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93551.

0.1 Msolution of urea, at a given temperature, is isotonic with

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0.1M NACL solution
0.1 M GLUCOSE solution
0.02 M KCL solution
0.1 `M BaCl_(2)` solution

Answer :B
93552.

0.1 M NH_4OH is 1% ionized. Find the extent of hydrolysis of 0.1 M NH_4 Cl .

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SOLUTION :`10^(-4)`
93553.

0.1 M NaOH was gradually added to 50 ml of aqueous of CH_(3)COOH.Find pH of the solution at the equivalent point of the reaction. [ log 5 = 0.70]

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Solution :CONCENTRATION of the salt formed
`(0.1 xx 50)/(100)= (0.1)/(2)= 0.05 [LOG C= log 5 xx 10^(-2)= 0.7 -2.0 = -1.30]`
`pH= 7+ (1)/(2) [pKa + log C]= 7 + (1)/(2) [4.7 +(-1.30)] =7 + (1)/(2) [3.40]= 8.70`
93554.

0.1 M NaCl and 0.05 M BaCl_(2) solutons are separated by a semi-permeable membrane in a container. For this system choose the correct answer

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There is no movement of any solution ACROSS the membrane
Water flows from `BaCl_(2)` solution towards NaCl solution
Water flows from NaCl solution towards `BaCl_(2)` solution
OSMOTIC pressure of 0.1 M NaCl is lower than the osmotic pressure of `BaCl_(2)` (Assume complete dissociation)

Solution :Applying `pi V = iCRT`
i=2 for NaCl
i=3 for `BaCl_(2)`
`pi V_(NaCl)=2xx0.1 RT=0.2 RT`
`pi V_(BaCl_(2))=3xx0.05 RT =0.15 RT`
As `pi V_(NaCl)gt pi V_(BaCl_(2))`. So, water from `BaCl_(2)` towards `NaCl_(2)` solution.
93555.

0.1 M NaCl solution is placed in two different cells having cell constant 0.5 and 0.25 cm^(-1) respectively. Which of the two will have greater value of specific conductance?

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Solution :Specific conductance `kappa=1/rho*1/A`
Specific conductance `1/rho` is directly PROPORTIONAL to cell constant `1/A`.
`therefore` The cell with higher cell constant has greater value of specific conductance. i.e., The cell with 0.5 `CM^(-1)` cell constant will have greater value of specific conductance.
93556.

0.1 M NaCl and 0.1 M CH_(3)COOH are found to have osmotic pressures of P_(1) and P_(2) respectively then what is the correct ststement ?

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`P_(1)gtP_(2)`
`P_(1) if P_(2)`
`P_(1)`LT`P_(2)`
`P_(1)=P_(2)=0` atm.

Solution :`NACL` DISSOCIATES completely while `CH_(3)COOH` dissociates to a SMALL extent. Hence, `P_(1) gt P_(2).`
93557.

0.1M KI and 0.2 M AgNO_(3) are mixed in 3:1 volume ratio . The deperession in freezing point of the resulting solution will be 0.1 x (Assume Kf of H_(2)O=2Kg//"mol").

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`3.72K`
`1.86K`
`0.93K`
`0.279K`

ANSWER :D
93558.

0.1 M NaCl and 0.1 M CH_(3)COOH are kept in separate containers. If their osmotic pressures are P_(1) and P_(2) respectively then what is the correct statement ?

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`P_(2)gtP_(2)`
`P_(2)=P_(2)`
`P_(2)ltP_(2)`
`P_(2)=P_(2)=0 ATM,

Solution :Since NaCI is a stronger electrolyte than `CH_(3)COOH`, it will DISSOCIATE to freater EXTENT, and release ION (PARTICLE). Therefore, `P_(1)gtP_(2)`.
93559.

0.1 M HCl and 0.1 M H_(2)SO_(4), each of volume 2 ml are mixed and the volume is made up to 6 ml by adding 2ml of 0.01 N NaCl solution. The pH of the resulting mixture is

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1.17
`1.0`
0.3
log 2 - log 3

Solution :MILLIMOLES of `H^(+) = 0.1 xx 2 + 0.1 xx 2 xx 2 = 0.6`
TOTAL VOLUME in ML = 6
`pH = -log [H^(+)] = -log ((0.6)/(6)) = -log 0.1 = 1.0`.
93560.

