S-Block Elements By- Manas Mahajan ALKALI METALS.
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Transcript of S-Block Elements By- Manas Mahajan ALKALI METALS.
S-Block Elements
By- Manas Mahajan
ALKALI METALS
Chapter summary
• Introduction• Characteristic properties of the s-block
elements .• Variation in properties of the s-block
elementsof the First Group(Alkali Metals). • Physical Properties
Members of the s-Block Elements
Li Be
Na
K
Rb
Cs
Fr
Mg
Ca
Sr
Ra
Ba
IA IIA
IA Alkali metals
IIA Alkaline Earth metals
Characteristic properties of s-block elements
• Metallic character• Low electronegativity• Basic oxides, hydroxides• Ionic bond with fixed oxidation states• Characteristic flame colours• Weak tendency to from complex
Metallic character
• High tendency to lose e- to form positive ions
• Metallic character increases down both groups
Electronegativity
• Low nuclear attraction for outer electrons
• Highly electropositive
• Small electronegativity
Group I Group II
Li 1.0 Be 1.5
Na 0.9 Mg 1.2
K 0.8 Ca 1.0
Rb 0.8 Sr 1.0
Cs 0.7 Ba 0.9
Fr 0.7 Ra 0.9
Characteristic flame colours
Na+ Cl- (g) Na (g) + Cl (g)Na(g) Na* (g)[Ne]3s1 [Ne]3p1
Na*(g) Na(g) + h (589nm, yellow)
Flame test
HCl(aq) sample
Li deep redNa yellowK lilacRb bluish redCs blue
Ca brick redSr blood redBa apple green
Variation in properties of elements
• Atomic radii• Ionization enthalpies• Hydration enthalpies• Melting points• Reactions with oxygen, water, hydrogen and
chlorine
Atomic radii (nm)Li 0.152 Be 0.112
Na 0.186 Mg 0.160
K 0.231 Ca 0.197
Rb 0.244 Sr 0.215
Cs 0.262 Ba 0.217
Fr 0.270 Ra 0.220
Li
Fr
Be
Ra
Ionization EnthapyGroup I 1st I.E. 2nd I.E.
Li 519 7300
Na 494 4560
K 418 3070
Rb 402 2370
Cs 376 2420
Group I 1st I.E. 2nd I.E. 3rd I.E.
Be 900 1760 14800
Mg 736 1450 7740
Ca 590 1150 4940
Sr 548 1060 4120
Ba 502 966 3390
Ionization Enthalpy
Li Na
KRb
Cs
1st I.E.
300
400
500
600
500
1000
1500
2000
Be
CaBa
Be+
Ca+
Ba+
1st IE
2nd IE
Ionization Enthalpy
Group I
1. Have generally low 1st I.E. as it is well shielded from the nucleus by inner shells.
2. Removal of a 2nd electron is much more difficult because it involves the removal of inner shell electron.
3. I.E. decreases as the group is descended. As atomic radius increases, the outer e is further
away from the well-shielded nucleus.
Hydration Enthalpy
M+(g) + aqueous M+(aq) + heat
M+
-600
-300
Li+ Na+ K+ Rb+ Cs+
Hydration Enthalpy
-600
-300
Li+ Na+ K+ Rb+ Cs+ Be2+ Mg2+ Ca2+ Sr2+ Ba2+
-2250
-2000
-1750
-1500
Hydration Enthalpy
General trends:1. On going down both groups, hydration enthalpy decreases. (As the ions get larger, the charge density of the ions decreases, the electrostatic attraction between ions and water molecules gets smaller.)
2. Group 2 ions have hydration enthalpies higher than group 1. ( Group 2 cations are doubly charged and have smaller sizes)
Ionization Energy
• Amount of energy required to remove an electron from the ground state of a gaseous atom or ion.– First ionization energy is that energy required to
remove first electron.– Second ionization energy is that energy required
to remove second electron, etc.
Trends in First Ionization Energies
• As one goes down a column, less energy is required to remove the first electron.– For atoms in the same
group, Zeff is essentially the same, but the valence electrons are farther from the nucleus.
Ionization Enthalpy of Alkali Metals
• ionization enthalpy decreases down the group from Li to cs because as we move down a group the number of valence electrons goes increasing separating the electrons away from the nucleus ,there is an increasing shielding of the nuclear charge by the inner shell electrons and thus the removal of electrons requires less energy as we move down.
