InterviewSolution
This section includes InterviewSolutions, each offering curated multiple-choice questions to sharpen your knowledge and support exam preparation. Choose a topic below to get started.
| 93051. |
100 ml 0.2 M Na_(2)Ais titrated with 100ml 0.03 M HCl. Calculate pH of final solution. pKa_(1)(H_(2)A)=5""pKa_(2)(H_(2)A)=9 |
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Answer» 2 0.5 `0.5-x ""x""x` `K_(A)=(1)/(100)LN.(0.5)/(0.25)=(ln2)/(100)` Rate `=KP_(A) = (ln2)/(100)xx0.3=2.1xx10^(-3)"atm"//"sec"` |
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| 93052. |
100 mL 0.1 M solutions of ammonium acetate is diluted by adding 100 mL of water. The pH of the resulting solution will be (pK_(a) of acetic acid is nearly equal to pK_(a) of NH_(4)OH) |
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Answer» 4.9 `PH = 7 + (1)/(2)(pK_(a) -pK_(B)) = 7` as `pK_(a) ~~ pK_(b)`. |
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| 93053. |
100 ml, 0.05 M CuSO_4 solution is electrolysed by using current of 0.965 Å for 100 min.Find the pH of solution at the end of electrolysis. |
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Answer» After 1000 second when total `Cu^2+` discharge then `H^+` and `OH^(-)` discharge equally so pH will not change further. `Cu^(+2)+2e^(-)to Cu` `n_(Cu^(+2))/1=n_(E^(-))/2=Q/(2F)=(it)/(2F)` `(0.925xxt)/(2xx96500)=(0.05xx100)/1000` t=1000 sec `(n_(H^+))_("excess")=(n_(OH^(-)))_("discharge")=n_(e^(-))=Q/F=(it)/(F)=(0.965xx1000)/96500=10^(-2)` `n_(H^+)=(MV)/1000` `10^(-2)=(Mxx100)/1000implies M=10^(-1)` `[H^+]=10^(-1)` `pH= -"log" 10^(-1)=1` |
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| 93054. |
100 mg of a protein is dissolved in just enough water to make 10.0 mL of solution. If this solution has an osmotic pressure of 13.3 mm Hg at 25^(@)C, what is the molar mass of protein? |
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| 93055. |
100 grams of each P_(4)O_(6) and KMnO_(4)^(-) were mixed in hydrochloric acid solution to from H_(3)PO_(4) and MnCl_(2). Which reagentis left unreacted and how much of it is left ? |
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Answer» Solution :`MN^(2+) + 5E^(-) rarr Mn^(2+)` Thus milliequivalents of `KMnO_(4) = (100 xx 5 x 1000)/(158) = 3164.56` `(P^(3+))_(4) rarr 4P^(5+) + 8e^(-)` Thus MILLI equivalents of `P_(4)O_(6) = (100 xx 8 xx 1000)/(220) = 3638` Therefore `P_(4)O_(6)` is excess. Excess milliequivalents of `P_(4)O_(6) = 473.44` Weight of `P_(4)O_(6)` left unreacted `(437.44 xx 0.220)/(8) = 12.03 g` |
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| 93056. |
10.0 gram-atom of an alpha-active radioisotope is disintegrating in a sealed container. In one hour, the He gas collected at STP is 11.2 litres. Calculate the half-life of the isotope supposing each nucleus yielding one He atom. |
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| 93057. |
100 gms of 118% oleum reacted with excess water. How much H_(2)SO_(4) is formed? |
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Answer» SOLUTION :`SO_(3)+H_(2)SO_(4) to H_(2)S_(2)O_(7), H_(2)S_(2)O_(7)+H_(2)O to 2H_(2)SO_(4)` `SO_(3)` is absorbed in `98%` conc. `H_(2)SO_(4)` to get oleum. Oleum `[H_(2)S_(2)O_(7)]` is diluted with water to get `H_(2)SO_(4)` 118% of oleum `to` 100 gm `"?" larr 100%`, 118grams. |
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| 93058. |
1.00 gm of a non-electrolyte solute dissolved in 50 gm of benzene lowered the freezing point of benzene by 0.40 K. K_(f) for benzene is 5.12 kg mol^(-1). Molecular mass of the solute will be |
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Answer» `256 g mol^(-1)` = 256 gm/mol Hence, molecular mass of the SOLUTE `= 256 gm mol^(-1)` |