0.1 M copper sulphate solution in which copper electrode is dipped at 25^@C. Calculate the electrode potential of copper. [Given E_(Cu^(2+)|Cu)^@ = 0.34]

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Solution :Given that
`[CU^(2+)] = 0.1 M`
`E_(Cu^(2+)|Cu)^@ = 0.34`
`E_("cell") = ?`
Cell reaction is `Cu^(2+) (aq) + 2r^(-) to Cu(s)`
`E_("cell") = E^(@) - (0.0591)/n log ([Cu])/([Cu^(2+)]) = 0.34 - (0.0591)/2 log 1/(0.1)`
`- 0.34 - 0.0296 = 0.31 V`.
93561.

0.1M copper sulphate solution in which copper electrode is dipped at 25^(@)C. Calculate the electrode potential of copper. [Given: E_(Cu^(2+)"|"Cu)^(@)=0.34]

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SOLUTION :Give that
` [Cu^(2+)] = 0.1M `
` E_(Cu^(2+|Cu^(@) = 034 `
` E_("cell") = ? `
Cell reaction is
` Cu_(aq)^(2+) + 2e^(-) to Cu_((s))`
` E_("cell")= E^(@) - ( 0.0591)/N log ([Cu])/([Cu^(2+)])`
` = 0.34 (0.0591)/2 log 1/(0.1)`
= 0.34 - 0.0294
0.31 V
93562.

0.1 M acetic acid solution is titrated against 0.1M NaOH solution. What would be the difference in Ph between 1/4 and 3/4 stages of neutralisation of acid :

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2 LOG 3/4
2log1/4
log1/3
2log3

Answer :D
93563.

0.1 litre so.ution is made by mixing 4 gram NaOH, 20 millimoles of H_(2)SO_(4), 40 millimoles of HCl and 20 millimoles of HNO_(3) what is the pH of solution.

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ANSWER :7
93564.

0.1 g atom of radioactive isotope ""_ZX^A (half-life 5 days) is taken. How many number of atoms will decay during eleventh day?

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SOLUTION :`N_0 = 0.1 atom`
`t = 10" daysand" t_(1//2) = 5` days
`LAMBDA = 2.303/t log""N_0/N`
`0.693/5 = 2.303/10 log""0.1/N`
`:.`Amount left after 10 days = 0.0250 g atom
Similarly if t = 11 days
`0.693/5 = 2.303/11 log""0.1/N`
`:.` Amount left after 11 days = 0.0218 g atom
`:.` Amount decayed in 11th DAY =0.0250- 0.0218
`= 3.2xx 10^(-3)` g atom
`=3.2 XX 6.023 xx 10^23 xx 10^(-3)" atoms" = 1.93 xx 10^21` atoms
93565.

01. ampere current is passed for 10 second through copper and silver voltameters . The metal that is deposited more is

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Cu
Ag
both (a) and (B)
no EFFECT

SOLUTION :`w ALPHA E` : provided Q is constant `, E_(Ag)^(@) GT E_(Cu)^(@)`
93566.

0.092 g of a compound with the molecular C_(3)H_(8)O_(3) on reaction with an excess CH_(3)MgI gives 67.00mL of methone at STP. The number of active hydrogen atoms present in a molecule of the compound is

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four
three
two
one

Solution :`ROH+CH_(3)MgIrarrCH_(4)+Mg(OR)I`
According to the above reaction EVERY one mole of a compound contaning one active `H` atom PER molecule releases one mole of `CH_(4)` GAS at `STP`. Thus, number of moles of `CH_(4)` gas realesed per mole of compound should be an indicator of the number of active HYDROGEN atoms per molecule of compound.
`n_(CH_(4))=(Vol. of CH_(4) at STP)/(22,400 mL mol^(-1))`
`=0.003 mol`
`n_("compound")=("mass")/("molar mass)"=(0.092g)/(92 g mol^(-1))`
`=0.001 mol`
This implies that `1` mol of compound releases `3` mols of `CH_(4)` gas i.e. there are `3` active hydrogen atoms present in a molecule of the compound.
93567.

