AP Chemistry Cumulative Review

AP Chemistry Cumulative Review

memorize.aimemorize.ai (lvl 286)
Section 1

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+1, except if bonded to Alkali Metal -1

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Cards (528)

Section 1

(50 cards)

+1, except if bonded to Alkali Metal -1

Front

Oxidation # of Hydrogen

Back

Bronsted-Lowry Acid

Front

H + donor

Back

different # of neutrons

Front

Isotope

Back

H2, F2, N2, O2, Cl2, Br2, I2

Front

Diatomic Molecules

Back

1)Assign Oxidation #s 2) Half Reaction 3) Balance Moles 2) Balance add e- to balance Oxidation #s (RED-OX = reduction on left, Oxidation on right) 4) Add H+ or OH - to balance charge 5) Add H2O to balance hydrogens 4) Balance electrons by multiplying until half reactions are equal 5) Add together & check

Front

How to Balance a Redox Equation

Back

End Point

Front

In a titration, the point where the indicator changes (just after moles of solid are equal to moles of base)

Back

Acid + Base --> Salt + Water

Front

Neutralization Reaction (general format) (net ionic of which is always (H+) + (OH-) --> (H2O))

Back

electrolyte

Front

Substance that, when dissolved, is conductive

Back

-1

Front

Oxidation # of Halogens

Back

0

Front

Oxidation # of Compounds

Back

actual yield/theoretical yield x 100%

Front

% yield

Back

p+

Front

proton (symbol)

Back

Allotrope

Front

An element with several different forms, each with different properties (i.e. graphite & diamond)

Back

Atomic Mass Unit

Front

The weighted average of all the isotopes that an atom can have (in g/mol)

Back

M1V1=M2V2

Front

Formula used when diluting stock solution (to find amount of water or stock needed)

Back

Arrhenius Base

Front

Ionizes to produce OH- Ions

Back

Solute

Front

Substance being dissolved in a solution (lower [ ])

Back

Monoprotic

Front

Donates a single H+ Ion (... other prefixes also)

Back

1) Convert to moles 2) divide by lowest moles 3) if any halfs, double all values 4) plug into Compound

Front

How to Find an Empirical Formula Given Grams

Back

Ionic Compounds

Front

Compound in which there is a bond between two non-metals; when naming them you use the numerical prefixes (may NOT be reduced i.e. S2F4 may not become SF2)

Back

Volume Metric Flask & Pipet

Front

Tools NEEDED for dilution

Back

charge

Front

Oxidation # of Ions

Back

Solvent

Front

Substance in which something is dissolved in a solution (higher [ ])

Back

Molecule

Front

2 or more covalently bonded atoms

Back

charge

Front

Oxidation # of Polyatomic Ions

Back

Arrhenius Acid

Front

Ionizes to produce H+ ions

Back

1) multiply each AMU by the percentage that represents that isotopes occurrence in nature 2) then add all the AMUs together.

Front

How to Find a Weighted Average

Back

Cation

Front

positive ion

Back

period

Front

Horizontals on the periodic table

Back

# protons (atom is defined by this)

Front

Atomic #

Back

1) Assume percentages are g (where you have 100 g) 2) convert to moles 3) divide by lowest value 4) plug into compound

Front

How to Find an Empirical Formula Given Percentages

Back

Metalliods

Front

Elements on staircase on periodic table

Back

-2, with peroxide -1

Front

Oxidation # of Oxygen

Back

0

Front

Oxidation # of free elements

Back

Bronsted-Lowry Base

Front

H+ Acceptor

Back

n0

Front

neutron (symbol)

Back

Covalently w/in themselves, Ionicly bonded w/ each other

Front

Polyatomic Ions (bonding)

Back

Molecular Compounds

Front

Compound in which there is a bond between a metal and a non-metal; when naming, pay attention to ionic charges on periodic table (may be reduced)

Back

Oxidation is Loss Reduction is Gain

Front

OIL RIG

Back

Molar Mass of Element/ Total Molar Mass

Front

% Composition Formula

Back

Solution

Front

A homogeneous mixture with 1 phase

Back

Ionic

Front

All _________ compounds are electrolytes

Back

moles of solute/ L of solution

Front

Molarity (M)

Back

e-

Front

electron (symbol)

Back

Amphoteric

Front

a single substance that may be an acid or a base (i.e. water)

Back

Molecular

Front

All (though really not all, but for our purposes all) ________ compounds are NOT electrolytes

Back

Anion

Front

negative ion

Back

# protons + # neutrons

Front

Mass #

Back

group

Front

Verticals on the periodic table

Back

precipitate

Front

A solid or gas that can be formed when 2 or more aqueous reactants come together

Back

Section 2

(50 cards)

M = square root (3RT/mm)

Front

Kinetic Energy of an individual particle formula

Back

Closed System

Front

Type of system in which the energy may escape, but the mass is conserved

Back

Thermochemistry

Front

The heat changed in a chemical reaction.

