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Bohr relationship

O. Lund, J. Hansen, S. Brunak and J. Bohr, Relationship between protein structure and geometrical constraints. Protein Sci. 5 (1996), 2217-2225. [Pg.223]

Bohr relationship, 95 Boltzmann distribution law, 51, 52 Bond clevage, Norrish Type I, 238 Norrish Type II and III, 240 Bond dissociation energy, 6 Bond length, 29, 93 Born-Oppenheimer approximation, 29, 97... [Pg.187]

For nearly half a century, Mendeleev s periodic table remained an empirical compilation of the relationship of the elements. Only after the first atomic model was developed by the physicists of the early twentieth century, which took form in Bohr s model, was it possible to reconcile the involved general concepts with the specificity of the chemical elements. Bohr indeed expanded Rutherford s model of the atom, which tried to connect the chemical specificity of the elements grouped in Mendeleev s table with the behavior of electrons spinning around the nucleus. Bohr hit upon the idea that Mendeleev s periodicity could... [Pg.31]

The mathematical relationship (4) is the one Bohr was able to deduce. Current quantum mechanical methods also deduce this relationship, of course, but with a model that is in fundamental discord with the one used by Bohr. [Pg.261]

According to the correspondence principle as stated by N. Bohr (1928), the average behavior of a well-defined wave packet should agree with the classical-mechanical laws of motion for the particle that it represents. Thus, the expectation values of dynamical variables such as position, velocity, momentum, kinetic energy, potential energy, and force as calculated in quantum mechanics should obey the same relationships that the dynamical variables obey in classical theory. This feature of wave mechanics is illustrated by the derivation of two relationships known as Ehrenfest s theorems. [Pg.43]

This is precisely the relationship that was required when Bohr assumed that the angular momentum of the electron is quantized for the allowed orbits. [Pg.16]

However, in the sodium atom, An = 0 is also allowed. Thus the 3s —> 3p transition is allowed, although the 3s —> 4s is forbidden, since in this case A/ = 0 and is forbidden. Taken together, the Bohr model of quantized electron orbitals, the selection rules, and the relationship between wavelength and energy derived from particle-wave duality are sufficient to explain the major features of the emission spectra of all elements. For the heavier elements in the periodic table, the absorption and emission spectra can be extremely complicated - manganese and iron, for example, have about 4600 lines in the visible and UV region of the spectrum. [Pg.285]

This section started with the discovery of Soddy and Fajans on radioactive decay around 1910 and the relationship of radioactive decay to the periodic table. At this point in the history, we understand the periodic table and we understand the role of isotopes in the periodic table. We have not yet understood the structure of the modern Table, i.e. first row two elements, second row eight elements, etc. That understanding can be based on Bohr theory of the hydrogen atom originally developed in 1911 and is summarized in Bohr s famous article in Zeitschrift fur Physik (Bohr 1922). [Pg.24]

An overview of a scientific subject must include at least two parts retrospect (history) and the present status. The present status (in a condensed form) is presented in Chapters 2 to 21. In this section of the overview we outline (sketch) from our subjective point of view the history of electrochemical deposition science. In Section 1.2 we show the relationship of electrochemical deposition to other sciences. In this section we show how the development of electrodeposition science was dependent on the development of physical sciences, especially physics and chemistry in general. It is interesting to note that the electron was discovered in 1897 by J. J. Thomson, and the Rutherford-Bohr model of the atom was formulated in 1911. [Pg.3]

The dependence of the elastic pressure on the density can be expressed approximately by a power function p = Bpn, usually called polytropic. It could alternatively be considered that the force centers are repelled according to the relationship F = a/(3n-2) as assumed in the Bohr theory of crystal lattices. The thermal motion, at this degree of compression, consists of small oscillations. To each vibrational degree of freedom there corresponds an energy RT (per mole). The total oscillatory energy equals cvT, where cv is independent of the volume in this approximation... [Pg.552]

If the electron is now brought from the first into the second orbit, then an amount of energy must be expended, equivalent to E2 — Ev If, on the other hand, the electron moves from state 2 to state 1, then an amount of energy E2 — Ex is set free, which, according to Bohr, is released as monochromatic radiation of a frequency given by the relationship v = E2 — Ej) jh, in which h is Planck s constant. [Pg.4]

The energy levels of the hydrogen atom are found to be determined solely by the principal quantum number, and their relationship is the same as found for a Bohr... [Pg.21]

The absorption or emission of energy in an electromagnetic spectrum occurs in discrete packets of photons. The relationship between the energy of a photon and the frequency appropriate for the description of its propagation is given by the famous Bohr equation ... [Pg.77]

Moseley s empirical relationship reveals a behavior that is in agreement with the Rydberg-Bohr equation, because the energy levels linked with the outer electron transitions are significantly... [Pg.155]

Bohr was able to show that there is a clear relationship between the energy absorbed by (or released from) atoms. To do this he used the equation (provided for you on the AP test)... [Pg.64]

The molar magnetic susceptibility, xm> is related to a quantity of more interest to the chemist, the Bohr magneton number (or magnetic dipole moment in Bohr magneton units), designated p. The relationship is ... [Pg.409]

It was the analysis of the line spectrum of hydrogen observed by J. J. Balmer and others that led Neils Bohr to a treatment of the hydrogen atom that is now referred to as the Bohr model. In that model, there are supposedly allowed orbits in which the electron can move around the nucleus without radiating electromagnetic energy. The orbits are those for which the angular momentum, mvr, can have only certain values (they are referred to as quantized). This condition can be represented by the relationship... [Pg.18]

It should be noted that this relationship is identical to Bohr s assumption about stable orbits... [Pg.19]

From Bohr s theory it could thus be deduced that the element of atomic number 72 cannot be a Rare Earth, but that it must exhibit a relationship to zirconium. Von Hevesy and Coster did not, as so many others had done, look for the missing element in minerals of the Rare Earths but came across hafnium, as was expected theoretically, in fairly large quantities (about 1 %) in the majority of minerals containing zirconium and in all preparations of zirconium which had been considered pure up till then. [Pg.13]

In Bohr s model of the hydrogen atom, the circular orbits were determined by the quantum number more accurately, by the square of the quantum number n. No other orbits were allowed. By changing the orbits from circles to ellipses, Sommerfeld introduced a second radius, which gave him another variable to play with. So it was that Sommerfeld generalized Bohr s quantum condition for electron orbits in terms of the two quantum numbers n and k. His analysis led him to establish a relationship between the two quantum numbers namely, the quantum number n set the upper limit on the quantum number k, but k could have smaller values as follows ... [Pg.48]


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See also in sourсe #XX -- [ Pg.95 ]




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