8.2 Hybrid Atomic Orbitals

8.2 Hybrid Atomic Orbitals

  • One way to explain how chemical bonds form in diatomic molecules is by thinking in terms of overlap of atomic orbitals.
    • To understand how stable bonds are formed, we need a more detailed model.
    • The water molecule has one oxygen atom bonding to two hydrogen atoms.
    • The bond angle is not 90deg as shown by the evidence.
    • The real-world observations of a water molecule do not match the predictions of the valence bond theory model.
  • This isn't consistent with the evidence.
  • Waves combine to create new mathematical descriptions that have different shapes when atoms are bound together.
  • There are four equivalent hybrid orbitals that point toward the corners of a tetrahedron in the oxygen atom.
    • The bond angle should be a result of the overlap of the O and H orbitals.
    • Valence bond theory must include a hybridization component to give accurate predictions because of the observed angle of 104.5deg.
  • In order to make the geometry easier to see, some orbitals may be drawn in a balloon shape instead of a lump.
  • The experimental structure is consistent with this description.
  • There are no hybrid orbitals in isolated atoms.
    • They are formed from bonds of covalently bonding atoms.
  • The shapes and orientations of hybrid orbitals are very different from the atomic ones.
  • A set of hybrid orbitals is created.
    • The number of hybrid orbitals in a set is the same as the number of atomic orbitals in the set.
  • A set of hybrid orbitals are equivalent in shape and energy.
  • The type of hybrid orbitals depends on the electron-pair geometry of the atom.
  • S bonds are formed when hybrid orbitals overlap.
    • P bonds are formed by un hybridized orbitals.
  • We will discuss the common types of hybrid orbitals in the following sections.
  • A central atom with no lone pairs of electrons in a linear arrangement of three atoms is an example.
    • There are two regions of electron density in the molecule.
    • Two of the Be atom's four orbitals will mix to accommodate the two electron domains.
    • The number of hybrid orbitals is always equal to the number of atomic orbitals.
    • The half-filled hybrid orbitals will overlap with the chlorine atoms to form two identical s bonds.
  • The hybrid orbital is oriented in one direction.
  • We show the electronic differences in an isolated Be atom and in a bonded Be atom in a diagram.
    • The diagram has energy at the top.
    • One upward arrow is used to indicate one electron in an orbital and two upward arrows are used to indicate two electrons of opposite spin.
  • The newly created orbitals are occupied by the valence electrons.
    • The unpaired electron on a chlorine atom pairs up with the hybrid electron on a chlorine atom when they overlap.
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    • Other examples include the mercury atom in the linear HgCl2 molecule, the zinc atom in Zn(CH3)2, which has a linear C-Zn-C arrangement, and the carbon atoms in HCCH and CO2.
  • The University of Wisconsin-Oshkosh has orbitals in three dimensions.

  • There are 2 hybridized orbitals with respect to each other.
  • We will use these representations when the view is too crowded to see.
  • 2 hybrid orbitals are sometimes used in crowded figures.
  • The molecule is trigonal and has three bonds to hydrogen atoms.
  • BH3 has a trigonal structure.
  • Three s bonds are formed in BH3 by the overlap of the three half-filled hybrid orbitals.
  • This includes the molecule with a lone pair on the central atom, as well as the molecule with two single bonds and a double bond connected to the central atom, such as the molecule with two single bonds and a double bond connected to the central atom.
  • The electrons that point in one direction are contained in a region of electron density.

  • There are 3 hybridized orbitals with respect to each other.
  • A molecule of methane, CH4, consists of a carbon atom surrounded by four hydrogen atoms.
    • Each carbon electron pairs with a hydrogen electron when the C-H bonds form, and the four valence electrons of the carbon atom are distributed equally in the hybrid orbitals.
  • A C-H s bond is created by overlap of each of the hybrid orbitals.
  • A sigma bond is formed by 3 orbitals of the carbon atom.
    • The formation of four strong, equivalent covalent bonds between the carbon atom and each of the hydrogen atoms resulted in the creation of the methane molecule, CH4.
  • A s bond is formed between the two carbon atoms.
    • The orientation of the two CH3 groups is not fixed relative to each other.
    • There is evidence that shows rotation around bonds.
  • A single pair of electrons can be held by 3 hybrid orbitals.
    • The nitrogen atom in ammonia is surrounded by three bonding pairs and a single pair of electrons.
    • 3 hybridized with one hybrid.
  • There are two lone pairs and two bonding pairs of electrons in the water.
    • Two of the hybrid orbitals were occupied by lone pairs and two by bonding pairs.
    • Since lone pairs occupy more space than bonding pairs, structures that contain lone pairs have slightly distorted bond angles.
    • The observed angles in ammonia and water are slightly different.

  • There are five P-Cl bonds in a molecule of PCl5 and they are directed toward the corners of a trigonal bipyramid.
  • There are two lone pairs of electrons on the central atom, and two lone pairs on the T-shape shown.
  • A molecule of sulfur has six bonding pairs of electrons and a single sulfur atom.
    • The central atom has no lone pairs of electrons.
    • Two hybrid orbitals directed towards different corners of an Octahedron.
  • The structure around sulfur is made up of 2 orbitals.
    • The minor part of each orbital is not shown for clarity.
  • The number of regions of electron density surrounding an atom is used to determine the atom's hybridization.
  • The arrangements are the same as those predicted by the theory.
    • There are two theories that give an explanation for how the shapes of molecule are formed.
  • Determine the structure of the molecule.
  • The number of regions of electron density around an atom is determined by the number of bonds, radicals, and lone pairs that count as one region.
  • The set of hybridized orbitals should be assigned to this geometry.
  • The shapes of hybridized orbital sets are the same as the electron-pair geometries.
    • There are 2 orbitals arranged in a trigonal fashion.
  • It is important to remember that hybridization was created to rationalize observed geometries.
    • The model works well for molecules with small central atoms, in which the valence electron pairs are close together.
    • There are fewer repulsions for larger central atoms.
    • They do not need hybridized orbitals to explain the observed data because their compounds exhibit structures that are not consistent with the theory.
    • Sulfur and H2S have the same Lewis structure.
    • It has a smaller bond angle, which shows less hybridization on sulfur than oxygen.
    • There is a need to explain the structures.
  • Ammonium sulfate is important.
  • There are four regions of electron density in sulfate.
  • Nitrogen is sometimes used as a source of urea.