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87201.

A solution of a metal ion when treated with KI gives a red precipitate which dissolves in excess KI to give a colourless solution. Moreover, the solution of metal ion on treatment with a solution of cobalt (II) thiocyanate gives rise to a deep blue crystalline precipitate. the metal ion is

Answer»

`Pb^(2+)`
`HG^(2+)`
`Cu^(2+)`
`Co^(2+)`

Solution :`Hg^(2+)+2KItoHgI_(2)darr+underset("red PPT")(2K^(+))`
`HgI_(2)+2KItoK_(2)HgI_(4)`
`Hg^(2+)+Co^(2+)+underset("deep BLUE crystalline")(4SCN^(-)toCoHg(SCN)_(4)darr"")`
87202.

A solution of a metal ion when treated with KI gives a red precipitate which dissolves in excess KI to give a colourless solution. Morever, the solution of metal ion on treatment with a solution of cobalt (II) thiocyanate gives rise to a deep blue crystalline precipitate. The metal ion is :

Answer»

`Pb^(2+) `
`Hg^(2+) `
`CU^(2+)`
`Co^(2+)`

SOLUTION :`Hg^(2+) (aq) + 2KI (aq) to underset("(Scarlet RED)")(HgI_2 (s)) + 2K^(+) (aq)`
`HgI_2(s) + 2KI (aq) to K_2[HgI_4](aq)`
`Co^(2+)(aq) + Hg^(2+) (aq) + 4SCN^(-) (aq) to underset("DEEP blue ")(Co[Hg(SCN)_4])(s)`
87203.

A solution of a metal ion when treated with KI gives a red precipitate which dissolves in excess KI to give a colourless solution.Moreover, the solution of metal ion on treatment with a solution of cobalt (II) thiocyanate gives rise to a deep blue crystalline precipitate.The metal ion is:

Answer»

`Pb^(2+)`
`Hg^(2+)`
`Cu^(2+)`
`Co^(2+)`

SOLUTION :`Hg^(2+)+2I^(-)to HgI_(2)DARR` (scarlet/red)
`HgI_(2)+2I^(-)("excess")to[HgI_(4)]^(2-)`(soluble complex)
`Hg^(2+) +Co(SCN)_(2) to Co[Hg(SCN)_(4)]darr` (DEEP blue)
87204.

A solution of A is mixed with an equal volume of a solution of B containing the same number of moles, and the reaction A + B = C occurs. At the end of 1h, A is 75% reacted. How much of A will be left unreacted at the end of 2 h if the reaction is (a) first order in A and zero order in B, (b) first order in both A and B , and (c) zero order in both A and B ?

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SOLUTION :(a) 6.25, (B) 14.3, (C )0%
87205.

A solution of A and B with 30 moles present of A is in equilibrium with its vapour which contain 60 mole percent of A. Assuming that the solution and the vapour behave ideally, calculate the ratio of the vapour pressures of pure A and pure B.

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Solution :`{:("In solution",x_(A)=0.30, therefore, x_(B)=0.70),("In the vapour phase,",y_(A)=0.60,therefore,y_(B)=0.40):}`
But`y_(A)=(p_(A))/("TOTAL V.P.")=(p_(A))/(p_(A)+p_(B))=(x_(A)p_(A)^(@))/(x_(A)p_(A)^(@)+x_(B)p_(B)^(@))=(0.30p_(A)^(@))/(0.30p_(A)^(@)+0.70p_(B)^(@))=0.60"...(i)"`
`y_(B)=(p_(B))/(p_(A)+p_(B))=(x_(B)p_(B)^(@))/(x_(A)p_(A)^(@)+x_(B)p_(B)^(@))=(0.70p_(B)^(@))/(0.30p_(A)^(@)+0.70p_(B)^(@))=0.40"...(II)"`
Dividing EQN. (i) by eqn. (ii), `(0.30p_(A)^(@))/(0.70p_(B)^(@))=(0.60)/(0.40) or (p_(A)^(@))/(p_(B)^(@))=(0.60)/(0.40)xx(0.70)/(0.30)=3.5`
87206.

A solution of a 0.4 g sample of H_(2)O_(2) reactedwith 0.632g of KMnO_(4)in the pressure of sulphuricacid.Calculatedthe percentage purity of the sample of H_(2)O_(2) .

