AP Chemistry Exam Review

AP Chemistry Exam Review

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Section 1

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Cards (137)

Section 1

(50 cards)

mass number

Front

The sum of an atom's neutrons and protons

Back

Energy Levels

Front

s-subshell holds two electrons p-subshell holds six electrons d-subshell holds 10 electrons f-subshell holds 14 electrons

Back

Ionic Bonds

Front

An ionic solid is held together by the electrostatic attractions between ions that are next to one another in a lattice structure. Occurs between a metal and a nonmetal; electrons are not shared, they are given up by one atom and accepted by another. Substances with ionic bonds are usually solids at room temperature and have very high melting and boiling points. Ex. NaCl

Back

Substitutional alloy

Front

Forms between atoms of similar radii Ex. Atoms of zinc are substituted with copper atoms to create an alloy

Back

Gases will most likely act as ideal under what conditions?

Front

High temperature and low pressure

Back

Network (Covalent) Bonds

Front

In a network solid, atoms are held together in a lattice of covalent bonds. They are very hard and have very high melting and boiling points. Ex. The most commonly seen network solids are compounds of carbon (such as diamond or graphite) and silicon (SiO₂ quartz)

Back

Periodic Trends

Front

Across the periods - atomic radius decreases - ionization energy increases - electronegativity increases Down the periods - atomic radius increases - ionization energy decreases - electronegativity decreases

Back

Factors Affecting Melting Points of Ionic Substances

Front

1. Charge on ions - a greater charge leads to a greater bond energy Ex. MgO will have a higher melting point than NaCl 2. Size of ions - smaller ions will have greater attraction Ex. LiF will have a greater melting KBr

Back

Moles

Front

grams/molar mass

Back

electron configuration

Front

The complete description of the energy level and subshell that each electron on an element inhabits

Back

Different types of bonds and their relative melting and boiling points (from highest to lowest)

Front

1. Network Covalent Bonds 2. Ionic Bonds (based on Coulombic attraction) a. Greater Ion Charge b. Smaller Atom Size 3. Covalent Bonds (based on molecular polarity) a. Hydrogen Bonds b. Non-Hydrogen Bond Dipoles c. London Dispersion Forces (temporary dipoles) i. Large molecules are more polarizable because they have more electrons.

Back

Atomic Radius Trends

Front

Atomic radius decreases across a period Atomic radius increases down a group Cations are smaller than their atoms Ions are larger than their atoms

Back

Incomplete Octets

Front

Some atoms are stable with less than eight electrons in their outer shell. - Hydrogen only requires two electrons - Boron is considered to be stable with only six electrons, as in BF₃

Back

Double Bond

Front

Bond designation: One sigma and one pi Bond order: Two Bond length: Intermediate Bond energy: Intermediate

Back

London Dispersion Forces

Front

Forces that occur between all molecules. These very weak attractions occur because of the random motions of electrons on atoms within molecules. At a given moment, a nonpolar molecule might have more electrons on one side than on the other, given it an instantaneous polarity. Molecules with more electrons will experience will experience greater London dispersion forces, and therefore have generally higher melting and boiling points. London forces are even weaker than dipole-dipole forces, so substances that have only London dispersion forces melt and boil at extremely low temperatures and tend to be gases at room temperature.

Back

Aufbau principle

Front

States that when building up the electron configuration of an atom, electrons are placed in orbitals, subshells, and shells in order of increasing energy.

Back

Hydrogen Bonds

Front

Much stronger than dipole-dipole forces. Substances that have hydrogen bonds have higher melting and boiling points. Ex. water, H₂O and ammonia, NH₃ *Water is less dense as a solid than as a liquid because its hydrogen bonds force the molecules in ice to form a crystal structure, which keeps them apart than they are in the liquid form

Back

Converting from moles to liters

Front

I mole of gas = 22.4 L

Back

Triple Bond

Front

Bond designation: One sigma and two pi Bond order: Three Bond length: Shortest Bond energy: Greatest

Back

ionization energy

Front

The amount of energy necessary to remove an electron from an atom.

Back

Hund's Rule

Front

States that when an electron is added to a subshell, it will always occupy an empty orbital if no one is available. Electrons always occupy orbitals singly if possible and pair up only if no empty orbitals are available.

