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93451.

0.44 g of a colourless oxide of nitrogen occupies 224 ml at STP. The compound is :

Answer»

`N_2O`
NO
`N_2O_2`
`NO_2`

ANSWER :A
93452.

0.436g of acetyl derivative of a polyhydric alcohol (molecular mass =92) required 0.336g KOH for hydrolysis. Calculate the number of hydroxy gropus in the alcohol.

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Solution :We known that , `(w)/(w) (M+42n)=56 N`
where w is the amount of alkali, W amount ofacetyl DERIVATIVE, M is the molecular mass of alcohol and n NUMBER of HYDROXYL groups.
`(0.336)/(0.436)(92+42n)=56n`
or `92+42n=(0.436)/(0.336)xx56n=(218)/(3)n`
or `276+126n=218n`
or `n=3 ` ( The alcohol is trihydric. )
93453.

0.42g of an organic compound containing C, H, O and N gave on combustion 0.924g of CO_(2) and 0.243g of water. 0.208 g of the substance when distilled with NaOH gave NH_(3), which required 30 mL of (N/20) H_(2)SO_(4) solution for neutralization. Calculate the amount of each element in 0.42g of the compound.

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SOLUTION :Carbon Moles of C in `CO_(2)=1 xx` moles of `CO_(2)`
`=1 xx (0.924)/(44)= 0.021`
Weight of `C= 0.021 xx 12= 0.252g`
HYDROGEN Moles of H in `H_(2)O = 2 xx` moles of `H_(2)O`
`=2 xx (0.243)/(18)= 0.027`
Weight of `H= 0.027 xx 1= 0.027g`
NITROGEN m.e. of `H_(2)SO_(4)= (1)/(20) xx 30= 1.5`
`therefore` m.e. of `NH_(3)= 1.5`
Eq of `NH_(3)= (1.5)/(1000)= 0.0015`
moles of `NH_(3)= 0.0015`
Now moles of N in `NH_(3)=1 xx` moles of `NH_(3)= 0.0015`
Weight of N in 0.208g of the compound = `0.0015 xx 14`
=0.021g
`therefore` weight of N in 0.42g of the compound `=(0.021)/(0.208) xx 0.42` = 0.042g
Oxygen `therefore` TOTAL weight of C, H and `N= (0.252 + 0.027 + 0.042)g`
=0.321g
`therefore`weight of `O= 0.42- 0.321`
= 0.099g
93454.

0.400 g of an acid HA (mol. mass = 80) was dissolved in 100 g of water. The solution showed a depression of freezing point of 0.12 K. What will be the dissociation constant (in multiple of 10^(-3) ) of the acid at about 0°C? Given K_f (water) = 1.86 K Kg "mol"^(-1)(Assume molarity of solution a molality)

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Solution :MOLALITY (m) of solution `=(0.4 xx 1000)/(80 x 100) = 0.05`
`DeltaT_(f)` (normal) `=K_(f) xx m = 1.86 xx 0.05 = 0.093` K
Van.t Hoff factor,
`i=(DeltaT_(f) ("OBSERVED"))/(DeltaT_(f)("normal")) = 0.12/0.093 = 1.290`
`HA + H_(2)O `ALPHA =(i-1)/(n-1) = (1.290-1)/(2-1) = 0.29`
`K_(a) = (Calpha^(2))/(1-alpha) = (0.05 xx (0.29)^(2))/(1-0.29) = 5.92 xx 10^(-3)`
93455.

0.4 gm of He in a bulb at a temperature of 'T' K had a pressure of 'P' atm. When the bulb was immersed in hotter bath at a temperature 50K more than the first one, 0.08 gm of gas had to be removed to restore the original pressure. Then value of 'T' is:

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100K
200K
300K
500K

Solution :Since P and V is CONSTANT
`n_(i)T_(i)=n_(F)T_(f)`
`(0.4)/(4)xx(T)=((0.4-0.08))/(4)xx(T+50)`
`5T=4(T+50)`
T=200K
93456.

0.4 g of NaOH present in one litre solution shows the pH:

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12
2
6
10

Answer :A
93457.

0.3g of a compound on combustion gave 0.54g of water and 0.88g of carbon dioxide. Find the percentage of carbon and hydrogen in the compound

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ANSWER :80%, 20%
93458.

