Previous Year Paper

JEE Mains 2 Apr 2026 Shift 1 (Previous Year Paper)

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Mathematics Section A (20 questions)

Question 1

Let α,α+2,α∈Z \alpha, \alpha + 2, \alpha \in \mathbf{Z} , be the roots of the quadratic

equation x(x+2)+(x+1)(x+3)+(x+2)(x+4) x(x + 2) + (x + 1)(x + 3) + (x + 2) (x + 4)

+.....+(x+n−1)(x+n+1)=4n +.....+ (x + n - 1) (x + n + 1) = 4n for some n∈N n \in \mathbf{N} .

Then (n+α) (n + \alpha) is equal to :

  1. AOption (a)

    0

  2. BOption (b)

    1

  3. COption (c)

    2

  4. DOption (d)

    3

View answer & explanation

Correct answer

Answer: (c)C.

2

Why this answer is correct

Given that:

α,α+2,α∈Z \alpha, \alpha + 2, \alpha \in \mathbf{Z} , are the roots of the quadratic equation:

x(x+2)+(x+1)(x+3)+(x+2)(x+4)+…+(x+n−1)(x+n+1)=4n x(x + 2) + (x + 1)(x + 3) + (x + 2) (x + 4) + \ldots + (x + n - 1) (x + n + 1) = 4n , where n∈N n \in \mathbf{N} .

Calculation:

nx2+x(2+4+6+…+2n)+(1⋅3+…+(n−1)(n+1))=4n nx^2 + x(2 + 4 + 6 + \ldots + 2n) + (1 \cdot 3 + \ldots + (n - 1)(n + 1)) = 4n

⇒ nx2+n(n+1)x+n(n−1)(2n+5)6=4n nx^2 + n(n + 1)x + \frac{n(n - 1)(2n + 5)}{6} = 4n

⇒ x2+(n+1)x+(n−1)(2n+5)6=4 x^2 + (n + 1)x + \frac{(n - 1)(2n + 5)}{6} = 4

Discriminant must be a perfect square:

D=(n+1)2−4×(n−1)(2n+5)6 D = (n + 1)^2 - 4 \times \frac{(n - 1)(2n + 5)}{6}

⇒ D=122−2n26=20−(n2−13) D = \frac{122 - 2n^2}{6} = 20 - \left( \frac{n^2 - 1}{3} \right)

For a perfect square:

n2−13=16 \frac{n^2 - 1}{3} = 16

⇒ n=7 n = 7

Substitute n=7 n = 7 into the equation:

x2+8x+8×156−5=0 x^2 + 8x + \frac{8 \times 15}{6} - 5 = 0

⇒ x2+8x+15=0 x^2 + 8x + 15 = 0

Roots: x=−3,−5 x = -3, -5

α=−5,α+2=−3 \alpha = -5, \alpha + 2 = -3

α+n=7−5=2 \alpha + n = 7 - 5 = 2

∴ The correct answer is option (3).

Question 2

Let x and y be real number such that

50(2x1+3i−y1−2i)=31+17i,i=−1 50 \left( \frac{2x}{1 + 3i} - \frac{y}{1 - 2i} \right) = 31 + 17i, i = \sqrt{-1} . Then the

value of 10(x−3y) 10(x - 3y) is :

  1. AOption (a)

    20

  2. BOption (b)

    31

  3. COption (c)

    35

  4. DOption (d)

    75

View answer & explanation

Correct answer

Answer: (d)D.

75

Why this answer is correct

Given that:

50(2x1+3i−y1−2i)=31+17i50\left(\frac{2x}{1+3i}-\frac{y}{1-2i}\right)=31+17i

Calculation:

50(2x1+3i−y1−2i)=31+17i50\left(\frac{2x}{1+3i}-\frac{y}{1-2i}\right)=31+17i

⇒ 11+3i=1−3i10\frac{1}{1+3i}=\frac{1-3i}{10} and 11−2i=1+2i5\frac{1}{1-2i}=\frac{1+2i}{5}

⇒ 10x−30xi−10y−20yi=31+17i10x-30xi-10y-20yi=31+17i

⇒ Real part: 10(x−y)=3110(x-y)=31, Imaginary part: −30x−20y=17-30x-20y=17

⇒ x=0.9,;y=−2.2x=0.9,;y=-2.2

⇒ 10(x−3y)=7510(x-3y)=75

∴ The correct answer is option (4).

Question 3

Let α,β∈R \alpha, \beta \in \mathbf{R} be such that the system of linear

equations

x+2y+z=5 x + 2y + z = 5

2x+y+αz=5 2x + y + \alpha z = 5

8x+4y+βz=18 8x + 4y + \beta z = 18

has no solution. Then βα \frac{\beta}{\alpha} is equal to :

  1. AOption (a)

    -4

  2. BOption (b)

    4

  3. COption (c)

    8

  4. DOption (d)

    -8

View answer & explanation

Correct answer

Answer: (b)B.

4

Why this answer is correct

Given that:

x+2y+z=5 x + 2y + z = 5

2x+y+αz=5 2x + y + \alpha z = 5

8x+4y+βz=18 8x + 4y + \beta z = 18

Calculation:

Δ=∣121 21α 84β∣=0 \Delta = \begin{vmatrix} 1 & 2 & 1 \ 2 & 1 & \alpha \ 8 & 4 & \beta \end{vmatrix} = 0

Δ=1(β−4α)−2(2β−8α)+1(0)=0 \Delta = 1(\beta - 4\alpha) - 2(2\beta - 8\alpha) + 1(0) = 0

β−4α−4β+16α=0 \beta - 4\alpha - 4\beta + 16\alpha = 0

−3β+12α=0 -3\beta + 12\alpha = 0

4α=β 4\alpha = \beta

βα=4 \frac{\beta}{\alpha} = 4

∴ The correct answer is option (2).

Question 4

Let A=[12 1α] A = \begin{bmatrix} 1 & 2 \ 1 & \alpha \end{bmatrix} and B=[33 β2] B = \begin{bmatrix} 3 & 3 \ \beta & 2 \end{bmatrix} .

If A2−4A+I=O A^2 - 4A + I = O and B2−5B−6I=O B^2 - 5B - 6I = O , then

among the two statements :

(S1) : [(B−A)(B+A)]T=[1315 710] [(B - A)(B + A)]^T = \begin{bmatrix} 13 & 15 \ 7 & 10 \end{bmatrix}

and

(S2) : det (adj(A + B))=−5 \text{det (adj(A + B))} = -5 ,

  1. AOption (a)

    only (S1) is correct

  2. BOption (b)

    only (S2) is correct

  3. COption (c)

    both (S1) and (S2) are correct

  4. DOption (d)

    both (S1) and (S2) are wrong

View answer & explanation

Correct answer

Answer: (b)B.

only (S2) is correct

Why this answer is correct

Given that:

A=[12 1α],;A2−4A+I=O A = \begin{bmatrix} 1 & 2 \ 1 & \alpha \end{bmatrix}, ; A^2 - 4A + I = O

B=[33 β2],;B2−5B−6I=O B = \begin{bmatrix} 3 & 3 \ \beta & 2 \end{bmatrix}, ; B^2 - 5B - 6I = O

Calculation:

Trace of A:\text{Trace of } A: ; α+1=4⇒α=3\alpha + 1 = 4 \Rightarrow \alpha = 3

Determinant of B:\text{Determinant of } B: ; det(B)=6−3β=−6⇒3β=12⇒β=4\text{det(B)} = 6 - 3\beta = -6 \Rightarrow 3\beta = 12 \Rightarrow \beta = 4

B - A = \begin{bmatrix} 2 & 1 \ 3 & -1 \end{bmatrix}, ; B + A = \begin{bmatrix} 4 & 5 \ 5 & 5 \end{bmatrix}

(B - A)(B + A) = \begin{bmatrix} 2 & 1 \ 3 & -1 \end{bmatrix} \begin{bmatrix} 4 & 5 \ 5 & 5 \end{bmatrix} \Rightarrow \begin{bmatrix} 13 & 15 \ 7 & 10 \end{bmatrix}

\text{adj(A + B)} = \begin{bmatrix} 5 & -5 \ -5 & 4 \end{bmatrix}, ; det(adj(A + B))=\text{det(adj(A + B))} = (5)(4) - (-5)(-5) = 20 - 25 = -5

∴ The correct answer is option (3).

Question 5

Let A be the set of first 101 terms of an A.P., whose first term is 1 and the common difference is 5 and let B be the set of first 71 terms of an A.P.,

whose first term is 9 and the common difference is 7. Then the number of elements is A∩B A \cap B , which are divisible by 3, is :

  1. AOption (a)

    4

  2. BOption (b)

    5

  3. COption (c)

    6

  4. DOption (d)

    7

View answer & explanation

Correct answer

Answer: (b)B.

5

Why this answer is correct

Given that:

AP1 (Set A)=1,6,11,16,…,101 terms \text{AP}_1 \text{ (Set A)} = { 1, 6, 11, 16, \dots, 101 \text{ terms} }

AP2 (Set B)=9,16,…,71 terms \text{AP}_2 \text{ (Set B)} = { 9, 16, \dots, 71 \text{ terms} }

D=L.C.M. d1,d2=35 D = \text{L.C.M. } { d_1, d_2 } = 35

1st Common term=16 1^{\text{st}} \text{ Common term} = 16

Calculation:

16+(n−1)⋅35≤499 16 + (n - 1) \cdot 35 \leq 499

⇒ n≤14.8 n \leq 14.8

⇒ n=14 n = 14

A∩B=16,51,86,121,156,191,226,261,296,331,366,401,436,471 A \cap B = { 16, 51, 86, 121, 156, 191, 226, 261, 296, 331, 366, 401, 436, 471 }

Divisible by 3:

=51,156,261,366,471 = { 51, 156, 261, 366, 471 }

∴ The correct answer is option (2).

Question 6

The number of seven-digit numbers, that can be formed by using the digits 1, 2, 3, 5 and 7 such that each digit is used at least once, is ;

  1. AOption (a)

    15400

  2. BOption (b)

    17800

  3. COption (c)

    16800

  4. DOption (d)

    29400

View answer & explanation

Correct answer

Answer: (c)C.

16800

Why this answer is correct

Given that:

5C1×7!3!+5C2×7!2!2! {}^5C_1 \times \frac{7!}{3!} + {}^5C_2 \times \frac{7!}{2!2!}

Calculation:

5C1×7!3!=5×50406=5×840=4200 {}^5C_1 \times \frac{7!}{3!} = 5 \times \frac{5040}{6} = 5 \times 840 = 4200

5C2×7!2!2!=10×50404=10×1260=12600 {}^5C_2 \times \frac{7!}{2!2!} = 10 \times \frac{5040}{4} = 10 \times 1260 = 12600

⇒ 4200+12600=16800 4200 + 12600 = 16800

∴ The correct answer is option (3).

Question 7

The number of elements in the set

S = \left{ (r, k) : k \in \mathbf{Z} \text{ and } {}^{36}C_{r+1} = \frac{6({}^{35}C_r)}{(k^2 - 3)} \right} , is

  1. AOption (a)

    2

  2. BOption (b)

    4

  3. COption (c)

    8

  4. DOption (d)

    16

View answer & explanation

Correct answer

Answer: (b)B.

4

Why this answer is correct

Given that:

36Cr+1=6(35Cr)k2−3 {}^{36}C_{r+1} = \frac{6({}^{35}C_r)}{k^2 - 3}

Calculation:

36r+1⋅35Cr=6⋅35Crk2−3 \frac{36}{r+1} \cdot {}^{35}C_r = 6 \cdot \frac{{}^{35}C_r}{k^2 - 3}

⇒ k2−3=r+16 k^2 - 3 = \frac{r+1}{6}

⇒ k2=r+196 k^2 = \frac{r+19}{6}

0≤r≤35 0 \leq r \leq 35

⇒ 3.1≤r+196≤9 3.1 \leq \frac{r+19}{6} \leq 9

⇒ k2=4,9 k^2 = 4, 9

⇒ k=±2,±3 k = \pm 2, \pm 3

⇒ (r,k)=(5,±2),(35,±3) (r, k) = (5, \pm 2), (35, \pm 3)

∴ The correct answer is option (2).

Question 8

If the mean of the data

Class5-1010-1515-2020-2525-3030-35
Frequency2k2854k+15

is 21, then k is one of the roots of the equation :

  1. AOption (a)

    2x2−23x−10=0 2x^2 - 23x - 10 = 0

  2. BOption (b)

    4x2−35x+24=0 4x^2 - 35x + 24 = 0

  3. COption (c)

    2x2−19x−10=0 2x^2 - 19x - 10 = 0

  4. DOption (d)

    2x2−35x+98=0 2x^2 - 35x + 98 = 0

View answer & explanation

Correct answer

Answer: (c)C.

2x2−19x−10=0 2x^2 - 19x - 10 = 0

Why this answer is correct

Given that:

21=15+12.5k+490+1215+27.5+27.5k+162.590+2k 21 = \frac{15 + 12.5k + 490 + 1215 + 27.5 + 27.5k + 162.5}{90 + 2k}

Calculation:

21(90+2k)=15+12.5k+490+1215+27.5+27.5k+162.5 21(90 + 2k) = 15 + 12.5k + 490 + 1215 + 27.5 + 27.5k + 162.5

⇒ 1890+42k=1910+40k 1890 + 42k = 1910 + 40k

⇒ 42k−40k=1910−1890 42k - 40k = 1910 - 1890

⇒ 2k=20 2k = 20

⇒ k=10 k = 10

k k satisfies the equation 2x2−23x−10=0 2x^2 - 23x - 10 = 0 .

∴ The correct answer is option (1).

Question 9

Let the mid points of the sides of a triangle ABC be (52,7) \left( \frac{5}{2}, 7 \right) , (52,3) \left( \frac{5}{2}, 3 \right) and (4, 5). If its incentre is (h, k), then 3h + k is equal to :

  1. AOption (a)

    11

  2. BOption (b)

    12

  3. COption (c)

    13

  4. DOption (d)

    14

View answer & explanation

Correct answer

Answer: (c)C.

13

Why this answer is correct

Given that:

Midpoints: (52,7),(52,3),(4,5) \text{Midpoints: } \left( \frac{5}{2}, 7 \right), \left( \frac{5}{2}, 3 \right), (4, 5)

Incentre: (h,k) \text{Incentre: } (h, k)

Calculation:

I=(249,5) I = \left( \frac{24}{9}, 5 \right)

⇒ h=249=83,;k=5 h = \frac{24}{9} = \frac{8}{3}, ; k = 5

⇒ 3h+k=3×83+5=8+5=13 3h + k = 3 \times \frac{8}{3} + 5 = 8 + 5 = 13

∴ The correct answer is option (3).

Question 10

Let an ellipse x2a2+y2b2=1 \frac{x^2}{a^2} + \frac{y^2}{b^2} = 1 , a < b, pass through the point (4, 3) and have eccentricity 53 \frac{\sqrt{5}}{3} . Then the length of its latus rectum is :

  1. AOption (a)

    453 \frac{4\sqrt{5}}{3}

  2. BOption (b)

    25 2\sqrt{5}

  3. COption (c)

    753 \frac{7\sqrt{5}}{3}

  4. DOption (d)

    853 \frac{8\sqrt{5}}{3}

View answer & explanation

Correct answer

Answer: (d)D.

853 \frac{8\sqrt{5}}{3}

Why this answer is correct

Given that:

x2a2+y2b2=1,;a<b\frac{x^2}{a^2} + \frac{y^2}{b^2} = 1,; a < b

(4,3)(4, 3) lies on the ellipse

e=53e = \frac{\sqrt{5}}{3}

Calculation:

e2=1−a2b2⇒a2b2=1−e2=1−59=49e^2 = 1 - \frac{a^2}{b^2} \Rightarrow \frac{a^2}{b^2} = 1 - e^2 = 1 - \frac{5}{9} = \frac{4}{9}

⇒a2b2=49…(1)\Rightarrow \frac{a^2}{b^2} = \frac{4}{9} \dots (1)

16a2+9b2=1…(2) \frac{16}{a^2} + \frac{9}{b^2} = 1 \dots (2)

From (1) and (2):

a2=20,;b2=45a^2 = 20,; b^2 = 45

LR=2a2b=2(20)35=853LR = \frac{2a^2}{b} = \frac{2(20)}{3\sqrt{5}} = \frac{8\sqrt{5}}{3}

∴ The correct answer is option (4).

Question 11

If sin⁡(π18)sin⁡(5π18)sin⁡(7π18)=K \sin\left(\frac{\pi}{18}\right) \sin\left(\frac{5\pi}{18}\right) \sin\left(\frac{7\pi}{18}\right) = K , then the value of sin⁡(10Kπ3) \sin\left(\frac{10K\pi}{3}\right) is :

  1. AOption (a)

    3+122 \frac{\sqrt{3} + 1}{2\sqrt{2}}

  2. BOption (b)

    3−12 \frac{\sqrt{3} - 1}{\sqrt{2}}

  3. COption (c)

    32 \frac{\sqrt{3}}{2}

  4. DOption (d)

    12 \frac{1}{2}

View answer & explanation

Correct answer

Answer: (a)A.

