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A Level Chemistry CIE
2. Inorganic Chemistry
CONTENTS
2.1 The Periodic Table: Chemical Periodicity
2.1.1 Period 3 Elements: Physical Properties
2.1.2 Period 3 Elements: Structure & Bonding
2.1.3 Period 3 Oxides
2.1.4 Period 3 Oxides & Hydroxides: Acid/Base Behaviour
2.1.5 Period 3 Chlorides
2.1.6 Period 3 Elements: Electronegativity & Bonding
2.1.7 Period 3 Chlorides & Oxides
2.1.8 Chemical Periodicity of Other Elements
2.2 Group 2
2.2.1 Reactions of Group 2 Elements
2.2.2 Reactions of Group 2 Oxides, Hydroxides & Carbonates
2.2.3 Thermal Decomposition of Nitrates & Carbonates
2.2.4 Group 2: Physical & Chemical Trends
2.2.5 Group 2: Trends in Solubility of Hydroxides & Sulfates
2.3 Group 17
2.3.1 Physical Properties of the Group 17 Elements
2.3.2 Chemical Properties: Halogens & Hydrogen Halides
2.3.3 Reactions of the Halide Ions
2.3.4 The Reactions of Chlorine
2.4 Nitrogen & Sulfur
2.4.1 Nitrogen and its Compounds
2.4.2 Nitrogen Oxides
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All elements are arranged in the order of increasing atomic number from left to right
Atomic radius
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The atomic radius is the distance between the nucleus and the outermost electron YOUR NOTES
of an atom
The atomic radius is measured by taking two atoms of the same element,
measuring the distance between their nuclei and then halving this distance
In metals this is also called the metallic radius and in non-metals, the covalent
radius
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The graph shows a decrease in atomic radii of Period 3 elements across the period
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The diagram shows that across Period 3, the elements gain extra electrons in the
same principal quantum shell
Ionic radius
The ionic radius is the distance between the nucleus and the outermost electron of
an ion
Metals produce positively charged ions (cations) whereas nonmetals produce
negatively charged ions (anions)
The cations have lost their valence electrons which causes them to be much
smaller than their parent atoms
Because there are less electrons, this also means that there is less shielding of the
outer electrons
Going across the period from Na+ to Si4+ the ions get smaller due to the
increasing nuclear charge attracting the outer electrons in the second principal
quantum shell nucleus (which has an increasing atomic number)
The anions are larger than their original parent atoms because each atom has
gained one or more electrons in their third principal quantum shell
This increases the repulsion between electrons, while the nuclear charge is still
the same, causing the electron cloud to spread out
Going across P3- to Cl- the ionic radii decreases as the nuclear charge increases
across the period and fewer electrons are gained by the atoms (P gains 3 electrons,
S 2 electrons and Cl 1 electron)
Ionic radii of ions of Period 3 elements table
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Ions of Period 3 elements with increasing positive charge (metals) and increasing of
outer electrons across the period
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The diagram shows the electron configuration of the ions of Period 3 elements and
their relative sizes
Melting point
Melting points of the elements across Period 3 table
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Ions of Period 3 elements with increasing positive charge (metals) and increasing of
outer electrons across the period
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Ions of Period 3 elements with increasing positive charge (metals) and increasing of
outer electrons across the period
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The above trends can be explained by looking at the bonding and structure of the YOUR NOTES
elements
Bonding & structure of the elements table
The table shows that Na, Mg and Al are metallic elements which form positive ions
arranged in a giant lattice in which the ions are held together by a 'sea' of
delocalised electrons around them
Metal cations form a giant lattice held together by electrons that can freely move
around
The electrons in the ‘sea’ of delocalised electrons are those from the valence shell
of the atoms
Na will donate one electron into the ‘sea’ of delocalised electrons, Mg will donate
two and Al three electrons
As a result of this, the metallic bonding in Al is stronger than in Na
This is because the electrostatic forces between a 3+ ion and the larger number of