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Solution :`{:(2KMnO_(4),+3H_(2)SO_(4),+5H_(2)O_(2) ,to K_(2)SO_(4),+2MnSO_(4),+8H_(2)O,+5O_(2)),("+7",,,,"+2",,):}`
Eq . Wt . Of `KMnO_(4) = (" mol.wt")/("change in ON per mole ") = 158/5 = 31/6`
Again from the above reaction we see that
2 moles of `KMnO_(4)` combine with 5 moles of `H_(2)O_(2)`
Again from the above reaction we see that
2 moles of `KMnO_(4)` combine with 5 moles of `H_(2)O_(2)`
or 1 equivalentof `KMnO_(4)` combines with `1/2 ` molesof `H_(2)O_(2)`
` :. ` equivalentwt. of `H_(2)O_(2) = (" mol .wt")/2 = 34/2 = 17 `
Now , m.e of `H_(2)O_(2)` = m.e of `KMnO_(4)`
oreq. of `H_(2)O_(2)`= eq. of `KMnO_(4)`
`x/17=(0.632)/(31.6) "" ` ....(EQN . 4I)
x being the amount of `H_(2)O_(2)` is GRAMS ,
x = 0.34 g
Percentage of `H_(2)O_(2)` in the sample = `(0.34)/(0.4) xx 100 = 85 % `
87207.

A solution of 7 g of a non-volatile solute in 250 g of water boils at 100.26^(@)C. Find the molecular mass of th solute K_(b) for water is 0..52 K kg mol^(-1) .

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Solution :Elevation in BOILING point, `DeltaT_(b)=100.26-100=0.26^(@)C=0.26 K`
`M_(B)=(K_(B)xxW_(B))/(DeltaT_(b)xxW_(A))=((0.52" K kg mol"^(-1))XX(7g))/((0.26 K)xx(0.250" Kg"))=56" g mol"^(-1)`
87208.

A solution of 6.2 g ethylene glycol is dissolved in 55 g of water (Kf=1.86-kg "mol2"^(-1)), is cooled to -3.72^(@)C. What is the weight (in grams) of the ince separated from the solution ?

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87209.

A solution of 3.0xx10^(4) kg of comphor (C_(6)H_(16)O) in 25.3xx10^(-3) kg of cholorform boils at 61.3^(@)C if K_(b) for chloroform is 3.83 k kg "mol"^(-1). Calculate the boiling of chloroform. (b) Two liquids (A) and (B) form an idal solution. At 300 K thevapour pressure of solution containing 1 mole of A and 3 moles of B is 550 of Hg. At the same temperature if one moel of B is added to this solution. the vapour pressure of the solution increases by 10 mm of Hg. Determine the vapour of A and B.

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Solution :(i) `60.86^(@)C`
(ii) `P_(A)^(@)=400` MM and
`P_(A)^(@)=600 mm`
87210.

A solution of 500 ml of 0.2 M KOH and 500ml of 0.2 M HCl is mixed and stirred, the rise in temperature is T_(1). The experiment is repeated using 250ml each of solution, the temperature raised is T_(2). Which of the following is true

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`T_(1)=T_(2)`
`T_(1)=2T_(2)`
`T_(1)=4T_(2)`
`T_(2)=9T_(1)`

Solution :Suppose HEAT evolved in `I^(st)` case is `Q_(1)` and that in the `II^(ND)` case it is `Q_(2)`. Then `Q_(2)=(1)/(2)Q_(1)`
But `Q_(1)=1000T_(1) and Q_(2)=500T_(2)`
`therefore500T_(2)=(1)/(2)xx1000 T_(1)i.e.T_(2)=T_(1)`.
87211.

A solution of 1.73g of 'A' in 100 "cc" of water is found to be isotonic with a 3.42% (wt./vol.) solution of sucrose (C_(12)H_(22)O_(11)). Calculate molecular weight of A. (C_(12)H_(22)O_(11)=342)

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SOLUTION :We know that the isotonic SOLUTIONS have the same molar CONCENTRATION (i.e., moles/lit)
LET the molecular WEIGHT of A be M
Moles of `A=(1.73)/(M)`
`:.` molar conc.of A (moles/litre) `=(1.73)/(M)xx(1000)/(100)=(17.3)/(M)`
Molar conc.of sucrose `=(3.42)/(342)xx(1000)/(100)=0.1`
`:.(17.3)/(M)=0.1`, `M=173`
87212.

A solution of 1.25 g of 'P' in 50 g of water lowers freezing point by 0.3^(@) C. Molar mass of 'P' is 94.K_("(water)") = 1.86 K kg mol^(-1). The degree of association of ‘P’in water is

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0.8
0.6
0.65
`75%`

SOLUTION :1.25 g of P in 50 GO `H_2O implies ` 25 g in 1000 g of `H_2O`
MOLALITY `=(25)/(94)`
`Delta t = i xx K_(p) xx m`
`0.3 = ixx1.86 xx (25)/(94)`
`i=(94 xx 0.3)/(1.86 xx 25) = 0.6064`
` alpha = (i-1)/((1)/(n)-1) = (0.6064 -1)/((1)/(2)-1)=(-0.3936)/(-0.5) = 0.787=78.7% = 80%`
87213.

