P

NEET - 2025
Mark Group Date : 27/04/2025
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Answer Key Version - P (NEET - 2 0 2 5 )

Physics Chemistry
01. 4 12. 1 23. 3 34. 3 45. 2 46. 2 57. 4 68. 1 79. 3 90. 1

02. 1 13. 2 24. 1 35. 2 47. 2 58. 1 69. 2 80. 1

03. 3 14. 1 25. 1 36. 4 48. 2 59. 1 70. 1 81. 1

04. 3 15. 3 26. 1 37. 1 49. 1 60. 1 71. 1 82. 2

05. 4 16. 2 27. 2 38. 4 50. 4 61. 2 72. 4 83. 4
06. 1 17. 2 28. 2 39. 4 51. 4 62. 4 73. 1 84. 2
07. 1 18. 2 29. 1 40. 2 52. 4 63. 3 74. 1 85. 1
08. 1 19. 2 30. 1 41. 1 53. 1 64. 3 75. 2 86. 4
09. 1 20. 1 31. 2 42. 2 54. 3 65. 2 76. 1 87. 3
10. 1 21. 1 32. 3 43. 4 55. 2 66. 3 77. 3 88. 4

11. 1 22. 3 33. 2 44. 3 56. 1 67. 1 78. 2 89. 4

Botany Zoology
91. 3 101. 2 111. 2 121. 2 131. 4 136. 3 146. 2 156. 3 166. 3 176. 3
92. 3 102. 4 112. 4 122. 2 132. 2 137. 2 147. 4 157. 4 167. 1 177. 4
93. 3 103. 3 113. 4 123. 4 133. 3 138. 2 148. 1 158. 2 168. 3 178. 3
94. 1 104. 4 114. 4 124. 2 134. 3 139. 2 149. 2 159. 4 169. 4 179. 3
95. 4 105. 2 115. 3 125. 3 135. 1 140. 2 150. 1 160. 3 170. 1 180. 4
96. 2 106. 3 116. 1 126. 1 141. 3 151. 3 161. 1 171. 1
97. 3 107. 1 117. 3 127. 3 142. 2 152. 2 162. 4 172. 3
98. 4 108. 1 118. 2 128. 3 143. 3 153. 2 163. 2 173. 3
99. 2 109. 3 119. 3 129. 4 144. 3 154. 2 164. 3 174. 4
100. 4 110. 4 120. 3 130. 2 145. 4 155. 2 165. 1 175. 3

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09. (1) For the same value of current, the higher
PHYSICS value of voltage is required for higher fre-
01. (4) quency. Hence, option (1) is true.
1 2 1 2
L   T1   meter   sec 
n2  n1  1  T   10  10. (1)
 L2   2  km   hr 
1 2
 m   sec 
n2  10  3    129600. Since total charge remains same
10 m   3600sec 
2CV  CV  2CV ' KCV '
02. (1)
03. (3) 3V
V ' .
K 2
value of one division of main scale x
LC   .
no.of divisions of vernier scale n
04. (3) 5 N force will not produce any tension
in spring without support of other 5 N
force. So here the tension in the spring will
be 5 N only.
05. (4) In the arrangement shown, the
unpolarised light is incident at polarising 11. (1)
angle of 90° – 37° = 53°. The reflected light
is thus place polarised light. When plane
polarised light is passed through Nicol
prism (a polarise or analyser), the intensity
gradually reduced to zero and finally
increases. r  10 2 sin 450  10 m
06. (1) Since charge and potential remains T sin 450  m2 r
same C ' = C T cos 450  mg
A 0 A0
 2 r g 10
t d tan 450    tan 450  1
(d  l )  t  g r 10
K
t 2 2
l t  0    1 rad/s  T=   2 sec
K  1

2  20 
1.6  2   0  K  5. 12. (1) h  10m, h1  1  100 h   0.8h
K  
07. (1)
h1  e2 h  e  0.8  0.89 .

