Ionic compound aqueous solutions

In an aqueous solution, ionic compounds are completely dissociated into ions. For example, an aqueous solution of barium nitrate, Ba(N03)2, contains Ba + ions and NO3 ions. If aqueous solutions of ionic compounds are mixed, some ions may interact to form an insoluble product called a precipitate. For example, if aqueous solutions of barium nitrate and sodium sulfate are mixed, insoluble barium sulfate will precipitate. The complete formula equation for this reaction is written as follows. 

In aqueous solution, ionic solids dissolve as the negative ends and the positive ends of the water molecules hecome oriented with the corresponding oppositely charged ions that make up the ionic compound, pulling them away from the solid into solution. 

Many of the reactions of halogens can be considered as either oxidation or displacement reactions the redox potentials (Table 11.2) give a clear indication of their relative oxidising power in aqueous solution. Fluorine, chlorine and bromine have the ability to displace hydrogen from hydrocarbons, but in addition each halogen is able to displace other elements which are less electronegative than itself. Thus fluorine can displace all the other halogens from both ionic and covalent compounds, for example... 

The most common oxidation state of niobium is +5, although many anhydrous compounds have been made with lower oxidation states, notably +4 and +3, and Nb can be reduced in aqueous solution to Nb by zinc. The aqueous chemistry primarily involves halo- and organic acid anionic complexes. Virtually no cationic chemistry exists because of the irreversible hydrolysis of the cation in dilute solutions. Metal—metal bonding is common. Extensive polymeric anions form. Niobium resembles tantalum and titanium in its chemistry, and separation from these elements is difficult. In the soHd state, niobium has the same atomic radius as tantalum and essentially the same ionic radius as well, ie, Nb Ta = 68 pm. This is the same size as Ti ... 

The most numerous cases of homogeneous catalysis are by certain ions or metal coordination compounds in aqueous solution and in biochemistry, where enzymes function catalyticaUy. Many ionic effects are known. The hydronium ion and the hydroxyl ion OH" cat-... 

The theory of rate measurements by electrochemistry is mathematically quite difficult, although the experimental measurements are straightforward. The techniques are widely applicable, because conditions can be found for which most compounds are electroactive. However, many questionable kinetic results have been reported, and some of these may be a consequence of unsuitable approximations in applying theory. Another consideration is that these methods are mainly applicable to aqueous solutions at high ionic strengths and that the reactions being observed are not bulk phase reactions but are taking place in a layer of molecular dimensions near the electrode surface. Despite such limitations, useful kinetic results have been obtained. 

Table 5.1 lists some of the atomic properties of the Group 2 elements. Comparison with the data for Group 1 elements (p. 75) shows the substantial increase in the ionization energies this is related to their smaller size and higher nuclear charge, and is particularly notable for Be. Indeed, the ionic radius of Be is purely a notional figure since no compounds are known in which uncoordinated Be has a 2- - charge. In aqueous solutions the reduction potential of... 

The oxide (p. 1209), chalcogenides (p. 1210) and halides (p. 1211) have already been described. Of them, the only ionic compound is HgF2 but other compounds in which there is appreciable charge separation are the hydrated salts of strong oxoacids, e.g. the nitrate, perchlorate, and sulfate. In aqueous solution such salts are extensively hydrolysed (HgO is only very weakly basic) and they require acidification to prevent the formation of polynuclear hydroxo-bridged species or the precipitation of basic salts such as Hg(OH)(N03) which contains infinite zigzag chains ... 

Some ionic compounds are soluble, others are not. Consider what happens when we pour a solution of sodium chloride (a strong electrolyte) into a solution of silver nitrate (another strong electrolyte). A solution of sodium chloride contains Na+ cations and Cl anions. Similarly, a solution of silver nitrate, AgNO, contains Ag+ cations and NO, anions. When we mix these two aqueous solutions, a white precipitate, a cloudy, finely divided solid deposit, forms immediately. Analysis shows that the precipitate is silver chloride, AgCl, an insoluble white solid. The... 

Write the net ionic equation for the formation of each of the following insoluble compounds in aqueous solution ... 

Why Do We Need to Know This Material The techniques described in this chapter provide rhe tools that we need to analyze and control the concentrations of ions in solution. A great deal of chemistry is carried out in solution, and so this material is fundamental to understanding chemistry. The ionic compounds released into waterways by individuals, industry, and agriculture can impair the quality of our water supplies. However, these hazardous ions can be identified and removed if we add the right reagents. Aqueous equilibria govern the stabilization of the pH in blood, seawater, and other solutions encountered in biology, medicine, and the environment. 

Apart from the three broad categories of student conceptions discussed above, students displayed several inappropriate conceptions relating to the stractural properties of substances. For example, 14% of students suggested that Mg + ions were present in magnesium ribbon. A second example involved the chemical reaction between copper(II) oxide powder and dilute sulphuric acid. In this instance, 25% of students suggested that Cu + ions were present only in aqueous solution but not in the solid and liquid states. This view was rather unexpected because students had earlier been introdnced to ionic and covalent compounds. It is likely that students had merely rote-learned the general rale without sufficient understanding that ionic solids are formed between metallic and non-metallic elements. 

The stability of chalconide (ionic) compounds decreases from oxygen to tellurium treatment with water produces XH- with X = O or S (hydroxyl and thiol radicals, respectively), but XH2 with X = Se or Te. On warming, aqueous solutions of HS evolve hydrogen sulfide, evidencing that the hydrosulfide ion is much less stable than hydroxide. 

Ionic compounds such as halides, carboxylates or polyoxoanions, dissolved in (generally aqueous) solution can generate electrostatic stabilization. The adsorption of these compounds and their related counter ions on the metallic surface will generate an electrical double-layer around the particles (Fig. 1). The result is a coulombic repulsion between the particles. If the electric potential associated with the double layer is high enough, then the electrostatic repulsion will prevent particle aggregation [27,30]. 

A number of other attempts have been made to account for the properties of concentrated aqueous solutions of ionic compounds by procedures that represent further improvements on the simple Debye-Huckel approach. However, they lie outside the scope of the present chapter. The important point to emphasize is that the concentrated aqueous solutions that are generally employed in the preparation of AB cements tend to exhibit significant ion-ion interactions such interactions lead to significant deviations from ideality which may be accounted for by substantial extension of the ideas of simple dilute solution theory. 

Fig. 8. Correlation between Pearson s hardness parameter (7P) derived from gas-phase enthalpies of formation of halide compounds of Lewis acids (19), and the hardness parameter in aqueous solution (/A), derived from formation constants of fluoride and hydroxide complexes in aqueous solution (17). The Lewis acids are segregated by charge into separate correlations for monopositive ( ), dipositive (O), and tripositive ( ) cations, with a single tetrapositive ion (Zr4+, ). The /P value for Tl3+ was not reported, but the point is included in parentheses to show the relative ionicity of Tl(III) to ligand bonds. 

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