AP Chemistry Review Terms (Rosenfeld)

AP Chemistry Review Terms (Rosenfeld)

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Section 1

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Graham's Law of Effusion

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Last updated

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Mar 1, 2020

Cards (150)

Section 1

(50 cards)

Graham's Law of Effusion

Front

Effusion of a gas is INVERSELY proportional to the SQUARE ROOT of the molar mass r₁/r₂ =√M₂/M₁

Back

Alkali metals

Front

Group 1 metals

Back

End point

Front

point at which the titrated solution changes color

Back

Common Weak Base Reaction

Front

H⁺+NH₃→NH₄+

Back

Hund's Rule

Front

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

Back

Number of Molecules in a Mole

Front

6.022x10^23

Back

Experimental yield

Front

the actual amount of product produced in an experiment

Back

Law of Conservation of Mass

Front

mass reactants = mass products

Back

Standard Temperature and Pressure

Front

0.00°C, 1 atm (273 K)

Back

Titrant

Front

buret solution used in titration

Back

6.63x10⁻³⁴Js

Front

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

Back

Heisenberg Uncertainty Principle

Front

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

Back

Volume of 1 mole of Gas @STP

Front

22.4L

Back

Kinetic Energy per Molecule Equation

Front

1/2mv²

Back

Transition metals

Front

elements in groups 3-12

Back

Indicator

Front

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

Back

Alkaline earth metals

Front

Group 2 metals

Back

Strong Bases

Front

Group 1 and heavier Group 2 bases

Back

Molarity

Front

mol/L, concentration of a solution

Back

lambda

Front

wavelength symbol

Back

Dalton's Law of Partial Pressure Equation

Front

Ptotal=Pa+Pb+Pc....

Back

Strong Acids

Front

HCl, HBr, HI, HNO₃, HClO₄, H₂SO₄

Back

Aufbau Principle

Front

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

Back

E

Front

=h(frequency)

Back

Reduction agent

Front

the reactant that is being oxidized, brings about reduction

Back

Common Weak Acid Reaction

Front

HF+ OH⁻→H₂O

Back

Strong Acid Strong Base Overall Reaction

Front

H⁺+OH⁻→H₂O

Back

Linear Geometry (2 possibilities)

Front

AX₂, AX₂E₃

Back

Percent Yield Equation

Front

experimental yield/theoretical yieldx100

Back

Percent Error Equation

Front

theoretical yield-experimental yield/theoretical yieldx100

Back

Molality

Front

mol/kg of solvent, used in calculating colligative properties

Back

nu

Front

frequency symbol

Back

Soluble Ions

Front

Group 1, Ammonium, Nitrates, Acetates, Sulfates (+Halides)

Back

3.0x10⁸m/s

Front

speed of light, C

Back

Pressure

Front

force per unit area

Back

Oxidizing agent

Front

the reactant that is being reduced, brings about oxidation

Back

Insoluble Ions

Front

Carbonates, Hydroxides, Oxides, Phosphates, Sulfides

Back

standard solution

Front

a solution used in titrations whose concentration is known

Back

Oxidation

Front

loss of electrons, increase in oxidation #

Back

Pauli Exclusion Principle

Front

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

Back

Reduction

Front

gain of electrons, decrease in oxidation #

Back

Analyte

Front

solution in flask being titrated

Back

Excess reactant

Front

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

Back

Theoretical yield

Front

amount of product produced when limiting reactant is used up

Back

Equivalence Point

Front

point where acid completely neutralizes base, moles of H+ = moles of OH-

Back

Density

Front

mass/volume

Back

Mole Fraction

Front

mols A/total mols (also known as XA)

Back

1 atm in mmHg and torr

Front

760 mmHg, 760 torr

Back

C =

Front

=lambda(nu) (aka. wavelength x frequency)

Back

Limiting reactant

Front

reactant that's completely used up in a chemical reaction

Back

Section 2

(50 cards)

Catalyst

Front

lowers activation energy

Back

Colligative Properties (What properties change with addition of solute?)

Front

vapor pressure lowering, boiling point elevation, freezing point depression

Back

Activation Energy

Front

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

Back

Heat of Vaporization

Front

energy required for liquid→gas

Back

Network Covalent solids

Front

- atoms joined by a continuous network of covalent bonds - high melting points - nonconductors of electricity - insoluble in water - Ex: diamond, graphite, quartz (compare to molecular solids)

Back

System

Front

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

Back

Hydrogen Bonding

Front

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

Back

Trigonal Pyramidal

Front

AX₃E

Back

Bent (2 possibilities)

Front

AX₂E, AX₂E₂

Back

Square Pyramidal

Front

AX₅E

Back

Single Bond (# sigma and/or pi)

Front

1 sigma bond

Back

Octahedral

Front

AX₆

Back

Deposition

Front

gas to solid

Back

T-shape

Front

AX₃E₂

Back

Metallic solids

Front

- metal cations held together by electrons not attached to any particular metal cation - high electrical conductivity - conduct heat - ductile and malleable -insoluble in water -high range of melting and boiling points

Back

Melting Point

Front

point at which solid→liquid occurs

Back

Base

Front

puts OH⁻ into solution = ACCEPTS protons

Back

Molecular Substances

Front

-nonconductors of electricity -insoluble in water -low melting and boiling points (covalent)

Back

Trigonal Planar

Front

AX₃

Back

Triple Bond (# sigma and/or pi)

Front

1 sigma bond, 2 pi bonds

Back

Seesaw

Front

AX₄E

Back

Exothermic

Front

negative enthalpy, heat flows into surroundings, favorable for deltaG

Back

Rate

Front

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

Back

Dipole-Dipole forces

Front

-electrostatic force between the positive and negative ends of a polar molecule -stronger than London forces, but weaker than H bonding

Back

Endothermic

Front

positive enthalpy, heat flows into system, not favorable for deltaG

Back

Q>K (Favors forward or reverse reaction?)