0.396 gm of a bromoderivative of a hydrocarbon (A) when vapourized occupied 67.2 ml at NTP. On reaction with aqueous NaOH, (A) gives (B). (B) when passed over alumina at 250^(@)C gives a neutral compound (C ), while at 350^(@)C it gives a hydrocarbon (D): (D) when heated with HBr gives an isomer of (A). When (D) is treat with conc. H_(2)SO_(4) and the product is diluted with water and distilled, (E) is obtained. Identify (A) to (E) and explain the reaction involved.

Answer»

Solution :Molecular WEIGHT of `A=(0.369xx22.4xx1000)/(67.2)=123`
(A) is a bromoderivative, so it may be written as R - Br.
`M_(RBr)=123`, So, R = 43 `because` Br = 80 (Atomic weight)
i.e. `C_(n)H_(2n+1)=43`
or `12n+2n+1=43`
or n = 3
`THEREFORE A=C_(3)H_(7)Br`
So, the POSSIBLE structures of (A) are `CH_(3)CH_(2)CH_(2)BrorCH_(3)-UNDERSET(Br)underset(|)(CH)-CH_(3)`
The reactions are as follow.

Since (D) gives an isomer of (A) on HBr addition, hence
(A) = `CH_(3)CH_(2)CH_(2)Brand(E)=CH_(3)underset(OH)underset(|)(CH)CH_(3)`
93459.

0.395g of an organic compound by Carius method for the estimation of S gave 0.582g of BaSO_(4). The percentage of S in the compound is :

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`20.24%`
`35.62%`
`12.24%`
`40.65%`

Solution :`underset(233)(BaSO_(4))-=underset(32)(S)`
`233g` of `BaSO_(4)` contain SULPHUR `=32g`
`0.582g` of `BaSO_(4)` contain sulphur
`=(32)/(233)xx0.582`
Percentage of sulphur
`=(32xx0.582)/(233xx0.395)xx100=20.24%`
93460.

0.38 gm of a silver salt of a dibasic acid on ignition gave 0.27 gm of silver. Molecular mass of acid is x xx 10 gm then x value is

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Solution :`E=("weight of SILVER salt")/("weight of silver") xx 108 -107`
93461.

0.38 g sample of NaNO_3is dissolved in 250 mlflask. The molarity of the solution is

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0.018 M
0.095 M
0.260 M
0.016 M

Solution :Moles of `NaNO_3 = (0.38)/(85)`
MOLARITY`= ( (0.38)/(85) XX 1000)/(250) = 0.018 M `
93462.

0.36g of Mg combines with chlorine to produce 1.425 g of mangesium chlorine 9.50g of another sample of anhydrous magnesium chloride gave, on electrolysis 2.24 litre of chlroine at NTP. Show that these data agree with the law of constant proportions.

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SOLUTION :Mass of 2.24 LITRE of CHLORINE at NTP`=(71)/(22.4)xx2.24=7.1`
93463.

0.36g of an organic compound containing sulphur produced H_(2)SO_(4) by Carius method, which on treatment with BaCl_(2) produced quantitatively 0.2330g of BaSO_(4). Calculate the percentage of S in the compound. (Ba= 137, S= 32, O= 16)

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SOLUTION :Moles of S in `BaSO_(4) = 1 XX` moles of `BaSO_(4)`
`=(0.2330)/(233)= 0.001 (BaSO_(4)= 233)`
WEIGHT of `S= 0.001 xx 32G`
`=0.032g`
% of `S= (0.032)/(0.36) xx 100= 8.89%`
93464.

0.369g of a bromo derivative of a hydrocarbon (A) when vaporised occupied 67.2mL at NTP. (A), on reaction with aqueous NaOH, gives (B). (B), when passed over alumina at 250^(@)C, gives a neutral compound (C ) while at 300^(@)C, it gives a hydrocarbon (D). (D), when heated with HBr gives an isomer of (A). When (D ) is treated with concentrated H_(2)SO_(4) and the product is diluted with water and distilled, (E ) is obtained Identify (A) to (E ).

Answer»

SOLUTION :
93465.

0.3605 g of a metal is deposited on the electrode by passing 1.2 ampere current for 15 minutes through its salt. Atomic weight of the metal is 96. what will be its valency?

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SOLUTION :CALCULATE the WT. deposited by 96500 coulombs. This will be the equivalent wt.
Then valency=At. Wt/Eq. wt.\
93466.

