Lattice Energy Flashcards

1
Q

definition of lattice energy

A

enthalpy change when one mole of ionic compound is formed from its gaseous ions under standard conditions

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2
Q

enthalpy change of lattice energy

A

exothermic

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3
Q

Na+(g) + Cl-(g) → NaCl (s) is an example of

A

lattice energy

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4
Q

what does large exothermic value for lattice energy mean

A

more stable and strong ionic bonding

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5
Q

suggest reason for difference in LE between calcium oxide and iron (II) oxide

A

iron has smaller ionic radius = high charge density

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6
Q

key words for mentioning lattice energy difference (4)

A

ionic radius
charge density
electrostatic attraction between cation and anion
charge on ion

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7
Q

definition of enthalpy change of atomisation

A

enthalpy change when one mole of gaseous atoms are formed from its element under standard conditions

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8
Q

enthalpy change of atomisation

A

endothermic

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9
Q

why is enthalpy change of atomisation endothermic

A

energy must be supplied to break the bonds holding atom together

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10
Q

Li(s) –> Li(g) is an example of

A

enthalpy change of atomisation

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11
Q

definition of enthalpy change of hydration

A

the enthalpy change when one mole of gaseous ions dissolves in sufficient water to form an infinitely dilute solution

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12
Q

enthalpy change of hydration

A

exothermic

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13
Q

trends in enthalpy change of hydration

A

more exothermic with smaller ions

high charge density makes stronger bonds with water molecule

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14
Q

definition of enthalpy change of solution

A

the energy absorbed or released when one mole of an ionic solid dissolves in sufficient amount of water to form an infinitely dilute solution

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15
Q

enthalpy change of solution (aq)

A

exo/endo (little changes)

large values are insoluble

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16
Q

definition of first ionisation energy

A

enthalpy change when one electron is removed from each atom in one mole of gaseous atoms under standard conditions

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17
Q

enthalpy change of first ionisation energy

A

endothermic

18
Q

why is first ionisation eneergy endothermic

A

energy needed to overcome the force of attraction between outer electrons and nucleus

19
Q

why is first ionisation energy of calcium less positive than its second ionisation energy

A

electron lost is closer to the nucleus
electron lost from positive ion
outer electron more firmly attracted to the nucleus

20
Q

definition of first electron affinity

A

enthalpy change when one mole of electrons is added to one mole of gaseous atoms to form one mole of gaseous 1- ions under standard conditions

21
Q

enthalpy change of first electron affinity

A

exothermic

22
Q

why is first electron affinity exothermic

A

electron experience attraction to the nucleus, energy absorbed to overcome repulsion

23
Q

Cl(g) + e → Cl- (g) is an example of

A

first electron affinity

24
Q

definition of second electron affinity

A

enthalpy change when one mole of electrons is added to one mole of gaseous 1- ions to form one mole of gaseous 2- ions under standard conditions

25
enthalpy change of second electron affinity
endothermic
26
why is second electron affinity endothermic
ion and electron both negative + energy required to overcome repulsion
27
O- (g) + e → O2-(g) is an example of
second electron affinity
28
factors affecting electron affinity
nuclear charge distance shielding from electrons (shielding + distance offsets)
29
what does low electron affinity mean
more wanting to give up its electron and has weak pull on valence of electrons
30
trend of electron affinity with halogens
becomes less negative (further away from outer shell = less energy released)
31
why is fluorine a less exothermic value than chlorine
very small and pushing in electron require some energy - crowded speace = less energy released
32
look at born haber cycle ok
ok
33
definition of enthalpy change of formation
enthalpy change when ionic compound formed from its elements under standard conditions
34
enthalpy change of what (2) in born haber cycle
formation | lattice
35
factors affecting lattice energy
ion size | charge on ions
36
definition of polarising power
ability of cation to attract e and distort an anion
37
describe ion polarisaion
small cation has high charge density and able to distort large anion
38
describe trend of thermal stability of group 2 carbonates/nitrates
increasing stability increasing ionic size = low charge density polarising ability on nitrate decreases
39
trend of solubility of sulphates
less soluble down the group lattice energy and hydration energy both decrease hydration decreases more enthalpy of solution more endothermic
40
equation for E.sol
E.latt - E.hyd
41
trend of solubility of hydroxides
more soluble lattice and hydration energy both decrease lattice energy decreases more enthalpy change of solution less endothermic