Chapter 3 S Block elements Notes
Class :XII Chapter
#03
CHEMISTRY of 'S' BLOCK
Manufacturing Of Sodium By Down's Process
Introduction:
J.C.Down
developed a process of preparing sodium metal by electrolysis of fussed sodium
chloride. This process is called "Down's Process". Electrolysis of
sodium chloride is carried out in Down's cell.
Raw Materials:
Fused
sodium chloride is used as electrolyte in this process. Since sodium chloride
has melting point 801oC, therefore some amount of calcium chloride
is used to lower the melting point of sodium chloride to about 600oC.
Construction
Of Down's Cell:
The
Down's cell is made up of steel lined with fire bricks. The cell has central
graphite anode & a surrounding iron cathode. The two electrodes are
separated by means of iron gauze diaphragm to prevent reaction between chlorine
gas & sodium metal.
2Na
+ Cl2 2NaCl
Liquid
Sodium metal collects in the inverted trough under oil and then tapped off
through iron vessel,
Working Of
Down's Cell:
When
electricity is passed through the molten mixture of sodium chloride and calcium
chloride, Na+ & Cl- move towards their respective
electrodes & form neutral particles.
At
Cathode Na+ + e- Na
At
Anode 2Cl- Cl2 + e-
Some calcium ions are
also reduced into calcium metal at cathode they can easily be separated by
means difference in their densities.
Reactions Of Alkali Metals And Alkaline Earth Metals
Alkali
metals and alkaline earth metals have one and town electrons in their outer
most shell respectively therefore they readily loose their electrons to attain
the stable configuration of Noble gases and hence very reactive and acts as
reducing agent.
Reaction With Hydrogen:
Alkali metals and Alkaline earth metals reacts with hydrogen at 250oC
to form ionic hydrides.
M
+ H2 2MH (M = Alkali metal)
M
+ H2 M2H (M = Ca, Sr, Ba)
Reactions With Nitrogen:
Alkali metals
and Alkaline earth metals react with nitrogen to form nitride except Be.
6M
+ N2 2M3N (M = Alkali metal)
3M + N2 M3N2 (M = Alkaline earth metal except Be)
Reactions With Oxygen:
Alkali
metals and Alkaline earth metals react with oxygen to form variety of compound
like oxide, peroxide and super oxide. The product depends upon the metal and
conditions.
Li
+ O2 2Li2O (Lithium oxide)
2Na
+ O2 Na2O2 (Sodium peroxide)
M
+ O2 MO2 (Super oxides M= K, Rb, Cs)
2M + O2 2MO (Oxides M= Be, Mg, Ca)
M
+ O2 MO2 (Peroxides M = Sr, Ba)
Reactions With Halogens:
Alkali metals
and Alkaline earth metals react with halogens to form halides.
2M + X2 2MX (M = Alkali metal)
M
+ X2 MX2 (M = Alkaline earth metals)
Reaction With Water:
Alkali
metals and Alkaline earth metals react with water violently. They react with
water to form hydrogen gas and an alkali. Be and Mg form a protective coating
of hydrated metal oxide on their surface and are protected form extensive
corrosion.
2M
+ 2H2O 2MOH + H2 (M = Alkali metals)
M
+ H2O M(OH)2
+ H2 (M = Ca, Sr, Ba)
M
+ H2O MO
+ H2 (M = Be, Mg)
Magnesium
reacts with boiling water to form hydrogen gas.
Mg + H2O Mg(OH)2 + H2
Industrial Preparation Of Sodium Carbonate Solvay
Process
Introduction:
Sodium
Carbonate is generally called Soda Ash of washing soda and Sodium bicarbonate
is also known as Baking soda. Ammonia-Solvay process is used for the
preparation of sodium carbonate in industries.
In
1860s Ernest Solvay developed a process for preparation of Sodium Carbonate.
Almost all of the sodium carbonate and sodium bicarbonate produced in the world
is manufactured by Solvay Process.
Raw Materials:
Raw
materials used in this process are as follows.
1.
Sodium chloride (Brine Solution)
2.
Ammonia gas
3.
Lime stone (for producing CO2)
Ammonia-Solvay Process:
This process
consists of three steps.
Step # 01 Ammoniation of Brine
Step # 02 Carbonation of Ammoniated Brine.
Step # 03 Conversion to Na2CO3.