0.0833 mol of carbohydrate of empirical formula CH_(2)O contain 1 gof hydrogen. The molecular formula of the carbohydrate is

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`C_(5)H_(10)O_(5)`
`C_(3)H_(4)O_(3)`
`C_(12)H_(22)O_(11)`
`C_(6)H_(12)O_(6)`

Solution :`:' 0.0833` mole carbohydrate has hydrogen `= 1g`
`:.` 1 mole carbohydrate has hydrogen
`= 1/(0.0833) =12g`
EMPIRICAL Formula `(CH_(2)O)` has hydrogen `= 2g`
Hence ` n = (12)/(2)= 6`
Hence molecular formula of carbohydrate `= 2g`
Hence `n = 12/2 =6`
Hence molecular formula of carbohydrate `= (CH_(2)O)_(6)`
`= C_(6)H_(12)O_(6)`.
93568.

0.0852g of an organic halide (A) when dissolved in 2.0g of camphor, the melting point in the mixture was found to be 167^(@)C. Compound (A) when heated with sodium gives a gas (B). 280mL of gas (B) at STP weight 0.375g. What would be 'A' in the whole process? K_(f) for comphor=40, m.pt. of camphor=179^(@)C.

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`C_2H_5Br`
`CH_3I`
`(CH_3)_2CHI`
`C_3H_7Br`

Solution :`DeltaT=179-167=12, w=0.0852g, W=2g, K_f`=40, molecular WEIGHT of (A)
`=(1000xxK_fxxw)/(DeltaTxxW)=(1000xx40xx0.0852)/(12xx2)=142`
(A) undergoes Wurtz REACTION to form (B) i.e.
`(A) overset(Na)to(B)+NaX`
(B)is an ALKANE say `C_nH_(2n+2)`
`:'` 280 mL of (B) weighs 0.375 g at NTP
`:.` 22400 mL of (B) weighs `=(0.375xx22400)/280`
= 30 g at NTP
`:.` M.wt. of (B) =30,12n+2n+2n+2=30,n=2
Thus (B) si ethane and THEREFORE (A) is `CH_3X`.
The m.wt.of `CH_3X=142`
At. wt. of X = 127 `:.` X is iodine
Therefore alkyl ahlide is `CH_3I`. This reaction is `underset((A))(2CH_3I)underset("either")overset(Na)tounderset((B))(C_2H_6)`
93569.

0.06% (w/v) aqueous solution of urea is isotonic with:

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0.1 M glucose SOLUTION
0.01M glucose solution
0.6% glucose solution
0.06% glucose solution

Solution :0.06% (W/V) = 0.06 G in 100 mLi.e. 0.6 g in 1000 ML
`M =0.6/60 = 0.01M`
93570.

0.06 mole og KNO_(3) solid is added to 100 cm^(3) of water at 298 K. The enthalpy of KNO_(3) aq solution is 35.8 kJ mol^(-1). After the solute is dissolved the temperature of the solutions will be

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293 K
298 K
301 K
304 K

SOLUTION :On APPLYING `mC_(p)Delta T`.
93571.

0.05M NaOH solution offered a resistance of 31.69Omegain a conductivity cell at 298K. If the cell constant of the conductivity cell is 0.367cm^(-1)the molar conductivity of the NaOH solution is

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`232 Omega^(-1) cm^2 "mol"^(-1)`
`234 Omega^(-1) cm^2 "mol"^(-1)`
`231 Omega^(-1) cm^2 "mol"^(-1)`
`230 Omega^(-1) cm^2 "mol"^(-1)`

ANSWER :A
93572.

0.05 moles of AICI_3 is required to coagulate 500 ml of As_2S_3 sol. If its coagulation value is 10^x find x

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SOLUTION :`500 to 0.05 ` MOLES
`1000 to ?`
`0.1` moles = 100 MILLI moles = `10^2`
93573.

0.05 m urea solution will have freezing point (K_(f) = 1.86 K kg "mol"^(-1) )

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273.093 K
273.186 K
272.907 K
272.814 K

Answer :B::C
93574.

0.05 M NaOH solution offered a resistance of 31.6 ohm in a conductivity cell. If the cell constant of cell is 0.367cm^(-1) , calculate the molar conductivity of the solution,

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Solution :Molarity =0.05
`R=31.6Omega`
cell constant, `(l)/(a)=0.367cm^(-1)`
`^^_(m)=(Kxx1000)/("Molarity")`
`=((1)/(R)xx(l)/(a)xx1000)/("MOLARTIY")`
`=(1)/(31.6)xx(0.367xx1000)/(.05)`
`=(0.367xx1000)/(31.6xx0.05)`
`=232.2ohm^(-1)cm^(2)MOL^(-1)`
93575.

