Nand Foundation Academy, Shegaon: Xii - A Div
Nand Foundation Academy, Shegaon: Xii - A Div
JEE CELL
Chemistry
Total Questions : 50 Total Marks : 50
Roll No.
10-Oct-2019
XII - A Div 10:00 AM To 12:00 PM
This is to certify that, the entry of Roll No. has been correctly written and verified.
Note :
i) All Questions are compulsory
ii) Darken ( ) the appropriate circle(#) of the most correct option/response with black ball point pen.
States Of Matter
1) Ten grams of a gas occupies 2 L at N.T.P. At 5) A gas occupies a volume of 250 ml at 700 mm
what temperature will the volume of the same Hg pressure and 25◦ C. What additional
quantity of a gas become double at the same pressure is required to reduce the gas volume
pressure ? to its 4/5th value at the same temperature ?
A) 0.5 atm B) 0.8 atm 9) 3.2 g of oxygen and 0.2 g of hydrogen are
placed in a 1.12 L flask at 0◦ C. The total
C) 0.9 atm D) 1 atm pressure of the gas mixture will be
A) 1 atm B) 4 atm C) 3 atm D) 2 atm. A) 3 B) 2 C) 6 D) 4
10) A litre of gas is measured at 27◦ C. What volume 17) If the root mean square speed of helium is 4.75
will it occupy at −23◦ C ? m s−1 at 25◦ C, then its speed will become 9.50
m s−1 at
A) 1200 ml B) 1800 ml
A) 100◦ C B) 323◦ C C) 919◦ C D) 1192◦ C.
C) 883 ml D) 167 ml
18) 50 ml of hydrogen diffuses through a small hole
11) The ratio of the rate of diffusion of helium and from a vessel in 20 minutes. Time taken for 40
methane under identical conditions of pressure ml of oxygen to diffuse under similar conditions
and temperature will be : will be
12) At what temperature, will the rms velocity of a 19) The vapour density of a mixture containing NO2
gas at 50◦ C be doubled? and N2 O4 is 38.3 at 26.7◦ C. The number of
moles of NO2 in 100 g mixture is
A) 626 K B) 1019 K C) 200◦ C D) 1019◦ C
A) 0.437 B) 8.2 C) 3.62 D) 4.62
13) 0.6 L of an ideal gas weighs 1.80 g at 27◦ C and
1 atm pressure. ts approximate molar mass is : 20) A what temperature, the rate of effusion of N2
would be 1.625 times that of SO2 at 50◦ C ?
A) 36.9 B) 72.0 C) 147.6 D) 369
A) 135 K B) 373 K C) 546 K D) 303 K
14) The molecular velocity of any gas is :
21) 160 ml of a gas are collected over water at 25◦ C
A) inversely proportional to absolute and 768.8 mm Hg. If aqueous tension at 25◦ C is
temperature 23.8 mm Hg, then pressure of dry gas at 25◦ C is
:
B) directly proportional to square of
temperature A) 76.8 mm Hg B) 760mmHg
15) 56 g of N2 (molar mass = 28) are mixed with 44 A) pT/R B) pRT C) p/RT D) RT/p.
g of CO2 (molar mass = 44) and the pressure of
23) A 10 L flask at 300 K contains a gaseous
the resulting gaseous mixture is 3 atm. The
mixture of CO and CO2 at a total pressure of 2.0
partial pressure of N2 in the mixture is :
atm. If 0.2 mol of CO is present, the partial
pressure of CO2 is (Use R = 0.082 L atm
A) 1 atm B) 1.5 atm mol−1 K−1 )
C) 1/2 D) 2
Answer Sheet
1 C 2 B 3 C 4 A 5 B 6 D 7 C 8 A 9 B 10 C 11 B 12 D
13 B 14 C 15 C 16 D 17 C 18 B 19 A 20 B 21 C 22 C 23 C 24 B
25 C 26 B 27 A 28 B 29 A 30 B 31 D 32 B 33 A 34 A 35 C 36 A
37 C 38 C 39 A 40 B 41 A 42 B 43 C 44 A 45 C 46 B 47 D 48 C
49 B 50 C
Solution Sheet
V1 V
1) = 2 7) Volume occupied by 1 mol of gas at S.T.P.
T1 T2
(Charles law) = 22.4 L
4L × 273 Volume occupied by 0.25 mol of gas at S.T.P.
