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The document discusses the properties and reactions of Group 2 elements in the Periodic Table, including their electronic configurations, metallic radii, melting points, and densities. It explains the trends in reactivity, ionization energies, and the formation of ionic compounds, as well as their reactions with oxygen, water, and dilute acids. Additionally, it covers the thermal decomposition of carbonates and nitrates, and the industrial uses of Group 2 compounds such as calcium carbonate in cement production.
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Cambridge International AS Level Chemist
oy
‘The elements in Group 2 of the Periodic Table are
sometimes referred to as the As
they are in Group 2, the elements have atoms whose
electronic configurations end with two electrons in their
outermost principal quantum shell. These two outer
electrons occupy an ssubshell. Here are the electronic
configurations ofthe first five elements in Group 2:
Beryllium (Be) 1s°25*
Magnesium (Mg) 1s#2s'2p%3s?
Calcium (Ca) 1s#2s*2p®3s23p%4s?
Strontium (St) 1s22s?2p%3s*3p%3d?4s"4p%5s?
Barium (Ba) 1s!2s!2p®3st3p%3d!4s'apd!"5°5p%6e
One way of describing the size of an atom is its
metallic radius, The metallic radius is half the distance
between the nuclei in a giant metallic lattice (Figure 11.2).
See page 149 for other measures that describe the size
ofatoms.
Figure 11.2 The metallic radius gives us a measure of the size
of the atoms of metallic elements.
Look at the metallic radi of the Group 2 elements, shown
in Table 1.1, The atoms of Group 2 elements get larger
going down the group as the outer two electrons occupy a
new principal quantum shel further from the nucleus.
oun! ee ea
berylium (Be) 0122
magnesium (Mg 0.160
calcium (Ca) 0197
strontium (5 ozs
barium (Ba) 027
Table 11.1 The metallic radii of the Group 2 elements.
‘There are also general trends in other physical properties,
such as melting point and density, shown in Table 11.2 and
Figures 11.3 and 11.4
ees Atomic | Melting | Density
Sood number | point /*c | / gem?
beryllium (Be)
magnesium (Mg 2 650 174
calcium (Ca) 2 838 155
strontium (S4 38 768 26
barium (Ba) 56 m4 35
Table 11.2 The melting points and densities of the
Group 2 elements.Caceres)
ea
= 1000
£
2
500
o4 2 2% 38 36
Be Mg se Ba
‘Momic number
Figure 11.3 Melting points of the Group 2elements,
‘
as
e
2
31
o
of 2 » 2 3
fe My s ta
Aomicrumber
Figure 11.4 Densities of the Group 2 elements.
Cron
1a Lookat Figure1.3
1 Whatis the general tend in the melting points
going down Group 2?
Which element breaks the trend?
'b Explain why the atomsin Group2, asin any other
group, get larger with increasing atomic number.
‘€ Would you expect the2+ ions of Group 2 elements
tobe larger or smaller than their atoms? Explain
yyouranswer.
d_ Radium (Ra) isa radioactive element found below
barium atthe bottom of Group 2. Predict:
i itsmatting point
i itsdensity
Ii its metallicradius.
Reactions of Group 2 elements
‘The Group 2 metals form ionic compounds. When they
react, their atoms lose the two electrons from their
outermost s subshell and form an ion with the stable
electronic configuration of a noble gas. This creates a 2+
ion. For example, in the ionisation ofa magnesium atom
to a magnesium ion:
Mg —> Mg? + 2"
callonnumier
‘The metals act as reducing agents. Their atoms give away
electrons and so they are oxidised themselves as they react
to form their 2+ ions. The ionisation energies shown in
‘Table 11.3 show how easily the two outer electrons are
removed from the Group 2 atoms.
Corry we
element energy /kJmot | energy /kJmot
beryllium (Be) 900 1760
‘magnesium (Mg) 736 1450
calcium (Ca) 590 1150
strontium (Sr) 548 1060
barium (Ba 502 966
Table 11.3 The first and second ionisation energies of the
Group 2 elements.
‘The metals in Group [Link] more reactive as we go down the
‘group. As you can see from Table 11.3 it takes less energy
(eit gets easier) to remove the pair of outer electrons
going down Group 2, So, although the positive charge
con the nucleus increases down the group, the greater
shielding effect provided by extra inner shells of electrons
and the larger distance of the outermost electrons from
the nucleus outweigh the attraction of the higher nuclear
charge. This helps to explain the increase in reactivity
going down the group, as it gets easier for the atoms to
form their 2+ ions.Cambridge International AS Level Chemist
eae neko
‘The Group 2 metals burn in air, and more rapidly in
‘oxygen, forming white solid oxides. For example,
‘magnesium ribbon burns with a bright white flame
once ignited in a Bunsen flame (Figure 11.5}
2Mg{s) + 0,(¢) —> 2MgO(s)
Figure 11.5 Magnesium ribbon reacting with oxygen
inthe air.
