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Atomic halide

Several benzyl derivatives exhibit potentially hazardous properties arising from the activation by the adjacent phenyl group, either of the substituent or of a hydrogen atom. Halides, in particular, are prone to autocatalytic Friedel Crafts polymerisation if the aromatic nucleus is not deactivated by electron withdrawing substituents. [Pg.73]

Uncertainties 0,04 V or less. Abbreviations R refers to the HOCHiCH, alkyl group, DTH(SS) to oxidized dithiothre-itol, and HiNlOiC-LipCSS) and HO(0)C-Lip(SS) to oxidized lipoamide and lipoic acid, respectively. Values have been adjusted for small changes in f. s of standard reference couples, see text, ff" calculated from the data in the references indicated and recent halogen atom-halide system potentials, see text. [Pg.48]

Inorganic 7r-ligands such as carbonyl or nitrosyls generally follow the metal atom halides also follow the metal but precede carbonyls or nitrosyls. [Pg.9]

MarkownikofT s rule The rule states that in the addition of hydrogen halides to an ethyl-enic double bond, the halogen attaches itself to the carbon atom united to the smaller number of hydrogen atoms. The rule may generally be relied on to predict the major product of such an addition and may be easily understood by considering the relative stabilities of the alternative carbenium ions produced by protonation of the alkene in some cases some of the alternative compound is formed. The rule usually breaks down for hydrogen bromide addition reactions if traces of peroxides are present (anti-MarkownikofT addition). [Pg.251]

PPha, pyridine) organic groups (olefines, aromatic derivatives) and also form other derivatives, e.g. halides, hydrides, sulphides, metal cluster compounds Compounds containing clusters of metal atoms linked together by covalent (or co-ordinate) bands, metaldehyde, (C2H40) ( = 4 or 6). A solid crystalline substance, sublimes without melting at I12 1I5" C stable when pure it is readily formed when elhanal is left in the presence of a catalyst at low temperatures, but has unpredictable stability and will revert to the monomer, ft is used for slug control and as a fuel. [Pg.257]

Rokni M and Jaoob J FI 1982 Rare-gas halide lasers Applied Atomic Collision Physics, Vol 3, Gas Lasers ed FI S W Massey, E W MoDaniel, B Bederson and W L Nighan (New York Aoademio)... [Pg.829]

The heats of formation of the gaseous atoms, 4, are not very different clearly, it is the change in the bond dissociation energy of HX, which falls steadily from HF to HI, which is mainly res ponsible for the changes in the heats of formation. 6. We shall see later that it is the very high H—F bond energy and thus the less easy dissoeiation of H—F into ions in water which makes HF in water a weak aeid in comparison to other hydrogen halides. [Pg.73]

All the other aluminium halides are covalently bonded with aluminium showing a coordination number of four towards these larger halogen atoms. The four halogen atoms arrange themselves approximately tetrahedrally around the aluminium and dimeric molecules are produced with the configuration given below ... [Pg.153]

All Group IV elements form tetrachlorides, MX4, which are predominantly tetrahedral and covalent. Germanium, tin and lead also form dichlorides, these becoming increasingly ionic in character as the atomic weight of the Group IV element increases and the element becomes more metallic. Carbon and silicon form catenated halides which have properties similar to their tetrahalides. [Pg.195]

Towards a simple Lewis base, for example the proton, phosphine is a poorer electron donor than ammonia, the larger phosphorus atom being less able to form a stable covalent bond with the acceptor atom or molecule. Phosphine is, therefore, a much weaker base than ammonia and there is no series of phosphonium salts corresponding to the ammonium salts but phosphonium halides. PH4X (X = Cl, Br, I) can be prepared by the direct combination of phosphine with the appropriate hydrogen halide. These compounds are much more easily dissociated than ammonium halides, the most stable being the iodide, but even this dissociates at 333 K PH4I = PH3 -t- HI... [Pg.226]

Numerous ionic compounds with halogens are known but a noble gas configuration can also be achieved by the formation of a covalent bond, for example in halogen molecules, X2, and hydrogen halides, HX. When the fluorine atom acquires one additional electron the second quantum level is completed, and further gain of electrons is not energetically possible under normal circumstances, i.e... [Pg.312]

The dipole moments of the hydrogen halides decrease with increasing atomic number of the hydrogen, the largest difference occurring between HF and HCl, and association of molecules is not an important factor in the properties of FICl, HBr and HI. This change in dipole moment is reflected in the diminishing permittivity (dielectric constant) values from HF to HI. [Pg.327]

Iron(III) chloride forms numerous addition compounds, especially with organic molecules which contain donor atoms, for example ethers, alcohols, aldehydes, ketones and amines. Anhydrous iron(III) chloride is soluble in, for example, ether, and can be extracted into this solvent from water the extraction is more effective in presence of chloride ion. Of other iron(III) halides, iron(III) bromide and iron(III) iodide decompose rather readily into the +2 halide and halogen. [Pg.394]

Materials that contain defects and impurities can exhibit some of the most scientifically interesting and economically important phenomena known. The nature of disorder in solids is a vast subject and so our discussion will necessarily be limited. The smallest degree of disorder that can be introduced into a perfect crystal is a point defect. Three common types of point defect are vacancies, interstitials and substitutionals. Vacancies form when an atom is missing from its expected lattice site. A common example is the Schottky defect, which is typically formed when one cation and one anion are removed from fhe bulk and placed on the surface. Schottky defects are common in the alkali halides. Interstitials are due to the presence of an atom in a location that is usually unoccupied. A... [Pg.638]

The Alkyl Halides. Ethyl bromide and iodide (see below) are typical alkyl halides. Compounds of this class are of very great importance in synthetic work, owing to the reactivity of the halogen atom. This is illustrated by the following reactions ... [Pg.103]


See other pages where Atomic halide is mentioned: [Pg.272]    [Pg.45]    [Pg.205]    [Pg.45]    [Pg.79]    [Pg.415]    [Pg.272]    [Pg.45]    [Pg.205]    [Pg.45]    [Pg.79]    [Pg.415]    [Pg.28]    [Pg.79]    [Pg.179]    [Pg.199]    [Pg.226]    [Pg.254]    [Pg.265]    [Pg.276]    [Pg.279]    [Pg.345]    [Pg.375]    [Pg.378]    [Pg.267]    [Pg.304]    [Pg.124]    [Pg.898]    [Pg.2475]    [Pg.2475]    [Pg.2749]    [Pg.17]    [Pg.116]    [Pg.152]    [Pg.316]    [Pg.326]   
See also in sourсe #XX -- [ Pg.62 ]

See also in sourсe #XX -- [ Pg.133 ]




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Alkali halides helium atom scattering

Aryl halides Atom transfer reactions

Atom-molecule reactions studied in flow systems the hydrogen halide system

Atomic boron halides

Atomic charges carbonyl halides

Boron halides atomic carbon

Halides and Halogen Atoms as Hydrogen-Bond Acceptors

Halides atomic copper

Halides endohedral atoms

Halides metal atoms

Halides of 2 C-atoms

Halides, aryl atoms

Halogen atoms direct reactions with hydrogen halides

Heavy atom halides

Magnesium atoms alkyl halides

Metal atoms acyl halides

Metal atoms alkyl halides

Metal atoms aryl halides

Metal atoms reaction with aryl halides

Metal atoms silyl halides

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