Thursday, January 24, 2013

Chapter 4 - Bonding


Structure, giant covalent: Very hard but brittle. Very high m.p. and b.p. Do not conduct in any state. Insoluble.
Structure, giant ionic: Hard but brittle. High m.p. and b.p. Conduct when molten or aqueous, but not as solids.
Structure, giant metallic: Malleable, not brittle. M.p. and b.p. dependent on no. of valence e-. Good conductivity.
Structure, molecular covalent: Usually soft and malleable unless hydrogen bonded. Low m.p. and b.p. Do not conduct in any state. Often soluble in non-aqueous solvents, unless they can hydrogen bond to water.
Allotropes: Occur when an element can exist in different crystalline forms, such as in carbon, which can exist as graphite, fullerene and diamond.
Diamond is exceptionally hard because there is no plane of weakness in the molecule made up of sp3 hybridized carbon atoms. In graphite, the carbon atoms are sp2 hybridized. Remaining electrons after the three σ bonds, are delocalized, resulting in the fact that graphite is a good conductor of electricity.
Bond polarity: A polarity caused by a difference in electronegativity between the elements. The greater the difference, the greater the polarity.
Bond, π: Pi bond. A bond formed by the sideways overlap of p orbitals with electron densities concentrated above and below a line drawn through the two nuclei. Double bonds have one π bond, while triple bonds have two which are perpendicular to each other.
Bond, σ: Sigma bond. A bond formed by the head on overlap of atomic orbitals from two different atoms along the line drawn through the two nuclei, with electron densities concentrated along the line. Single, double and triple bonds have one σ bond.
Covalent bond: Bonding by the sharing of electrons. The electrons are shared and attracted by both nuclei resulting in a directional bond between the two atoms.
Dative bond: A bond in which both electrons come from one of the atoms. Also known as coordinate bond.
Ionic bond: A bond by which electrons are transferred from one atom to another to form ions with complete outer shells.
In an ionic compound the + and – ions are attracted to each other by the electrostatic force between them, and build up into a strong lattice. Have relatively high m.p. Ionic bonds occur between elements with a great difference (>1.8) in electronegativity.
Conductivity: The extent to which a substance can conduct electricity. Must possess electrons or ions that are free to move.
Delocalization: The sharing of one electron pair by more than two atoms.
Forces, dipole-dipole: Permanent electrostatic forces of attraction between polar molecules. Stronger than van der Waals’.
Forces, Hydrogen bonding: Occurs when hydrogen attached to a highly electronegative element (N, F, or O) is bonded to another highly electronegative element (N, F, or O). Stronger than dipole:dipole forces.
Forces, van der Waal’s: Temporary dipole forces due to momentary unevenness in spread of electrons. Weakest of intermolecular forces. Increase with increasing molar mass.
Hybridization: The mixing of atomic orbitals to create new orbitals of the same energy.
Metallic bonding: The valence electrons in metals become detached from the individual atoms so that the metals consist of a closely packed lattice of + ions in a ‘sea’ of delocalized electrons. Forces of attraction are between ions and electrons and not between the ions themselves, which means that metals are malleable and ductile.
Molecular polarity: Depends on both the bond polarity and the symmetry.
Resonance hybrid: Structures that arise from the possibility to draw a multiple bond in different positions equivalently. Can be better explained by delocalization.
Solubility: The extent to which one substance dissolves in another.
VSEPR theory: Valence Shell Electron Pair Repulsion theory. States that pairs of electrons arrange themselves around the central atom so that they are as far apart from each other as possible. Greater repulsion between lone pair of electrons than bonded pairs.
 
 
Information for this post came directly from http://liakatas.org/chemblog/?page_id=17