Back

Equivalence Point

Front

In a titration, the point where moles of acid are equal to moles of base (just before the indicator changes color)

Back

0 degrees C, 1 atm

Front

STP

Back

Open System

Front

Type of system in which the energy and mass may leave or enter

Back

Specific Heat (s)

Front

The energy required to raise 1 g of substance 1 degree C

Back

P of a =(X of a)(total pressure)

Front

Dalton's Law of Partial Pressures (to find partial pressure formula)

Back

Isolated System

Front

Type of system in which nothing is transfered (no mass or energy); ideal

Back

Average KE = 1/2(mass)(average speed of all particles)

Front

Average Kinetic Energy Formula

Back

X of a = moles a/total moles

Front

Mole Fraction

Back

0

Front

If heat capacity isn't mentioned, you can assume that q of cal is = ?

Back

Surroundings

Front

Everything in the universe that is not defined by you as part of the system

Back

Force = mass x acceleration

Front

Newton's Second Law

Back

rate gas A/rate gas B = square root (mm A/ mm B)

Front

Speed of Diffusion/Effusion formula

Back

Pressure of H2O must be Subtracted

Front

In ideal gas law problem, when it says "atmospheric" ...

Back

Calorimetry

Front

The measurement of heat changes

Back

Temperature

Front

Measure of the average kinetic energy of all the particles in a substance

Back

PV=nRT

Front

Ideal Gas Law Formula

Back

H

Front

Symbol for Enthalpy

Back

PEACe 1)each molecule is a Point in space 2)Elastic collisions 3) no force of Attraction 4) no energy lost or gained to Collisions

Front

Idea Gas Law (actual rules)

Back

rate gas A/rate gas B = square root (mm gas B/ mm gas A)

Front

Rate of Diffusion/Effusion formula

Back

C=(mass)(specific heat)

Front

Heat capacity formula

Back

Reducing Agent

Front

The reactant in the oxidizing reaction that forces the reduction reaction to occur

Back

q rxn = -(q of H2O + q of cal)

Front

q rxn = ?

Back

q

Front

Symbol for Total Heat absorbed or released

Back

1 atm = 760 mmHg = 101.3 kPa

Front

Pressure Units/Conversions

Back

Heat Capacity (C)

Front

The amount of energy/heat required to raise some substance 1 degree C

Back

Oxidizing Agent

Front

The reactant in the reduction reaction that forces the oxidation reaction to occur

Back

Delta H or Enthalpy Change

Front

Measure of the change in enthalpy

Back

Temperature

Front

Kinetic Energy is proportional to ______

Back

0.0821 atm L/mol K

Front

R in ideal gas law

Back

Barometer

Front

Instrument used to measure the pressure of atmospheric gas

Back

purple --> pink

Front

Colors of Reaction when (MnO4 -) --> (Mn2+)

Back

force x distance = work done

Front

Energy (definition)

Back

yellow --> green

Front

Colors of Reaction when (Cr2O7 2-) --> (Cr 3+)

Back

Atmospheric Pressure

Front

the weight exerted by a column of air or the pressure exerted by the Earth's atmosphere

Back

System

Front

What is defined by you taken from the whole universe

Back

Exothermic

Front

Releases/gives off heat (negative value)

Back

8.314 J/K mol

Front

R in instances that pertain to energy

Back

Constant Volume

Front

Bomb Calorimeter

Back

q cal = CAT

Front

q cal = ?

Back

AH

Front

Symbol for the heat absorbed or lost molecularly (PER MOLE)

Back

P1V1/N1T1=P2V2/N2T2

Front

Combined Gas Law Formula

Back

Endothermic

Front

Absorbs/takes in heat (positive value)

Back

Manometer

Front

Instrument used to measure the pressure of a not-atmospheric gas (open or closed system)

Back

Calorimeter

Front

A device used to measure Delta H

Back

Constant Pressure

Front

Coffee Cup Calorimeter

Back

q H2O = msAT

Front

q H2O = ?

Back

high pressure, low temperature

Front

Non-Ideal Gas Conditions

Back

Section 3

(50 cards)

Positive work value; work done on system

Front

When gas compresses ...

Back

∆H | ∆S is spontaneous...at high temperatures

Front

+ | +

Back

isothermal

Front

change that occurs at constant temperature

Back

London dispersion forces

Front

universal IMF for nonpolar molecules

Back

square planar

Front

AX4E2

Back

octahedral

Front

AX6

Back

Negative work value; work done by system

Front

When gas expands ...

Back

State Functions

Front

Function in which it doesn't matter HOW the changes take place, only that they do; you can use to formula Final - Initial ( i.e. energy, pressure, volume, temperature, sort of moles)

Back

AE= AH - RTAn

Front

Change in Energy = ? (in terms of constant pressure; for gasses)

Back

AE = q + w

Front

Change in Energy (AE) = ? (in terms of work)

Back

London dispersion forces

Front

larger molecules which have higher mass and therefore electron density have stronger...

