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2nd Year Chemistry Chapter 5 Test2nd Year · Chemistry · Punjab (PTB)
Q1. Multiple choice questions (Attempt all · 10 × 1 = 10)
Which of the following is explicitly mentioned as a factor affecting reactivity alongside bond energy?
What has primarily led to restrictions or banning of DDT in developed countries?
What is the overall reaction kinetics order followed by an SN1 mechanism?
What are the secondary products formed alongside ethene in the elimination reaction?
Which halogenoalkane is the most reactive based on bond energy?
What phosphorus-containing by-product is formed when an alcohol reacts with PCl5?
Which compounds were historically used as refrigerants but are now replaced due to ozone depletion?
What reagent is used alongside pyridine to prepare pure alkyl chlorides from alcohols?
What happens to the lone pair of electrons on the chlorine atom in a halogenoarene?
The first step in the SN1 mechanism acts as follows:
Q2. Short questions (Attempt any 6 of 8 · 6 × 2 = 12)
Why is the E2 reaction called bimolecular?
Explain the mechanisms which the chloroalkane will adopt while giving nucleophilic substitution reactions.
What is the natural source of bromomethane (CH3Br)?
Complete the following equation. C2H5Br + CH3COONa
Does 1-bromo-2,2-dimethylpropane undergo elimination reaction or not? Justify.
What is the role of iron chloride (FeCl3) during the chlorination of benzene?
Give two methods to convert methanol into chloromethane.
Differentiate between primary, secondary and tertiary halogenoalkanes.
Q3. Long questions (Attempt any 2 of 3 · 2 × 4 = 8)
Compare the reactivity of halogenoalkanes and halogenoarenes using chloroethane and chlorobenzene as examples.
Explain the SN2 mechanism of nucleophilic substitution reactions with a suitable example.
Describe the SN1 and SN2 mechanisms of nucleophilic substitution in halogenoalkanes.