Back

How intermolecular forces affect the phase of a substance

Front

1. Substances with weak intermolecular forces (LD), tend to be gases at room temperature. 2. Substances with strong intermolecular forces (HB) tend to be liquids at room temperature. 3. Because ionic bonds are generally significantly stronger tan intermolecular forces in covalent molecules, ionic substances are usually solid at room temperatures. Ionic substances do not experience intermolecular forces.

Back

Moles and Solutions

Front

Moles = (molarity)(liters of solution)

Back

Ionization energy

Front

The energy required to remove an electron from an atom.

Back

Avogadro's number

Front

6.022×10²³ particles per one mole

Back

Interstitial alloys

Front

Metal atoms with two different radii combine Ex. In steel, much smaller carbon atoms occupy the interstices of the iron atoms

Back

empirical formula

Front

- Represents the simplest ratio of one element to another in a compound - Start by assuming a 100 g sample - Convert percentages to grams - Convert grams into moles - Divide each mole value by the lowest of the values - These values become the subscripts

Back

molecular formula

Front

- Determine the molar mass of the empirical formula - Divide that mass into the molar mass x = m/e x = molar mass/ empirical mass - Multiply all subscripts in the empirical formula by the value of x

Back

Valence Shell Electron Pair Repulsion Model

Front

Electrons repel each other, so when atoms come together to form a molecule, the molecule will assume the shape that keeps its different electron pairs as far apart as possible.

Back

Electronegativity

Front

Refers to how strongly the nucleus of an atom attracts the electrons of other atoms in a bond.

Back

atomic number

Front

The same as the number of protons in the nucleus of an element; it is also the same as the number of electrons surrounding the nucleus of an element when it is neutrally charged.

Back

Formal Charge

Front

If more than one valid Lewis structure exists for a molecule, formal charge can be used to determine the more likely structure.

Back

Frequency and Wavelength

Front

c = λv Inversely proportional c = speed of light in a vacuum (2.998×10⁸ m/s) λ = wavelength of the radiation v = frequency of the radiation

Back

isotopes

Front

Atoms of an element with different numbers of neutrons

Back

Standard Temperature and Pressure (STP)

Front

Pressure = 1 atm Temperature = 273 K

Back

photoelectron spectra (PES)

Front

A chart of the amount of ionization energy for all electrons ejected from a nucleus. The y-axis describes the relative number of electrons that are ejected from a given energy level. The x-axis shows the binding energy of those electrons.

Back

Standard Enthalpy of Formation

Front

The amount of heat lost or gained when one mole of a compound is formed from its constituent elements.

Back

Expanded Octets

Front

In molecules that have d subshells available, the central atom can have more than eight valence electrons, but never more than twelve. - PCl₅ - SF₄ - XeF₄

Back

Heisenberg Uncertainty Principle

Front

States that it is impossible to know both the momentum of an electron at a particular instant.

Back

Enthalpy Change (Hess's Law for ΔH)

Front

The enthalpy change for a reaction is equal to the sum of the enthalpy of formation of all the products minus the sum of the enthalpy of formation of all the reactants.

Back

Energy and Electromagnetic Radiation

Front

ΔE = hv = hc/λ ΔE = energy change h = Planck's constant, 6.626×10⁻³⁴ J∙s v = frequency of the radiation λ = wavelength of the radiation c = the speed of light, 3.00×10⁸ m/s

Back

Covalent bonding

Front

Bonding in which two atoms share electrons. Each atom counts the shared electrons as part of its valence shell to achieve complete outer shells. The first covalent bond formed between two atoms is called a sigma bond.

Back

percent composition (mass percents)

Front

The percent by mass of each element that makes up a compound. It is calculated by dividing the mass of each element or component in a compound by the total molar mass for the substance.

Back

Resonance Forms

Front

Back

Single bonds

Front

Bond designation: One sigma Bond order: One Bond length: Longest Bond energy: Least

Back

Quantum Theory

Front

Max Planck figured out that electromagnetic energy is quantized. That is, for a given frequency of radiation (or light), all possible energies are multiples of a certain unit of energy, called a quantum (mathematically, that's E = hv). So, energy changes do not occur smoothly but rather in small but specific steps.

Back

Vapor Pressure

Front

Arises from the fact that molecules inside a liquid are in constant motion. If those molecules hit the surface of the liquid with enough kinetic energy, they can escape the intermolecular forces holding them to the other molecules and transition them into the gas phase. This is not to be confused with a liquid boiling. In order for vaporization to occur, no outside energy needs to be added.

