• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/45

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

45 Cards in this Set

  • Front
  • Back

Corresponding Units for k of each Overall Rxn Order:


0th, 1st, 2nd, 3rd

0th: Ms- 1st: s- 2nd: M-s- 3rd: M2-s-

0th Order Integrated Rate Law

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

1st Order Integrated Rate Equation

-kt = ln ( [A]t / [A]0 )

1st Order Rxn Equation

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


y = mx + b

1st Order Rxn Half Life



t 1/2 = ln(2) / k

2nd Order Integrated Rate Law

1/[A]t = kt + (1/[A]0)

Decay Rate

-(delta)N / (delta)t = kN


N= #of radioactive nuclei


k= decay constant

Activation Energy Equation


(For Two Temperatures)



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

The Arrhenius Equation


*Ea: Activation Energy


*R : Ideal Gas Constant (8.3145 J mol- K-)


*T : Temperature (K)



k = Ae ^(-Ea/RT)


*Ea goes UP, k goes DOWN


*Temperature goes UP, k goes UP

Kinetic Molecules Theory

average kinetic energy and thus the average speed of gas molecules depends on the absolute temp. (K)

Collision Theory

a bimolecular reaction occurs when 2 properly oriented molecules come together w/ a sufficiently energetic collision

Collision Rates

Collision Rates Increase when... Increased Concentration, Diameter, and Average Speed of Molecules

Increase Temperature

Increased Kinetic Energy

Increased Kinetic Energy

More Frequent Collisions

More Frequent Collisions

Increased Rate of Reaction

Elementary (RXN) Step

a single step in a Rxn mechanism that describes an individual molecular event

Overall (Rxn)

Describes the reaction stoichiometry and is a summation of all elemental steps in the reaction

Reactive Intermediate

Produced in one step and consumed in a subsequent step

Molecularity

a classification of an elementary reaction based on the # of molecules (or atoms) on the reactant side of the chemical equation

Unimolecular

One Reactant (always 1st order)

Bimolecular

Two Reactants

Termolecular

Three Reactants

Rate Determining Step (RDS)

slowest step in a reaction mechanism


(Rate of Step 1 = Rate of Overall)

[A] + [B] -> [AB]


Frequency of AB Collisions

*[A] molecules is proportional to Concentration of [B] molecules


*Doubling [ ] of A or B - Doubles AB frequency


*Doubling both [A] and [B] - Quadruples AB total frequency

Catalyst

a substance that increases the rate of the Rxn w/o itself being consumed in the Rxn


*Lowers Activation Energy (Ea)


*Not in the overall Rxn


Homogenous / Heterogenous Catalyst

Homog. : catalyst in same phase as reactants


Heterog. : catalyst in different phases

Chemical Equilibrium

a dynamic state where the [ ] of the reactants and the [ ] of the products remains constant


overtime

Reaction Quotient (Qc)

Q > 1 : more products


Q < 1 : more reactants


Q = 1 : equal [products] & [reactants]


Q = [products] / [reactants] =


[C]^c[D]^d / [A]^a[B]^b

K

ratios of products to


reactants at equilibrium


0 < K < 1 : more reactants


K ~ 1 : equal [ ]'s


K > 1 : more products

Q = K at Equilibrium

Q goes to K to show direction of RXN


Q < K : reaction goes left


Q > K : reaction goes right

Kp : the equilibrium


constant for partial


pressures


Kp = Kc(RT)^(delta N)


delta N: change in gasses in Rxn (c+d)-(a+b)


R : 0.08206 L atm mol- K- T : Temp. (K)



aA + bB -> cC + dD


Kp = (PC^c)(PD^d) / (PA^a)(PB^b)

LeChatelier's Principle

if a stress is applied to a Rxn mixture at


equilibrium, a net Rxn occurs to relax that stress.


1. Increase Reactants [ ], Rxn moves to right


Decrease Products [ ], Rxn moves to the right


2. Change Pressures/ Volumes


(1/2 volume, increases pressure, Rxn moves to side w/ least # of moles)


3. Change Temperatures


(increase T, decrease products, Exothermic


decrease T, increase products, Endothermic)

Bronsted Lowry Definitions


1. Acid


2. Base

1. Acid : (donator) any substance that can transfer a proton (H+) to another substance




2. Base : (acceptor) any substance that can accept a proton

Conjugates

One Proton Different


HA + B -> BH+ + A-


HA&A- (A/B Conjugate Pair)


B&BH+ (A/B Conjugate Pair)

Electrolytes

Most acids and bases are electrolytes


*Strong Acid/Base = Strong Electrolyte

Strong Acids

Binary:


HCl, HBr, HI




OXO Acids:


HNO3, H2SO4, HClO4, HClO3

Strong Acid

*MOST DISSOCIATION

Smallest Ka

*LEAST DISSOCIATION


*HIGHEST pH

Kc < 1


Kc > 1

Weak Acid/Base (PARTIAL DISSOCIATION)


Strong Acid/Base (STRONG DISSOCIATION)

Stronger Acid


Weaker Conjugate Base (and vice versa)

More Polar

Stronger Acid / Base

Short Strong Bond


(Difficult to Dissociate)

Long, Weak Bonds


(Easily Dissociate)

Higher Acid Strength


(O Atoms)

More # of Oxygen Atoms

pH Scale (pH = -log[H+] )

ACIDIC 0 < 7 < 14 BASIC


NEUTRAL

Weaker Acid will be ...

Less Acidic than Stronger Acid