Thermodynamics Flashcards

1
Q

ΔfH definition

A

Energy transferred when 1 mol of a compound is formed from its elements under standard conditions and all reactants and products being in their standard states

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2
Q

ΔatH definition

A

Enthalpy change when 1 mol of gaseous atoms is formed from its elements in their standard states

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3
Q

ΔsublimationH definition

A

enthalpy change for a solid metal turning to gaseous atoms and equals ΔatH

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4
Q

ΔdissH (bond dissociation) definition

A

standard molar enthalpy change when one mole of a covalent bond is broken into two gaseous atoms

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5
Q

First IE definition

A

ΔH required to remove 1 mol of e- from 1 mol gaseous atoms to form 1 mol gaseous ions with a 1+ charge

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6
Q

First electron affinity definition

A

ΔH when 1 mol of gaseous atoms gain 1 mol of electrons to form 1 mol of gaseous ions with a 1- charge

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7
Q

Why is first electron affinity exothermic for atoms that normally form 1- ions (group 7 for instance)

A

The ion is more stable than the atom
There is an attraction between the nucleus and the electron

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8
Q

Why is the second electron affinity for oxygen endothermic?

A

Energy is required to overcome the repulsive force between the negative ion and the electron

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9
Q

ΔlatformH definition

A

standard ΔH when 1 mol of a solid ionic crystal lattice is fromed from its consituent ions in gaseous form

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10
Q

ΔlatdissH definition

A

standard ΔH when 1 mole of an ionic crystal lattice forms its consituent ions in gaseous form

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11
Q

ΔhydH definition
(exo or endothermic?)

A

enthalpy change when 1 mol of gaseous ions become aqueous ions

always exothermic as bonds are formed between ions and water

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12
Q

ΔsolH definition

A

standard enthalpy change when 1 mol of an ionic solid dissolves in a large enough amount of water to ensure that the ions are well separated and do not interact with each other

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13
Q

Opposite of enthalpy of lattice formation?

A

enthalpy of lattice dissociation

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14
Q

Why use born haber cycles to calculate lattice enthalpies?

A

It cannot be determined directly

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15
Q

Which lattice enthalpy would point down in a born haber cycle?

A

formation

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16
Q

What’s always at the bottom row of a born haber cycle?

A

The solid compound

17
Q

What’s always at the top row of a Born Haber cycle?

A

positive ions, electrons and gaseous atoms (which turn into negative ions next)

18
Q

ΔatH(Cl2) is the same thing as…

A

the mean bond energy for Cl2

19
Q

Explain 2 trends in lattice enthalpies

A

ion size: the larger the ions, the less -ve the ΔlatformH will be, the weaker the lattice will be

ion charge: the bigger the charge, the greater the attraction so the stronger the lattice enthalpy (more -ve values)

20
Q

Perfect ionic model

A

assumed by theoretical lattice enthalpies
ions are 100% spherical and ionic
attractions are purely electrostatic

21
Q

What 4 things cause covalent character?

A

Small +ve ion
multiple +ve charges on +ve ion
large -ve ion
multiple -ve charges on -ve ion

22
Q

The more ________ the bigger the difference between the theoretical and born haber lattice enthalpies

A

covalent character

23
Q

Why would the born haber value be larger than the theoretical value for a compound?

A

if it has some covalent character
it tends towards giant covalent structure
lattice + is stronger than if it was 100% ionic

24
Q

What is different in the shapes of purely ionic ions and ions with covalent character?

A

purely ionic- 100% spherical
covalent character- electron charge cloud is distorted

25
Q

Substances with more ways of arranging their atoms and energy (more disordered) have a higher/lower entropy?

A

higher

26
Q

Why do solids have lower entropies than gases?

A

as the solid increases in temperature its entropy increases as particles vibrate more
gases move around even more–> more disordered

27
Q

At 0K substances have ______ entropy and the reason why

A

0

no disorder
particles are stationary

28
Q

When do significant increases in entropy occur?

A

change of state from s to l to g
increase in no of molecules from r to p

29
Q

entropy unit

A

JK−1mol−1

30
Q

ΔS =

A

Sprod - Sreact

31
Q

Gibbs free energy purpose

A

combines effect of entropy and enthalpy into 1 number

32
Q

ΔG=

A

ΔH-TΔS

ALWAYS USE S/1000

33
Q

ΔG units

A

KJmol-1

34
Q

ΔG has to be ____ve for a reaction to occur

A

-

35
Q

What is ΔG for melting/boiling? Why?

A

0

physical phase changes are equillibria

36
Q

If the reaction involves an increase in entropy what does increasing temperature do to ΔG?

A

makes it more likely that ΔG is negative and the reaction occurs

37
Q

If the reaction involves a decrease in entropy what would an increase in temperature do to ΔG

A

Less likely that ΔG is negative and the reaction is less likely to occur

38
Q

ΔG = ΔH - TΔS as a graph’s y, m, x and c values

A

ΔG as y
T as x
ΔH as c
-ΔS as m

39
Q

ΔG = ΔH - TΔS positive gradient means

A

ΔS is negative