Solutions

JEE Chemistry · 84 questions · Page 3 of 9 · Click an option or "Show Solution" to reveal answer

Q21
Two solutions A and B are prepared by dissolving 1 g of non-volatile solutes X and Y, respectively in 1 kg of water. The ratio of depression in freezing points for A and B is found to be 1 : 4. The ratio of molar masses of X and Y is
A 1 : 4
B 1 : 0.25
C 1 : 0.20
D 1 : 5
Correct Answer
Option B
Solution
ΔTf=ikf×m\Delta T_{f}=i k_{f} \times m
ΔTf(A)ΔTf(B)=14\frac{\Delta T_{\mathrm{f}(\mathrm{A})}}{\Delta \mathrm{T}_{\mathrm{f}(\mathrm{B})}}=\frac{1}{4}
i×Kf×1MA×1i×Kf×1MB×1=14\frac{\mathrm{i} \times \mathrm{K}_{\mathrm{f}} \times \frac{1}{\mathrm{M}_{\mathrm{A}}} \times 1}{\mathrm{i} \times \mathrm{K}_{\mathrm{f}} \times \frac{1}{\mathrm{M}_{\mathrm{B}}} \times 1}=\frac{1}{4}
MBMA=14\frac{M_{B}}{M_{A}}=\frac{1}{4}
MA:MB=4:1M_{A}: M_{B}=4: 1
Q22
In the depression of freezing point experiment A. Vapour pressure of the solution is less than that of pure solvent B. Vapour pressure of the solution is more than that of pure solvent C. Only solute molecules solidify at the freezing point D. Only solvent molecules solidify at the freezing point Choose the most appropriate answer from the options given below :
A A and C only
B A only
C A and D only
D B and C only
Correct Answer
Option C
Solution

In the depression of freezing point experiment only solvent molecules solidify and vapour pressure of solution decreases as some of the surface area is occupied by solute molecules, so less number of molecules will go in vapour form.

Q23
Identify the mixture that shows positive deviations from Raoult's Law
A (CH3)2CO+CS2\left(\mathrm{CH}_3\right)_2 \mathrm{CO}+\mathrm{CS}_2
B (CH3)2CO+C6H5NH2\left(\mathrm{CH}_3\right)_2 \mathrm{CO}+\mathrm{C}_6 \mathrm{H}_5 \mathrm{NH}_2
C CHCl3+C6H6\mathrm{CHCl}_3+\mathrm{C}_6 \mathrm{H}_6
D CHCl3+(CH3)2CO\mathrm{CHCl}_3+\left(\mathrm{CH}_3\right)_2 \mathrm{CO}
Correct Answer
Option A
Solution
(CH3)2CO+CS2\left(\mathrm{CH}_3\right)_2 \mathrm{CO}+\mathrm{CS}_2

Exibits positive deviations from Raoult's Law

Q24
What happens to freezing point of benzene when small quantity of napthalene is added to benzene?
A Increases
B Decreases
C Remains unchanged
D First decreases and then increases
Correct Answer
Option B
Solution

When a small quantity of naphthalene is added to benzene, the freezing point of benzene decreases.

This phenomenon is due to the colligative property known as freezing point depression.

The addition of a solute, such as naphthalene, disrupts the orderly arrangement of solvent molecules in the solid phase, thereby lowering the freezing point.

Mathematically, the decrease in freezing point (ΔTf\Delta T_f) can be represented by the equation:

ΔTf=iKfm\Delta T_f = i \cdot K_f \cdot m

where: ii is the van't Hoff factor (which is 1 for naphthalene as it does not dissociate in solution), KfK_f is the cryoscopic constant of the solvent (benzene), mm is the molality of the solution.