0.32g of a metal gave on treatment with an acid 112mL. Of hydrogen at NTP. Calculate equivalent mass of the metal:

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58
32
11.2
24

Solution :MASS of metal tthat DISPLACES 11200ml, HYDROGEN at STP will be its equivalent mass.
`therefore` Equivalent mass of metal`=(0.32)/(112)xx11200=32`
93467.

0.32 g of a metal on treatment with an acid gave 112 mL of hydrogen at NTP. Calculate the equivalent weight of the metal

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58
32
11.2
24

Solution :Equivalent WEIGHT of a metal is the mass of the metal which produces 11200 mL of `H_(2)` at NTP.
112 ml of `H_(2)` at NTP are PRODUCED from metal
`=0.32 g`
`therefore 11200` mL of `H_(2)` will be produced from metal
`=(0.32)/(112)xx11200`
= 32 g
93468.

0.31 gm of an ally Fe+ Cu was dissolved in excen dilute H_(2)SO_(4) and the solution was made up to100 ml . 20 ml of this soltin required 3 m of N/30 K_(2)Cr_(2)O_(7) solution for exact oxidation. The % purity (in closest value) of Fe in wire is ____________.

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ANSWER :9
93469.

0.30g of an organic compound contaiining C, H and Oxygen an combustion yields 0.44gCO_2 and 0.18g H_2O. If onemol of compound weight 60, then molecular formula of the compound is

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`C_2H_4O_2`
`C_4H_6O`
`C_3H_8O`
`CH_2O`

SOLUTION :Percentage of `C = 12/44 XX 0.44/0.30 xx 100 = 40%`
Percentage of `H= 12/18 xx 0.18/0.30 xx 100 = 6.6%`
Percentage of `O = 100-(40 + 6.6) = 53.4%`

Hence empirical formula `= CH_2O`
`n = ("Molecular mass")/("Emperical formula mass") =60/30 = 2`
`rArr ` Molecular formula of the compound` = (CH_2O)_2 = C_2H_4O_2`
93470.

0.30g of an organic compound containing C, Hand Oxygen on combustion yields 0.44g CO_(2) and 0.18g H_(2)O. If one mole of compound weighs 60, then molecular formula of the compound is

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`C_(3)H_(8)O`
`C_(2)H_(4)O_(2)`
`CH_(2)O`
`C_(4)H_(6)O`

Solution :PERCENTAGE of `C=(12)/(44)XX(0.44)/(0.30)xx100=40%`
Percentage of `=(2)/(18)xx(0.18)/(0.30)xx100=6.6%`
percentate of `O=100-(40+6.6)=53.4%`

Hence, EMPIRICAL formula `=CH_(2)O`
`n=("Molecular mass")/("Empirical formula mass")=(60)/(30)=2`
`rArr` Molecular formula of COMPOUND `=(CH_(2)O)_(2)`
`=C_(2)H_(4)O_(2)`
93471.

0.3 g of an acid is neutralised by 40 cm^(3) of 0.125 N NaOH. Equivalent mass of the acid is

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60
45
30
63

Solution :`40cm^(3)` of 0.125 N NAOH neutralise ACID = 0.3 g
`therefore 1000cm^(3)` of 1 N NaOH will neutralise acid
`=(0.3)/(40)xx(1000)/(0.125)g=60g`
`1000cm^(3)` of 1 N NaOH contain one g ram equivalent of NaOH. It will neutralise one gram equivalent of the acid.
Hence, equivalent WEIGHT of acid = 60
93472.

02g of a monobasic organic acid containing C, H and O on combustion gave 0.505g of CO_(2) and 0.0892 g of H_(2)O. 0.183g of this acid required 15cc of N/10 NaOH for exact neutralisation. Find the molecular formula of the acid.

