4.
Bonding
Ionic Bonding
Evidence for the existence of ions
X-ray diffraction: Electron density map of NaCl
These maps show the
likelihood of finding
electrons in a region
The ions are discrete or
separate, because the
electron density falls to zero
between the ions
The contours are lines of
equal electron density
The electron density map
does not, however, show the
edge of the ion and so it is
difficult to measure the
radius of the ion from an
electron density map
The maps show that for NaCl
The ions are arranged in a
regular pattern.
The chloride ions are larger than
the sodium ions
Physical properties of Ionic Compounds
high melting points ( there are strong attractive forces between the ions)
non conductor of electricity when solid (ions are held together tightly and can not move)
conductor of electricity when in solution or molten. ( ions are free to move)
brittle / easy to cleave apart
A little force will push the ions along and ions will be next to similar ions. There will be a force
of repulsion between like ions, pushing the layers apart
Migration of ions
-ve
+ve
-ve
+ve
Blue colour of
Cu2+ ions
migrate to the
negative
electrode
Yellow colour of
CrO42- ions
migrate to the
positive
electrode
A drop of potassium Manganate
solution, which is purple, is
placed on moist filter paper on a
microscope slide and the ends
of the slide are connected to a
24 V DC power supply. After ten
minutes the purple colour of the
MnO4- ion has migrated to the
positive electrode
CuCrO4
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Ionic Bonding
Metal atoms lose electrons to form +ve ions.
Non-metal atoms gain electrons to form -ve ions.
Mg goes from 1s2 2s2 2p63s2
to Mg2+ 1s2 2s2 2p6
O goes from 1s2 2s2 2p4 to
O2- 1s2 2s2 2p6
Ionic crystals have the structure of giant lattices of ions
An Ionic bond is the strong electrostatic force of attraction
between oppositely charged ions formed by electron transfer.
Ionic bonding is stronger and the melting points higher when the ions
are smaller and/ or have higher charges. E.g. MgO has a higher
melting point than NaCl as the ions involved (Mg2+ & O2- are smaller
and have higher charges than those in NaCl , Na+ & Cl- )
Ionic Radii
Positive ions are smaller compared to their atoms because it has one less shell of electrons and the
ratio of protons to electrons has increased so there is greater net force on remaining electrons
holding them more closely.
The negative ions formed from groups five to seven are larger than the corresponding atoms.
The negative ion has more electrons than the corresponding atom but the same number of protons. So the pull
of the nucleus is shared over more electrons and the attraction per electron is less, making the ion bigger.
N3- O2- F- and Na+ Mg2+ Al3+ all have the same
electronic structure (of the noble gas Ne)
Ionic
Radius
There are increasing numbers of protons from N to F
and then Na to Al but the same number of electrons.
The effective nuclear attraction per electron therefore
increases and ions get smaller
N3- O2- F- (Ne) Na+ Mg2+ Al3+
Within a group the size of the Ionic radii increases going down the group. This is because
as one goes down the group the ions have more shells of electrons.
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Definitions of enthalpy changes for stages involved in forming an ionic lattice
Enthalpy change of formation
The standard enthalpy change of formation of a compound is the energy transferred when 1
mole of the compound is formed from its elements under standard conditions (298K and
100kpa), all reactants and products being in their standard states
Na (s) + Cl2 (g)
NaCl (s)
[Hf = - 411.2 kJ mol-1]
Enthalpy of atomisation
The enthalpy of atomisation of an element is the enthalpy change when 1 mole of
gaseous atoms is formed from the element in its standard state
Na (s)
Na(g) [Hat = +148 kJ mol-1]
O2 (g)
O (g) [Hat = +249 kJ mol-1]
First Ionisation enthalpy
The first ionisation enthalpy is the enthalpy change
required to remove 1 mole of electrons from 1 mole
of gaseous atoms to form 1 mole of gaseous ions
with a +1 charge
Mg (g)
Mg+ (g) + e- [H IE 1]
First Electron Affinity
The first electron affinity is the enthalpy change that
occurs when 1 mole of gaseous atoms gain 1 mole of
electrons to form 1 mole of gaseous ions with a 1
charge
O (g) + e-
O- (g)
[Hea] = -141.1 kJ mol-1]
The first electron affinity is exothermic for atoms that
normally form negative ions because the ion is more
stable than the atom and there is an attraction
between the nucleus and the electron
Second Ionisation enthalpy
The second ionisation enthalpy is the enthalpy
change to remove 1 mole of electrons from one mole
of gaseous 1+ ions to produces one mole of gaseous
2+ ions.
