Solutions
When a certain amount of solid A is dissolved in $100 \mathrm{~g}$ of water at $25^{\circ} \mathrm{C}$ to make a dilute solution, the vapour pressure of the solution is reduced to one-half of that of pure water. The vapour pressure of pure water is $23.76 \,\mathrm{mmHg}$. The number of moles of solute A added is _____________. (Nearest Integer)
Explanation:
$ \frac{\mathrm{P}^0-\mathrm{P}_{\mathrm{S}}}{\mathrm{P}^0} \sim \frac{{ }^{\mathrm{n}} \text { solute }}{{ }^{\mathrm{n}} \text { solvent }} $
$ \frac{\mathrm{P}^0-\mathrm{P}^0 / 2}{\mathrm{P}^0}=\frac{{ }^{\mathrm{n}} \text { solute }}{{ }^{\mathrm{n}} \text { solvent }} $
${ }^{\mathrm{n}}$ solute $\sim \frac{{ }^{\mathrm{n}} \text { solvent }}{2}=\frac{100}{18 \times 2}=2.78 \mathrm{~mol}$
More accurate approach:
$ \frac{\mathrm{P}^0-\mathrm{P}_{\mathrm{S}}}{\mathrm{P}_{\mathrm{S}}}=\frac{{ }^{\mathrm{n}} \text { solute }}{{ }^{\mathrm{n}} \text { solvent }} $
$ \frac{\mathrm{P}^0-\mathrm{P}^0 / 2}{\mathrm{P}^0 / 2}=\frac{{ }^{\mathrm{n}} \text { solute }}{{ }^n \text { solvent }} $
${ }^n$ solute $={ }^n$ solvent $=\frac{100}{18}=5.55 \mathrm{~mol}$
The elevation in boiling point for 1 molal solution of non-volatile solute A is $3 \mathrm{~K}$. The depression in freezing point for 2 molal solution of $\mathrm{A}$ in the same solvent is 6 $K$. The ratio of $K_{b}$ and $K_{f}$ i.e., $K_{b} / K_{f}$ is $1: X$. The value of $X$ is [nearest integer]
Explanation:
Elevation in boiling point is given by
$\Delta \mathrm{T}_{\mathrm{b}}=\mathrm{K}_{\mathrm{b}} \mathrm{m}$
$ 3=\mathrm{K}_{\mathrm{b}} \times 1 $ ... (1)
Molality of $(A)$ in the same solvent $=2$
Depression in freezing point is given by
$ \begin{aligned} &\Delta \mathrm{T}_{\mathrm{f}}=\mathrm{K}_{\mathrm{f}} \mathrm{m} \\ &6=\mathrm{K}_{\mathrm{f}} \times 2 \quad\quad\quad{...(2)} \\ &\text { Dividing (1) by (2) } \\ &\frac{\mathrm{K}_{\mathrm{b}}}{\mathrm{K}_{\mathrm{f}}}=\frac{1}{\mathrm{X}}=\frac{1}{1} \\ &\therefore \quad \mathrm{X}=1 \end{aligned} $
Elevation in boiling point for 1.5 molal solution of glucose in water is 4 K. The depression in freezing point for 4.5 molal solution of glucose in water is 4 K. The ratio of molal elevation constant to molal depression constant (Kb/Kf) is _________.
Explanation:
1.2 mL of acetic acid is dissolved in water to make 2.0 L of solution. The depression in freezing point observed for this strength of acid is 0.0198$^\circ$C. The percentage of dissociation of the acid is ___________. (Nearest integer)
[Given : Density of acetic acid is 1.02 g mL$-$1, Molar mass of acetic acid is 60 g mol$-$1, Kf(H2O) = 1.85 K kg mol$-$1]
Explanation:
Moles of solute $($ acetic acid $)=\frac{1.2 \times 1.02}{60}$
As moles of solute are very less.
So, take molarity and molality the same.
$0.0198=\mathrm{i} \times 1.85 \times \frac{1.2 \times 1.02}{60 \times 2}$
$\mathrm{i}=1.05$
$\alpha=\frac{i-1}{n-1}=\frac{0.05}{1}= 0.05 = 5\text{%}$
2.5 g of protein containing only glycine (C2H5NO2) is dissolved in water to make 500 mL of solution. The osmotic pressure of this solution at 300 K is found to be 5.03 $\times$ 10$-$3 bar. The total number of glycine units present in the protein is ____________.
