Solutions

JEE Chemistry · 84 questions · Page 8 of 9 · Click an option or "Show Solution" to reveal answer

Q71
At 80oC, the vapour pressure of pure liquid ‘A’ is 520 mm Hg and that of pure liquid ‘B’ is 1000 mm Hg. If a mixture solution of ‘A’ and ‘B’ boils at 80oC and 1 atm pressure, the amount of ‘A’ in the mixture is (1 atm = 760 mm Hg)
A 52 mol percent
B 34 mol percent
C 48 mol percent
D 50 mol percent
Correct Answer
Option D
Solution

At

11

atmospheric pressure the boiling point of mixture is

80C.{80^ \circ }C.

At boiling point the vapour pressure of mixture,

PT=1{P_T} = 1

atmosphere

=760mmHg.= 760\,mm\,Hg.

Using the relation,

PT=PAXA+PBXB,{P_T} = P_A^ \circ {X_A} + P_B^ \circ {X_B},\,\,

we get

PT=520XA+1000(1XA){P_T} = 520{X_A} + 1000\left( {1 - {X_A}} \right)
{\left\{ \, \right.
PA=520mmHg,P_A^ \circ = 520mm\,\,Hg,
\,\,\,\,\,\,\,\,\,\,
PB=1000mmHg,XA+XB=1}\left. {P_B^ \circ = 1000\,mm\,Hg,\,{X_A} + {X_B} = 1} \right\}

or

\,\,\,\,\,\,\,\,\,\,
760=520XA+10001000XA760 = 520{X_A} + 1000 - 1000{X_A}\,\,

or

\,\,\,\,\,\,\,\,\,\,
480XA=240480{X_A} = 240

or

\,\,\,\,\,\,\,\,\,\,
XA=240480=12{X_A} = {{240} \over {480}} = {1 \over 2}

or

\,\,\,\,\,\,\,\,\,\,
5050

mol. percent i.e., The correct answer is

(d)(d)
Q72
The vapour pressure of water at 20oC is 17.5 mm Hg. If 18 g of glucose (C6H12O6) is added to 178.2 g of water at 20oC, the vapour pressure of the resulting solution will be
A 17.675 mm Hg
B 15.750 mm Hg
C 16.500 mm Hg
D 17.325 mm Hg
Correct Answer
Option D
Solution

NOTE : On addition of glucose to water, vapour pressure of water will decrease.

The vapour pressure of a solution of glucose in water can be calculated using the relation

PPSPS=Molesofglucoseinsolutionmolesofwaterinsolution{{{P^ \circ } - {P_S}} \over {{P_S}}} = {{Moles\,\,of\,\,glu\cos e\,\,in\,\,solution} \over {moles\,\,of\,\,water\,\,in\,\,solution}}

or

\,\,\,\,\,\,\,\,\,
17.5PSPS=18/180178.2/18{{17.5 - {P_S}} \over {{P_S}}} = {{18/180} \over {178.2/18}}

[as

\,\,\,\,\,\,\,\,\,
P=17.5{P^ \circ } = 17.5

] or

\,\,\,\,\,\,\,\,\,
17.5PS=0.1×PS9.917.5 - {P_S} = {{0.1 \times {P_S}} \over {9.9}}

or

\,\,\,\,\,\,\,\,\,
PS=17.325mmHg.{P_S} = 17.325\,mm\,Hg.

Hence (d) is correct answer.

Q73
What is the freezing point depression constant of a solvent, 50 g of which contain 1 g non volatile solute (molar mass 256 g mol1256 \mathrm{~g} \mathrm{~mol}^{-1} ) and the decrease in freezing point is 0.40 K ?
A 4.43 K kg mol14.43 \mathrm{~K} \mathrm{~kg} \mathrm{~mol}^{-1}
B 3.72 K kg mol13.72 \mathrm{~K} \mathrm{~kg} \mathrm{~mol}^{-1}
C 5.12 K kg mol15.12 \mathrm{~K} \mathrm{~kg} \mathrm{~mol}^{-1}
D 1.86 K kg mol11.86 \mathrm{~K} \mathrm{~kg} \mathrm{~mol}^{-1}
Correct Answer
Option C
Solution

To find the freezing point depression constant (Kf K_f ) of the solvent, we use the formula for freezing point depression: ΔTf=Kfm \Delta T_f = K_f \cdot m Given: The decrease in freezing point ΔTf\Delta T_f is 0.40 K.

The mass of the solute is 1 g and its molar mass is 256 g/mol.

The mass of the solvent is 50 g (or 0.050 kg).

