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48 Cards in this Set

  • Front
  • Back
molecular mass
sum of atomic masses of all atoms in molecule of substance
mole
quantity of a given substance that contains as many molecules as of atoms in exactly 12g of carbon12
molar mass
mass of one mole of a substance
avogadro's number
number of atoms in a mole
percent composition
mass percentage of each element in compound
empirical formula
simplist formula, written with smallest integers possible
molecular formula
multiple of empirical formula
VSEPR
Predicts shapes of molecules and ions
Assumes e- pars kept far away from each other
o Minimizes repulsion
Direction in space gives molecular geometry

localized bonding models
'rules' for vsepr
lewis dot structure
any resonance
sum of e- paris around central
minimize e- pair repulsion (lone pairs require more room)
dipole moment
quantitative measure of degree of charge separation in molecule

vector quantity ( magnitude and direction )
cis
molec same side, dipole likely

higher boiling point
trans
molec opp side, unlikely dipole

lower boiling point
intermolecular force
in liquid polar molecules orient so + end attracted to - end
increases energy required for liquid to break
increases boiling point
two theories stemming from quantum mechanics
valence bond theory
molecular orbital theory
valence bond theory
- an orbital onone atoms occupys portion of same region of space as orbital on another atom, orbitals overlap
- total number of electrons in both orbitals no more than 2
hybrid orbitals
apart of valence bond theory
describe bonding, obtained by taking combo of atomic orbitals from isolated atoms
number hybrid formed always = number atomic used
Sigma bond
cylindrical shape about bond axis, when two s orbitals overlap or other (ex p) does so along their axis ( imaginary line connecting nuclei
pi bond
electon distribution above and below bond axis, sidways overlap of two p orbitals
o When two parallel orbitals are still available after strong sigma formed
Molecular orbital theory:
which may spread over several atoms or the entire moleule

Structure of molecules similar to atoms

Each orbital has definite energy, ground state, fills lowest energy first

better than lewis bc combines atomic orbitals, molecular orbital formed 'covers' other atoms

limited to diatomic
bonding orbitals
molecular obitals that are concentrated in regions btwn nuclei

less energy
antibonding
zero values in region between nuclei

more energy
Molecular orbital theory:
which may spread over several atoms or the entire moleule

Structure of molecules similar to atoms

Each orbital has definite energy, ground state, fills lowest energy first

better than lewis bc combines atomic orbitals, molecular orbital formed 'covers' other atoms

limited to diatomic
bond order
molecular orbital theory

1/2 diff of [ bonded electrons - antibonded elecectrons]
bonding orbitals
molecular obitals that are concentrated in regions btwn nuclei

less energy
antibonding
zero values in region between nuclei

more energy
hunds rule
lowest energy arrangement of electrons in subshell obtained by putting electrons into separate orbitals of subshell w/ same spin before pairing electrons
aufbau principle
scheme used to reproduc electron configuration of ground states of atoms by successively filling subshells w/ electrons in specific order
bond order
molecular orbital theory

1/2 diff of [ bonded electrons - antibonded elecectrons]
hunds rule
lowest energy arrangement of electrons in subshell obtained by putting electrons into separate orbitals of subshell w/ same spin before pairing electrons
pauli exclusion principle
no tow electrons in atom can have same four quantum numbers
aufbau principle
scheme used to reproduc electron configuration of ground states of atoms by successively filling subshells w/ electrons in specific order
pauli exclusion principle
no tow electrons in atom can have same four quantum numbers
lewis dot shortcomings
assume electrons localized
dont deal w/ unpaired electrons
dont provide good information about bond energies
ionic bond
chem bond formed by attraction between + and - ions

each new ion often more stable than molec before
elements for octet rule
c, n, o, f

fails for h, b, and odd electron species, many w/ z> 10
coulumbs law
determines energy released when ions bond

attraction of opp charged ions

larger interaction of = greater melting point
lattice energy
change in energy from ionic solid separated to ions of gas phase

solid to gas = + value
gas to solid = - value
melting points
depend on strength of interaction between atoms or ions
ionic solids have high melting points because strong interaction between ions , more energy to vibrate and bonds and pull to farther distances
transition metals & valence eletrons
in ionic compounds, lose ns electrons first
then (n-1)d

because 2 lost are highest energy s electrons from atom
ionic radius
spherical region around nucleus which electrons are likely to be found

increases down column because of addition of electron shells

increases across table
anion radii vs cation
anion larger bc greater e- repulsion
isoelectric
same number and configuration of electrons
covalent bond:
chemical bond by sharign of electrons between atoms
valence bond theory
assume orbitals stay intact
valence only
bodn formed by overlatp of atomic orbitals

lewis dot
mo theory
atomic orbitals combine to form new molecular orbitals that cover entire molecue

atomic orbitals no longer exist once molecular orbitals formed
considers all electrons
ionic nomenclature
roman numerals, ide
ionization energy
min energy needed to remove electron

decreases as becomes easier to remove electron
electron affinity
enery change for process of adding electron

large negative indicates stable NEGATIVE ion FORMED ( large negative means wants badly)

small negative, doesnt want it