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Part Test 5 Neet Xi Solution

The document contains the answer key and solutions for a NEET Part Test-5 for Class XI, covering subjects Physics, Chemistry, and Biology. Each subject lists questions with corresponding answer choices and detailed solutions for selected questions. The answers are formatted in a structured manner, making it easy to reference specific questions and their solutions.

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0% found this document useful (0 votes)
12 views7 pages

Part Test 5 Neet Xi Solution

The document contains the answer key and solutions for a NEET Part Test-5 for Class XI, covering subjects Physics, Chemistry, and Biology. Each subject lists questions with corresponding answer choices and detailed solutions for selected questions. The answers are formatted in a structured manner, making it easy to reference specific questions and their solutions.

Uploaded by

Suresh
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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NEET ANSWER KEY & SOLUTION

PAPER CODE :- PART TEST-5


CLASS-XI

ANSWER KEY
PHYSICS
1. (B) 2. (A) 3. (B) 4. (C) 5. (C) 6. (D) 7. (C)
8. (A) 9. (A) 10. (D) 11. (A) 12. (D) 13. (D) 14. (A)
15. (C) 16. (C) 17. (A) 18. (B) 19. (D) 20. (A) 21. (A)
22. (A) 23. (D) 24. (D) 25. (A) 26. (C) 27. (C) 28. (C)
29. (C) 30. (B) 31. (B) 32. (A) 33. (A) 34. (D) 35. (D)
36. (D) 37. (B) 38. (C) 39. (A) 40. (A) 41. (C) 42. (B)
43. (D) 44. (A) 45. (D) 46. (D) 47. (D) 48. (A) 49. (D)
50. (D)

CHEMISTRY
51. (B) 52. (A) 53. (D) 54. (C) 55. (C) 56. (C) 57. (C)
58. (C) 59. (A) 60. (D) 61. (D) 62. (B) 63. (D) 64. (D)
65. (C) 66. (A) 67. (D) 68. (C) 69. (D) 70. (A) 71. (C)
72. (B) 73. (A) 74. (C) 75. (C) 76. (C) 77. (B) 78. (A)
79. (A) 80. (D) 81. (D) 82. (C) 83. (A) 84. (A) 85. (C)
86. (A) 87. (A) 88. (C) 89. (A) 90. (D) 91. (B) 92. (C)
93. (B) 94. (B) 95. (A) 96. (B) 97. (A) 98. (D) 99. (C)
100. (C)

BIOLOGY
101. (B) 102. (C) 103. (B) 104. (A) 105. (D) 106. (A) 107. (A)
108. (C) 109. (C) 110. (A) 111. (A) 112. (B) 113. (A) 114. (C)
115. (B) 116. (C) 117. (B) 118. (C) 119. (D) 120. (C) 121. (B)
122. (A) 123. (A) 124. (A) 125. (A) 126. (A) 127. (D) 128. (A)
129. (D) 130. (D) 131. (B) 132. (A) 133. (D) 134. (C) 135. (D)
136. (A) 137. (D) 138. (B) 139. (B) 140. (C) 141. (C) 142. (C)
143. (D) 144. (B) 145. (C) 146. (C) 147. (B) 148. (B) 149. (B)
150. (C) 151. (A) 152. (C) 153. (C) 154. (A) 155. (C) 156. (B)
157. (D) 158. (C) 159. (B) 160. (C) 161. (B) 162. (C) 163. (D)
164. (D) 165. (B) 166. (D) 167. (C) 168. (B) 169. (D) 170. (B)
171. (D) 172. (A) 173. (B) 174. (C) 175. (D) 176. (B) 177. (C)
178. (B) 179. (B) 180. (C) 181. (D) 182. (D) 183. (D) 184. (D)
185. (A) 186. (A) 187. (B) 188. (D) 189. (C) 190. (C) 191. (C)
192. (D) 193. (C) 194. (D) 195. (C) 196. (A) 197. (B) 198. (C)
199. (C) 200. (C)

