Physical Chemistry Key phrases Flashcards

1
Q

negative enthalpy - is this exothermic or endothermic? Why?

A

Exothermic because heat is being released into the surroundings, making the chemicals in the reaction more stable, releasing heat into the surroundings.

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2
Q

positive enthalpy - is this exothermic or endothermic? Why?

A

Endothermic because heat is taken into the chemicals from the surroundings, lowering the temperature of the surroundings

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3
Q

What has happened to the model of the atom over time?

A

Concept of an atom has changed from being a single undivided particle to having neutrons, protons and electrons in a sphere to the present day model where there are electron shells and a nucleus containing protons and neutrons.

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4
Q

Relative mass and charge of neutrons, protons and electrons

A

Protons: mass = 1, charge =+1
Neutrons: mass = 1, charge =0
Electrons: mass = 1/1840, charge = - 1

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5
Q

What are the symbols for mass number and atomic number?

A

Mass number is A
Atomic number is Z

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6
Q

How do you find the number of neutrons, protons and electrons?

A

Number of protons = atomic number,
Number of electrons = the atomic number - charge
Number of neutrons = mass number - atomic number

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7
Q

How do electron shells fill in electron configuration? What are the types of subshell and how many electrons can each hold?

A

Electrons fill in energy order filling the subshell before moving on to the next. although as s is further away in space but lower in energy than d from the 3d subshell onwards s fills and empties before d.

There are 4 types of electron subshell, s,p,d and f. s holds up to 2, p holds up to 6, d holds up to 10, f holds up to 14.

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8
Q

What’s an ionisation energy?

A

The minimum energy required to remove 1 mole of electrons from 1 mole of gaseous ions..

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9
Q

Full electron configuration vs short hand electron configuration

A

Full electron configuration shows all the electrons in their subshells. Short hand condenses the subshells into [noble gas] with electron configuration.

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10
Q

First ionisation energy - trend in period 3, reasons, and the exceptions.

A

Increases across a period as the nuclear charge increases and the atomic radius stays the same.

Exception - Al as Al has the first electron in 3p which is higher in energy then 2 s so easier to remove.
Exception - S - has the first spin pair repulsion in 3p

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11
Q

First ionisation energy - trend down group 2

A

decreases as atomic radius increases weakening attraction from outer electrons to the nucleus

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12
Q

Generic Equation for first ionisation/electron bombardment (with state symbols)

A

M(g) –> M(g) + e-

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13
Q

Key phrases to describe electron bombardment/impact

A

(for atoms/small molecules/molecules you want to make fragments of)
High energy electrons
From electron gun.
Fired at sample.
Knocks off one electron.
Has to happen in the gas phase.

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14
Q

Electrospray ionisation generic equation

A

M(g)+H+ –> MH+(g)

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15
Q

Electrospray ionisation key phrases

A

(for large molecules/molecules you don’t want to fragment)
Sample dissolved in volatile solvent
Injected as an aerosol through needle
Needle has a high positive charge
Sample gains a H+ ion

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16
Q

Key phrases - mass spec - acceleration

A

Positive ions are accelerated by a negative electric field to a constant kinetic energy

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17
Q

What happens in ion drift? Key phrases?

A

The positive ions with smaller m/z values will have the same kinetic energy as those with larger m/z and will move faster.

The heavier particles move slower

The ions are separated by different flight times

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18
Q

What happens in mass spec - detection - key phrases?

A

For each isotope the mass spectrometer can measure a m/z (mass/charge ratio)and an abundance.

Each ion of the same mass hits the detector plate at the same time.
Each ion gains an electron.

This flow of electrons is a current that is measured. The current is proportional to abundance.

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19
Q

How do you determine Mr from the mass spec read out? What’s the difference between electrospray and electron impact?

A

Look for the molecular ion peak, which is the peak furthest to the right of the graph that isn’t tiny.

For Electron impact/bombradment the m/z =Mr

If you’re using electrospray as well as the above you need to remember to take 1 away from the m/z to find the Mr

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20
Q

How to prepare a stock solution

A

Weigh out the desired mass of the compound into a weighing boat.
Record the mass of the compound + weighting boat. Add the compound into a beaker and reweigh the weighing boat and record this new mass. Dissolve the solid in 100cm3 water. Transfer the solution into a volumetric flask. Wash the container, stirring rod and funnel and add the washings to the volumetric flask. Fill the volumetric flask with distilled water, until the bottom of the meniscus is at the graduation mark . Invert.