Back

Coulomb's Law

Front

The amount of energy that an electron has depends on its distance from nucleus of an atom. While on the exam, you will not be required to mathematically calculate the amount of energy a given electron has, you should be able to qualitatively apply Coulomb's Law. Essentially, the greater the charge of the nucleus, the more energy an electron will have.

Back

Dipole-Dipole Forces

Front

Forces that occur when the positive end of one polar molecule is attracted to the negative end of another polar molecule. Molecules with greater polarity have higher melting and boiling points. Dipole-dipole attractions, however, are relatively weak, and these substances melt and boil at very low temperatures.

Back

Pauli Exclusion Principle

Front

States that the two electrons which share an orbital cannot have the same spin. One electron must spin clockwise, and the other must spin counterclockwise.

Back

Section 2

(50 cards)

Oxidizing agent

Front

Reactant that is reduced (gains electrons)

Back

Tetrahedral Geometry

Front

- Central atom has four electron pairs - Zero lone pairs - sp³ hybridization - 109.5° bond angle - Ex. CH₄, NH₄⁺, ClO₄⁻, SO₄²⁻, PO₄³⁻

Back

Activation Energy

Front

The amount of energy required to reach the transition state, the highest point on the graph. At this point, all reactant bonds have been broken, but no product bonds have been formed, so this is the point in the reaction with the highest energy and lowest stability.

Back

Reducing agent

Front

Reactant that is oxidized (loses electrons)

Back

Redox in a Galvanic Cell

Front

Oxidation takes place at the anode Reduction takes place at the cathode

Back

Gibbs Free Energy

Front

The amount of energy in a system that is available to do useful work. -ΔG is spontaneous +ΔG is nonspontaneous When ΔG = 0 the reaction is at equilibrium

Back

Bent Geometry

Front

- Central atom with three electron pairs - One lone pair - sp² hybridization - 120° bond angle - Ex. SO₂

Back

Solutes and Solvents

Front

"Like dissolves like" A basic rule to remember which solutes will dissolve in which solvents. Polar or ionic solutes (such as salt) will dissolve in polar solvents (such as water). Nonpolar solutes (such as oils) are best dissolved in nonpolar solvents. When an ionic substance dissolves, it breaks up into ions in a process called dissociation. Free ions in a solution are called electrolytes because they can conduct electricity.

Back

Graham's Law

Front

The rate of diffusion of a gas molecule is inversely proportional to the square root of that molecule's mass.

Back

If volume is constant

Front

As pressure increases, temperature increases

Back

Square Planar

Front

- Central atom has 6 electron pairs - Two lone pairs - d²sp³ hybridization - Ex. XeF₄, ICl₄⁻

Back

Catalysts

Front

Speed up a reaction by providing the reactants with an alternate pathway that has a lower activation energy. A catalyst lowers the activation energy, but it has no effect on the energy of the reactants, the energy of the products, or the ΔH of the reaction.

Back

Mole Fraction

Front

Mole fraction gives the fraction of moles of a given substance (S) out of the total moles present in a sample. Mole Fraction (Xa) = moles of substance S / total number of moles in solution

Back

Endothermic Reactions

Front

If the products have weaker bonds than the reactants, then the products have higher enthalpy than the reactants and are less stable; in this case, energy is absorbed by the reaction, or the reaction is exothermic.

Back

Trigonal Planar Geometry

Front

- Central atom with three electron pairs - Zero lone pairs - sp² hybridization - 120° bond angles - Ex. BF₃, SO₃, NO₃⁻, CO₃²⁻

Back

Density

Front

D = m/v

Back

Molarity (M)

Front

Expresses the concentration of a solution in terms of volume. M = moles of solute / liters of solution

Back

The Ideal Gas Equation

Front

PV = nRT R = .08206 Latm/molK

Back

Galvanic Cell (Voltaic Cell)

Front

In a galvanic cell, a favored redox reaction is used to generate a flow of current. Two half-reactions take place in separate chambers, and the electrons that are released by the oxidation reaction pass through a wire to the chamber where they are consumed in the reduction reaction. That's how the current is created. If the concentration of the products in a voltaic cell increases, the voltage decreases. If the concentration of the reactants increases, the voltage increases.

Back

Crystalline Solids

Front

Solid that has its atoms arranged in an orderly way.