Thus, the correct option is: Option B: Decreases

Q25
1.24 g of AX2 (molar mass 124 g mol−1) is dissolved in 1 kg of water to form a solution with boiling point of 100.015°C, while 25.4 g of AY2 (molar mass 250 g mol−1) in 2 kg of water constitutes a solution with a boiling point of 100.0260°C.Kb(H2O) = 0.52 kg mol−1Which of the following is correct?
A AX2 and AY2 (both) are completely unionised.
B AX2 and AY2 (both) are fully ionised.
C AX2 is completely unionised while AY2 is fully ionised.
D AX2 is fully ionised while AY2 is completely unionised.
Correct Answer
Option D
Solution

Mass of Ax2=1.24 gA x_2=1.24 \mathrm{~g} (solute) Molarmass of AX2=124 g mol1A X_2=124 \mathrm{~g} \mathrm{~mol}^{-1} Mass of water =1 kg=1 \mathrm{~kg} (solvent.)

Boiling point of water =100C=100^{\circ} \mathrm{C} Boiling point of water after adding solute AX2=100.0156CA X_2=100.0156^{\circ} \mathrm{C} Mass of AY2=25.4 gA Y_2=25.4 \mathrm{~g} (solute) Molarmass of AY2=250 g mol1A Y_2=250 \mathrm{~g~mol}^{-1} Mass of water =2 kg=2 \mathrm{~kg} (Solvent) Boiling point of water 100C\mp 100^{\circ} \mathrm{C} Boiling point of water after adding solute Ay2=100.0260CA y_2=100.0260^{\circ} \mathrm{C} Kb(H2O)=0.52 K kg mol1=0.520Ckgmol1\mathrm{K}_{\mathrm{b}}\left(\mathrm{H}_2 \mathrm{O}\right)=0.52 \mathrm{~K} \mathrm{~kg} \mathrm{~mol}{ }^{-1}=0.520^{\circ} \mathrm{C} \mathrm{kg} \mathrm{mol}^{-1} The ionisation of Ax2A x_2 and AY2A Y_2 can be determined by calculating Van't Hoff factor.

The phenomenon given in the question is elevation in boiling point.

The boiling point of solvent increases when another compound (solute) is added to it.

Relation: ΔTb=Kbim\Delta T_b=K_b \cdot i \cdot m

ΔTb=TbTb0\Delta T_b=T_b-T_b^0

ΔTb\Delta T_b \rightarrow Boiling point elevation TbT_b \rightarrow Boiling point of solution (solvent + solute) Tb0T_b^0 \rightarrow Boiling point of solvent KbK_b \rightarrow Molal elevation constant ii \rightarrow Van't Hoff factor

m Molality = Number of moles kg of solvent , Moles = Mass  Molarmass m \rightarrow \text{ Molality }=\frac{\text{ Number of moles }}{\mathrm{kg} \text{ of solvent }}, \text{ Moles }=\frac{\text{ Mass }}{\text{ Molarmass }}

For AX2A X_2 and AY2A Y_2 (solute), Van't Hoff factor represents how many particles a solute dissociates into when dissolved in a solvent (water).

For non-electrolytes, i=1i=1

AX2: Moles = mass  molarmass =1.249124 g mol1=0.01 mol Molality = Moles kg of solvent =0.01 mol1 kg=0.01 mol kg1ΔTb=Kb×i×mi=ΔTbkb×m=TbTb0Kb×m Substitute values as., \begin{aligned} &\begin{aligned} & A X_2: \\ & \text{ Moles }=\frac{\text{ mass }}{\text{ molarmass }}=\frac{1.249}{124 \mathrm{~g~mol^{-1}}}=0.01 \mathrm{~mol} \\ & \text{ Molality }=\frac{\text{ Moles }}{k_g \text{ of solvent }}=\frac{0.01 \mathrm{~mol}}{1 \mathrm{~kg}}=0.01 \mathrm{~mol} \mathrm{~kg}^{-1} \\ & \Delta T_b=K_b \times i \times m \\ & i=\frac{\Delta T_b}{k_b \times m} \\ &=\frac{T_b-T_b^0}{K_b \times m} \end{aligned}\\ &\text{ Substitute values as., } \end{aligned}
i=(100.0156C100C)0.52C kg mol1×0.01 mol kg1=0.0156C0.52×0.01C=3\begin{aligned} i & =\frac{\left(100.0156^{\circ} \mathrm{C}-100^{\circ} \mathrm{C}\right)}{0.52^{\circ} \mathrm{C} \mathrm{~kg} \mathrm{~mol}^{-1} \times 0.01 \mathrm{~mol} \mathrm{~kg}^{-1}} \\ & =\frac{0.0156^\circ \mathrm{C}}{0.52 \times 0.01{ }^{\circ} \mathrm{C}}=3 \end{aligned}

i=3i=3 means, there are 3 particles in solution after AX2A X_2 dissolved in water.

