Titration Flashcards

1
Q

F

A

Formal concentration:
about moles of “original chemical formula” in solution per liter

Note: Refer to F OF TITRANT!
(F will increase in any case, since titrant is keep being added)

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2
Q

Ve

A

Equivalence point:
the point where stoichiometric amount of titrant and analyte reacted

Conjugate base pair of analyte react with water to increase p().
Ex) WA,SB titrant: conjugate base of weak acid (weak base) react with water, inc. pH as it forms OH-.
See paint.

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3
Q

M

A

Molar concentration:

about moles of “each chemical species” in solution per liter

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4
Q

(1/2)Ve

A

Half of equivalence point:
the point where half of titrant was added to form the next compound.

the pt where half of titrant got deprotonated (if titrant was acid)

[HA]=[A-] if titrant was acid
[HB]=[B-] if titrant was base

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5
Q

Le Chatlier’s principle

A

Predict effect of change in chemical rxn in species

adding more reactant -> more product

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6
Q

Common ion effect

A

If there are ions of the same kind already dissolved in solution, then solubility of the ion is lower
than if there are no ions of same kind present in sol’n.

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7
Q

K

A

Equilibrium constant

K=( [C]^c [D]^d / [A]^a [B]^b )

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8
Q

Ka

A

Acid dissociation constant

HA-> H+ A-
Ka=( [H+][A-] ) /[HA]

∴ Bigger Ka means the acid dissociated to give out H+ more, and therefore indicates stronger acid

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9
Q

pH

A

-log[H+]

14-pOH

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10
Q

pKa

A

pKa=-log[Ka]

Note: just like smaller pH indicates stronger acid, smaller Ka indicates stronger acid.

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11
Q

Henderson-Hasselbalch equation

A

ONLY WORK FOR WEAK ACID OR BASE
pH=pKa+log([A-]/[HA])
pOH=pKb+log([BH+]/[B-])

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12
Q

Henderson-Hasselbalch equation at (1/2)Ve

A

pH=pKa if titrant was acid
pOH=pKb if titrant was base

∵log1=0
and the solution is either weak acid or base at (1/2)Ve

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13
Q

Mass balance

A

Formal concentration = all form of the species

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14
Q

Before Ve

A

[analyte] determines pH

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15
Q

After Ve

A

[titrant] determines pH

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16
Q

pF,pKa,pH

A

pH and pKa are smaller for stronger acid.
pF is small if much titrant is added (don’t relate to acidity)
UNLESS compare to pKa

17
Q

pF>7

AT Vi or Ve

A

pH=7

Since Not much F were added to solution, no pH change.
Q-what if starting pH was SA/SB, and not neutral water? Would I then need to calculate pH of starting species

18
Q

pKb given

A

DON’T do: 14-pKb to get pKa IF solution is base

DO: 14-pkb to get pKa IF solution is acid

19
Q

pKa less than pF

at Vi or Ve

A

Ka>F
strong-acid-like-behavior
(HA dissociates to give out H+ more)

pH=pF

m=1 (ignoring sign)

20
Q

pKa>pF

AT Vi or Ve

A

Ka is smaller than pF

pH is half of sum of pF and pKa, m=1/2(WA like)