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    Chemistry A Final Study Guide

    Chapter 8 Chemical Equations and Reactions

    types of reactionso synthesis

    A + XAX reactions of elements with O and S two reactants, one product metals with halogens oxides of active metals react with water to form hydroxides oxides of nonmetals react with water to form oxyacids

    o decomposition AXA + X electrolysis decomposition of a substance by an electric current decomp of metal carbonate products of metal oxide and CO2 decomp of metal hydroxide products of metal oxides and water decomp of metal chlorate products of metal chloride and oxygen decomp of acid products of nonmetal oxides and water

    o single displacement A + BYAY + B displacement of a metal in a compound by another metal displacement of hydrogen in water by a metal displacement of hydrogen in an acid by a metal displacement of halogens reactivity of halogens decreases down the group,

    therefore any halogen can replace any element below it

    o double displacement AX + BYAY + BX formation of a precipitate formation of a gas formation of water

    o combustion a reaction in which a substance combines with oxygen releasing a large amount of

    energy in the form of heat and light

    burning of hydrocarbons writing chemical equations in word and chemical formulas

    o identify elements in equationo write formula using compound nameso balance equation

    activity series and single displacement reactionso a list of elements arranged by the ease with which the elements undergo certain chemical

    reactions

    o usually determined in single displacement reactionso most active element placed at top and can replace any element below it but not above it

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    o trend in activity of halogens

    o reactivity of halogens decreases down the group, therefore any halogen can replace anyelement below it

    o they undergo synthesis reactions with many metalso form ionic compounds with group 1 and group 2 metals

    Chapter 9 Stoichiometry

    solving stoichiometry problems set up below

    mole ratio 2 2 1

    balanced equation 2HgO 2Hg + O2

    molesmass 95.2 g

    check

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    percent yield actual yield / theoretical yieldo theoretical yield max amount of product that can be produced from a given amount of

    reactant

    o actual yield measured amount of a product obtained from a reaction

    Chapter 10 States of Matter

    kinetic molecular theory foro solids

    strong intermolecular forces hold particles in relatively fixed positions with onlyvibrational motion

    definite melting point kinetic energy of particles overcomes the attractive forcesbetween them

    high density low incompressibility low rate of diffusion

    o liquids

    relative high density relative incompressibility transmits pressure equally in all directions particles close together and attractive forces between particles can slow diffusion surface tension force that tends to pull adjacent parts of a liquids surface together,

    decreasing surface area to the smallest possible size

    capillary action the attraction of the surface of a liquid to the surface of asolid

    o gases large particles that are far apart relative to their size collisions between gas particles and between particles and containers are elastic

    elastic collisions no net loss of kinetic energy particles are in continuous, random, rapid motion there are no forces of attraction between gas particles the temperature of the gas depends on the average kinetic energy of the particles of

    gas

    ideal gas hypothetical gas that perfectly fits all of the assumptions of the kinetic moleculartheory of gas

    o most gases exhibit ideal gas behavior when at high temperature and low pressureo noble gases and nonpolar diatomic molrcules show essentially ideal behavioro polar molecules deviate from ideal behavior

    intermolecular forces in liquidso dipole-dipoleo London dispersion forceso Hydrogen bonding

    properties ofo solids

    definite shape and volume crystalline solids crystals where particles are arranged in ordered geometric

    patterns

    ionic crystals positive and negative ions; electrostatic charge covalent network crystals each atom covalently bonded to its neighbor; in

    diamonds and oxides of transition metals

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    metallic crystals metal cations surrounded by a sea of electrons; cause ofhigh conductivity in metals

    covalent molecular crystals covalently bonded molecules held together byintermolecular forces

    o non polar weak London dispersion forceso polar dispersion forces, dipole-dipole, and hydrogen bonding

    amorphous solids particles randomly arranged; without shapeo liquids definite volume

    takes the shape of its container attraction between particles are caused by intermolecular forces stronger intermolecular forces and lower mobility than gases not bound in fixed positions particles have mobility/fluidity

    o gases expansion due to assumption of continuous, random, rapid motion and no forces

    of attraction between particles

    fluidity ability of gas particles to glide past each other; due to assumption thatthere are no forces of attraction between particles

    low density - due to assumption that particles are tiny and far apart compressibility - due to assumption that particles are tiny and far apart diffusion spontaneous mixing of two substances due to their random motion; due

    to assumption that particles are in continuous, random, rapid motion

    effusion process by which gases pass through a tiny opening; due to assumptionthat particles are in continuous, random, rapid motion

    liquid vapor equilibrium pressure exerted by a vapor in equilibrium with its correspondingliquid at a given temperature

    o smell indicator of vapor pressure; higher vapor pressure, the stronger the smello particles above average kinetic energy vaporized, they lose kinetic energy and go back into

    liquid

    o volatile liquid evaporates readily, weak intermolecular forceso non volatile molten ionic compounds

    vapor pressure curves

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    Chapter 11 Gases

    Daltons law of partial pressure total pressure of a mixture of gases is equal to the sum of thepartial pressures of the component gases

    gas lawso BoylesPV=k

    P1V1=P2V2 constant T, n

    o CharlesV=kT V1/T1= V2/T2 constant P, n

    o Gay LussacP=kT P1/T1= P2/T2 constant V, n

    o AvogadrosV=kn Avogadros number = 6.022 x 1023molecules, atoms, ions/mol

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    o combined gas law P1V1/T1= P2V2/T2 calculating molar mass of a gas

    o standard molar volume of a gas at STP, one mole of gas occupies 22.4 Lo multiply using 22.4 L/1 mol as the conversion

    ideal gas law PV=nRTo R = 0.08206 L x atm / mol x Ko used to calculate when there is no change