Step # 01 Ammoniation Of Brine:
This
step is carried out in ammoniating tower. In this step saturated solution of
sodium chloride or Brine is further saturated with ammonia, obtained from the
reaction of Ammonium Chloride and Calcium oxide. The brine is allowed to flow
down & ammonia passing up the tower. To ensure the proper saturation of
brine mushroom-shaped baffles plate is used to control the flow of brine.
Step # 02 Carbonation of Ammoniated Brine:
This
step is carried out in Carbonating tower also called "Solvay Tower".
In this tower ammoniated brine trickle down & carbon dioxide, obtained by
thermal decomposition of lime stone, going upward. The baffle plates are used
to control the flow of brine & break up carbon dioxide into small bubbles.
As a result NH4+ and HCO3- are
obtained.
Following reactions take place in Solvay
tower.
NH3
+ CO2 + H2O (NH4+1)2CO3-2
(NH4)2CO3
+ CO2 + H2O NH4HCO3
Na+Cl-
+ (NH4+)HCO3- NH4Cl
+ NaHCO3
The
bicarbonate ions form in a solution that has a high concentration of Na+
ions. Since sodium bicarbonate is slightly soluble in cold solution. These
reaction are exothermic the temperature rises which increases the solubility of
NaHCO3. Therefore lower part of tower is cooled down to increase
precipitation of NaHCO3. NaHCO3 Filtered off by vacuum
filtration.
Step # 03 Conversions to Na2CO3:
In
this step thermal decomposition of NaHCO3 gives anhydrous sodium
carbonate.
2NaHCO3 Na2CO3
+ H2O + CO2
Soda
ash is re-crystallized and yields deca hydrated sodium carbonate (Na2CO3.
10H2O) called "Washing Soda". CO2 obtained is
recycled to the carbonating tower.
Uses:
Sodium
carbonate has extensive uses.
1.
It is used in manufacturing of glass.
Na2CO3
+ SiO2 Na2SiO3
+ CO2
2.
Washing soda is used as water softener.
Ca+2
+ Na2CO3 CaCO3
+ 2Na+
3.
Sodium carbonate is used in preparations of soap, detergents, paper and
other chemicals.
Industrial Preparation Of Sodium Hydroxide
Castner-Kelner Process
Introduction:
Sodium
hydroxide is very important chemical in industries. It is also called Caustic
soda. Sodium hydroxide is prepared by electrolysis of Brine. This process is
called Castner-Kelner Process.
Process:
Castner-Kelner
process consist of two steps.
Step
# 01 Electrolysis of Brine
Step
# 02 Formation of Sodium hydroxide
Step # 01 Electrolysis Of Brine:
Electrolysis
of Brine is carried out in Castner-kelner cell.
Construction Of The Cell:
Castner-Kelner
cell is made up of steel tank. In the cell Titanium block are used as anode.
Flowing mercury is used as cathode to prevent the reaction between hydroxyl ion
and chlorine gas.
6OH-
+ Cl2 ClO3-
+ Cl- + 3H2O
When
electricity is passed through castner kelner cell at Titanium anode chloride
ions are oxidized to form chlorine gas.
2Cl- Cl2 + 2e-
At
flowing mercury cathode Na+ ions discharged to form sodium metal.
This sodium metal dissolved in mercury to form amalgam.
Na+
+ e- Na
Na
+ Hg Na/Hg
H+
ions in brine solution also attracted towards mercury but due to high voltage
of H+ ions on mercury surface, sodium ions are more easily
discharged on mercury surface.
Step # 02 Formation Of Sodium Hydroxide:
In
2nd step mercury containing sodium metal is taken to DENUDER. In
denuder sodium metal reacts with water to form sodium hydroxide and hydrogen
gas.
2Na/Hg
+ 2H2O 2NaOH + H2
+ Hg
In
denuder graphite blocks are used to control the flow of flowing mercury.
Disadvantages
Of The Process:
1.
This process consumes large quantity of electricity.
2.
Some mercury vapors may escape from the factory and contaminates sea
water, resulting in pollution of food chain.
Physical
Properties:
Physical
properties of sodium hydroxide are as follows.
1.
It is a white solid.
2.
It is deliquescent. (absorbs moisture from atmosphere and forms
solution)
3.
It melting point is 322oC with decomposition.
4.
It is highly soluble in water and evolves large quantity of heat when
it is dissolved.
Chemical
Properties:
Chemical
properties of sodium hydroxide are as follows.
1.
As An Alkali:
Sodium hydroxide
is a strong alkali and ionizes fully in its aqueous solutions. It neutralizes
acids to form salt and water.