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| 93059. |
100 g of sucrose solution in water is colled to -0.5^(@)C. What weight of ice would be separated out at this temperature if solution started to freeze at -0.38^(@)C? K_(f) for H_(2)O="1.86 K kg mol"^(-1). |
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Answer» Solution :Suppose 100 g of the solution contains `w_(2)` g of the SOLUTE and `w_(1)` g of the solvent. Then `w_(1)+w_(2)=100"…(i)"` `DeltaT_(f)=(1000xxK_(f)xxw_(2))/(w_(1)xxM_(2))` As the solution starts freezing at `-0.38^(@)C`. Hence, when `DeltaT_(f)=0.38^(@)` `0.38=(1000xx1.86xxw_(2))/(w_(1)xx342)"or"(w_(2))/(w_(1))=0.07"...(ii)"` Solving eqns. (i) and (ii), we get `w_(2)=6.6g, w_(1)=93.40 g` Now at `-0.5^(@)C`, some WATER SEPARATES out as ice but solute exists as such, i.e., `w_(2)=6.6g`. Let us caluclate water present `(w_(1))` `0.50=(1000xx1.86xx6.6)/(w_(1)xx342)"or"w_(1)=71.78` `therefore"Weight of iceseparated out "=93.40-71.78=21.62g` |
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| 93060. |
100 g of liquid A (molar mass 140 g mol^(-1)) was dissolved in 1000 g of liuquid B (molar mass 180 g mol^(-1)). The vapour pressure of pure liquid B was found to be 500 torr. Calculate the vapour pressure of pure liquid A and its vapour pressure in the solution if the total vapour pressure of the solution is 475 Torr. |
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Answer» Solution :NUMBER of moles of liquid A : `n_(A)=(100)/(140)=0.7143` mol Number of moles of liquid B : `n_(B)=(1000)/(180)=5.556` mol Then mole fraction of A, `x_(A)=(n_(A))/(n_(A)+n_(B))` `= (0.714)/(0.714+5.556)=0.114` And, mole fraction of B, `= x_(B)=1-0.114` = 0.8861 VAPOUR pressure of pure liquid B, `p_(B)^(0)=500` TORR Therefore, vapour presure of liquid B in the solution, `p_(B)=p_(B)^(0)x_(B)=500xx0.886` = 443 torr Total vapour pressure of the solution of liquid A in hte solution, `p_(A)=p_("total")-p_(B)` `= 475-433` = 32 torr Now,`p_(A)^(0)x_(A)` `p_(A)^(0)=(p_(A))/(x_(A))` `= (32)/(0.114)=280.5` torr Hence, the vapour pressure of pure liquid A is 280.7 torr. |
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| 93061. |
100 g of liquid A (molar mass "140g mol"^(-1)) was dissolved in 1000 g of liquid B (molar mass "180 g mol"^(-1)). The vapour pressure of pure liquid B was found o be 500 torr. Calculate the vapour pressure of pure liquid A and its vapour pressure in the solution if the total vapour pressure of the solution is 475 torr. |
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Answer» Solution :`"No. of moles of liquid A (solute)"=("100 G")/("140 g mol"^(-1))=(5)/(7)"MOLE"` `"No. of moles of lliquid B (solvent)"=("1000 g")/("180 g mol"^(-1))=(50)/(9)" mole"` `THEREFORE"Mole fraction of A in the solution "(x_(A))=(5//7)/(5//7+50//9)=(5//7)/(395//63)=(5)/(7)xx(63)/(395)=(45)/(395)=0.114` `therefore"Mole fraction of B in the solution "(x_(B))=1-0.114=0.886` `"Also, given"p_(B)^(@)="500 torr"` `"Applying Raoult's law,"p_(A)=x_(A)p_(A)^(@)=0.114xxp_(A)^(@)"...(i)"` `p_(B)=x_(B)p_(B)^(@)=0.886xx500="443 torr"` `p_("Total")=p_(A)+p_(B)` `475=0.114p_(A)^(@)+443"or"p_(A)^(@)=(475-443)/(0.114)="280.7 torr"` Substituting this value in eqn. (i) we get `""p_(A)=0.114xx"280.7 torr = 32 torr."` |
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| 93062. |
100 g of liquid A (molar mass 140 g "mol"^(-1) ) was dissolved in 1000 g of liquid B (molar mass 180 g "mol"^(-1) ). The vapour pressure of pure liquid B was found to be 500 torr. Calculate the vapour pressure of pure liquid A and its vapour pressure in the solution if the total vapour pressure of the solution is 475 torr. |