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21
Q

Key Phrases about Giant covalent lattices and the 4 common giant covalent lattices.

A

Diamond, Graphite, silicon and silicon dioxide are the 4 common giant covalent lattices.

Key phrases - Giant covalent lattice contain many strong covalent bonds which causes their properties. Covalent bonds have a shared pair of electrons.

graphite has delocalised electrons and van der Waals forces between layers

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22
Q

Coordinate/Dative bond

A

Special type of covalent bond where both electrons come from one atom called a coordinate bond or dative bond

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23
Q

Key phrases around giant ionic lattices and how to spot them.

A

How to spot them: They’re either containing ammonium (NH4+) or a metal and at least one non-metal.

Giant ionic lattices/(ionic bonds) have strong electrostatic attraction between oppositely charged ions. Larger ions and lower charges have weaker attraction.

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24
Q

Key phrases around giant metallic lattices and how to spot them

A

How to spot them - These compounds are just metals on their own.

The atoms lose their outer electrons causing the molecule to have delocalised electrons (forming metal cations)

Key phrase - Giant metallic lattices have strong electrostatic attraction between delocalised electrons and positively charged ions. Larger ions and lower charges have weaker attraction.

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25
Q

Giant ionic lattices - Properties

A

Properties
Ionic compounds conduct electricity when melted or in solution, have high melting points and are the second strongest structure and second strongest bond.

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26
Q

Giant Metallic lattice - Properties

A

Properties
Metallic compounds conduct electricity, have high melting points, are ductile, malleable and are the third strongest structure and third strongest bond.

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27
Q

Define electronegativity

A

Electronegativity is the ability of an atom to attract a bonding pair of electrons in a covalent bond.

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28
Q

What effects electronegativity? How to spot electronegative elements at a level?

A

Electronegativity is affected by having a smaller atomic radius and larger number of protons.

The most electronegative element is F. N, O and then Cl and the next most electronegative. This can be used to help compare electronegativity.

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29
Q

Simple molecular compounds -description

A

Simple molecular compounds are the most common crystal structure for covalent molecules. They have bonds holding atoms together to make molecules. The molecules are held together as solids and liquids by forces between the molecules.

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30
Q

Define polar bonds and what causes them/cancels them out

A

Polar bonds are bonds that have a permanent uneven distribution of electron density caused by a large difference in electronegativity. Symmetrical molecules the electronegative elements pull in equal and opposite directions so cancel.

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31
Q

Hydrogen bonding - What is it? Key phrases around it? Where is it between? How is it represented in diagrams?

A

Misnamed – this is not a bond but is the strongest intermolecular force
Key Phrases:
The electrostatic attraction in a hydrogen bond is between the lone pair on the N/O/F and the ∂+ hydrogen on a different molecule attached to a N/O/F. This attraction is between molecules

This is represented as a dotted line.

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32
Q

Permanent Dipole-Dipole forces key phrases and what cases them.

A

This kind of intermolecular force is caused by the large difference in electronegativity between two elements in a covalent bond. It is the second strongest intermolecular force.

This creates a polar bond where one of the elements is usually one of N/O/F/Cl. This, more electronegative, element is ∂-. The other element is less electronegative, such as C, H or other elements further to the left of the periodic table. This less electronegative element is ∂+.

The attraction is between molecules, this time between the ∂+ atom in one molecule and the ∂- in the other molecule. This is shown with a dotted line.

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33
Q

van der Waals’ forces key phrases/description

A

Key description
It is caused by a random movement of electrons causing a temporary dipole in that molecule (with a small d+ and d-). This partial charge then causes electron density to be attracted/repelled in other nearby molecules which induces a dipole in them.

Van Der Waals’ forces are the weakest intermolecular force, but the larger the surface area of the electron cloud (or the larger the molecule) the stronger this intermolecular force is as the size of the partial charge will increase. This can mean for large molecules van der waal’s forces are stronger between molecules than other intermolecular forces

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34
Q
A
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35
Q

Scaffold for doing melting point comparisons

A

When asked questions about melting points it’s essential to identify the crystal structure of the materials being compared. You need to discuss the forces/bonds that hold them together. The list below is in order of melting point from highest to lowest.
Diamond, graphite, silicon and silicon dioxide are giant covalent lattices (macromolecular). Bonds break to melt this.
metal and a non-metal is a giant ionic lattice, Forces of attraction are overcome.
Metals (usually alone) are giant metallic lattices. Forces of attraction are overcome.
2 or more non-metals bonded together tend to be simple molecular. Forces of attraction are overcome between molecules (chose most relevant of the three intermolecular forces)