Na+OH-
+ H+Cl- Na+Cl- + H2O
2.
Reaction With Ammonium Salts:
Sodium hydroxide
reacts with ammonium salts on warning and liberates ammonia.
NaOH
+ NH4Cl NH4+OH-
+ NaCl
3.
Reaction With Metal Ions:
It reacts with metal
ions and forms precipitate of insoluble metal hydroxides.
Fe+3
+ 3OH- Fe(OH)3
When precipitated hydroxides
are amphoteric, then they re-dissolve in excess of sodium hydroxide forming
complex.
Zn+2 + 2OH- Zn(OH)2
Zn(OH)2
+ 2OH- [Zn(OH)4]-2
Uses:
Sodium
hydroxide has following uses.
1.
It is used in preparation of phosphine, sodium chlorate(v)
2.
It is used in soap, rayon and paper.
3.
It is used to open drains due to its dissolving and caustic effects.
4.
It is used in textile for bleaching and dyeing processes.
5.
It is used in refining of petroleum.
6.
Its solution gives silky finish to mercerized cotton.
7.
It is used in laboratory as an alkali and for absorbing carbon dioxide.
Magnesium
Sulphate
Magnesium
sulphate occurs in nature as Kieserite (MgSO4. H2O). The
hepta hydrated magnesium sulphate (MgSO4. 7H2O) is
called EPSOM.
Preparation:
Magnesium
sulphate is prepared by the reaction of sulphuric acid on magnesium metal, its
oxide, hydrosice or carbonates.
Mg
+ H2SO4 MgSO4
+ H2
MgO
+ H2SO4 MgSO4
+ H2O
Mg(OH)2
+ H2SO4 MgSO4
+ 2H2O
MgCO3
+ H2SO4 MgSO4
+ H2O + CO2
Properties:
Magnesium
sulphate has following properties.
1.
Magnesium sulphate is a white crystalline solid.
2.
It is soluble in water.
3.
It loses its water molecules at 200oC to form anhydrous
magnesium sulphate.
MgSO4.
7H2O MgSO4
+ 7H2O
Uses:
Magnesium
sulphate has following uses.
1.
It is used in manufacturing of ceramics, paper, soap and cement.
2.
It is used as purgative in medicines.
Caustic Soda
Calcium Sulphate
Calcium
sulphate occurs in nature as dehydrate (CaSO4. 2H2O)
called GYPSUM.
Preparation:
Gypsum
can be prepared by the reaction dilute sulphuric acid with calcium carbonate or
chloride.
CaCO3
+ H2SO4 CaSO4
+ CO2 + H2O
CaCl2
+ H2SO4 CaSO4
+ 2HCl
Properties:
Calcium
sulphate has following properties.
1.
It is sparingly soluble in water, producing permanent hardness in
water.
2.
At 100oC gypsum is converted to hemi hydrated calcium
sulphate, which is called Plaster of Paris.
CaSO4.
2H2O (CaSO4)2
H2O + 2H2O
3.
At 200oC gypsum forms anhydrous calcium sulphate.
CaSO4.
2H2O CaSO4
+ 2H2O
Uses:
Calcium
sulphate has following uses.
1.
It is used in making of black board chalk.
2.
It is used as fertilizer for saline soil.
3.
It is used for filling and glazing of paper.
Bleaching Powder
Prof.
Odling suggested the formula of bleaching powder Ca(OCl)Cl with the help of
percentage composition of chlorine.
Preparation:
Bleaching
powder is prepared by Hasen clever process. In this process chlorine gas reacts
with slaked lime to form bleaching powder.
Ca(OH)2
+ Cl2 CaOCl2
+ H2O
Properties:
Bleaching
powder has following properties.
1.
It is a white amorphous solid with smell of chlorine gas.
2.
It dissolves in water and form chlorine gas.
CaOCl2 + H2O Ca(OH)2 +
Cl2
3.
It reacts with CO2 in the presence of moisture and form
hypochlorous acid which is responsible for bleaching action of Bleaching
powder.
CaOCl2
+ CO2 + H2O CaCO3
+ CaCl2 + 2HOCl
HOCl HCl + [O]
4.
It reacts with acid and librates chlorine gas.
CaOCl2
+ 2HCl CaCl2 + H2O + Cl2
Uses:
Bleaching
powder has following uses.
1.
It is used for bleaching of cotton, linen and paper pulp.
