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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]
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] SCl 2 + 2 C 2 H 4 → (ClC 2 H 4) 2 S
Energy densities table Storage type Specific energy (MJ/kg) Energy density (MJ/L) Peak recovery efficiency % Practical recovery efficiency % Arbitrary Antimatter: 89,875,517,874: depends on density: Deuterium–tritium fusion: 576,000,000 [1] Uranium-235 fissile isotope: 144,000,000 [1] 1,500,000,000
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
Toggle the table of contents. ... Molecular weight CAS No Helium-3: 3 He −269.96 ... Sulfuryl chloride fluoride: SO 2 ClF 7.1 −124.7 118.5
In inorganic chemistry, the sulfuryl group is a functional group consisting of a sulfur atom covalently bound to two oxygen atoms (S(=O) 2 X 2). It occurs in compounds such as sulfuryl chloride , SO 2 Cl 2 and sulfuryl fluoride , SO 2 F 2 .
The higher voltage drops back to 3.5 V soon as the bromine chloride gets consumed during the first 10–20% of the discharge. The cells with added bromine chloride are thought to be safer when abused. Li–SO 2 Cl 2 (IEC code: Y) Sulfuryl chloride: Lithium tetrachloroaluminate in sulfuryl chloride 3.7 V 3.95 V 330 720 Liquid cathode.
In the presence of aluminium chloride (AlCl 3), S 2 Cl 2 reacts with benzene to give diphenyl sulfide: 8 S 2 Cl 2 + 16 C 6 H 6 → 8 (C 6 H 5 ) 2 S + 16 HCl + S 8 Anilines (1) react with S 2 Cl 2 in the presence of NaOH to give 1,2,3-benzodithiazolium chloride (2) ( Herz reaction ) which can be transformed into ortho -aminothiophenolates (3 ...