Haloalkanes and Haloarenes is a Class 12 Chemistry chapter that carries about 4.2% of the Chemistry questions in NEET. Practise it with 45 questions covering 2 topics, each with an explanation.
Sample questions on Haloalkanes and Haloarenes with answers
8 questions from the practice bank, spread across the chapter's topics. The full set is in the app.
Question 1: Nomenclature of Haloalkanes
Allylic bromination of an alkene is carried out using:
- A Br₂ in CCl₄
- B NaBr
- C N-bromosuccinimide (NBS)
- D HBr
Answer: C. N-bromosuccinimide (NBS)
Why: NBS supplies a low concentration of bromine for substitution at the allylic position.
Question 2: SN1 and SN2 Reactions
A haloalkane that undergoes SN1 reaction at a chiral carbon gives mainly:
- A only an achiral product
- B a single product with inverted configuration
- C a racemic mixture
- D a single product with retained configuration
Answer: C. a racemic mixture
Why: The planar carbocation can be attacked from either face by the nucleophile, so both enantiomers form in equal amounts.
Question 3: Nomenclature of Haloalkanes
Chlorobenzene is less reactive than chloroethane towards nucleophilic substitution because:
- A the C–Cl bond has partial double bond character due to resonance, and carbon is sp² hybridised
- B chlorine is a better leaving group in chlorobenzene
- C the benzene ring is electron deficient
- D chlorobenzene is more polar
Answer: A. the C–Cl bond has partial double bond character due to resonance, and carbon is sp² hybridised
Why: The lone pair on chlorine delocalises into the ring, which strengthens and shortens the C–Cl bond.
Question 4: SN1 and SN2 Reactions
The order of reactivity of alkyl halides in an SN2 reaction is:
- A tertiary > secondary > primary > methyl
- B all equal
- C methyl > primary > secondary > tertiary
- D secondary > primary > methyl > tertiary
Answer: C. methyl > primary > secondary > tertiary
Why: Steric hindrance increases with substitution at the carbon.
Question 5: Nomenclature of Haloalkanes
A Grignard reagent is prepared by reacting an alkyl halide with magnesium in:
- A dry ether
- B water
- C dilute acid
- D aqueous alcohol
Answer: A. dry ether
Why: Moisture destroys it: RMgX + H₂O → RH + Mg(OH)X.
Question 6: SN1 and SN2 Reactions
Chloroform was once used as an anaesthetic, but its use was stopped because:
- A it is a reducing agent
- B it is slowly oxidised by air and light to poisonous phosgene
- C it is a solid
- D it is non-volatile
Answer: B. it is slowly oxidised by air and light to poisonous phosgene
Why: It is stored in dark bottles filled to the brim.
Question 7: Nomenclature of Haloalkanes
Iodoform (CHI₃) is used as:
- A a refrigerant
- B an anaesthetic
- C an antiseptic
- D a solvent in dry cleaning
Answer: C. an antiseptic
Why: It slowly releases iodine.
Question 8: SN1 and SN2 Reactions
The order of reactivity of alkyl halides in an SN1 reaction is:
- A secondary > tertiary > primary
- B primary > secondary > tertiary
- C all equal
- D tertiary > secondary > primary
Answer: D. tertiary > secondary > primary
Why: The rate depends on the stability of the carbocation formed.