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Answer» Solution : Number of moles of liquid A (solute) = `100/140 = 5/7 `mole Number of moles of liquid B (solvent) = `1000/180 = 50/9 `moles ` THEREFORE ` Mole fraction of A in the solution `(x_A) =(5//7)/(5//7 + 50//9) = (5//7)/(395//63) = 5/7 XX 63/395 = 45/395 = 0.114` ` therefore `Mole fraction of B in the solution (`x_B`) = 1 – 0.114 = 0.886 Also, given `p_B^0` = 500 torr Applying Raoult.s law and substituting the values, we have `p_A =x_A p_A^0 = 0.114 xx p_A^0` `p_B = x_B p_B^0 = 0.886 xx 500 = 443`torr `p_("total") =p_A + p_B` `475 = 0.114 p_A^0 + 443` `p_A^0 = (475 - 443)/(0.114) = 280.7` torr Vapour PRESSURE of A in the solution `p_A = 0.114 xx 280.7` torr = 32 torr. |
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| 93063. |
100 g of argon is allowed to expand from a pressure of 10 atm to 0.1 atm at 100^(@)C . Calculate the heat which is obsorbed, assuming ideal behaviour. |
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| 93064. |
100 g of a sample of HClsolution of relative density 1.17 contains 33.4 g of HCl . What volume of this HCl solution will be required to neutralise exactly5 litres of N/10NaOH solution ? |
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Answer» SOLUTION :Volume of HCl solution ` = 100/(1.17) mL ` `(" density " = ("mass")/("volume"))` Equivalents of HCl = `(33.4)/(36.5)` (eq.wt . Of HCl = 36.5) m.e of HCl ` = (33.4)/(36.5) xx 1000 "" … (Eqn . 3)` NORMALITY of HCl = `("m.e")/(" volume in mL") "" ....(Eqn .1)` ` =(33.4)/(36.5) xx 1000 xx (1.17)/100` ` = 10.7 ` N Now let the volumeof HCl, of normality calculated above , REQUIRED to neutralise exactly the given NaOH solution be v mL . Now let the volume of HCl , of normality calculated above , required to neutralise exactly the given ,naOH solution be v mL . m.e of HCl = m.e of NaOH `10.7 xx v = 1/10 xx 5000` ` 10 . 7xx v 1/10 xx 5000` `10.7 xx v = 500` ` :. "" v = 46.7 mL ` |
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| 93065. |
1.00 g of a non-electrolyte solute (molar mass 250g mol^(-1) was dissolved in 51.2 g of benzene. If the freezing point depression constant, K_(f) of benzene is 5.12 kh mol^(-1), the freezing point of benzene will be lowered by |
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Answer» 0.5 K `Delta T_(f)=(5.12xx1.0xx1000)/(250xx51.2)` `Delta T_(f)=0.4 K` |
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| 93066. |
1.00 g of a non electrolyte solute ( molar mass 250 " g mol"^(-1)) was dissolved in 51.2 g of benzene. If the freezing point depression constant, K_(f) of benzene is 5*12 K kg "mol"^(-1), the freezing point of benzene will be lowered by |
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Answer» Solution :`DELTA T_(f)=(K_(f)xx 1000 xx W_(2))/(M_(2)xxW_(1))` `(5*12xx1000xx1)/(51*2xx250)=0*4`. |
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| 93067. |
1.00 g of a non - electrolyte solute dissolved in 50 g of benzene lowered the freezing point of benzene by 0.40 K. The freezing point depression constnat of benzene is 5.12 K kg mol^(-1). Find the molar mass of the solute. |
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Answer» Solution :SUBSTITUTING the VALUES of various terms INVOLVED in following EQUATION, we get `M_(2)=(K_(f)xx w_(2)xx 1000)/(Delta T_(f)xx w_(1))` `M_(2)=(5.12"K kg mol"^(-1)xx1.00g xx 1000 g kg^(-1))/(0.40xx50 g)` `= 256g mol^(-1)` THUS, molar mass of the solute `= 256 g mol^(-1)` |
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| 93068. |
