Q 11 :

The vapour pressure vs. temperature curve for a solution–solvent system is shown below:

The boiling point of the solvent is ______ °C.         [2023]



(82)

The temperature at which vapour pressure of solvent becomes 1 atm is called normal B.P. of solvent. So, the boiling point of the solvent is 82°C.



Q 12 :

If the boiling points of two solvents X and Y (having same molecular weights) are in the ratio 2 : 1 and their enthalpy of vaporization are in the ratio 1 : 2, then the boiling point elevation constant of X is m times the boiling point elevation constant of Y. The value of m is ________ (Nearest Integer)            [2023]



(8)

ΔTb=Kbm

Kb=RTb 2×Msolvent1000×ΔHvap

(ΔTb)X(ΔTb)Y=[(Tb)X(Tb)Y]2×MXMY×ΔHYΔHX=(21)2(11)×21=8



Q 13 :

An aqueous solution of volume 300 cm3 contains 0.63 g of protein. The osmotic pressure of the solution at 300 K is 1.29 mbar. The molar mass of the protein is ________ g mol-1. Given: R = 0.083 L bar K-1 mol-1                              [2023]



(40535)

π=W/MVRT

or  M=W×R×Tπ×V=0.63×0.083×3001.29×10-3×300×10-3

or M=40535 g/mol



Q 14 :

Solutions of 12 g of non-electrolyte (A) prepared by dissolving it in 1000 mL of water exerts the same osmotic pressure as that of 0.05 M glucose solution at the same temperature. The empirical formula of A is CH2O. The molecular mass of A is ______ g. (Nearest integer)               [2023]



(240)

For isotonic solutions

π1=π2

C1=C2 (For non-electrolyte)

(12MA×1)=0.05

MA=240



Q 15 :

A solution is prepared by dissolving 0.3 g of a non-volatile non-electrolyte solute A of molar mass 60 g mol-1 and 0.9 g of a non-volatile non-electrolyte solute B of molar mass 180 g mol-1 in 100 mL H2O at 27°C. Osmotic pressure of the solution will be:

[Given: R = 0.082 L atm K-1 mol-1]                     [2026]

  • 1.23 atm

     

  • 1.47 atm

     

  • 2.46 atm

     

  • 0.82 atm

     

(3)

Mass of solute 'A'=0.3 g

Moles of solute 'A'=0.3 g60 g mol-1=1200 mol

Mass of solute 'B'=0.9 g

Moles of solute 'B'=0.9 g180 g mol-1=1200 mol

Total molarity of all solutes=2/200100×1000=110 M

∴  π=110×0.082×300

π=2.46 atm



Q 16 :

Elements P and Q form two types of non-volatile, non-ionizable compounds PQ and PQ2.When 1 g of PQ is dissolved in 50 g of solvent ‘A’, ΔTb was 1.176 K while when 1 g of PQ2 is dissolved in 50 g of solvent 'A', ΔTb was 0.689 K. (Kb of ‘A’=5 K kg mol-1). The molar masses of elements P and Q (in g mol⁻¹) respectively, are:   [2026]

  • 65, 145

     

  • 70, 110

     

  • 60, 25

     

  • 25, 60

     

(4)

(ΔTb)PQ=Kbm

1.176=5×1M1×100050

M1=85.03

(ΔTb)PQ2=5×1M2×100050=0.689

M2=145.13

Let molar mass of P & Q are MP and MQ respectively

MP+MQ=85.03

MP+2MQ=145.13

MP=24.93≈25

MQ=60.1≈60



Q 17 :

Consider the following aqueous solutions.    [2026]

I. 2.2 g Glucose in 125 mL of solution.
II. 1.9 g Calcium chloride in 250 mL of solution.
III. 9.0 g Urea in 500 mL of solution.
IV. 20.5 g Aluminium sulphate in 750 mL of solution.