Back

Reduction

Front

Electron gain

Back

Entropy

Front

A measure of molecular randomness, or disorder

Back

Cathode

Front

Where reduction occurs and the solution is becoming less positively charged, the positive cations from the salt bridge solution flow into the half-cell.

Back

Buffer Solution

Front

A solution consisting of a weak acid plus its conjugate base or a weak base plus its conjugate acid. This solution resists changes to its pH

Back

First Order Rate Laws

Front

Rate = k[A] The rate law for a first order reaction uses natural logarithms. The use of natural logarithms in the rate law creates a linear graph comparing concentration and time. The slope of the line is given by -k and the y-intercept is given by ln[A]₀

Back

Deviations From Ideal Behavior

Front

At low temperature and/or high pressure, gases behave in a less-than-ideal manner. This is because the assumptions made in the kinetic molecular theory become invalid.

Back

Half-life

Front

Describes the amount of time it takes for half of a sample to react.

Back

T-Shaped Geometry

Front

- Central atom has 5 electron pairs - Two lone pairs - dsp³ hybridization - Ex. ClF₃, ICl₃

Back

Specific Heat Capacity

Front

The amount of heat required to raise the temperature of one mass unit of a substance by 1.00°C

Back

Exothermic Reactions

Front

If the products have stronger bonds than reactants, then the products have lower enthalpy than the reactants and are more stable; in this case, energy is released by the reaction, or the reaction is exothermic.

Back

Spontaneous

Front

Not requiring an outside source of energy to proceed

Back

Anode

Front

Where oxidation occurs and the solution is becoming more positively charged, the negative anions from the salt bridge solution flow into the half-cell.

Back

Linear Geometry

Front

- Central atom with 2 electron pairs - Zero lone pairs - sp hybridization - Ex. BeCl₂ and CO₂ B - A - B

Back

Folded square, seesaw, distorted tetrahedron geometry

Front

- Central atom has 5 electron pairs - One lone pair - dsp³ hybridization - Ex. SF₄, IF₄⁺

Back

Solubility Rules

Front

1. Compounds with an alkali metal cation (Na⁺, Li⁺, K⁺, etc) or an ammonium cation (NH₄⁺) are always soluble. 2. Compounds with a nitrate (NO₃⁻) anion are always soluble.

Back

Bent Geometry

Front

- Central atom has four electron pairs - two lone pair - sp³ hybridization - 109.5° bond angle - Ex. H₂O, OF₂, NH₂⁻

Back

Amorphous Solid

Front

Solids whose particles have no orderly pattern.

Back

Dalton's Law

Front

Ptotal = Pa + Pb + Pc + ...

Back

Partial Pressure

Front

Pa = (Ptotal)(Xa) Xa = moles of gas A/total moles of gas

Back

Kinetic Molecular Theory

Front

- The kinetic energy of an ideal gas is directly proportional to its absolute temperature: The greater the temperature, the greater the average kinetic energy of the gas molecules. - There are no forces of attraction between the gas molecules in an ideal gas. - Gas molecules are in constant motion, colliding with one another and with the walls of their container without losing any energy.

Back

Oxidation

Front

Electron loss

Back

Solving Electroplating Problems

Front

1. If you know the current and time, you can calculate the charge in coulombs. I = q/t I = current (amperes, A) q = charge (coulombs, C) t = time (seconds, s) 2. Once you know the charge in coulombs, you know how many electrons were involved in the reaction. moles of electrons = (coulombs) / (96,500 coulombs/mol) 3. When you know the number of moles of electrons and you know the half-reaction for the metal, you can find out how many moles of metal plated out. 4. Once you know the number of moles of the metal, you can convert this to the number of grams of the metal.

Back

Linear Geometry

Front

- Central atom has 5 electron pairs - Three lone pairs - dsp³ hybridization - Ex. XeF₂, I₃⁻

Back

Boyle's Law (If temperature is constant)

Front

As pressure increases, volume decreases, and vice versa

Back

Trigonal Bipyramidal Geometry

Front

- Central atom has 5 electron pairs - Zero lone pairs - dsp³ hybridization - Ex. PCl₅, PF₅

Back

Trigonal Pyramidal Geometry

Front

- Central atom has four electron pairs - One lone pair - sp³ hybridization - 109.5° bond angle - Ex. NH₃, PCl₃, AsH₃, SO₃²⁻

Back

Enthalpy Change in Bonds

Front

When bonds are broken, energy is released. When bonds are formed, energy is absorbed.