T2 = = 546K = 22.4 × 0.25 = 5.6 L
2L
V1 V
2) = 2 at constant pressure 8) N2 (g) + 3H2 (g) −→ 2NH3 (g)
T1 T2
V 2V 1 vol 3 vol −→ 2 vol
= 10 mL 30 mL−→ 20 mL
300 T2
or T2 = 300 × 2 = 600 3.2
9) Moles of O2 = = 0.1
or = 600−273 = 327◦ C 32
0.2
W Moles of H2 = = 0.1
3) Moles of lighter gas= 2
4 nRT
W Pressure, p =
Moles of heavier gas= V
40 0.2 × 0.082 × 273
Mole fraction of lighter gas = =4 atm
W/4 1.12
= = 10/11 V V
W/4 + W/40 10) 1 = 2
Partial pressure of lighter gas T1 T2
V T
= Mole fraction x Total pressure or V2 = 1 2
10 T1
= × 1.1 = 1.0 atm 1000 × 250
11 =
300
=883 ml
s r
r (He) M (CH4 ) 16
4) n (CO) = n (N2 ) 11) r = = =2
p (CO) = p (N2 ) =1 atm (CH4 ) M (He) 4
√
r
1 3RT
Mole fraction of N2 , xN2 = = 0.5 12) ur.m.s = ∴ ur.m.s ∝ T
1+1 M
p (N2 ) = p × xN2 =1 × 0.5 = 0.5 atm. For ur.m.s to be doubled, temperature must be
raised by 4 times.
5) V1 = 250 ml., P1 = 700 mm Hg
4 T = (50 + 273) K = 323 K
V2 = 250 × ∴ 4T = 4 × 323 K= 1292 K
5
=200 mL.,P2 =? = (1292−273) C = 1019◦ C.
According to Boyle"s law, mRT 1.80 × 0.08 × 300
13) M = = = 72
P1 V1 = P2 V2 pV 1 × 0.6
250 × 700 √
or P2 = =875 mm Hg 14) Molecular velocity ∝ T
200
Additional pressure required 56
15) Moles of N2 = =2
= 875−700 28
= 175 mm Hg 44
Moles of CO2 = =1
RateofeffusionofH2 44
6) Mole fraction of
RateofeffusionOr 2 2 2
N2 = =
Mass (H2 ) /t 32 2+1 3
= = Partial pressure of
Mass (O2 ) /t 2
MassofH2 4 2
= N2 = × 3 =2 atm
MassofO2 1 3
or 4 : 1
s
r (H2 ) M (hydrocarbon) 22) pV = nRT
16) = n p
r (hydrocarbon) M (H2 ) =
√
r
M (hydrocarbon) v RT
3 3= ∴ No. of moles per litre = p/RT
2
√ 2 23) p = p(CO) + p(CO2 ) = 2.0 atm
M (hydrocarbon) = 3 3 × 2 = 54 0.2 × 0.082 × 300
For Cn H2n−2 , 12n + (2n − 2) = 54 p (CO) =
10
or n = 4 p(CO2 ) = 2 − 0.49 = 1.51 atm.
√
17) r.m.s. speed ∝ T 24) This is true only when pressure is constant.
r
4.75 298
= 25) 30/22.4 = 1.34 g L−1
9.50 T
4.75 2 298
26) p1 = p,
or =
9.50 T p2 = 2p,
or T = 1192 K T1 = T,
or T = 1192−273 =919◦ C T2 = 2T,
r
r (H2 ) 50/20 32 V1 = 5L,
18) = = V2 =?
r (O2 ) 40/t 2
50 t P1 V1 P V
or × =4 = 2 2
20 40 T1 T2
4 × 20 × 40 p1 V1 T2
or t = =64min or V2 =
50 T1 p 2
p × 5 × 2T
19) Molecular weight of mixture = = 5L
T × 2p
= 2 × vapour density
= 2 × 38.3 = 76.6
Let the mixture contains x of NO2 and (100−x) g dRT
27) p =
of N2 O4 M
x dx RT
Moles of NO2 = px =
46 Mx
100 dy RT
Moles of mixture= py =
76.6 My
Now, moles of NO2 and N2 O4 = Moles of px dx dy 2
mixture = = =4
x 100 100 py Mx My 1
+ = 2
46 92 76.6 r
100−92 r (SO2 ) 4 1
2x + 100−x = 28) = =
76.6 r (He) 64 4
100−x = 120.1
x = 120.1−100 = 20.1 29) Root mean square velocity is inversely
20.1 proportional to mass.