The correct increasing order of boiling point of these solutions will be:
[Given : Molar mass in g mol-1 : H = 1, C = 12, N = 14, O = 16, Cl = 35.5, Ca = 40, Al = 27 and S = 32]

  • III < I < II < IV

     

  • I < II < III < IV

     

  • II < III < I < IV

     

  • II < III < IV < I

     

(2)

ΔTb=i·kb·m

For dilute solution (M=m)

  Molarity i×m
(I) Mglucose=2.2180×1000125=0.098 0.098×1
(II) MCaCl2=1.9111×1000250=0.068 0.068×3
(III) Murea=960×1000500=0.3 0.3×1
(IV) MAl2(SO4)3=20.5342×1000750=0.08 0.08×5

 

Order of ΔTb=Al2(SO4)3>Urea>CaCl2>Glucose

So order of BP=Al2(SO4)3>Urea>CaCl2>Glucose

So Answer will be I<II<III<IV



Q 18 :

A substance ‘X’ (1.5 g) dissolved in 150 g of a solvent ‘Y’ (molar mass = 300 g mol-1) led to an elevation of the boiling point by 0.5 K. The relative lowering in the vapour pressure of the solvent ‘Y’ is ______ ×10-2. (nearest integer)

[Given : Kb of the solvent = 5.0 K kg mol-1]

Assume the solution to be dilute and no association or dissociation of X takes place in solution.         [2026]



(3)

ΔTb=i×Kb×m

0.5=i×m×5

i×m=0.55=0.1

i×a=151000

(where a = moles of solute)

Now,

P°-PsP°=iXsolute=i×aa+150300

=i×a12=15/10001/2=301000=3×10-2=3



Q 19 :

The osmotic pressure of a living cell is 12 atm at 300 K. The strength of sodium chloride solution that is isotonic with the living cell at this temperature is ______ g L-1. (Nearest integer)

Given : R = 0.08 L atm K-1 mol-1

Assume complete dissociation of NaCl

(Given : Molar mass of Na and Cl are 23 and 35.5 g mol-1 respectively.)           [2026]



(15)

π=iCRT

12=2×C×0.08×300

12=2×C×24

C=14 mole/L

then strength of NaCl solution

=14×58.5 g/L

=14.625 g/L

≈15 g/L



Q 20 :

A sample of sea water was found to contain 9.5%, w/w of MgCl2 and 5.85%, w/w of NaCl (Assuming complete ionization of salts) What will be the boiling point of sample?

( Kb for water =0.52 ,K-kg/mol, At. Wt of Mg = 24, Na = 23, Cl = 35.5)

  • 102.6°C

     

  • 103.07°C

     

  • 101.04°C

     

  • 100.52°C

     

(2)

In 100 gm solution

nMgCl2=0.1    nNaCl=0.1

After dissociation total moles=0.1×3+0.1×2=0.5

Wwater=100-9.5-5.85=84.65 gm

∴ ΔTb=0.52×0.5×100084.65=3.07°C

∴ Tb=103.07°C



Q 21 :

Molar depression constant for a solvent is 8.0 K kg mol-1. The depression in freezing point of the solvent for 0.03 mol kg-1 solution of K2SO4 is ______ ?

(Assume complete dissociation of the electrolyte)

  • 0.72 K

     

  • 0.24 K

     

  • 0.36 K

     

  • 0.12 K

     

(1)

K2SO4→2K++SO42-    i=3



Q 22 :

The freezing point of equimolal aqueous solutions will be highest for:

  • NaCl

     

  • Ca(NO3)2

     

  • AlCl3

     

  • C6H12O6

     

(4)

Depression in freezing point, ΔTf=iKfm. The value of van’t Hoff factor (i) is minimum for the glucose, which is a non-electrolyte. Hence, aqueous solution of glucose has highest freezing point.