1
SOLUTIONS
PHYSICS
1. (B) 10. (D)
Sol. x  a cos( t   ) ….(i) Sol. F   kx
dx
and v   a sin( t   ) ….(ii)
dt 11. (A)
Given at t  0 , x  1 cm and v   and   
Sol. Maximum acceleration  A2  A  4 2n2
Putting these values in equation (i) and (ii) we
1 1  0.01  4  ( )2  (60 )2  144  2 m / sec
will get sin   and cos  
a a
 1
2
1
2 12. (D)
 sin 2   cos 2         1
 a a Sol. E  m 2 A2  E  A2
2
 a  2 cm

2. (A) 13. (D)


Sol. Simple harmonic waves are set up in a string Sol. Let x be the point where K.E. = P.E.
fixed at the, two ends. 1 1
Hence m 2 ( A2  x 2 )  m 2 x 2
3. (B) 2 2
a1 10 2 A 4
Sol.    2x 2  A2  x    2 2cm
a2 25 5 2 2

4. (C)
14. (A)
Sol. It is given vmax  100 cm / sec , a = 10 cm.
Sol. F   kx  dW  Fdx   kxdx
100
 vmax  a     10 rad / sec W x 1 2
10 So  0
dW   0
 kx dx  W  U  
2
kx
Hence v   a 2  y 2  50  10 (10 )2  y 2
 y  5 3 cm 15. (C)
1
5. (C) m  2y 2
U 1 y2 a
2
Sol.  2   2  y
v max  a  a Umax 1 4 a 2
Sol. m a2 2
T 2
2   2
 v max   2 m / s
2 16. (C)
1 1
6. (D) Sol. Kinetic energy K  mv 2  ma 2 2 cos 2  t
2 2
a . 2 2a
Sol. v max  a   1
T T  m  2 a 2 (1  cos 2 t) hence kinetic energy
2
varies periodically with double the frequency of
7. (C)
S.H.M. i.e. 2 .
Sol. v   a2  y 2  10   a 2  (4 )2 and
8   a 2  (5 )2 17. (A)
2 
Accelerati on

2.0
 10 rad s 1
On solving  = 2     2  T   sec Sol.
Displaceme nt
T 0.02

8. (A) 18. (B)


Sol. Velocity is same. So by using v  a Sol. When a little mercury is drained off, the
 A11  A22  A33 position of c.g. of ball falls (w.r.t. fixed and) so
that effective length of pendulum increases
9. (A) hence T increase.
Sol. x  3 sin 2t  4 cos 2t. From given equation
 19. (D)
a1  3, a2  4, and  
2 T1 l1 2 l
Sol. T l   
 a  a12  a 22  3 2  4 2  5 T2 l2 T2 4l
 v max  a  5  2  10  T2  4 sec

2
20. (A) 29. (C)
Sol. No momentum will be transferred because, at
extreme position the velocity of bob is zero. 30. (B)
Sol. The distance between two points i.e. path
21. (A)
Sol. When external force is applied, one spring gets difference between them
extended and another one gets contracted by     v
      ( v  n)
the same distance hence force due to two 2 2 3 6 6n
springs act in same direction. 360
i.e. F  F1  F2    0 . 12 m  12 cm
6  500
  kx   k1 x  k 2 x  k  k1  k 2
31. (B)
22. (A) Co - efficient of t 100
Sol. v   2 m / sec .
m T m2 3 m2 Co - efficient of x 50
Sol. T  2  2   
k T1 m1 2 m
9 m2 32. (A)
 
4 m Sol. Both waves are moving opposite to each other
8
 m  kg  1 . 6 kg
5 33. (A)
Sol. Phase difference is 2 means constrictive
23. (D) interference so resultant amplitude will be
Sol. Potential energy of particle performing SHM is
maximum.
1
given by: PE  m 2y 2 i.e. it varies
2
parabolically such that at mean position it 34. (D)
becomes zero and maximum at extreme
position. 35. (D)
Sol. For producing beats, their must be small
24. (D) difference in frequency.
1
Sol. Spring constant 
Length of spring 36. (D)
k
 k' 
2
Imax  a1  a2  (5  3)2 16
n Sol.    
Imin  a1  a2 
 (5  3)2 1
Also, spring constant depends on material
properties of the spring.
Hence assertion is false, but reason is true. 37. (B)
Sol. From the given equations of progressive waves
25. (A) 1  500  and  2  506   n1  250 and

H 2 n 2  253
P vO 1 1
Sol. v  2    So beat frequency  n2  n1  253  250  3
 vH 2 o 2 16 4
beats per sec  Number of beats per min =
26. (C) 180.