negatively charged delocalised electrons is much larger compared to a 1+ ion and
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Si has the highest melting point due to its giant molecular structure in which each
Si atom is held to its neighbouring Si atoms by strong covalent bonds
P, S, Cland Ar are non-metallic elements and exist as simple molecules (P4, S8,
Cl2 and Ar as a single atom)
The covalent bonds within the molecules are strong, however, between the
molecules, there are only weak instantaneous dipole-induced dipole forces
It doesn’t take much energy to break these intermolecular forces
Therefore, the melting points decrease going from P to Ar (note that the melting
point of S is higher than that of P as sulphur exists as larger S8 molecules
compared to the smaller P4 molecule)
Electrical conductivity
The electrical conductivity decreases going across the Period 3 elements
Electrical conductivity decreases Period 3 elements table
Going from Na to Al, there is an increase in the number of valence electrons that
are donated to the ‘sea’ of delocalised electrons
Because of this, in Al there are more electrons available to move around through
the structure when it conducts electricity, making Al a better electrical conductor
than Na
Due to the giant molecular structure of Si, there are no delocalised electrons that
can freely move around within the structure
Si is therefore not a good electrical conductor and is classified as a semimetal
(metalloid)
The lack of delocalised electrons is also why P and S cannot conduct electricity
Exam Tip
Intermolecular forces are forces between moleculesIntramolecular forces
are forces within a molecule
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The sodium melts into a ball and moves across the water surface until it YOUR NOTES
disappears
Hydrogen gas is given off
The solution formed is strongly alkaline (pH 14) due to the sodium hydroxide
which is formed
The solution formed is weakly alkaline (pH 11) as the formed magnesium
hydroxide is only slightly soluble
When magnesium is heated, it reacts vigorously with steam (water) to make
magnesium oxide and hydrogen gas:
Mg(s) + H2O(g) → MgO(s) + H2(g)
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The Pauling scale shows the electronegativities of the elements in the periodic table.
Oxygen has a higher electronegativity than any of the Period 3 elements which is why
the Period 3 elements will have positive oxidation states and the oxygen a negative
oxidation state in the oxides of Period 3 elements
The Period 3 elements therefore have positive oxidation states in their oxides and
the oxygen has a negative oxidation state of -2
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Formulae of the oxides of the Period 3 elements & their oxidation states table
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Exam Tip
Since aluminium oxide does not react or dissolve in water, the oxide layer
protects the aluminium metal from corrosion.
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The acidic and basic nature of the Period 3 elements can be explained by looking
at their structure, bonding and the Period 3 elements’ electronegativity
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Structure, bonding & electronegativity of the Period 3 elements table YOUR NOTES
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The oxides of Na and Mg which show purely ionic bonding produce alkaline
solutions with water as their oxide ions (O2-) become hydroxide ions (OH-):
O 2-(aq) + H2O(l) → 2OH-(aq)
The oxides of P and S which show purely covalent bonding produce acidic
solutions with water because when these oxides react with water, they form an
acid which donates H+ ions to water
Eg. SO3 reacts with water as follows:
SO 3(g) + H2O(l) → H2SO 4(aq)
Al and Si are insoluble and when they react with hot, concentrated alkaline
solution they act as a base and form a salt
This behaviour is very typical of a covalently bonded oxide
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Al can also react with acidic solutions to form a salt and water YOUR NOTES
This behaviour is very typical of an ionic bonded metal oxide
This behaviour of Al proves that the chemical bonding in aluminium oxide is not
purely ionic nor covalent: it is amphoteric
Period 3 hydroxide
NaOH is a strong base and will react with acids to form a salt and water:
NaOH(aq) + HCl(aq) → NaCl(aq) + H2O(l)
Exam Tip
Electronegativity is the power of an element to draw the electrons towards
itself in a covalent bond.For example, in Na2O the oxygen will draw the
electrons more strongly towards itself than sodium does.