Back

+ ∆S

Front

gas > liquid > solid and (aq)>(s) cause...

Back

Hydrogen bonding

Front

IMF that occurs with FON

Back

T-shape

Front

AX3E2

Back

sublimation

Front

phase change from solid to gas

Back

methods of increasing rate

Front

raising heat, adding catalyst, heighten concentration, bigger surface area

Back

N=N.(0.5)^time/time half-life

Front

half-life equation

Back

endless

Front

Significant Digits of Conversion Factors

Back

w =-(P)(Change in V)

Front

work = ?

Back

∆H | ∆S is spontaneous...never

Front

+ | -

Back

+ ∆S

Front

greater # of moles of gas formed and greater volume formed cause...

Back

+ ∆S

Front

diatomic molecules forming mixed molecules, e.g. H2 + I2 -> 2HI, means...

Back

triple point

Front

temperature-pressure combination at which solid, liquid, and gas states appear

Back

critical point

Front

temperature-pressure point after which gas can no longer form liquid

Back

see-saw

Front

AX4E

Back

fusion

Front

melting

Back

effects of IMF

Front

boiling point, melting point, viscosity, vapor pressure, surface tension

Back

solid CO2

Front

chemical composition of dry ice

Back

are not

Front

For significant digits, leading zeros ____ significant

Back

are

Front

For significant digits, trailing zeros _____ significant

Back

∆H | ∆S is spontaneous...at low temperatures

Front

- | -

Back

Adding

Front

When ____ significant digits, round answer to least decimal place

Back

AH rxn = (Sum of AH of formation of products) - (Sum of AH of formation of reactants)

Front

Dirrect Method Formula

Back

viscosity

Front

thickness

Back

boiling point

Front

point at which vapor pressure=air pressure above

Back

Multiplying

Front

When _____ significant digits, round answer to least significant digit

Back

vapor pressure

Front

stronger IMF= lower... weaker IMF= higher...

Back

Dipole-dipole forces

Front

IMF that exists in polar molecules

Back

AH = q/moles

Front

Delta H (AH) = ?

Back

trigonal bipyramidal

Front

AX5

Back

∆Hvap

Front

energy needed to vaporize a mole of a liquid

Back

square pyramidal

Front

AX5E

Back

An = (moles of products that are gasses) - (moles of reactants that are gasses)

Front

Change in moles (An) =?

Back

equilibrium

Front

happens at lines in phase change charts

Back

∆H | ∆S is spontaneous...always

Front

- | +

Back

deposition

Front

phase change from gas to solid

Back

endless

Front

Significant Digits of counted things

Back

adiabatic

Front

change without heat transfer between the system and its surroundings

Back

0

Front

AH of formation for a substance in its stablest form (how it is found in nature)

Back

bond energy

Front

energy needed to break a bond

Back

Section 4

(50 cards)

prop-

Front

(organics) three carbons

Back

non-

Front

(organics) nine carbons

Back

blue-green

Front

when n=4 ->2, color=

Back

n (first quantum number)

Front

variable for energy of e-, goes from 1,2,3 on up

Back

d

Front

l=2

Back

dec-

Front

(organics) ten carbons

Back

m (third quantum number)

Front

variable for orientation of orbital (-1 through +1)

Back

Balmer Series

Front

spectrum of light when an electron drops to energy level n=2

Back

Effusion

Front

passage of gas through tiny orifice

Back

ionic

Front

... compounds are most conductive

Back

specific heat

Front

heat needed to change 1 g of substance to 1˚C

Back

first

Front

ln[A] vs. time is a ...-order reaction

Back

p

Front

l=1

Back

hex-

Front

(organics) six carbons

Back

entropy (S)

Front

degree of disorder in a system

Back

-ous acid

Front

if anion ends in -ite, acid name ends in...

Back

electron affinity

Front

energy involved in gaining an electron to become a negative ion

Back

blue-violet

Front

when n=5 ->2, color=

Back

but-

Front

(organics) four carbons

Back

third

Front

AP doesn't deal with ...-order reaction, don't pick it!

Back

d orbitals

Front

these orbitals are diagonal

Back

oct-

Front

(organics) eight carbons

Back

eth-

Front

(organics) two carbons

Back

s orbitals

Front

these orbitals are spherical

Back

s

Front

l=0

Back

l (second quantum number)

Front

variable for type of orbital

Back

Boltzmann distribution

Front

states molecules at a given temp. vary in kinetic energy along a bell-curve of molecular velocities

Back

Diffusion

Front

mixing of gases

Back

zero

Front

[A] vs. time is a ...-order reaction

Back

hydro-ic acid

Front

if anion ends in -ide, acid name ends in

Back

red

Front

when n=3 ->2, color=

Back

g solute/g solvent x 100

Front

mass percent

Back

heat capacity

Front

amount of heat needed to change a system by 1˚C

Back

C + 273

Front

calculation from K to C

Back

moles solute/kg solvent

Front

molality =

Back

hept-

Front

(organics) seven carbons

Back

rate law

Front

this MUST be determined experimentally

Back

pent-

Front

(organics) five carbons

Back

not spontaneous

Front

If K<1, then Gº>0 and reaction will be...at chemical equilibrium

Back

f

Front

l=3

Back

increasing

Front

entropy in the universe is always...

