The Morse oscillator modeling a different diatomic molecule has D = 324 kJ/mole and v =1240 cm¹. (Again, 11.9627 J/mole = 1 cm-¹.)M(a) What is the energy of the pictured eigenfunction? Report the energy in cm-¹ using theformula for the Morse oscillator energy levels.(b) How close to the dissociation limit is this state in kJ/mole, that is, what is the energydifference between this state and molecular dissociation?

Given dissociation energy Wavenumber,Also, from the expression of the dissociation energywhere is…

Answered: The Morse oscillator modeling a…

Similar questions

Which one of the following statements about the exchange energy of the few lowest excited states of helium, in which the two electrons are in different subshells, is incorrect? Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. b с d e In the absence of the exchange energy, the degeneracy between 1s¹2s¹ and 1s¹2p¹ configurations would only be lifted by relativistic corrections. For a given configuration and L the exchange energy favours (ie the energy is lower for) S-1 compared with S=0 O For a given configuration and L the exchange energy favours states that are spatially anti-symmetric The exchange energy gives larger shifts in the levels than relativistic corrections L, S remain good quantum numbers in the presence of the exchange energy
Please, I want to solve the question correctly, clearly and concisely
results. OAKL Consider a pne dimensional infinite-wall potential V = ∞ for > Land z<0, and V0 for There are two identical spin half fermions in this potential well and spin states are dened by) and 4) for spin up and down, respectively. a) (Very easy) Find the eigenvalues and the corresponding wave functions for the potential well. b) (Ensy) Write the full wave function for the fermions in singlet state with possible minimum energy. e) (Easy) Write the full wave function for the fermions in triplet state with possible minimum energy
(A) for internal energy using the Legendre transform. Show how the Gibbs free energy state function is derived from the state function (B) What are the conditions for G to act as a potential function? (C) Show the mathematical expression for G as a potential function.
Explain the reason that metal atomic chains have quantized G, different from bulk metals by comparing with the Schematic illustration of a diffusive and ballistic conductor.
A deuterium molecule (D2₂) at 30°K is known to be in the state, 1 /26 12/₂) = = |3|1, 1) + 4 |7, 3) + |7, 1) where , m) are eigenstates of the angular momentum operator. (a) If one were to measure L₂, what posible values one would get and what would be their associated probabilities? (b) Repeat (a) but for L². (c) What is the expectation value of the energy (E) of the molecule in this state, assuming purely rotational states. Take c= 30.4 cm-¹, where I=moment of inertia of D₂ and c=speed of light. Express your answer in eV. -
Write down the confi gurations for the ground states of calcium and aluminum. What are the LS coupling quantum numbers for the outside subshell electrons? Write the spectroscopic symbol for each atom
Please, I want to answer the question correctly and clearly for this question, the name of the course: Laser and its applications