GM
13. (2) v 
R
08. (1)
vA RB R 1
  
vB RA 4R 2
Wall  KE vB  2v A  6v
Wmg  Wsp  0 14. (1) For same material, specific resistance
is same.
1 15. (3) Here, m = 30 gram; a = 12 cm; T = 8 s; y
mxg sin   kx 2  0
2 = a = 12 cm
2mg sin 
Force, F  m 2 y  30  42 12  225 dyne
2
x
k 8

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2  2  1 23. (3) Force of attraction or repulsion per unit

16. (2) 2 I 0  4 I 0 cos or cos  length between two parallel wires carry-
2 2 2
ing currents I1 and I2 separated by distance
 1  1 1 
or cos 2  or 2  cos  or    . r is, F 
 0 2 I1 I 2
; so F = 1/r
2 2 4 2 4 r
17. (2) Given, r  3cm, V  0.3cm 3 24. (1) As the temperature rises the atoms of
the liquid become more mobile and the
pV coefficient of viscosity falls.
Bulk modulus = B   25. (1)
V
26. (1) From the equation of continuity
4
100  .r 3 A1v1  A2 v2
 3  4 3  103 atm .
0.3 Here, v1 and v2 are the velocities at two
ends of pipe, A1 and A2 are the area of pipe
at two ends
18. (2) v1 A2 (4.8) 2 9
   
v2 A1 (6.4) 2 16
27. (2)
28. (2) By COME
e mg 0
 mg    . Mg L MgL 1
0 e  0   Mv 2
2 4 2 2
1 MgL MgL
I1 Mv 2  
2 2 8
a
a
v 2 gL  3  3gL
19. (2)
I3    v 
I2 2 2  4 4
a
1 1
29. (1) sin c   r  h tan c  h 
μ  2 1
2
M  a
2   1 3
ma 2
I1 = I2 =     
2 2 r 7  7 3
6 24 4
2
7
  1
3
ma 2
So I 3  I1  I 2  30. (1)
12
31. (2) The emf induced between the centre and
20. (1) Resistance of each part = R / 10 the ring is
When 10 parts are connected in parallel,
1 1
then equivalent resistance e Bl 2   0.5  400  12 = 100 V
2 2
R /10 R
Req    0.01R. Q
10 100 32. (3) Thermal capacity = cm =  JK 1
T
21. (1)
22. (3) Here, n2 = 100 Hz m = 5 Q
Specific heat,  c   J kg 1 K 1
mT
n1  n2  m  100  5  105 Hz or 95 Hz
Q
When 1st fork n1 is loaded with wax, its latent heat = L   J kg 1
m
frequency decreases. As number of beats/
sec remains the same, the frequency of first internal energy U = Joule (J)
fork must be 105 Hz

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Choice (3) is correct.

25 1 1
  2  1   2  1  .
 t x 100 4 2
33. (2) Here, y  5sin 2    
 0.04 40 
42. (2)
Compare with the standard form of wave
equation

 2  t 2  x   2  2
y  r sin  
 T    40 Let the mass of a block is m. It will remains
stationary if forces acting on it are in
   40 cm equilibrium i.e.,
ma cos   mg sin   a  g tan 
34. (3)
43. (4)
35. (2) Between t = 0 and t = 2s
44. (3) From the first law of thermodynamics,
v = slope of x-t graph = 4/2 = 2 m/s
Q  U  W
t > 2, v = 0
For a cyclic process , U  0
p  p2  p1  0  mv  0  0.1 2 Q  W
 0.2kg m/s. Q  Q1  Q2  Q3  Q4
= 600 J – 400 J – 300 J + 200 J = 100 J
N  m2
36. (4)  0  4107 ,  0  8.85 1012 W  W1  W2  W3  W4
C2
= 300 J – 200 J – 150 J + W4
1 8 meter
= – 50 J + W4
so c     3  10 second .
0 0
Substitute the value of Q and W in eqn.
37. (1) (i),
38. (4) By conservation of momentum, we get 100 J = – 50J + W4 or W4 = 150 J.
 45. (2) The moment of inertia of the bar mag-
  v1 net
4m  0  mv1  3mv 2  v 2  
3
ml 2
 The ratio of de-Broglie wavelength of I
12
1 m2 v 2 1 Moment of inertia of each piece of magnet
particle 1 and 2 is   m v  3  3  1.
2 1 1 about an axis perpendicular to length pass-
ing through its centre
39. (4) At 45o range is maximum. At 15o and
2
75o ranges are equal as R  R90o   l
m 2 ml 2 1 l
40. (2) Y  A  B  A  B l      
2 12 12 8 8
(De-Morgan’s law) and magnetic dipole moment
41. (1) The de-Broglie wavelength associated M
with an electron accelerated through a M and time period of oscillation
2
12.27
potential of V volts is given as   Å I
V T  2
MB
1 V V
  2 or  2  1 1 I l /8
2 V1 V2  T   2  2
M B M /2B

