Chapter 3 - Bonding and Chemical Interactions

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Chemistry

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23 Terms

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incomplete octet
elements are more stable with
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expanded octet
elements are more stable with >8 e- in their valence shell
phosphorus (10)
sulfur (12)
chlorine (14)
etc
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ionic bonding
one + electrons from an atom with low ionization energy (most likely a metal) transferred to an atom with high electron affinity (typically a non metal), the resulting electrostatic attraction between opposite charges is what holds the ions together, and no electrons are shared between atoms (SIGNIFICANT DIFFERENT ELECTRONEGATIVITY)
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colavent bonding
electron pair is shared between two atoms, typically have similar values of electronegativity
\*\*coordinate covalent if the shared electrons are contributed by only one of the atoms

further in electronegativity the more ionic character
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covalent compound properties
low melting/boiling points
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bond energy
the greater the number of pairs of electrons shared between the atomic nuclei, the more energy required to break the bonds holding the atoms together
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polarity
occurs when two atoms have relatively different electronegativities, the atoms with higher electronegativity gets the larger share of electron density
- higher electronegativity, partial NEGATIVE
- lower electronegativity, partial POSITIVE
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non polar covalent bond
there is no separation of charge across the bond, difference in electronegative >0.5
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dipole moment
vector quantity of a polar covalent moment, electrons pulled more towards the atoms with higher electronegativity (giving it partial negative)
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formal charge equation
valance e - nonbonding (dots) - 0.5*bonding (lines)
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VSEPR model, 2 regions of e- density
linear, 180 degrees
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VSEPR model, 3 regions of e- density
trigonal planer, 120 degrees
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VSEPR model, 4 regions of e- density
tetrahedral, 109.5 degrees
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VSEPR model, 5 regions of e- density
trigonal bipyramidal, 90/120/180 degrees
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VSEPR model, 6 regions of e- density
octahedral, 90/180 degrees
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molecular orbit
two atoms bond to form a compound and the atomic orbitals interact
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sigma bonds
orbitals overlap head to head, linear, free rotation
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pi bond
orbitals overlap to create two parallel electron cloud densities, no free rotation
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van der Waals force
attractive or repulsive interactions of short lived and rapidly shifting dipoles created from rapid polarization and counter polarization of electron cloud density

* weakest of all intermolecular forces
* stronger in larger molecule and molecules of the same shape
* hydrocarbons typically participate in h
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diople-dipole interactions
present in liquid and solid phases
polar molecules tend to orient themselves that the partial charges of each dipole align opposite (ie partial postive next to partial negative)
- tend to lead to higher boiling/melting points than non polar bonds
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hydrogen bonds
unusually strong dipole dipole interaction
no sharing/transfer of electrons
H bonding to N, O, F has virtually no electron density, making it a prime target to interact with partial negative of N, O, F
unusually high boiling point
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polarity of dipole moment equation
p=qd

q = charge

d = distance
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coordinate covalent bond
When both electrons shared in bond are donated by one atom

transition metals can make these type of bonds

also known as divalent bond