1.00 g of a non-electrolyte solute dissolved in 50 g of benzene lowered the freezing point of benzene by 0.40 K. The freezing point depression constant of benzene is "5.12 K kg mol"^(-1). Find the molar mass of solute. |
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Answer» SOLUTION :Here, we are given `w_(2)=1.00 g, w_(1)=50, DeltaT_(f)=0.40 K, K_(f)="5.12 K kg MOL"^(-1)` Substituting these values in the formula `M_(2)=(1000K_(f)w_(2))/(w_(1)DeltaT_(f)),` we get `M_(2)=("1000 g kg"^(-1)xx"5.12 kg mol"^(-1)xx1.0g)/(50 g xx0.40 K)="256 g mol"^(-1)` |
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| 93069. |
100 cm^(3) of NH_(3) diffuses through a fine hole in 32.5 seconds. How much time will 60 cc of N_(2) take to diffuse under the same conditions ? |
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| 93070. |
100 cm^(3) of a given sample of H_(2)O_(2) gives 1000 cm^(3) of O_(2) at S.T.P. The given sample is |
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Answer» 10 VOLUME `H_(2)O_(2)` or 1mL of `H_(2)O_(2)` will give 10 mL of `O_(2)` of STP. Thus its volume strengthis 10 volume. |
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| 93071. |
100 cm^(3) of 1M CH_(3)COOH and 100 cm^(3) of 2 M CH_(3)OH were mixed to form an ester. The change in their intial rate if each solution is mixed with equal volume of water would be: |
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Answer» 4 TIMES |
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| 93072. |
100" cm"^(3)" of "1" M "CH_(3)COOH was mixed with 100" cm"^(3)" of "2" M "CH_(3)OH to form an ester. The change in the initial rate if each solution is diluted with equal volume of water would be |
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Answer» 4 times Rate `(r_(1)) = K[CH_(3)COOH][CH_(3)COH]` `= k(1)(2) = 2K` When each solution is DILUTED with equal volume of WATER, concentration of each is halved, Now, rate `r_(2) = k((1)/(2))((2)/(2)) =(k)/(2) therefore (r_(2))/(r_(1)) = (k//2)/(2k) = (1)/(4) = 0.25` or `r_(2) =0.25 r_(1)` |
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| 93073. |
100 cm^(3) of 0.1 N HCl solution is mixed with 100 cm^(3) of 0.2 N NaOH solution. The resulting solution is |
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Answer» 0.1 N and the solution is basic base`=0.2xx100=20` `THEREFORE` Solution will be basic. 0.1 N of HCl is NEUTRALISED by 0.1 N of NaOH and the remaining 0.1 N of NaOH is in 200 `cm^(3)` of solution. `therefore` Resulting normality`=0.5`N, basic. |
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| 93074. |
100 cm^3 of 1 M CH_3COOH was mixed with 100 cm^3 of 2 M CH_3OH to form an ester. The change in the initial rate if eachsolution is diliuted with equal volume of water would be |
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Answer» 0.5 TIMES |
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| 93075. |
10% (w/v) solution of sucrose (M.W = 342) is isotonic with 5% (w/v) solution of a solute X under identical conditions. The molecular weight of X is |
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Answer» 171 |
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| 93078. |
10% solution of urea is isotonic with 6% solution of a non-volatile solute X. What is the molecular mass of solute X? |
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Answer» `"6 G MOL"^(-)` |
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| 93079. |
10% solution of phenol is used as a |
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Answer» ANTISEPTIC |
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| 93080. |