3+122 \frac{\sqrt{3} + 1}{2\sqrt{2}}

Why this answer is correct

Given that:

K=sin⁡10∘sin⁡50∘sin⁡70∘ K = \sin 10^\circ \sin 50^\circ \sin 70^\circ

Calculation:

K=sin⁡10∘sin⁡50∘sin⁡70∘ K = \sin 10^\circ \sin 50^\circ \sin 70^\circ

⇒ K=14sin⁡30∘ K = \frac{1}{4} \sin 30^\circ

⇒ K=18 K = \frac{1}{8}

sin⁡10Kπ3=sin⁡(10×18×π3) \sin \frac{10K\pi}{3} = \sin\left( 10 \times \frac{1}{8} \times \frac{\pi}{3} \right)

⇒ sin⁡10Kπ3=sin⁡5π12 \sin \frac{10K\pi}{3} = \sin \frac{5\pi}{12}

⇒ sin⁡5π12=3+122 \sin \frac{5\pi}{12} = \frac{\sqrt{3} + 1}{2\sqrt{2}}

∴ The correct answer is option (1).

Question 12

Let S=x∈[−π,π]:sin⁡x(sin⁡x+cos⁡x)=a,a∈Z S = { x \in [-\pi, \pi] : \sin x (\sin x + \cos x) = a, a \in \mathbf{Z} } . Then n(S) is equal to :

  1. AOption (a)

    3

  2. BOption (b)

    6

  3. COption (c)

    7

  4. DOption (d)

    9

View answer & explanation

Correct answer

Answer: (d)D.

9

Why this answer is correct

Given that:

S=x∈[−π,π]:sin⁡x(sin⁡x+cos⁡x)=a,a∈Z S = { x \in [-\pi, \pi] : \sin x (\sin x + \cos x) = a, a \in \mathbf{Z} }

Calculation:

sin⁡x(sin⁡x+cos⁡x)∈[1−22,1+22] \sin x (\sin x + \cos x) \in \left[ \frac{1-\sqrt{2}}{2}, \frac{1+\sqrt{2}}{2} \right]

⇒ a=0,1 a = 0, 1 (since a∈Z a \in \mathbf{Z} )

Case 1: a=0 a = 0

sin⁡x(sin⁡x+cos⁡x)=0 \sin x (\sin x + \cos x) = 0

⇒ sin⁡x=0 \sin x = 0 or sin⁡x+cos⁡x=0 \sin x + \cos x = 0

sin⁡x=0⇒x=−π,0,π \sin x = 0 \Rightarrow x = -\pi, 0, \pi (3 solutions)

sin⁡x+cos⁡x=0⇒tan⁡x=−1⇒x=−π4,3π4 \sin x + \cos x = 0 \Rightarrow \tan x = -1 \Rightarrow x = -\frac{\pi}{4}, \frac{3\pi}{4} (2 solutions)

Total solutions for a=0 a = 0 : 3 + 2 = 5

Case 2: a=1 a = 1

sin⁡x(sin⁡x+cos⁡x)=1 \sin x (\sin x + \cos x) = 1

⇒ sin⁡2x+sin⁡xcos⁡x=1 \sin^2 x + \sin x \cos x = 1

⇒ 2sin⁡2x+2sin⁡xcos⁡x=2 2\sin^2 x + 2\sin x \cos x = 2

⇒ 1−cos⁡2x+sin⁡2x=2 1 - \cos 2x + \sin 2x = 2

⇒ sin⁡2x−cos⁡2x=1 \sin 2x - \cos 2x = 1

Squaring both sides:

sin⁡22x−2sin⁡2xcos⁡2x+cos⁡22x=1 \sin^2 2x - 2\sin 2x \cos 2x + \cos^2 2x = 1

⇒ 1−sin⁡4x=1 1 - \sin 4x = 1

⇒ sin⁡4x=0⇒4x=−4π,−3π,…,3π,4π \sin 4x = 0 \Rightarrow 4x = -4\pi, -3\pi, \dots, 3\pi, 4\pi

⇒ x=−π,−3π4,−π2,−π4,0,π4,π2,3π4,π x = -\pi, -\frac{3\pi}{4}, -\frac{\pi}{2}, -\frac{\pi}{4}, 0, \frac{\pi}{4}, \frac{\pi}{2}, \frac{3\pi}{4}, \pi

Total solutions for a=1 a = 1 : 4

Total solutions: 5+4=9 5 + 4 = 9

∴ The correct answer is option (4).

Question 13

If the point of intersection of the lines x+13=y+a5=z+b+17 \frac{x+1}{3} = \frac{y+a}{5} = \frac{z+b+1}{7} and x−21=y−b4=z−2a7 \frac{x-2}{1} = \frac{y-b}{4} = \frac{z-2a}{7} lies on xy-plane, then the value of a + b is :

  1. AOption (a)

    2

  2. BOption (b)

    5

  3. COption (c)

    7

  4. DOption (d)

    9

View answer & explanation

Correct answer

Answer: (c)C.

7

Why this answer is correct

Given that:

x+13=y+a5=z+b+17 \frac{x+1}{3} = \frac{y+a}{5} = \frac{z+b+1}{7}

x−21=y−b4=z−2a7 \frac{x-2}{1} = \frac{y-b}{4} = \frac{z-2a}{7}

Calculation:

3r1−1=r2+2⇒r2=3r1−3 3r_1 - 1 = r_2 + 2 \Rightarrow r_2 = 3r_1 - 3

7r1−b−1=0⇒b=7r1−1 7r_1 - b - 1 = 0 \Rightarrow b = 7r_1 - 1

7r2+2a=0⇒2a=−7r2⇒a=−72r2 7r_2 + 2a = 0 \Rightarrow 2a = -7r_2 \Rightarrow a = -\frac{7}{2}r_2

r2=3r1−3⇒a=−72(3r1−3)⇒a=−212r1+212 r_2 = 3r_1 - 3 \Rightarrow a = -\frac{7}{2}(3r_1 - 3) \Rightarrow a = -\frac{21}{2}r_1 + \frac{21}{2}

a+b=−212r1+212+7r1−1 a + b = -\frac{21}{2}r_1 + \frac{21}{2} + 7r_1 - 1

a+b=(−212+7)r1+(212−1) a + b = \left(-\frac{21}{2} + 7\right)r_1 + \left(\frac{21}{2} - 1\right)

a+b=142r1+192⇒r1=1 a + b = \frac{14}{2}r_1 + \frac{19}{2} \Rightarrow r_1 = 1

a+b=7+2=9 a + b = 7 + 2 = 9

∴ The correct answer is option (4).

Question 14

If a⃗ \vec{a} and b⃗ \vec{b} are two vectors such that ∣a⃗∣=2 |\vec{a}| = 2 and ∣b⃗∣=3 |\vec{b}| = 3 , then the maximum value of 3∣(3a⃗+2b⃗)∣+4∣(3a⃗−2b⃗)∣ 3\left| \left( 3\vec{a} + 2\vec{b} \right) \right| + 4\left| \left( 3\vec{a} - 2\vec{b} \right) \right| is :

  1. AOption (a)

    30

  2. BOption (b)

    36

  3. COption (c)

    60

  4. DOption (d)

    72

View answer & explanation

Correct answer

Answer: (c)C.

60

Why this answer is correct

Given that:

∣a⃗∣=2,;∣b⃗∣=3 |\vec{a}| = 2, ; |\vec{b}| = 3

E=3∣(3a⃗+2b⃗)∣+4∣(3a⃗−2b⃗)∣ E = 3\left| \left( 3\vec{a} + 2\vec{b} \right) \right| + 4\left| \left( 3\vec{a} - 2\vec{b} \right) \right|

Calculation:

E=39a2+4b2+12a⃗.b⃗+49a2+4b2−12a⃗.b⃗ E = 3\sqrt{9a^2 + 4b^2 + 12\vec{a}.\vec{b}} + 4\sqrt{9a^2 + 4b^2 - 12\vec{a}.\vec{b}}

⇒ a=2,;b=3,;a⃗.b⃗=6cos⁡θ a = 2, ; b = 3, ; \vec{a}.\vec{b} = 6 \cos \theta

⇒ E=336+36+12×6cos⁡θ+436+36−72cos⁡θ E = 3\sqrt{36 + 36 + 12 \times 6 \cos \theta} + 4\sqrt{36 + 36 - 72 \cos \theta}

⇒ E=372+72cos⁡θ+472−72cos⁡θ E = 3\sqrt{72 + 72 \cos \theta} + 4\sqrt{72 - 72 \cos \theta}

⇒ E=1821+cos⁡θ+2421−cos⁡θ E = 18\sqrt{2} \sqrt{1 + \cos \theta} + 24\sqrt{2} \sqrt{1 - \cos \theta}

⇒ E=36cos⁡θ2+48sin⁡θ2 E = 36 \cos \frac{\theta}{2} + 48 \sin \frac{\theta}{2}

⇒ Emax=(36)2+(48)2=1296+2304=3600=60 E_{\text{max}} = \sqrt{(36)^2 + (48)^2} = \sqrt{1296 + 2304} = \sqrt{3600} = 60

∴ The correct answer is option (3).

Question 15

Let a line L passing through the point (1, 1, 1) be perpendicular to both the vectors 2i^+2j^+k^ 2\hat{i} + 2\hat{j} + \hat{k} and i^+2j^+k^ \hat{i} + 2\hat{j} + \hat{k} . If P(a, b, c) is the foot of perpendicular from the origin on the line L, then the value of 34(a + b + c) is :

  1. AOption (a)

    50

  2. BOption (b)

    80

  3. COption (c)

    100

  4. DOption (d)

    120

View answer & explanation

Correct answer

Answer: (c)C.

100

Why this answer is correct

Given that:

L⃗ \vec{L} passes through point (1, 1, 1) and is perpendicular to 2i^+2j^+k^ 2\hat{i} + 2\hat{j} + \hat{k} and i^+2j^+k^ \hat{i} + 2\hat{j} + \hat{k} .

Calculation:

Direction vector of L⃗=∣i^j^k^ 122 221∣=−2i^+3j^−2k^ \text{Direction vector of } \vec{L} = \begin{vmatrix} \hat{i} & \hat{j} & \hat{k} \ 1 & 2 & 2 \ 2 & 2 & 1 \end{vmatrix} = -2\hat{i} + 3\hat{j} - 2\hat{k}

Equation of line: x−1−2=y−13=z−1−2=λ \frac{x-1}{-2} = \frac{y-1}{3} = \frac{z-1}{-2} = \lambda

Let P(a,b,c)≡(2λ+1,−3λ+1,2λ+1) P(a, b, c) \equiv (2\lambda + 1, -3\lambda + 1, 2\lambda + 1) be the foot of perpendicular from (0, 0, 0).

OM⃗⋅(−2i^+3j^−2k^)=0 \vec{OM} \cdot (-2\hat{i} + 3\hat{j} - 2\hat{k}) = 0

⇒ −2(2λ+1)+3(−3λ+1)−2(2λ+1)=0 -2(2\lambda + 1) + 3(-3\lambda + 1) - 2(2\lambda + 1) = 0

⇒ λ=−117 \lambda = -\frac{1}{17}

Substitute λ=−117 \lambda = -\frac{1}{17} :

a=−217+1,;b=317+1,;c=−217+1 a = \frac{-2}{17} + 1, ; b = \frac{3}{17} + 1, ; c = \frac{-2}{17} + 1

⇒ 34(a+b+c)=100 34(a+b+c) = 100

∴ The correct answer is option (3).

Question 16

If lim⁡x→2sin⁡(x3−5x2+ax+b)(x−1−1)log⁡e(x−1)=m \lim_{x \to 2} \frac{\sin(x^3 - 5x^2 + ax + b)}{(\sqrt{x-1} - 1)\log_e(x-1)} = m , then a + b + m is equal to:

  1. AOption (a)

    5

  2. BOption (b)

    6

  3. COption (c)

    8

  4. DOption (d)

    10

View answer & explanation

Correct answer

Answer: (b)B.

6

Why this answer is correct

Given that:

lim⁡x→2sin⁡(x3−5x2+ax+b)(x−1−1)log⁡e(x−1)=m \lim_{x \to 2} \frac{\sin(x^3 - 5x^2 + ax + b)}{(\sqrt{x-1} - 1)\log_e(x-1)} = m

Calculation:

∵ \because Denominator = 0 at x=2x = 2

⇒ \Rightarrow Numerator = 0 at x=2x = 2

⇒23−5(2)2+a(2)+b=0 \Rightarrow 2^3 - 5(2)^2 + a(2) + b = 0

⇒2a+b=12 \Rightarrow 2a + b = 12 ... (1)

m=lim⁡x→2sin⁡(x3−5x2+ax+b)(x3−5x2+ax+b)⋅(x3−5x2+ax+b)x−1−1x−1+1⋅log⁡e(1+(x−2))(x−2)⋅(x−2) m = \lim_{x \to 2} \frac{\frac{\sin(x^3 - 5x^2 + ax + b)}{(x^3 - 5x^2 + ax + b)} \cdot (x^3 - 5x^2 + ax + b)}{\frac{\sqrt{x-1} - 1}{\sqrt{x-1} + 1} \cdot \frac{\log_e(1 + (x-2))}{(x-2)} \cdot (x-2)}

⇒m=lim⁡x→22x3−5x2+ax+b(x−2)2 \Rightarrow m = \lim_{x \to 2} 2 \frac{x^3 - 5x^2 + ax + b}{(x-2)^2}

⇒m=lim⁡x→223x2−10x+a2(x−2) \Rightarrow m = \lim_{x \to 2} 2 \frac{3x^2 - 10x + a}{2(x-2)}

∵ \because Denominator = 0 at x=2x = 2

⇒ \Rightarrow Numerator = 0 at x=2x = 2

⇒3(2)2−10(2)+a=0 \Rightarrow 3(2)^2 - 10(2) + a = 0

⇒a=8 \Rightarrow a = 8

Substituting a=8a = 8 in (1):

2(8)+b=12 2(8) + b = 12

⇒b=−4 \Rightarrow b = -4

∴m=lim⁡x→22(6x−102) \therefore m = \lim_{x \to 2} 2 \left( \frac{6x - 10}{2} \right)

⇒m=2 \Rightarrow m = 2

∴a+b+m=8−4+2=6 \therefore a + b + m = 8 - 4 + 2 = 6

∴ The correct answer is option (2).

Question 17

If the curve y = f(x) passes through the point (1, e) and satisfies the differential equation dy = y (2 + logex) dx, x > 0, then f(e) is equal to :

  1. AOption (a)

    ee e^e

  2. BOption (b)

    ee2 e^{e^2}

  3. COption (c)

    e2e e^{2e}

  4. DOption (d)

    e2e e^{2^e}

View answer & explanation

Correct answer

Answer: (c)C.

e2e e^{2e}

Why this answer is correct

Given that:

dydx=y(2+ln⁡x) \frac{dy}{dx} = y(2 + \ln x)

Calculation:

∫1y,dy=∫(2+ln⁡x),dx \int \frac{1}{y} , dy = \int (2 + \ln x) , dx

⇒ ln⁡y=2x+xln⁡x−x+C \ln y = 2x + x \ln x - x + C

⇒ ln⁡y=x+xln⁡x+C \ln y = x + x \ln x + C

Given point (1, e): ln⁡e=1+1ln⁡1+C \ln e = 1 + 1 \ln 1 + C

⇒ 1=1+0+C⇒C=0 1 = 1 + 0 + C \Rightarrow C = 0

⇒ ln⁡y=x+xln⁡x \ln y = x + x \ln x

⇒ f(x)=y=ex+xln⁡x f(x) = y = e^{x + x \ln x}

⇒ f(e)=ee+e=e2e f(e) = e^{e + e} = e^{2e}

∴ The correct answer is option (3).

Question 18

The number of critical points of the function

f(x)={∣sin⁡xx∣,x≠0 1,x=0 f(x) = \begin{cases} \left| \frac{\sin x}{x} \right| & , \quad x \neq 0 \ 1 & , \quad x = 0 \end{cases} in the interval (−2π,2π) (-2\pi, 2\pi) is equal to:

  1. AOption (a)

    1

  2. BOption (b)

    3

  3. COption (c)

    5

  4. DOption (d)

    7

View answer & explanation

Correct answer

Answer: (c)C.

5

Why this answer is correct

Given that:

f(x)={∣sin⁡xx∣,x≠0 1,x=0 f(x) = \begin{cases} \left| \frac{\sin x}{x} \right| & , \quad x \neq 0 \ 1 & , \quad x = 0 \end{cases} , x∈(−2π,2π) x \in (-2\pi, 2\pi)

Calculation:

lim⁡x→0∣sin⁡xx∣=1=f(0) \lim_{x \to 0} \left| \frac{\sin x}{x} \right| = 1 = f(0) , hence f(x) f(x) is continuous.

f′(x)=ddx∣sin⁡xx∣=xcos⁡x−sin⁡xx2 f'(x) = \frac{d}{dx} \left| \frac{\sin x}{x} \right| = \frac{x \cos x - \sin x}{x^2}

f′(x)=0⇒tan⁡x=x f'(x) = 0 \Rightarrow \tan x = x

From the graph, there are 3 solutions to tan⁡x=x \tan x = x in (−2π,2π) (-2\pi, 2\pi) .

Additionally, f′(x) f'(x) does not exist at x=−π,π x = -\pi, \pi .

Total critical points = 3 (from tan⁡x=x \tan x = x ) + 2 (where f′(x) f'(x) does not exist) = 5.

∴ The correct answer is option (3).