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The diagram shows water molecules breaking down the giant ionic structure of NaCl
and MgCl2 to form hydrated ions
Aluminium chloride
Aluminium chloride exists in two forms:
AlCl3 as a giant lattice and with ionic bonds
Al2Cl6 as a dimer with covalent bonds
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When water is added to aluminium chloride the dimers are broken down and Al3+
and Cl- ions enter the solution
The highly charged Al3+ ion becomes hydrated and causes a water molecule that is
bonded to the Al3+ to lose an H+ ion which turns the solution acidic
The H+ and the Cl- form hydrogen chloride gas which is given off as white fumes
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The hydrated aluminium causes a water molecule to lose a H+ ion turning the
solution acidic
Silicon chloride
SiCl4 is hydrolysed in water, releasing white fumes of hydrogen chloride gas in a
rapid reaction
The SiO2 is seen as a white precipitate and some of the hydrogen chloride gas
produced dissolves in water to form an acidic solution
Phosphorus(V) chloride
PCl5 also gets hydrolysed in water
PCl5(s) + 4H2O(l) → H3PO 4(aq) + 5HCl(g)
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As the atomic number increases going across the period, there is an increase in YOUR NOTES
nuclear charge
Across the period, there is an increase in the number of valence shells however
the shielding is still the same as each extra electrons enters the same shell
As a result of this, electrons will be more strongly attracted to the nucleus causing
an increase in electronegativity across the period
Bonding & structure of Period 3 elements
The table shows that going from Al to S the bonding changes from metallic to
covalent and the structure changes from giant to simple structure
Na, Mg and Al are metallic elements which form positive ions arranged in a giant
lattice in which the ions are held together by a ‘sea’ of delocalised electrons
around them
Since Al donates three electrons into the sea of delocalised electrons to form an
ion with +3 charge, the electrostatic forces between the electrons and the
aluminium ion will be very strong
The electrons in the ‘sea’ of delocalised electrons are those from the valence shell
of the atoms
Na will donate one electron into the ‘sea’ of delocalised electrons, Mg will donate
two and Al three electrons
As a result of this, the metallic bonding in Al is stronger than in Na
This is because the electrostatic forces between a 3+ ion and the larger number of
negatively charged delocalised electrons are much larger compared to a 1+ ion
and the smaller number of delocalised electrons in Na
Since there are more electrons in a metallic lattice of aluminium compared to
sodium and magnesium, aluminium is a better electrical conductor
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Metal cations form a giant lattice held together by electrons that can freely move
around
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The diagram shows the giant molecular structure of silicon where silicon atoms are YOUR NOTES
held together by strong covalent bonds
Phosphorus, sulfur, chlorine argon re both non-metallic elements that exist as
simple molecules (P4 , S8 , Cl2 and Ar as single atoms)
The covalent bonds within the molecules are strong, however, between the
molecules there are only weak instantaneous dipole-induced dipole forces
It doesn’t take much energy to break these intermolecular forces
The lack of delocalised electrons means that these compounds cannot conduct
electricity
The diagram shows the simple molecular structure of phosphorus with covalent
bonds between the atoms
The diagram shows the simple molecular structure of sulfur with covalent bonds
between the atoms
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The table shows that Na, Mg and Al are metallic elements which form positive ions
arranged in a giant lattice in which the ions are held together by a ‘sea’ of
delocalised electrons around them
The electrons in the ‘sea’ of delocalised electrons are those from the valence shell
of the atoms
Na will donate one electron into the ‘sea’ of delocalised electrons, Mg will donate
two and Al three electrons
As a result of this, the metallic bonding in Al is stronger than in Na
This is because the electrostatic forces between a 3+ ion and the larger number of
negatively charged delocalised electrons is much larger compared to a 1+ ion and
the smaller number of delocalised electrons in Na
Because of this, the melting points increase going from Na to Al
Si has the highest melting point due to its giant molecular structure in which each
Si atom is held to its neighbouring Si atoms by strong covalent bonds
P, S, Cland Ar are non-metallic elements and exist as simple molecules (P4, S8,
Cl2 and Ar as single atom)
The covalent bonds within the molecules are strong, however between the
molecules there are only weak instantaneous dipole-induced dipole forces
It doesn’t take much energy to break these intermolecular forces
Therefore, the melting points decrease going from P to Ar (note that the melting
point of S is higher than that of P as sulphur exists as larger S8 molecules
compared to the smaller P4 molecule)
The presence of a ‘sea’ of delocalised electrons also determines whether the
element is a good conductor or not
Going across the period the electrical conductivity of the elements decreases due
to lack of delocalised electrons
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The electronegativities of the Period 3 elements therefore determines the chemical YOUR NOTES
bonding and structure of their chlorides and oxides
Going across Period 3, their chlorides and oxidised become more covalent and
their structure shifts from a giant ionic to a simple molecular structure
Their reactions with water become more vigorous as a result of this as it becomes
easier to hydrolyse the chlorides and oxides
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The diagram shows a flowchart of how to use the position and/or properties of an
element to make predictions about its behaviour
Answer
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Step 2: ‘The oxide does not dissolve in or react with aqueous sodium hydroxide’ YOUR NOTES
Since aluminium oxide does reaction with sodium hydroxide, element G cannot be
Group 13
Step 3:It forms an oxide which has a melting point of 1610 °C’
This suggests a giant molecular (covalent) structure which corresponds to Group
14
Step 4:Element X cannot be carbon (which is in Group 14) as carbon dioxide is a
gas whereas the element X oxide is a solid (with a melting point of 1610 °C)
Step 5: Element X is therefore a Group 14 element in Period 3 or lower
Note that this is an example of predicting the position of an element based on its
physical and chemical properties
Worked example: Predicting physical and chemical properties of selenium
Answer
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Answer
Answer 1:
Group 1 and 2 chlorides react with water to form colourless solutions of pH 6.5-7
Group 15 chlorides on the other hand react with water to form strong acidic
solutions
Element X therefore belongs to Group 15 of the Periodic Table
Answer 2:
The white fumes that are given off during this reaction is hydrogen chloride gas
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Group 2 reactions with dilute hydrochloric acid & dilute sulfuric acid chemical
equations
The reaction of all metals with oxygen follows the following general equation:
2M(s) + O 2(g) → 2MO(s)
The reaction of all metals with dilute H2SO4 follows the following general equation:
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Exam Tip
Learn the general equation for the reaction with oxygen, water and dilute
HCl/H2SO4 and the exceptions instead of memorizing the entire table!