Back

-ic acid

Front

if anion ends in -ate, acid name ends in...

Back

second

Front

1/[A] vs. time is a ...-order reaction

Back

violet

Front

when n=6 ->2, color=

Back

4.184

Front

specific heat of water

Back

spontaneous

Front

If K>1, then Gº<0 and reaction will be...at chemical equilibrium

Back

like

Front

like dissolves...

Back

meth-

Front

(organics) one carbon

Back

p orbitals

Front

these orbitals are perpendicular

Back

s (fourth quantum number)

Front

variable for spin of electron (+.5 or -.5)

Back

Section 5

(50 cards)

red/orange

Front

color of Ca (flame test)

Back

alkyne

Front

(organics) triple-bonded compound

Back

condensation

Front

organic reaction in which two functional groups come together, resulting in the release of water

Back

red

Front

color of Sr (flame test)

Back

Density

Front

mass/volume

Back

methoxy-

Front

ether prefix

Back

base

Front

metal oxide + H20 ->

Back

Alkali metals

Front

Group 1 metals

Back

ln (k1/k2) = (Ea/R)(1/T2-1/T1)

Front

equation to find Ea from reaction rate constants at two different temperatures

Back

phosphate, sulfide, carbonate, sulfate

Front

generally insoluble anions (names)

Back

green/yellow

Front

color of Ba (flame test)

Back

-ol

Front

ending for alcohols

Back

geometric isomers

Front

two molecules with identical connectivity but different geometries

Back

Transition metals

Front

elements in groups 3-12

Back

-oic acid

Front

carboxylic acid ending

Back

yellow

Front

color of Na (flame test)

Back

-al

Front

aldehyde suffix

Back

hydrolysis

Front

organic reaction in which water breaks apart a molecule (splitting into two hydroxides)

Back

Law of Multiple Proportions

Front

atoms combine in fixed whole # ratios

Back

Law of Conservation of Mass

Front

mass reactants= mass products

Back

activated complex (transition state)

Front

peak of energy diagram

Back

alcohol

Front

organic w/ -OH group

Back

mol

Front

6.022x10^23

Back

acid

Front

nonmetal oxide + H2O ->

Back

complex ions

Front

transition metals with ammonia, hydroxide, cyanide or thiocyanate form...

Back

diamagnetic

Front

elements which have all electrons paired and relatively unaffected by magnetic fields

Back

-oate

Front

ester suffix

Back

amine

Front

organic w/ -NH2

Back

blue

Front

color of Cs (flame test)

Back

oxide gas and water

Front

oxoacid solution (such as HSO4-) forms...

Back

purple

Front

color of K (flame test)

Back

allotrope

Front

different form of same element

Back

Ag+, Pb2+, Hg2+

Front

all cations are soluble with bromide, chloride and iodide EXCEPT

Back

insoluble

Front

hydroxides are soluble or insoluble?

Back

red

Front

color of Li (flame test)

Back

Amino-

Front

amine prefix

Back

Alkaline earth metals

Front

Group 2 metals

Back

-one

Front

ketone suffix

Back

Arrhenius equation

Front

to find activation energy use the...

Back

carbohydrates

Front

carbon, hydrogen, oxygen compounds

Back

0

Front

∆Hº of pure elements=

Back

Ag+, Pb2+, Hg2+, Sr2+, Ca2+, Ba2+

Front

all cations are soluble with sulfate EXCEPT

Back

k=Ae^(-Ea/RT)

Front

Arrhenius equation

Back

base and hydrogen gas

Front

pure metal or metal hydride + H20 ->

Back

alkene

Front

(organics) double-bonded compound

Back

Limiting reactant

Front

reactant that's completely used up in a chemical reaction

Back

ether

Front

organic w/ -O-

Back

hydrocarbons

Front

carbon & hydrogen compounds

Back

paramagnetic

Front

elements which have unpaired electrons and highly affected by magnetic fields

Back

alkane

Front

(organics) single-bonded compound

Back

Section 6

(50 cards)

Heisenberg Uncertainty Principle

Front

we cannot simultaneously determine an atom's exact path or location

Back

% error

Front

theoretical yield-experimental yield/theoretical yieldx100

Back

nu

Front

frequency symbol

Back

equivalence point

Front

point where acid completely neutralizes base

Back

standard solution

Front

a solution used in titrations whose concentration is known

Back

end point

Front

point at which the titrated solution changes color

Back

Molality

Front

mol/kg of solvent, used in calculating colligative properties

Back

22.4L

Front

volume of gas @STP

Back

Graham's Law

Front

effusion of a gas is inversely proportional to the square root of the molar mass

Back

soluble

Front

Group 1, Ammonium, Nitrates, Acetates, Sulfates, Halides

Back

Strong acid weak base rxn

Front

H⁺+NH₃→NH₄

Back

excess reactant

Front

reactant which doesn't get used up completely in a chemical reaction

Back

oxidation

Front

loss of electrons, increase in oxidation #

Back

mol Fraction

Front

mols A/ total mols, XA

Back

1/2mv²

Front

Kinetic Energy per molecule

Back

1 atm

Front

760 mmHg, 760 torr

Back

√3RT/M(in kg)