Physical Properties
• Silvery White• Soft & Light Metals• Due to large size , elements have low density• Low Melting & Boling Points indicates weak
bonding due to presence of only 1 valence electron .
• In order of increasing atomic number the alkali metals are:
• Lithium• Sodium
• Potassium• Rubidium • Caesium• Francium
Increasing atomic number
Alkali Metals
All alkali (group 1) metals react violently with water, forming Hydrogen gas and Hydroxides (pH above 7):
Alkali metals are:• Metals found in group 1 of the periodic
table.
• Soft when cut (compared to other metals).
• Metals with low melting points and densities.
• Powerful reducing agent and form univalent compounds.
• Metals which tarnish in air.
Properties of Alkali Metals
E.g.
Li2O
Na2O, Na2O2
K2O2, KO2
Rb2O2, RbO2
Cs2O2, CsO2
Oxides On cumbustion in excess of air, alkali metals form
1. Oxides- LiO2
2. Peroxides- Li2O2, NaO2
3. Superoxides- K2O2 ,Cs2O2
RbO2
E.g.LiOHNaOHKOHRbOHCsOH
Hydroxides
The oxides of the alkali metal are easily hydrolysed by addition of water.
E.g.:- LiO2 + H2O → LiOH
The alkali metals combine directly with halogens under appropriate conditions forming halides of general formula MX.
These halides can also be prepared by the action of aqueous halogen acids (HX) on metals oxides, hydroxides or carbonate.
All these halides are colourless, high melting crystalline solids having high negative enthalpies of formation.
Halides
M2O + 2HX → 2MX + H2O MOH + HX → MX + H2O M2CO3 + 2HX → 2MX + CO2 + H2O (M = Li, Na, K, Rb or Cs)
(X = F, Cl, Br or I)
Examples of halides
Salts of oxo-acids
Since the alkali metals are highly electropositive, therefore their hydroxides are very strong bases and hence they form salts with all oxoacids.
( H2CO3, H3PO4, H2SO4, HNO3, HNO2 etc) .
They are generally soluble in water and stable towards heat.
The carbonates (M2CO3) of alkali metals are remarkably stable upto 1273 K, above which they first melt and then eventually decompose to form oxides.
Li2CO3 , however is considerably less stable and decomposes readily.
Δ Li2CO3 → Li2O + CO2
This is presumably due to large size difference between Li+ and CO2-
3 which makes the crystal lattice unstable.
SODIUM CHLORIDE
The most abundant source of sodium chloride is sea water. Crude sodium chloride, generally obtained by crystallisation of brine solution, contains sodium sulphate, calcium sulphate, calcium chloride and magnesium chloride as impurities. Calcium chloride,CaCl2, and magnesium chloride MgCl2 are impurities because they are deliquescent(absorb moisture from the atmosphere).
To obtain pure sodium chloride–
Crude salt is dissolved in minimum amount of water and filtered to remove insoluble impurities.The solution is then saturated with hydrogen chloride gas.Crystals of pure sodium separate out.Calcium and magnesium chloride, being more soluble than sodium chloride, remains in solution.
USES OF NaCl −
1) It is used as a common salt or table salt for domestic purpose.
2) It is used for the preparation of Na2O2 , NaOH and Na2CO3.
SODIUM HYDROXIDE(CAUSTIC SODA),
NaOHSodium hydroxide is generally prepared
commercially by the electrolysis of sodium chloride in Castner −Kellner cell.
A brine soln. is electrolysed using a mercury cathode and a carbon anode. Sodium metal discharged at the cathode combines with
mercury to form sodium amalgam. Chlorine gas is evolved at the anode.
NaCl → Na+ + Cl¯
AT ANODE: Cl ¯ ─ e¯ → Cl Cl + Cl → Cl2
AT CATHODE: Na+ + e ¯ → Na+
Na + Hg → NaHg Amalgam
The amalgam is treated with water to give sodium hydroxide, mercury and hydrogen gas.
2NaHg + 2H2O→ 2NaOH + 2Hg + H2
PROPERTIES-1. NaOH is a white, translucent solid and it melts at 591K.2. it is readily soluble in water to give alkaline solution.3. Crystals of NaOH are deliquescent. It reacts with the CO2 in the atmosphere to form Na2CO3.