(Given : R = 0.083 L bar K$-$1 mol$-$1)
Explanation:
$ \pi=\mathrm{icR} \mathrm{T} $
$5.03 \times 10^{-3}=\frac{2.5}{M} \times \frac{1000}{500} \times 0.083 \times 300$
Molar mass of protein $=24751.5 \mathrm{~g} / \mathrm{mol}$
Number of glycine units in protein $=\frac{24751.5}{75}$
$ =330 $
The vapour pressures of two volatile liquids A and B at 25$^\circ$C are 50 Torr and 100 Torr, respectively. If the liquid mixture contains 0.3 mole fraction of A, then the mole fraction of liquid B in the vapour phase is ${x \over {17}}$. The value of x is ______________.
Explanation:
A solution containing 2.5 $\times$ 10$-$3 kg of a solute dissolved in 75 $\times$ 10$-$3 kg of water boils at 373.535 K. The molar mass of the solute is ____________ g mol$-$1. [nearest integer] (Given : Kb(H2O) = 0.52 K kg mol$-$1 and boiling point of water = 373.15 K)
Explanation:
$ \begin{aligned} &\mathrm{W}_{\text {solvent }}=75 \times 10^{-3} \mathrm{~kg} \\\\ &\Delta \mathrm{T}_{\mathrm{b}} =373.535-373.15 \\\\ &=0.385 \mathrm{~K} \\\\ &\mathrm{~K}_{\mathrm{b}}\left(\mathrm{H}_{2} \mathrm{O}\right) =0.52 \mathrm{~K} \mathrm{~kg} \mathrm{~mol}^{-1} \\\\ &\Delta \mathrm{T}_{\mathrm{b}} =\frac{\mathrm{K}_{\mathrm{b}} \times 10^{3} \times \mathrm{W}_{\text {solute }}}{\mathrm{M}_{\text {solute }} \times \mathrm{W}_{\text {solvent }}} \\\\ &\mathrm{M}_{\text {solute }} =\frac{0.52 \times 10^{3} \times 2.5 \times 10^{-3}}{75 \times 10^{-3} \times 0.385} \\\\ &=45.02 \\\\ & \approx 45 \end{aligned} $
2 g of a non-volatile non-electrolyte solute is dissolved in 200 g of two different solvents A and B whose ebullioscopic constants are in the ratio of 1 : 8. The elevation in boiling points of A and B are in the ratio ${x \over y}$ (x : y). The value of y is ______________. (Nearest integer)
Explanation:
$ \begin{aligned} &\frac{\left(\Delta T_{b}\right)_{A}}{\left(\Delta T_{b}\right)_{B}}=\frac{\left(k_{b}\right)_{A}}{\left(k_{b}\right)_{B}} \\\\ &=\frac{1}{8}=\frac{x}{y} \\\\ &\therefore y=8 \end{aligned} $
The osmotic pressure exerted by a solution prepared by dissolving 2.0 g of protein of molar mass 60 kg mol$-$1 in 200 mL of water at 27$^\circ$C is ______________ Pa. [integer value]
(use R = 0.083 L bar mol$-$1 K$-$1)
Explanation:
$\pi=\frac{2 \times 1000}{60 \times 10^{3} \times 200} \times .083 \times 300$
$\pi=0.00415 \mathrm{~atm}$
$\pi=415 \mathrm{~Pa}$
A 0.5 percent solution of potassium chloride was found to freeze at $-$0.24$^\circ$C. The percentage dissociation of potassium chloride is ______________. (Nearest integer)
(Molal depression constant for water is 1.80 K kg mol$-$1 and molar mass of KCl is 74.6 g mol$-$1)
Explanation:
$ \begin{aligned} &\mathrm{i}=\frac{0.24 \times 99.5 \times 74.6}{1.80 \times 0.5 \times 1000} \\\\ &=1.98 \\\\ &\alpha=\frac{\mathrm{i}-1}{\mathrm{n}-1}=\frac{0.98}{1}=0.98 = 98 \,\% \end{aligned} $
A company dissolves 'x' amount of CO2 at 298 K in 1 litre of water to prepare soda water. X = __________ $\times$ 10$-$3 g. (nearest integer)
(Given : partial pressure of CO2 at 298 K = 0.835 bar.
