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MOLECULAR POLARITY
Result from imbalance distribution of electric charge in the molecule
Due to the formation of partial positive and partial negative ends
Determined by bond polarity and shape
abt the entire molecule
BOND POLARITY
Determined by the electronegativity difference of the two bonded nonmetals
Symbolized by polar arrow
Molecules that contain polar bond are not always polar
only abt the bond
electronegativity difference
mostly ionic bonds - 1.7 or higher
polar covalent - greater than 0.4 to less than 1.7
mostly covalent - 0.4 or less
nonpolar covalent - 0
ionic bonds
polar but we don’t use polar arrows and partial charges
depicting polar bonds
unequal electron sharing can be depicted by a polar arrow which points to the more electronegative element and partial charges
δ+ +→ δ-
polar covalent bond
much more common than either pure ionic or pure covalent bonds
shared electron pair isn’t shared equally, but remains closer to one atom than the other
unequal electron sharing causes the more electronegative atom of the bond to be partially negative and the less electronegative atom to be partially positive
electron density shifts to more electronegative element
nonpolar covalent bond
equal sharing of electrons
no partial charges
lewis structures of molecules
same as the lewis structure of covalent compounds
need to be able to discern the central atom, bonding grps, and non-bonding grps
converting a molecular formula → lewis structure
Draw the skeletal formula (central atom and surrounding atoms)
Get total # of valence electrons and deduct the # used to form single bonds from all of the atoms
Divide remaining electrons by 2 and distribute those lone pairs to the surrounding atoms first, then the central atom
is the central atom doesn’t have full octet, change a lone pair of a surrounding atom into another bonding pair for the central atom to form a multiple bond
add brackets and charges in the case of polyatomic ions
for acids, H atoms are never bonded to the central atom, only the oxygen atom
central atom
less electronegative atom
appears only once in the formula (?)
hydrogen can never be a central atom
single bonds
are never between 2 surrounding atoms
multiple bonds
if there aren’t enough electrons for the central atom to attain an octet, a multiple bond is present
molecules that don’t follow the octet rule
molecules w/ electron deficient atoms
expanded valence shells
molecules w/ odd electron atoms
molecules w/ electron deficient atoms
molecules that have less than 8 valence electrons
B and Be are electron deficient most times
expanded valence shells
central atom w/ more than 8 valence electrons
can be atoms from period 3 and below (nonmetals?)
molecules w/ odd electron atoms
the lone electron / radical electron makes molecules very unstable and short-lived
happen due to d-orbitals
molecular shapes
the function of a molecule depends on its shape
Valence Shell Electron Pair Repulsion Theory (VSEPR Theory) and Molecular Shape (?)
each grp of valence electrons around a central atom is located as far as possible from others to minimize repulsions
a “grp” of electrons is only the # of electrons that occupies a localized region around an atom
a single bond, double bond, triple bond, lone pair, or single electron all count as a single grp each
electron grps (2 categories) are only those around the central atom (total # = bonding grps + nonbonding grps)
for multiple central atoms, one will be specified
bonding grps
single bonds, double bonds, or triple bonds
each are counted as 1 bonding grp
non-bonding grps
lone pair (around the central atom only) and lone electron
each are counted as 1 bonding grp
electron grp arrangement
depends in the total number of electron grps
defined by both bonding and non-bonding electron grps
linear
trigonal planar
tetrahedral
trigonal bipyramidal
octahedral
Does not always = the shape of the molecule
linear
2 electron grps around the central atom
180 degree ideal bond angle
trigonal planar
3 electron grps around the central atom
forms a triangle and lies flat on a plane
120 degrees ideal bonding angle
tetrahedral
4 electron grps around the central atom
109.5 degrees ideal bond angle
trigonal bipyramidal
5 electron grps around the central atom
triangle at the middle and 2 pyramids formed (1 top, 1 bottom)
120 degree ideal bond angle between 2 equatorial sides
90 degree ideal bond angle between an axial and equatorial side
has two different positions for electron groups, and two ideal bond angles
Equatorial-equatorial repulsions are weaker than axial-equatorial repulsions
Where possible, lone pairs in a five electron-group system occupy equatorial positions
