In Chem 465, we learn that the Hamiltonian of a rigid rotor is H=BJ2 where B is the rotational constant and J is the rotational angular momentum. The rotational energies are: E=BJ(J+1) 5 where J=0,1,2β¦ is the rotational angular momentum quantum number. Consider a perturbation: π»π»β = 1 2 πποΏ½π½π½Μ+ + π½π½ΜβοΏ½. where Ξ» is a constant. The operators π½π½Μ+ and π½π½Μβ have the following effects on the spherical harmonics πππ½π½ πππ½π½ : π½π½Μβπππ½π½ πππ½π½ = π½π½πππ½π½β1 πππ½π½β1 , π½π½Μβππ0 0 = 0 π½π½Μ+πππ½π½ πππ½π½ = (π½π½ + 1)πππ½π½+1 πππ½π½+1 (1) [5 pts] Prove that the first-order perturbation vanishes based on symmetry arguments. (2) [10 pts] For the ground rotational state (J=0), compute the second-order contribution to its energy due to the perturbation by the J=1 state. (3) [3 pts] For the ground rotational state (J=0), prove that the second-order contribution to its energy due to the perturbation by the J=2 state vanishes
Selection rules only permit transitions between consecutive rotational levels: ΞJ=JΒ±1, and require the molecule to contain a permanent dipole moment. Due to the dipole requirement, molecules such as HF and HCl have pure rotational spectra and molecules such as H2 and N2 are rotationally inactive.
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