10% sites of catalyst bed have adsorbed H_2. On heating, H_2 gas is evolved from sites and collected at 0.03 atm and 300K in a small vessel of 2.46 cm^3. Number of sites available is 7.2×(10)^(16) per cm^2 and surface area is 1000cm^2. The number of surface sites are occupied by one molecule of H_2 is [Given: N_A=6×(10)^(23)] |
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Answer» 1 |
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| 93081. |
10% sites of catalyst bed have adsorbed by H_2 on heating H_2 gas is evolved from sites and collected at 0.03atm and 300K in a small vessel of 2.46cm^3. No.of sites available is 5.4 xx 10^16 per cm^2 and surface area is 1000 cm^2. Findout the no.of surface sites occupied per molecule of H_2 (N_A = 6 x 10^23) |
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Answer» 1 No. of ABSORBED molecules of `H_2 = 3 xx 10^(-6) xx 6 xx 10^(23) = 18 xx 10^(17)` Total no. of SURFACE sites available `= 5.4 xx 10^(16) xx 1000 = 5.4 xx 10^(19) cm^2` No. of surface sites that is occupied by adsorption of `H_2 = 10/100 xx 5.4 xx 10^(19) = 5.4 xx 10^(18)` No. of surface sites occupied by one molecule `H_2 = (5.4 xx 10^(18))/(18 xx 10^(17)) = 3`. |
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| 93082. |
10% of a reactant decomposes in 1 hour, 20% in 2 hours and 30% in 3 hours. The order of the reaction is |
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Answer» 0 |
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| 93083. |
1^(0) -nitroalkane react with HNO_(2)gives |
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Answer» dinitroalkane |
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| 93084. |
10 moles of X, 12 mole of Y and 20 moles of Z are mixed to produce a final product P, according to the given balanced reaction - X + 2Y rarr I I + Z rarr Y + P then the maximum moles of P, which can be produced assuming that the products formed can also be reused in the reaction ? |
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Answer» Solution :`{:(,X,+,2Y,rarr,I,,I,+,Z rarr,Y,+,P,),("step - I",10,,12,,,"step - I",6,,20,,,,),(,10 - 6,,,,6,,0,,20 - 6,6,,6,),("step - II",4,,6,,0,"step - II",3,,14,0,,6,),(,4 - 3,,0,,3,,0,,14 - 3,3,,6 + 3,),("step - III",1,,3,,0,"step - III",1,,11,0,,9,),(,0,,3 - 2,,1,,0,,11 -1,1,,9 + 1,):}` `= 10`MOLES of P |
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| 93085. |
10 moles of a liquid L are 50% converted into its vapour at its boiling point (273^@C) and at a pressure of 1 atm.If the value of latent heat of vapourisation of liquid L is 273 L atm/mole , than which of the following statements is/are correct : Assume volume of liquid to be negligible and vapour of the liquid to behave ideally. |
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Answer» Work done by the system in the above process is 224 L atm `W=-P_(ext)(DeltaV)=-1` atm (224 L) =-224 L atm `:.` work done by system =224 L atm Enthalpy change `(DeltaH)=q=273xx5=1365 L atm` `DeltaS=(DeltaH_(VAP))/T=1365/546=2.5` L atm /K `DeltaU=q+W=1365-224=1141 L atm` |
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| 93086. |
10 mole of liquid 'A' and 20 mole of liquid 'B' is mixed in a cylindrical vessel containing a piston arrangement. Initially a pressure of 2 atm is maintained on the solution. Now, the piston is raised slowely and isothermally. Assume ideal behaviour of solution and A and B are completely miscible. P_(A)^(@) = 0.6 atm and P_(B)^(@) = 0.9 atm The pressure at which (1)/(3) theof the total amount (by mol) of liquid solution taken initially will be present in the vapour form is [Given: sqrt(57) = 7.55] |
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Answer» `0.783` |
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| 93087. |