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Ozonolysis
2 l T
T    54. (3)
2 MB 2
h
According to de Broglie equation,  
mv
CHEMISTRY Given, h = 6.6 × 10–34 J s, m = 0.66 kg,
46. (2) v = 100 m s–1
Heat of combustion  number of carbon 6.6  10 34
atoms in alkane.   1 1035 m
0.66 100
47. (2)
55. (2)
In Kolbe’s electrolysis alkanes and CO2
collected from anode side. Size, shape and orientation
56. (1)
48. (2)

2 5 H
Molar ratio of CO2 and N2O = : =2:5 > N > > C
44 44 O N
H H H H H F F F H H H
 Ratio of number of molecules will also
be 2 : 5. =0

49. (1) 57. (4)

Empirical formula weight = 12 + 2 × 1 = 14 Elements with electronic configuration 1
22.4 L of N2 = 28 g and 3 belong to second period and groups
17 and 16 respectively whereas the
28 elements with electronic configurations 2
 1 L of N2 = and 4 belong to third period and groups
22.4
17 and 16 respectively. Thus, the least
28 negative E.A. is of 3 due to electron-
Now, 1 L of organic gas = g electron repulsion in the compact 2p-
22.4
orbital. The more negative E.A. is of 4, then
 22.4 L of organic gas = 28 g 1 (halogen) and most negative is of 2
 Molecular weight of gas = 28 g (halogen). Hence, the correct order is 3 < 4
(Empirical weight)n = Molecular weight < 1 < 2.
58. (1)
28
n 2
14 O O

Molecular formula = CH3 C Cl

CH3

(Empirical formula)n = (CH2)2 = C2H4.
50. (4) 59. (1)
C–can’t form H-bond. Among the given compounds, Only (D)
compound is aromatic and obeys Huckel’s
51. (4)
rule.
N2 electrons – 14e–
60. (1)
No unpaired electrons.
q = 600 J, q = +ve when heat is absorbd by
52. (4) the system W = – 900 J
(A)-(III), (B)-(I), (C)-(IV), (D)-(II) ΔE = q + W
53. (1) ΔE = 600 – 900 = – 300 J

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61. (2) Ions which have unpaired electrons

exhibit colour in solution. Ti3+ has an outer
ΔG = +ve for non-spontaneous reactions electronic configuration of 4s0 3d1, i.e., 1
As ΔG = ΔH –T ΔS unpaired electron. Thus, its solution will
Thus ΔH should be positive and be coloured.
ΔS should be negative, thus, ΔG will be 70. (1)
positive at all temperature.
O
62. (4)
ph–CH=O+H2 CH–C–CH3
CaO is basic; CO2 is acidic; SiO2 is weakly
acidic. SnO2 is amphoteric. O
OH
63. (3) ph–CH=CH–C–CH3

Statement (3) is incorrect. It’s correct form
is as follows Most of the tetrahalides are 71. (1)
covalent in nature. If both (A) and (R) are correct and (R) is
64. (3) the correct explanation of (A).