Front

average speed of gas

Back

oxidizing agent

Front

the reactant that is being reduced, brings about oxidation

Back

linear

Front

AX₂, AX₂E₃

Back

reduction agent

Front

the reactant that is being oxidized, brings about reduction

Back

tetrahedral

Front

AX₄

Back

Hund's Rule

Front

within a sublevel, place one e⁻ per orbital before pairing them

Back

analyte

Front

solution in flask being titrated

Back

titrant

Front

buret solution used in titration

Back

wavelength

Front

determined by the formula h/m(in kg)v, (v=velocity)

Back

reduction

Front

gain of electrons, decrease in oxidation #

Back

strong bases

Front

Group 1 and heavier Group 2 bases

Back

1.38x10⁻²³J/K

Front

Boltzmann constant, used in calculating speed of gas per molecule

Back

weak acid strong base rxn

Front

HF+ OH⁻→H₂O

Back

Pauli Exclusion Principle

Front

each orbital can hold two e⁻s each w/ opposite spins

Back

Molarity

Front

mol/L, concentration of a solution

Back

Pressure

Front

force per unit area

Back

3.0x10⁸m/s

Front

speed of light, C

Back

experimental yield

Front

the actual amount of product produced in an experiment

Back

Aufbau Principle

Front

e⁻s fill the lowest energy orbital first, then work their way up

Back

lambda

Front

wavelength symbol

Back

insoluble

Front

Carbonates, Hydroxides, Oxides, Phosphates, Sulfides

Back

3/2RT

Front

Kinetic Energy per mol

Back

√3kT/m

Front

speed per molecule of gas

Back

trigonal planar

Front

AX₃

Back

indicator

Front

a weak acid that changes color at or near the equivalence point

Back

% yield

Front

experimental yield/theoretical yieldx100

Back

strong acids

Front

HCl, HBr, HI, HNO₃, HClO₄, H₂SO₄

Back

E

Front

#NAME?

Back

Standard Temperature and Pressure

Front

0.00°C, 1 atm

Back

strong acid strong base rxn

Front

H⁺+OH⁻→H₂O

Back

r₁/r₂

Front

=√M₂/M₁

Back

Dalton's Law

Front

Ptotal=Pa+Pb+Pc....

Back

Theoretical yield

Front

amount of product produced when limiting reactant is used up

Back

6.63x10⁻³⁴Js

Front

Planck's constant, used to calculate energy w/frequency

Back

Section 7

(50 cards)

seesaw

Front

AX₄E

Back

square planar

Front

AX₄E₂

Back

permanent gases

Front

substances w/ critical temperatures below 25°C

Back

vaporization

Front

liquid to gas

Back

endothermic

Front

positive enthalpy, heat flows into system

Back

supercritical fluid

Front

substances above the critical temperature and pressure in which the pressure is so high that density and flowing ability of a "gas" resembles that of a liquid

Back

1.86°C

Front

kf of water

Back

octahedral

Front

AX₆

Back

Hydrogen bonding

Front

unusually strong dipole forces found when H is bonded to N, O, or F

Back

Q>K

Front

reverse rxn occurs when

Back

bent

Front

AX₂E, AX₂E₂

Back

exothermic

Front

negative enthalpy, heat flows into surroundings

Back

LeChatelier's Principle

Front

If a system @equilibrium is stressed, the system will shift so as to reestablish equilibrium

Back

viscosity

Front

resistance to flow

Back

adhesion

Front

molecules' tendency to stick to the container

Back

ΔTf= kf x molality

Front

freezing point depression formula

Back

Cg=kPg

Front

Henry's Law, solubility of gases is directly proportional to the partial pressure of the gas

Back

freezing

Front

liquid to solid

Back

sublimation

Front

solid to gas

Back

system

Front

the part of the universe one is focused upon (in thermodynamics)

Back

melting point

Front

point at which solid→liquid occurs

Back

Q<K

Front

forward rxn occurs when

Back

rate

Front

how fast or slow a reaction occurs, becomes slower as it reaches equilibrium

Back

Van't Hoff factor

Front

for colligative properties for electrolytes, the # of mols of ions/ mols of solute

