3. Bonding Flashcards
Exceptions to octet rule
H, He, Li, Be, B
Within or after period 3
Does a molec with polar bond always polar?
Nope, depends on cancelled out dipole moments
London dispersion forces
When a covalent bond contains slight unequal sharing of e- leading to constant polarization and counter polarization; type of van der Waals force; weakest of intermolecular forces
LDF = only intermolecular force in noble gases, but LDF = present in ALL molec. LDF inc with bigger atoms b/c they have more e- to interact —> more polarizable
Ionic bonding vs covalent bonding vs coordinate covalent bonding vs heterolytic rxns
When 1+ e- of atom with low IE = transferred to atom with high EA; from crystal lattice - large, organized arrays of ions vs when e- pair = shared b/w atoms with similar electronegativity; if pair = shared unequally —> polar vs when shared e- = contributed by only one of two atoms (ex: when Lewis base gives e- pair to Lewis acid) vs opposite of coordinate covalent bonding: bond breaks and both e- go back to one of the products
Bond energy vs bond dissociation energy/bond enthalpy
AVG ENERGY required to break all bonds into isolated, gaseous states; the more e- shared —> the more energy needed to break it
The higher the bond energy —> the shorter the bond length (ex: triple bonds vs double bonds) vs THE ENERGY IT TAKES TO BREAK A SPECIFIC BOND IN A GAS PHASE; always pos b/c it requires energy
Know which bond is strongest b/w triple, double, single, sigma and pi bonds. Why is single bond stronger than sigma bonds?
I pretty much laid it out for you. S orbitals have more overlap than p orbitals
How to find formal charge? How to find valence e-?
# ve- in free atom minus # of ve- in bonded atom Group # on periodic table
Linear vs trigonal planar vs tetrahedral vs square planar vs trigonal bipyramidal vs octahedral angles and hybridization
180; sp vs 120; sp2 vs 109.5; sp3 vs 90; sp3d2 90,120,180; sp3d vs 90, 180; sp3d2, 6 sigma bonds and no lone pairs
Valence shell electron pair repulsion theory (VSEPR)
3D arrangement of atoms around a central atom is determined by repulsions b/w bonding and nonbonding e- pairs in valence shell of central atom
Electronic vs molecular geometry
Position of all bonding and lone e- pairs around central atom vs position of only bonding e- pair; uses coordination number - # of atoms that surround and bonded to central atom
Molecular orbital vs bonding orbital vs antibonding orbital
When 2 atoms form a cmpd —> atomic orbitals interact => molecular orbital vs signs of 2 atomic orbitals that are same vs 2 atomic orbitals that are different
Sigma bond vs pi bond
single bonds; head to head overlap, allows free rotation around axis vs double and triple bonds; parallel e- clouds overlap, doesn’t allow free rotation around axis
Which elements do H bonds?
F, O, N; H bonds = strongest type of dipole dipole interaction
How to determine higher bpts based on intermolecular forces?
Consider all the forces involved (dispersion forces, dipole-dipole, H bonds): Ionic bond = strongest, dispersion forces = weakest; if molec have 1+ type of forces —> higher bpt
How to determine largest dipole moment?
If linear and no dipoles cancel out —> strongest dipole moment. If bent or some dipoles cancel out —> weaker dipole moment