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Periodic Properties of the Elements

Periodic Properties of the Elements. The Periodic Table. The modern periodic table was developed in 1872 by Dmitri Mendeleev (1834-1907). A similar table was also developed independently by Julius Meyer (1830-1895).

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Periodic Properties of the Elements

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  1. Periodic Properties of the Elements

  2. The Periodic Table The modern periodic table was developed in 1872 by Dmitri Mendeleev (1834-1907). A similar table was also developed independently by Julius Meyer (1830-1895). The table groups elements with similar properties (both physical and chemical) in vertical columns. As a result, certain properties recur periodically.

  3. The Periodic Table Mendeleev left empty spaces in his table for elements that hadn’t yet been discovered. Based on the principle of recurring properties, he was able to predict the density, atomic mass, melting or boiling points and formulas of compounds for several “missing” elements.

  4. The Periodic Table

  5. The Periodic Table metal/non-metalline

  6. The Periodic Table The periodic table is based on observations of chemical and physical behavior of the elements. It was developed before the discovery of subatomic particles or knowledge of the structure of atoms. The basis of the periodic table can be explained by quantum theory and the electronic structure of atoms.

  7. Quantum Numbers In addition to n, the principal quantum number, there are three additional quantum numbers which describe the type of orbital ( l ) , the spatial orientation of the orbital (ml ), and the spin of the electron (ms ).

  8. Quantum Numbers The magnetic quantum number (ml ) specifies the spatial orientation of the orbital. An example is to distinguish between the px, py or pz orbitals.

  9. Electron Spin Each orbital, regardless of type, can contain zero, one or two electrons. If two electrons occupy the same orbital, they must spin in opposite directions. The spin is quantized, and can be expressed using quantum numbers, or simply specifying the spin as up or down or clockwise and counter-clockwise.

  10. The Pauli Exclusion Principle Quantum mechanics dictates that no two electrons in an atom can have the same four quantum numbers. Another way of stating the Pauli Exclusion Principle is that if electrons occupy the same orbital, they must have opposite spins.

  11. Multi-electron Atoms Orbitals of any type can be empty, or have 1 or two electrons. Experimental data indicate that if two electrons are in the same orbital, they will spin in opposite directions.

  12. Energy Levels In any atom or ion with only 1 electron, the principal quantum number, n, determines the energy of the electron. For n=2, the 2s and 2p orbitals all have the same energy.

  13. Energy Levels Likewise, the 3s, 3p and 3d orbitals are all degenerate, with the same energy.

  14. Energy Levels In a multi-electron atom, there is interaction between electrons. As a result of this interaction, the various subshells of a principal quantum level will vary in energy.

  15. Energy Levels

  16. Energy Levels

  17. Energy Levels The energy diagram for the first three quantum levels shows the splitting of energies.

  18. Energy Levels For a given value of n, the energies of the subshells is as follows: ns<np<nd<nf

  19. Energy Levels The subshells have different energies due to the penetrating ability for each type of orbital. Electrons in a 2s orbital can get nearer to the nucleus than those in a 2p orbital.

  20. Energy Levels The electrons in the 3s orbital (top diagram) have higher probability to be found near the nucleus, and thus greater penetrating ability than those in 3p or 3d orbitals.

  21. Multi-electron Atoms Electron configurations are a way of noting which subshells of an atom contain electrons. Although much of the periodic table was developed before the concept of electron configurations, it turns out that the position of an element on the periodic table is directly related to its electron configuration.

  22. Multi-electron Atoms

  23. Electron Configurations Write the complete electron configurations for nitrogen and zinc. How many unpaired electrons does each atom have? What is the short hand notation for each element.

  24. Hund’s Rule When electrons occupy degenerate orbitals, they occupy separate orbitals with parallel spins. This is the lowest energy, or ground state, configuration.

  25. Multi-electron Atoms The electron configurations for Cr and Cu differ from that expected based on their positions in the periodic table.

  26. Multi-electron Atoms Electron configurations also get less predictable for the elements near the bottom of the periodic table. With many quantum levels (n) occupied, the energy levels overlap and the lowest energy arrangement becomes more difficult to predict.