Back

Charles' Law (If pressure is constant)

Front

As temperature increases, volume increases

Back

Square Pyramidal

Front

- Central atom has 6 electron pairs - One lone pair - d²sp³ hybridization - Ex. BrF₅, IF₅

Back

Octahedral Geometry

Front

- Central atom has 6 electron pairs - Zero lone pairs - d²sp³ hybridization - Ex. SF₆

Back

Section 3

(37 cards)

Le Châtelier's Principle

Front

States that whenever a stress is placed on a system at equilibrium, the system will shift in response to that stress. If the forward rate increases, we say the reaction has shifted right, which will create more products. If the reverse rate increases, we say the reaction has shifted left, which will create more reactants.

Back

Half-life of a first order reactant

Front

Back

Equilibrium Constants

Front

Kc - constant for molar concentrations Kp - constant for partial pressures Ksp - solubility product (no denominator because the reactants are solids) Ka - acid dissociation constant for weak acids Kb - the base dissociation constant for weak bases Kw - the ionization of water (1 x 10⁻¹⁴)

Back

Heat of Formation, ΔH°f

Front

The change in energy that takes place when one mole of a compound is formed from its component pure elements under standard state conditions. ΔH°f for a pure element is zero. If ΔH°f for a compound is negative, energy is released when the compound is formed from pure elements, and the product is more stable than its constituent elements. That is, the process is exothermic. If ΔH°f for a compound is positive, energy is absorbed when the compound is formed from pure elements, and the product is less stable than its constituent elements. That is, the process is endothermic. ΔH° = ΔH°f products - ΔH°f reactants

Back

Equilibrium Constant, Keq

Front

The equilibrium constant tells you the relative amounts of products and reactants at equilibrium. The relationship between the concentrations of reactants and products in a reaction at equilibrium is given by the equilibrium expression, also called the law of mass action.

Back

Heat of Fusion

Front

Energy that must be put into a solid to melt it. This energy is needed to overcome the forces holding the solid together. Alternatively, the heat of fusion is the heat given off by a substance when it freezes. The intermolecular forces within a solid are more stable, and therefore, have lower energy than the forces within a liquid, so energy is released in the freezing process.

Back

Laws of Thermodynamics

Front

The first law of thermodynamics says that the energy of the universe is constant. The second law of thermodynamics says that if a process is favored in one direction, then it can't be favored in the reverse direction, and an increase in entropy promotes favored reactions.

Back

ΔG in Redox Reactions

Front

ΔG° = -nFE° ΔG° = Standard Gibbs free energy change (J/mol) n = the number of moles of electrons F = Faraday's constant, 96,500 coulombs/mole E° = Standard reaction potential (V, which is equivalent to J/C)

Back

How different values of enthalpy and entropy affect spontaneity

Front

Back

Le Châtelier's Principle with Temperature

Front

In an exothermic process: If the temperature goes up, the reaction will proceed in the backward direction (shifting away from the added energy). If the temperature goes down, the reaction will proceed in the forward direction (creating more energy). The reverse would be true in an endothermic reaction, as the energy would be part of the reactants.

Back

Specific Heat Equation

Front

q = mcΔT q = heat added (J or cal) m = mass of the substance (g or kg) c = specific heat ΔT = temperature change (K or °C)

Back

pH

Front

Back

Thermodynamically Favored Reactions

Front

A process that can occur without outside energy input.

Back

intermediates

Front

Substances that are produced but also fully consumed over the course of a reaction. Intermediates will always cancel out when adding up the various elementary steps in a reaction.

Back

Solubility Product (Ksp)

Front

The solubility product is a measure of the extent of a salt's dissociation in solution. The great the value of the solubility product for a salt, the more soluble the salt.

Back

Henderson Hasselbalch Equation

Front

Back

Common Ion Effect

Front

States that newly added ions will affect the equilibrium of a substance.