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Remember that:
oxide + water → hydroxide
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When some of Group 2 metals react with sulfuric acid rather than hydrochloric, an
insoluble sulfate forms
Going down the group, the Group 2 sulfates become less and less soluble
Calcium sulfate is sparingly soluble, but strontium sulfate and barium sulfate
are insoluble
Reactions of Group 2 oxides with acid
Group 2 sulfates also form when a Group 2 oxide is reacted with an acid
The insoluble sulfates form at the surface of the oxide, which means that the
solid oxide beneath it can’t react with the acid
This can be prevented to an extent by using the oxide in powder form and
stirring , in which case neutralisation can take place
Remember that:
oxide + dilute hydrochloric acid → salt + water
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Remember that:
hydroxide + dilute acid → salt + water
Remember that:
carbonate + dilute hydrochloric acid → salt + water + carbon dioxide
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X = Group 2 element
Going down the group, more heat is needed to break down the carbonates
HEAT
MgCO 3 ⎯⎯⎯⎯⎯⎯ MgO + CO 2
Going down Group 2, more heat is needed to break down the carbonate and
nitrate ions
The thermal stability of the Group 2 carbonates and nitrates therefore
increases down the group
The smaller positive ions at the top of the groups will polarise the anions
more than the larger ions at the bottom of the group
The small positive ion attracts the delocalised electrons in the carbonate
ion towards itself
The higher the charge and the smaller the ion the higher the polarising
power
The more polarised they are, the more likely they are to thermally decompose
as the bonds in the carbonate and nitrate ions become weaker
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The graph shows that both the first and second ionization energies decrease going
down the table
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The first ionisation energy is the energy needed to remove the first outer electron YOUR NOTES
of an atom
The second ionisation energy is the energy needed to remove the second outer
electron of an atom
The graph above shows that going down the group, it becomes easier to remove
the outer two electrons of the metals
Though the nuclear charge on the nucleus increases going down the group
(because there are more protons), factors such as an increased shielding effect
and a larger distance between the outermost electrons and nucleus outweigh the
attraction of the higher nuclear charge
As a result of this, the elements become more reactive going down the group as it
gets easier for the atoms to lose two electrons and become 2+ ions
This trend is shown by looking at reactions of the Group 2 metals:
With dilute hydrochloric acid: bubbles of hydrogen gas are given off much
faster indicating that the reactions become more vigorous
With oxygen hydrochloric acid: the metals get more reactive with oxygen down
the group (Ba is so reactive, that it must be stored in oil to prevent it from
reacting with oxygen in air)
Physical trends
Going down the group, the elements become larger as the outer two electrons
occupy a new principal quantum shell which is further away from the nucleus
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The atomic radius of the Group 2 elements increases going down the group due to YOUR NOTES
the addition of an extra principal quantum shell
The graph shows a increase in atomic radius going down the group
The melting point of the elements decreases going down the group as the outer
electrons get further away from the nucleus
This means that the attraction between the nucleus and the bonding electrons
decreases causing a decrease in melting point
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YOUR NOTES
The graph shows a decrease in melting point going down the group
As you go down the group, the density of the alkali earth metals increases
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Answer
Property 1:
The Group 2 oxides and hydroxides have general formula XO and X(OH)2 respectively
where X is the Group 2 element.