‘The magnesium oxide formed is basic in character, as
shown on page 156. Calcium oxide, CaO, reacts with
water to form calcium hydroxide. If water is dripped.
‘onto the surface of a lump of calcium oxide it causes
a vigorous reaction. It gives off so much heat that
some of the water boils offs the solid lump appears
to expand and cracks open:
Ca0(s) + H,0(l) —> Ca(OH), (3)
In excess water, some of the slightly soluble calcium
hydroxide dissolves to form a weakly alkaline
solution, The excess aqueous hydroxide ions in the
solution resultin its pH of 11:
a(oH),(s) "> ca*(aq) + 204-(aq)
In general, the reaction and dissolving of the Group 2
metal oxides in water is described by the following
ionic equation:
(5) + H,0(l) —> 20H (aq)
‘The Group 2 metals get more reactive with oxygen
going down the group. The larger atoms lose their
outer two electrons more readily than the smaller
atoms in the group. The reasons for this are given
beneath Table 11.3,
‘The greater reactivity of barium metal is llustrated
by the fact that it must be stored under oil to keep it
out of contact with air.
‘Some of the Group 2 metals burn with characteristic
flame colours. Itis the 2+ ions formed in the
reaction that cause the colours. We can test for
calcium, strontium and barium in compounds
using flame tests. A nichrome wire, cleaned with
concentrated hydrochloric acid, is dipped into a
sample of the salt to be tested and heated in a non-
luminous Bunsen flame:
calcium compounds give a brick-reé colour
strontium compounds give ascarlet/red colour
barium compounds give an apple-green colour.
ee nha)
We have seen on page 155 how magnesium reacts
very slowly with cold water but will eventually form a
weakly alkaline solution:
Mg(s) + 2H,0() —> Mg(OH),(aq) + H,(e)
Hot magnesium does react vigorously with water in
‘the form of steam to make magnesium oxide and
hydrogen gas (Figure 11.6):
Mg(s) + H,O(g) —> MgO(s) + H,(e)Caceres)
fee int ut cenun ls
Figure 11.6 An experiment showing magnesium reacting with steam, The steam is given off from mineral wool soaked
in water at the right-hand end ofthe test tube. The white magnesium oxide formed is visible inside the test tube and the
hydrogen gas produced in the reaction has been ignited at the end of the straight tube.
Calcium reacts more readily than magnesium with
water:
Ca(s) + 2H,0(l) —> Ca(OH),(aq) + H,(e)
This reaction forms a cloudy white suspension of
slightly soluble calcium hydroxide, The calcium
hydroxide that does dissolve makes the solution
weakly alkaline. The hydrogen gasis given off at a
steady rate. Going down the group, hydrogen gasis
released more and more rapidly by the reaction of
the element with water (Figure 11.7)
“The resulting solutions also get more alkaline going down the
‘group. We can explain this by looking at the solubility of
the hydroxides formed (see Table 11.4). Their solubility
Increases on going down Group 2. Therefore when adding
and stirring magnesium hydroxide in water to make a
saturated solution, then doing the same with barium
hydroxide and water, there will be a higher concentration
‘of hydroxide ions in the case of the saturated barium
hydroxide solution. This results in a higher pH value for
the barium hydroxide solution.
Gaeeues
Figure 11.7 Barium reacting vigorously with water.
Not all Group 2 compounds get more soluble on
descending the group. For example, their sulfates become
less soluble - so barium sulfate is much less soluble
than magnesium sulfate. (Infact the test for sulfate ions,
depends on the formation of a white precipitate of barium
sulfate, produced when barium chloride solution is added
toa solution of the compound being tested.)
You can read more about the reasons why the
Group 2 sulfates get less soluble going down the group on
page 267
magnesium hydroxide, MeOH)
calcium hydroxide, C
(OH),
strontium hydroxide, S(O),
barium hydroxide, BalOH), 15x10?
Table 11.4 Solubility of the Group 2 hydroxides in water,eae aed Res
Poy
Tae
2. a Writea balanced chemical equation, including
state symbols, forthe reaction of
strontium with oxygen
strontium oxide with water
Write a balanced chemical equation, including
state symbols, forthe reaction of barium
with water.
Predict the pH of the solution formed in
partbi.
‘€ Radium (Ra} isa radioactive element found below
barium atthe bottom of Group 2. Predict:
1 the formula ofits ion
the formula ofits oxide and hydroxide
itsfirstionisation energy
its reactivity compared with barium
the relative pH ofits saturated hydroxide
solution compared with a saturated solution
of calcium hydroxide
vi the solubility ofits sulfate compared with
strontium sulfate.
