Chem test 3
Hybridization of central atom
linear/linear sp trigonal planar/ trigonal planar/bent sp2 tetrahedral/tetrahedral/trigonal bypyrimadal/bent sp3
london dispersion forces
non polar molecules temporary dipoles are formed as a result of momentary uneven distribution of electrons stringest with large long molecules
ionic bond
oppositely charged ions , stringest with large charges and small bond lenghts
hydrogen binds
polar molecules with h bund to small electronegative atom , usually small dipole forced
dipole forces
polar molecules, partial charges not so as strong
Linear
sp
trigonal planar
sp2
trigonal bypyrimidal
sp3d
Octahedral
sp3d2
delocalization
the spreading of electron in alternating single and double bonds over 3+ atoms in a molecule
A π bond could be formed from the overlap of which two orbitals?
two unhybridized p orbitals
A molecule that contains delocalized electrons ________
will have at least two resonance structures.
Which of these molecules have delocalized electrons?
Draw the Lewis structure of each molecule and determine which has resonance. Resonance results in alternate ways to distribute electrons but still maintains a valid Lewis Structure. CO₃²⁻ has delocalized electrons. CO₃²⁻
bond order
You can calculate the bond order using this formula: BO=1/2 (numberofbondingelectrons−numberofantibondingelectrons) Benzene has σ and π bonds and the bond order will be a combination of both. To calculate bond order for σ bonds, there are 2 bonding electrons and 0 antibonding electrons.BO=1/2(2−0)=1 To calculate bond order for π bonds, there are 6 bonding electrons and 0 antibonding electrons. This is if there were six full pi bonds, but because this is a resonance structure it is divided by two.
The term 'delocalization' refers to
electrons being shared via π bonds between more than just two atoms.