Unit 9 Flashcards
Excited state electron location
in the excited state, the electron will have a higher probability of being found further from the nucleus
Comparison of Coulombic interactions for a 1-electron and 3-electron atom
In one-electron, electron only interacts with nucleus (positively charged, attractive). In 3-electron, electrons interact with nucleus (positively charged, attraction) and interact with electrons (negatively charged, repulsion)
Screening/Shielding
electrons interact with each other, atoms/ions are H-like but comparatively contracted depending on the degree of exposure to the nucleus
Z*(eff)
-net/effective nuclear charge that is “felt” by an electron of interest
-the net positive charge pulling the electrons towards the nucleus
-the higher the pull of the valence electrons, the higher the effective nuclear charge
Nuclear charge
Z(eff)= Z-S
Z= atomic number
S= shielding
Electron shielding
-electrons with the same n do not screen/shield effectively
-core electrons screen valence effectively
-for orbitals with same n value, the greater the number of secondary maxima, the greater the ability to penetrate the core electron density, and higher Z* felt by valence electrons
Graphing r^2R^2 (Radial Probability Density Plot)
-core electrons are in secondary maxima, with each n value being a maxima (descending in height)
-valence electrons are graphed, with increasing l value causing larger width and lower height
-2* maxima (n-l) are drawn within secondary maxima and increase in height and width, tells how much shielding occurs (how much orbital can penetrate core electron density)(the more peaks, the more an orbital can penetrate core)
core vs valence electrons (shielding)
-Core: feel most of positive nuclear charge, are not screened effectively by valence, do not screen each other effectively, shield valence effectively, more core= lower Z* (more screening)
-Valence: do not screen core or each other effectively, most often at larger r outside of core, more 2* maxima correlates to less shielding (higher Z*)
Z* trends in periodic table
-Z* increases left-right on PT (more protons are added, valence electrons do not shield effectively, so electrons feel greater positive charge)
-Z* increases top-bottom (more core orbitals are filled as n increases,
Ionization Energy
-minimum energy required to remove/eject an electron from the highest energy occupied valence orbital in gaseous state
-farther electron is from nucleus, the easier to pull it away (opposite of atomic radius trend, closer the electron is to nucleus, the harder it is to eject)
-electron is ejected with 0 kinetic energy
IE trends and calculations
-First IE:
-X(g) -> X+(g) + e-
-IE= -[-13.6eV(Z*^2/n^2)]
-Second IE:
-X+(g) -> X2+(g) + e-
-IE2> IE1 (removing electron leads to less screening, greater affinity of last electron to nucleus)
-IE increases left-right (En becomes more negative, requiring more energy to ionize), decreases top-bottom (En becomes less negative because n increases)
Electron Affinity (EA)
-minimum energy required to detach/remove/eject the highest energy valence electron from X- (singly charged anion) in gaseous state
-how much an atom wants to gain an electron
-noble gases are exception
-amount of energy released when an atom gains an electron (electron’s negative charge causes overall energy level to lower)
EA trends
-X-(g) -> X(g) + e-
-increases left-right (Z* increases, so element will hold onto electrons more), decreases top-bottom (n increases, En becomes less negative)
Atomic radii
-distance of valence shell of electrons from nucleus when atom is neutral
-sizes of atoms are determined by the volumes occupied by their electrons
Atomic radii trends
-atomic radius decreases left-right (Z* increases, meaning electrons feel greater positive attraction, total energy of orbital decreases, nucleus increases, and electrons contract more centrally)
-atomic radius increases top-bottom (n increases, more core electrons are added, total energy increases, spatial extent of orbital increases as well)