Henry's law constant for CO2 at 298 K = 1.67 kbar.
Atomic mass of H, C and O is 1, 12, and 6 g mol$-$1, respectively)
Explanation:
$P_{g}=\left(K_{H}\right) X_{g}$
where $X_{g}$ is mole fraction of gas in solution
$0.835=1.67 \times 10^{3}\left(\mathrm{X}_{\mathrm{CO}_{2}}\right)$
$\mathrm{X}_{\mathrm{CO}_{2}}=5 \times 10^{-4}$
Mass of $\mathrm{CO}_{2}$ in $1 \mathrm{~L}$ water $=1221 \times 10^{-3} \mathrm{~g}$
The osmotic pressure of blood is 7.47 bar at 300 K. To inject glucose to a patient intravenously, it has to be isotonic with blood. The concentration of glucose solution in gL$-$1 is _____________.
(Molar mass of glucose = 180 g mol$-$1, R = 0.083 L bar K$-$1 mol$-$1) (Nearest integer)
Explanation:
$(\pi=\mathrm{CRT})$
(Where C represents the concentration of glucose solution and $\pi$ represents osmotic pressure)
$\mathrm{C}=\frac{7.47}{0.083 \times 300}\left(\mathrm{~mol} \mathrm{~L}^{-1}\right)$
which in $\mathrm{gm} / \mathrm{L}=\frac{7.47}{0.083 \times 300} \times 180$
$ =54 \mathrm{gm} / \mathrm{l} $
Explanation:
Vapour pressure of pure water $\left(\mathrm{P}_{\mathrm{A}}^{\circ}\right)$ $ =60.000 \mathrm{~mm} \text { of } \mathrm{Hg} $
Also, $0.1 \mathrm{~mol}$ of an ionic solid is dissolved in $1.8 \mathrm{~kg}$ of water and salt remains $90 \%$ dissocated in the solution.
So, total number of moles $=0.01+0.09 a$ of non-volatile particles.
Now, mass of water $=1.8 \mathrm{~kg}=1.8 \times 1.8 \times 1000 \mathrm{~g}$
Molar mass of water $=18 \mathrm{~g}$
Moles of water $=\frac{1.8 \times 1000}{18}=100$ moles
Using the colligative property, relative lowering in vapour pressure,
$ \frac{\mathrm{P}_{\mathrm{A}}^{\circ}-\mathrm{P}_{\mathrm{A}}}{\mathrm{P}_{\mathrm{A}}^{\circ}}=x_{\mathrm{A}} $
$ \Rightarrow $ $\frac{60-59.724}{60} =\frac{0.01+0.09 a}{100} $
$ \Rightarrow $ $ \frac{0.276}{60} =\frac{0.01+0.09 a}{100} $
$ \Rightarrow $ $ \frac{27.6}{60} =0.01+0.09 a $
$ \Rightarrow $ $ 0.46 =0.01+0.09 a $
$ \Rightarrow $ $ 0.09 a =0.45 $
$ \Rightarrow $ $ a =\frac{0.45}{0.89} $
$ \Rightarrow $ $ a =5 $
So, the number of ions present per formula unit of the ionic salt is 5 .
