1
Q

Describe the greenhouse effect.

A
  • Most UV radiation from the sun is absorbed by gasses in the earth’s atmosphere.
  • Some is reflected back into space.
  • Some reaches the surface of Earth which is absorbed.
  • This heats up the surface of the earth and radiates IR back towards space.
  • Some IR escapes through the ‘IR window’, as they are not absorbed by the gases in the atmosphere.
  • Some IR is absorbed by gases in the troposphere and reemitted in all directions included back towards earth.
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2
Q

Give examples of greenhouse gasses?

A

CO₂
H₂O
CH₄

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3
Q

What happens when greenhouse gasses absorb radiation?

A
  • Their bonds in the molecules vibrate more.
  • The vibrational energy is transferred to neighbouring particles during collisions.
  • These particles now have more kinetic energy and their temperature starts to rise.
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4
Q

How can polar molecules be dissolved?

A

Using polar solvents.

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5
Q

What is the difference between hydration and solvation?

A
  • Hydration is dissolving with water as a solvent.

- Whereas solvation is dissolving with a non-water solvent.

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6
Q

What happens when a salt dissolves in water?

A
  • Water is polar.
  • Its 𝛿+ Hs are attracted to the negative ions
  • Its 𝛿- O is attracted to the positive ions.
  • The water molecules surround the ions during hydration.
  • This ion-dipole interaction must be stronger/as strong as the bond broken for it to dissolve.
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7
Q

Why might molecules like Al₂O₃ not dissolve in water?

A
  • The bond between Al and O ions are stronger than the ion-dipole interaction that would form.
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8
Q

How do some non-polar molecules dissolve in water?

A

Through hydrogen bonds.

e.g. alcohols disolving in water

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9
Q

Why don’t polar molecules like haloalkanes dissolve in water?

A
  • they have weak dipoles.

- so water will form a stronger intermolecular bond than with the haloalkane.

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10
Q

How can you dissolve a haloalkane?

A

Use a solvent that can interact via pertinent dipole-dipole interactions.

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11
Q

How do non-polar substances dissolve in non-polar solvents?

A
  • by forming instantaneous dipole-induced dipole forces.
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12
Q

What is the standard lattice enthalpy?

A

The energy change when 𝟭 𝗺𝗼𝗹𝗲 of an ionic compound is formed from its 𝗴𝗮𝘀𝗲𝗼𝘂𝘀 ions under 𝘀𝘁𝗮𝗻𝗱𝗮𝗿𝗱 𝗰𝗼𝗻𝗱𝗶𝘁𝗶𝗼𝗻𝘀.

(298K/100kPa)

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13
Q

What does the sign and magnitude of the standard lattice enthalpy tell you?

A
  • Always negative, as energy is released as bonds form.

- more negative = stronger bonding.

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14
Q

What is the enthalpy change of solution?

A

The energy change when 𝟭 𝗺𝗼𝗹𝗲 of an ionic compound is dissolved in the 𝗺𝗶𝗻𝗶𝗺𝘂𝗺 𝗮𝗺𝗼𝘂𝗻𝘁 𝗼𝗳 𝘀𝗼𝗹𝘃𝗲𝗻𝘁 to ensure 𝗻𝗼 𝗳𝘂𝗿𝘁𝗵𝗲𝗿 enthalpy change upon further dilution.

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15
Q

What is the enthalpy change of hydration?

A

The energy change when 𝟭 𝗺𝗼𝗹𝗲 of aqueous ions are formed from its 𝗴𝗮𝘀𝗲𝗼𝘂𝘀 ions under 𝘀𝘁𝗮𝗻𝗱𝗮𝗿𝗱 𝗰𝗼𝗻𝗱𝗶𝘁𝗶𝗼𝗻𝘀.

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16
Q

How is the lattice enthalpy, enthalpy of solution and enthalpy of hydration linked?

A

enthalpy of solution = enthalpy of hydration - lattice enthalpy.

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17
Q

What happens if the enthalpy change of hydration is larger (in magnitude) than the lattice enthalpy?

A
  • The enthalpy change of solution will be negative.
  • So the enthalpy change of solution will release energy.
  • So the process is exothermic.
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18
Q

How can you find the enthalpy change of solution practically?

A

Calorimetry.