10 mole of liquid 'A' and 20 mole of liquid 'B' is mixed in a cylindrical vessel containing a piston arrangement. Initially a pressure of 2 atm is maintained on the solution. Now, the piston is raised slowely and isothermally. Assume ideal behaviour of solution and A and B are completely miscible. P_(A)^(@) = 0.6 atm and P_(B)^(@) = 0.9 atm The minimum pressure for the existence of liquid solution is |
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Answer» `0.6atm` |
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| 93088. |
10 mole of liquid 'A' and 20 mole of liquid 'B' is mixed in a cylindrical vessel containing a piston arrangement. Initially a pressure of 2 atm is maintained on the solution. Now, the piston is raised slowely and isothermally. Assume ideal behaviour of solution and A and B are completely miscible. P_(A)^(@) = 0.6 atm and P_(B)^(@) = 0.9 atm The pressure below which the evaporation of liquid solution will start, is |
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Answer» `0.5 ATM` |
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| 93089. |
10 mole of liquid 'A' and 10 mole of liquid 'B' is mixed in a cylindrical vessel containing a piston arrangement. Initially a pressure of 2 atm is maintained on the solution. Now, the piston is raised slowly and isothermally. Assuming A and B tobe completely miscible and forming an ideal solution. P_(A)^(@) = 0.6atm and P_(B)^(@) = 0.9 atm The minimum pressure for the existance of liquid solution is : |
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Answer» `0.6` ATM |
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| 93090. |
10 mole of liquid 'A' and 10 mole of liquid 'B' is mixed in a cylindrical vessel containing a piston arrangement. Initially a pressure of 2 atm is maintained on the solution. Now, the piston is raised slowly and isothermally. Assuming A and B tobe completely miscible and forming an ideal solution. P_(A)^(@) = 0.6atm and P_(B)^(@) = 0.9 atm If 1/4 of the total amount of liquid solution taken initially is converted to vapour, then moles of A in the vapour will be : [Given : sqrt(2425) = 49.25] |
| Answer» ANSWER :A | |
| 93091. |
10 mol sampleof AgNO_(3)is dissolved in one lit of 1.00 M NH_(3)Is it possibleAgCl(s)form the solution by adding0.010molof NaCl ? |
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Answer» Solution :`K_(SP(AgCl)) = 1.8 xx10^(-10), K _(F[Ag(NH_(3))_(2)^(.)])= 1.6 xx10^(7)` ` {:("Ag"^(+),+,2NH_(3),hArr,[Ag(NH_(3))_(2)^(+)]),(0.10 M ,,1.00,,0),(x,,(1-0.20)M,,),(,,=0.80 M,,0.10 M ):}` It is assumed that all `Ag^(+)` ions have been complexed and only x amount is left `K_(f)= ([Ag(NH_(3))_(2)])/([Ag^(+)][NH_(3)]^(2)) RARR 1.6 xx10^(7) = (0.10)/(XX(0.80)^(2))` ` :. x = 9.8 xx10^(-9) M = [Ag^(+)] ` undissolved `[Cl^(-)] = 1.0 xx10^(-2) M ` ` :. [Ag^(+)] [Cl^(-)] = 9.8 xx10^(-9) xx1.0 xx10^(2) = 9.8 xx10^(-11) lt 1.8 xx10^(-10) [K_(sp(AgCl))] ` Hence , AgCl (s) will not precipitate |
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| 93092. |
10 mol of an ideal gas (gamma= 1.5)expands adiabatically from (400K,10L) to 20 L along following paths. Path A : Reversible Path B : One step expansion. Path C : Two step expansion. Path D : Free expansion Which is/are correct statement(s) ? |
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Answer» Final temperature attained along path B is maximum. `n_(Cvm)(T_(2)-T_(1))=w` `T_(2)=T_(1)+(w)/(n_(Cvm))` `w=-x` `T_(2)=T_(1)+(x)/(n_(Cvm))` x is minimum along path B. So `T_(2)` is maximum. Pathd-D `DeltaS_("total")=DeltaS_("SYSTEM")+DeltaS_("SURROUNDING")` `Delta_("total")=nC_(vm)ln .(T_(2))/(T_(1))+nRln.(V_(2))/(V_(1))+O` `T_(2)=T_(1)` (for free expansion) `DeltaS_("total")=10Rln2` Path A `DeltaS_("gas")=0` for reversible adiabatic process. Path-D `T_(2)=T_(1)+(w)/(n_(Cvm))w=0` `T_(2)=T_(1)=400K` |