Back

single bond

Front

1 sigma bond

Back

Bond enthalpy

Front

ΔH when 1 mol of bonds is broken in the gaseous state

Back

heat of vaporization

Front

energy required for liquid→gas

Back

pi=(nRT)/v

Front

osmotic pressure formula

Back

condensation

Front

gas to liquid

Back

ΔTb= kb x molality

Front

boiling point elevation formula

Back

cohesion

Front

molecules' tendency to stick to one another

Back

heat capacity

Front

heat required to raise the system 1°C

Back

boiling point

Front

point at which liquid→gas occurs

Back

P₁= X₁P₁°

Front

Raoult's Law, relations between vapor pressure and concentrations

Back

triple bond

Front

1 sigma bond, 2 pi bonds

Back

0.512°C

Front

kb of water

Back

London dispersion forces

Front

weakest IMFs, found in all molecules

Back

catalyst

Front

lowers activation energy

Back

heat of fusion

Front

energy required for melting to occur

Back

work

Front

all forms of energy except for heat

Back

double bond

Front

1 sigma bond, 1 pi bond

Back

deposition

Front

gas to solid

Back

trigonal bipyramidal

Front

AX₅

Back

t-shape

Front

AX₃E₂

Back

square pyramidal

Front

AX₅E

Back

surroundings

Front

the rest of the universe (in thermodynamics)

Back

trigonal pyramidal

Front

AX₃E

Back

melting

Front

solid to liquid

Back

activation energy

Front

the minimum energy that molecules must possess for collisions to be effective, Ea

Back

Colligative properties

Front

vapor pressure lowering, boiling point elevation, freezing point depression, osmotic pressure

Back

Section 8

(50 cards)

permanganate

Front

MnO₄¹⁻

Back

Weight

Front

amount of gravitational force exerted on an object

Back

anode

Front

half cell in which oxidation occurs

Back

Buffer

Front

a solution that resists a change in pH, contains both a weak acid and its conjugate base

Back

chlorite

Front

ClO₂¹⁻

Back

no precipitate forms

Front

if Q<Ksp

Back

conjugate acid

Front

the chemical formed when a base accepts a proton

Back

sulfite

Front

SO₃²⁻

Back

phosphate

Front

PO₄³⁻

Back

nitrate

Front

NO₃¹⁻

Back

ammonium

Front

NH₄¹⁺

Back

5% rule

Front

x can be ignored when % ionization is <5%

Back

oxalate

Front

C₂O₄²⁻

Back

chloride

Front

Cl¹⁻

Back

Mass

Front

a measure of resistance of an object to a change in its state of motion

Back

96,500

Front

Faraday's constant

Back

Scientific Method

Front

a method of investigation involving observation and theory to test scientific hypotheses

Back

chromate

Front

CrO₄²⁻

Back

bromate

Front

BrO₃¹⁻

Back

Bronsted-Lowry base

Front

proton acceptors, must have an unshared pair of e⁻s

Back

nitrite

Front

NO₂¹⁻

Back

Bronsted-Lowry acid

Front

proton donors

Back

Matter

Front

anything occupying space and with mass

Back

2nd law of thermodynamics

Front

the total entropy is always increasing, all systems tend towards maximum entropy

Back

entropy

Front

a measure of randomness or disorder

Back

chlorate

Front

ClO₃²⁻

Back

oxide

Front

O²⁻

Back

iodide

Front

I¹⁻

Back

carbonate

Front

CO₃²⁻

Back

acetate

Front

C₂H₃O₂¹⁻

Back

Law of Conservation of Mass

Front

matter can't be created nor destroyed

Back

salt bridge

Front

connects the 2 half cells in a voltaic cell

Back

voltaic cells

Front

uses a spontaneous redox rxn to generate electrical energy, consists of 2 half cells

Back

sulfide

Front

S²⁻

Back

1st law of thermodynamics

Front

the total energy of the universe is constant, all systems tend towards minimum energy

Back

1.0x10⁻¹⁴

Front

Kw

Back

spontaneity

Front

the likelihood that a rxn will occur "by itself"

Back

Arrhenius base

Front

puts OH⁻ into solution

Back

cathode

Front

half cell in which reduction occurs

Back

a precipitate forms

Front

if Q>Ksp

Back

perchlorate

Front

ClO₄¹⁻

Back

Arrhenius acid

Front

puts H⁺ into solution

Back

flouride

Front

F¹⁻

Back

hydroxide

Front

OH¹⁻

Back

conjugate base

Front

the chemical formed when an acid donates a proton

Back

3rd law of thermodynamics

Front

the entropy of a pure perfectly formed crystal @0K is 0

Back

sulfate

Front

SO₄²⁻

Back

Nernst Equation

Front

Ecell= E°cell -RT/nF x lnQ

Back

cyanide

Front

CN¹⁻

Back

dichromate

Front

Cr₂O₇²⁻

Back

Section 9

(50 cards)

Finding Empirical Formulas

Front

1.Calculate moles of each atom in molecule 2.Divide each mole number by smallest mole number 3.If necessary, multiply every mole number to get a whole number 4.Moles of each atom is subscript in empirical formula

Back

Kinetic Molecular Theory-FOR IDEAL GASES!!!