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Solution :Moles of `C=1 xx` moles of `CO_(2)= (0.505)/(44)=0.0115`
Wt. of `C= 0.0115 xx 12= 0.1380g`
Moles of `H=2 xx` moles of `H_(2)O=2 xx (0.0892)/(18)=0.0099`
wt of `H= 0.0099 xx1= 0.0099g`
Wt of O = wt of the compound -(wt. of C + wt. of H)
`=0.2 -(0.1380 + 0.0099)= 0.0521g`
Moles of `O= (0.0521)/(16)=0.0033`
`THEREFORE` moles of `C: H: O= 0.0115: 0.0099: 0.0033`
`=115: 99: 33`
`=3.5:3:1=7:6:2`
Empirical formula is `C_(7)H_(6)O_(2)`
Now, since the acid is monobasic, mol wt. = eq. wt
`therefore` EQUIVALENT of the acid `=(0.183)/("eq.wt")=(0.183)/("mol wt")`
`therefore` m.e. of the acid `=(0.183)/("mol. wt") xx 1000`
`=(183)/("mol.wt")`
m.e. of the BASE `=(1)/(10) xx 15=1.5`
`because` m.e. of the acid= m.e. of the base `(183)/("mol wt")=1.5 therefore` mol. wt.=122
Since the empirical formula weight, i.e., `84+6+32+122`, is equal to the molecular formula weight, the molecular formula of the acid is the same as the empirical formula. Hence the formula is `C_(7)H_(6)O_(2)`.
93473.

0.2964g of Cu was deposited on passage of a current of 0.5 amp for 30 min through a solution of copper sulphate. Calculate the atomic weight of Cu.

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ANSWER :63.56
93474.

0.2864 of Cu was deposited on passage of a current of 0.5 ampere for 30 minutes through a solution of copper sulphate. What is the electrochemical equivalent of copper ? "(1 F = 96500 coulombs)"

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Solution :Electrochemical equivalent (Z) is defined as the weight of the substance deposited by the passage of 1 coulomb of electricity.
`therefore z = ("wt. of Cu deposited")/("CHARGE in COULOMBS")`
`= ("wt. of Cu")/("current in AMPERE " xx " time in seconds")`
`= (0.2864)/(0.5 xx 30 xx 60)`
= 0.00032g/coulomb.
93475.

0.28 g of nitrogenous was subjected to Kjeeldahl's proicess to produce 0.17 g of NH_(3). The percentage of nitrogen in the organic compound id :

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5
10
50
80

Solution :N//A
93476.

0.2614g of an organic compound gave upon combustion 0.2324g of CO_(2) and 0.0950g of H_(2)O. 0.1195g of this compound gave 0.3470g of AgCl. If the vapour density of the substance is 49.5, calculate its molecular formula.

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SOLUTION :`(C_(2)H_(4)Cl_(2))`
93477.

0.261 g ofa sample of pyrolusite was heated with excess of HCl and the chlorine evolved was passed in a solution of Kl . The liberated iodine requuired 90 mL N/30Na_(2)S_(2)O_(3). Calculate the percentage of MnO_(2) in the sample.

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SOLUTION :N/A
93478.

0.25g of an organic compound on Kjeldahl's analysis gave enough ammonia to just neutralise 10cm^(3) of 0.5M H_(2)SO_(4). The percentage of nitrogen in the compound is

Answer»

`28`
`56`
`14`
`112`

Answer :B
93479.

0.2595g of an organic compound yielded quantitatively 0.35g of BaSO4. Find the percentage of sulphur in the compound. (Ba= 137.3, S= 32, O= 16)

Answer»


ANSWER :`18.5%`
93480.

0.2595 g of an organic substance in a quantitative analysis yielded 0.35 g of the barium sulphate. The percentage of sulphur in the subtance is

Answer»

`18.52 G`
`182.2 g`
`17.5 g`
`175.2 g`

Solution :`%` of `S = 32/233 XX (" w.t of " BaSO_(4))/(" w.t of ORGANIC COMPOUND") xx 100`
`= 32/233 xx (0.35)/(0.2595) xx 100 = 18.52% gm`.
93481.

0.25 mole of propane is subjected to combustion. If this reaction is used for making a fuel cell, the number of moles of electrons involved in each half cell for this amount of propane will be

Answer»

Solution :No of moles of electrons involved for 1 MOLE of `C_(3)H_(8)=20`
`therefore`. No. of moles of electrons involved for 0.25 mole of `C_(3)H_(8)=5`.
93482.

0.25 g of an element 'M' reacts with excess fluorine to produce 0.547g of the hexafluoride MF_(6). What is the element?gt

Answer»

Cr
Mo
S
Te

Answer :B
93483.

0.2475g of an organic compound on combustion gave 0.4950g of CO_(2) and 0.2025g of H_(2)O. Calculate the percentage of oxygen in the compound

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ANSWER :0.3637
93484.

