Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Of first and second periods

FIGURE 5.15 The ground-state electron configurations of first- and second-period atoms. Each horizontal line represents a specific atomic orbital. Arrows pointing up represent electrons with spin quantum number m, = +j and arrows pointing down represent electrons with spin quantum number m, = -j. [Pg.190]

Figure 11.15 shows how the electron clouds for the electrons of the atoms of first and second period elements are envisioned. Note that the electron charge waveforms for the electrons in different orbitals of each atom are all superimposed on each other. [Pg.427]

In a liquid the radius of the sphere of molecular interaction is R 3r, where r— radius of a molecule. Liquids are mainly formed by the elements of first and second periods of the system. For the second period we can write down R 3r = (n + l)r, where n— main quantum number. For both periods (first and second) we have R = ( + l)r 2.5 r. [Pg.67]

Electron Configurations of First and Second Period Elements... [Pg.2]

As it is, almost 99% of the human body consists of hydrogen, carbon, nitrogen, and oxygen, which are the members of the first and second period of our table of elements. It is perhaps easy to realize that the order of elements in the table reflects the... [Pg.21]

The pharmacokinetics and absolute oral systemic availability of zaleplon have been assessed in a partially randomized, single-dose, crossover study in 23 healthy subjects, who received intravenous infusions of zaleplon 1 and 2.5 mg during the first and second periods and were then randomly assigned to receive an oral dose of 5 mg or an intravenous infusion of 5 mg in a crossover design (7). The oral and intravenous doses of zaleplon were well tolerated. Somnolence, abnormal vision, diplopia, and dizziness were the most commonly reported adverse events. [Pg.440]

At the end of the first and second periods of heating it is well to dissolve the sublimed ammonium carbonate, by pouring 5-10 cc. of hot water back and forth through the condenser, and return the solution to the reaction mixture. [Pg.14]

The variation of the ionization potential in the groups of elements is also of significance. As a general rule the ionization potential decreases as the group is descended, i.e. as the atomic number increases and the difference in the first and second periods is considerable, e.g. [Pg.38]

The pharmacokinetics and absolute oral systemic availability of zaleplon have been assessed in a partially randomized, single-dose, crossover study in 23 healthy subjects, who received intravenous infusions of zaleplon 1 and 2.5 mg during the first and second periods and were... [Pg.3710]

New graphical representations of the exact molecular orbitals for Hj that make it easier to visualize these orbitals and interpret their meanings. These images provide a foundation for developing MO theory for the first- and second-period diatomic molecules. [Pg.1084]

We see that sp d hybridization uses an available d orbital in the outermost occupied shell of the central atom. The heavier Group VA elements—P, As, and Sb—can form five covalent bonds using this hybridization. But nitrogen, also in Group VA, cannot form five covalent bonds, because the valence shell of N has only one t and three orbitals (and no d orbitals). The set of t and orbitals in a given energy level (and therefore any set of hybrids composed only of t and p orbitals) can accommodate a maximum of eight electrons and participate in a maximum of four covalent bonds. The same is true of all elements of the second period, because they have only t and p orbitals in their valence shells. No atoms in the first and second periods can exhibit expanded valence. [Pg.333]

Figure 9-5 shows molecular orbital energy level diagrams for homonuclear diatomic molecules of elements in the first and second periods. Each diagram is an extension of the... [Pg.357]

Figure 9-5 Energy level diagrams for first- and second-period homonuclear diatomic molecules and ions (not drawn to scale). The sohd lines represent the relative energies of the indicated atomic and molecular orbitals, (a) The diagram for H2, Hc2, Li2, Bc2, B2, C2, and N2 molecules and their ions, (b) The diagram for O2, F2 and Nc2 molecules and their... Figure 9-5 Energy level diagrams for first- and second-period homonuclear diatomic molecules and ions (not drawn to scale). The sohd lines represent the relative energies of the indicated atomic and molecular orbitals, (a) The diagram for H2, Hc2, Li2, Bc2, B2, C2, and N2 molecules and their ions, (b) The diagram for O2, F2 and Nc2 molecules and their...
The electron distributions for the homonuclear diatomic molecules of the first and second periods are shown in Table 9-1 together with their bond orders, bond lengths, and bond energies. [Pg.359]

The accuracy of calculations on transition metal systems has lagged behind that of the first and second rows of the periodic table.One problem for the transition metal compounds is that an SCF wave function is often a much poorer representation of the system than for those compounds only composed of first- and second-row elements. In fact, for some transition metal systems, large CASSCF calculations are required even for a qualitatively correct description, and a quantitative description requires lengthy Cl expansions. In addition to extensive n-particle basis requirements, experience has shown that transition metals also require considerably larger one-particle basis sets than for the first and second rows. As transition metals have such stringent one- and n-particle requirements, FCI benchmark calculations and ANO basis sets have given considerable insight into how to improve the accuracy of calculations on transition metal systems. [Pg.138]

One important goal when deriving Lewis structures is to associate each atom with an octet of electrons, the same number of electrons found in the valence shells of the noble gases. In reality, only a few elements consistently achieve an exact octet of electrons in covalent compounds, but those that do are the important elements found in the first and second periods of the periodic table, most notably H, C, N, O, and F. Elements in the third and higher periods have more empty orbitals (d-orbitals) in their valence shells and can expand their capacity to accommodate as many as 10, 12, or even 14 electrons. Elements like P, S, I, and several others can form compounds like PC15, SFs, and IF7. Yet, these same elements form many compounds and ions with an octet of electrons in their valence shells. Other elements, like boron (Group IIIA), have only three valence electrons, and when all are used to form bonds, as in BF3, boron ends up with only six electrons in its valence shell. [Pg.277]

It takes 10 electrons to complete the first and second periods (Is ls lp ). This leaves us 6 electrons to fill the 3 orbital and partially fill the 3p orbitals. Thus the electron configuration of S is... [Pg.277]

Next, we will consider Lewis structures for molecules with covalent bonds involving nonmetals in the first and second periods. The principle of achieving a noble gas electron configuration applies to these elements as follows ... [Pg.413]

The most common higher coordination number in these elements is six some of the fluorides of the first and second periods provide examples. [Pg.552]

The other exceptions to this rule involve compounds of boron and beryllium, which form compounds like BeHj and BF3, in which there are four and six electrons, respectively, in their completed valence shells. However, the octet rule applies to all of the other elements in the first and second periods of the Periodic Table, on whose compounds we will now focus our attention. [Pg.63]


See other pages where Of first and second periods is mentioned: [Pg.475]    [Pg.1180]    [Pg.601]    [Pg.279]    [Pg.208]    [Pg.579]    [Pg.612]    [Pg.87]    [Pg.328]    [Pg.318]    [Pg.174]    [Pg.112]    [Pg.361]    [Pg.538]    [Pg.33]    [Pg.475]    [Pg.1180]    [Pg.328]    [Pg.304]    [Pg.361]    [Pg.523]   
See also in sourсe #XX -- [ Pg.126 , Pg.127 , Pg.128 , Pg.129 ]




SEARCH



Diatomic Molecules of the First and Second Periods

© 2024 chempedia.info