Front

1.Volume of individual particles can be assumed to be zero 2.The particles are in constant motion, which causes pressure 3.Particles exert no forces on each other 4.The average kinetic energy of the particles is directly affected by temperature(K)

Back

Naming Binary Ionic Compounds

Front

Cation first, anion second

Back

Dalton's Law of Partial Pressures

Front

Ptotal=P1+P2+P3+...

Back

Net Ionic Equation

Front

only contains ions that change in reaction

Back

Second-Order Half Life

Front

1/([A]0*k)

Back

First-Order Rate Law

Front

r=k[A]

Back

Law of Definite Proportion

Front

a given compound always has exactly the same proportion of elements by mass

Back

Integrated Zero-Order Rate Law

Front

[A]=-kt + [A]0

Back

First-Order Half Life

Front

.69/k

Back

Gamma Ray-

Front

high-energy light

Back

Root Mean Square Velocity

Front

u(rms)=(3RT/M)^1/2

Back

Acids

Front

substances that form H+ when dissolved in water; proton donors

Back

R=

Front

0.0826Latm/Kmol

Back

Zero-Order Half Life

Front

[A]0/2k

Back

Zero-Order Rate Law

Front

r=k

Back

1atm=?mmHg/Torr

Front

760mmHg/Torr

Back

Chemical Bonds

Front

Force that holds atoms together

Back

If needed, indicate charge of metal(cation) by

Front

a Roman numeral

Back

Osmotic Pressure

Front

Osmotic pressure=MRT

Back

Decrease Volume and Increase Temperature

Front

Increase Pressure

Back

Increase Temperature

Front

Increase Volume

Back

Chemical Kinetics

Front

studies the rate at which a chemical process occurs and sheds light on its reaction mechanism

Back

Molal FP Depression Constant

Front

▲T=k*m(solute)

Back

Radioactivity

Front

Spontaneous emission of radiation

Back

STP

Front

0°C and 1 atm

Back

Integrated First-Order Rate Law

Front

ln[A]=-kt + ln[A]0

Back

Second-Order Rate Law

Front

r=k[A]^2

Back

Molal BP Elevation Constant

Front

▲T=k*m(solute)

Back

Overall Reaction Order

Front

n+m (these are orders of reactants)

Back

Law of Multiple Proportions

Front

when two elements form a series of compounds, the ratios of the masses of the second element that combine with 1g of the first element can always be reduced to whole numbers

Back

van't Hoff Factor

Front

i=moles of particles/moles of solute dissolved

Back

Integrated Rate Law

Front

expresses how the concentrations depend on time

Back

In covalent bonds, prefixes are used to tell

Front

amount of atoms present

Back

Molarity

Front

moles of solute/volume of soln(L)

Back

Normality

Front

(N) number of equivalents per liter of solution

Back

A monoatomic cation takes name from

Front

its element

Back

Beta Particles-

Front

high-speed electrons

Back

Isotopes

Front

atoms with the same number of protons but a different number of neutrons

Back

1atm=?Pa

Front

101,325 Pa

Back

Bases

Front

Substances that form OH- when dissolved in water; proton acceptors

Back

Ideal Gas Law

Front

PV=nRT

Back

R=

Front

8.31J/Kmol

Back

Integrated Second-Order Rate Law

Front

1/[A]=kt + 1/[A]0

Back

Joule

Front

SI unit of energy; Kg*m^2/s^2

Back

A monoatomic anion is named by taking

Front

its root and adding -ide

Back

Percent Yield

Front

Actual Yield/Theoretical Yield*100%

Back

Molality

Front

mol of solute/kg of solvent

Back

Alpha Particles-

Front

2+ charge

Back

Enthalpy of Solution

Front

▲Hsoln=▲H1+▲H2+▲H3+...

Back

Section 10

(50 cards)

Volt

Front

unit of electrical potential; J/C

Back

Q<K

Front

shift to right (Q?K)

Back

w(max)

Front

=▲G (work)

Back

▲G

Front

▲H-T▲S

Back

pH=

Front

=log[H+]

Back

▲Ssurr

Front

-▲H/T

Back

Equilibrium Expression

Front

K=[C]^l[D]^m/[A]^j[B]^k; products/reactants; solids don't count

Back

Equilibrium constant

Front

K

Back

Speed of light

Front

c=2.9979*10^8 m/s

Back

▲Suniv

Front

▲Ssys+▲Ssurr

Back

Entropy

Front

(S) the driving force for a spontaneous is an increase in entropy of the universe

Back

Cell Potential

Front

(Ecell) driving force of the electrons

Back

▲H°reaction

Front

Σn▲H°(products)-Σn▲H°(reactants)

Back

Reaction Quotient

Front

(Q) does the same as equilibrium expression, except it uses initial concentrations

Back

Principal Quantum Number

Front

(n) has values 1,2,3,...; tells energy levels

Back

Q=K

Front

at equilibrium (Q?K)