A solution of 1.25 g of P in 50 g of water lowers freezing point by 0.3^(@)C. Molar mass of P is 94 and K_(f) (water) = 1.86 "K kg mol"^(-1). The degree of association of P if it forms dimers in water is :

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0.8
0.6
0.65
0.75

Solution :`DeltaT_(f)=0*3^(@)C " " M_(B)=94"g mol"^(-1)`
`K_(f)=1*86"K kg mol"^(-1)""W_(B)=1*25g`
`a=?""W_(A)=50g`
In order to calculate `alpha`, .`i`. must be known
`DeltaT_(f)=(ixxK_(f)xxW_(B)xx1000)/(W_(A)xxM_(B))`
`0*3=(ixx1*86xx1*25xx1000)/(50xx94)`
or `i=(0*3xx50xx94)/(1*86xx1*25xx1000)=0*606`
It is GIVEN that P undergoes ASSOCIATION to form DIMER.
`{:(,2P,HARR,P_(2),),("Initial",1,,0,),("after association",1-alpha,,alpha//2,):}`
`:.` Total number of moles `=1-alpha+alpha//2`
`=1-alpha/2`
`i=("Observed number of moles")/("Normal number of moles")`
`i=(1-alpha//2)/(1)=1- alpha/2`
`0*606=1- alpha/2`
`0*606=(2-alpha)/(2)`
`1*212=2*alpha`
`alpha=2-1*212=0*788` or `78*8%`
`~~80%`
87214.

A solution of 12.5 g of an unknown solute in 170 g water gave a boiling point elevation of 0.63 K. Calculate the molar mass of the solute. (K_(b)=0.53 K kg mol^(-1)).

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Solution :`W_(B)=12.5g, W_(A)=0.170 kg, DeltaT_(b)=0.63 K, K_(b)=0.53" K kg MOL"^(-1), M_(B)=?`
`M_(B)=(K_(b)xxW_(B))/(DeltaT_(b)xxW_(A))=((0.53" K kg mol"^(-1))(12.5g))/((0.63 K)xx(0.170 kg))=61.85" g mol"^(-1)`.
87215.

A solution of 1.25 g of a non-electrolyte in 20 g of water freezing at 271.94. If K = 1.86 K molality-then the molecular wt. of the solute is:

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207.8 g/mol
179.79 g/mol
209.6 g/mol
109.6 g/mol

Answer :D
87216.

A solution of 1.25 g of a certain non-electrolyte in 20.0 g of water freezes at 271.94 K. Calculate the molecular mass of the solute, K_(f)for water is 1.86 K/m.

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Solution :`W_(B)=1.25g, W_(A)=0.02 KG, K_(f)-=1.86" K kg mol"^(-1),T_(f)^(@)=273 K`
`T_(f)=271.94 K, DeltaT_(f)=273-271.94=1.06 K, M_(B)=?`
`M_(B)=(K_(f)xxW_(B))/(DeltaT_(f)xxW_(A))=((1.86" K kg mol"^(-1))XX(1.25 G))/((1.06 K)xx(0.02 kg))=109.67" g mol"^(-1).`
87217.

A solution of 10^(-3)M each in Mn^(2+), Fe^(2+), Zn^(2+) and Hg^(2+) is heated with 10^(-16) M sulphide ion. If K_(sp) of MnS, FeS, ZnS and HgS are 10^(-15), 10^(-23), 10^(-20) nd 10^(-54) respectively which one will precipitate first ?

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FeS
MnS
HGS
ZnS

Solution :HgS which has LARGER `K_(SP)` VALUE.
87218.

A solution of 1.25 g of a non-electrolyte in 20 g of water freezing at 271.9K with its molal depression constant , then the molecular wt. of the solute is:

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207.8 g/mol
179.79 g/mol
209.6 g/mol
105.68 g/mol

Answer :D
87219.

A solution of 1 molal concentration of a solute will have maximum boiling point elevation when the solvent is

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ETHYL ALCOHOL
ACETONE
BENZENE
Chloroform

Answer :C
87220.

A solution of 0.2g of a compoundcontaining Cu^(2+) and C_(2)O_(4)^(2-) ions on titration with 0.02" M " KMnO_(4) in presence of H_(2)SO_(4) consumes 22.6 mL of theoxidant .The resultant solution is neutralised with Na_(2)CO_(2) acidfied with dilute acetic acid and treated with excess KI . The liberated I_(2) required 11.3 mL of0.05Na_(2)S_(2)O_(3) solution for complete reduction . Findout the mole ratio ofCu^(2+) " to " C_(2)O_(4)^(2-)in the compound. Writedown the balanced redoxreactions involvedin the above titrations .