Question 19

Let [.] denote the greatest integer function. Then the value of ∫03ex+e−x[x]!dx \int_0^3 \frac{e^x + e^{-x}}{[x]!} dx is:

  1. AOption (a)

    e2+e3−1e2−1e3 e^2 + e^3 - \frac{1}{e^2} - \frac{1}{e^3}

  2. BOption (b)

    12(e2+e3−1e2−1e3) \frac{1}{2} \left( e^2 + e^3 - \frac{1}{e^2} - \frac{1}{e^3} \right)

  3. COption (c)

    e2+e3−12e2−12e3 e^2 + e^3 - \frac{1}{2e^2} - \frac{1}{2e^3}

  4. DOption (d)

    12(e2+e3)−1e2−1e3 \frac{1}{2} (e^2 + e^3) - \frac{1}{e^2} - \frac{1}{e^3}

View answer & explanation

Correct answer

Answer: (b)B.

12(e2+e3−1e2−1e3) \frac{1}{2} \left( e^2 + e^3 - \frac{1}{e^2} - \frac{1}{e^3} \right)

Why this answer is correct

Given that:

∫03ex+e−x[x]!,dx\int_{0}^{3}\dfrac{e^x+e^{-x}}{[x]!},dx

Calculation:

∫03ex+e−x[x]!,dx\int_{0}^{3}\dfrac{e^x+e^{-x}}{[x]!},dx

⇒ ∫01(ex+e−x),dx+∫12(ex+e−x),dx+12∫23(ex+e−x),dx\int_{0}^{1}(e^x+e^{-x}),dx+\int_{1}^{2}(e^x+e^{-x}),dx+\dfrac{1}{2}\int_{2}^{3}(e^x+e^{-x}),dx

⇒ \(\left[e^x-e^{-x}\right]{0}^{1}+\left[e^x-e^{-x}\right]{1}^{2}+\dfrac{1}{2}\left[e^x-e^{-x}\right]_{2}^{3}\)

⇒ (e−1e)+(e2−e−1e2+1e)+12(e3−e2−1e3+1e2)\left(e-\dfrac{1}{e}\right)+\left(e^2-e-\dfrac{1}{e^2}+\dfrac{1}{e}\right)+\dfrac{1}{2}\left(e^3-e^2-\dfrac{1}{e^3}+\dfrac{1}{e^2}\right)

⇒ 12(e2+e3−1e2−1e3)\dfrac{1}{2}\left(e^2+e^3-\dfrac{1}{e^2}-\dfrac{1}{e^3}\right)

∴ The correct answer is option (2).

Question 20

Let y = y(x) be the solution curve of the differential equation (1+sin⁡x)dydx+(y+1)cos⁡x=0,y(0)=0 (1 + \sin x) \frac{dy}{dx} + (y + 1) \cos x = 0, y(0) = 0 . If the curve y = y(x) passes through the point

(α,−12) \left( \alpha, \frac{-1}{2} \right) , then a value of α \alpha is :

  1. AOption (a)

    π6 \frac{\pi}{6}

  2. BOption (b)

    π4 \frac{\pi}{4}

  3. COption (c)

    π3 \frac{\pi}{3}

  4. DOption (d)

    π2 \frac{\pi}{2}

View answer & explanation

Correct answer

Answer: (d)D.

π2 \frac{\pi}{2}

Why this answer is correct

Given that:

(1+sin⁡x)dydx+(y+1)cos⁡x=0,;y(0)=0 (1 + \sin x) \frac{dy}{dx} + (y + 1) \cos x = 0, ; y(0) = 0

Calculation:

∫dyy+1=−∫cos⁡x1+sin⁡xdx \int \frac{dy}{y+1} = -\int \frac{\cos x}{1+\sin x} dx

⇒ ln⁡(y+1)=−ln⁡(1+sin⁡x)+C \ln(y+1) = -\ln(1+\sin x) + C

⇒ y+1=eC1+sin⁡x y+1 = \frac{e^{C}}{1+\sin x}

Using y(0)=0 y(0) = 0 :

⇒ 1+1=eC1+sin⁡0 1+1 = \frac{e^{C}}{1+\sin 0}

⇒ C=0 C = 0

⇒ y+1=11+sin⁡x y+1 = \frac{1}{1+\sin x}

Given y=−12,;x=α y = -\frac{1}{2}, ; x = \alpha :

⇒ −12+1=11+sin⁡α -\frac{1}{2} + 1 = \frac{1}{1+\sin \alpha}

⇒ 12=11+sin⁡α \frac{1}{2} = \frac{1}{1+\sin \alpha}

⇒ 1+sin⁡α=2 1+\sin \alpha = 2

⇒ sin⁡α=1 \sin \alpha = 1

⇒ α=π2 \alpha = \frac{\pi}{2}

∴ The correct answer is option (4).

Mathematics Section B (5 questions)

Question 21

If the domain of the function f(x)=log⁡(0.6)(∣2x−5x2−4∣) f(x) = \sqrt{\log_{(0.6)} \left( \left| \frac{2x - 5}{x^2 - 4} \right| \right)}

is (−∞,a]∪b∪[c,d)∪(e,∞) (-\infty, a] \cup {b} \cup [c, d) \cup (e, \infty) , then the value of

a + b + c + d + e is ____________.

  1. AOption (a)
  2. BOption (b)
  3. COption (c)
  4. DOption (d)
View answer & explanation

Correct answer

Answer: (a)A.

Why this answer is correct

Given that:

log⁡0.6∣2x−5x2−4∣≥0 \log_{0.6} \left| \frac{2x - 5}{x^2 - 4} \right| \geq 0

∣2x−5x2−4∣≤1 \left| \frac{2x - 5}{x^2 - 4} \right| \leq 1

x≠52 x \neq \frac{5}{2}

−1≤2x−5x2−4≤1 -1 \leq \frac{2x - 5}{x^2 - 4} \leq 1

(x+1)2−10(x−2)(x+2)≥0 \frac{(x+1)^2 - 10}{(x-2)(x+2)} \geq 0

x∈(−∞,−1−10]∪(−2,2)∪[−1+10,∞) x \in (-\infty, -1-\sqrt{10}] \cup (-2, 2) \cup [-1+\sqrt{10}, \infty)

(x−1)2(x−2)(x+2)≥0 \frac{(x-1)^2}{(x-2)(x+2)} \geq 0

x∈(−∞,−2)∪(2,∞)∪1 x \in (-\infty, -2) \cup (2, \infty) \cup {1}

Calculation:

(1)∩(2)∩(3) (1) \cap (2) \cap (3)

x∈(−∞,−1−10]∪1∪[−1+10,52)∪(52,∞) x \in (-\infty, -1-\sqrt{10}] \cup {1} \cup \left[ -1+\sqrt{10}, \frac{5}{2} \right) \cup \left( \frac{5}{2}, \infty \right)

a+b+c+d+e=−2+1+5=4 a + b + c + d + e = -2 + 1 + 5 = 4

Question 22

If ∑k=1nak=6n3 \sum_{k=1}^n a_k = 6n^3 , then ∑k=16(ak+1−ak36)2 \sum_{k=1}^6 \left( \frac{a_{k+1} - a_k}{36} \right)^2 is equal to ________.

  1. AOption (a)
  2. BOption (b)
  3. COption (c)
  4. DOption (d)
View answer & explanation

Correct answer

Answer: (a)A.

Why this answer is correct

Given that:

a1+a2+…+an=6n3 a_1 + a_2 + \ldots + a_n = 6n^3

a1+a2+…+an+an+1=6(n+1)3 a_1 + a_2 + \ldots + a_n + a_{n+1} = 6(n+1)^3

Calculation:

an+1=6(n+1)3−6n3 a_{n+1} = 6(n+1)^3 - 6n^3

⇒ an+1=6((n+1)−n)((n+1)2+n2+n(n+1)) a_{n+1} = 6((n+1)-n)((n+1)^2 + n^2 + n(n+1))

⇒ an+1=6(1)(3n2+3n+1) a_{n+1} = 6(1)(3n^2 + 3n + 1)

⇒ an=6(3(n−1)2+3(n−1)+1) a_n = 6(3(n-1)^2 + 3(n-1) + 1)

⇒ an=6(3n2−3n+1) a_n = 6(3n^2 - 3n + 1)

⇒ ∑k=16(6(3k2+3k+1)−6(3k2−3k+1)36)2 \sum_{k=1}^6 \left( \frac{6(3k^2 + 3k + 1) - 6(3k^2 - 3k + 1)}{36} \right)^2

⇒ ∑k=16(36k36)2=∑k=16k2=6×7×136=91 \sum_{k=1}^6 \left( \frac{36k}{36} \right)^2 = \sum_{k=1}^6 k^2 = \frac{6 × 7 × 13}{6} = 91

Question 23

Let a, b, c ∈1,2,3,4 \in {1, 2, 3, 4} . If the probability, that

ax2+22bx+c>0 ax^2 + 2\sqrt{2} bx + c > 0 for all x ∈R \in \mathbf{R} , is mn \frac{m}{n} ,

gcd (m, n) = 1, then m + n is equal to ________.

  1. AOption (a)
  2. BOption (b)
  3. COption (c)
  4. DOption (d)
View answer & explanation

Correct answer

Answer: (a)A.

Why this answer is correct

Given that:

8b2−4ac<0⇒2b2<ac8b^2 - 4ac < 0 \Rightarrow 2b^2 < ac

Calculation:

Total combinations of b,a,cb, a, c:

1×4+1×3+1×4+1×4+1×2+1×2=191 \times 4 + 1 \times 3 + 1 \times 4 + 1 \times 4 + 1 \times 2 + 1 \times 2 = 19

Valid combinations satisfying 2b2<ac2b^2 < ac:

2+3+4+4+2+2=172 + 3 + 4 + 4 + 2 + 2 = 17

Required probability:

1764=mn\frac{17}{64} = \frac{m}{n}, where m=17,n=64m = 17, n = 64

m+n=17+64=81m + n = 17 + 64 = 81

Question 24

Let a circle C have its centre in the first quadrant, intersect the coordinate axes at exactly three points and cut off equal intercepts from the coordinate

axes. If the length of the chord of C on the line x + y = 1 is 14 \sqrt{14} , then the square of the radius of C is ________.

  1. AOption (a)
  2. BOption (b)
  3. COption (c)
  4. DOption (d)
View answer & explanation

Correct answer

Answer: (a)A.

Why this answer is correct

Given that:

r2=(142)2+(r−12)2 r^2 = \left( \frac{\sqrt{14}}{2} \right)^2 + \left( r - \frac{1}{\sqrt{2}} \right)^2

Calculation:

r2=72+(r−12)2 r^2 = \frac{7}{2} + \left( r - \frac{1}{\sqrt{2}} \right)^2

⇒ r2=72+r2−2r+12 r^2 = \frac{7}{2} + r^2 - \sqrt{2}r + \frac{1}{2}

⇒ 2r=4 \sqrt{2}r = 4

⇒ r=22 r = 2\sqrt{2}

⇒ r2=8 r^2 = 8

Question 25

If α=∫023log⁡2(x2+4)dx+∫242x−4dx \alpha = \int_0^{2\sqrt{3}} \log_2 (x^2 + 4) dx + \int_2^4 \sqrt{2^x - 4} dx , then α2 \alpha^2 is

equal to ________.

  1. AOption (a)
  2. BOption (b)
  3. COption (c)
  4. DOption (d)
View answer & explanation

Correct answer

Answer: (a)A.

Why this answer is correct

Given that:

∫abf(x)dx+∫f(a)f(b)f−1(x)dx=bf(b)−af(a) \int_a^b f(x) dx + \int_{f(a)}^{f(b)} f^{-1}(x) dx = bf(b) - af(a)

α=(23)(4)−(0)(2) \alpha = (2\sqrt{3})(4) - (0)(2)

Calculation:

α=83 \alpha = 8\sqrt{3}

α2=192 \alpha^2 = 192

Chemistry Section A (20 questions)

Question 26

The mass of iron converted into Fe3O4 \text{Fe}_3\text{O}_4 by the action of 18 g of steam is :

(Given : Molar mass of H, O and Fe are 1, 16 and 56 g mol−1 \text{g mol}^{-1} respectively)

Assume iron is present in excess :

  1. AOption (a)

    2.1 g

  2. BOption (b)

    4.2 g

  3. COption (c)

    21 g

  4. DOption (d)

    42 g

View answer & explanation

Correct answer

Answer: (d)D.

42 g

Why this answer is correct

CONCEPT:

Stoichiometry of the Reaction

  • Stoichiometry refers to the quantitative relationship between reactants and products in a chemical reaction.
  • In the given reaction:

3Fe(s) + 4H2O(g) → Fe3O4(s) + 4H2(g)

  • From the balanced chemical equation:
  • 3 moles of Fe react with 4 moles of H2O.
  • The molar ratio of Fe to H2O is 3:4.
  • Molar masses:
  • Molar mass of Fe = 56 g/mol
  • Molar mass of H2O = 18 g/mol

EXPLANATION:

  • Given mass of steam (H2O) = 18 g
  • Number of moles of steam:

nsteam = ⅛18 = 1 mol

  • From the stoichiometric ratio, moles of Fe required:

nFe = ¾

  • Mass of Fe required:

Mass of Fe = nFe × Molar mass of Fe

= ¾ × 56

= 42 g

Therefore, the mass of iron converted into Fe3O4 by the action of 18 g of steam is 42 g.

Question 27

What is the energy (in J atom−1 \text{J atom}^{-1} ) required for the following process?

Li2+(g)→Li3+(g)+e− \text{Li}^{2+}\text{(g)} \rightarrow \text{Li}^{3+}\text{(g)} + \text{e}^-

(Take the ionization energy for the H atom in the ground state as 2.18×10−18 J atom−1 2.18 \times 10^{-18} \text{ J atom}^{-1} )

  1. AOption (a)

    8.72×10−18 8.72 \times 10^{-18}

  2. BOption (b)

    1.962×10−18 1.962 \times 10^{-18}

  3. COption (c)

    1.962×10−17 1.962 \times 10^{-17}

  4. DOption (d)

    6.54×10−17 6.54 \times 10^{-17}

View answer & explanation

Correct answer

Answer: (c)C.

1.962×10−17 1.962 \times 10^{-17}

Why this answer is correct

CONCEPT:

Ionization Energy and Its Dependence on Nuclear Charge (Z)

  • The ionization energy is the energy required to remove an electron from an atom or ion in its gaseous state.
  • For hydrogen-like ions (single electron systems like Li2+ \text{Li}^{2+} ), the ionization energy can be calculated using the formula:

E=EH×Z2 \text{E} = \text{E}_{\text{H}} \times \text{Z}^2

  • Here:
  • EH \text{E}_{\text{H}} is the ionization energy of a hydrogen atom in its ground state.
  • Z \text{Z} is the atomic number of the element.

EXPLANATION:

  • The given reaction is:

Li2+(g)→Li3+(g)+e− \text{Li}^{2+}\text{(g)} \rightarrow \text{Li}^{3+}\text{(g)} + \text{e}^-

  • Here, Li2+ \text{Li}^{2+} is a hydrogen-like ion with a single electron in its orbit. Its ionization energy can be calculated using the formula:

E=EH×Z2 \text{E} = \text{E}_{\text{H}} \times \text{Z}^2

  • The ionization energy of hydrogen, EH=2.18×10−18 J atom−1 \text{E}_{\text{H}} = 2.18 \times 10^{-18} \text{ J atom}^{-1} .
  • The atomic number of lithium, Z=3 \text{Z} = 3 .
  • Substitute the values into the formula:

ELi2+=2.18×10−18×(3)2 \text{E}_{\text{Li}^{2+}} = 2.18 \times 10^{-18} \times (3)^2

ELi2+=2.18×10−18×9 \text{E}_{\text{Li}^{2+}} = 2.18 \times 10^{-18} \times 9

ELi2+=1.962×10−17 J atom−1 \text{E}_{\text{Li}^{2+}} = 1.962 \times 10^{-17} \text{ J atom}^{-1}

Therefore, the energy required for the process is 1.962×10−17 J atom−1 1.962 \times 10^{-17} \text{ J atom}^{-1} .

Question 28

Given below are two statements :

Statement (I) : The correct sequence of bond lengths in the following species is: O2+<O2<O2−<O22− \text{O}_2^+ < \text{O}_2 < \text{O}_2^- < \text{O}_2^{2-}

Statement (II) : The correct sequence of number of unpaired electrons in the following species is: O2>O2+>O2−>O22− \text{O}_2 > \text{O}_2^+ > \text{O}_2^- > \text{O}_2^{2-}

In the light of the above statements, choose the correct answer from the options given below :

  1. AOption (a)

    Both Statement I and Statement II are true

  2. BOption (b)

    Both Statement I and Statement II are false

  3. COption (c)

    Statement I is true but Statement II is false

  4. DOption (d)

    Statement I is false but Statement II is true

View answer & explanation

Correct answer

Answer: (c)C.

Statement I is true but Statement II is false

Why this answer is correct

CONCEPT:

Bond Order and Unpaired Electrons in Molecular Orbital Theory

  • Bond Order:

Bond Order = (Number of bonding electrons - Number of antibonding electrons)⁄2

  • The bond order is a measure of the number of chemical bonds between a pair of atoms. It is given by the formula:
  • A higher bond order corresponds to a shorter and stronger bond, while a lower bond order corresponds to a longer and weaker bond.
  • Unpaired Electrons:
  • The number of unpaired electrons in a molecule is determined based on the electronic configuration of its molecular orbitals.
  • Molecules with unpaired electrons are paramagnetic, while those without unpaired electrons are diamagnetic.

