PRACTICE PROBLEMS Give the electronic configurations and term symbols of the first excited electronic states of the atoms up to Z = 10.

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1 PRACTICE PROBLEMS 2 1. Based on your knowledge of the first few hydrogenic eigenfunctions, deduce general formulas, in terms of n and l, for (i) the number of radial nodes in an atomic orbital (ii) the number of angular nodes (iii) the total number of nodes 2. Recall that a filled or half-filled p, d or f shell has spherical symmetry. Accordingly, go through the periodic table from Z = 36 to Z = 54 and predict which atomic ground states will have spherically-symmetrical electronic distributions (multiplet-s term symbols). 3. Give the electronic configurations and term symbols of the first excited electronic states of the atoms up to Z = Using an optimized variational wavefunction of the form ψ (r 1, r 2 ) = e α(r 1+r 2 ) estimate the ground-state energy of Li Calculate the energy of the hypothetical 1s 3 state of the Li atom using the optimized variational wavefunction ψ (1, 2, 3) = e α(r 1+r 2 +r 3 ) Neglect electron spin, of course. Compare with the experimental groundstate energy, E 0 = hartrees. Comment on the applicability of the variational theorem. 6. After separation of variables in the H + 2 obeys the differential equation d dµ (µ2 1) dm dµ + problem, the function M(µ) ) (A + 2Rµ + 14 R2 Eµ 2 λ2 µ 2 M(µ) = 0 1 where A is a constant, R is the internuclear distance, λ is the angular momentum quantum number, and E is the energy, a negative number for 1

2 bound states. Find the asymptotic solution of the above equation as µ. 7. Predict the electronic configuration and term symbol for the ground state of the superoxide ion O 2 and of the peroxide ion O Propose electron configurations and term symbols for the two lowest singlet excited states of O Give the electron configuration, term symbol and bond order for the ground state of each of the following species: N + 2, N 2 and N The overlap integral between a 1s and a 2pσ orbital on nuclei separated by a distance R (in bohr) is given by S = ) (R + R 2 + R3 3 e R Determine the value of R which gives the maximum overlap. (It may be of interest that the internuclear distance in HF equals 0.916Å.) 11. Carry out a Hückel calculation on the allyl radical CH 2 = CH CH 2 Determine, in terms of the empirical parameters α and β, the energies of the π-molecular orbitals, the resonance stabilization energy and the frequency of the lowest-energy electronic transition. 2

3 ANSWERS 1. Hydrogenic orbital ψ nl has n l 1 radial nodes, l angular nodes, n 1 total nodes. 2. Z=36 Kr [Kr] 1 S 0 Z=37 Rb [Kr]5s 2 S 1/2 Z=38 Sr [Kr]5s 2 1 S 0 Z=42 Mo [Kr]5s4d 5 7 S 3 Z=43 Tc [Kr]5s 2 4d 5 6 S 5/2 Z=46 Pd [Kr]4d 10 1 S 0 Z=47 Ag [Kr]5s4d 10 2 S 1/2 Z=48 Cd [Kr]5s 2 4d 10 1 S 0 Z=51 Sb [Kr]5s 2 4d 10 5p 3 4 S 3/2 Z=54 Xe [Kr]5s 2 4d 10 5p 6 1 S 0 3. Z=1 H 2s 2 S 1/2 or $2p 2 P 1/2 Z=2 He 1s2s 3 S 1 Z=3 Li 1s 2 2p 2 P 1/2 Z=4 Be 1s 2 2s2p 3 P 0 Z=5 B 1s 2 2s2p 2 4 P 1/2 Z=6 C 1s 2 2s 2 2p 2 1 P 1 3

4 Z=7 N 1s 2 2s 2 2p 3 2 S 1/2 Z=8 O 1s 2 2s 2 2p 4 1 P 1 Z=9 F 1s 2 2s2p 6 2 S 1/2 Z=10 Ne 1s 2 2s 2 2p 5 3s 3 P 0 4. Variational energy formula: E(α) = α 2 2Z 5 8 α Minimum for α = Z 5/16, E = (Z 5/16) 2. For Z = 3, E = hartrees. 5. Components of above energy formula: each electron has KE = α 2 /2, nuclear attraction PE = Zα. Each electron pair has repulsion PE = 5α/8. For Li, with 3 electrons and 3 pairs, E(α) = 3 2 α2 3Zα α Minimum for α = Z 15/24 gives E = hartrees. Lower than E 0 = but wavefunction is ILLEGAL! 6. As µ the largest terms are those containing µ 2. Thus Cancel µ 2 and find solution µ 2 M (µ) R2 Eµ 2 M(µ) 0 M(µ) const e R Eµ/2 7. O 2 has configuration...3σ 2 g1π 4 u1π 2 g 3 Σ g O 2 has configuration...3σ2 g1π 4 u1π 3 g 2 Π g 4

5 O 2 2 has configuration... 3σ 2 g 1π4 u 1π4 g 1 Σ + g 8. Both excited states have same configuration as ground state,... 3σ 2 g 1π4 u 1π2 g, but with the following occupancy of 1π g orbitals: 1 Σ + g and 1 g The plus superscript in the first term symbol is rather tricky. Don t worry about it. But if you insist... two-electron singlet spin state has antisymmetric spin function, thus must have symmetric orbital function like π x (1)π y (2) + π y (1)π x (2) which doesn t change sign upon transformation φ φ. Singlet oxygen and other active oxygen species are involved in biochemical lipid oxidations. 9. N π 4 u3σ 2 g 1 Σ + g BO=3 N π 4 u3σ g 2 Σ + g BO=2.5 N π 4 u 3σ2 g 1π g 2 Π g BO= Setting ds/dr = 0 find maximum at R = bohrs or = Å. 11. Secular determinant x x x = x3 2x = 0 where x = (α E)/β. Roots x = 0, ± 2, thus E = α 2β, α, α + 2β. Remember both α and β are negative. Ground state energy (3 electrons) = 2(α+ 2β)+α = 3α+2 2β. One localized π-orbital plus one unpaired electron would have energy = 2(α+β) + α = 3α+2β. Resonance stabilization energy = (2 2 2)β =.828 β =.828 β. Lowest energy electronic transition given by hc λ = 2 β 5