First, calculate the molality (m m ): Molality is defined as the moles of solute per kilogram of solvent.

Calculate moles of solute: Moles of solute=1g256g/mol=1256mol \text{Moles of solute} = \dfrac{1 \, \text{g}}{256 \, \text{g/mol}} = \dfrac{1}{256} \, \text{mol} Calculate molality (m m ): m=1256mol0.050kg=1256×0.050mol/kg m = \dfrac{\dfrac{1}{256} \, \text{mol}}{0.050 \, \text{kg}} = \dfrac{1}{256 \times 0.050} \, \text{mol/kg} Now, substitute into the formula to find Kf K_f : 0.4=Kf1256×0.050 0.4 = K_f \cdot \dfrac{1}{256 \times 0.050} Solving for Kf K_f : Kf=0.4256×0.050=5.12K kg/mol K_f = 0.4 \cdot 256 \times 0.050 = 5.12 \, \text{K kg/mol} Thus, the freezing point depression constant of the solvent is 5.12K kg/mol 5.12 \, \text{K kg/mol} .

Q74
Solute A associates in water. When 0.7 g of solute A is dissolved in 42.0 g of water, it depresses the freezing point by 0.2^\circC. The percentage association of solute A in water, is : [Given : Molar mass of A = 93 g mol-1. Molal depression constant of water is 1.86 K kg mol-1.]
A 50%
B 60%
C 70%
D 80%
Correct Answer
Option D
Solution

Since, ΔTf=ikfm\Delta \mathrm{T}_{\mathrm{f}}=\mathrm{ik}_{\mathrm{f} m}

m=0.793×1000420.2=i×1.86×0.7×100093×42i=0.6α=i11n1=0.61121=0.8\begin{aligned} &m=\frac{0.7}{93} \times \frac{1000}{42} \\\\ &0.2=i \times 1.86 \times \frac{0.7 \times 1000}{93 \times 42} \\\\ &i=0.6 \\\\ &\alpha=\frac{i-1}{\frac{1}{n}-1}=\frac{0.6-1}{\frac{1}{2}-1}=0.8 \end{aligned}

Hence, the percentage association of solute AA is 80%80 \%.

Q75
Given below are two statements : one is labelled as Assertion (A) and the other is labelled as Reason (R). Assertion (A) : At 10^\circC, the density of a 5 M solution of KCl [atomic masses of K & Cl are 39 & 35.5 g mol-1 respectively], is 'x' g ml-1. The solution is cooled to -21^\circC. The molality of the solution will remain unchanged. Reason (R) : The molality of a solution does not change with temperature as mass remains unaffected with temperature. In the light of the above statements, choose the correct answer from the options given below :
A Both (A) and (R) are true and (R) is the correct explanation of (A).
B Both (A) and (R) are true but (R) is not the correct explanation of (A).
C (A) is true but (R) is false.
D (A) is false but (R) is true.
Correct Answer
Option A
Solution

Molality and Mass are temperature Independent so on changing temp., molality and mass remain unchanged.

Q76
A solution of two miscible liquids showing negative deviation from Raoult's law will have :
A increased vapour pressure, increased boiling point
B increased vapour pressure, decreased boiling point
C decreased vapour pressure, decreased boiling point
D decreased vapour pressure, increased boiling point
Correct Answer
Option D
Solution

Negative Deviation from Raoult's Law Negative deviation means the intermolecular forces of attraction between the molecules of the two liquids (A-B) are stronger than the forces between molecules of the pure liquids (A-A and B-B).

This stronger attraction makes it harder for molecules to escape into the vapor phase.

Effect on Vapor Pressure and Boiling Point Vapor Pressure : Since the molecules are held more tightly, the vapor pressure of the solution will be lower than expected from Raoult's law.

Decreased vapor pressure.

Boiling Point : A lower vapor pressure means you need to increase the temperature further to reach atmospheric pressure, where boiling occurs.

Therefore, the boiling point of the solution will be higher than expected.

Increased boiling point.

Answer The correct answer is Option D: decreased vapor pressure, increased boiling point.