2.
It is used for sterilization of drinking water.
3.
It is used for the preparation of chloroform.
Sodium Chloride
Occurance:
Sodium
chloride is also known as common salt or table salt. It occurs as Rock salt.
Large deposits of rock salt are found in Pakistan at Khewra. It also occurs
in sea water to the extent of about 3%. The salt is mined as solid or pumped
from under ground deposit as a saturated solution known as Brine.
Purification:
In
tropical regions, sodium chloride is obtained by the solar evaporation of sea
water; the impurities such as calcium and magnesium are removed by treating sea
water with sodium carbonate and sodium hydroxide to precipitate these metals.
Ca+2Cl2-(aq)
+ Na+2CO3-2(aq) CaCO3
+ 2Na+Cl-(aq)
Mg+2Cl2-(aq)
+ 2Na+OH-(aq) Mg(OH)2 + 2Na+Cl-(aq)
This
purified product is fit for industrial use but requires further purification
for its use as table salt.
Uses:
Sodium
chloride has following uses.
1.
It is an essential part of our daily life.
2.
It is used as food preservative.
3.
In chemical industry it is used in the manufacture of sodium metal,
chlorine gas, sodium hydroxide, sodium carbonate, sodium hypochlorite (I),
sodium chlorate(V).
4.
It is used in glazing earthen ware.
5.
It is used in regeneration of water softener.
6.
It is used in salting out of soap.
Reasons
1)
Lithium and Beryllium markedly differ from other member of their
family.
Reason:
Due to their small atomic
size, charge density of Li+ ion and Be++ ions are higher
than their group members. These high charge densities result strong polarizing
effect and high heats of hydration.
2)
First ionization enthalpies of Alkali metals and Alkaline earth metals
are generally low. However, ionization enthalpies of IIA elements are higher
than IA group elements.
Reason:
Alkali metal and Alkaline
earth metals have one and two electrons in their valence orbits respectively.
They loose their valence electrons to have the stable configuration of
preceding noble gas. Hence 1st ionization enthalpies of IA and IIA group
elements are generally low.
Since each Alkaline earth
metal has one extra proton than corresponding alkali metal. This higher nuclear
charge attracts electrons more strongly; hence increase the ionization
enthalpies of IIA group.
3)
Ionization potential decreases Lithium to Cesium.
Reason:
Down the group from Lithium
to Cesium, atomic size increases due to increasing number of orbits. Therefore
valence electrons, in heavier atoms of IA group, are loosely attracted by
nucleus and hence low ionization energy is required to remove valence
electrons.
4)
Alkali metals have larges covalent radii.
Reason:
Alkali metals have smallest
nuclear charge in their respective periods and force of attraction of nucleus
on valence electrons is weakest. Therefore they have largest covalent radii.
5)
Alkali metals and Alkaline earth metals easily form cations.
Reason:
Alkali metals and Alkaline
earth metal, having large atomic size and low ionization potential, easily lose
their valence electrons to attain the electronic configuration of preceding
noble gas and form cations of +1 and +2 charges respectively.
K K+ + e-
[Ar] 4s1 [Ar]
Ca Ca+ + e-
[Ar] 4s2 [Ar]
4s1
Ca+ Ca++ + e-
[Ar] 4s1 [Ar]
6)
Na+ ions are smaller than sodium atom.
Reason:
Sodium like other alkali
metals looses its valence electron, forming Na+ ion, to attain
stable electronic configuration of Neon. After removal of electrons third orbit
is empty and in Na+ ion number of protons exceeds number of
electrons. Therefore strong hold of nucleus over electrons causes decrease in
size of sodium ion than sodium atom.
7)
Alkaline earth metal ions are more strongly hydrated than alkali metal
ions.
Reason:
Hydration of ions depends
upon charge density and ionic radii. Due to small ionic radii and more positive
charge on ions of group IIA, strong electric field is produced around these
ions. Therefore Alkaline earth metal ions are more strongly hydrated than
Alkali metal ions.
8)
Li+ ions are more readily hydrated than K+ ions.
Reason:
Hydration depends upon
charge density of the ion Lithium with small ionic radii, has high chare
density as compared to K+ ion. Therefore Li+ ions are
more readily hydrated than potassium ion.
9)
Alkali metals are powerful reducing agent.
Reason:
Substances having tendency
to loose electrons are called reducing agent. Alkali metal wit their largest
size and low ionization potential values, can easily loose their electrons.