    Chapter 14 Acids

    electrolytes all aqueous acids are electrolytes naming acids

    o ate ico ite - ous

    acid-base theorieso Arrhenius

    acid increases concentration of hydrogen ions (H+) strong acid releases lots of H+; completely ionize in aqueous solution weak acid releases few H+in aqueous solution

    base increases concentration of hydroxide ions (OH-) strong bases dissociate in water strong bases are strong electrolytes

    o Bronsted-Lowry acid molecule or ion that is a proton donor base molecule or ion that is a proton acceptor Bronsted-Lowry acid-base reaction protons are transferred from one reactant (the

    acid) to another (the base)

    o Lewis acid atom, ion, or molecule that accepts an electron pair to form a covalent bond

    any compound where the central atom has three valence electrons can reactas a Lewis acid

    base atom, ion, or molecule that donates an electron pair to form a covalent bond Lewis acid-base reaction formation of one or more covalent bonds between an

    electron pair donor and electron pair receiver

    conjugate acid-base pairso conjugate base of an acid the species that remains after a Bronsted-Lowry acid has given

    up a proton

    o conjugate acid of a base the species that remains after a Bronsted-Lowry base has gaineda proton

    o conjugate acid-base pairs in equilibrium both the forward and reverse reactions occuro

    strong acid weak baseo weak acid strong base

    amphoteric can act as either acid or baseChapter 15 Acid Base Titration

    calculating pHo pH = -log [H30+]o [H30+] = 10-pH

    titration calculationo MAVA= MBVB

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    Chapter 16 Reaction Energy

    temperature the measure of the average kinetic energy of the particles in a sample of matter heat energy transferred between samples of matter because of a difference in temperatures specific heat the amount of energy required to raise the temperature of one gram of a substance

    by 1 degree C or 1 K

    o Cp= q / m x To specific heat = heat transferred / mass x T

    H enthalpy change amount of energy absorbed or released by a system as heat during aprocess at constant pressure

    o H = HproductsHreactantso enthalpy change depends on number of moles

    Hesss Law the overall change in enthalpy change in a reaction is equal to the sum of enthalpychanges for the individual steps in the process

    o Hesss Law problem write steps of equation with H balance equations to cancel out

    **if multiply equation, make sure you multiply H what cant cancel should be final equation add H to find total H

    entropy measure of the randomness of the particles in a systemo represented by So measured in kJ / (mol x K)o positive S system increases more randomo negative S system decreases more orderedo solid particles in fixed positions low entropyo liquid particles close together a bit higher in entropyo gas particles far apart and in random, rapid motion high entropy

    spontaneous reactionsH S G Is this reaction spontaneous?negative positive negative yes, at all temperatures

    negative negative positive or negative only if T < H / S

    positive positive positive or negative only if T > H / S

    positive negative positive never

    o reaction spontaneous if G < 0 Gibbs free energy enthalpy-entropy function at a particular temperature and constant pressure

    that assesses the tendency of a reaction to proceed in a particular direction

    o G = H TS *at a constant temperature and pressureChapter 17 Reaction Kinetics

    reaction mechanism step by step sequence of reactions by which overall chemical changes occur intermediates species that appear in some steps but not in the net equation homogeneous reaction reactants and products exist in a single case collision theory set of assumptions regarding collisions and reactions activation energy minimum energy required to transform reactants into an activated complex

    o required to merge valence electrons and to loosen bonds sufficiently for molecules to reacto has to overcome repulsive forces between molecules

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    activated complex transitional structure that results from an effective collision; it persists whileold bonds are breaking and new bonds are forming

    o not an intermediate factors affecting reaction rate

    o nature of reactants reaction rate depends on particular reactants and bonds involvedo surface area

    heterogeneous reactions involve reactants in two different phases; reactions canonly occur when surfaces are in contact

    increase in surface area increases rate of heterogeneous reactionso temperature an increase in temperature increases average kinetic energy of particles and

    can result in a greater number of effective collisions

    energy of collisions must be equal to or greater than activation energyo concentration in homogeneous reactions, reaction rates depend on concentration of the

    reactants

    depends in slowest step in reaction mechanismo presence of catalysts

    catalysts substance that changes the rate of a reaction without itself being permanentlyconsumed; does not appear as a product

    o provides alternate pathway of lower energy where the potential energy is lowered and mayhelp to form an activated complex that requires lower activation energy

    rate limiting step if the reaction proceeds in a series of steps, the slowest-rate step is the ratelimiting step

    writing a rate lawo rate law an equation that relates reaction rate and concentrations of reactantso determined by how concentration affects the reaction rateo R = k [A]n[B]mo k = specific rate constanto [A] and [B] molar concentrations

    Chapter 18 Chemical Equilibrium reversible reactions a reaction in which the products can react to reform the reactants equilibrium conditions pressure, concentration, temperature equilibrium constant K = [C]c[D]d/ [A]a[B]b

    o independent of initial concentrationso dependent on temperature

    Le Chtliers principle a system subjected to stress will shift in the direction that tends to relievethe stress

    reactions running to completion when ions are removed from the reaction either as a gas orprecipitate causing the reaction to cease