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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.
1,3-Dichloropropane; 2,2-Dichloropropane; See also. Dichloropropene This page was last edited on 28 June 2024, at 04:27 (UTC). Text is available under the ...
Protonolysis is the cleavage of a chemical bond by acids. Many examples are found in organometallic chemistry since the reaction requires polar M δ+-R δ-bonds, where δ+ and δ- signify partial positive and negative charges associated with the bonding atoms.
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.
The common mechanism is a free radical chain reaction, where the addition of oxygen gives rise to hydroperoxides and their associated peroxy radicals (ROO•). [5] Typically, an induction period is seen at the start where there is little activity; this is followed by a gradually accelerating take-up of oxygen, giving an autocatalytic reaction ...
1,3-Dichloropropane This page was last edited on 26 August 2022, at 19:57 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 License ...
1,3-Dichloropropane is a compound of chlorine, hydrogen, and carbon. It may be found as a contaminant in soil fumigants containing 1,3-dichloropropene. [2]