Mg+ (g)
Mg 2+ (g) + e- [H IE2 ]
Second Electron Affinity
The second electron affinity is the enthalpy change
when one mole of gaseous 1- ions gains one
electron per ion to produce gaseous 2- ions.
O (g) + e-
O2- (g)
[Hea = +798 kJ mol-1]
The second electron affinity for oxygen is
endothermic because it take energy to overcome
the repulsive force between the negative ion and
the electron
First Electron affinity values will become less exothermic as you go down Group 7 from chlorine
to iodine because the atoms get bigger and have more shielding so it becomes less easy to
attract electrons to the atom to form the negative ion
Enthalpy of lattice formation
The Enthalpy of lattice formation is the standard enthalpy change when 1 mole
of an ionic crystal lattice is formed from its constituent ions in gaseous form.
Na+ (g) + Cl- (g)
NaCl (s)
[H Latt = -787 kJ mol-1]
Trends in Lattice Enthalpies
The strength of a enthalpy of lattice formation depends on the following
factors
1.
The sizes of the ions:
The larger the ions, the less negative the enthalpies of lattice
formation (i.e. a weaker lattice). As the ions are larger the charges
become further apart and so have a weaker attractive force
between them.
2.
The lattice enthalpies become
less negative down any group.
e.g. LiCl, NaCl, KCl, RbCl
The charges on the ion:
The bigger the charge of the ion, the greater the attraction between
the ions so the stronger the lattice enthalpy (more negative values).
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e.g group 1 halides (eg NaF KI) have
lattice enthalpies of around 700 to 1000
group 2 halides (eg MgCl2) have lattice
enthalpies of around 2000 to 3500
group 2 oxides eg MgO have lattice
enthalpies of around 3000 to 4500
kJmol-1
BORN HABER CYCLES
The lattice enthalpy cannot be determined directly. We calculate it indirectly by making use of changes
for which data are available and link them together in an enthalpy cycle the Born Haber cycle
Born Haber cycle: sodium Chloride
Na+ (g) + e-
Pay attention to state symbols
and direction of arrows.
Cl (g)
HEa(Cl)
Hat (Cl)
Na+ (g) + Cl- (g)
Na+(g) + e- + Cl2(g)
H lattice formation
(NaCl)
HIE 1(Na)
Na (g)
Usually all pieces of data are given except
the one that needs to be calculated
+ Cl2(g)
Hat (Na)
Na (s) + Cl2(g)
Hf (NaCl)
NaCl (s)
By applying Hesss law the heat of formation equals to the sum of everything else
Hf =HatNa + HIENa+ HatCl + HEaCl + Hlatt formation
Rearrange to give Hlatt formation = Hformation - (HatmNa + HIENa + HatmCl + HEaCl )
Hlattice formation =-411 (+107 + 496 + 122 + -349) = -787 kJmol-1
Born Haber cycle: magnesium Chloride
Mg2+ (g) + 2e- +
2x Hat (Cl)
Mg2+
(g) +
2e-
The data for the Hat (Cl) could
also be given as the bond energy
for E(Cl-Cl ) bond.
2Cl (g)
2 xHEa(Cl)
Mg2+ (g) + 2Cl- (g)
+ Cl2(g)
HIE 2(Mg)
Mg+ (g) + e-
Remember :
E(Cl-Cl ) = 2 x Hat (Cl)
Note in this example the first and
second ionisation energies of
magnesium are needed as Mg is
a +2 ion
+ Cl2(g)
HIE 1(Mg)
H lattice formation
Mg (g)
+ Cl2(g)
Hat (Mg)
Mg (s) + Cl2(g)
Hf (MgCl2)
MgCl2 (s)
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Born Haber cycle: calcium oxide
Ca2+ (g) + 2e- +
Ca2+ (g)
O (g)
Hat (O)
Ca2+ (g) + 2e- + O2(g)
HEa1(O)
+ O2- (g)
HEa2(O)
Ca2+ (g) + e- + O- (g)
Notice the second electron affinity for
oxygen is endothermic because it
take energy to overcome the
repulsive force between the
negative ion and the electron
HIE 2(Ca)
Ca + (g) + e- + O2(g))
HIE 1(Ca)
Ca (g)
+ O2(g)
H lattice formation
Hat (Ca)
Ca (s) + O2(g)
Hf (CaO)
CaO (s)
Perfect Ionic Model
Theoretical lattice enthalpies assumes a perfect ionic model where the ions are 100% ionic and
spherical and the attractions are purely electrostatic.
