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Punjab (PTB) · Chapter test · Free

2nd Year Chemistry Chapter 5 TestHALOGENOALKANES

30 marks · 40 minutes · 21 questions. Covers: CHAP 21: HALOGENOALKANES.

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2nd Year Chemistry Chapter 5 Test

2nd Year · Chemistry · Punjab (PTB)

Name: ____________Roll No: ________Class/Section: ________Date: ________Total marks: 30Time: 40 minutes

Q1. Multiple choice questions (Attempt all · 10 × 1 = 10)

  1. Which of the following is explicitly mentioned as a factor affecting reactivity alongside bond energy?

    1. Boiling point

    2. Surface area

    3. Bond polarity

    4. Molecular geometry

  2. What has primarily led to restrictions or banning of DDT in developed countries?

    1. High manufacturing cost

    2. Persistence in the environment

    3. Lack of effectiveness

    4. Bad odor

  3. What is the overall reaction kinetics order followed by an SN1 mechanism?

    1. Zero order

    2. First order

    3. Second order

    4. Third order

  4. What are the secondary products formed alongside ethene in the elimination reaction?

    1. H2O and NaBr

    2. H2 and NaBr

    3. O2 and NaBr

    4. HBr only

  5. Which halogenoalkane is the most reactive based on bond energy?

    1. R–F

    2. R–Cl

    3. R–Br

    4. R–I

  6. What phosphorus-containing by-product is formed when an alcohol reacts with PCl5?

    1. H3PO3

    2. POCl3

    3. P2O5

    4. PH3

  7. Which compounds were historically used as refrigerants but are now replaced due to ozone depletion?

    1. Chlorofluorocarbons (CFCs)

    2. Hydrofluorocarbons (HFCs)

    3. Polyvinyl chloride (PVC)

    4. Polytetrafluoroethylene (PTFE)

  8. What reagent is used alongside pyridine to prepare pure alkyl chlorides from alcohols?

    1. Thionyl chloride

    2. Phosphorus trichloride

    3. Hydrochloric acid

    4. Phosphorus pentachloride

  9. What happens to the lone pair of electrons on the chlorine atom in a halogenoarene?

    1. It remains localized

    2. It is lost to the catalyst

    3. It is delocalised into the ring

    4. It forms a coordinate bond

  10. The first step in the SN1 mechanism acts as follows:

    1. Rate-determining step

    2. Ionization step

    3. Nucleophilic attack

    4. Deprotonation step

Q2. Short questions (Attempt any 6 of 8 · 6 × 2 = 12)

  1. Why is the E2 reaction called bimolecular?

  2. Explain the mechanisms which the chloroalkane will adopt while giving nucleophilic substitution reactions.

  3. What is the natural source of bromomethane (CH3Br)?

  4. Complete the following equation. C2H5Br + CH3COONa 

  5. Does 1-bromo-2,2-dimethylpropane undergo elimination reaction or not? Justify.

  6. What is the role of iron chloride (FeCl3) during the chlorination of benzene?

  7. Give two methods to convert methanol into chloromethane.

  8. Differentiate between primary, secondary and tertiary halogenoalkanes.

Q3. Long questions (Attempt any 2 of 3 · 2 × 4 = 8)

  1. Compare the reactivity of halogenoalkanes and halogenoarenes using chloroethane and chlorobenzene as examples.

  2. Explain the SN2 mechanism of nucleophilic substitution reactions with a suitable example.

  3. Describe the SN1 and SN2 mechanisms of nucleophilic substitution in halogenoalkanes.