0.05 M NaOH solution offered a resistance of 31.6 ohm in a conductivity cell. If the cell constant of cell is 0.367cm^(-1), calculate the molar conductivity of the solution.

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Solution :MOLARITY =0.05
`R=31.6Omega`
Cell consatant, `(L)/(a)=0.367cm^(-1)`
MOLAR conductivity,
`Delta_(m)=(Kxx1000)/("Molarity")`
`=((1)/(R)xx(l)/(a)xx100)/("Molarity")`
`=(1)/(31.6)xx(0.367xx1000)/(0.5)`
`=(0.367xx1000)/(31.6xx0.05)`
`=232.2ohm^(-1)cm^(2)MOL^(-1)`
93576.

0.04 N solution of a weak acid has a specific conductance 4.23 xx10^(-4)" mho.cm"^(-1). The degree of dissociation of acid at this dilution is 0.0612. Calculate the equivalent conductance of weak acid at infinite solution.

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Solution :Specific CONDUCTANCE `kappa=4.23xx10^(-4)"mho.cm"^(-1)`
`lambda_(C )=(kappa1000)/(C )=(4.23xx10^(-4)xx1000)/(0.04)`
`=10.575"mho.cm"^(2).EQ^(-1)`.
`alpha=0.0612=(lambda_(C ))/(lambda_(oo))=(10.575)/(lambda_(oo))`
`therefore lambda_(oo)="172.79 mho. cm"^(2)."gm. equiv."^(-1)`.
93577.

Specific conductance of 1 M KNO_(3) solution is observed to be 5.55 times 10^(-3)mho cm^(-1). What is the equivalent conductance of KNO_(3) when one litre of the solution is used?

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Solution :Specific conductance `kappa=4.23xx10^(-4)"mho.CM"^(-1)`
`lambda_(C )=(kappa1000)/(C )=(4.23xx10^(-4)xx1000)/(0.04)`
`=10.575"mho.cm"^(2).eq^(-1)`.
`alpha=0.0612=(lambda_(C ))/(lambda_(oo))=(10.575)/(lambda_(oo))`
`THEREFORE lambda_(oo)="172.79 mho. cm"^(2)."GM. equiv."^(-1)`.
93578.

0.04 g of pure NaOH is dissolved in 10 litof distilled water. The pH of the solution is:

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9
10
11
12

Answer :B
93579.

0.037 g of an alcohol was added to methyl magnesium iodide and the gas evolved at STP, occupies the volume 11.2 cm^(3). On dehydration, the alcohol gives an alkene. The alkene upon ozonolysis produces acetone as one of its products. The alcohol gives the carboxylic acid upon oxidation with same number of carbon atom. The alcohol is ...

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n-butyl ALCOHOL
Isopropyl alcohol
Isobutyl alcohol
Sec. Butyl alcohol

Solution :The molecular mass of
`R- OH= (22400 xx 0.037)/(11.2)= 74 g`
`:. C_(n)H_(2n+2)O= 74 IMPLIES 12n +(2n+2)+16= 74`
`implies n=4`
`to` The possible alcohols are n-butyl alcohol, isobutyl alcohol, sec. Butyl alcohol and tertiary butyl alcohol. As the alcohol gives the carboxylic acid with same number of carbon atoms UPON oxidation, the option (d) is ruled out. Also, option (b) is ruled out as the alcohol is of 4-carbon atoms.
The one of the products of ozonolysis of Alkene is acetone. Thus, alkene has = `C(CH_(3))_(2)` GROUP. Thus, alkene must be isobutylene, i.e., `(CH_(3))_(2) = CH_(2)`. So, the given alcohol is isobutyl alcohol.
93580.

0.037 g of an alcohol, ROH was added to CH_(3)MgI and the gas evolved measured 11.2 cm^(3) at N.T.P. What is the molar mass of alcohol ? On dehydration, ROH gave an alkene which on ozonolysis gave acetone as one of the products. ROH on oxidation easily gave an acid containing the same number of carbon atoms. give the structure of ROH and of acid with proper reasoning.