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36
Q

Method of calculating the number of bonding pairs and lone pairs

A

number of electrons = group number + bonds - charge
electron pairs = number of
electrons/2
number of lone pairs = electron pairs - bond pairs

Use coordination number for complexes not shapes

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37
Q

List of the key shapes of molecules, their bond angle and examples and bond angles - 2 bonding pairs

A
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38
Q

List of the key shapes of molecules, their bond angle and examples and bond angles - 3 bonding pairs

A
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39
Q

List of the key shapes of molecules, their bond angle and examples and bond angles - 4 bonding pairs

A
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40
Q

List of the key shapes of molecules, their bond angle and examples and bond angles - 2 bonding pairs 2 lone pairs

A
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41
Q

List of the key shapes of molecules, their bond angle and examples and bond angles - 3 bonding pairs 1 lone pair

A
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42
Q

List of the key shapes of molecules, their bond angle and examples and bond angles - 5 bonding pairs

A
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43
Q

List of the key shapes of molecules, their bond angle and examples and bond angles - 6 bonding pairs

A
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44
Q

List of the key shapes of molecules, their bond angle and examples and bond angles - 4 bonding pairs with d8 electrons or 2 lone pairs

A
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45
Q

Define enthalpy change

A

Enthalpy change (∆H) is the heat energy change measured under conditions of constant pressure.

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46
Q

What are standard conditions?

A

100 kPa,
298 K,

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47
Q

What’s Hess’ law

A

Enthalpy change is independent of the route taken

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48
Q

What are collisions and successful collisions?

A

Collisions - When particles hit into each other

Successful collisions - When particles hit into each other and react as particles
have energy greater than or equal to the activation
energy

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49
Q

Define activation energy

A

The minimum energy required for a reaction to occur

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50
Q

Define Catalyst

A

A chemical that lowers the activation energy by providing an alternate reaction pathway, without being used up.

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51
Q

Effect of changing temperature on rate?

A

As temperature increases/decreases the number of particles with energy equal to or greater than the activation energy increases/decreases. This greatly increases/decreases the frequency of successful collisions.

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52
Q

Effect of changing pressure in gases, concentration in liquids or surface areas in solids?

A

Closer/More/more spread out particles
The number of collisions increases so the number of successful collisions increases in proportion. (reverse also true)

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53
Q

Effect of having added a catalyst to rate of reaction?

A

The proportion of particles with energy equal to or greater than the activation energy increases so the number of successful collisions increases.

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54
Q

Key features of a Maxwell Boltzmann distribution?

A
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55
Q

Define mean bond enthalpy

A

The average enthalpy change when 1 mole of a specific bond is broken in the gas phase.

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56
Q

Why are values from calorimetry inaccurate? (3 reasons)

A

Heat loss/incomplete combustion/heat absorbed by equipment

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57
Q

Explain why values from mean bond enthalpy calculations differ from those determined using Hess’s law

A

Values from Hess’s law are for specific chemicals, where as values from mean bond enthalpies are averaged over a wide variety of compounds.

58
Q

What is dynamic equilibrium?

A

forward and reverse reactions proceed at equal rates
the concentrations of reactants and products remain constant

59
Q

What is Le Chatelier’s Principle?

A

The equlibrium will shift to oppose the change

60
Q

Scaffold for applying Le Chatelier’s Principle.

A

The equilibrium will shift to the ______ side to oppose _______ by _______.

May also need to comment on yield – the more to the right of the equilibrium the bigger the yield.

61
Q

What variable is the only variable that Kc/Kp/Ka/Kw and k depend on

A

Temperature

62
Q

What’re the key rules for calculating oxidation state?

A

Oxidation states are a measure of how many electrons have been lost
Elements have an oxidation state of 0,
Chemicals in compounds will usually have the oxidation state of their group number, except for the chemical you’re asked to work out in the exam
Helpful to remember H is +1 and O is -2 except for in peroxide which is +1
The more electronegative element is always negative.

63
Q

How to balance a redox equation

A

Construct half equation
Balance the Subject of the half equation (using big numbers)
Balance the Oxygens by adding in water (H2O)
Balance the hydrogens by adding in H+
Balance the overall charge on each side of the equation by adding in electrons (e-)
Subject
Oxygens
Hydrogens
Charge

64
Q

What is oxidation and reduction?