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19
Q

Describe calorimetry to find the enthalpy change of solution practically

A
  • In a polystyrene cup add the solvent and measure the initial temperature of the solvent,
  • measure out your solid solute in a weighing boat using scales.
  • add the solute to the solvent and stir. Put a lid over the polystyrene cup (leave a hole in the lid to keep the thermometer in.
  • Note down the maximum temperature reached after the solute was added.
  • use the equation E = mcΔT to work out the enthalpy.
    (mass in grams, T can be in any unit).
  • Work out the moles of solute added by doing moles = mass/Mr
  • Divide this by the energy to find the enthalpy change of solution.
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20
Q

Why might the enthalpy change of the solution from a practical be different than the actual value?

A
  • heat lost to surroundigns.
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21
Q

What affects the lattice enthalpy?

A
  • Size of ions (ionic radii)

- Size of change (bigger difference in charge = stronger bond).

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22
Q

How do the ionic radii affect the lattice enthalpy?

A
  • The smaller the ionic radii, the stronger the electrostatic attraction between ions.
  • as smaller ions can pack together more closely.
  • and so have a larger charge density.
  • Thus more energy is required to overcome the stronger forces.
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23
Q

How does the size of charge affect the lattice enthalpy?

A
  • Bigger the charge on an ion, the stronger the electrostatic attraction between ions.
  • Thus more energy is required to overcome these forces.
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24
Q

What is entropy?

A

The measure of disorder in a system.