M M+ + e-
(M= Li, Na, K, Rb, Cs)
Therefore Alkali metals are
powerful reducing agent.
10) Li+/Li couple has
exceptionally high negative electrode potential.
Reason:
Substances, having tendency
to loose electrons, have highly negative values of standard electrode
potential. Li+/Li couple has very high negative electrode potential
value because high value of heat of hydration for Lithium eases the oxidation
of Li and Li+.
11) Alkali metal can not be used
in voltaic cells.
Reason:
High negative values of
standard electrode potential of Alkali metals indicate ease of oxidation. Since
in voltaic cells water is used as solvent and Alkali metals are readily
oxidized in water. Therefore they can not be used in voltaic cells.
12) Alkaline earth metals are
harder than Alkali metals.
Reason:
Alkali metals and Alkaline
earth metals form positively charged M+ and M++ ions
respectively. Due to the greater charge attraction of metal ions and electron
gas of Alkaline earth metal crystal, they are much harder than Alkali metals.
13) In manufacturing of Sodium,
the two electrodes are separated by Iron-gauze diaphragm.
Reason:
In manufacturing of Sodium,
Sodium deposits on cathode in molten state and Chlorine gas is obtained on
anode. Iron diaphragm is used to separate cathode from anode to prevent
reaction between molten sodium and chlorine gas.
2Na
+ Cl2 2NaCl
14) Alkali metals are highly
reactive.
Reason:
Since all Alkali metals have
one electron in their valence shell. They have great tendency to loose their
electron to attain electronic configuration of preceding noble gas. Therefore
Alkali metals are highly reactive.
15) Na+ ions are
discharged at cathode in preference to H+ ion in the manufacturing
of Sodium hydroxide.
Reason:
In the manufacturing of
NaOH, Na+ ions are more easily deposited on mercury cathode.
Na+
+ e- Na
Na
+ Hg Na/Hg
Due to high voltage of H+
ion on the surface of mercury, Na+ ions are more easily deposited on
mercury cathode.
16) How the given reaction is
avoided during preparation of Sodium hydroxide.
6OH- + Cl2 ClO3-
+ Cl- + 3H2O
Reason:
In the preparation of NaOH,
NaOH obtained on cathode and Chlorine gas on anode. To prevent above reaction
floating mercury is used as cathode.
17) Zinc hydroxide is soluble in
excess of Sodium hydroxide.
Reason:
If NaOH in excess reacts
with insoluble Zinc hydroxide as a result complex compound
Tetrahydroxozincate(II) ion is formed which is soluble in water.
Zn(OH)2
+ 2OH- [Zn(OH)4]-
Tetrahydroxozincate(II)
18) Plaster of Paris is used in
making plaster coats and moulds.
Reason:
Plaster of Paris when mixed
with water sets with expansion in few minutes. This setting with expansion
property helps in use of Plaster of Paris in plaster coats and moulds.
Group Trends
Atomic Radii OR Atomic Size:
It may be defined as,
“The distance between
the outer electrons and nucleus is called Atomic radii or Atomic size.”
Atomic size is measured by diffraction of x-rays through substance in
solid state. It is measured in Ao (Angstrom).
1Ao
= 10-10 m = 10-8 cm
Factors Affecting Atomic
Size:
There are three
factors which may affect the atomic size.
1)
Number of Shell:
Increase in number of shell
will increase distance between outer electrons and nucleus (Atomic size).
Therefore down in a group atomic size increases due to increase in number of
shell in an atom. Greater increase in atomic size occurs due to increase in
number of shell.
2)
Nuclear Charge:
Due to increase in nuclear
charge the attraction between outer electrons and nucleus is increased, which
will cause a decrease in atomic size. Therefore atomic size decreases across in
a period with increasing nuclear charge. Small variation in atomic size of
elements occurs due to variation in their nuclear charge.
3)
Screening Effect of
Shielding Effect:
Electrons in inner shells
will tend to shield electrons in outer most shell from nucleus therefore
effective nuclear charge is less than actual nuclear charge; this effect of
inner electrons is called Screening or Shielding effect.
Shielding effect of inner
electrons will weaken the force of attraction between outer electrons and
nucleus therefore increases due to increase in inner electrons therefore atomic
size increases down in a group.
Ionization Potential
Definition:
It may be defined as,
"The minimum amount
of energy required to remove one mole of electrons from one mole of gaseous
atoms of the element to from one mole of gaseous cations is called Ionization
Potential."
