acids and bases Flashcards

1
Q

What is an acid base equilibira?

A

In this essay I will argue
that, although mental states are physical things, they are not identical to brain states and thus
type identity theory is incorrect.

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2
Q

Define a Bronsted Lowry acid

A

A proton donor

Eg NH4+

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3
Q

Define a Bronsted Lowry base

A

A proton acceptor

Eg OH-

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4
Q

Define concentration

A

how many moles are in a given volume of solution

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5
Q

Define acid strength

A

The strength is a measure of how ionised the acid is in solution

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6
Q

What’s the difference between a strong acid and a weak acid?

A

A strong acid will fully ionise in solution whereas a weak acid will partially ionise in solution.

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7
Q

What is pH

A

a measure of the concentration of hydrogen ions in solution.

As the concentration of hydrogen ions for a strong acid is very high, yet the concentration of hydrogen ions for a strong alkali is very low a logarithmic scale must be used.
So,
pH = -log10[H+].

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8
Q

equation to determine [H+] with ph

A

[H+] = 10^–pH

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9
Q

Write an equation for the dissossiation of sulfuric acid in water

A

H2SO4(l) → 2H+(aq) + SO42–(aq)

Diprotic acid

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10
Q

What causes a solution to be acidic?

A

H+ (hydrogen ion), or more accurately H3O+ (hydroxonium ion), protons react with H2O to form it.

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11
Q

Explain the dissociation of water

A

Water very slightly dissociates into its ions according to the following equation:
2H2O(l) ⇋ H3O+(aq) + OH-(aq)

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12
Q

Write an equation for the ionisation of water

A

2H2O ⇌ H3O+ + OH
//
H2O ⇌ H++ OH-

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13
Q

Explain the nature of the formation of hydroxonium and OH- ions

A

hydroxonium ion is a very strong acid, and the hydroxide ion is a very strong base. As fast as they are formed, they react to produce water again.

The net effect is that an equilibrium is set up.

2H2O(l) ⇋ H3O+(aq) + OH-(aq)

At any one time, there are incredibly small numbers of hydroxonium ions and hydroxide ions present. (The H2O is in large excess)

Water very slightly dissociates

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14
Q

Derive Kw using the equation for the ionisation of water

A

H2O ⇌ H++ OH-
Keq = [H+] [OH-]/ [H2O]
Keq [H2O] = [H+][OH-]
[H2O] is so large compared to [H+] and [OH-] that Keq[H2O] can be considered to be constant
Keq[H2O] = Kw
Therefore, Kw = [H+][OH-]

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15
Q

What is the difference between ionising and dissassociating?

Just an NB

A

Ionisation is the process that involves the formation of ions whereas dissociation is the process of breaking up of a moiety into its constituent atoms, molecules and ions

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16
Q

What ius the value of Kw at room temperature (25 *C)

A

1 x 10 ^-14

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17
Q

What is the forward reaction of the ionisation of water

A

endothermic

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18
Q

Is the forward or backward reaction favoured when temperature of water is increased?

A

Forward, because its endothermic.. so more [H+] is produced so becomes more acidic, pH decreases

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19
Q
A
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20
Q

What physical factors affect the value of Kw? How do they affect it?

A

Temperature only- if temperature is increased, the equibilibium moves to the right so Kw increases and the pH of opure water decreases.

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21
Q

Why is pure water still neutral, even if pH does not equal 7?

A

[H+]=[OH-]

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22
Q

What is the realtionship between pH and conc of H+?

A

Lower pH= higher concentration of H+

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23
Q

If two solutiuons have a pH difference of 1, what is the difference in [H+]?

A

A factor of 10

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24
Q

Why does pure water have a pH of 7?

A

That question is actually misleading! In fact, pure water only has a pH of 7 at a particular temperature - the temperature at which the Kw value is 1.00 x 10-14 mol2 dm-6.

In pure water at room temperature the Kw value tells you that:
[H+] [OH-] = 1.00 x 10-14

But in pure water, the hydrogen ion (hydroxonium ion) concentration must be equal to the hydroxide ion concentration. For every hydrogen ion formed, there is a hydroxide ion formed as well.

That means that you can replace the [OH-] term in the Kw expression by another [H+].

[H+]2 = 1.00 x 10-14

Taking the square root of each side gives:

[H+] = 1.00 x 10-7 mol dm-3

Converting that into pH:

pH = - log10 [H+]

pH = 7

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25
Q

How would you calculate pH of 0.0500 mol dm-3 Ba(OH)2

A

[OH-]= 0.05 x 2
[H+] = kw/ [OH-]
[H+] = 10^-14/ 0.1
pH = -log [H+]
pH= -log [1.00 x 10^-13]
pH = 13.00

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26
Q

How would you calculate [H+] of [Ba(OH)2] with pH 13.30?

A

[H+] = 10 ^-pH
[H+] = 10 ^-13.3 = 5.01x10^-14
[OH-] = Kw/[H+]
[OH-]=10^-14/ 5.01x10^-14 = 0.2
[Ba(OH)2] = 0.2 x 1/2 = 0.100 mold dm^-3

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27
Q

Give examples of strong monoprotic acids

A

HCl, HNO3

28
Q

Give examples of strong diprotic acids

A

H2SO4

29
Q

Give examples of strong triprotic acids

A

H3PO4

30
Q

Give examples of strong monobasic bases

A

NaOH KOH

31
Q

Give examples of strong diprotic bases

A

Ca(OH)2
Ba(OH)2

32
Q

Give examples of weak monobasic bases

A

ammonia
methylamine

33
Q

Give examples of strong dirpotic bases

A

1,2-diaminoethane

34
Q

Give examples of weak acids

A

mono - ethanoic
di - ethandioic
tri - citiric

35
Q

What is Ka

A

acid dissociation constant
Weak acids and bases only dissocaite partially in water therefore the reaction has an equilibirum dissassociation constant Ka