Differences between theoretical and Born Haber (experimental) lattice enthalpies
The Born Haber lattice enthalpy is the real experimental value.
When a compound shows covalent character, the theoretical and the born Haber lattice enthalpies
differ. The more the covalent character the bigger the difference between the values.
When the negative ion becomes distorted and more covalent we say it becomes polarised. The
metal cation that causes the polarisation is called more polarising if it polarises the negative ion.
Ionic with covalent
character
100% ionic
When 100 % ionic the ions are spherical.
The theoretical and the born Haber lattice
enthalpies will be the same
The polarising power of cation increases when
the positive ion is small
the positive ion has multiple charges
The charge cloud is distorted .The theoretical
and the experimental Born Haber lattice
enthalpies will differ
The polarizability of an anion depends
on its size. The bigger the ion the more
easily it is distorted
When a compound has some covalent character- it tends towards giant
covalent so the lattice is stronger than if it was 100% ionic. Therefore the
born haber value would be larger than the theoretical value.
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Why does Calcium chloride have the formula CaCl2 and not CaCl or CaCl3?
It is useful to draw out the born haber cycles for each potential case.
Theoretical lattice enthalpies have
been calculated for each case
We need to calculate an enthalpy of formation for each case.
The one with the most exothermic enthalpy of formation will be the one that
forms as it will be the most thermodynamically stable
Born Haber Cycle for CaCl
Ca+ (g) + eCa+
(g) +
e-
These get larger as the
positive charge on the
calcium ion becomes bigger.
+ Cl (g)
HEa(Cl)
Hat (Cl)
+ Cl2(g)
Ca+ (g) + Cl- (g)
HIE 1(Ca)
Ca (g)
H lattice formation
+ Cl2(g)
Hat (Ca)
Ca (s) + Cl2(g)
Theoretical lattice enthalpies
Hlatt CaCl = -719 kJ mol-1
Hlatt CaCl2 = -2218 kJ mol-1
Hlatt CaCl3 = -4650 kJ mol-1
The enthalpy of formation
is largely a balance of the
ionisation energy and
lattice enthalpy.
Hf (CaCl) is -163.1 kJ mol-1.
This is exothermic.
Hf (CaCl) = -163.1 kJmol-1
CaCl (s)
Born Haber Cycle for CaCl2
Ca2+ (g) + 2e- + 2Cl (g)
2 xHat (Cl)
2 xHEa(Cl)
HIE 2(Ca)
Ca2+ (g) + 2Cl- (g)
Ca2+ (g) + 2e- + Cl2(g)
Ca+ (g) + e- + Cl2(g)
HIE 1(Ca)
Ca (g)
H lattice formation
+ Cl2(g)
The enthalpy of formation is
therefore more exothermic.
This is the most stable form
Hat (Ca)
Ca (s) + Cl2(g)
The increased ionisation
enthalpy to form Ca2+ is
more than compensated for
by the stronger lattice
enthalpy of formation
Hf (CaCl2) = -739.2 kJmol-1
CaCl2 (s)
Born Haber Cycle for CaCl3
Ca3+ (g) + 3e- +
3Cl (g)
3 xHat (Cl)
Ca3+ (g) + 3e- + 1.5 Cl2(g)
3 xHEa(Cl)
Ca3+ (g)
Ca2+ (g) + 2e- + 1.5 Cl2(g)
Ca+ (g) + e- + 1.5Cl2(g)
Ca (g)
+1.5 Cl2(g)
HIE 3(Ca)
+ 3Cl- (g)
H lattice formation
HIE 2(Ca)
The big increase in ionisation
enthalpy to remove the 3rd
electron is not compensated
for by the stronger lattice
enthalpy of formation
The enthalpy of formation is
therefore endothermic. This is
the least stable form
HIE 1(Ca)
Hat (Ca)
Ca (s) + 1.5 Cl2(g)
CaCl3 (s)
Hf (CaCl3) = +1541.7 kJmol-1
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Covalent Bonding
A covalent bond strong and is caused by the electrostatic attraction
between the bonding pair of electrons and nuclei.
