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Types of solutions :
The homogeneous mixture of two or more components is called solution.
A binary solution contains one solute and one solvent.
The component which is present in large quantity is called solvent while the component
which is present in small quantity is called solute.
Solute + solvent Solution
Based on the physical state of solute and solvent, solutions are 9 types.
Type of solution Solute Solvent Example
Gaseous solutions Gas Gas Air
Liquid Gas CHCl3 in N2
Solid Gas Camphor in N2
Liquid solutions Gas Liquid O2 in water
Liquid Liquid Alcohol in water
Solid Liquid NaCl in water
Solid solutions Gas Solid H2 in palladium
Liquid Solid Hg in Na
Solid Solid Alloys like brass, bronze etc.,
Concentration terms :
Mass percentage (w/w) :
The of a component is given by,
Mass of the component
Mass % of a component = 100
Total mass of solution
Eg. 10% sucrose (w/w) means, 10g of sucrose is dissolved in 90g of water where the
total mass of the solution is 100g.
Volume percentage (V/V) ;
Volume of the component
Volume % of a component = 100
Total volume of solution
Eg. 10% (V/V) ethanol means, 10ml of ethanol is dissolved in 90ml of water resulting
in 100ml of solution.
Mass/volume percentage :
10% (w/v) glucose means 10g of glucose is present in 100ml of solution.
Parts per million (ppm) :
Number of parts of component
Parts per milliion = 106
Total number of parts of all components of solution
Molarity (M) :
* The number of moles of solute dissolved in one litre of solution at a given temperature
is called molarity.
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* Molarity depends upon the temperature because the molarity expression contains
volume term.
* Molarity (M) = n/V
n Number of moles of solute
V Volume of solution in lit.
w 1000
* Molarity (M) =
GMW V
W weight of the solute in grams
GMW gram molecular weight of the solute
V Volume of the solution in ml.
* For dilution :
M1V1 = M2V2
M1 Molarity of concentrated solution
V1 Volume of concentrated solution
M2 Molarity of dilute solution
V2 Volume of dilute solution
Volume of water to be added V2 – V1.
Molality (m) :
* The number of moles of the solute dissolved in one kg of the solvent is called molality.
* Units of molality : Mol. kg 1
* Molality is independent of temperature because the expression of molality does not
contain volume term.
Number of moles of solute
* Molality (m) =
Mass of solvent in kg
W1 1000
GMw W2
W1 weight of solute in grams
W2 weight of solvent in grams
GMw gram molecular weight of solute.
Mole fraction :
* The ratio of the number of moles of a component to the total number of moles of all
the components of solution is called mole fraction of that component.
Let n1 is the number of moles of solute and n2 is the number of mole of solvent.
Then,
n1
mole fraction of solute X 1
n1 n2
and,
n2
mole fraction of solvent X 2
n1 n2
2
* Sum of the mole fractions of solute and solvent is equal to one.
* Mole fraction has no units.
* Mole fraction is independent of temperature because its expression contains only weight
terms.
Solubility :
* The maximum amount of substance that can be dissolved in a specified amount of
solvent at a specified temperature is called solubility.
Solubility of a solid in a liquid :
1) Polar compounds are soluble in polar solvents while non-polar solutes are soluble
in non-polar solvents.
2) The solution which cannot dissolve some more solute at a given temperature is
called saturated solution.
3) The solution which is capable of dissolving some more solute at a given temperature
is called unsaturated solution.
4) The solution which contains more solute than that required for saturated at a given
temperature is called supersaturated solution.
Supersaturated solutions are meta stable.
5) (i) If the lattice energy of a substance is higher than its hydration energy, then the
dissolution process is endothermic and the solubility of that compound increases with raise in
temperature.
(ii) If the lattice energy of a substance is lower than its hydration energy, then the
dissolution process is exothermic and the solubility of that compound decreases with raise in
temperature.
6) Pressure does not affect the solubility of a solid in a liquid.
Solubility of a gas in a liquid :
1) The solubility of gases increases with increase of pressure.
2) According to Henry’s law, at a constant temperature the solubility of a gas in a
liquid is directly proportional to the pressure of the gas.
(OR)
The partial pressure of the gas in vapour phase (P) is directly proportional to the
mole fraction of the gas (X) in the solution.
PX
(OR) P = KH.X
Where KH is called Henry’s law constant.
* A plot of partial pressure of the gas versus mole fraction of the gas in solution gives a
straight line passing through the origin. Slope is equal to Henry’s law constant.
* Higher the value of KH at a given pressure, the lower is the solubility of the gas in the
liquid.
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* As temperature increases, the KH value increases, ie, the solubility of a gas decreases
with increase in temperature.
Applications of Henry’s law :
1. The soda water bottles are sealed under high pressure to increase the solubility of CO2
in soda water.
2. When scuba divers go into the deep sea, due to increase in pressure the solubility of
the gases in blood increases. When divers come out towards surface, the pressure
gradually decreases and dissolved gases release from blood by forming bubbles of
nitrogen in blood. This blocks capillaries and creates a medical condition called bends.