A

Oxidation – is loss of electrons,
Reduction – is gain of electrons,

65
Q

What’s an oxidising and reducing agent?

A

Reducing agent – is a chemical that causes reduction and is itself oxidised,
Oxidising agent - is a chemical that causes oxidation and is itself reduced,

66
Q

How are half equations combined?

A

multiply half equations until there is the same number of electrons in each half equation (one set of electrons is in the reactants and one in the products so these should cancel).

67
Q

How do cells work?

A

Reaction between two metals
and their ions in solution, the more
reactive metal is reduced
The more reactive electrode’s
metal atoms become ions, donating
electrons through wires to the less
reactive electrode where ions in the
solution gain electrons and become
part of the metal electrode

68
Q

What’s a salt bridge used for? What’s a common salt bridge?

A

Salt bridge completes the circuit
KNO3 is the standard chemical for a
salt bridge

69
Q

What’s the standard hydrogen electrode? What are the conditions? What kind of electrodes should be used?

A

Platinum electrodes should be used when another electrode
won’t work as they’re a gas/liquid/mix of ions

All ions should have a concentration of 1 moldm-3,
Pressure should be 100 kPa,
Temperature should be 298 K

70
Q

What are the rules for making a cell diagram?

A

The solid vertical line represents the boundary between phases e.g. solid (electrode) and solution (electrolyte) *The double line represents the salt bridge between the two half cells
*the voltage produced is indicated *the more positive half cell is written on the right if possible (but this is not essential)
If a system does not include a metal that can act as an electrode, then a platinum electrode must be used and included in the cell diagram. It provides a conducting surface for electron transfer. A platinum electrode is used because it is unreactive and can conduct electricity. (surface are of the electrodes has no impact on the reaction)

71
Q

How to calculate the emf of a cell from a cell diagram?

A

emf = E°right - E°left

72
Q

How to calculate the emf of a cell with no diagram?

A

emf = Ered - Eox
(This assumes that the cell is feasible)

73
Q

What does a negative emf tell you?

A

that the cell’s reaction isn’t feasible

74
Q

Define emf

A

Cell emf is the maximum potential difference between two electrodes of a cell

75
Q

What’s the electrode potential of a standard hydrogen electrode in V?

A

0 V

76
Q

What’s the emf of the measured electrode in the standard hydrogen electrode equal to? Why?

A

emf = E°right

The standard hydrogen is on the left because that means the electrochemical potential of that cell is the value read on the voltmeter. This is because hydrogen’s E0 = 0

77
Q

What’s the electrochemical series?

A

The electrochemical series is the list of electrochemical potentials in numerical order
The series is shown as equilibrium (even though it usually just has straight common forward arrows)

78
Q

Scaffold for using the electrochemical series?

A

The golden rule – Most positive is reduced
Use this rule to identify the equation to examine,
reducing agents are on the right, oxidising agents are on the left,
Then select the chemical that is being the oxidising agent or the reducing agent in that chemical .

79
Q

Scaffold for writing equations using electrochemical series

A

The golden rule – the most positive is reduced for discharging cells, reverse for recharging cells,
Reducing agents are on the right and oxidising agents are on the left.
Electrons must cancel

80
Q

Non-rechargeable cells - key info

A

Electrochemical cells can be used as a commercial source of energy.
No cell of any type is necessarily at standard conditions.
There are issues around disposal so there are waste issues.
Contain chemicals that get used up over time and eventually their emf drops to 0 as the energy gets converted into other forms (light/heat etc).

81
Q

Key facts about rechargeable cells

A

The cells chemicals can be restored by charging them and causing the reaction to reverse.
There’s less waste, it’s cheaper in the long run and has lower environmental impact. There are still some waste issues at end of life of cell.
Discharging follows the golden rule for electrochemistry (most positive is reduced)
Recharging is the opposite to the golden rule the most positive is oxidised, the most negative is reduces during recharging

82
Q

Half equations for the lithium ion cell, charging and discharging equations,

A

Positive electrode:
Li+ + CoO2 + e– → Li+[CoO2]–

Negative electrode: Li → Li+ + e–

In use: CoO2 + Li  LiCoO2
Charging: LiCoO2  CoO2 + Li

83
Q

Equation for hydrogen fuel cells

A
84
Q

What is a fuel cell?

