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Transition elements ionization energies

Ionization energy. As ionization energies go, the values found for the transition elements are neither very high nor very low. They are all rather similar in magnitude. The sequential increase in nuclear charge, which would tend to increase the ionization energy, seems to be almost offset by the extra screening of the nucleus provided by the added electrons. [Pg.399]

C08-0023. Iron and cobalt form compounds that can be viewed as containing cations, but nickel does not. Use the ionization energies in Appendix C to predict which other transition metal elements are unlikely to form stable cations with charges greater than +2. [Pg.552]

Transition metals tend to have higher melting points than representative metals. Because they are metals, transition elements have relatively low ionization energies. Ions of transition metals often are colored in aqueous solution. Because they are metals and thus readily form cations, they have negative standard reduction potentials. Their compounds often have unpaired electrons because of the diversity of -electron configurations, and thus, they often are paramagnetic. Consequently, the correct answers are (c) and (e). [Pg.577]

Table 5.7 Ionization energies amd their MADs (eV) computed with the best basis sets for transition metal elements. Table 5.7 Ionization energies amd their MADs (eV) computed with the best basis sets for transition metal elements.
The first ionization energies of the elements are plotted in Figure 1.4. There is a characteristic pattern of the values for the elements Li to Ne which is repeated for the elements Na to Ar, and which is repeated yet again for the elements K, Ca and A1 to Kr (the s- and p-block elements of the fourth period). In the latter case, the pattern is interrupted by the values for the 10 transition elements of the d-block. The fourth period pattern is repeated by the fifth period elements, and there is an additional... [Pg.9]

The transition from positive ions with low oxidation states, via insoluble oxides with intermediate oxidation states, to oxoanions with high oxidation states, is caused by the competition between ionization energies, lattice enthalpies and enthalpies of hydration, similar to the discussion of the variations of ionic forms of the p-block elements given in Section 6.1. Further discussion occurs in Section 7.5.3. [Pg.127]

Calculate the sum of the first two ionization energies for the first-series transition elements, and account for the general trend. [Pg.907]

In group B elements (transition and inner transition metals), there are no fixed jumps between the two consecutive ionization energies. That is why we cannot talk about the relationships of ionization energies of these elements. [Pg.49]


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See also in sourсe #XX -- [ Pg.737 , Pg.738 , Pg.738 , Pg.739 ]

See also in sourсe #XX -- [ Pg.739 , Pg.740 , Pg.740 ]

See also in sourсe #XX -- [ Pg.1094 ]




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Ionizing element

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