RT
Sol. v  v T 38. (C)
M
i.e. if v is doubled then T becomes four times, Sol. At nodes pressure change (strain) is maximum
hence T2  4 T1  4(273  27)  1200 K  927 C
39. (A)
27. (C) Sol. Energy is not carried by stationary waves
Sol. At given temperature and pressure
1 v1 2 4 40. (A)
v     2 :1
 v2 1 1 Sol. The velocity of sound in solid is given by,
v  E /  . Though  is large for solids, but
28. (C) their coefficient of elasticity E is much larger
    (compared to that of liquids and gases). That is
Sol. Path difference      
2 2 3 6 why v is maximum in case of solid

3
41. (C) Finally when the sphere becomes empty, the
Sol. Frequency - Number of waves passing through resulting C.G. is the C.G. of sphere i.e. length
a point per unit time. becomes equal to the original length and hence
Wave length - Linear distance between starting the time period becomes equal to the same
and end point of 1 complete wave.
value as when it was full of water.
Wave number - No. of waves contained in unit
length
Speed - Linear distance travelled by a wave
l l
per unit time. C.G.

42. (B)

C.G. Resultant C.G.

46. (D)
Sol.
Sol. y  f (x 2  vt 2 ) doesn’t follows the standard
wave equation.

47. (D)
1  cos 2t
Sol. y  sin 2  t 
43. (D) 2
Sol. This is the special case of physical pendulum 2 
 Period, T  
2l 2 
and in this case T  2
3g The given function is not satisfying the
22 standard differential equation of S.H.M.
 T  2  3 .14  2 .31 sec  2 .4 sec
3  9.8 d 2y
   2 y . Hence it represents periodic
dx 2
44. (A) motion but not S.H.M.
Sol. We know that speed of velocity in air
v  T or v 2  T b 48. (A)
v12 T Sol. In the same phase  = 0 so resultant amplitude
Thus,  1 = a1  a2  2 A  A  3 A
v 22 T2
v12 0  2731
Or  49. (D)
 2v1 
2
T2 Sol. nA = Known frequency = 256, nB = ?
Or T2  1092K  1092  273 ºC  819ºC x = 2 bps, which is decreasing after loading
(i.e. x) known tuning fork is loaded so nA
Hence nA – nB = x ... (i)  Correct
45. (D)
nB – nA = x ... (ii)  Wrong
Sol. The given system is like a simple pendulum,
 nB = nA – x = 256 – 2 = 254 Hz.
whose effective length (l) is equal to the
distance between point of suspension and C.G.
(Centre of Gravity) of the hanging body. 50. (D)
When water slowly flows out the sphere, the Sol. When the bob is immersed in water its
C.G. of the system is lowered, and hence l  m    1 
effective weight =  mg  g   mg  
increases, which in turn increases time period      
(as T  l ).    1  T' g
After some time weight of water left in sphere  geff  g   
   T g eff
become less than the weight of sphere itself, so
the resultant C.G. gets clear the C.G. of sphere 
 T' T
itself i.e. l decreases and hence T increases. (  1)

4
CHEMISTRY
51. (B) 62. (B)
Sol. Kolbe's reaction is convenient for preparation
of alkanes containing even number of carbon
Sol.
atoms not odd.