Rate of electrophilic substitution reaction 72. (4)

 Electron donating group on benzene. MnO4– + 2H2O + 3e– 
 MnO2 + 4OH
–

65. (2) 73. (1)

Decreasing order of reactivity :
Tf  i  K f  m
If halogen is different : R-I>R-Br>R-Cl>R-
F Van’t Hoff factor, i = 2 for NaCl, m = 0.01
If halogen is same : 3o > 2o > 1o alkyl halide. hence Tf  0.02 K f which is maximum in
66. (3) the present in case.

N2O 4 2NO 2 Hence Tf is maximum or freezing point

Initial moles 1 0 is minimum.
At equilibrium (1-x) 2x 74. (1)
Total number of moles at equilibrium
K 2 Cr2 O 7  4H 2SO 4  K 2SO 4  Cr2 (SO 4 )3  4H 2 O  3[O]
= 1 – x + 2x = 1 + x [Na 2SO3  [O]  Na 2SO 4 ]  3
67. (1) K 2 Cr2 O 7  3Na 2SO3  4H 2SO 4  3Na 2SO 4  K 2SO 4
 Cr2 (SO 4 )3  H 2 O
pH = pOH = pKw or Cr2 O  3SO  8H  3SO  2Cr 3  4H 2 O
2 2  2
7 3 4

pOH = 14 – 4.7 = 9.3, pOH = –log [OH ] = –

9.3 75. (2)

[OH–] = 5 × 10–10 [Xe]4f7 6s2, [Xe]4f7 5d1 6s2 and [Xe] 4f9 6s2
68. (1) 76. (1)
Statements I, II and III are correct while IV
OH O
and V are incorrect. Their while correct Cu 573 K
form are
IV. The correct order of ionic radii of +3 77. (3)
oxidation state is Bi3+ > Sb3+ > As3+.
O O
69. (2) C6H5NH2 + Cl–C–C6H5
NaOH
C6H5NH–C–C6H5
–HCl
Aniline Benzoyl chloride Benzanilide
Ti3+ (Z = 22)

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78. (2) 88. (4)

The solution containing n-heptane and Volume of the acid taken
ethanol shows non-ideal behaviour with
positive deviation from Raoult’s law. This = 50 mL of 0.5 M H2SO4
is because the ethanol molecules are held = 25 mL of 1 M H2SO4
together by strong H-bonds, however the
Volume of alkali used for neutralization
forces between n-heptane and ethanol are
of excess acid
not very strong, as a result they easily
vapourise showing higher vapour prssure = 60 mL of 0.5 M NaOH = 30 mL of 1 M
than expected. NaOH

79. (3) Now 1 mole of H2SO4 neutralizes 2 moles

of NaOH,
[C][D] [C]2 [D]2 (i.e., H2SO4 + 2NaOH  Na2SO4 + H2O)
K1  ; K2  , t he r e f or e
[A][B] [A]2 [B]2
 30 mL of 1 M NaOH = 15 mL of 1 M
K2 = K12 Since, on multiplying equations H2SO4
by any stoichiometric coefficient, standard
electrode potential value does not get  Volume of acid used by NH3 = 25 – 15 =
multiplied, therefore x = y. 10 mL

80. (1) 1.4  M  B  V

Now %N =
Mass of the substance taken
[Ni(H2O)6]2+
1.4  1  2  10
81. (1) =  56 .
0.5

3d1xy ,3d1yz ,3d1xz 89. (4)

Assertion is incorrect but the reason is
82. (2)
correct.
Reaction of diazonium salts with Cu/HBr
90. (1)
is called Gattermann reaction.
CH3COOH = weak acid
83. (4)
NaOH = strong base
The correct form of statement-I is :
Point of equivalent will be attained at a
Lactose on hydrolysis results galactose +
glucose. pH range of 7.5 to 10 suitable indicator
= Phenolphthalein.
84. (2)
Minus signs are for reactants and positive
signs for products. Dividing numbers are
the coefficients.

85. (1)
(i)-(c), (ii)-(e), (iii)-(d), (iv)-(a), (v)-(b)
86. (4)
P-4, Q-1, R-2, S-3

87. (3)
SnS is soluble in yellow ammonium
sulphide.

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