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| 93093. |
10 mL of tap water containing ca^(2+) and Mg^(2+) in the presence of HCO_(3)^(-)was properly buffered and the indicator mureside added . The sample was dilutedand heated to 60^(@)C.Titration with 0.01M EDTA solution changed the indicator colour at 7.50 mL . This complexed Ca^(2+) only . A second 10.mL sample was made basic and Erio T indicator added . Titration with 0.01M EDTAsolutionchanged the indicator colourat 13.02 mLUndertheseconditions both ca^(2+) and Mg^(2+) are complexed . If the 10 mLof water samplewere to be evaporated to dryness , what weight of CaCO_(3)+ MgCO_(3) would be formed? |
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Answer» Solution :All EDTA cmplxesare FORMED on a ONE to one basis with dipositive ions . Mole f `Ca^(2+) +MG^(2+) ` = mole of `CaCO_(3)` + mole of `MgCO_(3)` `= (0.01 xx13.02)/(1000) = 13 xx 10^(-5)` Mole of `Ca^(2+) ` mole of `CaCO_(3)` `= (0.01 xx 7.50)/1000 = 7.50 xx10^(-5)` ` :. ` mole of `MgCO_(3) = 13 xx 10^(-5) - 7.50 xx10^(-5) = 5.5 xx 10^(-6)` ` :. `weight of `CaCO_(3) +MgCO_(3)= 7.50 xx10^(-5) xxx100 + 5.5 xx10^(-5) xx 84` ` = 1.21 xx 10^(-2) g ` `(CaCO_(3) = 100 , MgCO_(3)=84)` |
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| 93094. |
10ml of sulphuric acid solution (sp.gr.=1.84) contains 98% weight of pure acid. Calculate the volume of 2.5 M NaOH solution required to just neutralise the acid. |
| Answer» SOLUTION :`147.2` ML | |
| 93095. |
10 mL of mixture containing carbon monoxide and nitrogen required 7mL, oxygen to form CO_(2) and NO, on combustion The volume of N_(2) in the mixture will be: |
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Answer» 7/2mL `N_(2)(g)+O_(2)(g)rarr2NO(g)` `X+y=10` `(x)/(2)+y=7` Solving eqs, i and II, `x=6` and y=4 |
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| 93096. |
10mlof NaHC_(2)O_(4) is oxidized by 10 ml of 0.02 M MnO_(4)^(-) . Therefore, 10 ml of NaHC_(2)O_(4) can be neutralized by |
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Answer» 10 ML of `0.1` M NaOH |
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| 93097. |
10ml of liquid 'A' is mixed with 10ml of liquid 'B' the volume of the resultant solution is 19.9 ml. What type of deviation expected from Raoult's law? |
| Answer» SOLUTION :NEGATIVE DEVIATION. | |
| 93098. |
10 mL of liquid carbon disulphide (sp. Gravity 2.63) is burnt in oxygen. Find the volume of the resulting gases measured at S.T.P. |
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Answer» `{:(UNDERSET(76g)(CS_(2))+3O_(2)rarr underset("3 moles")(ubrace(CO_(2)+2SO_(2)))),(""=3xx22.4" L at STP"):}` |
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| 93099. |
10 mL of liquid 'A' is mixed with 10 mL of liquid 'B', the volume of the resultant solution is 19.9 ml. What type of deviation expected from Raoult's law ? |
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Answer» SOLUTION :NEGATIVE DEVIATION from Raoul.s LAW or -ve deviation from Raoult.s law. |
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| 93100. |
10 mL of HCl solution gave 0.1435 g of AgCl when treated with excessof AgNO_(3). Find the normality of the acid solution [Ag = 108] |
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Answer» SOLUTION :`"CL present in 0.1435 g AgCl"=(35.5)/(143.5)xx0.1435g=0.0355g` `"HCL containing 0.0355 g Cl"=(36.5)/(35.5)xx0.0355g=0.0365g=(0.0365)/(36.5)"g eq."="0.001 g eq."` |
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