Buffers, Titrations, Solubility Flashcards

1
Q

common ion effect

A

the shift in the position of an equilibrium upon addition of a substance that provides an ion already involved in that equilibrium

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2
Q

buffers

A

solutions that resist changes in pH when limited amounts of acid or base are added

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3
Q

where does the buffer’s resistance to change in pH arise from?

A

the presence of appreciable concentrations of weak acids and its conjugate (weak) base

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4
Q

addition of OH- to a buffer

A

the acid in the buffer will neutralise added strong base

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5
Q

addition of H3O+ to a buffer

A

the base in the buffer will neutralise added strong acid

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6
Q

a good buffer contains

A

the conjugate acid and base in similar amounts
- source of protons: eg HA to neutralise incoming bases
- sink of protons : eg A- to neutralise incoming acids

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7
Q

Henderson-Hasselbach equation

A

the equation highlights that the pH of a buffer solution has a value close to the pKa of the weak acid

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8
Q

how to make a buffer

A
  1. select a weak acid with a pJa similar to desired pH
  2. A) mix equal amounts of acid and its conjugate base or B) start with the weak acid and neutralise half of it with a strong base
  3. adjust to desired pH by adding small amounts of strong acid/base
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9
Q

buffer capacity

A

the molar amount of acid or base which the buffer can handle without significant changes in pH

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10
Q

why can’t buyers tolerate the addition of infinite amounts of strong acid or base?

A

after enough external acid or base has been added to deplete the base or acid in the system, the buffer is destroyed

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11
Q

how would you approach quantitative problems of neutralisation and buffers?

A
  1. figure out which major species remain after any strong acids/bases act
    - assume these reactions go to completion
    - it’s often convenient to work in amount (moles)
  2. determine the concentrations of any minor species that the major species generate via equilibrium reactions
    - work in concentrations (volume is constant)

how?
have both an acid and its conjugate base -> buffer -> HH
have only a weak acid/base -> acid/base dissociation -> ICE
have either H3O+ or OH- directly remaining from step 1 -> done

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12
Q

titrant

A

known concentration

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13
Q

analyte

A

unknown concentration solution

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14
Q

equivalence point

A

point at which stoichiometrically equivalent quantities of acid and base have been mixed together

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15
Q

strong acid/strong base titration

A
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16
Q

weak acid/strong base

A
17
Q

acid-base indicator

A

a substance that changes colour in a specific pH range. indicators exhibit pH-dependent colour changes because they are weak acids and have different colours in their acid (Hln) and conjugate base (In-) forms

HIn + H2O <–> H3O+ + In-

18
Q

strong base/strong acid

A
19
Q

weak base/strong acid

A
20
Q

solubility

A

amount of solute that dissolves in a given amount of solvent (mol/L)

21
Q

formula for ionic compounds dissociating into ions in solution as they dissolve

A
22
Q

saturated solution

A

we’ve added enough solid so that some remains at the equilibrium, where ions are (re)crystallising and dissolving at the same rates.

23
Q

equilibrium constant (ion-product) expression

A

solubility product, Ksp

24
Q

Ksp

A

a measure of how much of an ionic compound has dissolved at equilibrium
= [M^n+]^m[X^y-]^x

25
Q

Precipitation of ionic compounds

A

AB (s) <–> A+ (aq) + B-(aq)
-> dissolution
<- precipitation

Ksp = [A+]eq[B-]eq
Qsp = [A+]t[B-]t

26
Q

compare Qsp to Ksp

A

Qsp>Ksp: solution is supersaturated and precipitation will occur
Qsp=Ksp: solution is saturated and equilibrium exists already
Qsp<Ksp: solution is unsaturated and dissolution will occur

27
Q

how does pH affect solubility

A

if the compound contains the conjugate anion of a weak acid, the addition of a strong acid will increase solubility