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Mock Test 9 Paper 1 - BTK - A
Mock Test 9 Paper 1 - BTK - A
Mock Test 9 Paper 1 - BTK - A
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Mock Test-9–Paper-1 (100400.1)-PCM-IITJEE-2
Physics PART – I
SECTION – A
1. The rms voltage is found by parametrising the voltage
V t 0 t 1 sec .
V 0
V0 / 2 1 t 2 sec .
1/ 2 1/ 2
1 2 1 1 V 2 2 7
Vrms = V 2 (t)dt = V02 t 2 dt 0 dt = V0
2 0 2 0 4 1 24
ab
3. The median of the triangle between a and b is given
2
2 a b a b
Location of centre of mass =
3 2 3
Now v = v vi v f v
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Mock Test-9–Paper-1 (100400.1)-PCM-IITJEE-3
V2 3
v = t
2a
v v2 3
=
t 2a
5. F = ma
2
v2
mg = m a2t
r
2
v2
at = 2 g2 = 4 m/s2
r
6. Consider the FBD of the bottle after shaping and beeping on the balance.
Now after shaping the suspended particles being heavier will again start
setfling down. Thus the centre of mass of the system must have a
downward acceleration.
Now: Mg N = Ma
N = Mg Ma < Mg
Mg
Thus weight recorded is less than W.
N
I
7. Radiation pressure = P
c
1 a 3
Area of Hexagon = a 6 a
2 2
F = pA cos
3 3a2 I 3 9a2 3 9a2I
=
2 c 2 4 2 4c
Power
8. I=
4 r 2
Power = 4r2.I= 4 (50)2 10-8 = 3.14 10-4 Watt
2
1 p0 B
also I= We know that v =
2 v
2
B 1 p0 v
= | I=
v2 2 B
2IB 2 10 8 1.6 10 5
p0 = = 3.07 10-3 N/m2
v 340
9. For ammeter
99 Ig = (I – Ig) 1 or I = 100 Ig . . . (i)
Ig is the full scale deflection current of the galvanometer and I is the range of ammeter
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Mock Test-9–Paper-1 (100400.1)-PCM-IITJEE-4
99
i Ig
G
1
For the circuit in figure-1
12 V
= 3 A r = 1.01 .
99 1
2r
99 1
For voltmeter, range
V = Ig (99 + 101) V = 200 Ig . . . (2)
Also resistance of the voltmeter = 99 + 101 = 200
200 2
In figure –2 resistance across the terminals of the battery R1 = r + = 2.99
202
99 101
G
Ig
V
12
Current drawn from the battery, I1 = = 4.01 A
2.99
4
Voltmeter reading V = 12 – I1 r = 12 – 4.01 1.01
5
5
V = 7.96 = 9.95 V
4
9.95
Using (2), Ig = = 0.05 A
200
Using (1), range of the ammeter
I = 100 Ig
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Mock Test-9–Paper-1 (100400.1)-PCM-IITJEE-5
11. Initially the charges on the plates will be distributed as shown. P.d across the plates is given by
Q1 Q2
and is independent of the charge on the outer surfaces. Thus, when capacitor is
2C
discharged, the charges on the outer surface do not change. Charge on the inner surface decreases
according to
Q1+Q2 Q1+Q2
2 2
Q1-Q2 Q2-Q1
2 2
t
Q1 Q 2 RC
the equation q = e
2
t
Q1 Q 2 Q1 Q 2 RC
Total charge on the left plate q = e
2 2
t
Q1 Q 2 Q1 Q 2 RC
And total charge of the right plate q2 = e .
2 2
7
13. y2 = (5 )2 x 2 = (3 2)2 (7 x)2 x 7x
3
x = 4 y = 3 T 2 5
y
g 32
14. y
ydA , choosing a horizontal strip at a height y of thickness dy, dA = dy a y
evaluating
b
dA
3
the integrals, we get y b . (since here a = 1)
10
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Mock Test-9–Paper-1 (100400.1)-PCM-IITJEE-6
Similarly x
xdA . For this we choose a vertical strip at a distance x from the origin of thickness dx.
dA
3
dA = kx2dx. Now evaluating the integrals, we get x .