EXPLANATION:

  • The electronic configurations of the molecular orbitals for the given oxygen species are as follows:
  • O+2O2+

: Bond Order = 2.5, Unpaired Electrons = 1

  • O2O2

: Bond Order = 2, Unpaired Electrons = 2

  • O−2O2−

: Bond Order = 1.5, Unpaired Electrons = 1

  • O2−2O22−

: Bond Order = 1, Unpaired Electrons = 0

  • Statement I: The bond length is inversely proportional to the bond order. Therefore, the correct sequence of bond lengths is:

O+2<O2<O−2<O2−2O2+<O2<O2−<O22−

This makes Statement I true.

  • Statement II: The number of unpaired electrons decreases in the following order:

O2>O+2>O−2>O2−2O2>O2+>O2−>O22−

This makes Statement II true.

Conclusion: Both Statement I and Statement II are true.

Question 29

Consider the following data

(i) 2Al(s)+6HCl(aq)→Al2Cl6(aq)+3H2(g)+ 2\text{Al(s)} + 6\text{HCl(aq)} \rightarrow \text{Al}_2\text{Cl}_6\text{(aq)} + 3\text{H}_2\text{(g)} +  1200 kJ/mol.

(ii) H2(g)+Cl2(g)→2HCl(g)+164 kJ/mol. \text{H}_2\text{(g)} + \text{Cl}_2\text{(g)} \rightarrow 2\text{HCl(g)} + 164 \text{ kJ/mol.}

(iii) HCl(g)+aq→HCl(aq)+83 kJ/mol. \text{HCl(g)} + \text{aq} \rightarrow \text{HCl(aq)} + 83 \text{ kJ/mol.}

(iv) Al2Cl6(s)+aq→Al2Cl6(aq)+663 kJ/mol. \text{Al}_2\text{Cl}_6\text{(s)} + \text{aq} \rightarrow \text{Al}_2\text{Cl}_6\text{(aq)} + 663 \text{ kJ/mol.}

The enthalpy of formation of anhydrous solid

Al2Cl6 \text{Al}_2\text{Cl}_6 is :

  1. AOption (a)

    −648 kJ mol−1 -648 \text{ kJ mol}^{-1}

  2. BOption (b)

    −1350 kJ mol−1 -1350 \text{ kJ mol}^{-1}

  3. COption (c)

    −2002 kJ mol−1 -2002 \text{ kJ mol}^{-1}

  4. DOption (d)

    −1527 kJ mol−1 -1527 \text{ kJ mol}^{-1}

View answer & explanation

Correct answer

Answer: (d)D.

−1527 kJ mol−1 -1527 \text{ kJ mol}^{-1}

Why this answer is correct

CONCEPT:

Enthalpy of Formation (ΔfH \Delta_{\text{f}}H )

  • The enthalpy of formation (ΔfH \Delta_{\text{f}}H ) of a compound is the change in enthalpy when 1 mole of a compound is formed from its constituent elements in their standard states under standard conditions.
  • To calculate the enthalpy of formation for a reaction, the enthalpy changes (ΔrH \Delta_{\text{r}}H ) from individual steps involved in the reaction can be summed up using Hess's Law.
  • Hess's Law states that the total enthalpy change for a reaction is the sum of the enthalpy changes for the individual steps that lead to the reaction.

EXPLANATION:

  • Given data:
  • Step (i): \( 2\text{Al(s)} + 6\text{HCl(aq)} \rightarrow \text{Al}_2\text{Cl}_6\text{(aq)} + 3\text{H}2\text{(g)} \), \( \Delta{\text{r}}H_1 = -1200 , \text{kJ/mol} \)
  • Step (ii): \( \text{H}_2\text{(g)} + \text{Cl}2\text{(g)} \rightarrow 2\text{HCl(g)} \), \( \Delta{\text{r}}H_2 = -164 , \text{kJ/mol} \) (multiplied by 3: −164×3,kJ/mol -164 \times 3 , \text{kJ/mol} )
  • Step (iii): HCl(g)+aq→HCl(aq) \text{HCl(g)} + \text{aq} \rightarrow \text{HCl(aq)} , ΔrH3=−83,kJ/mol \Delta_{\text{r}}H_3 = -83 , \text{kJ/mol} (multiplied by 6: −83×6,kJ/mol -83 \times 6 , \text{kJ/mol} )
  • Step (iv): \( \text{Al}_2\text{Cl}_6\text{(aq)} \rightarrow \text{Al}_2\text{Cl}6\text{(s)} + \text{aq} \), \( \Delta{\text{r}}H_4 = +663 , \text{kJ/mol} \)
  • Target reaction: 2Al(s)+3Cl2→Al2Cl6(s) 2\text{Al(s)} + 3\text{Cl}_2 \rightarrow \text{Al}_2\text{Cl}_6\text{(s)}
  • Using Hess's Law:
  • ΔfH=ΔrH1+ΔrH2+ΔrH3+ΔrH4 \Delta_{\text{f}}H = \Delta_{\text{r}}H_1 + \Delta_{\text{r}}H_2 + \Delta_{\text{r}}H_3 + \Delta_{\text{r}}H_4
  • ΔfH=−1200−(164×3)−(83×6)+663 \Delta_{\text{f}}H = -1200 - (164 \times 3) - (83 \times 6) + 663
  • ΔfH=−1200−492−498+663 \Delta_{\text{f}}H = -1200 - 492 - 498 + 663
  • ΔfH=−1527,kJ/mol \Delta_{\text{f}}H = -1527 , \text{kJ/mol}

Therefore, the enthalpy of formation (ΔfH \Delta_{\text{f}}H ) of anhydrous solid Al2Cl6 \text{Al}_2\text{Cl}_6 is −1527,kJ/mol -1527 , \text{kJ/mol} .

Question 30

19.5 g of fluoro acetic acid (molar mass = 78 g mol-1) is dissolved in 500g of water at 298 K. The depression in the freezing point of water was 1°C. What is \( \text{K}{\text{a}} \) of fluoro acetic acid ? (For water, \( \text{K}{\text{f}} = 1.86 \text{ K kg mol}^{-1} \)). Assume molarity and molality to have the same values.

  1. AOption (a)

    10−6 10^{-6}

  2. BOption (b)

    4×10−4 4 \times 10^{-4}

  3. COption (c)

    3×10−5 3 \times 10^{-5}

  4. DOption (d)

    3×10−3 3 \times 10^{-3}

View answer & explanation

Correct answer

Answer: (d)D.

3×10−3 3 \times 10^{-3}

Why this answer is correct

CONCEPT:

Freezing Point Depression and Degree of Dissociation

  • The depression in the freezing point of a solution is given by the equation:

ΔTf = iKfm

where:

  • ΔTf = depression in freezing point
  • i = van't Hoff factor
  • Kf = molal freezing point depression constant
  • m = molality of the solution
  • The van't Hoff factor, i, is related to the degree of dissociation (α) by the formula:

i = 1 + (n - 1)α

where:

  • n = number of ions produced per molecule upon dissociation
  • α = degree of dissociation
  • The dissociation constant (Ka) is given by the formula:

Ka = (Cα²) / (1 - α)

where:

  • C = concentration of the solute
  • α = degree of dissociation

EXPLANATION:

  • Given data:
  • Mass of fluoroacetic acid = 19.5 g
  • Molar mass of fluoroacetic acid = 78 g mol-1
  • Mass of water = 500 g = 0.5 kg
  • ΔTf = 1°C
  • Kf = 1.86 K kg mol-1
  • Calculate the number of moles of fluoroacetic acid:

= 19.5 / 78 = 0.25 mol

  • Calculate the molality (m):

m = Number of moles of solute / Mass of solvent in kg

= 0.25 / 0.5 = 0.5 mol kg-1

  • ΔTf = iKfm

1 = i × 1.86 × 0.5

i = 1 / 1.86 × 0.5 = 2 / 1.86

  • i = 1 + α (since fluoroacetic acid dissociates into 2 particles: H+ and CH2FCOO-)

2 / 1.86 = 1 + α

α = 2 / 1.86 - 1 = 0.075

  • Ka = Cα² / 1 - α

Here, C = molality = 0.5 mol kg-1

Ka = 0.5 × (0.075)² / 1 - 0.075

Ka = 0.5 × 0.005625 / 0.925 = 0.0028125 / 0.925

Ka ≈ 3 × 10-3

Therefore, the dissociation constant (Ka) of fluoroacetic acid is approximately 3 × 10-3.

Question 31

The solubility product constants of Ag2CrO4 \text{Ag}_2\text{CrO}_4 and AgBr \text{AgBr}  are 32x and 4y respectively at 298 K.  The value of (molarity of Ag2CrO4molarity of AgBr) \left( \frac{\text{molarity of Ag}_2\text{CrO}_4}{\text{molarity of AgBr}} \right) can be expressed as :

  1. AOption (a)

    2x3y \frac{2\sqrt[3]{\text{x}}}{\text{y}}

  2. BOption (b)

    2xy 2\sqrt{\frac{\text{x}}{\text{y}}}

  3. COption (c)

    xy \sqrt{\frac{\text{x}}{\text{y}}}

  4. DOption (d)

    x3y \frac{\sqrt[3]{\text{x}}}{\sqrt{\text{y}}}

View answer & explanation

Correct answer

Answer: (d)D.

x3y \frac{\sqrt[3]{\text{x}}}{\sqrt{\text{y}}}

Why this answer is correct

CONCEPT:

Solubility Product and Molarity Relation

  • The solubility product constant (Ksp K_{\text{sp}} ) represents the equilibrium constant for the dissolution of a sparingly soluble salt.
  • The molarity of ions in solution can be derived from the solubility product constant using the stoichiometric relationship between the ions and the salt.

EXPLANATION:

  • For Ag2CrO4 \text{Ag}_2\text{CrO}_4 :
  • The dissociation equation is:

Ag2CrO4⇌2Ag++CrO42− \text{Ag}_2\text{CrO}_4 \rightleftharpoons 2\text{Ag}^+ + \text{CrO}_4^{2-}

  • The solubility product is given by:

Ksp=[Ag+]2[CrO42−] K_{\text{sp}} = [\text{Ag}^+]^2[\text{CrO}_4^{2-}]

  • If the molarity of Ag2CrO4 \text{Ag}_2\text{CrO}_4 is S1 S_1 , then:
  • [Ag+]=2S1 [\text{Ag}^+] = 2S_1
  • [CrO42−]=S1 [\text{CrO}_4^{2-}] = S_1
  • Substitute these values into the solubility product equation:

Ksp=(2S1)2(S1) K_{\text{sp}} = (2S_1)^2(S_1)

Ksp=4S13 K_{\text{sp}} = 4S_1^3

  • Given Ksp=32x K_{\text{sp}} = 32x , solve for S1 S_1 :

4S13=32x 4S_1^3 = 32x

S1=2x1/3 S_1 = 2x^{1/3}

  • For AgBr \text{AgBr} :
  • The dissociation equation is:

AgBr⇌Ag++Br− \text{AgBr} \rightleftharpoons \text{Ag}^+ + \text{Br}^-

  • The solubility product is given by:

Ksp=[Ag+][Br−] K_{\text{sp}} = [\text{Ag}^+][\text{Br}^-]

  • If the molarity of AgBr \text{AgBr} is S2 S_2 , then:
  • [Ag+]=S2 [\text{Ag}^+] = S_2
  • [Br−]=S2 [\text{Br}^-] = S_2
  • Substitute these values into the solubility product equation:

Ksp=S22 K_{\text{sp}} = S_2^2

  • Given Ksp=4y K_{\text{sp}} = 4y , solve for S2 S_2 :

S22=4y S_2^2 = 4y

S2=2y1/2 S_2 = 2y^{1/2}

  • Calculate the ratio (S1S2) \left( \frac{\text{S}_1}{\text{S}_2} \right) :

S1S2=2x1/32y1/2 \frac{\text{S}_1}{\text{S}_2} = \frac{2x^{1/3}}{2y^{1/2}}

S1S2=x3y \frac{\text{S}_1}{\text{S}_2} = \frac{\sqrt[3]{x}}{\sqrt{y}}

Therefore, the ratio (molarity of Ag2CrO4molarity of AgBr) \left( \frac{\text{molarity of Ag}_2\text{CrO}_4}{\text{molarity of AgBr}} \right) is x3y \frac{\sqrt[3]{x}}{\sqrt{y}} .

Question 32

An electrochemical cell is constructed using half cells in the direction of spontaneous change Fe(OH)2(s)+2e−→Fe(s)+2OH−(aq) E0=−0.88V \text{Fe(OH)}_2(\text{s}) + 2\text{e}^- \rightarrow \text{Fe(s)} + 2\text{OH}^-(\text{aq}) \text{ E}^0 = -0.88\text{V}  and AgBr(s)+e−→Ag(s)+Br−(aq) E0=+0.07V \text{AgBr(s)} + \text{e}^- \rightarrow \text{Ag(s)} + \text{Br}^-(\text{aq}) \text{ E}^0 = +0.07\text{V}  Which of the following option is correct ?

  1. AOption (a)

    Overall reaction Fe(s)+2OH−(aq)+2AgBr(s)⇌Fe(OH)2(s)+2Ag(s)+2Br−(aq) \text{Fe(s)} + 2\text{OH}^-(\text{aq}) + 2\text{AgBr(s)} \rightleftharpoons \text{Fe(OH)}_2(\text{s}) + 2\text{Ag(s)} + 2\text{Br}^-(\text{aq})

  2. BOption (b)

    Ecell0=−0.95V \text{E}^0_{\text{cell}} = -0.95\text{V}

  3. COption (c)

    Fe is reduced in the electrochemical cell

  4. DOption (d)

    Ecell0 \text{E}^0_{\text{cell}} is an extensive property

View answer & explanation

Correct answer

Answer: (a)A.

Overall reaction Fe(s)+2OH−(aq)+2AgBr(s)⇌Fe(OH)2(s)+2Ag(s)+2Br−(aq) \text{Fe(s)} + 2\text{OH}^-(\text{aq}) + 2\text{AgBr(s)} \rightleftharpoons \text{Fe(OH)}_2(\text{s}) + 2\text{Ag(s)} + 2\text{Br}^-(\text{aq})

Why this answer is correct

CONCEPT:

Standard Cell Potential (E0cell)

  • The standard cell potential (E0cell) is the difference in the standard reduction potentials of the cathode and the anode in an electrochemical cell.
  • The standard cell potential can be calculated using the equation:

E0cell = E0cathode - E0anode

EXPLANATION:

  • In the given reaction:

Fe(s) + 2OH-(aq) + 2AgBr(s) → Fe(OH)2(s) + 2Ag(s) + 2Br-(aq)

  • Iron (Fe) is oxidized to Fe(OH)2, so Fe is the anode.
  • Silver bromide (AgBr) is reduced to Ag, so AgBr is the cathode.
  • Given standard reduction potentials:
  • E0AgBr = +0.07 V (for AgBr(s) + e- → Ag(s) + Br-(aq))
  • E0Fe = -0.88 V (for Fe(OH)2(s) + 2e- → Fe(s) + 2OH-(aq))
  • Using the standard cell potential equation:
  • E0cell = E0cathode - E0anode
  • = 0.07 V - (-0.88 V)
  • = 0.07 V + 0.88 V
  • = 0.95 V
  • Key points to note:
  • Fe is oxidized in the reaction, not reduced.
  • E0cell is not an extensive property; it is an intensive property, as it does not depend on the amount of material.

Therefore, the correct overall reaction is:

Fe(s) + 2OH-(aq) + 2AgBr(s) → Fe(OH)2(s) + 2Ag(s) + 2Br-(aq)

The standard cell potential (E0cell) is 0.95 V.

Question 33

\( \text{t}{100%} \) is the time required for the 100% completion of the reaction while \( \text{t}{1/2} \) is the time required for 50% of the reaction to be completed. Which of the following option correctly represents the relation between \( \text{t}{100%} \) and \( \text{t}{1/2} \) for zero and first order reactions respectively ?

  1. AOption (a)

    \( \text{t}{100%} = (\text{t}{1/2})^2 \) and \( \text{t}{100%} = (\text{t}{1/2})^\infty \)

  2. BOption (b)

    \( \text{t}{100%} = 2\text{t}{1/2} \) and \( \text{t}{100%} = (\text{t}{1/2})^\infty \)

  3. COption (c)

    \( \text{t}{100%} = 2\text{t}{1/2} \) and \( \text{t}{100%} = (2\text{t}{1/2})^2 \)

  4. DOption (d)

    \( \text{t}{100%} = (\text{t}{1/2})^\infty \) and \( \text{t}{100%} = 2\text{t}{1/2} \)

View answer & explanation

Correct answer

Answer: (b)B.

\( \text{t}{100%} = 2\text{t}{1/2} \) and \( \text{t}{100%} = (\text{t}{1/2})^\infty \)

Why this answer is correct

CONCEPT:

Zero-order and First-order Reaction Time Relationships

  • For a zero-order reaction, the rate of reaction is constant and independent of the concentration of the reactant.
  • For a first-order reaction, the rate of reaction is proportional to the concentration of the reactant.
  • The times required for 50% completion (\( \text{t}{1/2} \)) and 100% completion (\( \text{t}{100%} \)) of the reaction differ for zero-order and first-order reactions.

