Enthalpy, Rates and equilibrium, Equilibrium 2, Enthalpy and Entropy Flashcards

Chapter 9,10,19,22

1
Q

Enthalpy definition

A

A measure of the heat energy in a system.

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2
Q

Law of conservation of energy

A

Energy cannot be created or destroyed, only transferred. The total energy of a chemical system remains constant.

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3
Q

Activation energy

A

Minimum amount of energy required for a reaction to occur

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4
Q

Standard conditions

A

Standard pressure- 100kPa
Standard temperature- 25°C (25+273= 298K)
Standard concentration- 1mol/dm³

Standard state- physical state of a substance under standard conditions.

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5
Q

Standard enthalpy of reaction

A

The enthapy change that accompanies a reaction in the molar quantities shown in the equation in standard conditions, with all reactants and products in their standard states.

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6
Q

Standard enthalpy of formation

A

The enthalpy change when *1 mole of a substace** is formed from its constituent elements under standard conditions, with all reactants and products in their standard states.

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7
Q

Enthalpy change of combustion

A

Enthalpy change when 1 mole of a substance reacts completely with oxygen, under standard conditions, with all reactants and products in their standard states.

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8
Q

Enthalpy change of neutralisation

A

The enthapy change when 1 mol of water is formed in a neutralisation reaction between an acid and a base, in standard conditions, with all reactants and products in their standard states.

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9
Q

Why can calorimetry be inaccurate?

A
  • heat loss to surroundings
  • incomplete combustion of fuel
  • evaporation of alchohol (fuel) from wick
  • not in standard conditions

All apart from last cause results to be less exothermic.
Look at flashcards to see how to draw graph for enthalpy of neutralisation.

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10
Q

Average bond enthalpy

Equation

Why only an average?

A

The enthalpy change to break 1 mole of a specified bond in a gaseous molecule.
Always endothermic.

Total(bond enthalpy in reactants)- total(bond enthalpy in products)

Bond enthalpy found from the mean enthalpy of the same bond in different molecules.

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11
Q

Hess’s Law

A

The enthalpy change of a reaction is independent of the route taken.

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12
Q

Rate of reaction definition

A

How fast a reaction is being used up/ change in concentration over time.

Rate greatest at start, as reactant at highest concentration.
Slows down, as reactants are being used up.
Reactants completely used up so rate is 0.

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13
Q

Factors affecting rate of reaction

A

Concentration (or pressure when reactants are gas)

Temperature

Use of a catalyst

Surface area

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14
Q

How does each factor affect the rate of reaction?

A

Concentration/pressure - more molecules per unit/volume, more successful collisions.
Temperature- greater kinetic energy, more successful collisions, more with activation energy
Catalysts- provides an alternate reaction pathway with lower activation energy so more particles have activation energy, more successful collisions.
Surface area- more area for particles to collide with.

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15
Q

What makes a collision effective

A

Particles should collide with correct orientation
Particles must have enough energy to overcome activation energy barrier.

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16
Q

Catalysts definition

Types- method

Advantages of catalysts.

A

Substance that increases the rate of reaction without being used up in reaction. Provided an alternate reaction pathway, with lower activation energy.

Homogenous- when all reactants are in same phase
Heterogenous- reactants are in different phases

Homogenous:
Reactant react with catalyst to form intermediate. Intermediate breaks down to form product and regenerates catalyst.

Heterogenous:
Reactant molecules are adsorbed (weakly bonded) onto surface of catalyst, where reaction occurs. Product leaves catalyst by desorption.

Reduces energy demand and lowers temperatures- reduces energy costs and increases sustainability by reducing combustion of fossil fuels, so reduction of CO2 emmissions.

Increases yield of desired products with fewer by-products.

17
Q

Examples of catalysts

A

Homogenous:
Ozone depletion, cl. radical 2O3<–>3O2

Heterogenous:
Hydrogenation of alkene, Ni catalyst
Haber process, Fe catalyst

18
Q

Boltzman distribution curve
- increasing temperature
- using a catalyst

A

Shows the spread of energies (Fraction of molecules with energy vs Energy)
Curve not symmetrical as particles with very high energies skew the results to the right

  • more particles at higher energies, more particles with activation enery, more successful collisions
  • More particles with energy more than the activation energy, so frequency of successful collisions increases
19
Q

Le Chatelier’s principle

A

If an external change occurs to a reaction at equilibrium, the position of equilibrium will move to oppose the change.

20
Q

Dynamic equilibrium is reached when

A
  • In a closed system
  • Forward and backward rate are equal
  • The concentration of products and reactants are constant
21
Q

Increasing pressure

A

Moves to least moles of gas.

22
Q

Enthalpy of atomisation

A

The enthalpy change when 1 mole of gaseous atoms is formed from its element in its standard state.

23
Q

First ionisation energy

A

The energy required to remove 1 electron from each atom in 1 mole of gaseous atoms, to form 1 mole of gaseous 1+ ions.

24
Q

First electron affinity

A

The enthalpy change when 1 electron is added to each atom in 1 mole of gaseous atoms, to form 1 mole of gaseous -1 ions.

25
Q

Lattice enthalpy

A

Enthalpy change when 1 mole of an ionic crystal lattice is formed from its constituent ions in gaseous form.

Measure of ionic bond strength.

26
Q

Enthalpy of hydration

A

Enthalpy change when 1 mole of gaseous ions dissolve in H2O to become 1 mole of aqeous ions.

27
Q

Enthalpy of solution

A

Enthalpy change when 1 mole of a solute completely dissolves in water.

28
Q

The more exothermic lattice enthalpy is,

A

The more exo, the stronger the ionic bonds

29
Q

Factors affecting lattice enthalpy/ enthalpy of hydration

A
  • ionic radius increases, distance between ions increases, attraction decreases, lattice enthalpy less exo
  • ionic charge increases, attraction between ions increases, more exo

(in enthalpy of hydration, its attraction between ions and water)

30
Q

Entropy
Factors affecting entropy

Why does Ne(g) have greater entropy than Ne(l)

Units and equation for standard entropy

A

The dispersal of energy/ the level of disorder in a chemical system
Entropy increases when: increase in number of molecules, changes state (s–> l –> g)

In gas state atoms are more disordered, atoms have greater energy

J/K/mole
standard entropy= entropy of products- entropy of reactants

31
Q

Feasibility definition

A

Whether a reaction is likely to happen and is energetically feasible (spontaneous)
Free energy change must be -ve.

32
Q

Gibb’s Free energy change

A

ΔG = ΔH – TΔS

free energy change ΔG= kJ/mol
enthalpy change ΔH= kJ/mol
T= K
Standard entropy change ΔS= J/K/mole (convert to kJ/K/mol by dividing by 1000)

33
Q

Free energy change during change of state

A

ΔG = 0

y=mx+c
ΔG = (-ΔS)T + ΔH

Energy limitations: Some reactions have -ve ΔG, but still don’t occur:
- reaction rate may be very slow
- reaction may require large activation energy