Chemical Equilibrium Flashcards

1
Q

Ksp

A
  • dissosiation constant
  • higher Ksp= more soluble compound
  • experimentally found, obtained from a chart
  • coefficients turn into exponents
  • ICE tbl (MOLES) to find
  • NO SOLIDS OR PURE LIQUIDS
    concentration of reactant(s)
  • [A+]^a[B-]^b
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2
Q

Common Ion Affect

A
  • more of ions already in solution added lowers solubility of added reactant
  • ions already present limits dissociation of more of same ions being added
  • Ksp decreases, equilibrium shifted to reactants side of reaction
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3
Q

Acid in water

A
  • strong completely dissociates
  • will form water with OH and shift equilibrium to products side
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4
Q

Q < Ksp

A
  • less than
  • no ppt formed
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5
Q

Q > Ksp

A
  • greater than
  • ppt formed
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6
Q

Q

A
  • reaction quotient
  • relative amount products and reactants present
  • changes as approach equilibrium
  • [X]^x[Y]^y
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7
Q

2 types of gravimetric analysis

A
  • precipitation
  • volatilization
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8
Q

Precipitation

A
  • solid generated from liquid phase medium
  • precipitate “falls out” of supernatant (water above) via the use of excess of reagent
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9
Q

Volatilization

A
  • gas comes out of solid or liquid medium
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10
Q

Precipitating agents

A
  • specific
    -selective
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11
Q

Specific precipitating agent

A
  • reacts w/ only one chemical species
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12
Q

Selective precipitating agent

A
  • reacts w/ limited # of chemical species
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13
Q

4 qualifications to make good ppt

A
  • easily filtered/washed (larger particles)
  • low solubility
  • unreactive w/ atmosphere
  • known composition
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14
Q

Colloidal suspension

A
  • v small [(10^-7 - 10^-4) cm diameter] particles
  • hard to filter/centrifuge
  • fix via recrystallization
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15
Q

Crystalline suspension

A
  • larger particles
  • settle spontaneously
  • easy to centrifuge and filter
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16
Q

Goal and methods to control particle size (4)

A
  • goal: maximize crystalline ppt particles
  • recrystallization
  • slow addtn of ppt agent
  • using dilute solutions
  • induce nucleation and particle growth
17
Q

Coprecipitation

A

-when soluble compound removed from solution during ppt formation
- minimize via recrystallization, washing of ppt, or increase of analyte concentration

18
Q

Surface adsorption

A
  • coprecipitation issue
  • ions stay on surface of solid
  • wash and decant to fix
19
Q

Mixed crystal formation

A
  • one of ions in solid crystal lattice replaced by another
  • caused by formation occurring too quickly
  • recrystallize or digest ppt to fix
20
Q

Occlusion

A
  • crystals grow too fast and trap counterions
  • use dilute solutions slowly or recrystallize to fix
21
Q

Mechanical entrapment

A
  • crystals grow too close together and grow together/ trap pockets of solution
  • use dilute solutions slowly or recrystallize to fix
22
Q

Recrystallization

A
  • boil ppt in supernatant/ wash
  • allow to cool slowly and bigger crystals form
23
Q

Like dissolves

A

like

24
Q

Like attracts

A

like

25
Q

Polyatomic ions in solution

A
  • stay as polyatomic ions in solution, no further dissociation
26
Q

Ksp increase

A
  • equilibrium shifts towards products side of reaction
27
Q

Typical rxn of ions of interest

A

Ca(OH)2 (s) ——–Ca 2+ (aq)+ 2 OH - (aq)