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the production of thymoquinone from thymol and carvacrol

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Figure 3.1. Position <strong>of</strong> transition metals in <strong>the</strong> periodic table.<br />

(Source: Solomons 1988)<br />

Ano<strong>the</strong>r difference between <strong>the</strong> main group metals <strong>and</strong> transition metals can be<br />

seen in <strong>the</strong> formulas <strong>of</strong> <strong>the</strong> compounds <strong>the</strong>y form. The main group metals tend to form<br />

salts (such as NaCl, Mg3N2, <strong>and</strong> CaS) in which <strong>the</strong>re are just enough negative ions to<br />

balance <strong>the</strong> charge on <strong>the</strong> positive ions. The transition metals form similar compounds<br />

(e.g., FeCl3, HgI2, or Cd(OH)2), but <strong>the</strong>y are more likely than main group metals to form<br />

complexes, such as <strong>the</strong> FeCl4 - , HgI4 2- , <strong>and</strong> Cd(OH)4 2- ions, that have an excess number<br />

<strong>of</strong> negative ions. A third difference between main group <strong>and</strong> transition-metal ions is <strong>the</strong><br />

ease with which <strong>the</strong>y form stable compounds with neutral molecules, such as water or<br />

ammonia (Morrison 1992).<br />

3.2. Electronic Configuration<br />

The electronic configuration <strong>of</strong> <strong>the</strong> atoms <strong>of</strong> <strong>the</strong> first row transition elements are<br />

basically <strong>the</strong> same. It can be seen in <strong>the</strong> Table 3.1, <strong>the</strong>re is a gradual filling <strong>of</strong> <strong>the</strong> 3d<br />

orbitals across <strong>the</strong> series starting <strong>from</strong> sc<strong>and</strong>ium. This filling is not regular, since for<br />

chromium <strong>and</strong> copper <strong>the</strong> population <strong>of</strong> 3d orbitals increase by <strong>the</strong> acquisition <strong>of</strong> an<br />

electron <strong>from</strong> <strong>the</strong> 4s shell. For chromium, both <strong>the</strong> 3d <strong>and</strong> 4s orbitals are occupied, but<br />

nei<strong>the</strong>r is completely filled in preference to <strong>the</strong> o<strong>the</strong>r. This suggests that <strong>the</strong> energies <strong>of</strong><br />

<strong>the</strong> 3d <strong>and</strong> 4s orbitals are relatively close for atoms in this row. In copper, <strong>the</strong> 3d level is<br />

full, but only one electron occupies <strong>the</strong> 4s orbital. This suggests that in copper <strong>the</strong> 3d<br />

orbital energy is lower than <strong>the</strong> 4s orbital. Thus <strong>the</strong> 3d orbital energy has passed <strong>from</strong><br />

higher to lower as we move across <strong>the</strong> period <strong>from</strong> potassium to zinc. However, <strong>the</strong><br />

whole question <strong>of</strong> preference <strong>of</strong> an atom to adopt a particular electronic configuration is<br />

11

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