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33 Cards in this Set

  • Front
  • Back

Strong Acids

HCl, HBr, HI, HNO3, ClO4, H2SO4

Strong Bases

hydroxides of Group IA, IIA

Common Salts

Strong electrocytes

Rate law

- (change in concentration of reactants) / time

Rate law 2

k (A)m (B)n

Arrehnius Equation

k=pZe -Ea/RT

Collision State Theory

maxwell-Roltzman distribution curve

Transition State Theory

Intermediate = produced then consumed


Catalyst = consumed then produced

Zero Order Rate law

Ax = -kt + A0

Zero Order shape

Ax = -kt + A0

Zero Order half life

A0/ 2k

1st Order Rate law

Ln Ax = -kt + ln A0

1st Order graphical representation

Ln Ax = -kt + ln A0

2nd Order rate law

1/A0 - 1/Ax = -Kt




1/Ax = Kt + 1/A0

2nd Order graphical representation

1/A0 - 1/Ax = -Kt


1/Ax = Kt + 1/A0

half life for 1st Order

ln2/K

half life for 2nd Order

1 / Ao K



1st Order simplified to A

A = A0 e -kt

mole fraction

mole solvent / mole solvent + mol solution

mass percent

g solvent / g solution

molality

moles solvent / g solution

conditions necessary hydrogen bonding

a H atom is covalently bonded to a small, Highly EN non metal




and simultaneously attracted to another non metal of a neighboring molecule

Average rate vs instantaenous rate

average is change over time and assumes that rate is constant. Initial rate is during an extremely short time before reverse reaction

higher lattice energy

in more insoluble in water

Necessary conditions for Eq reaction

1. reversible


2. rate of forward rxn and reversible rxn is same

What is System?

an isolated setting

K equilibrium Constant

Kf/Kr = reactants / products = K

Rxn quotient Q > K

reverse

Rxn quotient Q < K

forward

Q = K

Equilibruim

Solution of salts :


strong base and weak acid

pH > 7

solution of salts :


strong acid and weak base

pH < 7


sd