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Solution :At the first stage , `C_(2)O_(4)^(2-) ` is oxidisedto `CO_(2)` by the OXIDANT `KMnO_(4)`
`{:(5C_(2)O_(4)^(2-)+2MnO_(4)^(-)+16H^(+)to,10CO_(2)+2Mn^(2+)+3H_(2)O),("+7","+2"):}`
` :. ` normalityof `KMnO_(4)` solution= `0.02 xx (7-2) = 0.1 N `
At the second stage `Cu^(2+)`liberates `I_(2)` from KI and this LIBERATED `I_(2)` requires
11.3 mL of `0.05 " M " Na_(2)S_(2)O_(3)` solution for complete reaction .
`{:(2Cu^(2+)+2I^(-)to,2Cu^(+)+I_(2)),(2S_(2)O_(3)^(2-)+I_(2) to ,S_(4)O_(6)^(2-)+2I^(-)),(" +4"," +5"):}`
Normalityof `Na_(2)S_(2)O_(3)` solution ` = 0.05 (5-4) = 0.05 N `
Now , `(" m.e of "Cu^(2+))/( "m.e of " C_(2)O_(4)^(2-))= (" m.e of"Na_(2)S_(2)O_(3))/("m.e of"KMnO_(4)) = (0.05 xx 11.3 )/(0.1 xx 22.3) = 1/4 `
As `{:(Cu^(2+)to,Cu^(+)and,C_(2)O_(4)^(2-) to,2CO_(2)),(+2,+1,+6,+8):}`
` :. ("mmol of "Cu^(2+)xx1)/("mmol of"C_(2)O_(4)^(2-)xx2) =1/4`
or `("mole of "Cu^(2+))/(" mole of " C_(2)O_(4)^(2-)) = 1/2 `
87221.

A solution of 0.2 g of a compound containing Cu^(2+) "and" C_(2)O_(4)^(2-) ions on titration with 0.02 M KMnO_(4) in presence of H_(2)SO_(4) consumes 22.6 mL of the oxidant. The resultant solution is neutralized with Na_(2)CO_(3) acidified with dil. acetic acid and treated with excess KI. The liberated iodine requires 11.3 mL of 0.5 M Na_(2)S_(2)O_(3) solution for complete reduction. Find out the mole ratio of Cu^(2+) "to" C_(2)O_(4)^(2-)in the compound. Write down the balanced redox reactions involved in the above titrations.

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Solution :Let 'a' moles of `Cu^(2+)` and 'b' moles of `C_(2)O_(4)^(2-)` be PRESENT in solution
(i) The solution is oxidised by `KMnO_(4)` with only `C_(2)O_(4)^(2-)`
`Mn^(7+) + 5 E^(-) rarr Mn^(2+)`
`C_(2)^(6+) rarr 2C^(4+) + 2e^(-)`
Meq. of `C_(2)O_(4)^(2-)` = Meq. of `KMnO_(4)`
`b XX 2 xx 1000 = 0.02 xx 5 xx 2.26 `
`b = 1.13 xx 10^(-3)`
(ii) After oxidation of `C_(2)O_(4)^(2-)` the resulting solution is neutralized by `Na_(2)CO_(3)` acidified with dilute `CH_(3)COOH`and then treated with excess of KI. The liberated `I_(2)` REQUIRED `Na_(2)S_(2)O_(3)` for itsneutralization,
i.e. `Cu^(2+) overset("KI")to I_(2) overset(Na_(2)S_(2)O_(3))to Na_(2)S_(4)O_(6) + I^(-)`
Meq. of `Cu^(2+)` = Meq. of `I_(2)` liberated = Meq. of `Na_(2)S_(2)O_(3)` used
Meq. of `Cu^(2+)` = Meq. of `Na_(2)S_(2)O_(3)` used
`a xx 1 xx 1000 = 11.3 xx 0.5 xx 1`
`a = 5.65 xx 10^(-3)`
Molar ratio of `Cu^(2+)//C_(2)O_(4)^(2-) = a/bimplies 5.65 xx 10^(-3)/(1.13 xx 10^(-3)) = 5/1 `
Hence, molar ratio of `Cu^(2+) , C_(2)O_(4)^(2-) = 5 : 1`
Involved reactions are : `2 MnO_(4)^(-) + 5 C_(2)O_(4)^(2-) + 16H^(+) rarr 2MN^(2+) + 10 CO_(2) + 8H_(2)O`
`2Cu^(2+) + 4I^(-) rarr Cu_(2)I_(2) + I_(2)`
`I_(2) + 2S_(2)O_(3)^(2-) rarr 2I^(-) + S_(4)O_(6)^(2-)`
87222.

A solution of 0.20 g of a non-electrolyte in 2 g of water freezes at 271.14 K . If K_(f) = 1.86 K "molality"^(-1)then the molar mass of the solute is :

Answer»

207.8 g//mol
179.79 g//mol
200.8 g//mol
100.0 g//mol

Solution :`DELTA T_(F)=(1000_(f) XX W_(2))/(M_(2) W_(1))`
or `1.86=(1000 xx 1.86 xx 0.20)/(M_(2) xx 20)`
`:. M_(2) = (1000 xx 1.86 xx 0.20)/(1.86 xx 20 )=100.0`
87223.

