halogenation is a chemical reaction which introduces one or more halogens into a chemical compound. Halide-containing compounds are pervasive, making this type of transformation important, e.g. in the production of polymers, drugs. [1]