Question

State hunds rule with a spectrum

Answer 1

A set of guidelines, known as Hund's rules, help us determine the quantum numbers for the ground states of atoms. The hydrogenic shells fill up giving well defined states for the closed shells. As we add valence electrons we follow Hund's rules to determine the ground state. We get a great simplification by treating nearly closed shells as a closed shell plus positively charged, spin holes. For example, if an atom is two electrons short of a closed shell, we treat it as a closed shell plus two positive holes.)

Couple the valence electrons (or holes) to give maximum total spin. Now choose the state of maximum (subject to the Pauli principle. The Pauli principle rather than the rule, often determines everything here.) If the shell is more than half full, pick the highest total angular momentum state otherwise pick the lowest .

This method of adding up all the spins and all the Ls, is called LS or Russel-Saunders coupling. This method and these rule are quite good until the electrons become relativistic in heavy atoms and spin-orbit effects become comparable to the electron repulsion (arond Z=40). We choose the states in which the total and the total are good quantum numbers are best for minimizing the overlap of electrons, and hence the positive contribution to the energy.

For very heavy atoms, we add the total angular momentum from each electron first then add up the Js. This is called j-j coupling. For heavy atoms, electrons are relativistic and the spin-orbit interaction becomes more important than the effect of electron repulsion. Thus we need to use states in which the total angular momentum of each electron is a good quantum number.

We can understand Hund's rules to some extent. The maximum spin state is symmetric under interchange, requiring an antisymmetric spatial wavefunction which has a lower energy as we showed for Helium. We have not demonstated it, but, the larger the total the more lobes there are in the overall electron wavefunction and the lower the effect of electron repulsion. Now the spin orbit interaction comes into play. For electrons with their negative charge, larger increases the energy. The reverse is true for holes which have an effective postive charge.

A simpler set of rules has been developed for chemists, who can't understand addition of angular momentum. It is based on the same principles. The only way to have a totally antisymmetric state is to have no two electrons in the same state. We use the same kind of trick we used to get a feel for addition of angular momentum; that is, we look at the maximum z component we can get consistent with the Pauli principle. Make a table with space for each of the different states in the outer shell. We can put two electrons into each space, one with spin up and one with spin down. Fill the table with the number of valence electrons according to the following rules.

Make as many spins as possible parallel, then compute and call that . Now set the orbital states to make maximum , and call this , but don't allow any two electrons to be in the same state (of and ). Couple to get as before. This method is rather easy to use compared to the other where addition of more than two angular momenta can make the symmetry hard to determine.

for more details visit :https://en.wikipedia.org/wiki/Hund%27s_rules  
(in the above website u will be able to understand it more clearly ).

Answer 2

Answer:It states that electron pairing in the degenerate orbitals does not take place until all available orbitals orbitals contains one elelctron each.

Explanation: WKT there are three p orbitals , five d orbitals and seven f orbitals. According to this rule , pairing of electrons in these orbitals starts only when the 4th, 6th and 8th electron enters the p,d and f orbitals respectively.