A solution of 0.10 M of a weak electrolyte is found to be dissociated to the extent of 1.20% at 25^@C . Find the dissociation constant of the acid.

Answer»

SOLUTION :GIVEN that `a=1.20%=1.20/100=1.2 TIMES 10^-2`
`K_a=a^2c=(1.2 times 10^-2)^2 (0.1)`
`=1.44 times 10^-4 times 10^-1=1.44 times 10^-5`
87224.

A solution of 0.1 M KMnO_(4) is used for the reaction S_(2)O_(3)^(2-) + 2MnO_(4)^(-) + H_(2)O to MnO_(2)+SO_(4)^(2-) + OH^(-) What volume of solution in ml will be required to react with 0.158 gm of Na_(2)S_(2)O_(3)?

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SOLUTION :N/A
87225.

A solution of 0.01M Cd^(2+) contains 0.01IM NH_(4),OH. What conc. of NH _(4)^(+) form NH_(4)Cl is necessry to prevent precipitation of Cd(OH)_(2) ? K_(sp), of Cd(OH)_(2), = 2.0 xx 10^(-14) , K_(sp)of NH_(4)OH 1.8 xx 10^(-5) if answer is 1.272xx 10^(-x) mol/ltr then x =__________ ?

Answer»


ANSWER :1
87226.

A solution of (+) -2-chloro-2-phenylethane in toluene racemises slowly in the presence of small amount of SbCl_5 , due to the formation of

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Carbanion
Carbene
Free-radical
CARBOCATION

Solution :`SbCl_5` is USED for the FORMATION of carbocation
87227.

A solution of (+)-2-chloro-2-phenylethane in toluene racemises slowly in the presence of small amounts of SbCl_5, due to the formation of:

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Carbanion
Carbene
Free radical
Carbocation

Answer :D
87228.

A solution of (-) - 1 - chloro - 1 pheylethane in toluene raceimess slowly in the presence of a small amount of SbCI_(5), due of the formation of-

Answer»

FREEE radical
carbanion
carbene
carbocation

Answer :D
87229.

A solution of (-)-1- chloro -1- phenylethane in toluene racemises slowly in the presence of a small amount of SbCl_(5), due to the formation of

Answer»

FREE radical
carbene
carbocation
carbanion

Answer :C
87230.

A solution of (-)-1-chloro-1-penylethane in toluene racemises slowly in presence of a small amount of SbCl_(5) due to the formation of

Answer»

FREE radical
carbanion
carbene
CARBOCATION

Solution :In presence of `SbCl_(5)`, (-)-1-chloro-1-phenylethane forms a carbocation as shown:
`CH_(3)-CHCl-C_(6)H_(5)+SbCl_(5)to[CH_(3)-overset(+)(C)H-C_(6)H_(5)]SbCl_(6)^(-)`
Since the carbocation is a planar species, therefore, it can be attacked by `SbCl_(6)^(-)` EITHER from the top or the BOTTON face with equal EASE. as a result, a 50:50 mixture of two enantiomers of 1-chloro-1-phenylethane are formed, i.e., (-)-1-chloro-1-phenylethane undergoes racemization due to the formation of a carbocation intermediate.
87231.

A solution of (-)-1-chloro-1-phenylenthane is toluene racemises slowly in the presence of small amount of SbCl_(5), due to the formation of

Answer»

CARBANION
CARBENE
carbocation
free radical

ANSWER :C
87232.

A solutionmay contain any of the following ions: Fe^(2+),Ni^(2+), Cr^(3+),Zn^(2+),Mn^(2+) Based on the experiment and result therein , which of the ions would be present? Indicate any wrong infornation if any….. a. The original solution is treated with with (NH_(4)),S(a subestitate is obtain b. The ppt for (a) dissolves in regain c. The fitrate after sepration ppt in (a) is treated with NaOH and H_(2)O_(2) A dark ppt , is separate filtrate is colourless. e. The solution from (d) is turned with aq NH_(3) A dark ppt forms f. The ppt from (e) is solution in HCI (aq) and solutiondevelops an latense red colour whentreated with SCN^(Theta) (aq)

Answer»

Solution :Precipitate can be of `NiS`
b. `NiS` dissolves in aqua regain
c.Precipitatecan be of `Fe(OH)_(3)`
d.`Fe(OH)_(3)` is SOLUBLE in `HCI`(aq) giving (yellow) coloured soluble of `FeCI_(3)`
e.This step is INCORRECT since filtrate of (c ) isalreadly colourlessincdicatingabsence of `Cr^(2+)`
f. This confims `Fe^(3+)` by forming intense redcolour `Fe^(3+) + SCN^(THETA) rarr [Fe(SCN)]^(2+)`
Thus, `{:(Fe^(3+),-"confirmed"),(Ni^(2+),-"probable"),(Zn^(2+)Mn^(2+)Cr^(3+),-"ABSENT"):}`
87233.

