B5 Energetics 2 Flashcards

1
Q

Define Lattice Enthalpy

A

The enthalpy change when 1 mole of an ionic compound is formed from its ions in their gaseous state
under standard conditions

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2
Q

is lattice enthalpy exo or endo

A

exo

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3
Q

state and explain whether Nacl or Mgcl2 will have the highest melting point

A
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4
Q

what are the 2 ways of calculating lattice enthalpy

A

Experimental values - born harder cycles - using known energy changes from experiments

Theoretical changes - calucted using physics caluculations- assume ions are perfect spheres

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5
Q

Draw a Born- Harber cycle

A
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6
Q

standard enthalpy of formation

A

enthalpy change when one mole of a compound is formed from its elements in their standard states under standard conditions

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7
Q

standard enthalpy of atomisation

A

enthalpy change when one mole of a gaseous atoms forms from its element in its standard state under standard conditions

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8
Q

is standard enthalpy of atomisation exo or endo

A

always endothermic

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9
Q

standard enthalpy of atomisation equations

A
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10
Q

Atomisation equation for iodine

A
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11
Q

First ionisation enthalpy

A

enthalpy change when one electron is removed from each atom in one mole of gaseous atoms to form +1 ions

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12
Q

First ionisation enthalpy equation

A
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13
Q

second ionisation enthalpy

A

enthalpy change when one electron is removed from each +1 ion in one mole of gaseous +1 ions to form +2 ions

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14
Q

second ionisation enthalpy equation

A
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15
Q

first electron affinity

A

enthalpy change when one electron is added to one mole of gaseous atoms to form -1 ions

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16
Q

First electron affinity of chlorine equation

A

-ve

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17
Q

is second electron affinity exo or endo

A

endo

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18
Q

Born harber cycle of sodium chloride

A
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19
Q

write an equation for the standard enthalpy change of atomisation of bromine

A
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20
Q

What must you remember when using born harber cycle

A

state symbols

definitions

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21
Q

write the equation of the second electron affinity of oxygen - state and explain whether this will be endothermic or exothermic

A

endothermic

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22
Q

When must data be multiplied by 2 in a Born-Haber Cycle

A

When the product has a molar mass of two

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23
Q

When calculating lattice enthalpy from a Born-Haber Cycle, how should the equation be structured

A

With enthalpy of formation on the left-hand side of the equation, and the route on the right

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24
Q

Going clockwise round a Born-Haber cycle, what is the order of the processes

A

Atomisations, Ionisations, Electron Affinities, Lattice Enthalpy

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25
Q

What must be remembered with electrons in Born-Haber Cycles

A

The electrons produced by ionisation energies are used in the affinities

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26
Q

what happens when we put ionic compounds into solution

A

ions are separated from the lattice and surrounded by water molecules

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27
Q

write an equation to show the lattice enthalpy of sodium chloride

A
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28
Q

the charge on water molecules are attracted to the charge on the ions, these interactions are known as

A

ion - dipole interactions

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29
Q

when ions are separated from the lattice and surrounded by water molecules they are considered to be

A

in solution (aq) and hydrated

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30
Q

Define Enthalpy Change of Solution

A

enthalpy change when one mole of a solute dissolves in water to give a very dilute solution - avoids ions interacting

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31
Q

Define Enthalpy Change of Hydration

A

enthalpy change for forming a solution of ions from 1 mol of gaseous ions
Na + (g) + aq —> Na+ (aq)

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32
Q

is enthalpy change of hydration exo or endo

A

exo -ve

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33
Q

Enthalphy of hydration will depend on

A

ionic radius
charge

  • charge density

more negative
more exothermic

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34
Q

How do we calculate Enthalphy change of solution

A
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35
Q

Draw a solution enthalpy cycle, with general terms

36
Q

Draw a solution enthalpy cycle, for sodium chloride

37
Q

explain this entalphy level diagram

38
Q

explain this entalphy level diagram

39
Q

explain this enthalpy level diagram

40
Q

what about non polar solvents

41
Q

describe an experiment you could conduct to determine the enthalpy change of solution of NACl

42
Q

factors that effect standard lattice enthalpy

A

charge size,
ionic radius
- charge density

43
Q

factors that effect standard lattice enthalpy key words

A

charge
ionic radius
lattice entalphy
attraction

46
Q

Design an experiment to determine the enthalpy change of solution of magnesium chloride (MgCl2) - you should include appropriate measurements to use and names of all equipment used. Include details on how to make your experiment accurate and how to conduct the calculation required. (6 marks)

A

a)
1. measure water with named appropriate apparatus (measuring cylinder)
2. suitable volume/mass in the range 10 - 200cm3/g
3. into insulated container/polystyrene cup
4. add known mass of MgCl2(s)
5. use of ‘before and after’ weighing method
b)
1. record initial temperature (min 2 measurements)
2. record T at regular timed intervals for 5+ mins/until trend seen
3. plot T vs time
c)
1. extrapolate lines to when solid added (to find initial and final T)
2. Tfinal - Tinitial
3. Q=mc change in T
4. amount = mass/Mr
5. change Hsoln = -q/8.39x10-3

47
Q

What is the effect on deltaT, and the enthalpy change of solution, when the volume of water in an experiment is doubled

A

deltaT will half, as the same amount of energy is transferred to double the volume of water. Enthalpy of solution stays the same as the ratio of energy releases: moles is the same, and so the same energy is released per mole.