∴ Moles of NO2 = = 0.437
v46 Therefore, hydrogen having lowest mass will
u 3RT (N ) have highest r.m. s. velocity.
u 2
r (N2 ) u
28
20) = 1.625 = tu
r (SO2 ) 3R × 323
r 64
16 × T (N2 )
1.625 =
7 × 323
∴ T (N2 ) = 373K
21) Pressure of dry gas
= Pressure of gas collected over water −
Aqueous tension
= 745−23.8 =721.2 mm
pV
30) Compressibility factor (Z)= 36) Applying Boyle"s law,
RT
For one mole of a real gas van der Waals Pressure of gas A in 2L flask
equation 1000 × 600
= =300 torr.
a 2000
p + 2 (V − b) = RT Pressure of gas B in 2L flask
V
At low pressure 500 × 800
= =200 torr.
V
−b a≈V (b can be neglected) 2000
Total pressure = 300 + 200 = 500 torr
p + 2 V = RT
V
a 37) Let p1 = 100 mm Hg.
pV + = RT
V Increase in pressure
a 1
pV = RT − = 100 × =1
V 100
pV a p2 = 100 + 1 = 101 mm Hg
= 1−
RT VRT Let V1 = V and V2 = ?
a
∴ Z = 1− p1 V1 = p2 V2
VRT
p V 100 × V 100
31) van or V2 = 1 1 = = V
der a
Waals equation is : p2 101 101
p + 2 (V − b) = RT 100
V V− V
a Decrease in volume = 101
At high pressure, 2 can be neglected so that V
V
p(V − b) = RT 100
1−
pV − pb = RT 101
pV pb =V =1/101%
or − =1 V r
RT RT 8RT
pV pb pb 38) Average volocity =
or = 1+ ∴ z = 1+ πM
RT r RT RT Most probable velocity =
r MB Average velocity at, T1 K
32) A =
rB MA
r = Most Probable velocity at T2 K
V/20 MB 9.0 × 104 cms−1
=
V/10r 49 R = 8.314 × 107 ergs K−1 moL−1 ,
1 MB M
= s = 44 Averae velocity at T1 K
2 49 8 × 8.13 × 107 × T1
1 = 9.0 × 104
∴ MB = 49 × = 12.25 3.14 × 44
s 4
r (CH4 ) d (O2 )
r
32 √ 81 × 108 × 3.143 × 44
33) = = = 2:1 T1 =
r (O2 ) d (CH4 ) 16 8 × 8.314 × 107
= 1682.5 Kr
nRT 2 × 0.082 × 546 2 × 8.314 × 107 × T2
34) p = = =2 atm Similarly, = 9.0 × 104
V 44.8 44
35) r.m.s. r
speed at 140 K = x 81 × 108 × 44
T2 =
3R × 140 2 × 8.314 × 107
∴x= = 2143 K.
Mr
3R × 560
at, 560K, x0 =
M 39) V1 = 283 ml,
x0
r
560 T1 = 273 + 10 = 283 K
= =2
x 140 V2 = ?
0
x =2
T2 = 273+ 20 = 293 K
At constant P,
V1 V
= 2
T1 T2
V T
or V2 = 1 2
T1
283 × 293
V2 = = 293ml
283
s
rH2 MHydrocarbon √
40) = =3 3
rHydrocarbon MH2
r
MHydrocarbon √
∴ =3 3
2
MHydrocarbon
= 27
2
MHydrocarbon = 2 × 27 = 54
∴ n = 4 and hydrocarbon is C4 H6
41) Units of "a" =L2 atm. mol−2
1L = 1 dm3
Hence units of "a" = dm6 atm mol−2
1
42) Mean free path, l ∝
r r p r
2RT 8RT 3RT
43) C∗ = ,C = ,C =
M πM M
C∗ : C : C = 1 : 1.128: 1.225
44) Temp, changes from 293 K to 313 K.
Average K.E. ∝ T
KE (40◦ C) 313
∴ ◦
=
KE (20rC) 293
4g/t 2
45) =
x/t 32
(x is r
the amount of H2 diffused and t is the time)
4 1 1
= =
x 16 4
∴ x = 16 g
r r
3RT 3R × 300
46) =2
M M
or T = 1200 K = 927◦ C
r
r (gas) 32 1
47) = =
r (O2 ) 128 2
dRT 1.5 × 0.08 × 300
48) M = = = 36
r p 1
r MB
49) A =
rB r MA
MB
4=
r M A
MA 1
or =
MB 16
50) Because of the formation of solid NH4 Cl