Back

Theory of Relativity

Front

E=mc^2

Back

Le Chatelier's Principle

Front

if a change is imposed on a system at equilibrium, the position of the equilibrium will shift in a direction that tends to reduce that change

Back

▲G°

Front

▲H°-T▲S°

Back

Law of Conservation of Energy

Front

energy can't be created nor destroyed

Back

Angular Momentum Quantum Number

Front

(ℓ), has values from 0 to (n-1); tells shape of atomic orbitals

Back

Specific Heat Capacity

Front

J/°Cg or J/Kg

Back

Aufbau Principle

Front

as protons are added to the nucleus, electrons are similarly added

Back

Acid Dissociation Constant

Front

Ka=[products]^m/[reactants]^n

Back

▲E

Front

q+w

Back

Buffered Solution

Front

a solution that resists a change in its pH

Back

Quantum Model

Front

electrons in a hydrogen atom move around the nucleus only in circular orbits

Back

ℓ=0

Front

s orbital

Back

ℓ=4

Front

g orbital

Back

Nodes

Front

where there are no electrons

Back

Pauli Exclusion Principle

Front

in a given atom no two electrons can have the same set of four quantum numbers

Back

Electron Spin Quantum Number

Front

(msubs) can only be +1/2 or -1/2

Back

Quantum Mechanical Model

Front

involves quantum numbers

Back

Magnetic Quantum Number

Front

(mℓ) has values from -ℓ to ℓ, including zero; tells orientation of the orbital relative to other orbitals

Back

c=

Front

λv

Back

Work

Front

force acting over distance

Back

Solubility Product

Front

(Ksp) an equilibrium expression

Back

ℓ=2

Front

d orbital

Back

Galvanic Cell

Front

a device in which chemical energy is changed to electrical energy

Back

G

Front

G°+RTln(Q)

Back

Heat

Front

the transfer of energy between two objects due to temperature difference

Back

Cathode

Front

where reduction occurs

Back

Hund's Rule

Front

the lowest energy configuration for an atom is the one having the max number of unpaired electrons allowed by the Pauli principle in a set of degenerate orbitals

Back

ℓ=3

Front

f orbital

Back

Molar Heat Capacity

Front

J/°Cmol or J/Kmol

Back

Quantum Numbers

Front

describe various properties of one orbital

Back

ℓ=1

Front

p orbital

Back

Anode

Front

where oxidation occurs

Back

Hess's Law

Front

in going from a particular set of reactants to a particular set of products, the change in enthalpy is the same whether the reaction takes place in one step or in a series of steps

Back

Q>K

Front

shift to left (Q?K)

Back

Section 11

(28 cards)

Valence Electrons(assigned)

Front

(# of lone pair e-)+1/2(# of shared e-)

Back

Antibonding Molecular Orbital

Front

higher in energy than the atomic orbitals of which it is composed

Back

Bond Energy

Front

energy required to break a bond

Back

LE Model

Front

assumes that a molecule is composed of atoms that are bound together by sharing pairs of electrons using the atomic orbitals of the bound atoms

Back

Tetrahedral

Front

109.5°, sp^3

Back

Resonance

Front

when more than one valid Lewis structure can be written for a particular molecule; represented by double-headed arrows

Back

Ampere

Front

(A), C/s

Back

Faraday

Front

96,485 C/mol e-

Back

Polar Covalent Bond

Front

bond in which atoms aren't so different that electrons are completely transferred but are different enough that unequal sharing occurs

Back

Counterions

Front

anions or cations as needed to produce a compound with non net charge

Back

Pi Bond

Front

occupies the space above and below a sigma bond

Back

Coordination Compound

Front

consists of a complex ion, a transition metal with attached ligands, and counterions

Back

Bond Order

Front

# bonding e- - # antibonding e-/2

Back

Electronegativity

Front

ability of an atom in a molecule to attract shared electrons to itself

Back

Lone Pair

Front

pairs of electrons localized on an atom

Back

Trigonal Bipyramidal

Front

90°&120°, dsp^3

Back

Hybridization

Front

the mixing of native atomic orbitals to form special orbitals for bonding

Back

Bonding Pairs

Front

electron pairs found in the space between the atoms

Back

Linear

Front

180°, sp

Back

Dipole Moment

Front

a molecule having a center of positive charge and a center of negative charge

Back

Molecular Orbitals (MOs)

Front

similar to atomic orbitals, except between molecules

Back

Sigma Bond

Front

the line running between the atoms

Back

Ligand

Front

a neutral molecule/ion having a lone e- pair that can be used to form a bond to a metal ion

Back

Octahedral

Front

90°, d^2sp^3

Back

▲H

Front

Σ(bonds broken)-Σ(bonds formed)

Back

London Dispersion Forces

Front

the intermolecular attractions resulting from the constant motion of electrons and the creation of instantaneous dipoles

Back

Trigonal Planar

Front

120°, sp^2

Back

Formal Charge

Front

(# of valence e- on free atom) - (# of valence e- assigned to atom in molecule)

Back