A

Fuel cells are somewhat different to other cells.
They have a continuous supply of the chemicals into the cell and so neither run out of chemicals nor need re-charging.
There are acid versions of the cell but their overall equation is the same so the emf of the cell is the same.

85
Q

Using fuel cells as a fuel source, drawbacks and benefits.

A

Drawbacks:
Hydrogen is hard to transport and store easily as it is a gas.
Hydrogen is flammable and explosive (but this is true of most fuels).
Hydrogen is usally made using fossil fuels.
High cost of hydrogen fuel.

Benefits:
Only waste product is water,
Do not need recharging,
very efficient.

86
Q

Enthalpy of formation definition and symbol

A

deltaHf

Enthalpy change when one mole of a substance is formed from its constituent elements with all substances in their standard states

87
Q

Definition and symbol Enthalpy of combustion

A

Enthalpy change when one mole of a substance undergoes complete combustion in oxygen with all substances in standard states

88
Q

Enthalpy of neutralisation definition and symbol

A

Enthalpy change when 1 mole of water is formed in a reaction between an acid and alkali under standard conditions

89
Q

Definition - First Ionisation enthalpy

A

First ionisation energy = enthalpy change when each atom in one mole of gaseous atoms loses one electron to form one mole of gaseous 1+ ions.

90
Q

Definition Second ionisation enthalpy

A

Second ionisation energy = enthalpy change when each ion in one mole of gaseous 1+ ions loses one electron to form one mole of gaseous 2+ ions.

91
Q

Define first electron affinity

A

First electron affinity = enthalpy change when each atom in one mole of gaseous atoms gains one electron to form one mole of gaseous 1– ions.

92
Q

Define second electron affinity

A

Second electron affinity = enthalpy change when each ion in one mole of gaseous 1– ions gains one electron to form one mole of gaseous 2– ions.

93
Q

Define Enthalpy of atomisation

A

Enthalpy change when one mole of gaseous atoms is produced from an element in its standard state.

94
Q

Define Hydration Enthalpy

A

Enthalpy change when one mole of gaseous ions become hydrated (dissolved in water).

95
Q

Define Enthalpy of solution

A

Enthalpy change when one mole of an ionic solid dissolves in an amount of water large enough so that the dissolved ions are well separated and do not interact with each other.

96
Q

Define bond dissociation enthalpy

A

Enthalpy change when one mole of covalent bonds is broken in the gaseous state.

97
Q

Define Lattice enthalpy of formation

A

Enthalpy change when one mole of a solid ionic compound is formed from its constituent ions in the gas phase

98
Q

Define Lattice enthalpy of dissociation

A

Enthalpy change when one mole of a solid ionic compound is broken up into its constituent ions in the gas phase

99
Q

Define Enthalpy of vaporisation

A

Enthalpy change when one mole of a liquid is turned into a gas

100
Q

Define Enthalpy of fusion

A

Enthalpy change when one mole of a solid is turned into a liquid

101
Q

Golden rules for making born haber cycles

A

Make only one change at a time,
Start by making compounds gasesous atoms if you can,
Remove electrons from positive ion one mole at a time until the desired charge is reached,
Add electrons one mole at a time until the desired charge is reached.

102
Q

What’s the equation to calculate enthalpy of solution from a Hess cycle?

A

enthalpy of solution = lattice enthalpy of dissociation + enthalpy of hydration

103
Q

Calculating values from calorimetry?

A

List the values in the question
Convert the units
Find q from q=mc∆T
Find ∆H using ∆H=q/1000/n
Put in the sign

104
Q

Scaffold for calculating values from born haber cycles

A

Identify each enthalpy change in the Born-Haber cycle and label them with symbols
Put in the data for each enthalpy change you’ve identified and make sure you’ve put in multipliers where needed. (all enthalpy definitions use one mole, bond dissociation enthalpy = 2xatomisation enthalpy)
Change the sign on any arrows in the cycle not moving in the same direction
Construct an equation by adding up all the enthalpies and making it equal zero
Rearrange equation to find unknown
Put numbers into your equation to solve

105
Q

What is the perfect ionic model?

A

The perfect ionic model suggests that all ions are perfectly spherical and the charge is found in the centre (point charges)
Larger anions bonded to small cations tend to have more covalent character as smaller cations distorts (polarises) the electron density of the larger anion
The bigger the difference between the lattice enthalpy and the theoretical value the more covalent character. More covalent character the stronger the ionic bond.

106
Q

What does the size of the lattice enthalpy of formation/dissociation tell you about the compound?