4
GMm GMh
16. h ' h = h 2
R CR
GM
h ' h 1 2
C R
' GM
or, 1 2
cR
' GM
17. 1 2
cR
GM '
1
c 2R
'
GRS
GMm
18. Total energy h
R
GMh
= h
Rc 2
Now from black hole this must be negative
GM
h 1 2
0
Rc
GM
1
Rc 2
SECTION –C
T v v 1 T
1. v= ; w =
m m
v 3v 5 nd
For organ pipe: op = ; pipe (2 overtone) = 2m ; =
2 4
p RT RT
where, v S = = 360 m/s
M M
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Mock Test-9–Paper-1 (100400.1)-PCM-IITJEE-7
3 360
op = = 270 Hz
4
w - op = 5 w = 275 Hz
1 302.5
275 =
2 m = 3/2 ; = 2/3
m = 10-3 kg/m
2. The ray will suffer TIR on face BC and will then hit B
face AC normally.
60°
60°
A C
fe ( a g 1) a
3.
fa a g a
20 (1.5 1) a
10 1 .5
3 = 1.5 a t = 10 sec.
2 1 1
4.
E = (13.6 eV) Z Z 2 2 Z 2
Z 2 ( Z 2) 2 4Z 1 13.6
= 13.6 Z 2 2
=
Z 22 eV
h2 h
Now energy of electron is k = ; we have Or, k = 6eV
22m 2mk
4Z 1 13.6
So, = 10.2 eV
Z 22
Or,
Z 1 3 (Z2) (3Z+2) = 0
Z 22 16
So, the value of Z = 2 (neglecting the negative/ fractional value)
hc
5. Energy of photon corresponding ot wavelength E =
hc ( 6.6 10 34 ) (3 10 8 ) 1
Emax = 7
= 3.1 eV
min 4 10
1.6 10 19
From Einstein's equation for photoelectric effect
Emax = + (Ek) max
(Ek)max = Emax - = 3.1 2.1 = 1 eV
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Mock Test-9–Paper-1 (100400.1)-PCM-IITJEE-8
The photoelectron with charge e mass m and maximum velocity bends in a circle of radius r
mv 2
BeV =
r
mv 2mE k
r=
Be Be
For ammeter reading to be zero, no electron should reach the collector plate.
For which r d
2mEk
d
Be
2mE k -5
B Bmin = 2.25 10 Tesla.
ed
1 1 1
6. sin = [x (2 1)] = (n (2 1)]= 6
[n 500 109 20 106 ]
d d 10 10
n
n
sin = 2 1 Hence = sin1 2 40 1
40
| sin | 1
n
12 1 1
40
20 [ n – 40] 20
20 n 60 Hence number of maxima = 41
nRT
7. U
1
nRT
W Where is a constant
1
W nRT / 1
2 / 3 where 5 / 3 , 2
U nRT / 1
800
The radius of the track = m
2
Mg
10. Buoyant force =
2
Apply work energy theorem
1 ML2 2 MgL Mg 2 L MgL Mg L MgL
2 3 2 2 2 4 4
3g
2L
L 3gL
So, vcm =
2 8
Chemistry PART – II
SECTION – A
1. D
pKa for the compound A, B, C and D are respectively 9.98, 9.48, 8.81 and 8.48.
2. A
PCl2 PCl 1 atm
P
rate
m
PCl2 PCl 1.2 1
1/ 2
1/2
1
71 35.5 64 2
PCl2
PCl 0.9
2
PCl2 0.34
PCl = 0.66
2
Kp
0.66 1.28 atm
0.34
3. C
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Mock Test-9–Paper-1 (100400.1)-PCM-IITJEE-10
7 7
4 4
2 2
5 5 1 HOAc
1 3 OTs 3 OTs
6 2 6 OAc AcO
H H H H
50% 50%
4 5
3 7
6
2 1
The solvolysis of exo-isomers (option C) is 350 times faster than that of endo-isomers (option D).