  • It is the number of ways energy can be shared out in a system.
  • Given the letter S.
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25
Why do gases have a larger entropy than solids?
- Gases are more disordered. - So there are more ways to arrange the atoms/energy than in a solid. - And so it has a higher entropy.
26
How does the number of particles affect the entropy of a reaction?
- If there are more moles of a particle then there are more ways energy can be distributed. - and so the entropy has increased.
27
How is the entropy change calculated?
ΔₛᵧₛS = S(products) - S(reactants) Unit: JK⁻¹mol⁻¹
28
How can the total entropy change be calculated?
ΔₜₒₜS = ΔₛᵧₛS + ΔₛᵤᵣᵣS ΔₛᵤᵣᵣS = -ΔH/T (convert ΔH to Jmol⁻¹)
29
What must be true for a reaction to be feasible?
The total entropy change must be positive or zero.
30
What is solubility?
The maximum amount of solid that will dissolve in a solvent. Units: gdm⁻³
31
What is the 'point of saturation'?
The point where water (or a solvent) can no longer hold any more solute.
32
How do you get moldm⁻³ from gdm⁻³
divide by Mr of solid as mole = mass/Mr
33
What is the solubility product (Kₛₚ)?
- The equilibrium constant for a sparingly soluble product in a saturated solution.
34
What is the formula for Kₛₚ? Use the general equation AₓBᵧ₍ₛ₎ ⇌ xAʸ⁺₍ₐᵩ₎ + yBˣ⁻₍ₐᵩ₎
Same as K𝒸 but only the aqueous products... Kₛₚ = [Aʸ⁺₍ₐᵩ₎]ˣ [Bˣ⁻₍ₐᵩ₎]ʸ (always include state symbols)
35
How would you work through the following question... Calculate the solubility product of Li₂CO₃ when the solubility of the is 13.3gdm⁻³ at 20ᵒC.
1. write Kₛₚ expression using the reaction. Li₂CO₃₍ₛ₎ ⇌ 2Li⁺₍ₐᵩ₎ + CO₃²⁻₍ₐᵩ₎ Kₛₚ = [Li⁺₍ₐᵩ₎]² [CO₃²⁻₍ₐᵩ₎₎] 2. work out the solubility of Li₂CO₃ in moldm⁻³ 13. 3/Mr(Li₂CO₃) = 13.3/74 = 0.18moldm⁻³ 3. We know 1 mol of Li₂CO₃ dissocaites to form 2 moles of Li⁺ and 1 mole of CO₃²⁻ therfore... [Li⁺₍ₐᵩ₎] = 0.18 x 2 =0.36 [CO₃²⁻₍ₐᵩ₎] =0.18 4. Put into equation Kₛₚ = 0.36² x 0.18 = 0.023 5. Work out units. Kₛₚ = (moldm⁻³)² x (moldm⁻³) = (moldm⁻³)³ = (mol³dm⁻⁹) Answer = 0.023mol³dm⁻⁹
36
What is a feature of Brønsted-Lowry acid?
- proton donors.
37
How do H⁺ ions actually exist in water?
As hydroxonium ions (H₃O⁺)
38
What is a feature of Brønsted-Lowry base?
- proton acceptors
39
Give a general equation for a Brønsted-Lowry acid in water?
HA₍ₐᵩ₎ + H₂O₍ₗ₎ ⇌ H₃O⁺₍ₐᵩ₎ + A⁻₍ₐᵩ₎
40
Give a general equation for a Brønsted-Lowry base in water?
B₍ₐᵩ₎ + H₂O₍ₗ₎ ⇌ BH⁺₍ₐᵩ₎ + OH⁻₍ₐᵩ₎
41
Where is the position of equilibrium in weak acids, and what does this mean?
- More to the left. - So backwards reaction is favoured. - So dissociate poorly - Therefore not too many H⁺ produced.
42
Where is the position of equilibrium in strong acids, and what does this mean?
- More to the right. - So forward reaction is favoured strongly. - So dissociate almost completely. - Therefore many H⁺ produced.
43
Where is the position of equilibrium in strong bases, and what does this mean?
- More to the right. - So forward reaction is favoured strongly. - So dissociate almost completely. - Therefore many OH⁻ produced.
44
Where is the position of equilibrium in weak bases, and what does this mean?
- More to the left. - So backwards reaction is favoured. - So dissociate poorly. - Therefore not too many OH⁻ produced.
45
What happens to protons in acid-base reactions?
They are exchanged.
46
What is the role of water in the following reaction... | HA₍ₐᵩ₎ + H₂O₍ₗ₎ ⇌ H₃O⁺₍ₐᵩ₎ + A⁻₍ₐᵩ₎
- acts as a base. | - as it accepts protons.
47
What is a conjugate acid?
A species that has gained a proton.
48
What is a conjugate base?
A species that has lost a proton.
49
What are the conjugate pairs in the following reaction... | HA + B ⇌ BH⁺ A⁻
- HA and A⁻ are pairs with HA as the acid and A⁻ as the base. - B and BH⁺ are pairs with B as the base and BH⁺ as the acid.
50
What assumptions can you make about the concentrations in... - A neutral solution? - A strong acid?
- Neutral solution: [H⁺] = [OH⁻] | - Strong Acids: [H⁺] = [Acid]
51
What is the pH equation?
pH = -log₁₀[H⁺] [H⁺] = 10⁻ᵖᴴ
52
What must you factor in when finding the pH of acids like H₂SO₄
- Two protons are produced for every 1 acid. | - Therfore [H⁺] = 2[Acid]