Q77
Liquid 'M' and liquid 'N' form an ideal solution. The vapour pressures of pure liquids 'M' and 'N' are 450 and 700 mmHg, respectively, at the same temperature. Then correct statement is: (xM = Mole fraction of 'M' in solution ; xN = Mole fraction of 'N' in solution ; yM = Mole fraction of 'M' in vapour phase ; yN = Mole fraction of 'N' in vapour phase)
A xMxN<yNyN{{{x_M}} \over {{x_N}}} < {{{y_N}} \over {{y_N}}}
B (xM – yM) < (xN – yN)
C xMxN=yNyN{{{x_M}} \over {{x_N}}} = {{{y_N}} \over {{y_N}}}
D xMxN>yMyN{{{x_M}} \over {{x_N}}} > {{{y_M}} \over {{y_N}}}
Correct Answer
Option D
Solution
PM0P_M^0

= 450 mmHg and

PN0P_N^0

= 700 mmHg \therefore

PM0P_M^0

<

PN0P_N^0

Also we know,

PMP_M

=

PM0P_M^0
XMX_M

=

YMY_M
PTP_T

\Rightarrow

PM0P_M^0

=

YMXM(PT){{{Y_M}} \over {{X_M}}}\left( {{P_T}} \right)
PNP_N

=

PN0P_N^0
XNX_N

=

YNY_N
PTP_T

\Rightarrow

PN0P_N^0

=

YNXN(PT){{{Y_N}} \over {{X_N}}}\left( {{P_T}} \right)

As,

PM0P_M^0

<

PN0P_N^0

\Rightarrow

YMXM(PT){{{Y_M}} \over {{X_M}}}\left( {{P_T}} \right)

<

YNXN(PT){{{Y_N}} \over {{X_N}}}\left( {{P_T}} \right)

\Rightarrow

YMXM{{{Y_M}} \over {{X_M}}}

<

YNXN{{{Y_N}} \over {{X_N}}}

\Rightarrow

YMYN{{{Y_M}} \over {{Y_N}}}

<

XMXN{{{X_M}} \over {{X_N}}}
Q78
A mixture of ethyl alcohol and propyl alcohol has a vapour pressure of 290 mm at 300 K. The vapour pressure of propyl alcohol is 200 mm. If the mole fraction of ethyl alcohol is 0.6, its vapour pressure (in mm) at the same temperature will be
A 360
B 350
C 300
D 700
Correct Answer
Option B
Solution
PA=?,P_A^ \circ = ?,\,\,

Given

PB=200mm,xA=0.6P_B^ \circ = 200mm,\,\,{x_A} = 0.6
xB=10.6=0.4,P=290{x_B} = 1 - 0.6 = 0.4,\,\,P = 290
P=PA+PB=PAxA+PBxBP = {P_A} + {P_B} = P_A^ \circ {x_A} + P_B^ \circ {x_B}
290=PA×0.6+200×0.4\Rightarrow 290 = P_A^ \circ \times 0.6 + 200 \times 0.4

\therefore

\,\,\,\,\,\,\,\,
PA=350mmP_A^ \circ = 350mm
Q79
An aqueous solution of a salt MX2 at certain temperature has a van’t Hoff factor of 2. The degree of dissociation for this solution of the salt is :
A 0.33
B 0.50
C 0.67
D 0.80
Correct Answer
Option B
Solution

Let us assume that degree of dissociation is α\alpha.

MX2M2++2X+(1α)α2α\begin{array}{lll}{M{X_2}} & { \to {M^{2 + }} + } & {2X + } \\ {(1 - \alpha )} & \alpha & {2\alpha } \end{array}

Thus, after dissociation total number of moles formed (n) = 3. Now, we know degree of dissociation is

α=i1n1=2131=0.50\alpha = {{i - 1} \over {n - 1}} = {{2 - 1} \over {3 - 1}} = 0.50
Q80
The vapour pressure of acetone at 20oC is 185 torr. When 1.2 g of a non-volatile substance was dissolved in 100 g of acetone at 20oC, its vapour pressure was 183 torr. The molar mass (g mol-1) of the substance is:
A 64
B 128
C 488
D 32
Correct Answer
Option A
Solution

Using relation,

PPsPs=w2M1w1M2{{{P^ \circ } - {P_s}} \over {{P_s}}} = {{{w_2}{M_1}} \over {{w_1}{M_2}}}

where

w1,{w_1},
M1={M_1} =

mass in

gg

and mol. mass of solvent

w2,M2={w_2},{M_2} =

mass in

gg

and mol. mass of solute Let

M2=x{M_2} = x
P=185torr;Ps=183torr{P^ \circ } = 185\,\,torr;\,\,{P_s} = 183\,torr
185183183=1.2×58100x{{185 - 183} \over {183}} = {{1.2 \times 58} \over {100x}}

(Mol. mass of acetone

=58=58

)

x=64x=64

\therefore

\,\,\,\,\,

Molar mass of substance

=64=64
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