Explanation:
$\Delta$Tb = i Kb m
$\Delta$Tb = ${1 \over 2}$ $\times$ 2.6 $\times$ ${{1.22/{M_w}} \over {100/1000}}$ .... (1)
With Acetone as solvent
$\Delta$Tb = i Kb m
0.17 = 1 $\times$ 1.7 $\times$ ${{1.22/{M_w}} \over {100/1000}}$ ..... (2)
(1) / (2)
${{\Delta {T_b}} \over {0.17}} = {{{1 \over 2} \times 2.6 + {{1.22/{M_w}} \over {100/1000}}} \over {1 \times 1.7 \times {{1.22/{M_w}} \over {100/1000}}}}$
$\Delta$Tb = ${{0.26} \over 2}$
$\Delta$Tb = 13 $\times$ 10$-$2
$\Rightarrow$ x = 13
Explanation:
$ \Rightarrow \Delta {T_f} = {T_f} - {T_f}' = 1.86 \times {{10} \over 9}$
$ \Rightarrow {T_f}' = 273.15 - 1.86 \times {{10} \over 9}$
= 271.08 K
$ \simeq $ 271 K (nearest - integer)
[Given : Kf(H2O) = 1.86 K kg mol$-$1]
Explanation:
$\Rightarrow$ Mass of sucrose = (1000 $-$ x) gm
$\Rightarrow$ moles of sucrose = $\left( {{{1000 - x} \over {342}}} \right)$
$ \Rightarrow 0.75 = {{\left( {{{1000 - x} \over {342}}} \right)} \over {\left( {{x \over {1000}}} \right)}} \Rightarrow {x \over {1000}} = {{1000 - x} \over {342 \times 0.75}}$
$\Rightarrow$ 256.5x = 106 $-$ 1000x
$\Rightarrow$ x = 795.86 gm
$\Rightarrow$ moles of sucrose = 0.5969
New mass of H2O = a kg
$ \Rightarrow 4 = {{0.5969} \over a} \times 1.86 \Rightarrow $ a = 0.2775 kg
$\Rightarrow$ ice separated = (795.86 $-$ 277.5) = 518.3 gm
[Use : Molal Freezing point depression constant of water = 1.86 K kg mol$-$1]
Freezing Point of water = 273 K
Atomic masses : C : 12.0 u, O : 16.0 u, H : 1.0 u]
Explanation:
T$_f^o$ = 273 K
solvent : H2O(625 g)
Solute : 83 g of ethylene glycol
$\Rightarrow$ $\Delta$Tf = kf $\times$ m
$\Rightarrow$ $\left( {T_f^o - T_f^1} \right) = 1.86 \times {{83/62} \over {625/1000}}$
$ \Rightarrow 273 - T_f^1 = {{1.86 \times 83 \times 1000} \over {62 \times 625}} = {{154380} \over {38750}}$
$ \Rightarrow 273 - T_f^1 = 4$
$ \Rightarrow T_f^1 = 259$ K
(i) 0.10 M Ba3(PO4)2
(ii) 0.10 M Na2SO4
(iii) 0.10 M KCl
(iv) 0.10 M Li3PO4
Explanation:
(Round off to the nearest integer)
Explanation:

Now, $i = {{final\,moles} \over {initial\,moles}} = {{0.25a + 0.5a + 0.5a} \over {0.5a + 0.5a}}$
= 1.25 = 125 $\times$ 10$-$2
The molar mass of the biopolymer is _____________ $\times$ 104 g mol$-$1. (Round off to the Nearest Integer)
[Use : R = 0.083 L bar mol$-$1 K$-$1]
Explanation:
$\pi$ = osmotic pressure
C = molarity
T = Temperature of solution
let the molar mass be M gm/mol
2.42 $\times$ 10$-$3 bar = ${{\left( {{{1.46g} \over {Mgm/mol}}} \right)} \over {0.1l}} \times \left( {{{0.083l - bar} \over {mol - K}}} \right) \times (300K)$
$\Rightarrow$ M = 15.02 $\times$ 104 g/mol
[Given Kb for CCl4 is 5.0 K kg mol$-$1]
Explanation:
0.60 = 5 $\times$ $\left( {{{3/M} \over {100/100}}} \right)$
M = 250
(Henry's law constant for CO2 at 298 K is 1.67 $\times$ 103 bar)
Explanation:
Pgas = KH.Xgas
0.835 = 1.67 $\times$ 103 $\times$ ${{n(C{O_2})} \over {{{0.9 \times 1000} \over {18}}}}$
$ \Rightarrow $ n(CO2) = 0.025
Millimoles of CO2 = 0.025 $\times$ 1000 = 25
Explanation:
PT = xAPAo + xBPBo
= 0.6 $\times$ 90 + 0.4 $\times$ 15
= 54 + 6 = 60
xAPAo = yAPT
0.6 $\times$ 90 = yA(60)
$\Rightarrow$ yA = 0.9
yB = 0.1 = 1 $\times$ 10$-$1
$\therefore$ x = 1
Explanation:
Vapour pressure of pure methyl benzene, $p_B^o$ = 20 Torr
This mixture is equimolar, so number of moles of benzene,
nA = number of moles of methyl benzene, nB
Mole fraction of benzene in vapour phase, yA = ${{{p_A}} \over {{p_T}}}$ .... (i)
where pA is pressure of benzene in mixture.