EXPLANATION:

  • Zero-order Reaction:
  • For a zero-order reaction, the time required for the reaction to complete 100% is given by:

t100%=ak \text{t}_{100\%} = \frac{\text{a}}{\text{k}}

  • The time required for 50% completion is:

t1/2=a2k \text{t}_{1/2} = \frac{\text{a}}{2\text{k}}

  • By dividing \( \text{t}{100%} \) by \( \text{t}{1/2} \), we get:

\( \text{t}{100%} = 2\text{t}{1/2} \)

  • First-order Reaction:
  • For a first-order reaction, the time required for 100% completion is theoretically infinite, because the reactant concentration never truly reaches zero.
  • The time required for 50% completion is:

t1/2=ℓn 2k \text{t}_{1/2} = \frac{\ell\text{n } 2}{\text{k}}

  • Since t100% \text{t}_{100\%} is infinite, we represent the relationship as:

\( \text{t}{100%} = (\text{t}{1/2})^\infty \)

So, For a zero-order reaction, \( \text{t}{100%} = 2\text{t}{1/2} \).

  • For a first-order reaction, \( \text{t}{100%} = (\text{t}{1/2})^\infty \).

Therefore, the correct relationship is:

\( \text{t}{100%} = 2\text{t}{1/2} \) for zero-order reactions and \( \text{t}{100%} = (\text{t}{1/2})^\infty \) for first-order reactions.

Question 34

Given below are two statements :

Statement (I) : The first ionisation enthalpy of the elements Na, Mg, Cl and Ar follows the order Na > Mg > Cl > Ar

Statement (II) : Among Ca, Al, Fe and B, the third ionisation enthalpy is very high for Ca. In the light of the above statements, choose the

correct answer from the options given below :

  1. AOption (a)

    Both Statement I and Statement II are true

  2. BOption (b)

    Both Statement I and Statement II are false

  3. COption (c)

    Statement I is true but Statement II is false

  4. DOption (d)

    Statement I is false but Statement II is true

View answer & explanation

Correct answer

Answer: (d)D.

Statement I is false but Statement II is true

Why this answer is correct

CONCEPT:

Ionization Enthalpy

  • The ionization enthalpy is the energy required to remove an electron from the outermost shell of an isolated gaseous atom.
  • The first ionization enthalpy corresponds to the removal of the first electron, the second ionization enthalpy corresponds to the removal of the second electron, and so on.
  • Ionization enthalpy is influenced by factors such as atomic size, nuclear charge, shielding effect, and electron configuration.

EXPLANATION:

  • Statement (I): The first ionization enthalpy of the elements Na, Mg, Cl, and Ar follows the order Na > Mg > Cl > Ar.
  • This statement is false because the correct order of first ionization enthalpy is Na < Mg < Cl < Ar.
  • The trend in ionization energy across a period increases from left to right due to increasing nuclear charge and decreasing atomic size.
  • Na has the lowest ionization enthalpy, followed by Mg, Cl, and Ar, which has the highest due to its stable noble gas configuration.
  • Statement (II): Among Ca, Al, Fe, and B, the third ionization enthalpy is very high for Ca.
  • This statement is true.
  • Calcium (Ca) has a very high third ionization enthalpy because after losing two electrons, it attains a stable noble gas configuration (similar to Argon: [Ar]).
  • Removing a third electron from this stable configuration requires a significantly higher amount of energy.

So, Statement I is false but Statement II is true.

Question 35

Given below are two statements :

Statement (I) : Oxidising power of halogens decreases in the orderF2>Cl2>Br2>I2 \text{F}_2 > \text{Cl}_2 > \text{Br}_2 > \text{I}_2 , which is the basis of “Layer test”.

Statement (II) : “Layer test” to identify Br2 \text{Br}_2 and I2 \text{I}_2  in aqueous solution involves the oxidation of bromide or iodide into Br2 \text{Br}_2 or I2 \text{I}_2 respectively with , which is a type of displacement redox reaction.

In the light of the above statements, choose the correct answer from the options given below :

  1. AOption (a)

    Both Statement I and Statement II are true

  2. BOption (b)

    Both Statement I and Statement II are false

  3. COption (c)

    Statement I is true but Statement II is false

  4. DOption (d)

    Statement I is false but Statement II is true

View answer & explanation

Correct answer

Answer: (a)A.

Both Statement I and Statement II are true

Why this answer is correct

CONCEPT:

Oxidizing Power of Halogens

  • Oxidizing power refers to the ability of a substance to oxidize another substance, i.e., to accept electrons.
  • Among the halogens, the oxidizing power decreases down the group in the periodic table in the following order: F2 > Cl2 > Br2 > I2.
  • This trend is due to the decreasing standard reduction potentials of the halogens as we move down the group, making them less effective oxidizing agents.

Layer Test

  • The "Layer Test" is a chemical test used to identify halogens in aqueous solutions based on their relative oxidizing powers.
  • In this test, a more powerful oxidizing agent (e.g., Cl2) is used to oxidize halide ions (e.g., Br- or I-) to their molecular forms (Br2 or I2), which can then be detected by their characteristic colors.
  • For example:
  • Cl2 oxidizes bromide ions (Br-) to bromine (Br2), which appears as an orange-brown color in aqueous solution:

NaBr + Cl2-water → Br2 + NaCl

  • Cl2 also oxidizes iodide ions (I-) to iodine (I2), which appears as a violet color in organic solvents or a brown color in aqueous solution:

NaI + Cl2-water → I2 + NaCl

EXPLANATION:

  • Statement (I): "Oxidizing power of halogens decreases in the order F2 > Cl2 > Br2 > I2, which is the basis of 'Layer test'" is true. This is because fluorine has the highest oxidizing power, followed by chlorine, bromine, and iodine, consistent with their standard reduction potentials.
  • Statement (II): "'Layer test' to identify Br2 and I2 in aqueous solution involves the oxidation of bromide or iodide into Br2 or I2 respectively with Cl2, which is a type of displacement redox reaction" is also true. This statement correctly describes the chemical basis of the layer test, where Cl2, being a stronger oxidizing agent, displaces Br2 and I2 from their respective halide ions.
  • Since both statements are correct and Statement (II) explains the process mentioned in Statement (I), the correct interpretation is that both Statement I and Statement II are true.

Therefore, the answer is that both Statement I and Statement II are true.

Question 36

Which of the following sets includes all the species that will change the orange colour of K2Cr2O7 \text{K}_2\text{Cr}_2\text{O}_7 in acidic medium ?

  1. AOption (a)

    Fe2+,Sn2+,I−,S2− \text{Fe}^{2+}, \text{Sn}^{2+}, \text{I}^-, \text{S}^{2-}

  2. BOption (b)

    S2−,Fe3+,I−,C2O42− \text{S}^{2-}, \text{Fe}^{3+}, \text{I}^-, \text{C}_2\text{O}_4^{2-}

  3. COption (c)

    Fe2+,NO2−,SO2,Sn4+ \text{Fe}^{2+}, \text{NO}_2^-, \text{SO}_2, \text{Sn}^{4+}

  4. DOption (d)

    Fe3+,SO42−,S2−,Sn4+ \text{Fe}^{3+}, \text{SO}_4^{2-}, \text{S}^{2-}, \text{Sn}^{4+}

View answer & explanation

Correct answer

Answer: (a)A.

Fe2+,Sn2+,I−,S2− \text{Fe}^{2+}, \text{Sn}^{2+}, \text{I}^-, \text{S}^{2-}

Why this answer is correct

CONCEPT:

Oxidation-Reduction Reactions and Changes in Color

  • In an acidic medium, K2Cr2O7 \text{K}_2\text{Cr}_2\text{O}_7 (potassium dichromate) undergoes a reduction reaction. The dichromate ion Cr2O72− \text{Cr}_2\text{O}_7^{2-} is reduced to Cr3+ \text{Cr}^{3+} , causing a color change from orange to green.
  • This color change occurs when the dichromate ion reacts with a reducing agent, which donates electrons to reduce Cr2O72− \text{Cr}_2\text{O}_7^{2-} .
  • Common reducing agents include species that can themselves undergo oxidation, such as Fe2+,Sn2+,I−,S2− \text{Fe}^{2+}, \text{Sn}^{2+}, \text{I}^-, \text{S}^{2-} , etc.

EXPLANATION:

  • To determine which species will cause the color change of K2Cr2O7 \text{K}_2\text{Cr}_2\text{O}_7 in acidic medium, we need to identify species that act as reducing agents and undergo oxidation.
  • For the species in the given options:
  • Fe2+ \text{Fe}^{2+} : Oxidized to Fe3+ \text{Fe}^{3+} , donating electrons and reducing Cr2O72− \text{Cr}_2\text{O}_7^{2-} . Thus, it causes the color change.
  • Sn2+ \text{Sn}^{2+} : Oxidized to Sn4+ \text{Sn}^{4+} , donating electrons and reducing Cr2O72− \text{Cr}_2\text{O}_7^{2-} . Thus, it causes the color change.
  • I− \text{I}^- : Oxidized to I2 \text{I}_2 , donating electrons and reducing Cr2O72− \text{Cr}_2\text{O}_7^{2-} . Thus, it causes the color change.
  • S2− \text{S}^{2-} : Oxidized to sulfur (S \text{S} ), donating electrons and reducing Cr2O72− \text{Cr}_2\text{O}_7^{2-} . Thus, it causes the color change.
  • Other species, such as Fe3+ \text{Fe}^{3+} , Sn4+ \text{Sn}^{4+} , or SO42− \text{SO}_4^{2-} , cannot act as reducing agents in this context, as they are already in their oxidized states.

Conclusion: The species Fe2+,Sn2+,I−,S2− \text{Fe}^{2+}, \text{Sn}^{2+}, \text{I}^-, \text{S}^{2-} will change the orange color of K2Cr2O7 \text{K}_2\text{Cr}_2\text{O}_7 to green in acidic medium, as they are all capable of acting as reducing agents.

Question 37

Match List – I with List – II.

List – IList – II
Chromium (III) ComplexesΔ0(cm−1) \Delta_0(\text{cm}^{-1})
(en = ethylene diamine)
A. [Cr(CN)6]3− [\text{Cr(CN)}_6]^{3-} I. 15,060
B. [CrF6]3− [\text{CrF}_6]^{3-} II. 17,400
C. [Cr(H2O)6]3+ [\text{Cr(H}_2\text{O)}_6]^{3+} III. 22,300
D. [Cr(en)3]3+ [\text{Cr(en)}_3]^{3+} IV. 26,600

Choose the correct answer from the options given

below :

  1. AOption (a)

    a-I, b-II, c-III, d-IV

  2. BOption (b)

    a-II, b-III, c-IV, d-I

  3. COption (c)

    a-III, b-IV, c-I, d-II

  4. DOption (d)

    a-IV, b-I, c-II, d-III

View answer & explanation

Correct answer

Answer: (d)D.

a-IV, b-I, c-II, d-III

Why this answer is correct

CONCEPT:

Crystal Field Splitting Energy (CFSE) and Ligand Strength

  • The crystal field splitting energy (Δ0 \Delta_0 ) is directly proportional to the strength of the ligand in the spectrochemical series.
  • Stronger ligands cause greater splitting of the d-orbitals, resulting in higher Δ0 \Delta_0 values.
  • The spectrochemical series for the given ligands is as follows:

CN- > en (ethylene diamine) > H2O > F-

Thus, CN- is the strongest ligand, and F- is the weakest ligand.

  • Additionally, chelation (e.g., by ethylene diamine) increases the ligand strength compared to monodentate ligands of similar type.

EXPLANATION:

  • The given complexes are:
  • A. [Cr(CN)6]3− [\text{Cr(CN)}_6]^{3-}
  • B. [CrF6]3− [\text{CrF}_6]^{3-}
  • C. [Cr(H2O)6]3+ [\text{Cr(H}_2\text{O)}_6]^{3+}
  • D. [Cr(en)3]3+ [\text{Cr(en)}_3]^{3+}
  • The crystal field splitting energy (Δ0 \Delta_0 ) values are:
  • I. 15,060 cm-1
  • II. 17,400 cm-1
  • III. 22,300 cm-1
  • IV. 26,600 cm-1
  • Based on the ligand strength:
  • [Cr(CN)6]3− [\text{Cr(CN)}_6]^{3-} (CN-, strongest ligand) should have the highest splitting energy, i.e., Δ0 \Delta_0 = 26,600 , \text{cm}^{-1} \) (IV). - [Cr(en)3]3+ [\text{Cr(en)}_3]^{3+} (chelating ligand, moderate strength) should have the second-highest splitting energy, i.e., Δ0 \Delta_0 = 22,300 , \text{cm}^{-1} \) (III). - [Cr(H2O)6]3+ [\text{Cr(H}_2\text{O)}_6]^{3+} (H2O, weaker ligand) should have the second-lowest splitting energy, i.e., Δ0 \Delta_0 = 17,400 , \text{cm}^{-1} \) (II). - [CrF6]3− [\text{CrF}_6]^{3-} (F-, weakest ligand) should have the lowest splitting energy, i.e., Δ0 \Delta_0 $= 15,060 , \text{cm}^{-1} \) (I).

MATCHING:

Complex$ Δ0,(cm−1) \Delta_0 , (\text{cm}^{-1})
A. [Cr(CN)6]3− [\text{Cr(CN)}_6]^{3-} IV. 26,600
B. [CrF6]3− [\text{CrF}_6]^{3-} I. 15,060
C. [Cr(H2O)6]3+ [\text{Cr(H}_2\text{O)}_6]^{3+} II. 17,400
D. [Cr(en)3]3+ [\text{Cr(en)}_3]^{3+} III. 22,300

FINAL ANSWER:

A-IV, B-I, C-II, D-III

Question 38

Given below are two statements :

Statement (I) : 1,2,3-Trihydroxypropane can be separated from water by simple distillation.

Statement (II) : An azotropic mixture cannot be separated by fractional distillation.

In the light of the above statements, choose the correct answer from the options given below :

  1. AOption (a)

    Both Statement I and Statement II are true

  2. BOption (b)

    Both Statement I and Statement II are false

  3. COption (c)

    Statement I is true but Statement II is false

  4. DOption (d)

    Statement I is false but Statement II is true

View answer & explanation

Correct answer

Answer: (d)D.

Statement I is false but Statement II is true

Why this answer is correct

CONCEPT:

Distillation and Separation of Mixtures

  • Distillation is a separation technique based on the difference in boiling points of substances.
  • Simple distillation is effective when the boiling points of the components differ significantly, while fractional distillation is used for closer boiling points.
  • An azeotropic mixture is a mixture of two or more liquids that boils at a constant temperature and retains its composition in the vapor phase, making it impossible to separate by conventional fractional distillation.

EXPLANATION:

  • Statement (I): 1,2,3-Trihydroxypropane (commonly known as glycerol) cannot be separated from water by simple distillation because glycerol has a very high boiling point (approximately 290°C) compared to water (100°C). Moreover, glycerol decomposes at high temperatures, so it is typically separated by distillation under reduced pressure to avoid decomposition.
  • Statement (II): An azeotropic mixture cannot be separated by fractional distillation because the composition of the liquid and vapor phases remains constant during boiling, preventing further separation. This statement is true.
  • Based on the above analysis:
  • Statement (I) is false because glycerol cannot be separated from water by simple distillation.
  • Statement (II) is true because azeotropic mixtures cannot be separated by fractional distillation.

So, Statement I is false but Statement II is true.

Question 39

Given below are two statements :

Statement (I) : Benzyl chloride reacts faster in SN1 \text{S}_{\text{N}}1  mechanism than ethyl chloride.

Statement (II) : Ethyl carbocation intermediate is less stabilized by hyperconjugation than benzyl carbocation by resonance.

In the light of the above statements, choose the correct answer from the options given below :

  1. AOption (a)

    Both Statement I and Statement II are true

  2. BOption (b)

    Both Statement I and Statement II are false

  3. COption (c)

    Statement I is true but Statement II is false

  4. DOption (d)

    Statement I is false but Statement II is true

View answer & explanation

Correct answer

Answer: (a)A.

Both Statement I and Statement II are true

Why this answer is correct

CONCEPT:

Rate of SN1 Reaction

  • The rate of an SN1 reaction is directly proportional to the stability of the intermediate carbocation.
  • Carbocation stability is influenced by factors like resonance, hyperconjugation, and inductive effects.
  • Order of carbocation stability:

Ph-+CH2 > CH3-+CH2

  • Resonance stabilization is more effective than hyperconjugation in stabilizing carbocations.

EXPLANATION:

  • Statement (I): Benzyl chloride reacts faster in an SN1 mechanism than ethyl chloride.
  • This is true because the benzyl carbocation (Ph-+CH2) formed during the reaction is stabilized by resonance with the aromatic ring.
  • In contrast, the ethyl carbocation (CH3-+CH2) is stabilized only by hyperconjugation, which is less effective compared to resonance.
  • Statement (II): Ethyl carbocation intermediate is less stabilized by hyperconjugation than benzyl carbocation by resonance.
  • This is also true because the benzyl carbocation has multiple resonance structures, allowing delocalization of the positive charge over the aromatic ring, which provides significant stabilization.
  • On the other hand, the ethyl carbocation relies only on hyperconjugation, which provides limited stabilization compared to resonance.
  • Since both statements are true and align with the principles of carbocation stability, the correct answer is that both Statement (I) and Statement (II) are true.

Therefore, the stability of the benzyl carbocation due to resonance explains the faster reaction rate of benzyl chloride in the SN1 mechanism compared to ethyl chloride.

