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Aqueous Flashcards

Shivani Kershaw Chemistry NCEA Level 3 Englisch 47 Karten

Aqueous Flashcards

Karten in diesem Stapel (47)

  1. 1Define EquilibriumThe rate of the forward reaction
    Equals
    The rate of backwards reaction
  2. 2Define KsSolubility constant
    No unit
  3. 3Ks formulaKs = [C]c [D]d
  4. 4s formula (gL-1) given gmol-1 and mol L-1s = mol L-1 x gmol-1
  5. 5s formula (mol L-1) given gmol -1 and gL-1s = gL-1/gmol-1
  6. 61:1 ratio KsKs = (s) x (s)
    = s2
    s = square root Ks (mol L-1)
  7. 71:2 ratio Ks 2:1 ratio KsKs = (s) x (2s)2
    = 4s3
    s = 3square root Ks/4 (mol L-1)
  8. 8Define solubilityAmount of substance
    Dissolve in a given volume
    form saturated solution
  9. 9Describe Common Ion EffectIonic solution
    Added to a solution containing one of common ion
    Solubility is reduced
  10. 10Explain Common Ion EffectState common ion e.g Br-
    Br- added to solution
    Increase in [common ion]
    Reverse reaction favoured
    To restore equilibrium
    Decrease in [other ion] e.g Ag+
    Salt becomes less soluble e.g AgBr
  11. 11Complex Ions - NH3[Ag(NH3)2]+
    [Cu(NH3)4]+2
    [Zn(NH3)4]+2
  12. 12Complex Ions - OH-[Al(OH)4]-
    [Pb(OH)4]-2
    [Zn(OH)4]-2
  13. 13Complex Ion - cation (e.g Ag+) reacting with base NH3 addedProduce Complex Ion:
    Ag+ + 2NH3 >< [Ag(NH3)2]+
    Base added to the system (NH3)
    Reduces concentration of solution
    Product (Ag+) remove from equilibrium
    Ag2CO3 --> 2Ag+ + CO3^2-
    Increase in the forward reaction
    Equilibrium shifts to favour products
    More salt is dissolved e.g Ag2SO4 (s)
    Solubility is increased
  14. 14Complex Ion - cation (e.g Zn(OH)2) reacting with base OH- addedZnOH2 --> Zn2+ + 2OH-
    Small amount OH- added
    - decrease solubility
    - reaction moves to left
    - removes added product
    - produce more reactant
    Excess OH- added
    - react with cation
    - produce complex ion
    [Zn(OH)4]-2
    - reduces concentration of solution
    - product removed
    - reaction increase in forward direction
    - more salt dissolve
    - solubility increase
  15. 15Complex Ion - salt (e.g Ag2CO3) contains carbonate (CO3) when acid addedAcid added to system
    Reduces concentration of solution
    Dissociate into ions - cation and carbonate
    The acid reacts with carbonate (neutralises)
    Product (CO3) removed from equilibrium
    Ag2CO3 >< Ag+ + CO3^2-
    Increase in the forward reaction
    Equilibrium shifts to favour products
    More salt is dissolved
    Solubility is increased
  16. 16Describe Strong Acids/BasesDissociates completely
    Base - readily accepts H+
    Acid - readily donates H+
    A lot of particles per unit volume
  17. 17Describe Weak Acids/BasesPartially dissociates
    Base - partially accepts H+
    Acid - partially donates H+
    Few particles per unit volume
  18. 18Calculate conc from pH[C] = (10-pH)2/Ka
  19. 19Kb formulaKb = Kw/Ka
  20. 20Strong Acid Water Dissocation[C] = [D] > [H3O+] = [OH-]
    No additon of H3O+ or OH - pH remains neutral
    Acid fully dissociates into ions
  21. 21Strong Acid Water Dissocation when H+ added in ionisation[H3O+] = [C] > [OH-]
    Addition of H3O+ - pH decreases
    Ions added in dissociation
  22. 22Strong Base Water Dissocation when OH- added in ionisation E.g NaOH --> Na+ + OH-[OH-] = [Na+] > [H3O+]
    Addition of OH in ionisation - pH increases
    Solution basic
    Ions added in dissociation
  23. 23Explaining pH- depends on [H3O+] and [OH-] ratio
    - dissociation
    - pH is high [OH-] high
    - pH is low [H3O+] high
  24. 24Describe conductivityDepends on the concentration of ions
    Complete dissolve of ions