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Solution :(i) The molar mass of alcohol can be calculated as follows :

`11.2 cm^(3)` of `CH_(4)` are evolved from alcohol `=0.037 g`
`22400 cm^(3)` of `CH_(4)` are evolved from alcohol `=((0.037 g))/((11.2 cm^(3)))xx(22400 cm^(3))=74.0 g`.
(ii) General formula of alcohol `=C_(n)H_(2n+1)-OH`
`:.""12n+2n+1+17=74` or `14n+18=74`
`:.""14n=74-18=56` or `n=56//14=4`.
The molecular formula of alcohol `= C_(4)H_(9)OH`.
(iii) As the alcohol can be easily oxidised to ACID with the same number of carbon atoms, it is PRIMARY alcohol. Since on DEHYDRATION alcohol gives an alkene which upon ozonolysis gives acetone as ONE of the products, the alcohol must have `(CH_(3))_(2)CH-` group. Thus, the alcohol is isobutyl alcohol. The reactions involved a+re as follows :
`{:(""CH_(3)""CH_(3)""CH_(3)""H),("|""|""|""|"),(CH_(3)-CH-CH_(2)OH underset(-H_(2)O)overset(Conc. H_(2)SO_(4)//"heat")(rarr)CH_(3)-C=CH_(2)underset(Zn//H_(2)O)overset(O_(3))(rarr)CH_(3)-C=O+H-C=O),("Isobutyl alcohol""Isobutylene""Acetone""Formaldehyde"):}`
`{:(""CH_(3)""CH_(3)""CH_(3)),("|""|""|"),(CH_(3)-CH-CH_(2)OH underset(-H_(2)O)overset((O))(rarr)CH_(3)-CH-CHO overset((O))(rarr)CH_(3)-CH-COOH),("Isobutyl alcohol""Isobutyraldehyde""Isobutyric acid"):}`
93581.

0.037 g of an alcohol, ROH, was added to CH_3 MgIand the gas evolved measured 11.2 cm^3 at STP. What is the molecular weight of ROH? On dehydration, ROH gives an alkene which on ozonolysis gives acetone as one of the products. ROH on oxidation easily gives an acid containing the same number of carbon atoms. Give structures of ROH and the acid.

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SOLUTION :`C_4H_9OH, C_3H_2COOH`
93582.

0.025 g of starch sol is required to prevent the coagulation of 10 mL of gold sol when 1 mL of 10% NaCl solution is aded. What is the gold number of starch sol ?

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SOLUTION :Amount of starch sol needed to PREVENT the coagulation of gold sol = 0.025 g
= 25 mg. By DEFINITION, this REPRESENTS the gold NUMBER. Thus, gold number of starch = 25
93583.

0.023g of sodium metal is reacted with 100 cm^(3) of water. The pH of the resulting solution is :

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10
11
9
12

Solution :`M=(0.023xx1000)/(23xx100)=0.01M`
`NA^(+)+OH^(-)hArrNaOH`
`[OH^(-)]=0.01M=10^(-2)M," "pOH=-log(10^(-2))=2`
`pH+pOH=14`
`:." "pH=14-2rArrpH=12`.
93584.

0.02 mole of [Co(NH_(3))_(5)Br]Cl_(2) and 0.02 mole of [Co(NH_(3))_(5) Cl] SO_(4) are present in 200 cc of a solution X . The number of moles of the precipitates Y and Z that are formed when the solution X is treated with excess silver nitrate and excess barium chloride are respectively

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0.02 , 0.02
0.01 , 0.02
0.02 , 0.04
0.04 , 0.02

Solution :`[Counderset(0.02 "mole") underset(1"mole") ((NH_(3))_(5))Br]Cl_(2) + 2 underset(2 "MOLES")(AgNO_(3)) to [Co(NH_(3))_(5)underset(1 "mole")(Br)](NO_(3))_(2) + 2 Agunderset(2 "moles")(Cl)_((PPT)) (Y)`
`0.02 xx 2 = 0.04 ` mole
`[Co(NH_(3))_(5)underset(1 "mole")(Cl)]SO_(4) + underset(0.02 "moles")(BaCl_(2)) to [Co(NH_(3))_(5)underset(1 "mole")(Cl)] Cl_(2) + BaSO_(4)_("(ppt.)") underset(0.02 "moles")((Z))`
93585.

0.02 M monobasic acid dissociates 2% hence, pH of the solution is

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0.3979
1.3979
1.699
3.3979

Solution :`[H^(+)] = alpha.C = (2)/(100) xx 0.2, [H^(+)] = 4 xx 10^(-4)M`
`pH = -log [H^(+)] = 4 -log 4 , pH = 33979`.
93586.

