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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]
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.
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
The tables below provides information on the variation of solubility of different substances (mostly inorganic compounds) in water with temperature, at one atmosphere pressure. Units of solubility are given in grams of substance per 100 millilitres of water (g/100 ml), unless shown otherwise.
Further heating (180 °C) of potassium fluorosulfite with the sulfuryl chloride fluoride gives sulfuryl fluoride. KSO 2 F + SO 2 ClF → SO 2 F 2 + KCl + SO 2. Alternatively, sulfuryl chloride fluoride can be prepared without using gases as starting materials by treating sulfuryl chloride with ammonium fluoride or potassium fluoride in ...
Table of specific heat capacities at 25 °C (298 K) unless otherwise noted. [citation needed] Notable minima and maxima are shown in maroon. Substance Phase Isobaric mass heat capacity c P J⋅g −1 ⋅K −1 Molar heat capacity, C P,m and C V,m J⋅mol −1 ⋅K −1 Isobaric volumetric heat capacity C P,v J⋅cm −3 ⋅K −1 Isochoric ...
CSI is prepared by treating cyanogen chloride with sulfur trioxide, the product being distilled directly from the reaction mixture. [1] SO 3 + ClCN → ClSO 2 NCO. In this transformation, both the carbon and the nitrogen termini of CN are functionalized. The structure of CSI is represented as ClS(O) 2-N=C=O.
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