A

The larger in magnitude the value then the stronger the ionic bond is.

107
Q

What is entropy?
What keyword must you use when discussing entropy?

A

Entropy is a measurement of how disordered a system (chemical) is.

Disorder is an essential keyword

108
Q

Sketch the shape of an entropy graph and explain the shape of it.

A
109
Q

In what ways can entropy effect reactions?

A

Some reactions can be favoured by entropy (due to an increase in disorder)

If there is an increase in the total number of particles in the products compared to the reactants there is an increased in disorder so there’s an increase in entropy.

This can lead to an increase in the likelihood of a reaction taking place.

110
Q

What is Gibb’s free energy? (definition and equation)

A

Gibbs’ Free energy is the total energy available in a substance/substances that can be used in a chemical reaction

111
Q

How can we tell if a reaction is feasible?

A

Gibbs free energy change (∆G)can allow us to identify if a reaction is feasible or not. If ∆G is 0 or less then a reaction is feasible.

We can estimate the direction of Gibbs free energy change by looking at the equation and the direction of the values in it.

112
Q

What can the directions of entropy and enthalpy tell us about the feasibility of a reaction?

A
113
Q

How can Gibbs free energy link to straight line graphs?

A
114
Q

What is rate measured in?

A

The rate of a reaction is measured as the change in concentration per second (moldm-3s-1).

115
Q

Generic expression for rate of a reaction, including what possible orders are and what k depends on.

A

The rate of a chemical reaction is related to the concentration of reactants by a rate equation of the form:
Rate = k[A]m [B]n
Where m and n are the orders of reaction with respect to reactants A and B and k is the rate constant.
The orders m and n are restricted to the values 0, 1, and 2.
The rate constant k varies with temperature

116
Q

What is an overall order of reaction?

A

Overall order – is the total of the indices (total orders) in a rate equation

117
Q

What is a rate determining step?

A

The rate determining step is the slowest step in a reaction

118
Q

How can you identify a catalyst from a rate equation?

A

It’s in the rate equation but not in the overall rate equation.

119
Q

How do you identify the rate determining step?

A

If a chemical is not represented in the rate equation it’s not in the rate determining step.

The chemical can be represented by an intermediate.

120
Q

How can concentration time graphs be used to determine the order of a reaction?

A
121
Q

What’s an initial rate method?

A

Initial rate – rate measured over the first few seconds to keep concentration known, starting concentration(s) changed and rate measured again.

122
Q

What’s a continuous rate method?

A

Continuous rate – measured the change in concentration over time for the whole experiment

123
Q

How do rate concentrations graphs link to order of reactions?

A
124
Q

What do mole fractions add up to?

A

1

125
Q

What do partial pressures add up to?

A

The total pressure

126
Q

What effect does a catalyst have on the position of equilibria/yield/Kp/Kc? Why?

A

No effect, because catalysts increase the rate of forwards and reverse reactions equally

127
Q

What is a buffer?

A

A mixture of a weak acid and a weak base that resists small changes in pH

128
Q

How does a buffer resist small changes in pH?

A

The weak acid reacts with the added in OH- and the weak base can react with the added in H+

129
Q

Why is [H2O] incorporated into Kw?

A

Because the value is so large it is practically constant as it hardly changes.

130
Q

What is an equivalence point?

A

When the moles of the two compounds in a titration are equivalent in proportion so totally react.

131
Q

How should you select an indicator? What’s the limit on indicators?

A

This is where the indicator should be changing colour at to ensure an accurate colour change.

Indicators are mostly weak acids so if too much is added then that can make the titration inaccurate.

Indicators that change over the small range of weak acids/weak base titrations are very hard to select as the indicator must change colour over a very small pH range.

132
Q

Key phrase about symmetry and dipoles

A

Key phraseidea that dipole moments (or dipoles) cancel out due to symmetry

133
Q

Draw the structure of diamond

A
134
Q

Draw the structure of graphite

A
135
Q

Draw the structure of silicon

A
136
Q

Draw the structure of silicon dioxide

A
137
Q

Draw the structure of sodium chloride

A
138
Q

Draw the structure of sodium

A
139
Q

Draw the structure of ice

A
140
Q

Draw the structure of iodine

A
141
Q

Excess

A

When the moles of a compound is greater in proportion to their molar ratio than needed to react with other reactant.

142
Q

Limiting Reagent

A

When the moles of a compound is less in proportion to their molar ratio than needed to react with other reactant..