0.02 g equivalent of Ag was deposited in an electrolysis experiment. Find the quantity of charge passed. If the same charge is passed through a gold solution, 1.314 g of gold is deposited. Find the oxidation state of gold (Given atomic mass of Au =197 amu)

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SOLUTION :(a) CALCULATION of quantity of charge passed :
The reaction at cathode is :
`Ag^(+)(aq)+UNDERSET((96500" C"))underset(1Faraday)(E^(-)) to underset(1g equivalent) (Ag(s))`
1g equivalent of Ag was deposited on passing charge `=96500" C"`.
0.02g equivalent of Ag was deposited on passing charge `=((96500C))/((1g" equiv".))xx(0.02g " equiv".)=1930" C"`
(b) Calculation of oxidation state of gold
1.314g of gold is deposited on passing charge`=1930" C"`
197g of gold is deposited on passing charge `=((1930 C))/((1.314 g))xx(197 g)=289353" C"`
`=(289353)/(96500)=3F`.
`:.` The oxidation state of gold is +3
`AU^(3+)(aq)+underset((3F))(3e^(-)) to underset((197g))(Au(s))`
93587.

0.02 g of gelatin is required to protect 10 mL of gold sol from 10% NaCl, then find the gold number for gelatin. Report your answer by multiplying by 100.

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Solution :Gold NUMBER is MINIMUM amount of protective colloid which can protect 10 mL standard gold SOL from COAGULATION when 1 mL of `10% NaCl` is added.
93588.

0.0125 mol of sucrose is dissolved in 100 gm of water and it undergo partial inversion according to following equation C_12H_22O_11+H_2OtoC_6H_12O_6+C_6H_12O_6 If elevation in boiling point of solution is 0.104^@C calculate 1/10 mol percentage of sugar inverted (K_b,_(H_2O)=0.52).

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SOLUTION :`underset("Mol")(C_12H_22O_11)+underset(0.0125)(H_2O)tounderset(0)(C_6H_12O_6)+underset(0)(C_6H_12O_6)`
`0.0125-x " " x ""x`
`DeltaT_b=m_1K_b+m_2K_b+m_3K_b`
`m_1+m_2+m_3=0.104/0.52=0.2`
`(0.0125-x+x+x)/100 xx1000=0.2`
x=0.0075
mol % `=0.0075/0.0125xx100=60%`
`1/10th` of mol% =`60/10=6`
93589.

0.01 molar solutions of glucose, phenol and potassium chloride were prepared in water. The boiling points of

Answer»

`GLUCOSE solution = Phenol solution = Potassium CHLORIDE solution `
`Potassium chloride solution gt Glucose solution gt Phenol solution `
`Phenol solution gt Potassium chloride solution gt Glucose solution `
`Potassium chloride solution gt Phenol solution gt Glucose solution `

Solution :`underset("Boiling point DECREASING order"rarr.)(KCl gt C_(6)H_(5)OH gt C_(6)H_(12)O_(6))`
Potassium chloride is ionic compound and phenol formed phenoxide ion hence it shows greater boiling point then glucose.
93590.

0.01 M solution of KCl and BaCl_(2) are prepared in water. The freezing points of KCl is found to be -2^(@)C. What is the freezing point of BaCl_(2) to be completely ionized

Answer»

`-3^(@)C`
`+3^(@)C`
`-2^(@)C`
`-4^(@)C`

Solution :i for KCl = 2, i for `BaCl_(2)=3 because Delta T_(F) PROP i`
`(Delta T_(f)(KCl))/(Delta T_(f)(BaCl_(2)))=(2)/(3)rArr Delta T_(f)(BaCl_(2))=(3)/(2)xx2=3^(@)C`
`therefore` Freezing point of `BaCl_(2)=-3^(@)C`.
93591.

0.01 M solution each of urea, common salt and sodium sulphate are taken, the ratio of depression in freezing point of these solutions is

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`1:1:1`
`1:2:1`
`1:2:1`
`1:2:3`

Solution :It is the RATIO of numberof PARTICLEIN solution Urea = 1, common salt =2 , sodium sulphat = 3.
93592.

0.01 M solution each of urea, common salt and Na_(2)SO_(4) are taken, the ratio of depression of freezing point is :

Answer»

`1:1:1`
`1:2:1`
`1:2:3`
`2:2:3`

ANSWER :C
93593.

