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68908591fff493ab65fa7da7 - ## - Haloalkanes and Haloarenes - DPP 07 (Of Lec 09) - Lakshya NEET 2026

The document contains a series of questions and answers related to Organic Chemistry, specifically focusing on the reactions of haloalkanes and haloarenes. It includes multiple-choice questions about the stability of carbocations, products of reactions, and application of Markovnikov's rule. An answer key is provided at the end for reference.

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70 views3 pages

68908591fff493ab65fa7da7 - ## - Haloalkanes and Haloarenes - DPP 07 (Of Lec 09) - Lakshya NEET 2026

The document contains a series of questions and answers related to Organic Chemistry, specifically focusing on the reactions of haloalkanes and haloarenes. It includes multiple-choice questions about the stability of carbocations, products of reactions, and application of Markovnikov's rule. An answer key is provided at the end for reference.

Uploaded by

ayushsinrhn
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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NEET

Lakshya NEET (2026)


Organic Chemistry
DPP: 7
Haloalkanes and Haloarenes

Q1 Q4
Br2
CCl4
−−→ Products
+Br2 ⟶ CCl 4

Number of product(s) in the reaction is/are (A)


(A) 1 (B) 2
(C) 3 (D) 4

Q2 Br2

(1) −
−→ Meso − 2, 3 − dibromobutane ,
CCl4
(B)
identify reactant(1)
(A)

(B)
(C)

(C)

(D) All of these

Q5 Choose the correct statement regarding the


(D) formation of carbocations A and B given.

Q3 (A) Carbocation A is more stable and formed


relatively at slow rate.
(B) Carbocation B is more stable and formed
relatively at faster rate.
Product is (C) Carbocation A is more stable and formed
(A) A racemic mixture relatively at faster rate.
(B) A single enantiomer (D) Carbocation B is more stable and formed
(C) A pair of diastereomer relatively at slow rate.
(D) A chiral molecule

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Q6 The major product formed in the following (C)


reaction

(D) None is correct

Q10 Addition of HI on double bond of propene


HBr
yields isopropyl iodide and not n-propyl iodide
−→ Major product
as the major product, because addition proceeds
(A)
through
(A) A more stable carbonium ion
(B) (B) A more stable carbanion
(C) A more stable free radical
(D) None

(C) Q11 Ethylene reacts with Br2 to give 1, 2-


dibromoethane. The anti-addition takes place
due to the formation of the intermediate
(D)
(A) CH2 CH2 Br + CH+
2

(B)

(C) BrCH
+
= CH

(D)
Q7 The reaction
CH2 = CHCH 3 + HBr → CH3 CHBrCH 3

is
(A) Nucleophilic addition Q12 In the reaction C2 H5 CH = CH2 + H − X →

(B) Electrophilic addition Product. What is the product?


(C) Electrophilic substitution (A) C2 H5 − CH3

(D) Free radical addition (B) C2 H5 CH2 − CH2 X

(C) C2 H5 − CHX − CH3


Q8 The Markovnikov's rule is used in connection with
(D) CH3 − CH2 X − CH = CH2
(A) Stereochemistry of elimination reactions
(B) Stability of free radicals.
(C) Activity of enzymes
(D) Addition of acids to double bonds

Q9

which is predominate ; X is
(A)

(B)

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Answer Key
Q1 (B) Q7 (B)

Q2 (A) Q8 (D)

Q3 (C) Q9 (B)

Q4 (D) Q10 (A)

Q5 (B) Q11 (B)

Q6 (C) Q12 (C)

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