USES- The manufacture of soap, paper and no. of chemicals.In petroleum refiningIn textile industry for mercerising cotton fabricsAs laboratory reagentFor preparation of pure oils and fats
SODIUM HYDROGENCARBONATE(BAKING
SODA), NaHCO3
Sodium hydrogencarbonate is known as baking soda because it decomposes on heating to generate bubbles of carbon dioxide. It is made by saturating a solution of sodium carbonate with carbon dioxide. The white crystalline powder of sodium hydrogencarbonate , being less soluble, gets separated out.Na2CO3 + H2O + CO2 → 2NaHCO3
NaHCO3 is a mild antiseptic for skin infections. It is used in fire extinguishers.
BIOLOGICAL IMPORTANCE OF SODIUM AND POTASSIUMA typical 70 kg man contains about 90g of Na and 170g of K compared with only 5g of iron and 0.06g of copper.Potassium ions are present in higher concentration inside the cells than sodium ions and they are present outside the cell in blood plasma.Because of large concentration gradient inside and outside the cells, the transport of sodium ion into the cells is favoured. To pump out these ions again from the cell to maintain concentration gradient large driving force is carried out. The energy for this process is provided by ATP molecules.Thus both sodium and potassium ions are essential for living organisms.
Anomalous properties of Lithium
Lithium
Symbol – LiAtomic no. - 3Atomic Weight – 6.94uElectronic Configuration - 1s22s1
Group no. – 1Period no. – 2Group name – Alkali MetalsBlock name – ‘s’Standard State(298 K)- SolidColor – Silvery-white/grey Classification - Metallic
Anomalous Properties
• High melting & boiling point.• Much harder than other alkali metals.• Reacts with oxygen least readily to form normal
oxide(E.g. Li2O), whereas other alkali metals form peroxides and superoxides(E.g. MO2,M2O2).
4Li + O2 → 2Li2O• Unlike other alkali metals lithium reacts directly
with carbon to form an ionic carbide.
• The carbonates, hydroxides and nitrates of lithium decompose on heating unlike those of other alkali metals which are somewhat stable towards heat.
4LiNO3 → 2Li2O + 4NO2 + O2
2LiCO3 → 2Li2O + CO2
2LiOH → Li2O + H2O
• LiOH is a weaker base than hydroxides of other alkali metals.
• Unlike elements of group 1, Lithium forms nitride with nitrogen.
3Li + N → Li3N
• Lithium halides are have more covalent nature than halides of other members of group 1.
Due to appreciable covalent nature, the halides and alkyls of lithium are soluble in organic solvents.
Li + has very high hydration energy and charge/radius ratio, therefore it acts as an excellent reducing agent in solution.
Li +
Li +
Li+
Li +
• Small size of atom results in relatively high cohesive properties associated with relatively strong inter-metallic bonding; large atoms usually form weak bonds.
Diagonal Relationship
The properties of lithium are quite different from the properties of other alkali metals. On the other hand, it shows greater resemblance with magnesium, which is diagonally opposite element of it.
Similarly properties of Beryllium & Boron represent that of Aluminium & Silicon respectively.
The main reasons for the anomalous behavior of lithium are -:
The Reasons -: (i) The extremely small size of Lithium
& its ion. (ii) Greater polarizing power of lithium
ion ( Li+), due to its small size which result in the covalent character in its compounds.
(iii) Least electropositive character and highest ionization energy as compared to other alkali metals.
(iv) Non availability of vacant d-orbitals in the valence shell.
Some More ExamplesExamples For Diagonal Relationship
• Li and Mg form only normal oxides whereas Na forms peroxide and metals below Na, in addition, forms superoxide.
• Li is the only Group 1 element which forms nitride, (Li3N). Mg, as well as other Group 2 elements, also form nitride.
• Lithium carbonate, phosphate and fluoride are sparingly soluble in water. The corresponding Group 2 salts are insoluble. (Think lattice and solvation energies).
• Both Li and Mg form covalent organometallic compounds. LiMe and MgMe2 (of Grignard reagents) are both valuable synthetic reagents. The other Group 1 and Group 2 analogues are ionic and extremely reactive (and hence difficult to manipulate).
IONIZATION ENTHALPY.
