Schrodinger’s wave Equation
The vibrating string behaves like a wave. The motion of the electron is also like a sine wave. Let us consider a sine wave whose wavelength is ‘
This is the equation when the electron will move only in one direction. Now when an electron moves in the three-dimensional space x, y, and z axes, then
……….. (iii)
or
The total energy of a moving electron is sum of kinetic and potential energies, hence
(‘V’ is Potential energy)
Putting the value of v2 in equation (iv) we got

Significance of wave function :

2-

3. The probability of finding the electron in overall space from






In the first group of solutions, the probability of finding the electron

The second group of solutions depends upon ‘ ‘r‘ as well as on the direction in space along the x,y, and z axes.

Radial and Angular Functions ;



The Schrodinger wave equation.



R(r) is a function of radial part of the wave function whereas




Radial Probability distribution Curve :





The redial probability density for some orbitals of the hydrogen atom. The ordinate is proportional to and all distributions are to the same scale.
- The probability of finding the electron when r=0 ( 1.e. near the nucleus) is zero,
- Greater the value of principal quantum number ‘n’, the probability of finding the electron is farther from the nucleus.
- The probability of finding the electron for 18 orbital is at a distance of 0.529 A from the nucleus and is in good agreement with Bohr’s first circular orbit for the hydrogen atom. The probable distance for 2s or 2p orbital is 2,1 A.
Angular Probability distribution curve :
The angular function and
depend only on the direction in the three-dimensional space and is independent of the distance from the nucleus. The probability of finding the electron at a distance ‘r’ from the nucleus and in a given direction
.
Thus, is the probability of finding the electron in a given direction,
at any distance ‘ r ‘ from the nucleus to infinity. The angular part of the wave function arises (due to drawing on polar coordinates) and gives the shape of orbitals. They show a positive or negative sign relating to the symmetry of the angular function. For bonding, the overlap of orbital of a similar sign must take place.
1: It is easier to visualize the boundary surface of orbitals in the form of a solid shape having 90% of the electron density, For p – orbitals the electron density at the nucleus is zero. According to some texts, p-orbitals are two spheres that do not touch each other as shown in figure 1.09.
2: s–orbitals are spherically symmetrical and most of the electron density lie at the surface boundary of sphere. 2 s and 3 s also have a symmetrical sphere of increasing size. The drawing of 2p, 3p, 4p, 3d, 4d etc. also show the symmetry as shown in figure 1.09.
3: The probability of finding the electron towards direction is
and
. The diagram is figure are the angular part of the wave function.
4: d-orbitals are five in number in which dxy, dyz, dzx, and orbitals have the same shape but differ in their orientation. dxy, dyz, dzx lobes lie towards , yz and zx planes respectively,
lobes lying along and axes and lobes lie along the axis but the electron density also lies in the plane.