Back

Strong Acids

Front

HCl HBr HI HNO₃ HClO₄ H₂SO₄

Back

Second Order Rate Laws

Front

Rate = k[A]² The rate law for a second order reaction uses the inverses of the concentrations. The use of inverses in the rate law creates a linear graph comparing concentration and time. Notice that the line moves upward as the concentration decreases. The slope of the line is given by k and the y-intercept is given by 1/[A]₀

Back

Bond Energy

Front

The energy required to break a bond. Because the breaking of a bond is an endothermic process, bond energy is always a positive number. When a bond is formed, energy equal to the bond is released. ΔH° = Bond energies of bonds broken - bond energies of bonds formed ΔH° = reactants - products

Back

Changes in the Equilibrium Constant

Front

Shifts caused by concentration or pressure changes or temporary shifts, and do not change the value of the equilibrium constant itself. Because changing temperature also affects reaction kinetics by adding (or removing) energy from the equilibrium system, a change in temperature will also affect the equilibrium constant for the reaction itself, in addition to causing a shift.

Back

Strong Bases

Front

LiOH NaOH KOH Ba(OH)₂ Sr(OH)₂

Back

Heat capacity, Cp

Front

A measure of how much the temperature of an object is raised when it absorbs heat. An object with a high heat capacity can absorb a lot of heat without undergoing much of a change in temperature, whereas an object with a small heat capacity shows a large increase in temperature even if only a small amount of heat is absorbed.

Back

Comparing Q and K

Front

Back

Specific heat

Front

The amount of heat required to raise the temperature of one gram of a substance one degree Celsius.

Back

rate-determining step

Front

Refers to the slowest step of a reaction. Since the slowest step is the most important step in determining the rate of reaction, the slowest step and the steps leading up to it are used to see if the mechanism is consistent with the rate law for the overall reaction. The rate law for the entire reaction is equal to that of the slowest elementary step.

Back

Gibbs Free Energy, G

Front

A measure of whether or not a process will proceed without the input of outside energy. A process that occurs without outside energy is said to be thermodynamically favored. If ΔG is negative, the reaction is thermodynamically favored If ΔG is positive, the reaction is thermodynamically unfavored If ΔG = 0 the reaction is at equilibrium

Back

Values for Keq

Front

A large value for Keq means that products are favored over reactants at equilibrium A small value for Keq means that reactants are favored over products at equilibrium

Back

State Functions

Front

Enthalpy change (ΔH), entropy change (ΔS), and free-energy change (ΔG) are state functions. That means they all depend only on the change between the initial and final states of a system, not on the process by which the change occurs.

Back

Entropy, S

Front

A measure of randomness or disorder of the system; the greater the disorder of a system, the greater its entropy.

Back

Le Châtelier's Principle with Pressure

Front

When external pressure is increased, the reaction will shift to the side with fewer gas molecules.

Back

Phase Changes

Front

Melting - solid to liquid Freezing - liquid to solid Vaporization - liquid to gas Condensation - gas to liquid Sublimation - solid to gas Deposition - gas to solid

Back

Reaction Quotient, Q

Front

The quantitative application of Le Châtelier's Principle. It is determined using the law of mass action. The value for the reaction quotient can be compared to the value for the equilibrium constant to predict in which direction a reaction will shift from the given set of initial conditions. If Q<K reaction shifts right If Q>K reaction shifts left If Q=K reaction is at equilibrium

Back

Hess's Law

Front

States that if a reaction can be described as a series of steps, then ΔH for the overall reaction is simply the sum of the ΔH values for all the steps. When manipulating equations for use in the enthalpy calculations, there are three rules: 1. If you flip the equation, flip the sign on the enthalpy value 2. If you multiply or divide an equation by an integer, also multiply/divide the enthalpy value by that same integer 3. If several equations, when summed up, create a new equation, you can also add the enthalpy values of those component equations to get the enthalpy value for the new equations.

Back

Heat of Vaporization

Front

The energy that must be put into a liquid to turn it into a gas. This energy is needed to overcome the forces holding the liquid together. Alternatively, the heat of vaporization is the heat given off by a substance when it condenses. Intermolecular forces become stronger when a gas condenses; the gas becomes a liquid, which is more stable, and energy is released. As heat is added to a substance, the temperature of the substance can increase or the substance can change phases, but both changes cannot occur simultaneously. Therefore, when a substance is changing phases, the temperature of that substance remains constant.

Back

First Order vs. Second Order Reactions

Front

Back

Le Châtelier's Principle with Concentration

Front

When the concentration of a reactant is increased, the reaction will shift in the direction that allows it to use up the added substance. If reactants are added, the reaction shifts left. When the concentration of a species is decreased, the reaction will shift in the direction that allows it to create the substance that has been removed. If the reactants are removed, the reaction shifts right.

Back