20 - Acids, bases and pH Flashcards

1
Q

What is the Arrhenius model of acids?

A

-> acids dissociate and release H+ ion in (aq) solution
-> alalis dissociate and release OH- ions in (aq) solutions
-> H+ ions are neutralised by OH- to form water

H+(aq) + OH-(aq) —-> H2O (l)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is the Bronsted-Lowry model for acids and bases?

A

-> Bronsted-Lowry acid is a proton donor
-> Bronsted-Lowry base is a proton acceptor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is a conjugate acid-base pair?

A

Are two species that can be interconverted by the transfer of a proton

ie HC- and Cl-

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

In the reaction what is the conjugate acid and base?

HCl(aq) <—-> H+(aq) + Cl-(aq)

A

-> in the forward reaction HCl releases a proton to form Cl-, its conjugate base
-> in the reverse direction Cl- accepts a proton to form HCl, its conjugate acid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

HCl(aq) + OH-(aq) <—–> H2O(aq) + Cl-(aq)

What are the conjugate base pairs?

A

Acid 1 : HCl
Base 1 : Cl-

Acid 2 : H2O
Base 2 : OH-

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Reaction between HCl and H2O, what are its conjugate pairs?

A

HCl + H2O <—-> H3O+ + Cl-
A1 B2 A2 B1

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Why is the hydronium ion important

A

it is the active ingredient in any aqueous acid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Monobasic, dibasic and tribasic

A

refers to the number of H+ that cen be replaced per molecule in an acid-base reaction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

acid + metal

A

-> salt + hydrogen
redox

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are carbonates?
Acid + Carbonate

A

-> they are a base which can neutrlise acids

—> salt + water + CO2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

mathmatical relationship between [H+] and pH

A

pH = -log[H+]
[H+] = 10^-pH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

on a logarithmic scale, what dies a change in one pH represent?

A

a 10 times difference

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what happens when a strong acid is in (aq) solution?
what is this equation?

A

a strong monobasic acid completely dissociates
HA(aq) —> H+(aq) + A-(aq)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what is the relationship of [H+] and [HA] for a strong acid

A

[H+] = [HA]

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what is a weak acid?
give an equation

A

partially dissociates
HA <—> H+ + A-

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the acid dissociation constant Ka?
compare Ka pf a strong and weak acid

A

strong acids have a large Ka
-> the value of [H+][A-] is larger than [HA]

17
Q

mathmatical relationship between Ka and pKa

A

pKa = -logKa
Ka - 10^pKa

18
Q

what is the Ka equation of a weak acid, why is it this?

A

Ka= [H+]^2 / [HA]

-> when HA molecules dissociate H+ and A- are formed in equal quantities

19
Q

What are the approximations that have led to the simplification of the Ka equation?

A

Approximation 1
-> that the [H+] and [A-] are equal. Because the acid is in aqueous solution there is a small concentration due to the dissociation of water. However this is very small and can be neglected
[H+]eqm = [A-]eqm

Approximation2
-> the equilibrium concentration of HA is smaller than the undissociated concentration
[HA]eqm = [HA]start - [H+]eqm
-> as the dissociation of a weak acid is small you can assume that [HA]start> [H] and you can neglect any decrease in concentration of HA from dissociation
(Dissociation of HA is negligible )
[HA]eqm = [HA]start

20
Q

approximation in calculation involving weak acids

A

1) assumes that dissociation of water is negligible
-> [H+]eqm = {A-}eqm
-> at 25’c dissociation of water can be considered negligible if pH<6.
-> this approximation falls for very weak acids or dilute solutions

2) assumes that the concentrations of acid is much greater than the H= concentration at equilibrium
[HA]start» [H+]eqm
[HA]eqm = [HA]start - [H+]eqm approximate to
[HA]eqm = [HA]start
-> it holds for weak acids with a small Ka value
-> it breaks down wen [H+] becomes significant and there is a real difference between [HA]eqm and [HA]start - [H+]eqm
- it is not justified for stronger weak acids and for very dilute solutions

21
Q

how can the Ka of a weak acid be determined?

A
  • prepare a standard solution of the weak acid of a known concentration
  • measuring the pH of the standard solution using a pH meter
22
Q

Explain the ionisation of water
H2O + H2O

A
  • water ionies slightly acting as both an acid and a base

H2O + H2O <—> H3O- + OH-
A1 B2 A2 B1

23
Q

How do find the ionic product or water?

A

Ka = [H+][OH-] / [H2O]
Ka x [H2O] = [H+][OH-]
Ka x [H2O] = Kw

Kw = [H+][OH-]

24
Q

what is Kw

A

the ionic product of water
it is the ions in the water multiplied together

25
Q

what is the value of Kw at 298K

A

1 x 10^-14 mol2dm-6

26
Q

in an acidic solution of pH 3 [H+] = 10-3 moldm-3
what is the [OH-]

A

10-11

27
Q
A