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1,2-Dichloropropane is an intermediate in the production of perchloroethylene and other chlorinated chemicals. [4] It was once used as a soil fumigant, chemical intermediate, as well as an industrial solvent and was found in paint strippers, varnishes, and furniture finish removers but some of these uses have been discontinued.
1,3-Dichloropropene, sold under diverse trade names, is an organochlorine compound with the formula C 3 H 4 Cl 2. It is a colorless liquid with a sweet smell. It is a colorless liquid with a sweet smell.
At lower temperatures, the main product is 1,2-dichloropropane, but at 500 °C, allyl chloride predominates, being formed via a free radical reaction: CH 3 CH=CH 2 + Cl 2 → ClCH 2 CH=CH 2 + HCl An estimated 800,000 tonnes were produced this way in 1997.
1,2-Dichloropropane; 1,3-Dichloropropane; 2,2-Dichloropropane; See also. Dichloropropene This page was last edited on 28 June 2024, at 04:27 (UTC). Text is ...
Indeed, they would necessarily occupy disjoint volumes of space. The mixing of the products and reactants contributes a large entropy increase (known as entropy of mixing) to states containing equal mixture of products and reactants and gives rise to a distinctive minimum in the Gibbs energy as a function of the extent of reaction. [7]
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An example of a solvolysis reaction is the reaction of a triglyceride with a simple alcohol such as methanol or ethanol to give the methyl or ethyl esters of the fatty acid, as well as glycerol. This reaction is more commonly known as a transesterification reaction due to the exchange of the alcohol fragments.