A solution M is prepared by mixing ethanol and water. The mole fraction of ethanol in the mixture is 0.9. Given k_(f)("water")=1.86Kkg"mol"^(-1) k_(f)("ethanol")=2.0Kkg"mol"^(-1) k_(b)("water")=0.52Kkg"mol"^(-1) k_(b)("ethanol")=1.2Kkg"mol"^(-1) Standard f.p. of water = 273 K Standard f.p. of ethanol = 155.7 K Standard b.p. of water = 373 K Standard b.p. of ethanol = 351.5 K Vapour pressure of pure water = 32.8 mmHg Vapour pressure of pure ethanol = 40 mmHg Molecular weight of water = 18 g "mol"^(-1) Molecular weight of ethanol = 46 g "mol"^(-1) consider the solutions to be ideal dilute solutions and solutes to be nonvolatile and non-dissociative. The vapour pressure of the solution M is

Answer»

39.3 mmHg
36.0 mmHg
29.5 mmHg
28.8 mmHg

Answer :A
87234.

A solution M is prepared by mixing ethanol and water. The mole fraction of ethanol in the mixture is 0.9. Given k_(f)("water")=1.86Kkg"mol"^(-1) k_(f)("ethanol")=2.0Kkg"mol"^(-1) k_(b)("water")=0.52Kkg"mol"^(-1) k_(b)("ethanol")=1.2Kkg"mol"^(-1) Standard f.p. of water = 273 K Standard f.p. of ethanol = 155.7 K Standard b.p. of water = 373 K Standard b.p. of ethanol = 351.5 K Vapour pressure of pure water = 32.8 mmHg Vapour pressure of pure ethanol = 40 mmHg Molecular weight of water = 18 g "mol"^(-1) Molecular weight of ethanol = 46 g "mol"^(-1) consider the solutions to be ideal dilute solutions and solutes to be nonvolatile and non-dissociative. The f.p. of the solution M is

Answer»

268.7 K
268.5 K
234.2 K
150.9 K

Solution :SOLUTE is WATER and SOLVENT is ETHANOL
87235.

A solution made by dissolving 40 g NaOH 1000 g of H_(2)O is

Answer»

1 molar
1 normal
1 molal
NONE of the above

Solution :`M=(40)/(40xx1)=1` m SOL
87236.

A solution M is prepared by mixing ethanol and water. The mole fraction of ethanol in the mixture is 0.9. Given k_(f)("water")=1.86Kkg"mol"^(-1) k_(f)("ethanol")=2.0Kkg"mol"^(-1) k_(b)("water")=0.52Kkg"mol"^(-1) k_(b)("ethanol")=1.2Kkg"mol"^(-1) Standard f.p. of water = 273 K Standard f.p. of ethanol = 155.7 K Standard b.p. of water = 373 K Standard b.p. of ethanol = 351.5 K Vapour pressure of pure water = 32.8 mmHg Vapour pressure of pure ethanol = 40 mmHg Molecular weight of water = 18 g "mol"^(-1) Molecular weight of ethanol = 46 g "mol"^(-1) consider the solutions to be ideal dilute solutions and solutes to be nonvolatile and non-dissociative. Water is added to the solution M such that the mole fraction of water in the solution becomes 0.9. The b.p. of this solution is

Answer»

380.4 K
376.2 K
375.5 K
354.7 K

Solution :SOLUTE is ETHANOL and SOLVENT is WATER
87237.

A solution is preparedb mixind 8.5 of g CH_(2) Cl_(2) and 11.95 g of CHCl_(3). If vapour pressure of CH_(2)Cl_(2) and CHCl_(2) and CHCl_(3) at 298 K are 415 and 200 mmHg respectively. The mole fraction of CHCl_(3) in vapour form is: (Molar mass of Cl=35.5 g mol ^(-1))

Answer»

`0.162`
`0.675`
`0.325`
`0.486`

Solution :Molar mass os `CHCl_(3) = 119.5` g/mol
Molar mass of `CH_(2) Cl_(2) =85` g/mol.
molcs of `HCCl_(3 ) = (11.95)/( 119.5) =0.1` mol.
Moles of `CH_(2)Cl_(2)=(8.5)/(85)=0.1` mol
Molefraction of `ChCl_(3)=(0.1)/(0.2) =0.5` mol.
Mole fraction of `CH_(2) Cl_(2) =(0.1)/(0.2) = 0.5` mol.
Given-Vapour opressure of `CHCl_(3)=200 mm Hg = 0.263atm.` Vapour prcssure of `CH_(2) Cl_(2) =415 m m Hg = 0.546` ATM.)
(1 atm = 760 mm Hg)
`therefore P _(("above solution"))`
= Mole fractin of `CHCl_(4)xx` (Vapour PRESSURE of `CHCl_(3)`) + Mole fraction of `CH_(2) Cl_(2)xx ` (Vapour pressure of `CH_(2) Cl_(2)`)
`=0.5 xx0.263+ 0.5xx 546 =04045`
Mole fraction of `CHCl_(3)` in vapour from
`= (0.1315)/(0.4045) =0.325`
87238.

