YAKEEN (DROPPER NEET)

[NEET PATTERN] MINOR TEST– 03

Phase-2
DATED: 16/10/2022

ANSWER KEY
Que. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20
Ans. 2 3 4 2 2 4 1 2 3 2 2 4 1 2 2 2 4 1 2 4
Que. 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40
Ans. 3 2 4 1 1 4 2 3 2 2 2 1 1 2 2 1 2 3 4 1
Que. 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Ans. 3 1 2 3 2 2 2 2 2 1 4 1 4 4 2 2 2 4 3 1
Que. 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80
Ans. 4 2 3 3 4 2 4 3 1 3 4 2 2 4 2 4 2 3 4 1
Que. 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100
Ans. 1 1 4 1 3 1 4 1 2 2 2 2 1 3 1 1 4 3 3 2
Que. 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120
Ans. 1 4 2 2 1 3 1 4 3 4 4 4 3 4 3 2 3 1 4 3
Que. 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 139 140
Ans. 2 4 4 4 4 1 1 3 4 2 1 4 2 4 4 4 1 1 1 1
Que. 141 142 143 144 145 146 147 148 149 150 151 152 153 154 155 156 157 158 159 160
Ans. 1 4 1 4 1 4 4 4 4 2 4 3 1 1 2 2 1 3 4 3
Que. 161 162 163 164 165 166 167 168 169 170 171 172 173 174 175 176 177 178 179 180
Ans. 2 4 3 1 3 3 4 4 4 4 3 4 2 2 2 1 3 1 3 1
Que. 181 182 183 184 185 186 187 188 189 190 191 192 193 194 195 196 197 198 199 200
Ans. 4 2 3 2 2 3 3 2 2 4 2 2 1 3 4 1 4 1 3 3

[1]
 Hints & Solutions
1. (2)  ( d)
R=  R  2
Sn = 19 m (given) m
a R 
Sn = (2n – 1)  × 100 = 2 × 100 = 2 × 0.1 = 0.2%
2 R
a
19 m = (10 × 2 – 1)
2 12. (4)
a
19 = 19. ; a = 2 m/s2
2 13. (1)

2. (3) 14. (2)

In Ist part x  t so a constant velocity attain it.
15. (2)
After that x not vary so it is in rest. This situation Standard equation of projectile is
describe by option (3). g
y = (tan )x – 2 x2 …..(1)
2u cos 
2

3. (4) given equation is

g
y = 3x – x 2 …..(2)
4. (2) 2
Comparing (1) and (2)
5. (2) tan  = 3   = 60o
and 2u2cos2 = 2
1 1
u= = = 2 m/s
6. (4) cos  cos60

16. (2)
7. (1)
At any junction in the circuit 17. (4)
i = 0
18. (1)
8. (2)
R  2, (on stretching)
19. (2)
R     2 
2 2
= = =4
R     20. (4)
 R = 4R
21. (3)
9. (3)
22. (2)

23. (4)
From third equation of motion,
0 = u2 – 2aS
u2 u2
T  S= =
2a 2g
2
S1  u1   u 
2
10. (2)
6 + – + – – + + –  =   =   = 1/16
A B S2  u 2   4u 
–
2A+ 12V 9 4V 5
VA –2 × 6 – 12 – 2 × 9 + 4 – 2 × 5 = VB 24. (1)
 VA – VB = 48 V  Relative Acceleration is zero
 Relative velocity is constant
11. (2) Thus Relative path is straight line.

R= ,m=Ad
A 25. (1)

[2]
 dv x dx
ax = and vx = 50. (1)
dt dt
dv dy
ay = y and vy = 51. (4)
dt dt 2 2
O 1
3 1 3
26. (4) O
Propyl
27. (2)
IUPAC name : n-propylpropanoate
28. (3)
52. (1)
1 CH2
29. (2)
H3C–CH2–C–CH3
4 3 2
30. (2) IUPAC name : 2-methyl-1-butene

31. (2) 53. (4)

OH
32. (1)
Phenol
33. (1)
CH2CH2CH2CH3 Substituent
34. (2) IUPAC name : 3-butylphenol
35. (2) 54. (4)
CH–OH
36. (1)
Person finally reach at the point from where he CH3
starts i.e. xf – xi = 0 IUPAC name : 1-cyclopropylethanol
so displacement is zero and average velocity of
person is zero. 55. (2)
Alkene. It is only alkene out of all options
37. (2) represented by CnH2n. So for n = 4, C4H8.

38. (3) 56. (2)

Geminal diol and Vicinal diol are positional
39. (4) isomers of each other:
2 OH 2 1
1
40. (1)
OH OH
OH
41. (3) (A) (B)
Geminal Vicinal
Ethane-1,1-diol Ethane-1,2-diol
42. (1)
57. (2)
43. (2) Cl Cl Cl
Cl
44. (3)
Cl
45. (2)
Cl
58. (4)
46. (2) Has two dissimilar group attached to both ends of
double bond.
47. (2)
[It is one of essential condition to exhibit
48. (2) geometrical isomerism]

49. (2)
[3]
59. (3) C=C–C–C
Identical groups at terminal ends does not give C
G.I.
C
60. (1)
O 88. (1)
CH3 CH3 CH3
H3C–C–CH2–CH=CH–CH–CH3
H Cl H Cl Cl H
Cl H Cl Cl H H Cl
Stereoisomers = 22 = 4 CH3 CH3 CH3

61. (4) 89. (2)

(1) and (2) options have plane of symmetry and a = 3, b = 3
(1) also have centre of symmetry. a+b=3+3=6
(3) has centre of symmetry
(4) has absence of elements of symmetry 90. (2)
H
62. (2)
only structure (2) has centre of symmetry and two H
Cl
chiral centres
Cl POS
63. (3) only 1 plane of symmetry (P.O.S.)
Cl CH = CH–Cl
n=6 91. (2)
Cl CH = CH–F
CH3 CH3
No. of stereoisomers = 26 
O
O
64. (3)
H
Different in rings are ring chain isomers.
92. (2)
65. (4) H
In (1) terminal carbon valency are ⊥ to each H3C Br
other. So no geometrical isomerism. H3 C Cl
In (2) the absence of double bond in chain. H
In (3) similar groups. (Absence of elements of symmetry)

66. (2) 93. (1)

C  C – C – C – C ; C  C – C –C
C

67. (4)
Factual IUPAC name : 4-(1,1-dimethylethyl)-5-
ethyloctane.
86. (1) [Note: 1. When substituents are at equivalent
C≡N positions, lowest locant is given to that subsituent
which comes first in the alphabetical order.
2. While deciding the alphabetical order of the
IUPAC name : Benzenecarbonitrile various substituents, the name of the complex
substituent is considered to begin with the first
87. (4) letter of the complete name.]
C=C–C–C–C–C ; C=C–C–C–C ; C=C–C–C–C
C C
C CC
C=C–C–C–C ; C=C–C–C ; C=C–C–C

C C

[4]