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The Electron Configurations of Ions

To get the electron configuration of ions, a new rule is followed. We first write the electron configuration of the neutral atom. Then, for positive ions, we remove the electrons in the subshell with highest principal quantum number first. Note that these electrons might not have been added last, because of the n + / rule. Nevertheless, the electrons from the shell with highest principal quantum number are removed first. For negative ions, we add electrons to the shell of highest principal quantum number. (That shell has the electrons added last by the n +1 rule.)... [Pg.264]

How does the electron configuration of ions derived from representative elements give them stability ... [Pg.321]

Be able to write the electron configurations of ions. (Section 7.3)... [Pg.278]

The electron configurations of ions derived from representative elements follow a common pattern. What is the pattern, and how does it relate to the stability of these ions ... [Pg.357]

The electron configurations of ions consisting of only one atom can be shown in the same way as illustrated for atoms above. For the lighter elements, the electron... [Pg.142]

We began to consider the electron configurations of ions in Section 7.4. In light of our examination of ionic bonding, we will continue with that discussion here. The energetics of ionic bond formation helps explain why many ions tend to have noble-gas electron configurations. For example, sodium readily loses one electron to form Na, which has the same electron configuration as Ne ... [Pg.280]

Because many ionic compounds are made up of monatomic anions and/or cations, it is helpful to know how to write the electron configurations of these ionic species. The procedure for writing the electron configurations of ions requires only a slight extension... [Pg.249]

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]

As befits the electron configuration of elemental calcium, the metal is very reactive, readily losing two valence electrons to form the dispositive ion. In aqueous solution and ia its compounds, is colorless. Most calcium compounds ate white, unless the cation is paired with a colored anion. The ion... [Pg.406]

The chemistry of Cr(III) in aqueous solution is coordination chemistry (see Coordination compounds). It is dominated by the formation of kineticaHy inert, octahedral complexes. The bonding can be described by Ss]] hybridization, and HteraHy thousands of complexes have been prepared. The kinetic inertness results from the electronic configuration of the Cr ion (41). This type of orbital charge distribution makes ligand displacement and... [Pg.135]

In general, octahedral complexes of transition-metal ions possessing 0, 1, or 2 electrons beyond the electronic configuration of the preceding noble gas, ie, i/, (P configurations, are labile. The (P systems are usually inert the relative lability of vanadium(II) may be charge and/or redox related. [Pg.170]

The unique nature of the electronic configuration of copper, which contributes to its high electrical and heat conductivity, also provides chemical properties intermediate between transition and 18-sheU elements. Copper can give up the 4s electron to form the copper(I) ion [17493-86-6] or release an additional electron from the >d orbitals to form the copper(Il) ion [15158-11-9]. [Pg.195]

What Are the Key Ideas Bond formation is accompanied by a lowering of energy. That lowering of energy is due to the attractions between oppositely charged ions or between nuclei and shared electron pairs. The electron configurations of individual atoms control how the atoms combine with one another. [Pg.181]

What Do We Need to Know Already This chapter draws on many of the principles introduced in the preceding chapters. In particular, it makes use of the electron configurations of atoms and ions (Sections 1.13 and 2.1) and the classification of species as Lewis acids and bases (Section 10.2). Molecular orbital theory (Sections 3.8 through 3.12) plays an important role in Section 16.12. [Pg.776]

Fig. 4.—A diagram representing the electronic configurations of certain complex ions. Each circle represents a single-electron positional eigenfunction, each dot an electron. Fig. 4.—A diagram representing the electronic configurations of certain complex ions. Each circle represents a single-electron positional eigenfunction, each dot an electron.
Table 1-2. The electronic configurations of the transition-metal ions in the divalent and triva-lent states. Table 1-2. The electronic configurations of the transition-metal ions in the divalent and triva-lent states.
The electron configurations of atomic ions are written using the same procedure as for neutral atoms, taking into account the proper number of electrons. An anion has one additional electron for each unit of negative charge. A cation has one fewer electron for each unit of positive charge. [Pg.529]


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