53
How does pure water exist in reality?
In equilibrium with its ions... 2H₂O ⇌ H₃O⁺ + OH⁻ which simplifies to... H₂O ⇌ H⁺ + OH⁻
54
Use the equilibrium of pure water to derive Kw.
H₂O ⇌ H⁺ + OH⁻ Kc = [H⁺] [OH⁻] / [H₂O] Water dissociated very weakly, therefore, we can assume the concentration of water is a constant. So we can multiply out [H₂O] on both sides to get... Kw = [H⁺] [OH⁻]
55
What assumptions can we make when using Kw for pure water and Kw at standard conditions?
Kw = 1x10⁻¹⁴ (this is at standard conditions and will change if the temperature changes.) In pure water... [H⁺] = [OH⁻] therefore... Kw = [H⁺]²
56
How do you work out the pH of strong bases?
- strong bases dissociate to produce OH⁻. - Kw = [H⁺] [OH⁻] - therefore... [H⁺] = Kw / [OH⁻] - then put into pH equation
57
What constant is used to help work out the pH of weak acids?
Ka
58
Use the equilibrium of weak acids to derive Ka.
- HA ⇌ H⁺ + A⁻ - Kc = [H⁺] [A⁻]/[Ha] - Only a small amount of weak acids dissociates so... [HA₍ₐᵩ₎]equilibrium ≈ [HA₍ₐᵩ₎]start - Ka = [H⁺] [A⁻]/[Ha]ₛₜₐᵣₜ - The dissociation of acid is much greater than of water so we can assume all the H⁺ comes from the acid so... [H⁺₍ₐᵩ₎] ≈ [A⁻₍ₐᵩ₎] - Ka = [H⁺]²/[Ha]ₛₜₐᵣₜ
59
How do you work out the pH of a weak acid?
- Ka = [H⁺]²/[Ha]ₛₜₐᵣₜ - [H⁺]² = Ka x [Ha]ₛₜₐᵣₜ - [H⁺] = √(Ka x [Ha]ₛₜₐᵣₜ) - then put into pH equation
60
What is pKa?
Another way of measuring the strength of an acid equations: pKa = -log₁₀Ka Ka = 10⁻ᵖᴷᵃ
61
What is a buffer?
A chemical that resists a change in pH when small amounts of acid or base are added.
62
What are acidic buffers?
- something that resist the change of pH in order to keep a solution below pH7 - it is made from a weak acid and it's salt.
63
Ethanoic acid (CH₃COOH) can be used as a buffer with sodium ethanoate (CH₃COO⁻Na⁺). Describe what happened when an acid is added?
- Ethanoic acid is a weak acid in equilibrium... CH₃COOH₍ₐᵩ₎ ⇌ CH₃COOH₍ₐᵩ₎ + H⁺ - Because it is a weak acid its equilibrium lies far to the left so the concentrations are... CH₃COOH₍ₐᵩ₎ ⇌ CH₃COOH₍ₐᵩ₎ + H⁺ [High] [Low] [Low] - Sodium ethanoate dissociates fully in equilibrium... CH₃COO⁻Na⁺ ⇌ CH₃COO⁻ + Na⁺ - So its equilibrium lies far to the right and ist concentration are... CH₃COO⁻Na⁺ ⇌ CH₃COO⁻ + Na⁺ [Low] [High] [High] - When an acid is added its H⁺ react with a negative ion. - This is CH₃COO⁻ from the sodium ethanoate equation, as there is a high concentration of these. - This produces more CH₃COOH using the additional H⁺ returning the pH to normal and shifting the equilibrium to the left.
64
Ethanoic acid (CH₃COOH) can be used as a buffer with sodium ethanoate (CH₃COO⁻Na⁺). Describe what happened when a base is added?
- Ethanoic acid is a weak acid in equilibrium... CH₃COOH₍ₐᵩ₎ ⇌ CH₃COOH₍ₐᵩ₎ + H⁺ - Because it is a weak acid its equilibrium lies far to the left so the concentrations are... CH₃COOH₍ₐᵩ₎ ⇌ CH₃COOH₍ₐᵩ₎ + H⁺ [High] [Low] [Low] - Sodium ethanoate dissociates fully in equilibrium... CH₃COO⁻Na⁺ ⇌ CH₃COO⁻ + Na⁺ - So its equilibrium lies far to the right and its concentration are... CH₃COO⁻Na⁺ ⇌ CH₃COO⁻ + Na⁺ [Low] [High] [High] - When a base is added its OH⁻ ions react with a positive charge. - This is not the Na⁺ however as this will create a base and will dissociate back to OH⁻. - So this reacts with the H⁺. - Because there is a low contraction of H⁺ as this is used up, it shifts the equilibrium of the ethanoic acid equation to the right. - This drives the forward reaction and so produces more H⁺ to return the pH to normal
65
How would you work through the following question... Calculate the pH of a buffer that contains 2.35x10⁻² mol of methanoic acid and 1.84x10⁻² mol of sodium methanoate in a 1dm³ solutions. The value of Ka at 25°C for methanoic acid is 1.78x10⁻⁴
- Write Ka expression from the equilibrium equation. HCOOH₍ₐᵩ₎ ⇌ H⁺₍ₐᵩ₎ + HCOO⁻₍ₐᵩ₎ Ka = [H⁺][HCOO⁻] / [HCOOH] - we assume that salts dissociate fully and weak acids dissociate poorly so... [salt] = [A⁻] AND [HA₍ₐᵩ₎]equilibrium ≈ [HA₍ₐᵩ₎]start - [H⁺] = Ka x [HCOOH] / [HCOO⁻] - [H⁺] = 1.78x10⁻⁴ x 2.35x10⁻²) / 1.84x10⁻² - [H⁺] = 2.27x10⁻⁴ moldm⁻³ - plug into pH equitation - pH = 3.64