${p_A} = \mathop {p_A^o{\chi _A}}\limits_{Mole\,fraction} = p_A^o \times {{{n_A}} \over {{n_A} + {n_B}}} = p_A^o \times {{{n \over A}} \over {2{n \over A}}} = {{p_A^o} \over 2}$
pT is total pressure,
${p_T} = p_A^o{\chi _A} + p_B^o{\chi _B} = {p_A} + {p_B}$ (pressure of methyl benzene)
${p_T} = {{p_A^o} \over 2} + {{p_B^o} \over 2} = {{p_A^o + p_B^o} \over 2}$
Putting in above equation (i),
${y_A} = {{{{70} \over 2}} \over {{{(70 + 20)} \over 2}}} = {{70} \over {90}}$
yA = 0.78 = 78 $\times$ 10$-$2
[Use : Kb for water = 0.52 K kg mol$-$1 Boiling point of water = 100$^\circ$C]
Explanation:
= 100.52 $-$ 100
= 0.52
$ \therefore $ $\Delta$Tb = Kb (iM)
$ \Rightarrow $ 0.52 = i $\times$ 0.52 $\times$ 2
$ \Rightarrow $ i = ${1 \over 2}$
We know,
i = 1 + $\left( {{1 \over n} - 1} \right)\beta $
here, $\beta$ = degree of dimerization
n = number of particle associated
n = 2 for dimerization
$ \therefore $ ${1 \over 2} = 1 + \left( {{1 \over 2} - 1} \right)\beta $
$ \Rightarrow \beta = 1$
$ \therefore $ % association = 100
[Given : Molal depression constant of water = 1.85 K kg mol$-$1 Freezing point of pure water = 0$^\circ$ C]
Explanation:
$ \Rightarrow $ 3.885 = i $\times$ 1.85 $\times$ 2
$ \Rightarrow $ i = 1.05
Also, we know,
i = 1 + (n $-$ 1) $\alpha$
here n = number of particle obtained upon the dissociation of one particle.
$HA\rightleftharpoons H^{+}+A^{-} $
here from one particle HA we get two particle H+ and A$-$.
$ \therefore $ n = 2
So, i = 1 + (2 $-$ 1)$\alpha$
$ \Rightarrow $ 1.05 = 1 + $\alpha$
$ \Rightarrow $ $\alpha$ = 0.05 = 50 $\times$ 10$-$3
Explanation:
Effective molality = 0.6 + 1.6 + 0.4 = 2.6 m
As elevation in boiling point is a colligative property which depends on the amount of solute. So, to have same boiling point, the molality of two solutions should be same.
Molality of non-electrolyte solution = molality of ${K_4}[Fe{(CN)_6}]$ = 2.6 m
Now, 18.1 weight per cent solution means 18.1 g solute is present in 100 g solution and hence, (100 $-$ 18.1) = 81.9 g water.
$Molality = {{(Mass\,of\,solute/Molar\,mass\,of\,solute)} \over {Mass\,of\,solvent\,in\,kg}} \times 1000$
Now, $2.6 = {{18.1/M} \over {81.9/1000}}$
where, M is the molar mass of non-electrolyte solute
Molar mass of solute, M = 85
[Given : Henry's law constant = KH = 8.0 $\times$ 104 kPa for O2. Density of water with dissolved oxygen = 1.0 kg dm$-$3 ]
Explanation:
The oxygen dissolved in water has a partial pressure of 20 kPa in the vapor phase above the water. To find the molar solubility of oxygen in water, we use Henry's Law, which states:
$ \text{Partial pressure} (P_g) \propto \text{Solubility} $
This can be mathematically expressed as:
$ P_g = K_H \times \text{Solubility} $
Where:
$ P_g $ is the partial pressure of oxygen, given as 20 kPa.
