Chem Bonding Flashcards
covalent bond
Electrostatic forces of attraction between the shared electron and the positively charge nuclei due to the sharing of electrons through overlapping of orbitals
dative covalent bond
an atom donates a lone pair of electrons into an empty orbital of another atom for sharing
factors affecting strength of covalent bond
- bond order
as bond order increases, the number of bonding electrons within the inter-nuclei region increases. the electrostatic forces of attraction for these electrons increases - effectiveness overlap of orbitals
the larger the atom, the larger and more diffused the orbitals, the less effective the overlap of orbitals and the weaker the covalent bond - polarity of covalent bond
the greater the difference in electronegativities of the bonding atoms, the more polar the bond, the stronger the attractive forces between the S+ and S- that strengthens the covalent bond
ionic bond
strong electrostatic forces of attraction between oppositely charged ions in giant ionic lattice structure
Factors affecting strength of bonds
- Charge of ions
- Ionic radius
Greater charge of ions, smaller ionic radius, the stronger the ionic bond.
difference in charge is more important than difference in ionic radius
metallic bonds
strong electrostatic forces of attraction between the metal cations and sea of delocalised electrons in giant metallic lattice structure
factor affecting strength of metallic bond
- charge density of the metal cation
greater the charge and the smaller the size of the ion, the stronger the metallic bond - the number of valence electrons
the large number of valence electrons implies that the large number of sea of delocalised electrons
Instantaneous dipole- induced dipole
esfoa between temporary diploles. exist in all simple covalent molecules and noble gases
strength of id-id
- no of electrons
the larger the no of electron, the more polarisable is the electron cloud, resulting in stronger idid - surface area of molecules (isomers)
straight chain molecule has a larger surface of interaction for more extensive id-id than a branched isomer
permanent dipole-permanent dipole
esfoa between polar dipoles which exist between polar molecules
strength of pdpd
magnitude of net dipole moment
- difference in electronegativity
- arrangement of polar covalent bonds
hydrogen bonds
esfoa between electron-deficient H atom that is bonded to O, F or N atom and lone pair of electrons on a highly electronegative O, F or N atom
Strength of H-bonds
- Polarity of H-X bond
the more polar the H-X bind, the stronger the H-bond - extensiveness of inter-molecular H bonds
- number of H atoms bonded to N/O/F atom
- number of lone pairs on N/O/F atom
- presence of intramolecular H-bond
if solute is soluble in solvent
energy that is released from the solute-solvent interaction is sufficient to compensate for energy needed to overcome the solute-solvent and solvent-solute interactions.
why are ALCL3, ALBr3 and Be CL2 covalent compounds
they are simple molecule structure due to high charge density of cation and high polarisability of anion.