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  2. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    The orbital is not symmetric around the molecular axis and is therefore a pi orbital. The antibonding pi orbital (also asymmetrical) has four lobes pointing away from the nuclei. Both p y and p x orbitals form a pair of pi orbitals equal in energy and can have higher or lower energies than that of the sigma orbital.

  3. Molecular orbital - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital

    The symmetry properties of molecular orbitals means that delocalization is an inherent feature of molecular orbital theory and makes it fundamentally different from (and complementary to) valence bond theory, in which bonds are viewed as localized electron pairs, with allowance for resonance to account for delocalization.

  4. VSEPR theory - Wikipedia

    en.wikipedia.org/wiki/VSEPR_theory

    The methane molecule (CH 4) is tetrahedral because there are four pairs of electrons. The four hydrogen atoms are positioned at the vertices of a tetrahedron, and the bond angle is cos −1 (− 1 ⁄ 3) ≈ 109° 28′. [16] [17] This is referred to as an AX 4 type of molecule. As mentioned above, A represents the central atom and X represents ...

  5. Multiplicity (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Multiplicity_(chemistry)

    The highest occupied orbital energy level of dioxygen is a pair of antibonding π* orbitals. In the ground state of dioxygen, this energy level is occupied by two electrons of the same spin, as shown in the molecular orbital diagram. The molecule, therefore, has two unpaired electrons and is in a triplet state.

  6. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    The seventh lone pair must be placed on the nitrogen atom. Satisfy the octet rule. Both oxygen atoms currently have 8 electrons assigned to them. The nitrogen atom has only 6 electrons assigned to it. One of the lone pairs on an oxygen atom must form a double bond, but either atom will work equally well. Therefore, there is a resonance structure.

  7. Molecular orbital theory - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_theory

    However, in benzene the remaining six bonding electrons are located in three π (pi) molecular bonding orbitals that are delocalized around the ring. Two of these electrons are in an MO that has equal orbital contributions from all six atoms. The other four electrons are in orbitals with vertical nodes at right angles to each other.

  8. Orbital hybridisation - Wikipedia

    en.wikipedia.org/wiki/Orbital_hybridisation

    In ethene, the two carbon atoms form a σ bond by overlapping one sp 2 orbital from each carbon atom. The π bond between the carbon atoms perpendicular to the molecular plane is formed by 2p–2p overlap. Each carbon atom forms covalent C–H bonds with two hydrogens by s–sp 2 overlap, all with 120° bond angles. The hydrogen–carbon bonds ...

  9. Electron configuration - Wikipedia

    en.wikipedia.org/wiki/Electron_configuration

    The molecular orbitals are labelled according to their symmetry, [e] rather than the atomic orbital labels used for atoms and monatomic ions; hence, the electron configuration of the dioxygen molecule, O 2, is written 1σ g 2 1σ u 2 2σ g 2 2σ u 2 3σ g 2 1π u 4 1π g 2, [39] [40] or equivalently 1σ g 2 1σ u 2 2σ g 2 2σ u 2 1π u 4 3σ g ...