Carbocation has 3 pair of electrons. 63. (D)


Sol. Isobutyl chloride give
52. (A)
Sol. Alkyne and diene are functional isomers

53. (D)
Sol. Alicyclic compounds are Aliphatic cyclic
compounds. 64. (D)
Sol. When D or H atoms are with O, S, N then D
54. (C)
atom or H-atom replaces MgBr in respective
1 RMgX.
Sol. pKb 
I effect C2H5MgBr always gives C2H5D or C2H6.

55. (C) 65. (C)


Sol. Basicity in aqueous medium of –NH3 aqueous Sol. 3° carbon would be fastest because abstraction
follows the order: of hydrogen will be fast.
2° > 1° > 3°
66. (A)
56. (C) Sol. C2H4Cl + alc. KOH  CH2 = CH2
Sol. Stability ()bond ()
67. (D)
57. (C)
Sol. Cstability order [3° > 2° > 1°]
Sol.
58. (C)

Sol. 68. (C)


Sol. Lindlar's catalyst consist of CaCO3,
(CH3COO)2Pb, quinoline, and BaSO4 etc. This
(Acidic nature –M efect) is used for further reduction to stop.
59. (A) 69. (D)
Sol.
Sol.

70. (A)
60. (D)
Sol. Because of allyilc position of Br. It forms Sol.
stable allylic carbocation after removal of Br.

61. (D) 71. (C)


Sol. HCl does not form Anti Markovnikov's
Product with propene, because formation of Cl
is energetically unfavourable.

Sol. 72. (B)

Sol.

So all can exhibit tautomerism.


5
73. (A) 81. (D)
Sol. CH3 – CH2 – CH2 – Br has no chiral centre.
Sol.
Alkylation can also be done using Grignard has one chiral centre.
reagent.
has one chiral centre
so B & C options are correct.
74. (C)
82. (C)
Sol. If 2 atoms attached to double bond have same
atomic number then the relative priority of
Sol. groups is determined by similar comparision of
atomic number of next elements. Thus
preference order is OCH3 > OH > COOH >
CHO
This reaction is electrophilic addition reaction.
83. (A)
75. (C)

Sol.
Sol.

84. (A)

Sol.

(S) (horizontal lower priority)


76. (C)
85. (C)
Sol.

Sol.
They both are chain isomer

77. (B)
Meso tartaric acid The fischer projection is
unstable also due to internal compensation.
Sol.
Methyl propyl Isopropyl 86. (A)
Thioether Methyl thioether
 Position isomer Sol.

78. (A)
Sol. Geometrical isomerism exists due to restricted 87. (A)
Sol. Conformers (eclipsed and staggered form)
rotation and type compound
88. (C)
Sol. Unsaturated compounds have double or triple
79. (A)
bonds
Sol.
89. (A)
Total geometrical isomers = 21 = 2
 cis-trans isomerism = 2 Sol.

80. (D) Total 1° hydrogen atoms are those which are


Sol. Methyl 2-Methyl hepta(2Z, 5E) dienoate. attached to 1° carbon atom vice versa for 3°.
6
90. (D) 96. (B)
Sol. In homologous series general formula is same,
all the members have similar chemical Sol.
properties, adjacent members differ in
molecular mass by 14 and Homologous series  COOH group is main functional group.
members have different physical properties
Suffix = oic acid Prefixes for other - chloro ,
due to difference in weight
methyl, hydroxy,oxo Parent chain-hept-4-ene
91. (B)
Sol. 2–ethyl prop – 2 – enoic acid 97. (A)

Sol.

92. (C) 2–Ethyl butan-1-ol

98. (D)
Sol.

Sol.
3–Chloro–5–fluoro 3, 5 – dimethyl heptane.
Isopropyl methanoate
93. (B)

Sol. 99. (C)


O
2–Hydroxy propane – 1,2,3. tricarboxylic acid. Sol. In , the functional group is –

94. (B)
OH
COOH. The numbering is done from R.H.S. to
Sol.
give minimum number to carbon atom bearing
95. (A) the functional group

100. (C)
Sol. Sol. Assertion : - correct, Reason-false
all asymmetric molecules are optically active

2–methoxy–4–nitro benzene carbaldehyde

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