The strength of covalent bond can be demonstrated by the high melting points of giant atomic
structures like diamond and graphite. They have high melting points because they contain many
strong covalent bonds in a macromolecular structure. It takes a lot of energy to break the many
strong bonds.
The X-ray diffractions for the hydrogen
molecule show high concentration of negative
charge between H nuclei. This negative charge
is strongly attracted by both nuclei so attractive
interactions exceed repulsive ones
In a covalent compound there is significant electron
density between the atoms
Electron Configuration Diagrams
..
Dative Covalent bonding
A Dative covalent bond forms when the
shared pair of electrons in the covalent bond
come from only one of the bonding atoms. A
dative covalent bond is also called co-ordinate
bonding.
Common examples you should be able to
draw that contain dative covalent bond (e.g.
NH4+, H3O+, NH3BF3)
The dative covalent bond acts like
an ordinary covalent bond when
thinking about shape so in NH4+
the shape is tetrahedral
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O
H
H
H
Cl
Cl
Cl
The direction of the arrow
goes from the atom that is
providing the lone pair to the
atom that is deficient
Metallic bonding
Metals consist of giant lattices of metal ions in a sea of delocalised electrons
Definition: A metallic bond is the electrostatic force of attraction between the
positive metal ions and the delocalised electrons
sodium
The three main factors that affect the strength of a metallic bond are:
1. Number of protons/ Strength of nuclear attraction.
The more protons the stronger the bond
2. Number of delocalised electrons per atom (the outer shell electrons are delocalised)
The more delocalised electrons the stronger the bond
3. Size of ion.
The smaller the ion, the stronger the bond.
Metals have high melting points because the strong electrostatic forces between positive ions
and sea of delocalised electrons require a lot of energy to break
Example
Mg has stronger metallic bonding than Na and hence a higher
melting point. The Metallic bonding gets stronger because in Mg
there are more electrons in the outer shell that are released to the
sea of electrons. The Mg ion is also smaller and has one more
proton. There is therefore a stronger electrostatic attraction
between the positive metal ions and the delocalised electrons
and higher energy is needed to break bonds.
magnesium
Metals can conduct electricity well because the delocalised electrons can move through the structure
Metals are malleable because the positive ions in the lattice are all identical. So the planes of ions
can slide easily over one another. The attractive forces in the lattice are the same whichever ions are
adjacent
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Bonding and Structure
Bonding
Structure
Ionic : electrostatic force of
attraction between
oppositely charged ions
Examples
Giant Ionic Lattice
Sodium chloride
Magnesium oxide
Covalent : shared pair of
electrons
Simple molecular:
With intermolecular forces (van der
Waals, permanent dipoles, hydrogen
bonds) between molecules
Iodine
Ice
Carbon dioxide
Water
Methane
Covalent : shared pair of
electrons
Macromolecular:
giant molecular structures.
Diamond
Graphite
Silicon dioxide
Silicon
Metallic: electrostatic
force of attraction between
the metal positive ions and
the delocalised electrons
Giant metallic
lattice
Magnesium, Sodium
(all metals)
Only use the words molecules and intermolecular forces when talking about simple molecular substances
Property
Ionic
Molecular (simple)
Macromolecular
Metallic
boiling and
melting
points
high- because
of giant lattice
of ions with
strong
electrostatic
forces
between
oppositely
charged ions.
low- because of
weak intermolecular
forces between
molecules (specify
type e.g van der
waals/hydrogen
bond)
high- because of
many strong covalent
bonds in
macromolecular
structure. Take a lot
of energy to break the
many strong bonds
high- strong electrostatic forces
between positive ions and sea of
delocalised electrons
Solubility in
water
Generally
good
generally poor
insoluble
insoluble
conductivity
when solid
poor: ions
cant move/
fixed in lattice
poor: no ions to
conduct and
electrons are
localised (fixed in
place)
diamond and sand:
poor, because
electrons cant move
(localised)
graphite: good as free
delocalised electrons
between layers
good: delocalised electrons can
move through structure
conductivity
when molten
good: ions can
move
poor: no ions
poor
(good)
general
description
crystalline
solids
mostly gases and
liquids
solids
shiny metal
Malleable as the positive ions in
the lattice are all identical. So the
planes of ions can slide easily
over one another
-attractive forces in the lattice are
the same whichever ions are
adjacent
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