Chlorides nomenclature

Recently, a three-component 1,2,4-triazole synthesis involving Nef-Huisgen cascade was developed." Thus addition of acyl chloride 22 to isocyanide 23 (Nef reaction) generated the imidoyl chloride [nomenclature... 

Sulfonyl chloride 178 also has the common name oimesyl chloride. Another very common derivative is 4-methylbenzenesulfonyl chloride (179), also called />am-toluenesulfonyl chloride, which is also called tosyl chloride) (nomenclature for benzene-containing compounds is discussed in Chapter 21). This particular compound is introduced here because it so common and clearly fits into this section. Thionyl bromide (SOBrg) converts sulfonic acids to the corresponding sulfonyl bromide. This reaction is exactly analogous to the reactions with carboxylic acids. 

The lUPAC rules permit alkyl halides to be named m two different ways called func twnal class nomenclature and substitutive nomenclature In functional class nomencla ture the alkyl group and the halide (fluoride chloride bromide or iodide) are desig nated as separate words The alkyl group is named on the basis of its longest continuous chain beginning at the carbon to which the halogen is attached... 

This chapter concerns the preparation and reactions of acyl chlorides acid anhydrides thioesters esters amides and nitriles These com pounds are generally classified as carboxylic acid derivatives and their nomenclature is based on that of carboxylic acids... 

Berzehus (19) further appHed and amplified the nomenclature introduced by Guyton de Morveau and Lavoisier. It was he who divided the elements into metalloids (nonmetals) and metals according to their electrochemical character, and the compounds of oxygen with positive elements (metals) into suboxides, oxides, and peroxides. His division of the acids according to degree of oxidation has been Httie altered. He introduced the terms anhydride and amphoteric and designated the chlorides in a manner similar to that used for the oxides. 

The Stock Oxidation-Number System. Stock sought to correct many nomenclature difficulties by introducing Roman numerals in parentheses to indicate the state(s) of oxidation, eg, titanium(II) chloride for TiCl2, iron(II) oxide for FeO, titanium(III) chloride for TiCl, iron(III) oxide for Fe203, titanium(IV) chloride for TiCl, and iron(II,III) oxide for Fe O. In this system, only the termination -ate is used for anions, followed by Roman numerals in parentheses. Examples are potassium manganate(IV) for K2Mn02, potassium tetrachloroplatinate(II) for K PtCl, and sodium hexacyanoferrate(III) for Na3Fe(CN)3. Thus a set of prefixes and terminations becomes uimecessary. 

The nomenclature of macromolecules can be compHcated when there is Httle or no regularity in the molecules for such molecules, the stmctural details may also be uncertain. In cases where the macromolecule is a polymeric chain with some uncertainties about regularity in its stmcture, a simple expedient is to name the polymer after the monomer that gave rise to it. Thus there are source-based names such as poly(vinyl chloride). 

In the/flc isomer, the three chloride ions are located on the corners of one of the triangular faces of the octahedron. In the mer isomer, the three chloride ions are located around an edge (meridian) of the octahedron. The IUPAC system of nomenclature does not use this approach. A summary of the IUPAC procedures is presented in the book by Huheey, Keiter, and Keiter that is cited in the references listed at the end of this chapter. 

The prefix (RS) is used to denote a racemic modification. For example, (RS)-Sec butyl chloride. The symbols R and S are applied to compounds whose absolute stereochemistry has been determined. However, while applying the nomenclature to projection formulae of compounds containing several asymmetric centres Cahn, Ingold. Pielog procedures are supplemented by the following conversion rule. 

Section 7.8). Other classes of derivatives are thus most conveniently prepared from the sulfonyl chloride. Reaction with an alcohol leads to formation of a sulfonate ester. Two common sulfonyl chloride reagents employed to make sulfonate esters from alcohols arep-toluenesulfonyl chloride, known as tosyl chloride, and methanesulfonyl chloride, known as mesyl chloride (see Section 6.1.4). Note the nomenclature tosyl and mesyl for these groups, which may be abbreviated to Ts and Ms respectively. 

In Chapter 9 you see the basic structure of each of the carboxylic acids and Ccirboxylic acid derivatives. In this chapter we focus on the carboxylic acids and related compounds, such as esters, acyl chlorides, and acid anhydrides, and we also include some information on amides (see Chapter 13 for an additional examination of cimides). Before you can get into synthesis and reactions, though, you need to understand the structure and nomenclature of these compounds. 

Other commercial copolymers which are typically random are those of vinyl chloride and vinyl acetate (Vinylite), isobutylene and isoprene (butyl rubber), styrene and butadiene (SBR), and acrylonitrile and butadiene (NBR). The accepted nomenclature is illustrated by EP, which is designated poly-ethylene-co-propylene the co designating that the polymer is a copolymer. When the copolymers are arranged in a regular sequence in the chains, i.e., ABAB, the copolymer is called an alternating copolymer. A copolymer consisting of styrene and maleic anhydride (SMA) is a typical alternating copolymer. 

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