    - good conduct
    Partially dissolves (if weak substance)
    - bad conduct
  25. 25Calculate Ionic Product (precipitate)Calculate concentration of each ion
    - mol-1 of ion x inital ml/total ml
    IP = [calculated conc] x [calculated conc]
    Calculate IP no units
    Compare IP with given Ks
    - a precipitate forms or not?
  26. 26Comparing IP to KsIP < Ks < IP
  27. 27Define AcidProton (H+) donor
  28. 28Define BaseProton (H+) acceptor
  29. 29Calculate pH (given [H30+])-log [H30+]
  30. 30Calculate [H30+] (given pH)inv log - pH
  31. 31Calculate pH (given [OH-])Kw (1x10^-14)/[OH-] = [H30+]
    pH = -log [H30+]
  32. 32Calculate pH (weak acid)Ka = [C] [H30+]/[A] - H20 not included
    assume [C] = [H30+]
    [H30+]^2 = [A] x Ka
    [H30+] = square root [H30+]^2
    pH = -log [H30+]
  33. 33Calculate pH (weak base) (given Ka)Kb = Kw (1x10^-14)/Ka
    Kb = [C] [OH-]/[A] - H20 not included
    assume [C] = [OH-]
    [OH-]^2 = [A] x Kb
    [OH-] = square root [OH-]^2
    pOH = -log[OH-]
    pH = 14 - pOH
  34. 34Calculate pKa- log Ka
  35. 35Calculate Ka (given pKa)inv log - pKa
  36. 36Describe Buffer SolutionsAbsorbs the addition
    Small amounts
    Acids or base
    Without changing pH significantly
  37. 37Explain the role of the BufferNeutralise solution of acid by adding strong base
    Dissolve salt of conjugate base into solution of acid
  38. 38When is a Buffer Solution most effective?[Base] = [Acid]
    pH = pKa + log 10
    pH = pKa + log 10 [conjugate base]/[acid]
    pH = pKa
  39. 39Calculate pH of a Buffer Solution given KaKa = [H30+] [D] / [A]
    [H30+] = Ka x [A] / [D]
    pH = -log [H30+]
  40. 40Calculate pH of a Buffer Solution given pKa + conc of [A] and [D]pH = pKa - log [A] / [D]
    or
    pH = pKa + log [D] / [A]
  41. 41Define Equivalence PointAll of the weak acid has reacted with base being added
    Most vertical point on the graph
  42. 42Describe the features of a Titration Curve1. Start of pH of acid - initial pH due to starting acid or base
    2. E.P - weak acid has reacted with base
    3. Mid-point - half way in volume to E.P, pKa is pH of midpoint
    4. Buffer Zone - area 1 pH either side of mid-point
    5. After E.P - pH depends on conc of solution being added from burette
    Describe the features of a Titration Curve
  43. 43Calculate pH of a solution at Start Point (before base added)Equation
    Ka = 10 - pKa
    Ka = [H30+]^2 / [A]
    [H30+]^2 = Ka x [A]
    sqaure root [H30+]^2 = [H30+]
    pH = -log [H30+]
    pH = 3 sf
  44. 44Calculate volume of base at Equivalence PointEquation
    Calculate moles of substance where conc is given
    n = c x v (given)
    n(conc given) = n(base we want to know)
    v = n/c
    v(base) = ml (3 sf)
  45. 45Calculate Mid-Point of BufferpH = pKa
    v(base) /2 = ml 3sf
    pH = pKa when __ml of (base) has been added
  46. 46Calculate pH of Equivalence Point (after Mid-Point)v(base) + v(given) = ml 3 sf
    c(conc given initially) / new ml 3sf
    Kb = 1x10^14 / Ka
    Kb = [C] [OH-]/[A]
    Kb = [OH-]^2 /[c(conj base)]
    [OH-]^2 = Kb x [A] or [c(conj base)]
    sqaure root [OH-]^2 = [OH-]
    [H30+] = 1x10^-14 / [OH-]
    pH = - log [H30+]
    pH = 3 sf
  47. 47Calculate pH of a solution at Final Point (after base added)Amount added - E.P volume = excess volume
    Total volume caluclate (before v + added v)
    c(base) = excess v/total v X original conc of base
    [OH-] = c(base)
    [H30+] = 1x10^14 / [OH-]
    pH = -log [H30+]
    pH = 3 sf

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NCEA Level 3 Chemistry (Equilibrium) Karteikarten am Aqueous Flashcards, erstellt von Shivani Kershaw am 31/07/2018.
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