Question 40

In IUPAC nomenclature, the correct order of decreasing priority of functional group is :

  1. AOption (a)

    −CONH2,>C=O,−CHO,−NH2,−C≡C− -\text{CONH}_2, >\text{C} = \text{O}, -\text{CHO}, -\text{NH}_2, -\text{C} \equiv \text{C} -

  2. BOption (b)

    −CONH2,−COOCH3,−CHO,−NH2,−OH -\text{CONH}_2, -\text{COOCH}_3, -\text{CHO}, -\text{NH}_2, -\text{OH}

  3. COption (c)

    −CONH2,−CHO,>C=O,−NH2,−C≡C− -\text{CONH}_2, -\text{CHO}, >\text{C} = \text{O}, -\text{NH}_2, -\text{C} \equiv \text{C} -

  4. DOption (d)

    −CONH2,−CHO,−CN,−NH2,−C≡C− -\text{CONH}_2, -\text{CHO}, -\text{CN}, -\text{NH}_2, -\text{C} \equiv \text{C} -

View answer & explanation

Correct answer

Answer: (c)C.

−CONH2,−CHO,>C=O,−NH2,−C≡C− -\text{CONH}_2, -\text{CHO}, >\text{C} = \text{O}, -\text{NH}_2, -\text{C} \equiv \text{C} -

Why this answer is correct

CONCEPT:

IUPAC Nomenclature Priority of Functional Groups

  • In IUPAC nomenclature, the priority of functional groups is based on the specific rules established by IUPAC. The priority order is used to determine the principal functional group, which dictates the suffix of the compound name.
  • The priority order is determined based on the oxidation state of the carbon atom to which the functional group is attached. Functional groups with higher oxidation states have higher priority.
  • In general, the priority order from highest to lowest is:
  • Carboxylic acids (-COOH)
  • Esters (-COOR)
  • Amides (-CONH2)
  • Aldehydes (-CHO)
  • Ketones (>C=O)
  • Nitriles (-CN)
  • Alcohols (-OH)
  • Amines (-NH2)
  • Alkenes (C=C)
  • Alkynes (C≡C)

EXPLANATION:

  • Memonics: "Crazy Elephants Always Ask Kind Neighbors About Amazing Airplanes Always."
  • Functional groups provided in the question:
  • -CONH2 (Amide)
  • -CHO (Aldehyde)
  • C=O (Ketone)

  • -NH2 (Amine)
  • -C≡C- (Alkyne)
  • Based on the priority order of functional groups:
  • Amides (-CONH2) have the highest priority among the groups provided.
  • Aldehydes (-CHO) have the next highest priority.
  • Ketones (>C=O) follow aldehydes in priority.
  • Amines (-NH2) come after ketones.
  • Alkynes (-C≡C-) have the lowest priority among the given groups.
  • Thus, the correct decreasing order of priority is:

-CONH2, -CHO, >C=O, -NH2, -C≡C-

Therefore, the correct answer is Option 3.

Question 41

For the given molecule, “x”, the preferred site for the attack of the electrophile is :

  1. AOption (a)

    Predominantly at “r”

  2. BOption (b)

    “r” and “u”

  3. COption (c)

    “p” and “s”

  4. DOption (d)

    Predominantly at “u”

View answer & explanation

Correct answer

Answer: (d)D.

Predominantly at “u”

Why this answer is correct

CONCEPT:

Electrophilic Attack on Aromatic Compounds

  • Electrophilic substitution reactions occur when an electrophile replaces a substituent (usually a hydrogen atom) in an aromatic ring.
  • The position at which the electrophile attacks depends on the electron density of the aromatic ring and the nature of the substituents already present.
  • Electron-donating groups (+M or +I effect) increase electron density at certain positions, making them more favorable for electrophilic attack.
  • Electron-withdrawing groups (-M or -I effect) decrease electron density at specific positions, making them less favorable for electrophilic attack.

EXPLANATION:

  • In the given molecule, the nitrogen atom is attached to the aromatic ring and exhibits a +M (resonance donating) effect.
  • The +M effect of nitrogen increases the electron density at the ortho and para positions of the aromatic ring.
  • Among the labeled positions ("r", "u", "p", and "s"), position "u" is predominantly favored for electrophilic attack because it is para to the nitrogen atom, and the +M effect enhances the electron density at this position.
  • Position "r" also experiences an increase in electron density due to the +M effect, but it is less favorable than "u" because steric hindrance near the nitrogen may play a minor role in reducing reactivity at the ortho position.

Therefore, the preferred site for the attack of the electrophile is predominantly at "u" because of the +M nature of nitrogen.

Question 42

Match List-I with List-II.

 

List-IList-II
Mixture of CompoundsReagent used to distinguish
A. Diethyl amine + Ethyl amineI. Bromine water
B. Acetaldehyde + AcetoneII. CHCl3+KOH,Δ CHCl_3 + KOH, \Delta
C. Ethanol + PhenolIII. Neutral FeCl3 FeCl_3
D. Benzoic acid + Cinnamic acidIV. Ammonical silver nitrate

Choose the correct answer from the options given below :

  1. AOption (a)

    a-IV, b-II, c-I, d-III

  2. BOption (b)

    a-IV, b-II, c-III, d-I

  3. COption (c)

    a-II, b-IV, c-I, d-III

  4. DOption (d)

    a-II, b-IV, c-III, d-I

View answer & explanation

Correct answer

Answer: (d)D.

a-II, b-IV, c-III, d-I

Why this answer is correct

CONCEPT:

The question involves distinguishing between different chemical compounds in mixtures using specific reagents. The concept relies on the unique chemical reactions of these compounds with the reagents provided.

  • Phenol vs Ethanol: Phenol reacts with neutral FeCl3 FeCl_3 to give a violet color, whereas ethanol does not react with neutral FeCl3 FeCl_3 .
  • Diethyl amine vs Ethyl amine: Ethyl amine (a primary amine) reacts with CHCl3/KOH CHCl_3/KOH to give a carbylamine (foul-smelling test), whereas diethyl amine (a secondary amine) does not give this test.
  • Acetaldehyde vs Acetone: Acetaldehyde (an aldehyde) gives a positive test with ammonical silver nitrate (Tollens' test), forming a silver mirror, whereas acetone (a ketone) does not.
  • Benzoic acid vs Cinnamic acid: Cinnamic acid reacts with bromine water due to the presence of a double bond in its structure, whereas benzoic acid does not react with bromine water.

EXPLANATION:

  1. A. Diethyl amine + Ethyl amine: Ethyl amine (primary amine) reacts with CHCl3/KOH CHCl_3/KOH , producing a foul smell (carbylamine test). Diethyl amine (secondary amine) does not react. Therefore, the reagent used is II. CHCl3+KOH,Δ CHCl_3 + KOH, \Delta .
  2. B. Acetaldehyde + Acetone: Acetaldehyde gives a positive test with ammonical silver nitrate (Tollens' test), forming a silver mirror, whereas acetone does not. Therefore, the reagent used is IV. Ammonical silver nitrate.
  3. C. Ethanol + Phenol: Phenol reacts with neutral FeCl3 FeCl_3 to produce a violet color, whereas ethanol does not. Therefore, the reagent used is III. Neutral FeCl3 FeCl_3 .
  4. D. Benzoic acid + Cinnamic acid: Cinnamic acid reacts with bromine water due to the presence of a double bond, whereas benzoic acid does not. Therefore, the reagent used is I. Bromine water.

So the correct matching is A-II, B-IV, C-III, D-I

Mixture of Compounds (List-I)Reagent used to distinguish (List-II)
A. Diethyl amine + Ethyl amineII. CHCl3+KOH,Δ CHCl_3 + KOH, \Delta
B. Acetaldehyde + AcetoneIV. Ammonical silver nitrate
C. Ethanol + PhenolIII. Neutral FeCl3 FeCl_3
D. Benzoic acid + Cinnamic acidI. Bromine water

Question 43

Consider the three aromatic molecules (P, Q and R) whose structures have been given below :

The correct order regarding the reactivity of these compounds with Ph−N≡N Cl(−) Ph-N \equiv N \ Cl^{(-)} under optimum but slightly acidic medium is :

  1. AOption (a)

    P > Q > R

  2. BOption (b)

    R > P > Q

  3. COption (c)

    R > Q > P

  4. DOption (d)

    P > R > Q

View answer & explanation

Correct answer

Answer: (a)A.

P > Q > R

Why this answer is correct

CONCEPT:

Electrophilic Substitution Reaction (ESR) Reactivity

  • The reactivity of an aromatic compound towards electrophilic substitution reactions (ESR) depends on the electron density of the benzene ring.
  • Electron-donating groups increase the nucleophilicity of the benzene ring, enhancing its reactivity with electrophiles.
  • Electron-withdrawing groups decrease the nucleophilicity of the benzene ring, reducing its reactivity with electrophiles.

EXPLANATION:

  • Rate of ESR ∝ \propto  nucleophilicity of benzene ring.
  • The nucleophilicity of the benzene rings follows the order is P > R > Q
  • Thus, the reactivity of these compounds towards the diazonium salt in a slightly acidic medium is P > R > Q

Therefore, the correct order regarding the reactivity of these compounds with Ph−N≡N Cl(−) Ph-N \equiv N \ Cl^{(-)} is P > R > Q.

Question 44

Match List-I with List-II.

 

List-IList-II
VitaminName
A. Vitamin B1 B_1 I. Pyridoxine
B. Vitamin B2 B_2 II. Ascorbic acid
C. Vitamin B6 B_6 III. Thiamine
D. Vitamin CIV. Riboflavin

Choose the correct answer from the options given below :

  1. AOption (a)

    a-II, b-I, c-III, d-IV

  2. BOption (b)

    a-IV, b-III, c-II, d-I

  3. COption (c)

    a-III, b-IV, c-I, d-II

  4. DOption (d)

    a-I, b-III, c-II, d-IV

View answer & explanation

Correct answer

Answer: (c)C.

a-III, b-IV, c-I, d-II

Why this answer is correct

CONCEPT:

Vitamins and Their Chemical Names

  • Vitamins are organic compounds essential for various metabolic processes in the human body.
  • Each vitamin has a specific chemical name that represents its structure and function.
  • Matching vitamins with their chemical names helps in understanding their roles in human nutrition.

EXPLANATION:

  • The matching of vitamins with their chemical names is as follows:
  • Vitamin B1 (A): Its chemical name is Thiamine. Thiamine plays a crucial role in energy metabolism and nerve function.
  • Vitamin B2 (B): Its chemical name is Riboflavin. Riboflavin is involved in energy production and cellular function.
  • Vitamin B6 (C): Its chemical name is Pyridoxine. Pyridoxine is important for amino acid metabolism and neurotransmitter synthesis.
  • Vitamin C (D): Its chemical name is Ascorbic acid. Ascorbic acid is an antioxidant and is essential for collagen synthesis and immune function.

Therefore, the correct matching is: A - III, B - IV, C - I, D - II.

Question 45

A salt with few drops of conc. HCl gives apple green colour in flame test. The group precipitate of the salt is dissolved in acetic acid and treated with K2CrO4 K_2CrO_4 to give yellow precipitate. When the sodium carbonate extract of the salt solution is heated with conc. HNO3 HNO_3 and ammonium molybdate, it resulted a canary yellow precipitate. The cation and anion present in the salt are respectively.

  1. AOption (a)

    Ca2+ Ca^{2+} and SO42− SO_4^{2-}

  2. BOption (b)

    Ba2+ Ba^{2+} and PO43− PO_4^{3-}

  3. COption (c)

    Mn2+ Mn^{2+} and PO43− PO_4^{3-}

  4. DOption (d)

    Ba2+ Ba^{2+} and SO42− SO_4^{2-}

View answer & explanation

Correct answer

Answer: (b)B.

Ba2+ Ba^{2+} and PO43− PO_4^{3-}

Why this answer is correct

CONCEPT:

Flame Test and Identification of Ions

  • The flame test is used to identify certain metal ions based on the characteristic color they produce when heated in a flame.

  • Flame Colors:

  • Ba+2Ba+2

    produces an apple green color.

  • Ca+2Ca+2

    produces a brick red color.

  • Sr+2Sr+2

    produces a crimson red color.

  • Reactions for Identification:

  • Ba+2+CrO2−4→BaCrO4Ba+2+CrO42−→BaCrO4

: Yellow precipitate indicates the presence of Ba+2Ba+2

.

  • The sodium carbonate extract test with ammonium molybdate and concentrated nitric acid produces a canary yellow precipitate if PO3−4PO43−

    is present.

EXPLANATION:

  • From the flame test:
  • The apple green color in the flame test confirms the presence of Ba+2Ba+2

.

  • From the reaction with K2CrO4K2CrO4

:

  • The formation of a yellow precipitate confirms the presence of Ba+2Ba+2

    as BaCrO4BaCrO4

.

  • From the sodium carbonate extract test:

  • Heating the sodium carbonate extract with concentrated HNO3HNO3

    and ammonium molybdate produces a canary yellow precipitate, confirming the presence of PO3−4PO43−

.

  • Based on the observations:
  • The cation present in the salt is Ba+2Ba+2

.

  • The anion present in the salt is PO3−4PO43−

.

Therefore, the cation and anion present in the salt are Ba2+Ba2+

and PO3−4PO43−

respectively.

Chemistry Section B (5 questions)

Question 46

5.33 g of CrCl3⋅6H2O CrCl_3 \cdot 6H_2O , which is a 1 : 3 electrolyte, is dissolved in water and is passed through a cation exchanger. The chloride ions in the eluted solution, on treatment with AgNO3 AgNO_3 results in 8.61 g of AgCl. The ratio of moles of complex reacted and moles of AgCl formed is ________ ×10−2 \times 10^{-2} . (Nearest integer)

[Molar mass in g mol−1 mol^{-1} Cr : 52, Ag : 108, Cl : 35.5, H : 1, O : 16]

  1. AOption (a)
  2. BOption (b)
  3. COption (c)
  4. DOption (d)
View answer & explanation

Correct answer

Answer: (a)A.

Why this answer is correct

CONCEPT:

Coordination Chemistry and Precipitation Reaction

  • The given reaction involves a coordination complex [Cr(H2O)6]Cl3 [Cr(H_2O)_6]Cl_3 , which is a hexaaquachromium(III) chloride complex.
  • When this complex reacts with an excess of AgNO3 (silver nitrate), the chloride ions present outside the coordination sphere precipitate as AgCl (silver chloride).
  • The number of moles of AgCl precipitated depends on the number of chloride ions outside the coordination sphere of the complex.

EXPLANATION:

  • The reaction can be written as:

\( [Cr(H_2O)_6]Cl_3 + 3AgNO_3 \xrightarrow{excess} 3AgCl(s) + Cr(H_2O)_6_3 \)

  • In the given coordination complex [Cr(H2O)6]Cl3 [Cr(H_2O)_6]Cl_3 , all six water molecules are within the coordination sphere of the chromium ion, while the three chloride ions are outside the coordination sphere.
  • When reacted with excess AgNO3, each chloride ion forms a precipitate of AgCl:

Cl−+Ag+→AgCl(s) Cl^- + Ag^+ \rightarrow AgCl(s)

  • Thus, one mole of [Cr(H2O)6]Cl3 [Cr(H_2O)_6]Cl_3 reacts to produce 3 moles of AgCl precipitate.
  • The ratio of the moles of the complex reacted to the moles of AgCl precipitated is given as:

no. of moles of complex reactedno. of moles of AgCl precipitated×100 \frac{\text{no. of moles of complex reacted}}{\text{no. of moles of AgCl precipitated}} \times 100

= 13×100 \frac{1}{3} \times 100

= 33.3%

Therefore, the percentage of the moles of the complex reacted with respect to the moles of AgCl precipitated is 33.3%.

Question 47

Consider the isomers of hydrocarbon with molecular formula C5H10 C_5H_{10} . These isomers do not decolourise KMnO4 KMnO_4 solution. These isomers are subjected to chlorination with chlorine in presence of light to give monochloro compounds. The total number of monochloro compounds (structural isomers only) formed is ________.

  1. AOption (a)
  2. BOption (b)
  3. COption (c)
  4. DOption (d)
View answer & explanation

Correct answer

Answer: (a)A.

Why this answer is correct

CONCEPT:

Mathematical Addition

  • The addition of numbers is a fundamental arithmetic operation.
  • It involves combining two or more numbers to find their total.
  • The general form for addition is:

a + b = c, where c is the sum of a and b.

EXPLANATION:

Therefore, the sum of 1 + 4 + 4 + 2 + 3 is 14.

Question 48

One mole of an alkane (x) requires 8 mole oxygen for complete combustion. Sum of number of carbon and hydrogen atoms in the alkane (x) is ________.

  1. AOption (a)
  2. BOption (b)
  3. COption (c)
  4. DOption (d)
View answer & explanation

Correct answer

Answer: (a)A.

Why this answer is correct

CONCEPT:

Combustion of Alkanes

  • Alkanes are hydrocarbons with the general formula CnH2n+2 C_nH_{2n+2} .
  • When alkanes undergo combustion in the presence of oxygen (O2 O_2 ), they produce carbon dioxide (CO2 CO_2 ) and water (H2O H_2O ) as products.
  • The balanced chemical equation for the combustion of an alkane is:

CnH2n+2+(3n+12)O2→nCO2+(n+1)H2O C_nH_{2n+2} + \left( \frac{3n+1}{2} \right) O_2 \rightarrow nCO_2 + (n+1) H_2O

EXPLANATION:

  • In the given question, we are tasked with identifying the alkane based on the combustion equation.
  • The given combustion equation includes the term (3n+12) \left( \frac{3n+1}{2} \right) for the oxygen (O2 O_2 ) coefficient.
  • We are also provided with the condition 3n+12=8 \frac{3n+1}{2} = 8 .
  • Solving this equation:
  • 3n+12=8 \frac{3n+1}{2} = 8
  • 3n+1=16 3n+1 = 16 (multiplying both sides by 2)
  • 3n=15 3n = 15 (subtracting 1 from both sides)
  • n=5 n = 5 (dividing both sides by 3)
  • Since n=5 n = 5 , the alkane is C5H12 C_5H_{12} (pentane).
  • Substituting n=5 n = 5 into the combustion equation:

C5H12+8O2→5CO2+6H2O C_5H_{12} + 8O_2 \rightarrow 5CO_2 + 6H_2O

Therefore, the alkane is pentane (C5H12 C_5H_{12} ), and the number of oxygen molecules required for complete combustion is 8.

