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International Union of Pure and Applied Chemistry rules

The most definitive set of organic nomenclature rules currently in use were evolved through several international conferences and are known as the International Union of Pure and Applied Chemistry Rules (1UPAC rules). We first shall describe this system for naming the hydrocarbons known as alkanes—... [Pg.51]

The numbers 1,2, etc. in Scheme 18 were chosen for systematic reasons and are not in accord with International Union of Pure and Applied Chemistry rules. From these molecules, Type 1,2 and 2,3 have proved to be relevant to photochromism. For the azoderivatives Type 3,4, photochemical extrusion of N2 is possible this has been widely used in generating cyclopropanes.45 47... [Pg.241]

International Union of Pure and Applied Chemistry. Rules for the Nomenclature of Organic... [Pg.422]

As a general rule, adsorbates above their critical temperatures do not give multilayer type isotherms. In such a situation, a porous absorbent behaves like any other, unless the pores are of molecular size, and at this point the distinction between adsorption and absorption dims. Below the critical temperature, multilayer formation is possible and capillary condensation can occur. These two aspects of the behavior of porous solids are discussed briefly in this section. Some lUPAC (International Union of Pure and Applied Chemistry) recommendations for the characterization of porous solids are given in Ref. 178. [Pg.662]

After World War II the International Union of Chemistry became the International Union of Pure and Applied Chemistry (known in the chemical com munity as the lUPAC) Since 1949 the lUPAC has is sued reports on chemical nomenclature on a regular basis The most recent lUPAC rules for organic chem istry were published in 1993 The lUPAC rules often offer several different ways to name a single com pound Thus although it is true that no two com... [Pg.78]

Isopropyl group (Section 2 13) The group (CH3)2CH— Isotactic polymer (Section 7 15) A stereoregular polymer in which the substituent at each successive chirality center is on the same side of the zigzag carbon chain Isotopic cluster (Section 13 22) In mass spectrometry a group of peaks that differ in m/z because they incorporate differ ent isotopes of their component elements lUPAC nomenclature (Section 2 11) The most widely used method of naming organic compounds It uses a set of rules proposed and periodically revised by the International Union of Pure and Applied Chemistry... [Pg.1287]

As noted in the text, chemists overwhelmingly use the nomenclature system devised and maintained by the International Union of Pure and Applied Chemistry, or IUPAC. Rules for naming monofunctional compounds were given throughout the text as each new functional group was introduced, and a list of where these rules can be found is given in Table A.l. [Pg.1225]

In this book we use the Nomenclature of Organic Chemistry of the International Union of Pure and Applied Chemistry, 1979 Edition ( Blue book , IUPAC, 1979), the Revised Nomenclature for Radicals, Ions, Radical Ions, and Related Species (IUPAC, 1993), and additional rules applied by the Chemical Abstracts Service for the 1987-1991 Index Guide Chemical Abstracts, 1992). [Pg.5]

Although the definitions of isotactic, syndiotactic, and atactic polymers according to International Union of Pure and Applied Chemistry (IUPAC) rules are well established in terms of succession of mesa (m) or racemic (r) dyads,12 the symbolism of (+) and (—) bonds allows the easy treatments of possible configurations in cases of any complexity.1 Moreover, the (+) or (—) character of the bonds in a polymer chain is strictly related to the accessibility of gauche+ or gauche conformations of the bonds and, therefore, to the formation of right-handed or left-handed helical conformations.1... [Pg.73]

The Commission on Biochemical Nomenclature (CBN) of the International Union of Pure and Applied Chemistry (IUPAC) and of the International Union of Biochemistry and Molecular Biology (IUBMB) has issued many recommendations and rules on peptides and amino acids. These recommendations and rules concern nomenclature, notations, abbreviations, symbols, etc. (see www.chem.qmul.ac.uk/iupac/AminoAcid/ and www.chem.qmul.ac.uk/iubmb/). [Pg.253]

The International Union of Pure and Applied Chemistry (lUPAC) has set standard rules for naming organic compounds. The systematic (or lUPAC) names of alkanes and most other organic compounds follow the same pattern, shown below. [Pg.13]

The Commission of Nomenclature of the Macromolecular Division of lUPAC International Union of Pure and Applied Chemistry) formulated general rules for the nomenclature of polymers (relevant publications see Sect. 1.4.4). Selected recommendations are explained in the following paragraph. [Pg.6]

In general, organic compounds are given systematic names by using the order prefix-parent-suffix, where prefix indicates how many branching groups are present, parent indicates how many carbons are in the longest chain and suffix indicates the name of the family. Common names as weU as systematic names are used for alkanes and their derivatives. However, it is advisable to use systematic names or the lUPAC (International Union of Pure and Applied Chemistry) nomenclature, which can be derived from a simple set of rules. [Pg.62]

Simple binary and ternary compounds can be named by using a few simple rules, but systematic rules are required to name the millions of organic compounds that exist. Rules for naming compounds have been established by the International Union of Pure and Applied Chemistry (IUPAC). The IUPAC name stands for a compound that identifies its atoms, functional groups, and basic structure. Because of the complexity of organic compounds, thousands of rules are needed to name the millions of compounds that exist and the hundreds that are produced daily. The original intent of the IUPAC rules was to establish a unique name for each compound, but because of their use in different contexts and different practices between disciplines, more than one name may describe a compound. IUPAC rules result in preferred IUPAC names, but general IUPAC names are also accepted. [Pg.353]

Conventions for naming inorganic compounds are established by the International Union of Pure and Applied Chemistry (IUPAC) and are reviewed on a continuing basis. The following rules cover only the more commonly encountered complexes. [Pg.457]

Some of the rules of systematic nomenclature used in Chemical Abstracts and approved by the International Union of Pure and Applied Chemistry are collected here. Important trivial names are listed at the beginning of individual chapters. [Pg.13]

We will base our study on the system developed by the International Union of Pure and Applied Chemistry. The system is called the IUPAC Rules. There are other semi-systematic nomenclature systems, and many individual compounds are known by nonsystematic or trivial names. These names will be given along with the IUPAC names when such trivial names are commonly used. [Pg.11]


See other pages where International Union of Pure and Applied Chemistry rules is mentioned: [Pg.25]    [Pg.51]    [Pg.26]    [Pg.81]    [Pg.33]    [Pg.25]    [Pg.51]    [Pg.26]    [Pg.81]    [Pg.33]    [Pg.1]    [Pg.213]    [Pg.1286]    [Pg.205]    [Pg.1287]    [Pg.167]    [Pg.583]    [Pg.1]    [Pg.482]    [Pg.1662]    [Pg.607]    [Pg.366]    [Pg.192]    [Pg.117]    [Pg.565]    [Pg.287]    [Pg.199]    [Pg.177]    [Pg.181]    [Pg.2]   
See also in sourсe #XX -- [ Pg.235 ]




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