36
Q

Explain ka

A

We define a new constant as Ka =
Ka = [H+][A-]/[HA]

HA refers to the un-ionised acid molecule, and A- refers to the anion remainder after loss of a proton.
- A large Ka value means that a lot of the acid ionises in solution. (stronger acid)
- A small Ka value means that very little acid ionises in solution. (weaker acid)

37
Q

pKa=

A

pKa = – log Ka

38
Q

the stronger the acid:

A

the bigger Ka
the smaller pKa

39
Q

Basic titration method

A

Standard solution of acid/alkali prepared in volumetric flask

25 cm3 samples taken out with pipette and put into conical flask

Indicator + acid/alkali in conical flask

acid/alkali added from burette until permanent colour change

40
Q

How do you make a standard solution RP1

A
  • mass a weighing bottle/boat
  • add the correct mass of solid
  • pour the contents of the solid into a beaker
  • mass the weighing bottle/boat again (the difference in two recorded masses will provide the exact
    mass of the solid added to the beaker)
  • dissolve the solid in a little distilled water using a stirring rod
  • pour the solution into a volumetric flask using a funnel and stirring rod
  • wash the beaker several times, pouring the washings into the flask
  • top up to the mark carefully (drop-wise at the end)
  • swirl, invert and repeatedly shake to ensure it is homogenous (thoroughly mixed)
41
Q

What is a back titration?

A

Used where reaction between acid and base is slow (e.g. low solubility in water)

React an excess of an acid/base with the acid/base – some is leftover

Titrate the leftover acid/base to see how much leftover

42
Q

What is an indicator?

A

Weak acids which have a different colour to their conjugate bases.
HIn ⇌ H+ + In-
colour 1 ⇌ colour 2

43
Q

How do indicators work?

A

HIn ⇌ H+ + In-
low pH: equilibrium pushed left = colour 1
high pH: equilibrium pushed right = colour 2

44
Q

methyl orange
colour at low ph
range
colour at high pH

A

red
3.2-4.4
organge/yellow

45
Q

phenolphthalein
colour at low ph
range
colour at high pH

A

colourless
8.2-10.0
purple

46
Q

What is a titration curve

A

shows how pH of a solution changes in an acid-base reaction

47
Q

How is the neutralisation point identified

A

a large vertical section therough the equivalence point

48
Q

Define equivalence point

A

The point at which the exact volue of base has been added to just neutralise the acid or vice versa.

49
Q

strong acid-strong base
pH at equivalence:
suitable indicator:

A

7
phenolphthalien/methyl orange

50
Q

strong acid-weak base
pH at equivalence:
suitable indicator:

A

< 7 (4 )
methyl orange

51
Q

weak acid-strong base
pH at equivalence:
suitable indicator:

A

> 7 (9 )
phenolphthalein

52
Q

weak acid-weak base
pH at equivalence:
suitable indicator:

A

depends on the relative strength of th acid and base

53
Q

What is a buffer solution

A

solution that resists changes in pH when small amounts of acid pr alkali are added

NB- pH does change, just not by much

54
Q

Acidic buffer

A

buffers that have a pH lower than 7

55
Q

Basic buffer

A

buffers that have a solution higher than 7

56
Q

What is an acidic buffer made of?

A

mixture of a weak acid and one of its salts (ie HA and A-)

57
Q

What is key in an acidic buffer?

A

the [acid] and [salt] are much higher than the [H+]

58
Q

What are the two routes to make an acidic buffer?
+ how to calculate the pH of the buffer in each route

A

Route 1: mixture of weak acid and one of its salts (use [A-] and [HA] with Ka equation to calculate H+)
Route 2: Mixture oif an excess of weak acid and a strong base
(HA+OH—>A- +H2O to calulate left over HA and formed A- then use Ka)

59
Q

What is a basic buffer made of?

A

a mixture of a weak alkali and one of its salts

60
Q

What is the key in a basic buffer

A

the [base] and the [salt] are much higher than [OH-]

61
Q

What are the two routes to make an basic buffer?

A

Route 1: mixture of weak base and one of its salts
Route 2: mixture of an excess weak base and a strong acid

62
Q

How do buffer solutions work?

A

buffers pH depends on the ratio of [acid]:[salt] or [base]:[salt] so when small amounts of acid (H+) or base (OH-) are added the ratio remains roughly constant and so the pH hardly changes.

63
Q

What happens when you add a little acid to an acidic buffer?

A

HA⇌ H+ + A-
The added H+ is removed by reacting with A- to form more HA.
The [A- ]falls slightly and the [HA] rise slighty but as [HA] & [A-]&raquo_space; [H+] the ratio of [HA]:[A-] remains roughly constant.

64
Q

What happens when you add a little base to an acidic buffer?

A

HA⇌ H+ + A-
The added OH- reacts with H+ and so some HA breaks down to replace that H+

The [A- ]rises slightly and the [HA] falls slighty but as [HA] & [A-]&raquo_space; [H+] the ratio of [HA]:[A-] remains roughly constant.

65
Q

What happens when you add water to an acidic buffer?

A

The ratio of [HA]:[A-] remains constant so pH remains constant

66
Q

How do you calculate when acid is added to an acidic buffer

A
  • calc mol acid added
  • A-+H+–>HA before and after
  • plug into Ka
  • to get new H+
67
Q

How do you calculate when base is added to an acidic buffer

A

-calc mol OH- added
- HA+OH—>A- +H2O before and after
- calc [HA] and [A-] after
- plug into Ka to find H+

same pocess as finding pH of acidic buffer formed via routte 2