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NCERT Solutions for class 11 Chemistry | Chapter 13 Hydrocarbons

(1) Arrange the following in decreasing order of their boiling points.

(A) n–butane (B) 2–methylbutane (C) n-pentane (D) 2,2–dimethylpropane

[A] A > B > C > D
[B] B > C > D > A
[C] D > C > B > A
[D] C > B > D > A
Answer: C > B > D > A
(2) Arrange the halogens F2 , Cl2 , Br2 , I2 , in order of their increasing reactivity with alkanes.
[A] I2 < Br2 < Cl2 < F2
[B] Br2 < Cl2 < F2 < I2
[C] F2 < Cl2 < Br2 < I2
[D] Br2 < I2 < Cl2 < F2
Answer: I2 < Br2 < Cl2 < F2

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(3) The increasing order of reduction of alkyl halides with zinc and dilute HCl is
[A] R–Cl < R–I < R–Br
[B] R–Cl < R–Br < R–I
[C] R–I < R–Br < R–Cl
[D] R–Br < R–I < R–Cl
Answer: R–Cl < R–Br < R–I
(4) The correct IUPAC name of the following alkane is

[A] 3,6 – Diethyl – 2 – methyloctane
[B] 5 – Isopropyl – 3 – ethyloctane
[C] 3 – Ethyl – 5 – isopropyloctane
[D] 3 – Isopropyl – 6 – ethyloctane
Answer: 3,6 – Diethyl – 2 – methyloctane
(5) The addition of HBr to 1-butene gives a mixture of products A, B and C

The mixture consists of

[A] A and B as major and C as minor products
[B] B as major, A and C as minor products
[C] B as minor, A and C as major products
[D] A and B as minor and C as major products
Answer: A and B as major and C as minor products
(6) Which of the following will not show geometrical isomerism?

[A] (i)
[B] (ii)
[C] (iii)
[D] (iv)
Answer: (iv)
(7) Arrange the following hydrogen halides in order of their decreasing reactivity with propene.
[A] HCl > HBr > HI
[B] HBr > HI > HCl
[C] HI > HBr > HCl
[D] HCl > HI > HBr
Answer: HI > HBr > HCl
(8) Arrange the following carbanions in order of their decreasing stability.

[A] A > B > C
[B] B > A > C
[C] C > B > A
[D] C > A > B
Answer: B > A > C
(9) Arrange the following alkyl halides in decreasing order of the rate of β– elimination reaction with alcoholic KOH.

[A] A > B > C
[B] C > B > A
[C] B > C > A
[D] A > C > B
Answer: A > C > B
(10) Which of the following reactions of methane is incomplete combustion:

[A] (i)
[B] (ii)
[C] (iii)
[D] (iv)
Answer: (iii)
(11) Some oxidation reactions of methane are given below. Which of them is/are controlled oxidation reactions?

[A] (i)
[B] (ii)
[C] (iii)
[D] (iv)
Answer: C, D
(12) Which of the following alkenes on ozonolysis give a mixture of ketones only?

[A] (i)
[B] (ii)
[C] (iii)
[D] (iv)
Answer: C, D
(13) Which are the correct IUPAC names of the following compound?

[A] 5– Butyl – 4– isopropyldecane
[B] 5– Ethyl – 4– propyldecane
[C] 5– sec-Butyl – 4– iso-propyldecane
[D] 4–(1-methylethyl)– 5 – (1-methylpropyl)-decane
Answer: C, D
(14) Which are the correct IUPAC names of the following compound?

[A] 5 – (2′, 2′–Dimethylpropyl)-decane
[B] 4 – Butyl – 2,2– dimethylnonane
[C] 2,2– Dimethyl – 4– pentyloctane
[D] 5 – neo-Pentyldecane
Answer: A, D
(15) For an electrophilic substitution reaction, the presence of a halogen atom in the benzene ring _______.
[A] deactivates the ring by inductive effect
[B] deactivates the ring by resonance
[C] increases the charge density at ortho and para position relative to meta position by resonance
[D] directs the incoming electrophile to meta position by increasing the charge density relative to ortho and para position.
Answer: A, C
(16) In an electrophilic substitution reaction of nitrobenzene, the presence of nitro group ________.
[A] deactivates the ring by inductive effect.
[B] activates the ring by inductive effect.
[C] decreases the charge density at ortho and para position of the ring relative to meta position by resonance.
[D] increases the charge density at meta position relative to the ortho and para positions of the ring by resonance.
Answer: A, C
(17) Which of the following are correct?

[A] (i)
[B] (ii)
[C] (iii)
[D] (iv)
Answer: A, C
(18) Four structures are given in options (i) to (iv). Examine them and select the aromatic structures.

[A] (i)
[B] (ii)
[C] (iii)
[D] (iv)
Answer: A, C
(19) The molecules having dipole moment are __________.
[A] 2,2-Dimethylpropane
[B] trans-Pent-2-ene
[C] cis-Hex-3-ene
[D] 2, 2, 3, 3 - Tetramethylbutane.
Answer: B, C
(20) Assertion (A) : The compound cyclooctane has the following structural formula :

Reason (R) : (4n + 2) π electrons rule does not hold good and ring is not planar.

[A] Both A and R are correct and R is the correct explanation of A.
[B] Both A and R are correct but R is not the correct explanation of A.
[C] Both A and R are not correct.
[D] A is not correct but R is correct.
Answer: Both A and R are correct and R is the correct explanation of A.

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