Because of this divers feel more pain and dangerous to life.
To avoid bends, the tanks used by scuba divers are filled with air and helium because
helium is less soluble in blood.
3. At higher altitudes, the partial pressure of oxygen is low. Due to this the people living
there will have low concentration of oxygen in blood. Because of this they suffer with
anoxia by which they cannot think and work properly.
Vapour pressure of liquid-liquid solutions :
1. The pressure exerted by the vapour over the surface of the liquid when the liquid is
in equilibrium with its vapour at a given temperature is called vapour pressure of the
liquid P o .
(or) PA PAo . X A where PA is the vapour pressure of the pure liquid ‘A’.
o
similarly,
PB XA
(or) PB PBo . X B where PB is the vapour pressure of the pure liquid ‘B’.
o
PTotal PA PB
Non-ideal solutions :
* The solution which does not follow over the entire range of concentration is called
non-deal solution.
For the non-ideal solution with +ve deviation from Roult’s law :
1) It the A-B interactions are weaker than those between A-A and B-B, then this type of
solutions results.
2) For this solution,
Vmix ve
3) For this solution,
H mix ve
i.e., the solution is formed with the absorption of heat.
4) The solution shows more vapour pressure than expected and boils at a lower temperature
than expected.
PA PAo . X A , PB PBo . X B
and PT PAo . X A PBo . X B
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i.e., the solution is formed with the liberation of heat.
4) The solution shows less vapour pressure than expected and boils at an higher temperature
than expected.
i.e., PA PA . X A ; PB PB . X B
o o
and PT PA . X A PB . X B
o o
The property of a dilute solution which depends upon the number of particles of the
solute, irrestpective of their nature, present in the solution is called colligative property.
Lowering of vapour pressure, elevation of boiling point, depression of freezing point and
Osmatic pressure are the colligative properties.
1) When a non volatile solute is dissolved in a pure liquid, then the vapour pressure of the
liquid decreases. This decrease in vapour pressure is called lowering of vapour pressure
2) According to Raoult’s law, vapour pressure of the solution depends upon the mole fraction
of the solvent
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Here PA0 PA = lowering of the vapour pressure
PA0 PA
= Relative lowering of vapour pressure
PA0
Relative lowering of vapour pressure is equal to the mole fraction of the non-volatile
solute present in the solution
PA0 PA nB
XB
PA0
nA nB
PA0 PA nB
PA0 nA
PA0 PA wM
or
PA0 mW
To calculate the molar mass of given unknown solute (m) accurately following
expression can be used
PA0 PA wM
PA mW
When a non-volatile solute is added, then the boiling point of the liquid increases. This
increase in boiling point is termed as elevation of boiling point.
Reason: When a non-volatile solute is added, the vapour pressure of the liquid
decreases. To make the vapour pressure of the solution as 1 atm, higher temperature is
required where the solution boils. Hence boiling point elevates.
1 atm
solvent
solution
Tb0 Tb
T B.P of pure liquid
b
0
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Tb B.P of solution
Tb Tb0
Tb Tb Tb0
or Tb Kb . molality
where Kb is the molal boiling point elevation constant (or) Ebullioscopic constant.
Kb is given by
2
R.Tb0
Kb
1000.lv
Where Tb0 is the boiling point of pure liquid and lv is the latent heat of vapourisation
For water,
2 373 373
Kb
1000 540
0.515 K .mol 1.kg
0.52 K .mol 1.kg
1
* units of Kb= K .mol .kg
* When a non-volatile solute is added, then the freezing point of the solvent decreases. This
decrease in freezing point is termed as depression of freezing point.
Reason: When anon-volatile solute is added then the vapour pressure of the solvent
decreases and now it would become equal to that of solid solvent at lower temperature. Thus
the freezing point of the solvent decreases.
solvent
solution
vapour pressure
T Tf0
Temperature
f
(K)
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Tf0 F.P of pure solvent
T f F.P of solution
Tf Tf0 Tf
* For a dilute solution, the depression of freezing point is directly proportional to the
molality of the solution
T f molality
(or) T f K f .molality
where Kf is called molal freezing point depression constant (or) cryoscopic constant.
w 1000
T f K f .
m W
The depression in the freezing point observed when one mole of non-volatile non-
electrolyte solute is dissolved in one kg solvent is called Kf.
Kf is given by
2
R.T f0
Kf
1000.l f
0
Where T f is freezing point of pure solvent
2 273 273
For water, K f
1000 80
1
units of K f K.mol .kg
Osmotic pressure:
The minimum pressure that must be applied on solution to stop the osmotic flow of
solvent molecules is called osmotic pressure.
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V nRT
n
or RT
V
or CRT
w 1000
or R T
m V
T Absolute temperature
The solutions having same osmotic pressure at a given temperature are called isotonic
solutions.
1 c1.RT
& 2 c2 RT
If 1 2 then c1 c2
Among two solutions, the solution with higher osmotic pressure is called hypertonic
while the solution with lower osmotic pressure is called hopotonic.
