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Quantum number defined

The ability to assign a group of resonance states, as required for mode-specific decomposition, implies that the complete Hamiltonian for these states is well approxmiated by a zero-order Hamiltonian with eigenfunctions [M]. The ( ). are product fiinctions of a zero-order orthogonal basis for the reactant molecule and the quantity m. represents the quantum numbers defining ( ).. The wavefimctions / for the compound state resonances are given by... [Pg.1030]

The arrangement of electrons in an atom is described by means of four quantum numbers which determine the spatial distribution, energy, and other properties, see Appendix 1 (p. 1285). The principal quantum number n defines the general energy level or shell to which the electron belongs. Electrons with n = 1.2, 3, 4., are sometimes referred to as K, L, M, N,. .., electrons. The orbital quantum number / defines both the shape of the electron charge distribution and its orbital angular... [Pg.22]

The orbital angular-momentum quantum number, , defines the shape of the atomic orbital (for example, s-orbitals have a spherical boundary surface, while p-orbitals are represented by a two-lobed shaped boundary surface). can have integral values from 0 to (n - 1) for each value of n. The value of for a particular orbital is designated by the letters s, p, d and f, corresponding to values of 0, 1, 2 and 3 respectively (Table 1.2). [Pg.7]

The orbital or azimuthal quantum number (/) defines form (i.e., eccentricity of elliptical orbit cf Pauling, 1948) and indicates which sub-level is occupied by the electron. It assumes integer values between 0 and n —. ... [Pg.13]

Here wi, W2, W3 are parameters characterizing the representations of group Rj u, U2 stand for the corresponding quantities of group G2 v is the seniority quantum number, defined in a simpler way in Chapter 9. On the other hand, the eigenvalues of the Casimir operator of group i 2(+i may be expressed in the following way by v and S quantum numbers... [Pg.46]

We denote by G the set of all the experimentally observable quantities (called physical observables) which must be reproduced. Such quantities are, for instance, the collision energy, the quantum numbers defining the intramolecular state (vibrations and the principal quantum number of rotation), the total angular momentum etc... However, there are other dynamical variables which have a clear meaning in Classical Mechanics but correspond to no physical observable because of the Uncertainty Principle. We call them phase variables and denote them globally by g. The phase variables must be given particular values to obtain, at given G, a particular trajectory. Such variables are, for instance, the various intramolecular normal vibrational phases, the intermolecular orientation, the secondary rotation quantum numbers, the impact parameter, etc... Thus we look for relationships of the type qo = qq (G, g) and either qo = qo (G, g) or po = Po (G, g)... [Pg.29]

There are always 2n2 possible combinations of quantum numbers. We divide these into orbitals. Orbitals are maps of the probability of the electron being located at a certain region in space. They are designated by their angular momentum quantum numbers. The values of magnetic and spin quantum numbers define the electrons within an orbital. [Pg.55]

Each electron in an atom is defined by four quantum numbers n, l, m and s. The principal quantum number (n) defines the shell for example, the K shell as 1, L shell as 2 and the M shell as 3. The angular quantum number (/) defines the number of subshells, taking all values from 0 to (n — 1). The magnetic quantum number (m) defines the number of energy states in each subshell, taking values —l, 0 and +1. The spin quantum number fsj defines two spin moments of electrons in the same energy state as + and —f The quantum numbers of electrons in K, L and M shells are listed in Table 6.1. Table 6.1 also gives the total momentum (J), which is the sum of (7 + s). No two electrons in an atom can have same set quantum numbers (n, /, m, s). Selection rules for electron transitions between two shells are as follows ... [Pg.173]

Which quantum number defines a shell Which quantum numbers define a subshell ... [Pg.281]

Each set of three quantum numbers defines a particular atomic orbital, and, therefore, for n = 2, there are four atomic orbitals with the sets of quantum numbers ... [Pg.9]

GHz. This line was measured towards the cold, dark cloud L673 (2) and the molecular cloud M17-NW. The nitrogen nucleus has a spin of 1(N) = 1 / is the quantum number defining nuclear spin. An important spectroscopic effect of nuclear spin is quadrupole hyperfme structure. Consequently, the spectrum of the J= 1 -> 0 transition is split into three hyperfine components, indicated by the quantum number F F = J + I), which provides a spectral fingerprint for HCN. In order of increasing frequency, these transitions are labeled F= ->, F= —> 2, and F = 1 0. The intrinsic, or fundamental, intensity of the three... [Pg.370]

A wavefunction, ip, is a solution to the Schrodinger equation. For atoms, wavefunctions describe the energy and probabihty of location of the electrons in any region around the proton nucleus. The simplest wavefunctions are found for the hydrogen atom. Each of the solutions contains three integer terms called quantum numbers. They are n, the principal quantum number, I, the orbital angular momentum quantum number and mi, the magnetic quantum number. These simplest wavefunctions do not include the electron spin quantum number, m, which is introduced in more complete descriptions of atoms. Quantum numbers define the state of a system. More complex wavefunctions arise when many-electron atoms or molecules are considered. [Pg.18]

Magnetic quantum number (m,). Magnetic quantum numbers define the different spatial orientations of the orbitals. The values range from -/ to +/. For example, let s say the value of / is 1. So the magnetic quantum numbers will be -1, 0, and +1. The / value corresponds to p sublevel and the three magnetic quantum numbers correspond to the three atomic orbitals in the p subshell. [Pg.46]


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