axial
positioned vertically
equatorial
positioned at the middle (horizontal)
octahedral
6 electron grps around the central atom
forms 8 sides
90 degrees ideal bond angle always
molecular shape
3D arrangement of nuclei joined by the bonding grps
defined by the relative positions of the nuclei
classified using AXmEn
AXmEn
A - central atom
X - surrounding bonding grps
m - # of bonding grps
E - non-bonding valence electron grp
n - # of non-bonding grps
bond angle
angle formed by the nuclei of 2 surrounding atoms w/ the nucleus of the central atom
ideal and real
ideal bond angles
determined by basic geometry alone
similar electron grps around the central atom → real = ideal
real bond angles
deviate in many cases
more bonds
lone pair
presence of more electronegative atom
more bonds
more bonds → more repulsion → bond angle affected
real ≠ ideal bond angle
angle of multiple bond and other bonding pair → greater than ideal
angle of 2 bonding grps → less than ideal
lone pair
freedom of lone pair to move → more repulsion
angle of lone pair and bonding grp is greater than the ideal bond angle
angle of 2 bonding grp is less than the ideal bond angle
2 lone pairs may neutralize each other
presence of more electronegative atom
attracts bonding grps to itself
possible shapes
as long as there’s no lone pair, the name of the shape = EGA name
Shapes of Linear
only 1 shape total
Linear (AX2)
Shapes of Trigonal planar
2 shapes total
Trigonal planar (AX3)
Bent or v-shaped (AX2E)
Shapes of Tetrahedral
3 shapes total
Tetrahedral (AX4)
Trigonal Pyramidal (AX3E)
Bent or v-shaped (AX2E2)
Shapes of Trigonal Bipyramidal
4 shapes total
lone pairs are always equatorial
Trigonal Bipyramidal (AX5)
Seesaw (AX4E)
T-shaped (AX3E2)
Linear (AX2E3)
Shapes of Octahedral
3 shapes total
Octahedral (AX6)
Square Pyramidal (AX5E)
Square Planar (AX4E2)
pi bonds (π)
single bond in a double bond
middle bond of a triple bond
sigma bond (σ)
single bonds
chemical bonds
aka intramolecular forces
Intermolecular forces
forces of attraction that exist between molecules in a compound
aka Van der Waals Forces
aka secondary bonds
responsible for physical properties of matter (eg boiling pt)
weaker than chemical bonds
illustrated w/ dotted lines
Characteristics of IMF
weaker than primary bonds (ionic & covalent bonds)
strength of IMF affects the melting & boiling point as well as solubility of substances
causes the compound to exist in certain states of matter at a given temperature
weak IMF = gases at room temperature (ex: Helium gas)
very strong IMF = solids
Polar molecule
unequal distribution of charge as a result of its polar bonds and shape
aka dipole molecule bcs it has 2 poles (partial positive and partial negative)
Nonpolar molecule
equal distribution of charge which may be due to presence of nonpolar bonds and its shape
does not contain dipole
Polar molecules ex
Diatomic molecules which contain polar bonds
Shapes of these molecules are bent, trigonal pyramidal, seesaw, T-shaped, square pyramidal
contain one or more polar bonds and the individual bond dipoles do not cancel
Nonpolar molecules ex
Diatomic molecules which contain nonpolar bonds
Shapes of these molecules may be linear, trigonal planar, trigonal bipyramidal, square planar, tetrahedral, octahedral
Molecules that may contain polar bonds but are ALL cancelled
Molecules with carbon and hydrogen atoms in their chemical formula(hydrocarbons) or molecules with long chain of hydrocarbons
Types of IMF
dipole-dipole forces
hydrogen bonding
ion dipole force
london forces
dipole-dipole forces
between polar molecules
creates a higher boiling pt
polarizability
More electrons are further from the nucleus → Nucleus has less pull on far off electrons
more electrons and More negative charge = more polarizability
hydrogen bonding
special kind of dipole-dipole forces formed when a hydrogen atom bonded with highly electronegative such as N, O & F
resulting bond is highly polar with hydrogen (δ +)
ion dipole forces
interaction between ion and a polar molecule
ionic compound + dipole
Example: sodium chloride dissolved in water
London forces
exists among non-polar molecules
aka London Dispersion or Dispersion Forces
weak force and usually found among identical molecules such as O2 , N2 and Cl2 since there is no attraction among 2 opposite charges
all interacting molecules have london dispersion force
possible as long as 2 particles have a pt of contact
dependent on the size of atom or molecule: Larger atoms or molecules = electrons→ easier to induce them into temporary dipoles
increase with increasing molecular mass
IMF strength
Ion dipole > hydrogen bond > dipole-dipole > london dispersion