TTU Chem 1307 Exam 3 Notecards

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57 Terms

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Sublimation Energy

energy require to change state from solid to gas directly

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Angular Momentum Number (l)

An integer range from 0-(n-1) and indicates shape of orbital, multiple possible values of l

ex: if n=3, l= 0,1,2.
if n=1, l=0.

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Aufbau Principle

e- occupy the lowest energy orbitals first (1s2, then 2s2, then 2p6, then 3s2...etc.)

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Pauli Exclusion Principle

1. no two electrons in the same atom can have the same set of four quantum numbers
2. No more than 2 e- can occupy an orbital
3. e- that occupy same orbital must have different values for ms (ms= +1/2 and ms= -1/2)

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Periodic Trends: Atomic Radius

Highest in lower left corner, lowest in top right corner

<p>Highest in lower left corner, lowest in top right corner</p>
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Lattice Energy

(only have to know definition) The enthalpy change that takes place when a gaseous ion forms a solid ion

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Execptions to Electron Configuration

Copper - 4s1 3d10
Chromium - 4s1 3d5

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Change of Enthalpy (ΔH)

Used for heat transfer/capacity questions. Quantifies heat flow in or out of system.
ΔH = H(products) - H(reactants)

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Exothermic

Heat flows out of system (-ΔH)

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Endothermic

Heat flows into system (+ΔH)

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Heat calculation formula

q=mc∆T
q=heat absorbed or released by substance
m=mass
c=specific heat capacity
ΔT= change in temp. (final-initial)

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Specific Heat of H2O

c=4.184

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Calorimetry Solving Process

q=mcΔT, slove for water first, then use the q for the alloy equation. Flip sign (-/+) at the end of solving process.

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Bomb Calorimetry

energy of reaction = ΔT - Heat capacity of Calorimeter

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Hess's Law

using two reactions to achieve desired equation
rules: 1.if you reverse equation, reverse sign of ΔH associated with that equation, 2. if you multiple/divide equation, divde/multiple ΔH by the same

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Standard Enthalpy of Formation

ΔH(rxn) = Sum of ΔH products (ΔHfproducts) - Sum of ΔH reactants (ΔHfreactants)
element in standard form (Xe, H2, etc.) has an sum of ΔHf of zero
Most compounds have -ΔHf

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Wavelength (λ)

The distance between any point on a wave and the corresponding point on the next crest(or trough) of the next wave.

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Frequency (v)

The number of cycles of the wave in a give amount of time (ex:5.65x1o^14 Hz)

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Amplitude

The height of crest, or depth of trough, of a wave from the middle line.

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c = v x λ

Speed of light = frequency x wavelength

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Nanometers --> Meters conversion

10^-9

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Speed of light (c)

3.0 x 1o^8 m

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E = hv = hc/λ

energy of light (J)
h= planks constant
c= speed of light

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Plank's Constant (h)

6.626 x 10^-34

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Concept of Photoelectric Light

electrons are emitted as electromagnetic radiation(eg.light) hits the surface of a metal

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De Broglie's Equation

λ=h/mv
*mass is in Kg here, only here

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Bohr's Model of the Atom

"electron cloud model" Electrons occupy a definite amount of orbitals that require specific energies to occupy.

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Emission

Electrons moving from a higher shell to a lower shell emit energy(light)

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Absorption (Evolving) (Excited)

Electrons moving from a lower energy shell to a higher shell absorb energy to do so.

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Energy Level Formula

En = RH(1/n^2)
n = energy level outmost e is occupying, quantum number
RH = Rydberg's Constant

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Rydberg's Constant

-2.178 x 10^-18

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Heisenberg Uncertainty Principle

It is impossible to simultaneously know an electron's location AND speed of orbit

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Principle Quantum Number (n)

a positive integer(1,2,3..) indicating size and relative distance from nucleus, specifies the energy level

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Magnetic Quantum Number (ml)

Integer range from -l to 0 to +l, indicates orientation of the orbital in the space around the nuclues
ex: if l=2, ml= -2, -1, 0, 1, 2.

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Level (Shell)

denoted by (n), defined further by subshells

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Sublevel (Subshell)

designates the orbital shape, denoted by l quantum number
l= 0 -- s sublevel
l= 1 -- p sublevel
l= 2 -- d sublevel
1= 3 -- f sublevel

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Orbital shapes

s = spherical shaped
p = dumbbell shaped
d = clover leaf shaped

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Hund's Rule

when filling orbitals, e- go into separate orbitals with parallel spins until all of the orbitals are occupied by one e-, then they pair up.

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Valence Electrons

Electrons in the outermost energy level of an atom
ex: [Ne] 3s23p4 (everything following [Ne] is valence b/c it is not full)

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Periodic Trends: Ionization Energy

Lowest IE in left bottom corner, highest in right upper corner.

<p>Lowest IE in left bottom corner, highest in right upper corner.</p>
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Periodic Trends: Electron Affinity

Amount of energy required to add an e- to a gaseous ion/atom
Lowest in bottom left corner, highest in top right corner

<p>Amount of energy required to add an e- to a gaseous ion/atom<br>Lowest in bottom left corner, highest in top right corner</p>
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Ionic Bonds

Metal and nonmetal, >1.7 electronegativity difference

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Polar Covalent Bond

Nonmetals, 0.7-1.7 electronegativity difference

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(non-polar) Covalent Bond

Nonmetals >0.7 electronegativity difference

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Electronegativity

The ability of an atom in a molecule to attract shared electrons to itself
ex: H=2.1
B=2.0
C=2.5
N=3.0
O=3.5
S=2.5
F=4.0

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Bond Polarity

Difference in EN, results from an unequal distribution of electrons

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Molecular Polarity (dipole moement)

When the entire atom has a partially positive and partially negative charge.

Indicated by lewis structure, symmetric=nonpolar

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Isoelectric Ions

Ions with the same number of electrons in the configurations after incorporating ionic charges. ex. Al^3+ and O^2- are isoelectric

Ion size decreases as atomic number(z) increases when comparing isoelectric ions

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Ion size rules

1. Cations (positive ion) is smaller than parent atom
2. Anions (negative ions) are larger than parent atom (more e-)
3. Size generally decreases down a group

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Dissociation Energy

energy required to break apart a compound (breaks bond)

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Heat of formation

heat energy released or evolved when an electron is added to a neutral atom(Hf)

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Exceptions to Octet rule

more than octet- Anything after P can have more than 8 e- if it is the central atom

Less than octet- boron

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Resonance

occurs when two or more Lewis structures are valid and stable for a particular molecule

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Transition metals lose e- from --- orbital before --- orbital

s orbital before d orbital

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Formal charge

the difference between the number of valence electrons on a free atom and the number of electrons on the atom in the molecule (use lewis structures)

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Bond order

number of chemical bonds between a pair of atoms in a molecule
single
double
triple

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Bond energy

the energy required to break a bond
breaking bond - positive enthalpy
creating bond - negative enthalpy