Question 49

For reaction A → \rightarrow P, rate constant k = 1.5 ×103 s−1 \times 10^3 \ s^{-1} at 27°C. If activation energy for the above reaction is 60 kJ mol−1 mol^{-1} , then the temperature (in °C) at which rate constant, k = 4.5 ×103 s−1 \times 10^3 \ s^{-1} is ________. (Nearest integer)

Given : log 2 = 0.30, log 3 = 0.48, R = 8.3 J K−1 mol−1 K^{-1} \ mol^{-1} , ln 10 = 2.3

  1. AOption (a)
  2. BOption (b)
  3. COption (c)
  4. DOption (d)
View answer & explanation

Correct answer

Answer: (a)A.

Why this answer is correct

CONCEPT:

Arrhenius Equation and Activation Energy

  • The Arrhenius equation relates the rate constants of a reaction at two different temperatures with the activation energy of the reaction.
  • The equation is given as:

ℓn(K2K1)=EaR[T2−T1T1T2]ℓn(K2K1)=EaR[T2−T1T1T2]

  • Here:
  • K1K1

and K2

are the rate constants at temperatures T1

and T2

respectively.

  • Ea

is the activation energy of the reaction.

  • R

is the universal gas constant (8.3 J mol−1 K−1

).

  • T1

and T2

are the absolute temperatures in Kelvin.

EXPLANATION:

  • In the given question:
  • K1=1.5×103

, K2=4.5×103

  • Ea=60×103 J mol−1

, T1=300 K

  • Substitute these values into the Arrhenius equation:

ℓn(4.5×1031.5×103)=60×1038.3[T2−300300.T2]

  • Simplify the natural logarithm:
  • ℓn(4.5×1031.5×103)=ℓn 3
  • ℓn 3=1.0986
  • Rearrange the equation:

1.0986=60×1038.3[T2−300300.T2]

  • Calculate:
  • 60×1038.3=7228.92
  • 1.0986=7228.92[T2−300300.T2]
  • T2−300300.T2=1.09867228.92
  • T2−300300.T2=0.000152
  • T2−300=0.000152⋅300.T2
  • T2−300=0.0456⋅T2
  • T2−0.0456⋅T2=300
  • 0.9544⋅T2=300
  • T2=3000.9544
  • T2=314.4 K
  • Convert T2

to Celsius:

  • t=T2−273
  • t=314.4−273
  • t=41.4∘C

Therefore, the temperature T2

is 314.4 K, which corresponds to 41.4∘C

.

Question 50

At the transition temperature T, A ⇌ \rightleftharpoons B and ΔG∘=105−35 log T \Delta G^\circ = 105 - 35 \ log \ T where A and B are two states of substance X. The transition temperature in °C when pressure is 1 atm is ________. (Nearest integer)

  1. AOption (a)
  2. BOption (b)
  3. COption (c)
  4. DOption (d)
View answer & explanation

Correct answer

Answer: (a)A.

Why this answer is correct

CONCEPT:

Equilibrium and Gibbs Free Energy

  • At equilibrium under standard pressure conditions, the Gibbs free energy change (ΔG∘ \Delta G^\circ ) is zero.
  • The relationship between Gibbs free energy and equilibrium temperature can be expressed using thermodynamic principles.

EXPLANATION:

  • The given equation is:

105 – 35 log T = 0

  • We solve this equation to find the value of temperature (T T ):
  • Rearranging the equation:

35 log T = 105

  • Dividing both sides by 35:

log T = 105 / 35

log T = 3

  • Converting from logarithmic to exponential form:

T=103 T = 10^{3}

T=1000,K T = 1000 , \text{K}

  • Converting temperature from Kelvin to Celsius:

T(in ∘C)=T(in K)−273 T (\text{in } ^\circ \text{C}) = T (\text{in K}) - 273

T(in ∘C)=1000−273 T (\text{in } ^\circ \text{C}) = 1000 - 273

T(in ∘C)=727∘C T (\text{in } ^\circ \text{C}) = 727^\circ \text{C}

Therefore, the temperature at equilibrium is T=1000,K T = 1000 , \text{K} or T=727∘C T = 727^\circ \text{C} .

Physics Section A (20 questions)

Question 51

A particle is rotating in a circular path and at any instant its motion can be described as θ=5t440−t33 \theta = \frac{5t^4}{40} - \frac{t^3}{3} .

The angular acceleration of the particle after 10 seconds is ________ rad/s2 rad/s^2 .

  1. AOption (a)

    150

  2. BOption (b)

    120

  3. COption (c)

    130

  4. DOption (d)

    170

View answer & explanation

Correct answer

Answer: (c)C.

130

Why this answer is correct

θ=5t440−t33 \theta = \frac{5t^4}{40} - \frac{t^3}{3}

dθdt=540(4t3)−3t23=t32−t2 \frac{d\theta}{dt} = \frac{5}{40}(4t^3) - \frac{3t^2}{3} = \frac{t^3}{2} - t^2

α=d2θdt2=3t22−2t \alpha = \frac{d^2\theta}{dt^2} = \frac{3t^2}{2} - 2t

at t = 10

α=32(10)2−2×10=130rad/sec2 \alpha = \frac{3}{2}(10)^2 - 2 \times 10 = 130 rad/sec^2

Question 52

A parallel plate air capacitor has a capacitance C. When it is half filled as show in figure with a dielectric constant K = 5, the percentage increase in the capacitance is ________.

  1. AOption (a)

    33.34

  2. BOption (b)

    66.67

  3. COption (c)

    200

  4. DOption (d)

    400

View answer & explanation

Correct answer

Answer: (b)B.

66.67

Why this answer is correct

Initial capacitance

Ci=Aϵ0d=C C_i = \frac{A \epsilon_0}{d} = C

Final capacitance

C1=Aϵ0×5d2=10C C_1 = \frac{A \epsilon_0 \times 5}{\frac{d}{2}} = 10C

C2=Aϵ0d2=2C C_2 = \frac{A \epsilon_0}{\frac{d}{2}} = 2C

Cf=C1C2C1+C2=10×210+2C=53C C_f = \frac{C_1 C_2}{C_1 + C_2} = \frac{10 \times 2}{10 + 2} C = \frac{5}{3} C

% increase = 53C−CC×100=66.67 \frac{\frac{5}{3} C - C}{C} \times 100 = 66.67

Question 53

Heat is supplied to a diatomic gas at constant pressure. Then the ratio of ΔQ:ΔU:ΔW \Delta Q : \Delta U : \Delta W is______.

  1. AOption (a)

    2 : 3 : 5

  2. BOption (b)

    5 : 3 : 2

  3. COption (c)

    2 : 5 : 7

  4. DOption (d)

    7 : 5 : 2

View answer & explanation

Correct answer

Answer: (d)D.

7 : 5 : 2

Why this answer is correct

ΔQp=nCpΔT=72nRΔT \Delta Q_p = nC_p \Delta T = \frac{7}{2} nR \Delta T

ΔU=nCvΔT=52nRΔT \Delta U = nC_v \Delta T = \frac{5}{2} nR \Delta T

W = nRΔT nR \Delta T

ΔQ:ΔU:W::7:5:2 \Delta Q : \Delta U : W :: 7 : 5 : 2

Question 54

Two charged conducting spheres S1 and S2 of radii 8 cm and 18 cm are connected to each other by a wire. After equilibrium is established, the ratio of

electric fields on S1 and S2 spheres are ES1 and ES2 respectively. The value of ES1ES2 \frac{E_{S1}}{E_{S2}} is ________.

  1. AOption (a)

    32 \frac{3}{2}

  2. BOption (b)

    23 \frac{2}{3}

  3. COption (c)

    49 \frac{4}{9}

  4. DOption (d)

    94 \frac{9}{4}

View answer & explanation

Correct answer

Answer: (d)D.

94 \frac{9}{4}

Why this answer is correct

V1=V2 V_1 = V_2

\frac{kQ_1}{8} = \frac{kQ_2}{18} \quad \left{ V_{\text{surface}} = \frac{kQ}{R} \right}

Q1Q2=49 \frac{Q_1}{Q_2} = \frac{4}{9}

\frac{E_{S_1}}{E_{S_2}} = \frac{kQ_1}{r_1^2} \frac{r_2^2}{kQ_2} \quad \left{ E_{\text{surface}} = \frac{kQ}{R^2} \right}

=Q1Q2(r2r1)2=49(94)2=94 = \frac{Q_1}{Q_2} \left( \frac{r_2}{r_1} \right)^2 = \frac{4}{9} \left( \frac{9}{4} \right)^2 = \frac{9}{4}

Question 55

The equation of a plane progressive wave is given by

y=5cos⁡π(200t−x150) y = 5 \cos \pi \left( 200t - \frac{x}{150} \right) where x and y are in cm and

t is in second. The velocity of the wave is ________ m/s

  1. AOption (a)

    120

  2. BOption (b)

    150

  3. COption (c)

    200

  4. DOption (d)

    300

View answer & explanation

Correct answer

Answer: (d)D.

300

Why this answer is correct

v=coeff of tcoeff of x=2001150×100=300m/s v = \frac{\text{coeff of t}}{\text{coeff of x}} = \frac{200}{\frac{1}{150} \times 100} = 300\text{m/s}

Question 56

Two short electric dipoles A and B having dipole moment p1 and p2 respectively are placed with their axis mutually perpendicular as shown in the figure. The resultant electric field at a point x is making an angle of 60° with the line joining points O and x. The ratio of the dipole moments p2 / p1 is ________.

  1. AOption (a)

    32 \frac{\sqrt{3}}{2}

  2. BOption (b)

    23 2\sqrt{3}

  3. COption (c)

    13 \frac{1}{\sqrt{3}}

  4. DOption (d)

    3 \sqrt{3}

View answer & explanation

Correct answer

Answer: (b)B.

23 2\sqrt{3}

Why this answer is correct

E⃗A=2kp1x3(−i^) \vec{E}_A = \frac{2kp_1}{x^3} (-\hat{i}) {Axial point}

E⃗B=kp2x3(−j^) \vec{E}_B = \frac{kp_2}{x^3} (-\hat{j}) {Equatorial point}

Now : tan⁡θ=∣E⃗BE⃗A∣ \tan \theta = \left| \frac{\vec{E}_B}{\vec{E}_A} \right|

⇒tan⁡60∘=p22p1 \Rightarrow \tan 60^\circ = \frac{p_2}{2p_1}

⇒p2p1=23 \Rightarrow \frac{p_2}{p_1} = 2\sqrt{3}

Question 57

For the given circuit (shown in part (A)) the time dependent input voltage vin(t) and corresponding output vo(t) are shown in part (B) and part (C), respectively. Identify the components that are used in the circuit between points X and Y.

(A) Circuit used

Part(B) : Input voltage

Part(C) : Output voltage

  1. AOption (a)

  2. BOption (b)

  3. COption (c)

  4. DOption (d)

View answer & explanation

Correct answer

Answer: (b)B.

Why this answer is correct

will be updated soon.

Question 58

When a coil is placed in a time dependent magnetic field the power dissipated in it is P. The number of turns, area of the coil and radius of the coil wire are N, A and r respectively. For a second coils number of turns, area of the coil and radius of the coil wire are 2N, 2A and 3r respectively. When the first coil is

replaced with second coil the power dissipated in it is

2αP \sqrt{2} \alpha P . The value of α \alpha is ________.

  1. AOption (a)

    36

  2. BOption (b)

    1282 128\sqrt{2}

  3. COption (c)

    16

  4. DOption (d)

    64

View answer & explanation

Correct answer

Answer: (a)A.

36

Why this answer is correct

Sol. Power dissipated : P=ε2R P = \frac{\varepsilon^2}{R}

Induced emf ε=−NAdBdt \varepsilon = -NA \frac{dB}{dt}

Resistance of coil : R=ρℓπr2 R = \rho \frac{\ell}{\pi r^2}

Now : ℓ=N(2πRcoil) \ell = N(2\pi R_{coil})

Also : A=πRcoil2⇒Rcoil=Aπ A = \pi R_{coil}^2 \Rightarrow R_{coil} = \sqrt{\frac{A}{\pi}}

Thus ; R=ρN(2π)Aππr2 R = \frac{\rho N(2\pi) \sqrt{\frac{A}{\pi}}}{\pi r^2}

P=N2A2(dBdt)22ρNr2Aπ⇒P∝NA3/2r2......(1) P = \frac{N^2 A^2 \left( \frac{dB}{dt} \right)^2}{\frac{2\rho N}{r^2} \sqrt{\frac{A}{\pi}}} \Rightarrow P \propto NA^{3/2}r^2 ......(1)

P′∝(2N)(2A)3/2(3r)2......(2) P' \propto (2N)(2A)^{3/2}(3r)^2 ......(2)

(2)(1):P′P=362⇒P′=(2)(36)P \frac{(2)}{(1)} : \frac{P'}{P} = 36\sqrt{2} \Rightarrow P' = (\sqrt{2})(36)P

Thus : α=36 \alpha = 36

Question 59

Two identical long current carrying wires are bent into the shapes shown in the following figures. If the magnitude of magnetic fields at the centres P and Q of a semicircular arc are B1 B_1 and B2 B_2  respectively, then the ratio B1B2 \frac{B_1}{B_2} is ________.

  1. AOption (a)

    2+π1+π \frac{2 + \pi}{1 + \pi}

  2. BOption (b)

    1+π1−π \frac{1 + \pi}{1 - \pi}

  3. COption (c)

    2+π1−π \frac{2 + \pi}{1 - \pi}

  4. DOption (d)

    1+π2−π \frac{1 + \pi}{2 - \pi}

View answer & explanation

Correct answer

Answer: (a)A.

2+π1+π \frac{2 + \pi}{1 + \pi}

Why this answer is correct

Sol. B1=μ0I4πr×2+μ0I4r=μ0I4r(2π+1) B_1 = \frac{\mu_0 I}{4\pi r} \times 2 + \frac{\mu_0 I}{4r} = \frac{\mu_0 I}{4r} \left( \frac{2}{\pi} + 1 \right)

B2=μ0I4πr+μ0I4r=μ0I4r(1π+1) B_2 = \frac{\mu_0 I}{4\pi r} + \frac{\mu_0 I}{4r} = \frac{\mu_0 I}{4r} \left( \frac{1}{\pi} + 1 \right)

B1B2=2+π1+π \frac{B_1}{B_2} = \frac{2 + \pi}{1 + \pi}

Question 60

For a thin symmetric prism made of glass (refractive index 1.5), the ratio of incident angle and minimum deviation will be ________.

  1. AOption (a)

    3 : 4

  2. BOption (b)

    3 : 2

  3. COption (c)

    2 : 1

  4. DOption (d)

    1 : 2

View answer & explanation

Correct answer

Answer: (b)B.

3 : 2

Why this answer is correct

Sol. We have for thin prism minimum deviation :

δm=(μ−1)A \delta_m = (\mu - 1)A

⇒δm=(1.5−1)A⇒δm=A2 \Rightarrow \delta_m = (1.5 - 1)A \Rightarrow \delta_m = \frac{A}{2}

Also, i=A+δm2⇒i=A+A22⇒i=3A4 i = \frac{A + \delta_m}{2} \Rightarrow i = \frac{A + \frac{A}{2}}{2} \Rightarrow i = \frac{3A}{4}

Thus iδm=32 \frac{i}{\delta_m} = \frac{3}{2}

Question 61

Refer the figure given below. μ1 \mu_1 and μ2 \mu_2 are refractive indices of air and lens material. The height of image will be ________ cm.

  1. AOption (a)

    1

  2. BOption (b)

    0.5

  3. COption (c)

    1.2

  4. DOption (d)

    0.25

View answer & explanation

Correct answer

Answer: (a)A.

1

Why this answer is correct

Sol. μ2v−μ1u=μ2−μ1R \frac{\mu_2}{v} - \frac{\mu_1}{u} = \frac{\mu_2 - \mu_1}{R}

1.54v−1(−40)=1.54−1−20 \frac{1.54}{v} - \frac{1}{(-40)} = \frac{1.54 - 1}{-20}

1.54v=−140−0.5420 \frac{1.54}{v} = -\frac{1}{40} - \frac{0.54}{20}

1.54v=−2.0840 \frac{1.54}{v} = \frac{-2.08}{40}

v=−29.61 cm v = -29.61 \text{ cm}

hiho=μ1vμ2u=1(−29.61)1.54(−40)=0.48 \frac{h_i}{h_o} = \frac{\mu_1 v}{\mu_2 u} = \frac{1(-29.61)}{1.54(-40)} = 0.48

hi=0.48×2=0.96≈1cm h_i = 0.48 \times 2 = 0.96 \approx 1 \text{cm}

Question 62

For a certain metal, when monochromatic light of wavelength λ \lambda is incident, the stopping potential for photoelectrons is 3V0 3V_0 . When the same metal is illuminated by light of wavelength 2λ 2\lambda , then the stopping potential becomes V0 V_0 . The threshold wavelength for photoelectric emission for the given metal is αλ \alpha\lambda . The value of α \alpha is ________.

