Chemical reaction which removes a hydrogen halide from a substrate
Dehydrohalogenation to give an alkene
In chemistry, dehydrohalogenation is an elimination reaction which removes a hydrogen halide from a substrate. The reaction is usually associated with the synthesis of alkenes, but it has wider applications.
and 22 Related for: Dehydrohalogenation information
In chemistry, dehydrohalogenation is an elimination reaction which removes a hydrogen halide from a substrate. The reaction is usually associated with...
polyacetylene. Short, irregular segments of polyacetylene can be obtained by dehydrohalogenation of poly(vinyl chloride). Thermal conversion of precursor polymers...
Sodium amide, commonly called sodamide (systematic name sodium azanide), is the inorganic compound with the formula NaNH2. It is a salt composed of the...
is a chemical compound formed by the loss of hydrogen chloride (dehydrohalogenation) from DDT, of which it is one of the more common breakdown products...
In organic chemistry, an epoxide is a cyclic ether, where the ether forms a three-atom ring: two atoms of carbon and one atom of oxygen. This triangular...
reacts in a coupling reaction with epichlorohydrin, followed by dehydrohalogenation. Epoxy resins produced from such epoxy monomers are called glycidyl-based...
amine to dichlorocarbene, a reactive intermediate generated by the dehydrohalogenation of chloroform. Two successive base-mediated dehydrochlorination steps...
formation of urethane foams and epoxy resins. It is also useful in dehydrohalogenation reactions and Swern oxidations. Triethylamine is readily alkylated...
well. In the presence of a strong base, alkyl chlorides undergo dehydrohalogenation to give alkenes or alkynes. Alkyl chlorides react with magnesium...
while iodine is the least reactive of them all. The facility of dehydrohalogenation follows the reverse trend: iodine is most easily removed from organic...
also been detected on the Moon. This compound may be made by the dehydrohalogenation of 1,4-dichloro-2-butyne by potassium hydroxide (in alcoholic medium)...
Base-induced bimolecular dehydrohalogenation (an E2 type reaction mechanism). The optimum geometry for the transition state requires the breaking bonds...
triflate). When an alkyl halide is used, the reaction is called a dehydrohalogenation. For unsymmetrical products, the more substituted alkenes (those...
diastereoisomer predominates). An example of modest stereoselectivity is the dehydrohalogenation of 2-iodobutane which yields 60% trans-2-butene and 20% cis-2-butene...
[Specific proton acceptors as auxiliary bases in alkylation and dehydrohalogenation reactions]. Chemische Berichte (in German). 91 (2). Wiley-VCH: 380–392...
cycloaddition with dichloro ketene diazomethane insertion reaction dehydrohalogenation reaction with DMF Luche reduction to alcohol with sodium borohydride...
isobutyryl chloride is the subject of many reported transformations. Dehydrohalogenation of isobutyryl chloride with triethylamine gives 2,2,4,4-tetramethylcyclobutanedione...
chloramine with the formula C5H10NCl. The resulting chloramine undergoes dehydrohalogenation to afford the cyclic imine. 13C NMR: (CDCl3, ppm) 47, 27.2, 25.2[citation...
palladium(0) to give allylpalladium chloride dimer, (C3H5)2Pd2Cl2. Dehydrohalogenation gives cyclopropene. Allyl chloride is highly toxic and flammable...
5-Pentanediol with 3-bromopropionyl chloride gives the corresponding ester; dehydrohalogenation of the ester with triethylamine then gives the bis-acrylate (2)....
is disrupted due them being readily protonated by HCl released by dehydrohalogenation of PVC.[citation needed] Zweifel, Hans; Maier, Ralph D.; Schiller...
Global Information