Therefore, radium oxide is RaO and radium hydroxide is Ra(OH)2
Property 3:
Radium is below barium so its atomic radius is larger than the atomic radius of barium.
This means that radium’s outermost electrons are even further away and are therefore
even more easily removed than barium’s outermost electron pair.
The first ionization energy is between 450-480 kJ mol-1
Property 4:
Radium’s outermost electrons are even further away than in barium and are therefore
more easily removed making radium more reactive than barium.
Property 5:
The Group 2 hydroxides become more soluble going down the group.
Radium hydroxide will therefore be more soluble than calcium hydroxide.
Property 6:
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The Group 2 sulfates become less soluble going down the group. YOUR NOTES
Radium sulfate will therefore be less soluble than strontium sulfate.
Property 7:
The general equation for the reaction of Group 2 oxides with dilute hydrochloric acid
is:
XO(s) + 2HCl(aq) → XCl2(aq) + H2O(l)
Property 8:
Radium sulfate will be formed in this reaction, however the solubility of Group 2
sulfates decreases going down the group, therefore a white precipitate of radium
sulfate will be formed in this reaction
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The higher the concentration of OH- ions formed, the more alkaline the solution
The alkalinity of the formed solution can therefore be explained by the solubility
of the Group 2 hydroxides
Solubility of the Group 2 hydroxides table
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Going down the group, the solubility of the hydroxides increases which means that
the solutions formed from the reactions of the Group 2 metal oxides and water
become more alkaline going down the group
Group 2 sulfates
The solubility of the Group 2 sulfates decreasing going down the group
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The colours of the Group 17 elements get darker going down the group
Volatility
Volatilityrefers to how easily a substance can evaporate
A volatile substance will have a low melting and boiling point
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The melting & boiling points of the Group 17 elements increase going down the
group which indicates that the elements become less volatile
Going down the group, the boiling point of the elements increases which means
that the volatility of the halogens decreases
This means that fluorine is the most volatile and iodine the least volatile
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A covalent bond is formed by the orbital overlap of two atoms and the attraction of
electrons towards the nuclei; The bigger the atom, the weaker the covalent bond
The bond strength of the halogen molecules therefore decreases going down the
group
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The bond enthalpies decrease indicating that the bond strengths decrease going
down the group
Bond enthalpy is the heat needed to break one mole of a covalent bond
The higher the bond enthalpy, the stronger the bond
An exception to this is fluorine which has a smaller bond enthalpy than chlorine
and bromine
Fluorine is so small that when two atoms of fluorine get together their lone pairs
get so close that they cause significant repulsion counteracting the attracting
between the bonding pair of electrons and two nuclei
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The lone pairs on fluorine get so close to each other in a fluorine molecule that they YOUR NOTES
cause repulsion which decreases the bond strength
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The more electrons there are in a molecule, the greater the instantaneous dipole-
induced dipole forces
Therefore, the larger the molecule the stronger the van der Waals’ forces between
molecules
This is why as you go down the group, it gets more difficult to separate the
molecules and the melting and boiling points increase
As it gets more difficult to separate the molecules, the volatility of the halogens
decreases going down the group
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YOUR NOTES
Going down the group, the van der Waals’ forces increase due to an increased number
of electrons in the molecules which means that the volatility decreases
Exam Tip
Instantaneous induced – induced dipole forces are a type of van der Waals’
forces.
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The halogens’ ability to accept an electron (their oxidising power) therefore YOUR NOTES
decreases going down the group
With increasing atomic size of the halogens (going down the group) their
electronegativity, and therefore oxidising power, decreases
The chlorine has displaced the bromine from solution as it is more reactive
which can be summarised in the following ionic equation:
Cl2(aq) + 2Br-(aq) → 2Cl-(aq) + Br2(aq)
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The thermal stability of the hydrogen halide decreases going down the group as their
bonds become weaker due to the increased atomic radius of the halogens
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The diagram shows that going down the group the ionic radii of the halogens
increases
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YOUR NOTES
The reducing power of the halide ions increases going down the group
Exam Tip
The ionic radius is a measure of the size of an atom’s ion.