  1. AOption (a)

    1

  2. BOption (b)

    4

  3. COption (c)

    2

  4. DOption (d)

    3

View answer & explanation

Correct answer

Answer: (b)B.

4

Why this answer is correct

Sol. hcλ−ϕ=3eV0…(i) \frac{hc}{\lambda} - \phi = 3eV_0 \dots (i)

hc2λ−ϕ=eV0…(ii) \frac{hc}{2\lambda} - \phi = eV_0 \dots (ii)

hcλ−ϕ=3[hc2λ−ϕ] \frac{hc}{\lambda} - \phi = 3 \left[ \frac{hc}{2\lambda} - \phi \right]

ϕ=hc4λ \phi = \frac{hc}{4\lambda}

hcλ0=hc4λ \frac{hc}{\lambda_0} = \frac{hc}{4\lambda}

λ0=4λ \lambda_0 = 4\lambda

α=4 \alpha = 4

Question 63

An electromagnetic wave travelling in x-direction is described by field equation Ey=300sin⁡ω(t−xc) E_y = 300 \sin \omega \left( t - \frac{x}{c} \right) . If the electron is restricted to move in y-direction only with speed of 1.5×106 m/s 1.5 \times 10^6 \text{ m/s} then ratio of maximum electric and magnetic forces acting on the electron is ________.

  1. AOption (a)

    200

  2. BOption (b)

    150

  3. COption (c)

    400

  4. DOption (d)

    300

View answer & explanation

Correct answer

Answer: (a)A.

200

Why this answer is correct

Sol. Ey=300sin⁡ω(t−xv) E_y = 300 \sin \omega \left( t - \frac{x}{v} \right)

FM=qvB…(i) F_M = qvB \dots (i)

Fe=qE…(ii) F_e = qE \dots (ii)

FeFm=qEqvB=EvB=cv=3×1081.5×106=200 \frac{F_e}{F_m} = \frac{qE}{qvB} = \frac{E}{vB} = \frac{c}{v} = \frac{3 \times 10^8}{1.5 \times 10^6} = 200

Question 64

Angular momentum of an electron in a hydrogen atom is 3hπ \frac{3h}{\pi} , then the energy of the electron is ____ eV.

  1. AOption (a)
    • 1.51
  2. BOption (b)
    • 0.85
  3. COption (c)
    • 0.38
  4. DOption (d)
    • 0.28
View answer & explanation

Correct answer

Answer: (c)C.
  • 0.38

Why this answer is correct

Sol.  L = nh2π \frac{nh}{2\pi}

3hπ=nh2π \frac{3h}{\pi} = \frac{nh}{2\pi}

n = 6

E = −13.6n2 \frac{-13.6}{n^2} eV

= −13.662≈−0.38 \frac{-13.6}{6^2} \approx -0.38 eV

Question 65

A liquid drop of diameter 2 mm breaks into 512 droplets. The change in surface energy is α×10−6 \alpha \times 10^{-6} J. The value of α \alpha is ______. (Take surface tension of liquid = 0.08 N/m)

  1. AOption (a)

    10

  2. BOption (b)

    7

  3. COption (c)

    8

  4. DOption (d)

    11

View answer & explanation

Correct answer

Answer: (b)B.

7

Why this answer is correct

Sol.  V1=V2 V_1 = V_2

43πR3=512(43πr3) \frac{4}{3} \pi R^3 = 512 \left( \frac{4}{3} \pi r^3 \right)

R=(512)1/3r R = (512)^{1/3} r

1 = 8r

r = 18 \frac{1}{8} mm

ΔSE=SE2−SE1 \Delta SE = SE_2 - SE_1

= 512[T×4πr2]−[T×4πR2] 512 \left[ T \times 4\pi r^2 \right] - \left[ T \times 4\pi R^2 \right]

= 4πT[512r2−R2] 4\pi T [512r^2 - R^2]

= 4π(0.08)[512(18)2−12]×10−6≈7×10−6 4\pi (0.08) \left[ 512 \left( \frac{1}{8} \right)^2 - 1^2 \right] \times 10^{-6} \approx 7 \times 10^{-6}

α=7 \alpha = 7

Question 66

The dimensional formula of 12ϵ0E2 \frac{1}{2} \epsilon_0 E^2 (ϵ0 \epsilon_0 = permittivity of vacuum and E = electric field) is MaLbTc M^a L^b T^c . The value of 2a - b + c = ________.

  1. AOption (a)

    0

  2. BOption (b)

    1

  3. COption (c)

    -1

  4. DOption (d)

    2

View answer & explanation

Correct answer

Answer: (b)B.

1

Why this answer is correct

12ϵ0E2 \frac{1}{2} \epsilon_0 E^2 = Energy density

∴[12ϵ0E2]=ML2T−2L3=ML−1T−2 \therefore \left[ \frac{1}{2} \epsilon_0 E^2 \right] = \frac{ML^2T^{-2}}{L^3} = ML^{-1}T^{-2}

∴ \therefore a = 1, b = -1, c = -2

∴ \therefore 2a - b + c = 2 + 1 - 2 = 1

Question 67

The diameter of a wire measured by a screw gauge of least count 0.001 cm is 0.08 cm. The length measured by a scale of least count 0.1 cm is 150 cm. When a weight of 100 N is applied to the wire, the extension in length is 0.5 cm, measured by a micrometer of least count 0.001 cm. The error in the measured Young's modulus is α×109N/m2 \alpha \times 10^9 N/m^2 . The value of α \alpha is ________.

(Ignore the contribution of the load to Young's modulus error calculation)

  1. AOption (a)

    1.3

  2. BOption (b)

    1.65

  3. COption (c)

    0.13

  4. DOption (d)

    0.25

View answer & explanation

Correct answer

Answer: (b)B.

1.65

Why this answer is correct

Y = FℓAΔℓ \frac{F\ell}{A\Delta\ell}

∴ΔYY=ΔFF+Δℓℓ+2Δdd+Δ(Δℓ)Δℓ \therefore \frac{\Delta Y}{Y} = \frac{\Delta F}{F} + \frac{\Delta \ell}{\ell} + 2\frac{\Delta d}{d} + \frac{\Delta(\Delta\ell)}{\Delta\ell}

[A=πd24⇒ΔAA=2Δdd] \left[ A = \pi \frac{d^2}{4} \Rightarrow \frac{\Delta A}{A} = \frac{2\Delta d}{d} \right]

Since F is known exactly ⇒ΔF=0 \Rightarrow \Delta F = 0

ΔYY=0.1150+2×0.0010.08+0.0010.5=0.0277 \frac{\Delta Y}{Y} = \frac{0.1}{150} + \frac{2 \times 0.001}{0.08} + \frac{0.001}{0.5} = 0.0277

∴ΔY=0.0277Y \therefore \Delta Y = 0.0277 Y

Y = 100×1.5π4(0.08100)2×0.5×10−2=5.97×1010N/m2 \frac{100 \times 1.5}{\frac{\pi}{4} \left( \frac{0.08}{100} \right)^2 \times 0.5 \times 10^{-2}} = 5.97 \times 10^{10} N/m^2

∴ΔY=0.0277×5.97×1010N/m2=1.65×109N/m2 \therefore \Delta Y = 0.0277 \times 5.97 \times 10^{10} N/m^2 = 1.65 \times 10^9 N/m^2

Question 68

The velocity of a particle is given as

v⃗=−xi^+2yj^−zk^m/s \vec{v} = -x\hat{i} + 2y\hat{j} - z\hat{k} m/s . The magnitude of acceleration at point (1, 2, 4) is ________ m/s2 m/s^2 .

  1. AOption (a)

    6 \sqrt{6}

  2. BOption (b)

    9

  3. COption (c)

    33 \sqrt{33}

  4. DOption (d)

    0

View answer & explanation

Correct answer

Answer: (b)B.

9

Why this answer is correct

v⃗=−xi^+2yj^−zk^ \vec{v} = -x\hat{i} + 2y\hat{j} - z\hat{k}

a⃗=dv⃗dt=−dxdti^+2dydtj^−dzdtk^ \vec{a} = \frac{d\vec{v}}{dt} = -\frac{dx}{dt}\hat{i} + 2\frac{dy}{dt}\hat{j} - \frac{dz}{dt}\hat{k}

= −(−x)i^+2(2y)j^−(−z)k^=xi^+4yj^+zk^ -(-x)\hat{i} + 2(2y)\hat{j} - (-z)\hat{k} = x\hat{i} + 4y\hat{j} + z\hat{k}

∴a⃗ \therefore \vec{a} at (1,2,4) = i^+8j^+4k^ \hat{i} + 8\hat{j} + 4\hat{k}

∴∣a⃗∣=9m/s2 \therefore |\vec{a}| = 9 m/s^2

Question 69

The position of an object having mass 0.1 kg as a

function of time t is given as r⃗=(10t2i^+5t3j^)m \vec{r} = (10t^2\hat{i} + 5t^3\hat{j}) m .

At t = 1 s, which of the following statements are

correct?

A. The linear momentum p⃗=(2i^+1.5j^)kg.m/s \vec{p} = (2\hat{i} + 1.5\hat{j}) kg.m/s .

B. The force acting on the object F⃗=(2i^+3j^)N \vec{F} = (2\hat{i} + 3\hat{j}) N .

C. The angular momentum of the object about its

origin L⃗=15k^Js \vec{L} = 15\hat{k} Js .

D. The torque acting on the object about its origin

τ⃗=20k^Nm \vec{\tau} = 20\hat{k} Nm .

Choose the correct answer from the option given

below.

  1. AOption (a)

    A, B and C only

  2. BOption (b)

    B, C and D only

  3. COption (c)

    A, C and D only

  4. DOption (d)

    A, B and D only

View answer & explanation

Correct answer

Answer: (d)D.

A, B and D only

Why this answer is correct

Given r⃗=10t2i^+5t3j^⇒r⃗t=1=10i^+5j^ \vec{r} = 10t^2\hat{i} + 5t^3\hat{j} \Rightarrow \vec{r}_{t=1} = 10\hat{i} + 5\hat{j}

v⃗=dr⃗dt=20ti^+15t2j^⇒v⃗t=1sec=20i^+15j^ \vec{v} = \frac{d\vec{r}}{dt} = 20t\hat{i} + 15t^2\hat{j} \Rightarrow \vec{v}_{t=1sec} = 20\hat{i} + 15\hat{j}

a⃗=d2r⃗dt2=20i^+30tj^⇒a⃗t=1sec=20i^+30j^ \vec{a} = \frac{d^2\vec{r}}{dt^2} = 20\hat{i} + 30t\hat{j} \Rightarrow \vec{a}_{t=1sec} = 20\hat{i} + 30\hat{j}

∴P⃗=mv⃗=2i^+1.5j^ \therefore \vec{P} = m\vec{v} = 2\hat{i} + 1.5\hat{j}

F⃗=ma⃗=2i^+3j^ \vec{F} = m\vec{a} = 2\hat{i} + 3\hat{j}

τ⃗=r⃗×F⃗=20k^ \vec{\tau} = \vec{r} \times \vec{F} = 20\hat{k}

L⃗=r⃗×P⃗=5k^ \vec{L} = \vec{r} \times \vec{P} = 5\hat{k}

Question 70

A planet (P1) (P_1) is moving around the star of mass 2M in the orbit of radius R. Another planet (P2) (P_2) is moving around another star of mass 4M in a orbit

of radius 2R. Ratio of time periods of revolution of

P2 P_2 and P1 P_1 is ________.

  1. AOption (a)

    12 \frac{1}{2}

  2. BOption (b)

    2

  3. COption (c)

    4

  4. DOption (d)

    14 \frac{1}{4}

View answer & explanation

Correct answer

Answer: (b)B.

2

Why this answer is correct

From Kepler's law,

T2=4π2GMsr3 T^2 = \frac{4\pi^2}{GM_s}r^3

∴TP1=2πG(2M)R3/2 \therefore T_{P_1} = \frac{2\pi}{\sqrt{G(2M)}} R^{3/2}

TP2=2πG(4M)(2R)3/2 T_{P_2} = \frac{2\pi}{\sqrt{G(4M)}} (2R)^{3/2}

∴TP2TP1=(2)3/24=21×22×22=2 \therefore \frac{T_{P_2}}{T_{P_1}} = \frac{(2)^{3/2}}{\sqrt{4}} = \frac{\sqrt{2}}{1} \times \frac{2\sqrt{2} \times \sqrt{2}}{2} = 2

Physics Section B (5 questions)

Question 71

In single slit diffraction pattern, the wavelength of light used is 628 nm and slit width is 0.2 mm, the angular width of central maximum is α×10−2 \alpha \times 10^{-2}

degrees. The value of α \alpha is______.

View answer & explanation

Correct answer

Answer: 36Answer: 36

Why this answer is correct

Sol.  Angular width of central maxima θcm=2λd \theta_{cm} = \frac{2\lambda}{d}

= 2×628×10−90.2×10−3 \frac{2 \times 628 \times 10^{-9}}{0.2 \times 10^{-3}} rad.

= (628×10−5)×180π (628 \times 10^{-5}) \times \frac{180}{\pi} degrees

≈36×10−2 \approx 36 \times 10^{-2} degrees

∴ \therefore Answer : α=36 \alpha = 36

Question 72

A vessel contains 0.15 m3 of a gas at pressure 8 bar and temperature 140°C with cp=3R c_p = 3R and cv=2R c_v = 2R . It is expanded adiabatically till pressure falls to 1 bar. The work done during this process is ____ kJ. (R is gas constant)

View answer & explanation

Correct answer

Answer: 120Answer: 120

Why this answer is correct

Sol.  γ=CpCv=32 \gamma = \frac{C_p}{C_v} = \frac{3}{2}

∵P1V1γ=P2V2γ \because P_1 V_1^\gamma = P_2 V_2^\gamma

⇒V2=(P1P2)1/γV1 \Rightarrow V_2 = \left( \frac{P_1}{P_2} \right)^{1/\gamma} V_1

⇒V2=(81)2/3×0.15 \Rightarrow V_2 = \left( \frac{8}{1} \right)^{2/3} \times 0.15

⇒V2=0.6 m3 \Rightarrow V_2 = 0.6 \text{ m}^3

∵W=P1V1−P2V2γ−1 \because W = \frac{P_1 V_1 - P_2 V_2}{\gamma - 1}

= (8×0.15−1×0.61.5−1)×105=1.2×105 \left( \frac{8 \times 0.15 - 1 \times 0.6}{1.5 - 1} \right) \times 10^5 = 1.2 \times 10^5

⇒W=120 kJ \Rightarrow W = 120 \text{ kJ}

Question 73

1 μ \mu C charge moving with velocity

v⃗=(i^−2j^+3k^) m/s \vec{v} = (\hat{i} - 2\hat{j} + 3\hat{k}) \text{ m/s} in the region of magnetic field B⃗=(2i^+3j^−5k^) T \vec{B} = (2\hat{i} + 3\hat{j} - 5\hat{k}) \text{ T} . The magnitude of force acting on it is α×10−6 N \sqrt{\alpha} \times 10^{-6} \text{ N} . The value of α \alpha is ____.

View answer & explanation

Correct answer

Answer: 171Answer: 171

Why this answer is correct

Sol.  F⃗=q(v⃗×B⃗) \vec{F} = q(\vec{v} \times \vec{B})

= 1×10−6∣i^j^k^ 1−23 23−5∣ 1 \times 10^{-6} \begin{vmatrix} \hat{i} & \hat{j} & \hat{k} \ 1 & -2 & 3 \ 2 & 3 & -5 \end{vmatrix}

= 10−6[i^+11j^+7k^] 10^{-6} [\hat{i} + 11\hat{j} + 7\hat{k}]

⇒F⃗=171×10−6 N \Rightarrow \vec{F} = \sqrt{171} \times 10^{-6} \text{ N}

∴α=171 \therefore \alpha = 171

Question 74

A uniform wire of length l l of weight w is suspended from the roof with a weight of W at the other end. The stress in the wire at l3 \frac{l}{3} distance

from the top is (WA+2γwA) \left( \frac{W}{A} + \frac{2}{\gamma} \frac{w}{A} \right) , where, A is the cross sectional area of the wire. The value of γ \gamma is______.

View answer & explanation

Correct answer

Answer: 6Answer: 6

Why this answer is correct

Sol.  

σ=TA=W+w3A \sigma = \frac{T}{A} = \frac{W + \frac{w}{3}}{A}

⇒σ=WA+26wA \Rightarrow \sigma = \frac{W}{A} + \frac{2}{6} \frac{w}{A}

∴γ=6 \therefore \gamma = 6

Question 75

A tube is filled with water and a wooden cube 10 cm × \times 10cm × \times 10cm is placed in the water. The

wooden cube is found to float on the water with a part of it submerged in water. When a metal coin is

placed on the wooden cube, the submerged part is increased by 3.87 cm. The mass of the metal coin

is ____ gram. (Take water density as 1g/cm3 and density of wood as 0.4 g/cm3)

View answer & explanation

Correct answer

Answer: 387Answer: 387

Why this answer is correct

Sol.  

Weight of coin = Additional upthrust

⇒mcg=ρlVaddg \Rightarrow m_c g = \rho_l V_{add} g

⇒mc=1×3.87×(10)2 \Rightarrow m_c = 1 \times 3.87 \times (10)^2

⇒mc=387 gram \Rightarrow m_c = 387 \text{ gram}

75 questions in the full paper