Buffers, indicators and pH curves Flashcards

(18 cards)

1
Q

Acid

A

Proton donor

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2
Q

What is a buffer solution

A

A weak acid and the salt of that weak acid (e.g. CH3COOH and CH3COONa) or a weak alkali and the salt of that weak alkali (NH4OH and NH4Cl)

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3
Q

Add acid to an acid buffer (CH3COOH and CH3COONa)

A

There is a large reservoir of the acid and its conjugate base, when H+ is added equilibrium position backwards (H+ reacts with CH3COO-) and ratio of H+ to CH3COO- hardly changes so pH stays roughly constant

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4
Q

Add alkali to acid buffer

A

There is a large reservoir of the acid and its conjugate base, so OH- reacts with H+ to produce water, so equilibrium shifts forwards and CH3COOH reacts with water (ionises) into the salt and the H+ ratio of H+ to CH3COO- hardly changes so pH stays roughly constant

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5
Q

Why is HCOOH stronger than CH3COOH

A

The methyl group donates electron density to the o- making it more likely to re attract the H+, however the H group cannot donate electron density

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6
Q

Why is trichloroethanoic acid stronger than chloroethanoic acid

A

The chlorine atoms are very electronegative meaning electrons are drawn out of the OH group and H+ ions are much less likely to be re attracted since charge density is spread out

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7
Q
A
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8
Q
A
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9
Q

Base

A

Proton acceptor

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10
Q

Equivalence point

A

Number of moles of H+ = number of moles of OH-

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11
Q

Half equivalence point

A

Number of moles of acid salt = number of moles of acid

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12
Q

Significance of half equivalence point

A

pH = pKa

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13
Q

Salt of a strong acid and strong base

A

Weak conjugates, pH = 7

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14
Q

Salt of a weak acid and strong base

A

Salt is a strong conjugate base, pH > 7

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15
Q

Salt of a strong acid and weak base

A

Conjugate salt is fairly acidic, pH > 6

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16
Q

What determines choosing an ideal indicator

A

pKin should be equal to or as close as possible to the equivalence point of the titration

17
Q

Why are carboxylic acids acidic but alcohols which also contain an OH group are not?

A

Carboxylic acids are acidic because they can spread the delocalised charge (charge density is spread out) over the whole COO- group so they are less likely to be protonated again