Thermodynamics Flashcards

(39 cards)

1
Q

enthalpy of lattice formation

A
  • enthalpy change when one mole of a solid ionic compound
  • formed from it’s gaseous ions
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2
Q

A calculation of the enthalpy of lattice formation of silver iodide based on a perfect ionic model gives a smaller numerical value than the value calculated
Explain this difference

A
  • AgI contains covalent character
  • Bonds (holding the lattice together) are stronger
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3
Q

The enthalpy of lattice formation for caesium iodide in Table 1 is a value obtained by experiment. –1 The value obtained by calculation using the perfect ionic model is –582 kJ mol
Deduce what these values indicate about the bonding in caesium iodide.

A

(Almost/Mostly) purely/ perfectly ionic

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4
Q

State the meaning of the term periodicity.

A

Repeating pattern/trends (of physical or chemical properties/reactions)

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5
Q

State why there is a difference between theoretical and experimental values

A

covalent character

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6
Q

Explain why the hydration becomes less exothermic from Li+ to K+

A
  • size of ion increases from Li+ to K+
  • attraction between lone pair on O and + ion decreases
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7
Q

state meaning of enthalpy change

A
  • heat energy change at constant pressure
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8
Q

The enthalpy of hydration of Ca2+(g) is –1650 kJ mol–1 Suggest why this value is less exothermic than that of Mg2+(g)

A
  • Ca2+ (ion) bigger/lower charge to size ratio (than Mg2+)
  • weaker attraction/bond to (Oδ- in) water
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9
Q

explain why standard entropy value for CO2 is greater than carbon

A

CO2 / gas is more disordered (than solid)

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10
Q

State the temperature at which the standard entropy of aluminium is 0 J K–1 mol–1

A

0 K

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11
Q

standard enthalpy of formation

A
  • enthalpy change when one mole of a compound is formed from its elements
  • under standard conditions
  • reactants and products in standard states
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12
Q

standard enthalpy of combustion

A
  • enthalpy change when one mole of a compound
  • completely burned in oxygen
  • under standard conditions
  • reactants and products in standard states
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13
Q

standard enthalpy of atomisation

A
  • enthalpy change when one mole gaseous atoms are formed
  • from an element in its standard state
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14
Q

mean bond enthalpy

A
  • standard enthalpy change
  • when one mole of gaseous molecules each break a covalent bond
  • to form 2 free radicals
  • averaged over a range of compounds
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15
Q

first ionisation energy

A
  • standard enthalpy change when one mole of electrons
  • is removed from one mole of gaseous atoms
  • to form one mole of gaseous ions each with single positive charge
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16
Q

second ionisation energy

A
  • standard enthalpy change when one mole of electrons
  • is removed from one mole of gaseous 1+ ions
  • to form one mole of gaseous ions each with 2+ charge
17
Q

first electron affinity

A
  • standard enthalpy change when one mole of gaseous atoms
  • converted into one mole of gaseous ions
  • each with single negative charge
  • under standard conditions
18
Q

second electron affinity

A
  • standard enthalpy change when one mole electrons
  • added to one mole of gaseous ions
  • with single negative charge
  • to form one mole of ions with 2- charge
19
Q

lattice formation

A
  • enthalpy change when one mole of solid ionic compound
  • is formed from its gaseous ions
20
Q

lattice dissociation

A
  • enthalpy change when one mole of solid ionic compound
  • dissociates into its gaseous ions
21
Q

enthalpy of hydration

A
  • standard enthalpy change when one mole of gaseous ions
  • is converted into one mole of aqueous ions
22
Q

enthalpy of solution

A
  • standard enthalpy change when one mole of solute
  • dissolves in enough solvent to form solution with ions are enough apart not to interact with each other
23
Q

what does the perfect ionic model predict

A
  • ions act as point charges
  • ions are perfect spheres which cannot be distorted
  • ions show purely ionic bonding with no covalent character
24
Q

if a ionic compound has more exothermic lattice formation what does this suggest

A

covalent character

25
positive entropy change means
more disorder
26
negative entropy change means
more ordered
27
when is the reaction feasible
when Gibbs is less than or equal to 0
28
calculating temperature that reaction becomes feasible
T = enthalpy change/entropy change T = H/S
29
equation that links Gibbs to y=mx + c
Gibbs = -ST + H y = mx + c Gibbs = y-axis temp = x-axis gradient = -S y-intercept = H
30
In terms of electrostatic forces, suggest why the electron affinity of fluorine has a negative value.
- attraction between nucleus and extra electron - energy released when electron is gained
31
write equation for first electron affinity for chlorine
Cl (g) + e- ---> Cl- (g)
32
Explain why the bond enthalpy of a Cl–Cl bond is greater than that of a Br–Br bond
- bonding pair closer to nucleus/Cl smaller atom - so attraction is stronger
33
Suggest why the electron affinity of chlorine is an exothermic change.
- attraction between chlorine nucleus and extra electron
34
explain why there is a difference between the hydration enthalpies between magnesium and sodium ions
- Mg2+ smaller ion AND more highly charged - So more strongly attracted to water
35
state meaning of mean bond enthalpy of O-H bonds
- standard enthalpy change when 1 mole of O-H molecules break to form covalent bond - averaged over a range of compounds
36
explain why value of Kw increases as temperature increases
- [H2O] is constant - only partially dissociates
37
Explain why kw value increases as temperature increases
- breaking bonds is endothermic - equilibrium moves to right hand side
38
state why there is a difference between theoretical and experimental values
covalent character
39
explain why enthalpy of hydration becomes less exothermic from Li+ and K+
- ion size increases - weaker attraction between metal ion and O- on water