48
Q

What is the effect on deltaT, and the enthalpy change of solution, when the mass of the solid is doubled

A

deltaT will double, as double the amount of energy is being transferred to the same volume of water. Enthalpy of solution stays the same, as the ratio of energy released: moles is the same, and so the same amount of energy is released per mole.

49
Q

How does a greater ionic radius affect the attraction to ions

A

Weaker attraction to ions

50
Q

How does a smaller ionic radius affect the attraction to ions

A

Stronger attraction to ions

51
Q

How does a greater ionic charge affect the attraction to ions

A

Stronger attraction to ions

52
Q

How does a smaller ionic charge affect the attraction to ions

A

Weaker attraction to ions

53
Q

Explanation of comparing two lattice enthalpies with different ionic radii

A

Lattice enthalpy of X is more exothermic than Y. As ion X is smaller, so has a smaller ionic radius. Therefore attraction to Z- ions is stronger. So more energy is needed to break ionic bonds between ions.

54
Q

Explanation of comparing two lattice enthalpies with different ionic charge

A

Lattice enthalpy of X is more exothermic than Y. As X has a 2+ charge, compared to Y which has a 1+ charge. X has a greater ionic charge. Therefore attraction is stronger to Z- ions. So more energy is needed to break ionic bonds between ions.

55
Q

Dissolving energetically favourable

A

if Ah soln is negative dissolving is energetically favourable

56
Q

Define entropy

A

the number of different ways of arranging molecules and distributing energy

  • more random/ disordered –> higher entropy
57
Q

Describe and explain how entropy changes from (s) to (l) [or (l) to (g)]

A

Entropy increases as disorder increases. As liquid particles have more disorder than solid particles.

58
Q

Describe and explain how entropy changes from (l) to (s) [or (g) to (l)]

A

Entropy decreases as disorder decreases. As solid particles have less disorder than liquid particles.

59
Q

Describe and explain how entropy changes when there are more moles of gas as products

A

Entropy increases as disorder increases. As more gaseous molecules are produced.

60
Q

Describe and explain what happens to entropy when there are less moles of gas in the products

A

Entropy decreases as disorder decreases. As less gaseous molecules are produced.

61
Q

Equation to calculate deltaS

62
Q

Unit for entropy

A

J K-1 mol -1

remember to divide by 1000

63
Q

symbol for entropy

64
Q

if a system changes to become more random, energy can be spread out more

65
Q

entropy changes

66
Q

positive entropy change

A

solid - gas

less moles to more moles

in equations

67
Q

Units for deltaS

A

J K(-1) mol (-1)

68
Q

Free energy

A

overall energy change in a chemical reaction

  • The enthalpy change (ΔH) - This is the energy transfer between the chemical system and the surroundings

The entropy change at the temperature of reaction (TΔS) - This is the dispersal of energy within the system at a given temperature

69
Q

Gibb’s Free Energy Equation

70
Q

Gibb’s Free Energy Equation labeled

71
Q

What is crucial to do when calculating Gibb’s Free Energy

A

Always divide deltaS by 1000, so that it is in kJ

72
Q

What must be done when calculating Gibb’s free energy with the units

A

Divide deltaS by 1000 so it is in kJ

73
Q

Why must deltaS be divided by 1000 when using it in Gibb’s Free Energy equation

A

As deltaG is in kJ, and deltaS is in J

74
Q

Units for deltaG

A

kJ mol(-1)

75
Q

When is a reaction feasible

A

When deltaG is equal to/below zero

76
Q

When does the feasibility of a reaction change

A

When deltaG = 0

and find T

77
Q

Describe and explain how increasing temperature affects feasibility

A

Feasibility increases as temperature increases. As -TdeltaS becomes more negative than deltaH, so deltaG decreases.

78
Q

What is the gradient when Gibb’s Free Energy is graphical

79
Q

Explain how Gibb’s Free Energy is related graphically

80
Q

shown graphically

81
Q

Draw a graph and annotate where:
* Point where feasibility changes
* deltaH
* What the gradient represents

82
Q

2nd electron affinity is

83
Q

AG - for it be feasible

A

must be -ve

84
Q

why does a feasible reaction not get observed

A

kinetics are not taken into account, so that activation energy might be too high for it to actually occur

85
Q

if temp increase

A

-ve –> exothermci