17 Thermodynamics Flashcards

1
Q

Standard molar enthalpy of formation

A

Enthalpy change when one mole of a compound is formed from its constituent elements under standard conditions, all reactants and products in their standard states

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2
Q

Standard molar enthalpy change of combustion

A

Enthalpy change when one mole of substance is completely burnt in oxygen

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3
Q

Standard enthalpy of atomisation

A

Enthalpy change which accompanies the formation of one mole of gaseous atoms from the element in standard state under standard conditions

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4
Q

First ionisation energy

A

Standard enthalpy change when one mole of gaseous atoms is converted into a mole of gaseous ions each with a single positive charge

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5
Q

Second ionisation energy

A

Loss of a mole of electrons from a mole of singly positively charge ions

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6
Q

First electron affinity

A

Standard enthalpy change when one mole of gaseous ions each with a single negative charge

(Always negative as energy is given out when an electron is attracted to positively charged nucleus)

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7
Q

Second electron affinity

A

Enthalpy change when one mole of electrons is added to mole of gaseous ions each with a single negative charge to from ions each with two negative charges

(Always positive negative electron has to overcome the repulsion between the electron and negative ion)

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8
Q

Lattice enthalpy of formation

A

Standard enthalpy change when one mole of solid ionic compound is formed from its gaseous ions

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9
Q

Enthalpy of lattice dissociation

A

Standard enthalpy change when one mole of solid ionic compounds dissociated into its gaseous ions

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10
Q

Enthalpy of hydration

A

Standard enthalpy change when water molcules surround one mole of gaseous ions

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11
Q

Enthalpy of solution

A

Standard enthalpy change when one mole of solute dissolves completely in sufficient solvent to form a solution in which the molecules or ions are far enough apart not to interact with each other

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12
Q

Mean bond enthalpy

A

Enthalpy change when one mole of gaseous molecules each break covalent bonds to form two free radicals averaged over a range of compounds

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13
Q

Hess’s law

A

The enthaply change accompanying a chemical change is independent of the route by which the chemical change occurs

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14
Q

Trends in lattice enthalpies

A

Larger ions lead to smaller lattice enthalpies. This is because the opposite charges do not approach each other as closely when the ions are larger

Charge to size ratio increase

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15
Q

Explain why the enthalpy of lattice dissociation of potassium oxide is less endothermic than that of sodium oxide

A

The potassium ion is bigger to the electrostatic forces of attraction between ions is weak

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16
Q

Suggest why the electron affinity of fluorine has a negative value

A

The nucleus which is positive attracts the negative electron when an electron is gained energy is given out

17
Q

Explain why the theoretical enthalpy of lattice dissociation for silver fluoride is different form the experimental value that can be calculated using the born-harbour cycle

A

Theoretical value is calculated assuming that the bonding is perfecting ionic. Experimental value allows for the bonding to have some covalent character

18
Q

Why would the lattice dissociation for silver chloride be less than silver fluoride

A

Chloride ion is larger so the attraction between Cl- and Ag+ is weaker

19
Q

Define the term enthalpy of lattice dissociation

A

Enthalpy change when one mole of an compound is broken into its ions in the gaseous state

20
Q

Explain why the bond enthalpy of Cl-Cl bond is greater than that of a Br-Br bond

A

Bond pair is closer to the nucleus so attraction to bonding pair is stronger

21
Q

Explain the meaning of the term perfect ionic model

A

Ions can be regarded as point charges ( perfect spheres)

22
Q

Factors that increase polarisation

A

Positive ion small size and high charge

Negative ion larger size and high charge

23
Q

Spontaneous

A

Occurring as a result of a sudden impulse

24
Q

Entropy

A

A numerical measure of disorder in a chemical system

25
Q

Positive 🔺G

A

Means the reaction isn’t feasible at room tempeture

26
Q

Determining entropy change

A

At a boiling point water is equally likely to exist as liquid or vapour

🔺H = T🔺S

27
Q

Extracting metals

A

Extracting metals form their oxide ore is to heat them with carbon ( coke is cheap)

28
Q

Kinetic factors

A

Neither enthalpy change nor entropy changes tells us anything about how quickly or slowly a reaction is likely to go ( large activation energy)

29
Q

Partial pressure of A

A

Mole fraction of a ✖️ total pressure

30
Q

Mole fraction of A

A

Number of moles of A / total moles of gas

31
Q

Effect of pressure on gaseous equilibrium

A

Pressure only effects in there are a different number of moles

Increasing the pressure on a gas phase reaction will increase the rate at which equilibrium is reached because there would be more collisions

32
Q

Effect of temperature of a gaseous equilibrium

A

Increasing the temperature will also increase the rate of equilibrium is reach with a catalyst

33
Q

what does ∆H mean?

A

∆H, whilst important, is not suf cient to explain feasible change

34
Q

equation

A

∆G = ∆H – T∆S