A Solution is prepared by dissolvingcertain amountofsolute in 500 g water. The %by massof asolutionsis 2.38 . Calculate mass ofthe solute.

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Solution :Given : `W_(1)`= Massof a SOLVENT(water) = 500 g
`W_(2)` Massof a solute =?
%by MASS= % `(W//W) = 2. 38`
Let massof thesolute`=W_(2) =X g`
`:.` Massof the solution`= W_(1) + W_(2)= (500 + x) g`
Nowper centby massof solute `= ("massof solute")/("massof solution") xx 100`
`= ("mass of solute")/("mass ofsolvent+ massof solute") xx 100`
`:. 2.38= (X )/((500 + X)) xx 100`
`:. 2. 38(500 + X) =100 x`
`:. 2.38 xx 500 + 2.38 X =100 x`
`:.1190 + 2.38 X = 100 x`
`:.100 x -2.38 x= 1190`
`:. (100 -2.38) x= 1190`
`:. 97 .62 x = 1190`
`:. x = (1190)/(96.62) =12.19`
87239.

A solution is prepared by dissolving 26.3 g of CdSO_(4)in 1000 g of water. The depression in freezing point of the solution was forund to be 0.284 K. Calculate Van't Hoff factor. The cryoscopic constant for water is 1.86 K kg mol^(-1). (Given molar mass of CdSO_(4)=208 g mol^(-1).)

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Solution :`DeltaT_(F)=ixxK_(f)xxm=iK_(f)xxW_(B)/(M_(B)xxW_(A))`
`DeltaT_(f)=0.284 K, K_(f)=1.86" K kg mol"^(-1), W_(B)=26.3 g,`
`M_(B)=208.4" g mol"^(-1),W_(A)=1g.`
`i=(DeltaT_(f)xxM_(B)xxW_(B))/(K_(f)xxW_(B))=((0.28K)XX(208.4"g mol"^(-1))xx(1g))/((1.86" K kg mol"^(-1))xx(26.3g))=1.21.`
87240.

A solution is prepared by dissolving 10g of nonvolatile solute in 180g of H_(2)O. If the relative lowering of vapour pressure is 0.005, find the mol.wt. of the solute.

Answer»

SOLUTION :Suppose the mol.wt. of the solute is M.
Moles of solute `=(10)/(M)`
Mole of solvent `(H_(2)O)=(180)/(18)=10`
Mole fraction of solute `=(10//M)/((10)/(M)+10)=(1)/(M+1)`
We KNOW, RELATIVE lowering of VAP. Pressure `=` mole fraction of solute
`0.005=(1)/(M+1)`
`M=199`
87241.

A solution is prepared by dissolving 10 g of non-volatile solute in 200 g of water. It has a vapour pressure of 31.84 mm Hg at 308 K. Calculate the molar mass of the solute. [ Vapour pressure of pure water at 308 K = 32 mm Hg]

Answer»

Solution :APPLY the RELATION
`(p_1^0 - p_1)/(p_1^0) = (w_2 XX M_1)/(M_2 xx w_1)`

Substituting the values in the above relation, we have
`(32-31.84)/(32) = (10 xx 18)/(M_2 xx 200)`
`(0.16)/(32) = (180)/(200M_2)`
`M_2 = (180 xx 32)/(0.16 xx 200) = 180`
87242.

A solution is one molar in each of NaCl , CdCl_(2) , ZnCl_(2) and PbCl_(2) . To this , tin metal is added . Which of the following is true ? Given : {:(E_(Pb^(2+) |P)^(@) = -0.126 V "," E_(Sn^(2+)|Sn) = -0.136 V) , (E_(Cd^(2+)|Cd)^(@) = -0.40 V "," E_(Zn^(2+)|Zn)^(@)= -0.763 V), (E_(Na^(+) |Na)^(@) = -2.71 V):}

Answer»

Sn can REDUCE `NA^(+)` to Na
Sn can reduce `ZN^(2+)` to Zn
Sn can reduce `Cd^(2+) ` to Cd
Sn can reduce `Pb^(2+)` to Pb .

Solution :CHECK the spontaneity of each reaction by finding the E.M.F.
87243.