Ax21A++2X(1+2=3)A x_2 \rightarrow 1 A^{+}+2 X^{-} \quad(1+2=3)
Ax2 is completely ionised. AY2:\begin{aligned} &A x_2 \text{ is completely ionised. }\\ &A Y_2: \end{aligned}
 Moles = Mass  Molarmass =25.4 g250g mol=0.1016 mol Molality = Moles kgof1 solvent =0.1016 mol2 kg=0.050.8 mol kg1ΔTb=kb×l2×mi=ΔTbkb×m=TbTb0kb×m Substitute values as, \begin{aligned} &\begin{aligned} \text{ Moles } & =\frac{\text{ Mass }}{\text{ Molarmass }}=\frac{25.4 \mathrm{~g}}{250 \mathrm{g~mol}}=0.1016 \mathrm{~mol} \\ \text{ Molality } & =\frac{\text{ Moles }}{\mathrm{kgof}^{-1} \text{ solvent }}=\frac{0.1016 \mathrm{~mol}}{2 \mathrm{~kg}}=0.050 .8 \mathrm{~mol} \mathrm{~kg}^{-1} \\ \Delta T_b & =k_b \times \mathrm{l}^2 \times \mathrm{m} \\ i & =\frac{\Delta T_b}{k_b \times m} \\ & =\frac{T_b-T_b^0}{k_b \times m} \end{aligned}\\ &\text{ Substitute values as, } \end{aligned}
i=(100.0260C100C)0.52Ckgmol1×0.0508molkg1i = {{(100.0260^\circ C - 100^\circ C)} \over {0.52^\circ C\,kg\,mo{l^{ - 1}} \times 0.0508\,mol\,k{g^{ - 1}}}}

=0.0260C0.52×0.0508C=\dfrac{0.0260 ^\circ \mathrm{C}}{0.52 \times 0.0508 ^\circ \mathrm{C}} =0.98= 0.98 1\approx 1 i=1i=1 means AY2A Y_2 is completely unionised. Ay2A y_2 not give ionised particles when dissolved in water.

So, AX2A X_2 is completely ionised and AY2A Y_2 is completely unionised.

Answer: Option 4) Ax2A x_2 is fully ionised, AY2A Y_2 is completely unionised.

Q26
When a non-volatile solute is added to the solvent, the vapour pressure of the solvent decreases by 10 mm of Hg . The mole fraction of the solute in the solution is 0.2 . What would be the mole fraction of the solvent if decrease in vapour pressure is 20 mm of Hg ?
A 0.2
B 0.4
C 0.8
D 0.6
Correct Answer
Option D
Solution

When a non-volatile solute is added to a solvent, it causes the vapour pressure of the solvent to decrease.

In this scenario, when the vapour pressure decreases by 10 mm of Hg, the mole fraction of the solute in the solution is 0.2.

By understanding the relationship between vapour pressure change and mole fraction, we see that: The change in vapour pressure (PPP^{\circ} - P) is directly proportional to the mole fraction of the solute (XsoluteX_{\text{solute}}).

Therefore, if a 10 mm of Hg decrease corresponds to a mole fraction of 0.2, then a 20 mm of Hg decrease would correspond to a mole fraction of 0.4.

To find the mole fraction of the solvent (XsolventX_{\text{solvent}}), we use the formula: Xsolvent=1Xsolute X_{\text{solvent}} = 1 - X_{\text{solute}} Substituting the value we found: Xsolvent=10.4=0.6 X_{\text{solvent}} = 1 - 0.4 = 0.6 Thus, when the vapour pressure decreases by 20 mm of Hg, the mole fraction of the solvent is 0.6.

