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Ions, ionisation

Configuration Ground State Orbital Ion Ionised States Produced... [Pg.143]

Atomic number Element Atomic radius (s) Radius oj M ion (nm) Ionisation energies (kJ mol I 1st 2nd 3rd ... [Pg.30]

Ionisations 2, 3 and 5 are complete ionisations so that in water HCI and HNO3 are completely ionised and H2SO4 is completely ionised as a monobasic acid. Since this is so, all these acids in water really exist as the solvated proton known as the hydrogen ion, and as far as their acid properties are concerned they are the same conjugate acid species (with different conjugate bases). Such acids are termed strong acids or more correctly strong acids in water. (In ethanol as solvent, equilibria such as 1 would be the result for all the acids quoted above.) Ionisations 4 and 6 do not proceed to completion... [Pg.85]

The enthalpy changes AH involved in this equilibrium are (a) the heat of atomisation of the metal, (b) the ionisation energy of the metal and (c) the hydration enthalpy of the metal ion (Chapter 3). [Pg.97]

Liquid ammonia, which boils at 240 K, is an ionising solvent. Salts are less ionised in liquid ammonia than they are in water but, owing to the lower viscosity, the movement of ions through liquid ammonia is much more rapid for a given potential gradient. The ionisation of liquid ammonia... [Pg.109]

Element Ionisation energy (kj mof ) Metallic radius (nm) Ionic radius (nm) Heal oj laporibation at 298 K (kJ mol ) Hydration energy oj gaseous ion (kJ moI ) (V)... [Pg.120]

In liquid nitric acid, hydrogen bonding gives a loose structure similar to that of hydrogencarbonate ions. However, although pure nitric acid does not attack metals readily and does not evolve carbon dioxide from a carbonate, it is a conducting liquid, and undergoes auto-ionisation thus ... [Pg.240]

The electronic configuration of each halogen is one electron less than that of a noble gas, and it is not surprising therefore, that all the halogens can accept electrons to form X" ions. Indeed, the reactions X(g) + e - X (g), are all exothermic and the values (see Table 11.1), though small relative to the ionisation energies, are all larger than the electron affinity of any other atom. [Pg.310]

When hydrochloric acid is cautiously added to an aqueous solution containing both sodium nitrite and the sodium salt of sulphanilic acid, NaOsSCgH NH, the amino group of the latter undergoes normal diazotisation, giving the diazonium chloride (A). The latter, however, ionises in solution, giving sodium and chloride ions and the internal salt (B), which possesses two opposite charges and is therefore neutral this internal salt is stable under... [Pg.214]

So far the four metal ions have been compared with respect to their effect on (1) the equilibrium constant for complexation to 2.4c, (2) the rate constant of the Diels-Alder reaction of the complexes with 2.5 and (3) the substituent effect on processes (1) and (2). We have tried to correlate these data with some physical parameters of the respective metal-ions. The second ionisation potential of the metal should, in principle, reflect its Lewis acidity. Furthermore the values for Iq i might be strongly influenced by the Lewis-acidity of the metal. A quantitative correlation between these two parameters... [Pg.60]

Concentrated solutions are here considered to be those containing > c. 89 % by weight of sulphuric acid. In these solutions nitric acid is completely ionised to the nitronium ion. This fact, and the notion that the nitronium ion is the most powerful electrophilic nitrating species, makes operation of this species in these media seem probable. Evidence on this point comes from the effect on the rate of added water ( 2.4.2)... [Pg.15]

The continued effectiveness of the nitronium ion in relatively dilute solutions has been indicated by comparing the dependence of the rates on the concentration of sulphuric acid, with the acidity-dependence of the ionisation of model compounds. The (formerly or Cq) acidity... [Pg.21]

If it be assumed that the ionising characteristics of nitric acid are similar to those of the organic indicators used to define the scales of acidity, then a correspondence between the acidity-dependence of nitration and would suggest the involvement of the nitronium ion, whereas a correspondence with Hq would support the h)rpothesis that the nitric acidium ion were active. The analogies with and Hg are expressed in the first and last pairs of the followii equations respectively. The symbol AQ represents anthraquinone, the indicator originally used in this way for comparison with the acidity dependence of the rate of nitration of nitrobenzene ... [Pg.22]

There is increasing evidence that the ionisation of the organic indicators of the same type, and previously thought to behave similarly, depends to some degree on their specific structures, thereby diminishing the generality of the derived scales of acidity. In the present case, the assumption that nitric acid behaves like organic indicators must be open to doubt. However, the and /fp scales are so different, and the correspondence of the acidity-dependence of nitration with so much better than with Hg, that the effectiveness of the nitronium ion is firmly established. The relationship between rates of nitration and was subsequently shown to hold up to about 82 % sulphuric acid for nitrobenzene, />-chloronitrobenzene, phenyltrimethylammonium ion, and p-tolyltrimethylammonium ion, and for various other compounds. ... [Pg.22]