Front

Reverse rxn (Think products/reactants)

Back

Bond Enthalpy

Front

ΔH when 1 mol of bonds is BROKEN in the gaseous state (+broken, -formed)

Back

LeChatelier's Principle

Front

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

Back

Tetrahedral

Front

AX₄

Back

Trigonal Bipyramidal

Front

AX₅

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

Double Bond (# sigma and/or pi)

Front

1 sigma bond, 1 pi bond

Back

Sublimation

Front

solid to gas

Back

Square Planar

Front

AX₄E₂

Back

Viscosity

Front

resistance to flow

Back

Conjugate acid

Front

the chemical formed when a base accepts a proton

Back

Condensation

Front

gas to liquid

Back

Heat Capacity

Front

heat required to raise the system 1°C (C in q=mC∆T)

Back

Ionic solid

Front

- atoms joined by strong electrical forces between oppositely charged particles - high melting points - nonconducting as solids - conducting when molten or in solution - often water soluble -crystalline structures

Back

Heat of Fusion

Front

energy required for melting to occur

Back

Melting

Front

solid to liquid

Back

Adhesion

Front

molecules' tendency to stick to the container

Back

Boiling Point

Front

point at which liquid→gas occurs, where atmospheric pressure equals vapor pressure

Back

Freezing

Front

liquid to solid

Back

Vaporization

Front

liquid to gas

Back

Cohesion

Front

molecules' tendency to stick to one another

Back

Q<K (Favors forward or reverse reaction?)

Front

Forward rxn (Think products/reactants)

Back

London dispersion forces

Front

weakest IMFs, found in all molecules

Back

Acid

Front

puts H⁺ into solution = DONATES protons

Back

Surroundings

Front

the rest of the universe (in thermodynamics)

Back

Section 3

(50 cards)

Ammonium

Front

NH₄¹⁺

Back

Permanganate

Front

MnO₄¹⁻

Back

1st law of thermodynamics (Energy?)

Front

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

Back

Sulfide

Front

S²⁻

Back

Nitrate

Front

NO₃¹⁻

Back

Ka equation

Front

[H+][A-]/[HA]

Back

Cathode

Front

half cell in which reduction occurs (RED CAT)

Back

Chlorate

Front

ClO₃²⁻

Back

Sulfate

Front

SO₄²⁻

Back

Buffer

Front

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

Back

Phosphate

Front

PO₄³⁻

Back

Chloride

Front

Cl¹⁻

Back

Conjugate base

Front

the chemical formed when an acid donates a proton

Back

q in I=q/t

Front

Charge (Coulombs)

Back

Spontaneity

Front

the likelihood that a rxn will occur "by itself"

Back

Cyanide

Front

CN¹⁻

Back

t in I=q/t

Front

Time (SECONDS)

Back

I in I=q/t

Front

Current (Amperes)

Back

Half-life equation

Front

t1/2 = 0.693/k (First order reaction)

Back

∆G =

Front

=∆Gproducts-∆Greactants, =∆H -T∆S, =RTlnK, =-nFE⁰cell

Back

2nd law of thermodynamics (Entropy?)

Front

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

Back

0.08206 Latm/molK

Front

Gas Constant, R

Back

1.0x10⁻¹⁴

Front

Kw

Back

Kb equation

Front

[OH-][HB+]/[B]

Back

Iodide

Front

I¹⁻

Back

Entropy

Front

a measure of randomness or disorder (S)

Back

Kw

Front

Ka x Kb = 1.0x10⁻¹⁴

Back

Dichromate

Front

Cr₂O₇²⁻

Back

if Q>Ksp, does a precipitate form?

Front

a precipitate forms

Back

Chlorite

Front

ClO₂¹⁻

Back

62.36 Ltorr/molK

Front

Gas Constant, R (with Torr)

Back

Voltaic (or Galvanic) cells

Front

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

Back

Chromate

Front

CrO₄²⁻

Back

96,485 C/mol e-

Front

Faraday's constant

Back

3rd law of thermodynamics (Entropy at 0K?)

Front

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

Back

Carbonate

Front

CO₃²⁻

Back

A = abc

Front

Beer's Law, Absorbance = (molar absorptivity)(path length)(concentration)

Back

pOH

Front

-log[OH⁻], pH + pOH = 14

Back

Salt Bridge

Front

connects the 2 half cells in a voltaic cell (balances charge)

Back

if Q<Ksp, does a precipitate form?

Front

no precipitate forms

Back

Acetate

Front

C₂H₃O₂¹⁻

Back

Sulfite

Front

SO₃²⁻

Back

Fluoride

Front

F¹⁻

Back

Oxide

Front

O²⁻

Back

-1.602 x 10⁻¹⁹ Coulomb

Front

Charge of an electron

Back

Hydroxide

Front

OH¹⁻

Back

Perchlorate

Front

ClO₄¹⁻

Back

pH

Front

-log[H⁺], pH + pOH = 14

Back

Nitrite

Front

NO₂¹⁻

Back

Anode

Front

half cell in which oxidation occurs (AN OX)

Back