Q27
The size of a raw mango shrinks to a much smaller size when kept in a concentrated salt solution. Which one of the following processes can explain this?
A Osmosis
B Reverse osmosis
C Diffusion
D Dialysis
Correct Answer
Option A
Solution

Raw mango shrink in salt solution due to net transfer of water molecules from mango to salt solution due to phenomenon of osmosis.

Q28
On mixing, heptane and octane form an ideal solution. At 373 K, the vapour pressures of the two liquid components (heptane and octane) are 105 kPa and 45 kPa respectively. Vapour pressure of the solution obtained by mixing 25.0g of heptane and 35 g of octane will be (molar mass of heptane = 100 g mol–1 and of octane = 114 g mol–1)
A 72.0 kPa
B 36.1 kPa
C 96.2 kPa
D 144.5 kPa
Correct Answer
Option A
Solution
PTotal=PAxA+PBxB{P_{Total}} = {P_A}^ \circ {x_A} + {P_B}^ \circ {x_B}
=PHeptanexheptane+POctanexOctane= {P^ \circ }_{Hep\tan e}\,{x_{hep\tan e}} + {P^ \circ }_{Oc\tan e}\,{x_{Oc\tan e}}
=105×25/10025100+35114+45×35/11425100+35114= 105 \times {{25/100} \over {{{25} \over {100}} + {{35} \over {114}}}} + 45 \times {{35/114} \over {{{25} \over {100}} + {{35} \over {114}}}}
=105×0.250.25+0.3+45×0.30.25+0.3= 105 \times {{0.25} \over {0.25 + 0.3}} + 45 \times {{0.3} \over {0.25 + 0.3}}
=105×0.250.55+45×0.30.55= {{105 \times 0.25} \over {0.55}} + {{45 \times 0.3} \over {0.55}}
=26.25+13.50.55=72kPa= {{26.25 + 13.5} \over {0.55}} = 72\,kPa
Q29
Freezing point of a 4% aqueous solution of X is equal to freezing point of 12% aqueous solution of Y. If molecular weight of X is A, then molecular weight of Y is -
A 4A
B 2A
C 3A
D A
Correct Answer
Option C
Solution

For same freezing point, (

Δ\Delta

Tf)X = (

Δ\Delta

Tf)Y \Rightarrow kf mx = kf my \Rightarrow

4×1000A×96=12×1000M×88{{4 \times 1000} \over {A \times 96}} = {{12 \times 1000} \over {M \times 88}}

\Rightarrow M = 3.27A

\simeq

3A

Q30
1 g of a non-volatile non-electrolyte solute is dissolved in 100 g of two different solvents A and B whose ebullioscopic constants are in the ratio of 1 : 5. The ratio of the elevation in their boiling points, ΔTb(A)ΔTb(B){{\Delta {T_b}(A)} \over {\Delta {T_b}(B)}}, is :
A 5 : 1
B 1 : 0.2
C 10 : 1
D 1 : 5
Correct Answer
Option D
Solution

Given,

(kb)A(kb)B=15{{{{\left( {{k_b}} \right)}_A}} \over {{{\left( {{k_b}} \right)}_B}}} = {1 \over 5}
ΔTb(A)=kb(A)×\Delta {T_b}\left( A \right) = {k_b}\left( A \right) \times

Molality of A

ΔTb(B)=kb(B)×\Delta {T_b}\left( B \right) = {k_b}\left( B \right) \times

Molality of B Here, Molality of A = Molality of B = m

ΔTb(A)ΔTb(B)=(kb)A(kb)B×mm{{\Delta {T_b}\left( A \right)} \over {\Delta {T_b}\left( B \right)}} = {{{{\left( {{k_b}} \right)}_A}} \over {{{\left( {{k_b}} \right)}_B}}} \times {m \over m}

=

15{1 \over 5}
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