0.245 g of nitrogenous organic compound was Kjeldahlised and ammonia was absorbed in 10 ml of 0.1 N H_(2)SO_(4). The unreacted acid requires 3ml of 0.1N NaOH for complete neutralization. Calculate the percentage of nitrogen in the organic compound.

Answer»


SOLUTION :By Kjeldhal METHOD
93485.

0.2435 g of a complex gave 0.2870 g of AgCl when treated with a excess AgNO_(3) solution. The complex is

Answer»

`[Cr(NH_(3))_(4)Cl_(2)]Cl`
`[Cr(NH_(3))_(5)Cl_(2)]Cl_(2)`
`[Cr(NH_(3))_(3)Cl_(3)]`
`[Cr(NH_(3))_(6)Cl_(2)]Cl_(3)`

Solution :No. of moles of AGCL = `(0.287)/(143.5) = 0.002` moles
B can give 2 moles of AgCl.
93486.

0.220g of a sample of a volatile compound, containing carbon, hydrogen and chlorine yielded on combustion in oxygen 0.195g of CO_(2), 0.0804g of H_(2)O. 0.120g of the compound occupied a volume of 37.24mL at 105^(@)C and 768mm Hg pressure. Calculate the molecular formula of the compound.

Answer»

Solution :Moles of C in `CO_(2)=1 xx` moles of `CO_(2)= (0.195)/(44)=0.00443`
Weight of `C= 0.00443 xx 12=0.05316g`
Moles of H in `H_(2)O =2xx` moles of `H_(2)O= 2 xx (0.0804)/(18)= 0.00893`
Weight of `H= 0.00893 xx1= 0.00893g`
`therefore` weight of Cl= 0.22 `-(0.05316 + 0.00893)g= 0.15791g`
Moles of `Cl= (0.15791)/(35.5)= 0.00445`
Moles of `C: H: Cl= 0.00443: 0.00893: 0.00445`
`=443: 893: 445=1:2:1`
i.e., the empirical formula is `CH_(2)Cl`
Now, volume of the vapour of 0.12g of compound at NTP
`=(37.24 xx 768)/(378)xx (273)/(760)=27.18mL`
Moles of the compound `=(0.12)/(M)` (M = mol .wt)
`=(27.18)/(22400)`
`thereforeM = 99`
`therefore ("molecular formula weight")/("empirical formula weight")= (99)/(49.5)=2`
Hence, the empirical formula is `(CH_(2)Cl)_(2)`, i.e. `C_(2)H_(40Cl_(2)`
93487.

0.22 g sample of volatile compound, containing C, H and Cl only on combustion in O_2 gave 0.195 g CO_2 and 0.0804 g H2O. If 0.120 g of the compound occupied a volume of 37.24 mL at 105^@ and 768 mm of pressure, calculate molecular formula of compound.

Answer»

SOLUTION :`C_2H_4Cl_2`
93488.

0.2060 g of a substance gave 18.8mL of moist nitrogen at 17^(@)C and 756mm pressure. If the vapour tension at 17^(@)C is 14.5mm, find the percentage of nitrogen in the compound

Answer»


ANSWER :0.1056
93489.

0.21 g of an organic compound containing C, H, O and N gave upon combustion 0.462g of CO_(2) and 0.1215g of H_(2)O. The ammonia produced on distillation of 0.104g of this compound with NaOH, required 15mL of N/20 H_(2)SO_(4) for neutralisation. Find the empirical formula of the compound

Answer»

SOLUTION :`(C_(7)H_(9)NO_(2))`
93490.

0.2033 g of an organic compound in Dumas method gave 31.7m L of moist nitrogen at 14^(@)C and 758mm pressure. Calculate the percentage of nitrogen in the compound. (Aqueous tension at 14^(@)C=14mm, N= 14)

Answer»

Solution :Pressure due to nitrogen only `=758-14=744mm`
VOLUME of nitrogen at NTP `=(744 xx 31.7 xx 273)/(287 xx 760)`
=29.52mL
Mole of nitrogen `=(29.52)/(22400)`
Weight of nitrogen `(N_(2))= (29.52)/(22400) xx 28= 0.0369g`
% of nitrogen `=(0.0369)/(0.2033) xx 100`= 18.16%
93491.