Both the compound (C and D) give only exo acetate. The C6 – C1 bond is situated to the rear of the
ionizable group this facilating the ionization. This leads to non-classical carbonium ion that react with
acetic acid to yield the racemic mixture of acetate. No such anchimeric assistance available to the
endo-isomer which undergoes slow acetolysis through classical carbonium ions.
4. A
NH3 act as strong field ligand for Co2+ and Co3+ in the presence of strong field ligand Co+2 act as a
very good oxidizing agent.
2 3
Co NH3 5 H2 O Co NH3 6 e H2 O
NH3
Hence sp3 d2 LS d2 sp3 LS
d7 Co II d6 Co III
5. A
6. A
7. B
t 75% 34.65
t1/2 hour
2 2
0.693
K 4 102 hour
34.65 / 2
8. D
Compound P BeO
Compound Q BeCl2
Compound R Be(OH)2
9. B, C, D
I2Cl6 XeF4 K 2 Ni(CN)4 and Al2Br6
sp3 d2 sp3d2 dsp2 sp3
Cl Cl Cl
I I
Cl Cl
Cl
Planar molecule
Both the I atom are square planar due to lone pair repulsion.
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Mock Test-9–Paper-1 (100400.1)-PCM-IITJEE-11
10. B, C, D
(A) Work done by the gas is P1V1
25P1V1
(B) The maximum temperature attained by the gas during cycle
8R
(C) The heat absorbed by path PQ is (3P1V1)
5
(D) The net heat rejected by gas in path RP is P1V1
2
11. A, B
German silver – Cu, Zn, Ni
Dutch metal – Cu, Zn
Bronze – Cu, Sn
Kaolin – Al2O3.2SiO2.2H2O
12. A, B, C, D
O
H O P O H
H
P4 O6 H2O 4H3PO3
PCl3 3H2 O H3PO3 3HCl
4H3PO3
200o C
3H3PO4 PH3
H3PO3 with Co(NO3)2 gives violet blue ppt. while HPO3 can’t.
13. A, C, D
BeO is metal oxide and amphoteric in nature. OF2 is not an oxide rather oxyfluoride and neutral in
nature.
14. B
15. A
Solution for the Q. No. 14 to 15
H5C2 H O H O H
H5C2 H5C2
C C C Step I
C Step II
C
Faster epoxidation due to
H3C C4H9 Me C4H9
high reactivity of C C
Me O C4H9
P Q R
O
||
3 i H O
C4H9 COOH C2H5 C Me CO2
ii KMnO /H /
4
T S
H2 /Pt
C4H9 COOH
CH3 CH2 CH2 CH2 CH2 OH
Amyl alcohol
Compound (R) is optically active, it does not contains plane of symmetry and C2 – axis of symmetry. And also
it does not give neutral FeCl3 test.
16. C
Na2CO3 is thermally stable and cannot be decomposed at N.T.P.
17. B
Moles of NaOH is more as compare to NaHCO3 (a > b).
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Mock Test-9–Paper-1 (100400.1)-PCM-IITJEE-12
18. D
b = moles of NaHCO3 = 2 × CO2 = 0.02 mole
a = moles of NaOH = moles of NaHCO3 + moles of NaOH reacted with HCl at the end point.
= 0.02 + 0.05
= 0.07
Moles of Na2CO3 = c + moles of Na2CO3 formed from NaHCO3 and NaOH reaction.
Moles of BaCrO4 = c + moles of NaHCO3
c = 0.50 – 0.02
= 0.48
a + b + c = 0.02 + 0.07 + 0.48 = 0.57
SECTION – C
1. 8
1
K 2
H w K a2 K a1
K b
1
10 14 2
H 5 10 15 107
10
1
H 109 10 7 10 15 10 7 2
1
H 1016 10 22 2
1
H 1016 2 10 8
pH = 8
2. 8
Cl Cl
Br
Cl
MgCl
Mg / Ether
Ether
F
Number of chiral center in compound (F) are 4.