0.01 M NaCl solution is placed in two different cells having cell constant 0.5 and 0.25 cm^(-1) respectively. Which of the two will have greater value of specific conductance.

Answer»

SOLUTION :The SPECIFIC CONDUCTANCE values are same. Because the reaction (CATION) of CELL constant does not change.
93594.

0.01 M aqueous glucose solution is more concentrated than0.01 M aqueous glucose solution.

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93595.

0.01 m aqueous solution of K_(3)[Fe(CN)_(6)] freezes at -0.062^(@)C. What is the apparent percentage of dissociation ? (K_(f)" for water = 1.86 K kg mol"^(-1))

Answer»


Solution :`DeltaT_(f)"(observed)"=0.062^(@)C`
`DeltaT_(f)"(CALCULATED)"=K_(f)xxm=1.86xx0.01=0.0186^(@)C`
`therefore""i=(DeltaT_(f)"(observed)")/(DeltaT_(f)"(calculated)")=(0.062)/(0.0186)=3.33`
`{:(,""K_(3)[Fe(CN)_(6)]hArr3K^(+)+[Fe(CN)_(6)]^(3-)),("Initial","1 MOL "),("After disso.",""1-ALPHA""3alpha ""alpha "Total "= 1+3alpha):}`
`therefore""i=(1+3alpha)/(1) or alpha=(i-1)/(3)=(3.33-1)/(3)=0.777=77.7%`.
93596.

0.004 M Na_(2)SO_(4) is isotonic with 0.01 M glucose. Degree of dissociation of Na_(2)SO_(4) is

Answer»

0.75
0.5
0.25
0.85

Solution :`(1+2alpha)0.004=0.01`
93597.

0.004M Na_(2)SO_(4) is isotonic with 0.01M glucose. Degree of dissociation of Na_(2)SO_(4) is :

Answer»

`25%`
`50%`
`75%`
`85%`

Answer :C
93598.

0.001 mole of strong electrolyte Zn(OH)_2 is present in 200 mL of an aqueous solution. The pH of this solution is

Answer»

2
4
12
10

Solution :`Zn(OH)_2hArrZn^(2+) + 2OH^(-)`
`[OH^-] = 0.001xx2xx 1000/200`
`[OH^-]=1 XX 10^(-2)mol L^(-1)`
`POH=- log[OH^(-) ]= log(1 xx 10^(-2) )= + 2 LOG10`
`pOH=2, pH+POH= 14`
`pH +2=14 impliespH = 12`
93599.

0.001 mole each of Fe^(2+) and Cd^(2+) is present in one litre of 0.02M HCl, saturated with H_2S . Find whether each of these ions shall precipitate as sulphides. Calculate [Cd^(2+)] in the solution at equilibrium. K_a(H_2S) = 1 xx 10^(-21), K_(sp) (Cds) = 8 xx 10^(-27) , K_(sp) (FeS) = 3.7 xx 10^(-19)

Answer»

Solution :CDS precipitates , `[Cd^(2+) ] = 3.86 X 10^(-8) M`
93600.

0.00012% MgSO_(4) and 0.000111% CaCl_(2) is present in water. What is the measured hardness of water and millimoles of washing sodarequired to purigy water 1000 L water ?

Answer»

Solution :Basis of calculation = 100 g hard water
`MgSO_(4) = 0.00012g = (0.00012)/(120) ` mole
`CaCl_(2)=0.00012 g = (0.000111)/(111) ` mole `:. ` EQUIVALENT moles of `CaCO_(3)=((0.00012)/(120)+(0.000111)/(111))` mole
`:.` mass of `CaCO_(3)=((0.00012)/(120)+(0.000111)/(111))xx100=2xx10^(-4)g`
Hardness (in terms of ppm of `CaCO_(3)`)=`(2xx10^(-4))/(100)xx10^(6)=2`ppm
`CaCl_(2)+Na_(2)CO_(3)rarrCaCO_(3)+2NaCl`
`NaSO_(4)+Na_(2)CO_(3)rarrMgCO_(3)+Na_(2)SO_(4)`
`:.` Required `Na_(2)CO_(3)` for 100g of water `=((0.00012)/(120)+(0.000111)/(111))` mole
`=2xx10^(-6)` mole
`:.` Required `Na_(2)CO_(3)` for 1000 litre water `=(2xx10^(-6))/(100)xx(2)/(100)` mole (`:.` d=1g/mL)
`=(20)/(1000)` mole = 20 m mole