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  2. 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]

  3. 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.

  4. 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]

  5. Disulfur - Wikipedia

    en.wikipedia.org/wiki/Disulfur

    Disulfur is the diatomic molecule with the formula S 2. [2] It is analogous to the dioxygen molecule but rarely occurs at room temperature. This violet gas is the dominant species in hot sulfur vapors.

  6. Sulfur tetrachloride - Wikipedia

    en.wikipedia.org/wiki/Sulfur_tetrachloride

    It decomposes above −30 °C (242 K) to sulfur dichloride and chlorine.. SCl 4 → SCl 2 + Cl 2. It hydrolyzes readily: SCl 4 + H 2 O → SOCl 2 + 2 HCl. Sulfur tetrachloride reacts with water, producing hydrogen chloride and sulfur dioxide through the hydrolysis process.

  7. Addition reaction - Wikipedia

    en.wikipedia.org/wiki/Addition_reaction

    In organic chemistry, an addition reaction is an organic reaction in which two or more molecules combine to form a larger molecule called the adduct. [1] [2] An addition reaction is limited to chemical compounds that have multiple bonds. Examples include a molecule with a carbon–carbon double bond (an alkene) or a triple bond (an alkyne).

  8. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    Substitution reactions in organic chemistry are classified either as electrophilic or nucleophilic depending upon the reagent involved, whether a reactive intermediate involved in the reaction is a carbocation, a carbanion or a free radical, and whether the substrate is aliphatic or aromatic. Detailed understanding of a reaction type helps to ...

  9. VSEPR theory - Wikipedia

    en.wikipedia.org/wiki/VSEPR_theory

    VSEPR theory is used to predict the arrangement of electron pairs around central atoms in molecules, especially simple and symmetric molecules. A central atom is defined in this theory as an atom which is bonded to two or more other atoms, while a terminal atom is bonded to only one other atom.