A solution is obtained by mixing 300 g of 25% solution and 400 g of 40% solution by mus. Calculate the moss per centage of the resulting solution.

Answer»

Solution :MASS of solute in solution - I
= `(25)/(100 ) XX 300 ` g
= 75 g
Mass of solute in solution - II
= `(40)/(100) xx 400 ` g
160 g
Total mass of solute (I + II)
= 75 + 160 = 235 g
Total mass of solution = 300 + 400 = 700 g
mass percentage of solute in final solution
= `(235)/(70) xx 100 = 33.57%`
mass percentage of soluent in final solution
100 - 33.57
= 66.43%.
87244.

A solution is obtained by mixing 300 g of 25% solution and 400 g of 40% solution by mass.Calculate the mass percentage of the resulting solution.

Answer»

Solution : 300 g of 25% solution CONTAINS = 75 g SOLUTE
400 g of 40% solution contains = 160 g solute
Total solute = 75 + 160 = 235 g
Total solution = 300 + 400 = 700 g
PERCENTAGE of solute in the solution = `235/700 xx 100 = 33.5%`
Percentage of water in the solution = 100 - 33.5 = 66.5%.
87245.

A solution is obtained by mixing 200 ml 1 M CaCl_(2), 300 ml 2 M Na_(2)SO_(4) and 500 ml 1 M BaCl_(2) then which of the following is correct for the resultant solution obtained.

Answer»

`[CL^(-)] = 2.4 M`
`[Ca^(2+)] = 0.2 M`
`[SO_(4)^(2-)] = 0.1 M`
`[BA^(2+)] = 0.5 M`

Solution :`{:(Na_(2)SO_(4),+,BaCl_(2),rarr,2 NaCl,+,BaSO_(4),darr,,),(0.6 mol,,0.5 mol,,,,,,,),(0.1 mol,,-,,1 mol,,,,,):}`
`[Cl^(-)] = (2 xx 0.2 + 2) = 2.4 M`
`[Ca^(2+)] = 0.2 M`
`[SO_(4)^(2-)] = 0.1 M`
`[Ba^(2+)] = 0M`
87246.

A solution is obtained by mixing 300 g of 25% and 400 g of 40% solution by mass. Calculate the mass percentage of the resultng solution.?

Answer»

SOLUTION :`"300 g of 25% solution contains solute = 75 g,400 g of 40% solution contains solute = 160 g"`
`"Total solute "=160+75 = 235g,"Total solution "=300+400=700g`
`"Mass % of solute in the final solutieon"=(235)/(700)xx100=33.5%`
`"Mass % of solute in the final solutieon"=100-33.55=66.5%`.
87247.

A solution is obtained by mixing 100 ml of 1M NaCl, 100 ml of 1M MgCl_(2), 300 ml of 1M Mg (NO_(3))_(2) and finally diluted to 1000 ml. Which of the following is incorrect for final concentration of ions ?

Answer»

`[Na^(+)] = 0.1 M`
`Mg^(+2) = 0.4 M`
`[Cl^(-)] = 0.2 M`
`[NO_(3)^(-)] = 0.6 M`

Solution :`[Cl^(-)] = 0.1 + 0.2 = 0.3` mole/litre
87248.

A solution is obtained by dissolving 0.2 moles of urea in a litre water. Another solution is obtained by dissolving 0.4 moles of sugar in a litre of water at the same temperature. The lowering of vapour pressure to the first solution is.

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Same as that of the second SOLUTION
Half to that of the second solution
Double to that of the second solution
NONE

Solution :LOWERING of VAPOUR pressure depends on numbers of MOLES of solute
87249.

A solution is made by dissoving 40.5 g of C_(2)H_(5)OH until the total volume of the solution is 100 mL. What is the percentage volume of C_(2)H_(5)OH? The density of pure C_(2)H_(5)OH is 0.78 g/mL.

Answer»


SOLUTION :`"Intial mass of "C_(2)H_(5)OH=40.5 g.`
`"DENSITY of "C_(2)H_(5)OH=0.78 g//ML.`
`"Intial volume of solution "="Mass"/"Density"=((40.5g))/((0.78g//mL))=51.92 mL`
Final volueme of solution = 100 mL
`"PRECENTAGE volume of "C_(2)H_(5)OH=("Intial volume")/("Final volume")XX100=((51.92mL))/((100mL))xx100=51.92%`
87250.

A solution is 0.25% by mass. The weight of solvent containing 1.25g. Of solutes would be

Answer»

506g
498.75 G
580.25 g
581.25 g

Solution :MASS of solution =100 g. Mass of solute = 0.25 g.
:. Mass of SOLVENT =100-0.25 = 99.75 g.
0.25 of solute is PRESENT in 99.75g of solvent
:. 1.25 g. of solute will be present in
`(99.75 xx 1.25)/0.25 =498.75` g of solvent.