  27. Periodic Trends Many of the properties of atoms show clear trends in going across a period (from left to right) or down a group. In going across a period, each atom gains a proton in the nucleus as well as a valence electron.

  28. Periodic Trends The increase of positive charge in the nucleus isn’t completely cancelled out by the addition of the electron. Electrons added to the valence shell don’t shield each other very much. As a result, in going across a period, the effective nuclear charge (Zeff) increases.

  29. Effective Nuclear Charge The effective nuclear charge (Zeff) equals the atomic number (Z) minus the shielding factor (σ). Zeff= Z-σ

  30. Effective Nuclear Charge Zeff= Z-σ

  31. Effective Nuclear Charge Electrons in the valence shell are partially shielded from the nucleus by core electrons.

  32. Effective Nuclear Charge Electrons in p or d orbitals don’t get too close to the nucleus, so they are less shielding than electrons in s orbitals. As a result, effective nuclear charge increases across a period.

  33. Periodic Trends

  34. Periodic Trends In going down a group or family, a full quantum level of electrons, along with an equal number of protons, is added. As n increases, the valence electrons are, on average, farther from the nucleus, and experience less nuclear pull due to the shielding by the “core” electrons. As a result, Zeff decreases slightly going down a group.

  35. Trends- Atomic Radii Atomic radii are obtained in a variety of ways: 1. For metallic elements, the radius is half the internuclear distance in the crystal, which is obtained from X-ray data. 2. For diatomic molecules, the radius is half the bond length. 3. For other elements, estimates of the radii are made.

  36. Trends- Atomic Radii Atomic radii follow trends directly related to the effective nuclear charge. As Zeff increases across a period, the electrons are pulled closer to the nucleus, and atomic radii decrease. As Zeff decreases down a group, the valence electrons experience less nuclear attraction, and the radius increases.

  37. Trends- Atomic Radii Atomic size roughly halves across a period, and doubles going down a group.

  38. Electron Configurations of Ions The atoms of the main group elements (groups IA-VIIA) will form ions by losing or gaining electrons. The resulting ion will have the same electron configuration as a noble gas (group VIIIA). These configurations are usually very stable.

  39. Electron Configurations of Ions • Atoms or ions with the same electron configuration (or number of electrons) are called isoelectronic. For example, Na+, Mg2+, Ne, F-, and O2- are isoelectronic. The size will decrease with increasing positive charge. O2- > F- >Ne> Na+> Mg2+

  40. Electron Configurations of Ions When atoms lose electrons, the electrons are always removed from the highest quantum level first. For the first row of transition metals, this means that the electrons in 4s subshell are lost before the 3d subshell. Fe: [Ar]4s23d6 Fe2+: [Ar] 3d6 or [Ar]4s03d6

  41. Common Ionic Charges The charges of ions of elements in groups 1A-7A (the main groups) are usually predictable. Group 1A metals form +1 ions, group 2A metals form +2 ions, etc. The non-metals of group 5A have a -3 charge, those of group 6A have a -2 charge, and the halogens form ions with a -1 charge.

  42. Typical Ionic Charges

  43. Trends – Ionic Size Cations are always smaller than the neutral atom. The loss of one or more electrons significantly increases Zeff, resulting in the valence electrons being pulled closer to the nucleus.

  44. Ionic Size - Cations Within a group, assuming the same ionic charge, the size of the ion increases going down the group, due to more core electrons shielding the nucleus as n increases.

  45. Trends – Ionic Size Across period, the cations get more positive, and as a result, considerably smaller.

  46. Trends – Ionic Size Anions are always larger in size than the neutral atom. The addition of one or more electrons results in greater electron-electron repulsion, which causes the valence electrons to “spread out” a bit.

  47. Size of Anions

  48. Anions are always larger than the neutral atom.

  49. Size of Anions Within a group, assuming the same ionic charge, the size of the ion increases going down the group, due to more core electrons shielding the nucleus as n increases.

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