0.20 g of a hydrocarbon on combustion gave 0.66 g CO_2 . The percentage of hydrogen in the hydrocarbon is about :

Answer»

33
45
10
90

Answer :C
93492.

0.2 percent solution of phenol is a/an

Answer»

ANTISEPTIC
DISINFECTANT
antibiotic
antifertility drug

Answer :A
93493.

0.2% solution of Phenol is an :

Answer»

ANTIBIOTIC
ANTISEPTIC
Disinfectant
Analgesic

Answer :B
93494.

0.2 mole sample of hydrocarbon C_(x)H_(y) yields after complete combustion with excess O_(2) gas, 0.8 mole of CO_(2), 1.1 mole of H_(2)O Hence, hydrocarbon is

Answer»

`C_(4)H_(10)`
`C_(4)H_(6)`
`C_(4)H_(5)`
`C_(8)H_(16)`

ANSWER :A
93495.

0.2 molar solution of formic acid is ionized to 3.2 %. Its ionisation constant is :

Answer»

`9.6xx10^(-3)`
`2.05xx10^(-4)`
`1.25xx10^(-6)`
`4.8xx10^(-5)`

SOLUTION :`K_(a)=c alpha^(2), c = 0.2 M, alpha = (3.2)/(100)=0.032`
`K_(a)=0.2xx(0.032)^(2)=2.05xx10^(-4)`
93496.

0.2 molar solution of formic acid is ionized 3.2%. Its ionizationconstant is

Answer»

`9.6 XX 10^(-3)`
`2.1 xx 10^(-4)`
`1.25 xx 10^(-6)`
`4.8 xx 10^(-5)`

SOLUTION :`K_(a) = C ALPHA^(2) = 0.2 xx ((3.2)/(100))^(2) = 2.048 xx 10^(-4) = 2.1 xx 10^(-4)`.
93497.

0.2 molal acid HX is 20% ionised in solution K_"f" = 1.86 K "molality"^(–1). The freezing point of the solution is -

Answer»

– 0.45
– 0.90
– 0.30
–0.53

Answer :A
93498.

0.2 M NaOH is titrated with 100 ml 0.2 M CH_(3) COOH in a conducitivity cell. The data obtained were plotted as following The pH of solution in conductivity cell is 9 at point B. Calculate pH of conductivity cell when 100 ml 0.1 M HCl added in resulting solution present in conducitivity cell at point B.

Answer»


Solution :`CH_(3)COOH(AQ)+NaOH(aq)rarrCH_(3)COONA(g)+H_(2)O`
`{:(,(0.2xx100)/(1000),(0.2xx100)/(1000)," "0," "0),(," "0,0,0.02," "0.02):}`
`pH=9=(1)/(2)(pKw+pKa+log .(0.02)/(0.2))`
` 18=14+pKa-1`
`pKa=5`
`CH_(3)COONa(aq)+HCl(aq)rarrCH_(3)COOH(aq)+NaCl(aq)`
`{:(,0.02,(100xx0.1)/(1000)=0.01,0,0),(,0.01," "0,0.01,0.01):}`
Acidic buffer
`pH=pKa+log.(CB)/(CA)`
`pH=5+log.(0.01)/(0.01)`
`ph=5`
93499.

0.2maqueoussolutionof KC1freezes at - 0.680^(@)C. Calculatevan'tHofffactorand osmoticpressureof solutionat0. ^(@)C (K_(f)= 1 .86 Kkg "mol"^(-1))

Answer»

SOLUTION :van'tHofffactor=`1= 1.83 , pi_(OB) = 8.19 ATM`
93500.

0.2 m aqueous solution of a weak acid (HX) is 20% dissociated. The boiling point of this solution is ( K_(b) for water = 0.52 Km^(-1))

Answer»

`101.04^(@)C`
`100.104^(@)C`
`100.1248^(@)C`
`100.52^(@)C`

Solution :`{:("HX(AQ)",rarr,"H"^(+),+,"X"^(-)),(m(1-0.20),,m(0.20),,m(0.20)):}`
MOLAL CONC. of soln.
`=m(1-0.20)+0.20m +0.20m`
`=1.20m`
`DeltaT_(b)=K_(b) xx m`
`=0.52 xx 1.20(0.2)=0.1248`
Boiling point `=100.1248^(@)C`