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Manpreet Singh
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Cards (27)
Lattice enthalpy
measure of ionic bond
strength
used for
ionic
substances
dissociation
or
formation
enthalpy of lattice formation
enthalpy change when one mole of a solid
ionic substance
is formed from its
constituent
ions in a gaseous state under standard conditions
exothermic
M
g
2
+
(
g
)
+
Mg^{2+}(g)+
M
g
2
+
(
g
)
+
2
C
l
−
(
g
)
→
M
g
C
l
2
(
s
)
2Cl^-(g)\rightarrow MgCl_2(s)
2
C
l
−
(
g
)
→
M
g
C
l
2
(
s
)
enthalpy of lattice dissociation
enthalpy change when one mole of a solid ionic compound
dissociates
into its
gaseous
ions under standard conditions
endothermic
M
g
C
l
2
(
s
)
→
M
g
2
+
(
g
)
+
MgCl_2(s)\rightarrow Mg^{2+}(g)+
M
g
C
l
2
(
s
)
→
M
g
2
+
(
g
)
+
2
C
l
−
(
g
)
2Cl^-(g)
2
C
l
−
(
g
)
ionisation energy
energy required to remove one mole of
electrons
from one mole of atoms in their
gaseous
state under
standard conditions
to form one mole of 1+ ions
endothermic
M
g
(
g
)
→
M
g
+
Mg(g)\rightarrow Mg^+
M
g
(
g
)
→
M
g
+
(
g
)
+
(g)+
(
g
)
+
e
−
e^-
e
−
enthalpy of atomisation
enthalpy change
when
one mole
of
gaseous atoms
is formed form an
element
in its
standard state
under standard conditions
endothermic
1
2
I
2
(
s
)
→
I
(
g
)
\frac{1}{2}I_{2\ (s)}\rightarrow\ I_{(g)}
2
1
I
2
(
s
)
→
I
(
g
)
bond dissociation enthalpy
enthalpy change
when one mole of
covalent
bonds is broken in the
gaseous
state
endothermic
I
2
(
g
)
→
2
I
(
s
)
I_{2\ (g)}\rightarrow2I_{(s)}
I
2
(
g
)
→
2
I
(
s
)
enthalpy of electron affinity
enthalpy change
when one mole of
gaseous
atoms
gain
one mole of electrons to form one mole of 1- ions in their
gaseous
state under standard conditions
first is exothermic, second is endothermic
M
g
(
g
)
+
Mg_{(g)}+
M
g
(
g
)
+
e
−
→
M
g
(
g
)
−
e^-\rightarrow\ Mg_{(g)}^-
e
−
→
M
g
(
g
)
−
enthalpy change of hydration
enthalpy change when one mole of
gaseous
ions is
dissolved
in water to form one mole of
aqueous
ions under standard conditions
exothermic
M
g
(
g
)
2
+
→
M
g
(
a
q
)
2
+
Mg_{(g)}^{2+}\rightarrow Mg_{(aq)}^{2+}
M
g
(
g
)
2
+
→
M
g
(
a
q
)
2
+
enthalpy change of solution
enthalpy change when one mole of an ionic solid
dissolves
in enough water so that the dissolved ions no longer
interact
under standard conditions
exo/endo varies
N
a
C
l
(
s
)
→
N
a
(
a
q
)
+
NaCl_{(s)}\rightarrow Na_{(aq)}^+
N
a
C
l
(
s
)
→
N
a
(
a
q
)
+
+
+
+
C
l
(
a
q
)
−
Cl_{(aq)}^-
C
l
(
a
q
)
−
Calculating lattice enthalpies
cycle for group 2 elements
cycle for when first and second electron affinity
purely ionic model
all ions are
spherical
charge
evenly
distributed
100%
ionic
purely
electrostatic
theoretical
experimental
has
covalent
character
polarisation
non
spherical
experimental value different from theoretical
compound has
covalent
character
strength of
bonding
polarisation
trends in lattice enthalpies
larger
ions = smaller lattice enthalpies due to reduced
electrostatic force
of attraction
increases as size of
charge
increases due to more
energy
given out
factors affecting polarisation
positive ion =
small
size,
high
charge
negative ion =
large
size (easy to distort),
high
charge
enthalpy change of
solution
entropy
measure of
disorder
J
K
−
1
m
o
l
−
1
J\ K^{-1}mol^{-1}
J
K
−
1
m
o
l
−
1
symbol
S
what affects entropy
physical
state
( solid<liquid<gas)
dissolving
solid (dissolution)
number of
particles
(more = increase)
entropy
change
feasible reaction
reaction that takes place on its own
accord
, without energy being
supplied
to it
when is reaction feasible
when
Δ
G
\Delta G
Δ
G
is
negative
not guaranteed as may have high
E
a
E_a
E
a
or slow
rate
exothermic
gibbs free energy change
measure to predict
feasibility
when is
Δ
G
\Delta G
Δ
G
always negative
exothermic
and
positive
Δ
S
\Delta S
Δ
S
feasible
at any temperature
when is
Δ
G
\Delta G
Δ
G
always positive
endothermic
and
negative
Δ
S
\Delta S
Δ
S
not
feasible
at any temperature
free energy
graphs