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(general equation)
Ag +(aq) + X-(aq) → AgX(s)
(ionic equation)
X- is the halide ion in both equations
If the unknown solution contains halide ions, then a precipitate of the silver
halide will be formed (AgX)
A silver halide precipitate is formed upon addition of silver nitrate solution to halide
ion solution
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YOUR NOTES
Reaction of halide ions with silver nitrate & ammonia solutions table
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YOUR NOTES
(general equation)
Where X- is the halide ion
Reaction of chloride ions with concentrated sulfuric Acid
Concentrated sulfuric acid is dropwise added to sodium chloride crystals to
produce hydrogen chloride gas
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YOUR NOTES
Apparatus set up for the reaction of sodium chloride with concentrated sulfuric acid
The concentrated sulfuric acid oxidises HBr which decomposes into bromine and
hydrogen gas and sulfuric acid itself is reduced to sulfur dioxide gas:
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8HI (g) + H2SO 4 (l) → 4I2 (g) + H2S (s) + 4H2O (l)
Exam Tip
It gets easier to oxidise the hydrogen halides as you descend Group 17: the
halides become stronger reducing agents
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The ionic equation shows that the chlorine gets both oxidised and reduced
Chlorine gets oxidised as there is an increase in ox. no. from 0 to +1 in ClO-(aq)
The half-equation for the oxidation reaction is:
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YOUR NOTES
The ionic equation shows that the chlorine gets both oxidised and reduced
Chlorine gets oxidised as there is an increase in ox. no. from 0 to +5 in ClO3-(aq)
The half-equation for the oxidation reaction is:
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The disproportionation reaction of chlorine with water in which chlorine gets reduced
to HCl and oxidised to HClO
Exam Tip
Adding chlorine to a water supply is an effective way to make the water safe
to drink as it forms the sterilising agent HClO which in turn dissociates in
water into another sterilising agent, ClO-(aq)
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The diagram shows a triple covalent bond between two nitrogen atoms to achieve a
full outer shell of electrons
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YOUR NOTES
Since the electronegativity of the two nitrogen atoms is the same, the will pull the
electrons towards them equally so overall the molecule is nonpolar
Due to the lack of polarity, nitrogen gas is not attracted to or likely to react with
other molecules the way polar molecules would
Exam Tip
Nitrogen is very unreactive due to the lack of polarity and strength of its
triple bond.
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Basicity of ammonia
Ammonia can act as a Brønsted–Lowry base by accepting a proton (H+) using the
lone pair of electrons on the nitrogen atom to form an ammonium ion:
Since the position of the equilibrium lies well over to the left the ammonia solution
is only weakly alkaline
There is a higher concentration of ammonia molecules than hydroxide ions in
solution
Ammonia is therefore a weak base
Structure & formation of ammonium ion
The ammonium ion is formed by an acid-base reaction of ammonia with water:
NH3(aq) + H2O(l) ⇌ NH4+(aq) + OH-(aq)
The nitrogen in ammonia is covalently bonded to three hydrogen atoms and has
one lone pair of electrons causing the ammonia molecule to have a pyramidal
shape
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The nitrogen atom in ammonia uses its lone pair of electrons to form a dative YOUR NOTES
bond with a proton to form the ammonium ion
The ammonium ion has a tetrahedral shape in which all bonds have the same
length
Ammonium chloride (NH4Cl) and calcium hydroxide (Ca(OH)2) are mixed together
and then heated
NH4+ acts as an acid (proton donor) and OH- acts as a base (proton acceptor)
This acid-base reaction can be used to test if an unknown solution contains
ammonium ions
If the unknown solution does contain ammonium ions, it will react with calcium
hydroxide to form ammonia gas
This ammonia gas will turn damp red litmus paper blue
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YOUR NOTES
The diagram shows the apparatus set up for the preparation of ammonia gas from an
ammonium salt and calcium hydroxide
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YOUR NOTES
The diagram shows the formation of PAN from the photochemical reaction between
VOCs and nitrogen oxide
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The air also contains oxygen and tiny droplets of water that make up clouds
The nitrogen(IV) oxide (NO2) dissolves and reacts in water with oxygen as follows:
NO 2(aq) + H2O(l) + 1½O 2(g) → 2HNO 3(aq)
When the clouds rise, the temperature decreases, and the droplets get larger
When the droplet containing dilute nitric acid are heavy enough, they will fall down
as acid rain
The diagram shows the formation of acid rain by the oxidation of nitrogen(IV) oxide
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Nitrogen oxides can directly cause acid rain but can also act as catalysts in the
formation of acid rain
NO2 catalyses the oxidation of SO2 to SO3:
NO 2(g) + SO 2(g) → SO 3(g) + NO(g)
The regenerated NO2 molecule can get again oxidise another SO2 molecule to SO3
which will react with rainwater to form H2SO4
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