Chlorine functional group

It IS convenient m equations such as this to represent generic alcohols and alkyl halides as ROH and RX respectively where R stands for an alkyl group In addition to con venience this notation lets us focus more clearly on the functional group transformation that occurs the OH functional group of an alcohol is replaced as a substituent on car bon by a halogen usually chlorine (X = Cl) or bromine (X = Br)... 

Chlorination is carried out m a manner similar to brommation and provides a ready route to chlorobenzene and related aryl chlorides Fluormation and lodmation of benzene and other arenes are rarely performed Fluorine is so reactive that its reaction with ben zene is difficult to control lodmation is very slow and has an unfavorable equilibrium constant Syntheses of aryl fluorides and aryl iodides are normally carried out by way of functional group transformations of arylammes these reactions will be described m Chapter 22... 

Substitution. Substitution products retain the same nuclear configuration as naphthalene. They are formed by the substitution of one or more hydrogen atoms with other functional groups. Substituted naphthalenes of commercial importance have been obtained by sulfonation, sulfonation and alkah fusion, alkylation, nitration and reduction, and chlorination. 

Carbon Cha.in Backbone Polymers. These polymers may be represented by (4) and considered derivatives of polyethylene, where n is the degree of polymeriza tion and R is (an alkyl group or) a functional group hydrogen (polyethylene), methyl (polypropylene), carboxyl (poly(acryhc acid)), chlorine (poly(vinyl chloride)), phenyl (polystyrene) hydroxyl (poly(vinyl alcohol)), ester (poly(vinyl acetate)), nitrile (polyacrylonitrile), vinyl (polybutadiene), etc. The functional groups and the molecular weight of the polymers, control thek properties which vary in hydrophobicity, solubiUty characteristics, glass-transition temperature, and crystallinity. 

Deep fluorinalion of alkanes, ethers, acid fmlides, esters, alkyl chlorides, most ketones, ketals, orthoesters, and combinations of these functional groups produces principally the perfluonnated analogues (Table 2) Chlorine substituents (or chloro groups) usually survive fluorination... 

Although allylic brorninations and chlorinations offer a method for attaching a reactive functional group to a hydrocarbon framework, we need to be aware of two important limitations. For allylic halogenation to be effective in a particular- synthesis ... 

The Lead-Off Reaction Addition of HBr to Alkenes Students usually attach great-importance to a text s lead-off reaction because it is the first reaction they see and is discussed in such detail. 1 use the addition of HBr to an alkene as the lead-off to illustrate general principles of organic chemistry for several reasons the reaction is relatively straightforward it involves a common but important functional group no prior knowledge of stereochemistry or kinetics in needed to understand it and, most important, it is a polar reaction. As such, 1 believe that electrophilic addition reactions represent a much more useful and realistic introduction to functional-group chemistry than a lead-off such as radical alkane chlorination. 

Functional groups are either attached to the carbon backbone of a molecule or form part of that chain. Examples are the chlorine atom in chloroethane, CH3CH2CI, and the OFF group in ethanol, CFF CI OFi. Carbon-carbon multiple bonds, such as the double bond in 2-butene, are also often considered functional groups. Table 19.1 lists the most common functional groups. Double and triple carbon-carbon bonds were considered in Chapter 18. In the following eight... 

Linear polysiloxanes containing terminal function groups such as alkoxy groups, chlorine atoms are technically prepared by equilibration of cyclic polysiloxanes with functional silicone compounds291. ... 

The reactions of the six-membered chlorocyclophosphazene were studied with a number of aliphatic diamines (169 175), aromatic diamines (176), aliphatic diols (177-179), aromatic diols (180,181) and compounds containing amino and hydroxyl functional groups (169,170,182). This subject has been reviewed (11,16,20). There are at least five different reaction products that are possible (Fig. 19). Replacement of two chlorine atoms from the same phosphorus atom produces a spirocyclic product. Replacement of two chlorine atoms from two different phosphorus atoms in the same molecule produces an ansa product. Reaction of only one end of the difunctional reagent, resulting in the substitution of only one chlorine atom, leads to an open-chain compound. Intermolecular bridged compounds are formed when the difunc-... 

Polycondensation of difunctional oligomeric cyclodisilazanes with a,co-dihydroxypolysiloxanes proved to be another successful attempt to synthesize silazane modified polysiloxanes of improved thermostability. The cyclodisilazane oligomers IHa (see scheme below) are readily available from common and cheap materials, dichlorodimethylsilane and ammonia (fi). The chlorine atoms in these compounds can be easily exchanged to other functional groups, such as amino, hydroxyl, etc. 

Both the approaches discussed above are addressed to the desire for immobilization of the metal species, while the corrosive and volatile promoter must still be trapped and recycled. Recently, Webber et al. (28) have attempted to achieve immobilization of both the metal species and the promoter by attaching rhodium to a polymer functionalized with chlorinated thiophenol groups. This imaginative approach is presently plagued by both low reactivity and rhodium loss from the polymer surface. 

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