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Difluoroethene
Difluoroethene or Difluoroethylene can refer to any one of several isomeric forms of the organochloride with the molecular formula C2H2F2: There are three isomers: * 1,1-Difluoroethene * 1,2-Difluoroethene (''E'' and ''Z'') See also *Difluoroethane *Dichloroethene Dichloroethene or dichloroethylene, often abbreviated as DCE, can refer to any one of several isomeric forms of the organochloride with the molecular formula C2H2Cl2: There are three isomers: * 1,1-Dichloroethene *1,2-Dichloroethene (''E'' and ''Z' ... {{Chemistry index Organofluorides Haloalkenes ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
1,1-Difluoroethene
1,1-Difluoroethylene, also known as vinylidene fluoride, is a hydrofluoroolefin. It is a flammable gas. Global production in 1999 was approximately 33,000 metric tons. It is primarily used in the production of fluoropolymers such as polyvinylidene fluoride. Preparation 1,1-Difluoroethylene can be prepared by elimination reaction from a 1,1,1-trihaloethane compound, for example, loss of hydrogen chloride from 1-chloro-1,1-difluoroethane:. : or loss of hydrogen fluoride from 1,1,1-trifluoroethane: : See also * 1,2-Difluoroethylene *Perfluoroisobutene Perfluoroisobutene (PFIB) is the perfluorocarbon counterpart of the hydrocarbon isobutene and has the formula (CF3)2C=CF2. An alkene, it is a colorless gas that is notable as a highly toxic perfluoroalkene. Few simple alkenes are as toxic. Safet ... References {{DEFAULTSORT:Difluoroethylene, 1, 1- Organofluorides Vinylidene compounds ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Difluoroethane
Difluoroethane may refer to: * 1,1-Difluoroethane * 1,2-Difluoroethane See also * Difluoroethene * Dichloroethane Dichloroethane can refer to either of two isomeric organochlorides with the molecular formula C2H4Cl2: * 1,1-Dichloroethane (ethylidene chloride) * 1,2-Dichloroethane (ethylene dichloride) See also *Dichloroethene *Difluoroethane Difluoroethane m ... {{Short pages monitor ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Isomer
In chemistry, isomers are molecules or polyatomic ions with identical molecular formulae – that is, same number of atoms of each element – but distinct arrangements of atoms in space. Isomerism is existence or possibility of isomers. Isomers do not necessarily share similar chemical or physical properties. Two main forms of isomerism are structural or constitutional isomerism, in which ''bonds'' between the atoms differ; and stereoisomerism or spatial isomerism, in which the bonds are the same but the ''relative positions'' of the atoms differ. Isomeric relationships form a hierarchy. Two chemicals might be the same constitutional isomer, but upon deeper analysis be stereoisomers of each other. Two molecules that are the same stereoisomer as each other might be in different conformational forms or be different isotopologues. The depth of analysis depends on the field of study or the chemical and physical properties of interest. The English word "isomer" () is a back-for ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Organochloride
An organochloride, organochlorine compound, chlorocarbon, or chlorinated hydrocarbon is an organic compound containing at least one covalent bond, covalently bonded atom of chlorine. The chloroalkane class (alkanes with one or more hydrogens substituted by chlorine) provides common examples. The wide structural variety and divergent chemical properties of organochlorides lead to a broad range of names, applications, and properties. Organochlorine compounds have wide use in many applications, though some are of profound environmental concern, with 2,3,7,8-Tetrachlorodibenzodioxin, TCDD being one of the most notorious. Physical and chemical properties Chlorination reaction, Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular dam ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Dichloroethene
Dichloroethene or dichloroethylene, often abbreviated as DCE, can refer to any one of several isomeric forms of the organochloride with the molecular formula C2H2Cl2: There are three isomers: *1,1-Dichloroethene *1,2-Dichloroethene (''E'' and ''Z'') See also *Dichloroethane Dichloroethane can refer to either of two isomeric organochlorides with the molecular formula C2H4Cl2: * 1,1-Dichloroethane (ethylidene chloride) * 1,2-Dichloroethane (ethylene dichloride) See also *Dichloroethene *Difluoroethane Difluoroethane m ... {{Chemistry index Organochlorides Haloalkenes ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Organofluorides
Organofluorine chemistry describes the chemistry of the organofluorines, organic compounds that contain the carbon–fluorine bond. Organofluorine compounds find diverse applications ranging from Lipophobicity, oil and hydrophobe, water repellents to pharmaceuticals, refrigerants, and reagents in catalysis. In addition to these applications, some organofluorine compounds are pollutants because of their contributions to ozone depletion, global warming, bioaccumulation, and toxicity. The area of organofluorine chemistry often requires special techniques associated with the handling of fluorinating agents. The carbon–fluorine bond Fluorine has several distinctive differences from all other substituents encountered in organic molecules. As a result, the physical and chemical properties of organofluorines can be distinctive in comparison to other organohalogens. # The carbon–fluorine bond is one of the strongest in organic chemistry (an average bond energy around 480 kJ/molKirsch ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