$ K_H $ is Henry's law constant for $ \text{O}_2 $, provided as $ 8.0 \times 10^4 \, \text{kPa} $.
Substituting the given values into the equation:
$ 20 \times 10^3 = (8.0 \times 10^4) \times \text{Solubility} $
Solving for solubility:
$ \text{Solubility} = \frac{20 \times 10^3}{8.0 \times 10^4} $
$ \text{Solubility} = 0.25 \times 10^{-1} $
$ \text{Solubility} = 25 \times 10^{-5} \, \text{mol dm}^{-3} $
Thus, the molar solubility of oxygen in water rounds to 25 × 10-5 mol dm-3.
Explanation:
${X_B} = {2 \over 3}$
$P_A^o = 21kPa$
$P_B^o = 18kPa$
${P_{total}} = P_A^o{X_A} + P_B^o{X_B}$
$ = 21 \times {1 \over 3} + 18 \times {2 \over 3}$
$ = 7 + 12$
$ = 19 kPa$
[Given : Molal elevation constant of water Kb = 0.5 K kg mol$-$1 boiling point of pure water = 100$^\circ$C]
Explanation:
$ \therefore $ For AB2, n = 3
i = 1 + (n $-$ 1)$\alpha$
= 1 + (3 $-$ 1) $\times$ 0.1
= 1.2
Now, $\Delta$Tb = Kb (im)
$ \Rightarrow $ Tb $-$ T$_b^o$ = 1.2 $\times$ 0.5 $\times$ 10
$ \Rightarrow $ Tb $-$ 100 = 6
$ \Rightarrow $ Tb = 106
Explanation:
Assuming $100 \%$ association ( $\alpha=1$ ),
$ \Rightarrow i=1-\alpha\left(1-\frac{1}{n}\right)=\frac{1}{n}[\because \alpha+1] $
Now, $\Delta T_f=K_f \times m \times i$
$ 0-(0.93)=1.86 \times \frac{w_B \times 1000}{w_A \times M_B} \times \frac{1}{n} $
$\left[\because w_B=\right.$ mass of $\mathrm{PhCOOH}=12.2 \mathrm{~g}$
$w_A=$ mass of $\mathrm{H}_2 \mathrm{O}=100 \mathrm{~g}$
$M_B=$ molar mass of $\left.\mathrm{PhCOOH}\right]$
$=122 \mathrm{~g} \mathrm{~mol}^{-1}$
$=1.86 \times \frac{12.2 \times 1000}{100 \times 122} \times \frac{1}{n}$
$ \begin{aligned} \Rightarrow n &=\frac{1.86 \times 12.2 \times 1000}{0.93 \times 100 \times 122}=2 \end{aligned} $
$\therefore$ Number of benzoic acid molecules associated, $n=2$
Explanation:
moles of NaOH = molarity × volume (in litre)
= 0.1 × 0.1
= 0.01 moles
The balanced equation is
SO2 + 2NaOH $ \to $ Na2SO3 + H2O
$ \therefore $ Here NaOH is limiting Reagent.
