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Rules for Molecular Lewis Structures
Halogens can never have double or triple bonds (doesn’t mean it can’t have more than one single bond if central atom)
Fluorine + Hydrogen must always be at the END of the molecule. only one bond is permitted
- F: most electronegative, H: least electronegativity
Carbon must have four bonds unless Carbon Monoxide (3 bonds)
Cl, Br, I can have more than one single bond around them if they are central atoms are to have an expanded octet (Z>=14)
oxygen never bonded to oxygen unless peroxide
oxygen bonded to hydrogen as many times as permissible for acids
If theoretical < available, what to do first
First, always check the central atom to see if the Z>=14.
End of Lewis Structures, what to do?
Count up total # of electrons
Check Bond # for each atom.
Polyatomic Lewis Structures
if negative charge, add electrons to total
if positive charge, subtract electrons from total
NEVER FORGET BRACKETS AND CHARGE AT THE END
Addendum to maximum number of bonds rule
Discrepancy regarding the maximum number of bonds for the central atom (8 - group number), if you must place a multiple bond and it goes over the bond max, O P S and N can handle this situation.
Resonance
phenomenon that occurs when two or more Lewis Structures, that differ only in the placement of the multiple bond, can arise from the same skeletal structure
each contributing structure is separated by double headed arrow
Only occurs when you can be place the bond equally and identically to the other locations.
Occurs as a result of Delocalized Bonding (a pair of electrons is spread over a number of atoms rather being confined between two specific atoms.
Resonance Hybrid
a blend of all contributing structures
contributing structures are all the possible Lewis structures that can be made through Resonance
the more contributing structures a molecule has, (ions too), the more stable the molecule.
Formal Charge
Hypothetical charge the atom in a molecule would have if we could redistribute the electrons in the bond evenly between the atoms.
FC = valence e - #ofnonbondinge - (1/2)(bonding electrons)
To check formal charge calculations
determine the sum of the formal charges for whole strcture
sum must equal zero if a molecule, sum of FC in an ion must equal charge of Ion
Not actual charge of the atoms, just a bookkeeping procedure
What formal charges are preferable?
all formal charges of the atoms in the molecule are zeros is more perferable than one where some formal charges are not zero
if the lewis structure must have nonzero formal charges, the arrangement with the smallest nonzero formal charges is perferable
lewis structures are preferable when adjacent formal charges are zero or of the opposite sign
IMPORTANT: if lewis structure contains a negative formal charge (not all zero), the dominant lewis structure is the one in whpich the negative formal charge is assigned to the more electronegative atom.
VSEPR
Valence Shell Electron Pair Repulsion Theory
a model used to predict the shapes of molecules and polyatomic ions from Lewis Structures
Valence shell electrons repel each other (Coulombic Repulsive Interactions) so they spread out to minimize the repulsion and attain best possible shape/arrangement around central atom and surrounding atoms
‘AXE’ arrangement, A stands for central atom, X stands for # of bonds (where double and triple count as 1), E stands for pairs of non-bonding electrons around central atom
AX2
Linear, Bond Angle = 180 degrees
AX2E1
Bent, Bond Angle = less than 120 degrees
AX2E2
Bent, Bond Angle = 104.5 degrees
AX2E3
Linear, Bond Angle = 180 degrees
AX3
Trigonal Planar, Bond Angle = 120 degrees
AX3E1
Trigonal Pyramidal, Bond Angle = 107.5 degrees
AX3E2
T-Shape, Bond Angle = 90 degrees
AX4
Tetrahedral, Bond Angle 109.5 degrees
AX4E1
Sea-Saw, Bond Angle = Complex
AX4E2
Square Planar, Bond Angle = 90 degrees
AX5
Trigonal Bipyramidal, Bond Angle = 90 degrees and 120 degrees
AX5E1
Square Pyramidal, 90 degrees
AX6
Octahedral, Bond Angle = 90 degrees
Hybridization (Valence Bond Theory)
a theory that explains the mixing of atomic orbitals when atoms form bonds, leading to the formation of hybrids
five possible hybrids that can be made, sp, sp2, sp3, dsp3, d2sp3, (2-6)
hybrid depends on the shape of molecule (molecular geometry)
To figure out what hybridization was used to form the particular molecule
create lewis structure
Apply VESPR
look at central atom; pairs of non-bonding electrons around the atom + how many bonds (triple + double, count as 1)
Vectors and how they are used
line segments have both magnitude and direction, (in chem - used to represent a dipole between two atoms)
magnitude, using a value, just the intensity of the pull between the atoms.
direction comes from the pull between the two atoms involved in a polar bond
How are vectors used
going EQUAL (in magnitude) but opposite in direction, the two dipoles (vectors) cancel out
- they cancel only If the pull is the same in each direction (meaning same atom attached to central atom
going in same general direction additive (angle between vectors < 120 degrees) (as if one pull in that general direction)
Dipole Moment
the measurement of the polarity of a molecule.
symbol: u
essentially, a polar molecule has a dipole moment which measures the overall polarity
Polar Molecules vs Nonpolar Molecules
Polar molecules have at least one dipole that is not get opposed (cancelled out)
Nonpolar molecules are made entirely of nonpolar bonds or made up of several polar bonds which are equal but in opposite direction, cancelling each other out.
Consequence of being polar vs nonpolar?
Polar molecules feel attraction toward external magnetic/electrical fields; this is the opposite reaction that occurs for nonpolar molecules
additionally, like (only polar molecules or only nonpolar molecules) dissolves eachother.