When blood cells are placed in 0.9% (w/v) aq.NaCl solution, then blood cells
collapse due to loss of water by osmosis. People taking a lot of salt experience water retention
in tissue cells and intercellular spaces because of osmosis. The resulting puffiness or swelling
is called edema.
To account for the degree of association or degree of dissociation, van’t Hoff introduced
a factor (i), known as Vant Hoff factor.
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Vant Hoff factor (i) is given by
i>1
i 1
n 1
i<1; Normal molar mass < experimental molar mass and observed colligative property <
normal colligative property.
1 i
1 1/ n
PA0 PA n
0
i B
PA nA
Tb Kb .molality.i
T f K f .molality.i
C .RT .i
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Mass of glucose
(b) Number of moles of glucose =
Molar mass
10
0.0555
180
Mass of water
Number of moles of water =
Molar mass
90
5
18
Number of moles of glucose
Mole fraction of glucose =
Total moles
0.0555
5.0555
= 0.011.
Number of moles of water
Mole fraction of water =
Total moles
5
5.0555
= 0.989.
(c) w 10, GMW 180
weight 100
Volume of solution =
density 1.2
w 1000 10 1000
Molarity(M) = 1.2
GMW V 180 100
= 0.667 M.
8. If N2 gas is bubbled through water at 293K, how many milli moles of N2 gas would
dissolve in 1 litre of water? Partial pressure of N2 is 0.987bar and Henry’s law
constant of N2 at 293K is 76.48 k bar.
X N2 ?
P KH .X
P 0.987
(or) X N2
K H 76.48 103
1.28 105
nN2 nN
X N2 2
nN2 nH 2O nH 2O
nN2 X N2 nH2O
1000
1.29 105 7.17 104
18
= 0.717 milli mole.
9. If the solubility of H2S in water at STP is 0.195m, calculate Henry’s law constant.
Solution : 0.195 m = 0.195 mole H2S in 1 kg water.
1000
nH 2 S 0.195, nH 2O 55.55
18
P kH .X H2S
14
1
kH P / X H2S
0.195(0.195 55.55)
= 285.87 atm.
10. Henry’s law constant for CO2 in water is 1.67 108 Pa at 298K. Calculate the quantity
of CO2 in 500 ml of soda water when packed under 2.5atm CO2 pressure at 298K.
P o Ps w M
Solution :
Pso m W
1.013 1.004 2 18
1.004 m 98
m = 40.98 g/mol.
13. Heptane and octane form ideal solution. At 372K, the vapour pressure of the two
liquids are 104.2k Pa and 46.8k Pa respectively. What will be the vapour pressure of
a mixture of 26 g of heptane and 35 g of octane.
15
Mass
Solution : No. of moles of heptane =
Molar mass
26
0.260
100
35
Number of moles of octane = 0.307
114
No. of moles of heptane
Mole fraction of heptane =
Total moles
0.26
0.458
0.26 0.307
No. of moles of octane
Mole fraction of octane =
Total moles
0.307
0.542
0.26 0.507
Vapour pressure of the solution (PS ) PAo . X A PBo . X B
= 105.2 (0.458) + 46.8(0.542)
= 48.287 + 25.319
= 73.606k Pa.
14. The vapour pressure of two liquids A and B are 450mm of Hg and 700 mm of Hg
respectively at 350K. Find out the composition of the liquid mixture if total vapour
pressure is 600 mm of Hg. Also find the composition in the vapour phase.
Solution : PS PAo ( X A ) PBo ( X B )
but X A X B 1
(or) X B 1 X A
600 450( X A ) 700(1 X A )
450 X A 700 700 X A
(or) 250 X A 700 600 100
100
XA 0.4
250
and X B 1 0.4 0.6
In liquid phase A and B are in 4 : 6 mole ratio.
Tb Kb . molality. i
w 1000
=K b i
m W
1.8 1000
0.88 2.53 1
m 90
2.53 1.8 1000
m 58 g/mol
0.88 90
18. Calculate the weight of ascorbic acid (Vitamin C, C6H8O6) to be dissolved in 75g of
acetic acid to lower its melting point by 1.5o C . K f 3.9K. Kg. mol 1
17
19. Calculate the osmotic pressure in Pascals exerted by a solution prepared by
10 1000
1.4 103 2
122.5 250
0.0042875
2
(or) 0.0655
18
i 1 i 1
(or) 0.0655 =
n 1 2 1
(or) i 1.0655
T f K f . molality. i
10 1000
1.86 1.0655
122.5 250
0.647 0.65K .
23. Determine the amount of CaCl2 (i = 2.47) dissolved din 2.5 lit of water such that its
osmotic pressure is 0.75 atm at 270 C .
Solution : 0.75 atm, T = 27 + 273 = 300 K
Molar mass (m) = 40 + 71 = 111
V = 2.5 lit, R = 0.0821 lit. atm. K 1. mol 1
CRT . i
w 1000
R T. i
m V
.m.V
w
1000 R T i
0.75 111 2500
1000 0.0821 300 2.47
3.421g .
24. Determine the osmotic pressure of a solution prepared by dissolving 25 mg of K2SO4
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