ch. 17 &19 test Flashcards

1
Q

the common ion effect

A

whenever a weak electrolyte and a strong electrolyte containing a common ion are together in solution, the weak electrolyte ionizes less than if would if it were alone in solution.

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2
Q

buffers

A

solutions of a weak conjugate acid-base pair that resist drastic changes in pH

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3
Q

henderson-hasselback equation

A

pH=pKa+log([A-]/[HA])

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4
Q

addition of a strong acid or a strong base to a buffer is…

A

a neutralization reaction

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5
Q

titration of a strong acid w/ a strong base

A

S

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6
Q

titration of a strong base w/ a strong acid

A

backwards S

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7
Q

titration of a weak acid w/ a strong base

A

S shifts up

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8
Q

more soluble salt

A

has an anion that is the conjugate base of a weak acid.

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9
Q

unchanged solubility salt

A

has anion that is the conjugate base of a string acid

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10
Q

complex ion formation

A

metal ions can act as lewis acids and form complex ions with lewis base in the solvent

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11
Q

formation of what increases the solubility of certain salts?

A

complex ions

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12
Q

Amphoterism

A

amphoteric oxides and hydroxides are soluble in strong acids or base, because they can act either as acids or bases

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13
Q

metals with amphoterism behavior

A

Al^+3, Cr^+3, Zn^+3, and Sn^+2

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14
Q

Q=Ksp

A

the system is at equilibrium and the solution is saturated

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15
Q

Q<Ksp

A

more solid can dissolve, no precipitate forms

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16
Q

Q>Ksp

A

a precipitate will form

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17
Q

first law of thermodynamics

A

energy cannot be created or destroyed

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18
Q

enthalpy

A

is the heat absorbed or released by a system during a constant-pressure process

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19
Q

entropy

A

is a measure of the randomness in a system

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20
Q

spontaneous process

A

proceed without any outside assistance

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21
Q

experimental factors that affect spontaneous processes

A

temperature and pressure

22
Q

reversible process

A

the system changes so that the system and surroundings can be returned to the original state by exactly reversing the process. this maximizes work done by a system on the surroundings

23
Q

irreversible process

A

cannot be undone by exactly reversing the change to the system or cannot have the process exactly followed in reverse.

24
Q

second law of thermodynamics

A

the entropy of the universe increases in any spontaneous process.

25
Q

entropy equation

A

ΔS= Sfinal-Sinitial or ΔS=qrev/T(constant T)

26
Q

reversible process

A

ΔS univ=ΔSsys +ΔSsurr=0

27
Q

irreversible process

A

ΔS univ=ΔSsys +ΔSsurr>0

28
Q

microstate

A

a single possible arrangement of position nd kinetic energy of molecules

29
Q

Boltzman equation

30
Q

entropy increases with

A

the number if microstates of a system

31
Q

translational

A

movement of the entire molecule from one place to another

32
Q

vibrational

A

periodic motion of atoms within a molecule

33
Q

rotational

A

rotation of the molecule about an axis

34
Q

the number of microstates possible for a system increase with

A
  • an increase in volume
  • an increase in temperature
  • an increase in the number of atoms/molecules
35
Q

entropy of a system increases for process where

A
  • gases form from either solids or liquids
  • liquids or solutions form from solids
  • the number of gas molecules increases during a chemical reaction
36
Q

factors that affect entropy

A
  1. physical state
  2. amount of substance more ->greater
  3. temp. higher->greater
  4. vol./pressure: higher vol. lower pressure -> greater
  5. size: larger -> greater
37
Q

third law of thermodynamics

A

the entropy of a pure crystalline substance at absolute zero is 0.

38
Q

entropy change equation

A

ΔS= ΣΔS^o(products)- ΣΔS^o(reactants)

39
Q

ΔS^o

A

is the standrad moalr entropy and n and m coefficients of the balanced chemical equation

40
Q

ΔS^o bullet points

A
  • is not zero for the elements
  • values of (g) > (l) > (s)
  • increase with molar mass and number of atoms
41
Q

ΔSsurr=

42
Q

Gibbs free energy

A

enthalpy and entropy can be used to predict whether a reaction is spontaneous using the states function ΔG

43
Q

ΔG=

44
Q

ΔG>0

A

the forward reaction is spontaneous

45
Q

ΔG=0

A

the system is at equilibrium

46
Q

ΔG<0

A

the reaction is non spontaneous but spontaneous in the reverse direction

47
Q

ΔG^o=

A

ΣΔGf^o(products)- ΣΔGf^o(reactants)

48
Q

when -ΔH & +ΔS

A

spontaneous at all temperatures

49
Q

when +ΔH & -ΔS

A

non spontaneous at all temperatures

50
Q

when -ΔH & -ΔS

A

Spontaneous at low Temp; nonspontaneous at high temp

51
Q

when +ΔH & +ΔS

A

spontaneous at high temp; nonspontaneous at low temp