Q 23 :

Solution A is prepared by dissolving 1 g of a protein (molar mass =50000 g mol-1) in 0.5 L of water at 300 K. Its osmotic pressure is x bar. Solution B is made by dissolving 2 g of same protein in 1 L of water at 300 K. Osmotic pressure of solution B is y bar. Entire solution of A is mixed with entire solution of B at same temperature. The osmotic pressure of resultant solution is z bar. x, y and z respectively are:

(R=0.083 L bar mol-1 K-1)                  [2026]

  • 9.96×10-4,  9.96×10-4,  9.96×10-4

     

  • 9.96×10-4,  9.96×10-4,  19.92×10-4

     

  • 4.98×10-4,  4.98×10-4,  9.96×10-4

     

  • 4.98×10-4,  4.98×10-4,  4.98×10-4

     

(1)

Osmotic pressure π=CRT

Solution A:

x=150000×0.5×0.083×300 bar=9.96×10-4 bar

Solution B:

y=250000×1×0.083×300 bar=9.96×10-4 bar

Solution A + Solution B:

z=(1+2)50000×(0.5+1)×0.083×300 bar=9.96×10-4 bar



Q 24 :

At 27°C, 0.1 M, 1 L K4[Fe(CN)6] aqueous solution and 0.1 M, 1 L FeCl3 aqueous solution are placed in a container separated by a semi permeable membrane AB. Assume complete dissociation of both the solutes. Which of the following statement is correct?           [2026]

[IMAGE 202]

  • Blue color is formed on both sides.

     

  • Ionic solutes in aqueous solution can pass through semi-permeable membrane.

     

  • Solution on side 'y' is hypotonic.

     

  • To cause the reverse flow of solvent during osmosis, external pressure (any value) should be applied to side 'x'.

     

(3)

(1) (2)

4FeCl3+3K4[Fe(CN)6]→Fe4[Fe(CN)6]3(Prussian blue)+12KCl

Above reaction does not occur as solute molecules do not pass through semi permeable membrane.

(3) K4[Fe(CN)6]→4K++[Fe(CN)6]4- (i=5), assuming 100% ionization

πK4[Fe(CN)6]=iCRT=5×0.1RT=0.5RT

FeCl3→Fe3++3Cl- (i=4), assuming 100% ionization

πFeCl3=iCRT=4×0.1RT=0.4RT

Solution with lesser osmotic pressure (Y) is hypotonic.

(4) For reverse osmosis to occur, pressure to be applied on X side should be more than difference in osmotic pressure of the two compartments.



Q 25 :

A non-volatile, non-electrolyte solid solute when dissolved in 40 g of a solvent, the vapour pressure of the solvent decreased from 760 mm Hg to 750 mm Hg. If the same solution boils at 320 K, then the number of moles of the solvent present in the solution is ______ . (Nearest integer)

[Given: boiling point of the pure solvent = 319.5 K, Kb of the solvent =0.3 K kg mol-1]                [2026]



(5)

PA°-PAPA°=xB (mole fraction of solute)

760-750760=xB

xB=176

xA (mole fraction of solvent)

=1-xB=1-176=7576

Molality (m)=xB×1000xAMA=ΔTb=mKb

                      =(1/76)×1000(75/76)×MA=1×100075×MA

ΔTb=mKb

320-319.5=1×100075×MA×0.3

MA=8 g mol-1

Number of moles of solvent

=Given massMolar mass=(408) mol=5 mol.



Q 26 :

20 g hemoglobin in a 1 L aqueous solution (A) at 300 K is separated from pure water by semi permeable membrane. At equilibrium the height of solution in a tube dipped in a solution (A) is found to be 80.0 mm higher than the tube dipped in water.

The molar mass of hemoglobin is _______  kg mol-1. (Nearest integer)

(Given: g=10 ms-2, R=8.3 kPa dm3 K-1 mol-1, density of solution = 1000 kg m-3)               [2026]



(62)

Osmotic pressure π=hρg

=80×10-3 m×1000 kg m-3×10 ms-2

=800Pa=0.8kPa

Also π=CRT=WsoluteMsoluteVsolution×RT

π=CRT

=20gMsolute×1 dm3×8.3 kPa dm3 K-1 mol-1×300 K

0.8 kPa=20 gMsolute×1 dm3×8.3 kPa dm3 K-1 mol-1×300 K

Msolute=20 g0.8 kPa×1 dm3×8.3 kPa dm3 K-1 mol-1×300 K

            =62250 g mol-1=62.25 kg mol-1