2 mole NaOH produces 1 mole Na2SO3
0.01 mole NaOH produces ${1 \over 2}$ $ \times $ 0.01 mole Na2SO3
$ \therefore $ Moles of Na2SO3 = 0.005 mole
Na2SO3 $ \to $ 2Na+ + SO32-
van’t Hoff factor (i) = 3
Moles of H2O = ${{36} \over {18}}$ = 2 moles
Accoding to Relative Lowering of Vapour :
${{P_{{H_2}O}^o - {P_S}} \over {P_{{H_2}O}^o}} = {{i{n_{N{a_2}C{O_3}}}} \over {{n_{{H_2}O}} + i{n_{N{a_2}C{O_3}}}}}$
[ ${{n_{N{a_2}C{O_3}}}}$ << ${{n_{{H_2}O}}}$ ]
${{P_{{H_2}O}^o - {P_S}} \over {P_{{H_2}O}^o}} = {{i{n_{N{a_2}C{O_3}}}} \over {{n_{{H_2}O}}}}$
$ \Rightarrow $ ${{24 - {P_S}} \over {24}} = {{3 \times 0.005} \over 2}$
$ \Rightarrow $ 24 – PS = 0.18
$ \Rightarrow $ PS = 23.82
Lowering in pressure ($\Delta $P) = 0.18 mm of Hg
= 18 × 10–2 mm of Hg
[Kb = 0.52 K kg mol$-$1]
Explanation:
As AB is a binary electrolyte,
$\therefore$ AB $\rightleftharpoons$ A+ + B$-$, n = 2
$i = 1 + \alpha (n - 1) = 1 + {{75} \over {100}}(2 - 1) = 1.75$
Given, $\Delta$Tb = 2.5 K
Kb = 0.52 K kg mol$-$1
$\therefore$ $\Delta$Tb = Kb $\times$ m $\times$ i
$ \Rightarrow m = {{\Delta {T_b}} \over {{K_b} \times i}} = {{2.5} \over {0.52 \times 1.75}}$
$ = 2.74 \simeq 3$ mol/kg
[Given Kb for (H2O) = 0.52 K kg mol$-$1]
Explanation:
No. of ions = 2 + 3 = 5
i = 1 + (n $-$ 1) $\alpha $
= 1 + (5 $-$ 1) $\times$ 0.6
= 1 + 4 $\times$ 0.6 = 1 + 2.4 = 3.4
$\Delta {T_b} = {K_b} \times m \times i = 0.52 \times 1 \times 3.4 = 1.768^\circ $ C
$\Delta {T_b} = {({T_b})_{solution}} - {[{({T_b})_{{H_2}O}}]_{Solution}}$
$1.768 = {({T_b})_{solution}} - 100$
${({T_b})_{solution}} = 101.768^\circ $ C
$ = 375$ K
Explanation:
Given,
$T_f^o = 5.5^\circ C$
${K_f} = 5.12^\circ C/m \Rightarrow m = 200g$
${m_{solute}} = 10g$
Molar mass of solute ${C_4}{H_{10}} = 12 \times 4 + 10 = 58$
Solute (C4H10) is non-dissociative;
$\therefore$ i = 1
$\therefore$ $\Delta {T_f} = i{K_f}\,m$
$ \Rightarrow (T_f^o - T_f^1) = 1 \times 5.12 \times {{(10/58)} \over {(200/1000)}}$
$5.5 - T_f^1 = {{5.12 \times 5 \times 10} \over {58}} \Rightarrow T_f^1 = 1.086^\circ C$
or $T_f^1 \approx 1^\circ C$
The value of x is ________. (Rounded off to the nearest integer)
[Kf(H20) = 1.86 K kg mol-1]
Explanation:

Here, $i = {{Final\,moles} \over {Initial\,moles}}$
i = 1 $-$ $\alpha$ + $\alpha$ + $\alpha$ $\Rightarrow$ i = 1 + $\alpha$
Formula used for freezing point; $\Delta$Tf = i Kfm
Here, Kf = freezing constant of H2O
Kf(H2O) = 1.86 K kg mol$-$1
m = molarity
$\Delta$Tf = i Kfm
0.5 = (1 + $\alpha$) (1.86)${{(9.45/94.5)} \over {(500/1000)}}$
${5 \over {3.72}}$ = 1 + $\alpha$ $\Rightarrow$ ${5 \over {3.72}}$ $-$ 1 = $\alpha$
$\Rightarrow$ $\alpha$ $ = {{1.28} \over {3.72}} = {{32} \over {93}} = 0.344$
Percentage of dissociation = 34.4%
Explanation:
Boiling point of solution $=100.1^{\circ} \mathrm{C} =\mathrm{X} $
Explanation:
$\mathrm{Ag}^{+}$and $\mathrm{Cl}^{-}$combine to form $\mathrm{AgCl}$ precipitate
$ \begin{array}{cccc} & \mathrm{Ag}^{+}(\mathrm{aq})+ & \mathrm{Cl}^{-}(\mathrm{aq}) \longrightarrow & \mathrm{AgCl}(\mathrm{s}) \\\\ \mathrm{t}=0 & 0.05 \mathrm{~m} & 0.1 \mathrm{~m} \\\\ \mathrm{t}=\infty & 0 & 0.05 \mathrm{~m} \end{array} $
In final solution total concentration of all ions :
$ \begin{aligned} & {\left[\mathrm{Cl}^{-}\right]+\left[\mathrm{NO}_3^{-}\right]+\left[\mathrm{Ba}^{2+}\right]=0.05+0.05+0.05} \\\\ & \begin{aligned} \Delta \mathrm{T}_{\mathrm{b}} & =0.5 \times 0.15 \\\\ & =0.15 \mathrm{~m} \\\\ & =0.075^{\circ} \mathrm{C} \end{aligned} \end{aligned} $
B.P. of solution ' $\mathrm{B}$ ' $=100.075^{\circ} \mathrm{C}$
B.P. of solution ' $\mathrm{A}^{\prime}=100.1^{\circ} \mathrm{C}$
$|y|=100.1-100.075$
$ =0.025=2.5 \times 10^{-2} $
[Given, molar mass of A = 100 g mol–1; B = 200 g mol–1; C = 10,000 g mol–1]
The following inferences are made :
(A) X has higher intermolecular interactions compared to Y.
