10 - Acids And Bases Flashcards

1
Q

Arrhenius acids and bases

A

Defined by dissolution in water to excess of H+ or OH-

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2
Q

Bronstead-Lowry acids and bases

A

Defined by donation or reception of H+

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3
Q

Lewis acids and bases

A
  • defined by donation or reception of electron pairs

- acids accept electron pair

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4
Q

Amphoteric species

A
  • reacts like acid in basic environment and vice versa

- amphiprotic may behave as BL acid or base: water and polyvalent species

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5
Q

Consistency of equilibrium constants

A
  • only temperature dependent

- otherwise 100% constant

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6
Q

Log and other mathematical properties

A
Log1=0
Log10=1
Log100=2
Log1000=3
Logxy=logx+logy
-log(n x 10^-m)=(-logn)-log(10^-m)=m-logn=m-0.n

(because n is between 1 and 10, -logn will be between 0 and 1)

(6x10^-3)^2 = 36x10^-6

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7
Q

Water dissociation constant and K of WA and WB

A

Kw [water disossiation constant] =[H3O+][OH-]=10^-14

  • weak acids defined by Ka less than 1
  • weak bases defined by Kb less than 1
  • conjugate of a strong acid of base is inert
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8
Q

Hydrolysis and neutralization reactions

A
  • hydrolysis: salt ions react with water to give back acid and base
  • neutralization reactions form salt and sometimes water
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9
Q

Titrations

A
  • oft carried out between acids/bases or oxidation/reduction pairs
  • titrant (known [] and volumes) added to titrand (known volume, unknown [])
  • WAWB titrations rarely performed
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10
Q

equivalence points

A
  • for SASB titration, equivalence point will be at 7 but that isn’t always the case: otherwise, leans toward stronger of reactants
  • equivalence point may be observed by use of an indicator
  • equivalence point generally has steepest point on curve for any titration
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11
Q

SASB titrations

A

Flat- vertical - flat

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12
Q

WA (titrand) SB (titrant)

A
  • more gradual initial curve, vertical, flat
  • starting point is farther from zero than SASB
  • SA (titrant) and WB (titrand) is inverse
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13
Q

Polyvalent titration curve

A
  • equivalence points at steep segments

- half equivalence points (corresponding to pka values) between equivalence points at flat segments

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14
Q

Buffers

A
  • generally composed of WAWB conjugate pair
  • big flat parts of curve
  • greatest buffering capacity is about 1pH range within pKa of acid of buffer
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15
Q

Henderson-Hasselbalch

A
  • pH=pKa+log[A-][HA]
  • greater [], same ratio increase buffering capacity - less of a pH change with addition of A or B
  • use normality / equivalence equation to get []: N1V1=N2V2
  • optimal buffering occurs when pH = pKa
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