3. 6
a
E1 0.0591pKa log
b
b
E 2 0.0591 pKa log
a
E1 = 0.0591 (pH) E2 = 0.0591(pH)for (SHE)
E1 + E2 = 0.0591[2 × pKa]
E1 E 2
pKa pH 6.0
2 0.0591
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Mock Test-9–Paper-1 (100400.1)-PCM-IITJEE-13
4. 3
Acidic CrO3, Mn2O7, SiO2
Basic MnO, CrO
Amphoteric SnO2, Ga2O3, MnO2, Cr2O3, BeO.
5. 5
+ N
N N
N N N
N
C C
N N
C
N
+
N
N
6. 5
Tf iK f m
i = 1.0215
NH3 H2 O
NH4 OH
0.1 2
Kb 4.72 10 5
1
As i 1
7. 4
A
B C
0
P x xy xy
C
B D
xy yx y
0
Peq. P x y 2P 0
0
x y P
Ceq. x y
2
A eq. P0 x
(x = 3y)
2
K P1 K C1 x y 4
0
K P2 K C2 P x .y 1
8. 8
O
R O R NH
C
Acetals O R , sucrose (C H O ), Caprolactum do not give any ppt. or
R 12 22 11
9. 3
Ssurr 0, for ideal solution, and non ideal solution.
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Mock Test-9–Paper-1 (100400.1)-PCM-IITJEE-14
10. 6
O Br Br
Br
HBr
Br Na / ether
O
O Br Br
SECTION – A
n 1
1 1
1 x x 8 ..... x 2 x 6 x10 ..... dx
4
2. lim
n
r 0
=
4r 1 4r 3
0
1 2 1
1 x 1 1
= 1 x 4
dx =
4 1 x 2
dx tan1 x 0
1 x 4
0 0
2x y 1 x 2y 3z 0
3.
3x y z 2 4x 5y 2z 3 0
x y z
Line is parallel to
1 2 3
So, (2 + ) 1 + (1 – 2) 2 + 3 3 = 0
2
3
(3 + 4) 1 + (–1 + 5) 2 + (1 – 2) 3 = 0
1
2
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Mock Test-9–Paper-1 (100400.1)-PCM-IITJEE-15
/4 /4
sec x sec x
4. I e tan x sec x sec x tan x 1 dx e sec 2 xdx
0 0
2 2
5. Let AG = 2x, GD = x and DF = y then xy = 4 and 2x(3x + y) = 36 and 2(9x + 4) = 36 + AC
7. Put 3x = t
2t
2 tan1 t sin1
1 t2
2 tan1 t t 1
2t
sin1 2
2 tan1 t 1 t 1
1 t 1
2 tan t t 1
–1 3x 1
1 1
x
3 3
9. (x2 – 1) + y(y – 2) = 0 A
y = –x
(x2 – 1) + x(x + 2) = 0 3 1 1 2
2x2 + 2x – 1 = 0
2
,
2
S
(1, 2)
2 4 8
x
4 A P 1 1
,
1 3 2 2
x
2 (–1, 0)
1 3 1 3
,
2 2
2 x
10. e x f x x (0, 1)
e
2 1 1
13. m
1 1 2
1 1
2 5 5 2
m1
1 1 2 5 1
1
2 5
1 1
2 5
m2
1 1
1
2 5
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Mock Test-9–Paper-1 (100400.1)-PCM-IITJEE-16
SECTION – C
6 6
y 2 4y 8
3. A xP xL dy =
2y 7 dy
4
0 0
1 1 1
6. 1 4 1 1 8 1 1 3 11 4 = 9 – 3 – 3 = 3
1 1 2
7. 7 3
C3 4 4 C1 6 3
C2 3 4C2 5 C1 23 4
C3
= 2240 – {1620 – 240 + 4} = 856
= 856 – all 4 red balls goes to one
= 856 – 24 = 832
4 2
8. Focus is ,
5 5
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