THE REACTIVITY OF THESE METALS INCREASES DOWN THE GROUP.
THE ALKALI METALS ARE HIGHLY REACTIVE. CAUSINGCONTRIBUTING FACTORS ARE LARGE SIZE AND LOW
CHEMICAL PROPERTIEES
1. REACTIVITY TOWARDS AIR -
1. ALKALI METALS TARNISH IN DRY AIR DUE TO FORMATION OF THEIR OXIDES.
2. THEY BURN IN OXYGEN VIGOURSLY.
3. THEY REACT WITH MOISTURE FORMING HYDROXIDES.
EX-4LI+O2 2LI2O
2NA+O2 NA2 O2
M+O2 MO2
OXIDATION STATE- +1
LITHUIM IS AN EXEPTIONREACTING DIRECTLY WITH NITROGEN OF AIR TO FORM THE NITRIDE.
DUE TO THEIR HIGH REACTIVITY TO AIR AND WATER THEY ARE KEPT IN KEROSENE OIL.
2. REACTIVITY TOWARDS WATER-2M+2H2O 2M+2OH+H2
THE ALKALI METALS REACT WITH H2O TO FORM HYDROXIDE AND H2.REACTION WITH H2O IS EXPLOSIVE FOR ALKALI METALS.
3. REACTIVITY TOWARDS HALOGENS- THE ALKALI METALS READILY REACT VIGOURSLY WITH HALOGENS TO FORM IONIC HALIDES,M+X-.LITHUIM HALIDES ARE CONVALENT DUE TO POLARISATION.
5. REDUCING NATURELITHUIM-STRONGESTSODIUM-LEAST POWERFUL REDUCING AGENT.
A) M - M (SUBLIMATION ENTHALPY)B) M=+M+E- (IONISATION ENTHALPY)C)+M+H2O=M+ (HYDRATION ENTHALPY)
SOLUTION IN LIQUID AMMONIA.
THE ALKALI METALS DISSOLVE IN LIQUID AMMONIA GIVING DEEP BLUE SOLUTIONS - CONDUCTING IN NATURE.THE PRODUCTS OF THIS REACTION ARE -
1.HYDROGEN.2. AMIDE ION.
THIS REACTION TAKES PLACE AT SLIGHTLY ELEVATED TEMPERATURES OR IN THE PRESENCE OF CATALYST.WHEN LIQUID AMMONIA IS EXPOSED TO LIGHT OF
SPECTRA REGION OF UV LIGHT THERE IS NO OBSERVABLE CHANGE.
WHEN METTALIC SOLUTION ARE SO EXPOSED,REACTION OCCURS.THIS REACTION IN PRESENCE OF UV IS COMPLETE PHOTOCHEMICAL REACTION. REACTION-
+M + E- + NH3 MNH2 +1/2H2
THE BLUE COLUR IS DUE TO THE AMMONIATED ELECTRON WHICH ABSORBS ENERGY IN VISIBLE REGION OF LIGHT IMPARTING BLUE COLOUR TO SOLUTION. THE SOLUTION IS PARAMAGNETIC.
IN CONCENTRATED SOLUTION THE BLUE COLOUR CHANGES TO BRONZE COLOUR AND BECOME DIMAGNETIC.
1.LITHUIM IS USED TO MAKE ALLOYS.EX-WITH LEAD TO MAKE WHITE METAL,BEARINGS FOR MOTORS ENGINES,WITH ALUMINIUM TO MAKE AIRCRAFTS PARTS AND WITH MAGNESIUM TO MAKE ARMOUR PLATES.
LITHUIM IS ALSO USED TO MAKE ELECTROCHEMICAL CELLS.
USES
2. SODIUM IS USED TO MAKE A Na or Pb ALLOY NEEDED TO MAKE PbMe4. used as anti-knock additives to petrol.
Liquid sodium metal is used as a coolant in fast breeder nuclear REACTORS. 3. POTASSIUM HAS A VITAL ROLE IN BIOLOGICAL SYSTEMS.
POTASSIUM CHLORIDE IS USED AS A FERTILISER.
POTASSIUM HYDROXIDE IS USED AS AN EXCELLENT ABSORBENT OF CARBON DIOXIDE.
4.CAESIUM IS USED IN DEVISING PHOTOELECTRIC CELLS.