(B) X has lower intermolecular interactions compared to Y.
(C) Z has lower intermolecular interactions compared to Y.
The correct inference (s) is / are :
[Assume 100% ionisation of the complex and CaCl2, coordination number of Cr as 6, and that all NH3 molecules are present inside the coordination sphere]
Explanation:
$\Delta $Tb = i Kb m = 3 × Kb × 0.05 = 0.15 Kb
Molality of CrCl3.xNH3 = 0.10 m
$\Delta $Tb' = i Kb $ \times $ 0.10
Given, $\Delta $Tb' = 2$\Delta $Tb
$ \Rightarrow $ i Kb $ \times $ 0.10 = 0.15 Kb
$ \Rightarrow $ i = 3
Co-ordination number of Cr is 6.
[Cr(NH3 )x.Cl6-x]Cl3-6+x $ \to $ [Cr(NH3 )xCl] + (3-6+x)Cl–
i = 3 = 1 + 3 - 6 + x
$ \Rightarrow $ x = 5
the glucose solution is x $ \times $ 10–3 atm. x is _____. (nearest integer)
Explanation:
For Glucose: $\pi $2 = 0.2 atm, v2 = 2 L
$\pi $mix = ${{{\pi _1}{v_1} + {\pi _2}{v_2}} \over {{v_1} + {v_2}}}$
= ${{0.1 \times 1 + 0.2 \times 2} \over {1 + 2}}$
= ${{0.5} \over 3}$ = ${{500} \over 3} \times {10^{ - 3}}$
= 167 $ \times $ 10-3 atm
Explanation:
550 = $P_1^o$$ \times $${1 \over 4}$ + $P_2^o$$ \times $${3 \over 4}$
$ \Rightarrow $ 2200 = $P_1^o$ + 3$P_2^o$ ....(1)
On addition of 1 more mole of n-heptane
560 = $P_1^o$$ \times $${1 \over 5}$ + $P_2^o$$ \times $${4 \over 5}$
$ \Rightarrow $ 2800 = $P_1^o$ + 4$P_2^o$ ....(2)
From (1) and (2),
$P_1^o$ = 400, $P_2^o$ = 600
Explanation:
Let molar mass of protein B = y g/mol
$\pi $A = osmotic pressure of protein A = ${{0.73} \over x} \times {{1000} \over {250}} \times RT$
$\pi $B = osmotic pressure of protein B = ${{1.65} \over y} \times {1 \over 1} \times RT$
Given $\pi $A = $\pi $B
$ \Rightarrow $ ${{0.73} \over x} \times {{1000} \over {250}} \times RT$ = ${{1.65} \over y} \times {1 \over 1} \times RT$
$ \Rightarrow $ ${x \over y}$ = ${{0.73} \over {0.25 \times 1.65}}$ = 1.77
= 177 $ \times $ 10-2
(Given, Kf (water) = 2.0 K kg mol–1,
R = 0.08 dm3 atm K–1 mol–1)
Explanation:
$\Delta $Tf = Kf.m = 2 × 0.5
$ \therefore $ Temperature of solution = –1°C = 272 K
$ \therefore $ Final volume of ideal gas = ${{nRT} \over P}$
= ${{0.1 \times 0.08 \times 272} \over 1}$
= 2.18 L