Using Table 114 and the relative atomic mass
data on page 473, calculate the mass of calcium
hydroxide that will dissolve in 50g of water at 298K.
Reaction of Group 2 carbonates with
water and with dilute acids
The carbonates of magnesium, calcium, strontium and
barium are al insoluble in water. However, they all react
in dilute aci, forming a salt and water and giving off
carbon dioxide gas. For example, with dilute sulfuric acid
MgCO,() + H,SO aq) —> Mg8O,(ag) + H,00)
+ CO,(g)
‘The magnesium sulfate salt formed in the reaction above
is soluble in water so remains in aqueous solution, and no
solid will remain in excess dilute sulfuric acid, However,
the sulfates ofthe other Group 2 elements tend to form an
insoluble sulfate layer on the carbonate, preventing further
reaction after the intial effervescence of carbon dioxide
gas is seen.
With dilute nitric acd, all the nitrate sats formed are
soluble in water, For example:
CaCO,(9) + 2HNO (aq)
> Ca(NO)),(ag) + H,00) + COs)
‘The reactions with dilute hydrochloric acid also form
soluble salts, the chlorides. For example:
BaCO,(9) + 2HCKaq) —> BaCl, (ag) + H,0() + CO,(g)
Thermal decomposition of
Group 2 carbonates and nitrates
‘The carbonates and nitrates ofthe Group 2 elements
decompose when heated. The carbonates break down to
form the metal oxide and give off carbon dioxide gas.
For example:
MgCo,(9) “S Mgow) + Cog)
“The temperature at which thermal decomposition takes
place increases going down Group 2.
“The Group 2 nitrates also undergo thermal
decomposition. For example:
2Ca(NO,)(6) ““ 2Ca06) + 4NO,{g) + 0,18)
A brown gas s observed when a Group 2 nitrate is heated. This
is toxic nitrogen dioxide, NO, (nitrogen(IV) oxide).
As with the carbonates, a higher temperature is needed
to thermally decompose the nitrates as Group 2
is descended.
You can read an explanation of the trend in the
thermal stability ofthe Group 2 carbonates and nitrates,
‘on page 264.
CEs
3. a Writea balanced symbol equation for the reaction
‘of barium carbonate with dilute nitric acid,
b_ Which one ofthe three compounds listed will
decompose at the lowest temperature?
1 calcium carbonate, strontium carbonate,
barium carbonate
barium nitrate, calcium nitrate, magnesium
nitrate
€ Writea balanced chemical equation, including
state symbols, forthe thermal decomposition of:
i strontium carbonate
barium nitrate,Caceres)
Some uses of Group 2
compounds
We have just seen how the Group 2 carbonates decompose
‘on heating. Limestone is made up mainly of caleium
carbonate. There are many types of limestone, which
provide useful rocks for building. They can be shaped
into blocks that can be stuck to each other using mortar.
Previously this mortar was made using lime and sand.
‘Now it is more usual to use cement and sand, although the
‘cement is made from lime see below. Marble is another
form of calcium carbonate used as a building material, for
‘example to make expensive tiles.
However, most calcium carbonate is used to make
‘cement. The first stage in the manufacture of cement isthe
roasting of limestone in alime kiln (Figure 11.8).
At the high temperatures in the kiln, calcium carbonate
decomposes to form calcium oxide (also alld lime
‘or quicklime):
€aC0,9) > caw + €0,(g)
‘The calcium oxide made in the lime kiln goes on to be
roasted with clay to make cement. Cement can be mixed.
with sand and small pieces of rock to make concrete, the
most widely used building material in the world. Its tensile
strength can be improved by letting the concrete set with
iron rods running through it 5
Slaked lime (calcium hydroxide, Ca(OH), is also Figure 11.8 navotatngtin ly, caletum carbonate
used by farmers to raise the pH of acidic soil. Caleium
Lndergoes thermal decomposition to form calcium oxide and
hydroxide is basic, soit will react with and neutralise acid, pron dioxide i
raising the pH of the soil
4 a Howis limestone turned intolimein industry?
b_ Which major construction materials are made
from cement?
‘© Both calcium carbonate and magnesium oxide
hhave giant ionic structures. Why is magnesium
‘oxide used to line furnaces but calcium carbonate
isnot?
4d When lightning strikes during a thunderstorm,
the rain that fallsisa dilute solution of ritric
‘acid (HNO,), Use a balanced chemical equation,
including state symbols, to show how slaked lime
{calcium hydroxide) added to soil can neutralise
nitric adi.