Ionization potential is the measure
of strength of electrostatic attractions between nucleus and outer electrons.
Ionization potential is measured in KJ/mole.
When first electron is removed from
the atom the energy required is called 1st I.P.
When electron is removed form singly
charged cation then the amount of energy is called 2nd I.P.
Factors Affecting Ionization Potential:
There are three factors on which
ionization potential of elements.
1) Atomic Size:
Increase in atomic size of elements will cause
increase in distance between the nucleus and outer electrons. This wills weak
the force of attraction and therefore removal of outer electrons becomes easier
and ionization potential decreases. Down in a group ionization potential
decreases with increasing atomic size. Hence element at the top of each group
has highest value of I.P. and element at the bottom has least value.
2) Nuclear Charge:
Increase in nuclear charge will cause stronger
attraction between nucleus and outer electrons therefore ionization potential
increases with increasing nuclear charge across in a period. Hence element at
the left most in periodic table has least value of I.P. and element at the
right most in periodic table has highest value of I.P.
3) Screening Effect OR Shield Effect:
Electrons in inner shells will tend to shield
electrons in outer most shell from nucleus therefore effective nuclear charge
is less than actual nuclear charge; this effect of inner electrons is called
Screening or Shielding Effect.
Shielding effect of inner electrons will weaken the force
of attraction between outer electrons and nucleus therefore increase in
shielding effect decreases ionization potential. Down in a group shielding
effect increases due to increase in inner electrons therefore ionization potential
decreases down in a group.
Electro-Negativity
Definition:
"The
ability of an atom to attract shared pair of electrons to itself is called
Electro-negativity."
Electro-negativity depends upon the electrostatic attraction between outer
electrons and nucleus.
Factors
Affecting Electro-Negativity:
Electro-Negativity
depends upon following factors.
1. Atomic Size:
Increase in
atomic size of elements will cause increase in distance between the nucleus and
outer electrons. This wills weak the force of attraction and as result electro
negativity decreases. Down in a group electro negativity decreases with
increasing atomic size. Hence element on the top of each group has highest and
element at the bottom has lowest electro negativity.
2. Nuclear Charge:
Increase in
nuclear charge will cause stronger attraction between nucleus and outer
electrons therefore electro negativity increases with increasing nuclear charge
across in a period. Hence element at left most of the periodic table has least
value of electro negativity in that period and element at the right most has
highest value.
Heat Of Hydration
Definition:
"The
process in which water molecules surround other substance is called
Hydration."
"The
amount of heat released during hydration is called Heat of Hydration."
The
heat of hydration depends upon the charge density of the ions present. More the
charge density more will be the attraction of ions with water molecules,
therefore ions having more charge density has more heat of hydration.
Charge
density of the ion depends upon the size of charge and volume of ions, since
alkaline earth metal ions have more charge and less volume than alkali metal
ions therefore alkaline earth metal ions more easily hydrated than alkali
metal.
Electrode Potential
Definition:
"The
potential difference between metal and its salt solution is called Electrode
potential."
Electrode
potential is the measure of the conversion of metal and its ion. Ease of
conversion causes high electrode potential.
Alkali
metals and alkaline earth metals are strong reducing agent. The values of
electrode potentials are used to predict the ease of conversion of metal into
its ion. Electrode potentials of these metals are more negative because these
metals undergo oxidation very easily.
Electrode
potential of Lithium couple (Li+/Li) has exceptionally high value of
electrode potential because Lithium has very value of heat of hydration which
promotes the oxidation of Lithium into its ion.
The
electrode potential decreases down the group due to increase in atomic size.
The increase in atomic size will decrease ionization potential, due to which
metal are easily into their ions.
Density,
Melting Point & Boiling Point:
Density,
melting point and boiling point of a substance depends upon inter molecular
attractions between their particles. Stronger the attractions more will be the
density, melting point and boiling point.
Density of elements in
a group increases down in a group with increasing inter atomic attraction
between their atoms in the crystal. Therefore element at the top of each group
has least density and element at the bottom has highest density.
Alkaline
earth metals are denser than alkali metals due to the presence of M+2
ions in their structure which causes greater inter atomic attraction.
Melting
and boiling point also depends upon inter atomic attractions. Down in a group
melting and boiling point decreases due to decrease in inter atomic attraction.
Melting
and boiling point of alkaline earth metals are more than alkali metals because
alkaline earth metals have more inter atomic attractions than alkali metals.
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