Second-order rate coefficients for nitration in sulphuric acid at 25 °C fall by a factor of about 10 for every 10 % decrease in the concentration of the sulphuric acid ( 2.4.2). Since in sulphuric acid of about 90% concentration nitric acid is completely ionised to nitronium ions, in 68 % sulphuric acid [NO2+] io [HNO3]. The rate equation can be written in two ways, as follows ... [Pg.27]

The relative abilities of nitromethane, sulpholan, and acetic acid to support the ionisation of nitric acid to nitronium ions are closely similar to their efficiencies as solvents in nitration. Raman spectroscopy showed that for a given concentration of mixed acid (i i nitric and sulphuric acids) the concentration of nitronium ions in these three solvents varied in the order nitromethane > sulpholan > acetic acid. The concentration of mixed acid needed to permit the spectroscopic detection of nitronimn ions was 25 %, 50 % and 60 % in the three solvents, respectively (see 4.4.3). [Pg.39]

If we consider the effect of nitrous acid upon zeroth-order nitration in organic solvents we must bear in mind that in these circumstances dinitrogen tetroxide is not much ionised, so the measured concentration of nitrous acid gives to a close approximation the concentration of dinitrogen tetroxide. Further, the negligible self-ionisation of nitric acid ensures that the total concentration of nitrate ions is effectively that formed from dinitrogen tetroxide. Consequently as we can see from the equation for the ionisation of dinitrogen tetroxide ( 4.3.1),... [Pg.56]

For a base the stoichiometric second-order rate constant which should be observed, imder conditions where ionisation to the nitronium ion is virtually complete, namely > 90 % H2SO4, if nitration were limited to the free base and occurred at every encounter with a nitronium ion, would be ... [Pg.154]

Ridd - has reinterpreted the results concerning the anticatalysis of the first-order nitration of nitrobenzene in pure and in partly aqueous nitric acid brought about by the addition of dinitrogen tetroxide. In these media this solute is almost fully ionised to nitrosonium ion and nitrate ion. The latter is responsible for the anticatalysis, because it reduces the concentration of nitronium ion formed in the following equilibrium ... [Pg.221]

Mode of Motion. Nicotine, anabasine, and imidocloprid affect the ganglia of the insect central nervous system, faciUtating transsynaptic conduction at low concentrations and blocking conduction at higher levels. The extent of ionisation of the nicotinoids plays an important role in both their penetration through the ionic barrier of the nerve sheath to the site of action and in their interaction with the site of action, which is befleved to be the acetylcholine receptor protein. There is a marked similarity in dimensions between acetylcholine and the nicotinium ion. [Pg.269]

Lead (qv) is a member of Group 14 (IVA) of the Periodic Table because it has four electrons in its outer, or valence, shell. However, the usual valence of lead is +2, rather than +4. The two s electrons have higher ionisation energies. As a result, tetravalent lead exists as a free, positive ion only in minimal concentrations. Furthermore, the bivalent or plumbous ion differs from the other Group 14 bivalent ions, such as the starmous ion of tin, because Pb " does not have reducing properties. [Pg.67]

Ionisation of the basic chromium salt results in the formation of complex ions such as L A The... [Pg.85]

The reactor coolant pH is controlled using lithium-7 hydroxide [72255-97-17, LiOH. Reactor coolant pH at 300°C, as a function of boric acid and lithium hydroxide concentrations, is shown in Figure 3 (4). A pure boric acid solution is only slightly more acidic than pure water, 5.6 at 300°C, because of the relatively low ionisation of boric acid at operating primary temperatures (see Boron COMPOUNDS). Thus the presence of lithium hydroxide, which has a much higher ionisation, increases the pH ca 1—2 units above that of pure water at operating temperatures. This leads to a reduction in corrosion rates of system materials (see Hydrogen-ION activity). [Pg.191]

Tandem mass spectrometry or ms/ms was first introduced in the 1970s and gained rapid acceptance in the analytical community. The technique has been used for stmcture elucidation of unknowns (26) and has the abiUty to provide sensitive and selective analysis of complex mixtures with minimal sample clean-up (27). Developments in the mid-1980s advancing the popularity of ms/ms included the availabiUty of powerhil data systems capable of controlling the ms/ms experiment and the viabiUty of soft ionisation techniques which essentially yield only molecular ion species. [Pg.405]


See other pages where Ions, ionisation is mentioned: [Pg.194]    [Pg.392]    [Pg.398]    [Pg.17]    [Pg.302]    [Pg.406]    [Pg.194]    [Pg.392]    [Pg.398]    [Pg.17]    [Pg.302]    [Pg.406]    [Pg.13]    [Pg.29]    [Pg.34]    [Pg.134]    [Pg.139]    [Pg.139]    [Pg.361]    [Pg.94]    [Pg.122]    [Pg.212]    [Pg.21]    [Pg.50]    [Pg.59]    [Pg.127]    [Pg.542]    [Pg.546]    [Pg.549]    [Pg.192]    [Pg.197]   
See also in sourсe #XX -- [ Pg.117 , Pg.123 , Pg.635 , Pg.664 ]

See also in sourсe #XX -- [ Pg.7 , Pg.123 , Pg.635 , Pg.664 ]




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