🧪 Reaction Mechanism Quiz – Basic to Advanced
Q1. Which type of bond fission leads to the formation of free radicals?
✅ Correct Answer: C
In homolytic cleavage, both atoms get one electron each, forming free radicals.
In homolytic cleavage, both atoms get one electron each, forming free radicals.
Q2. Which intermediate is formed during the SN1 reaction?
✅ Correct Answer: C
SN1 involves the formation of a carbocation intermediate in the rate-determining step.
SN1 involves the formation of a carbocation intermediate in the rate-determining step.
Q3. Which of the following is the most stable carbocation?
✅ Correct Answer: D
3° carbocations are most stable due to hyperconjugation and inductive effect.
3° carbocations are most stable due to hyperconjugation and inductive effect.
Q4. SN2 reaction mechanism involves:
✅ Correct Answer: C
SN2 is a single-step reaction with backside attack leading to inversion of configuration.
SN2 is a single-step reaction with backside attack leading to inversion of configuration.
Q5. Which reaction follows Markovnikov’s rule?
✅ Correct Answer: C
Electrophilic addition to alkenes usually follows Markovnikov’s rule.
Electrophilic addition to alkenes usually follows Markovnikov’s rule.
Q6. Which reaction mechanism involves anti-periplanar geometry?
✅ Correct Answer: B
E2 reactions require anti-periplanar arrangement of leaving group and hydrogen.
E2 reactions require anti-periplanar arrangement of leaving group and hydrogen.
Q7. Which of the following is not a reactive intermediate?
✅ Correct Answer: C
Ester is a compound, not an intermediate. Others are reactive intermediates.
Ester is a compound, not an intermediate. Others are reactive intermediates.
Q8. What is the rate law for an SN2 reaction?
✅ Correct Answer: C
SN2 is bimolecular, depends on both substrate and nucleophile concentration.
SN2 is bimolecular, depends on both substrate and nucleophile concentration.
Q9. Which is the correct stability order of free radicals?
✅ Correct Answer: B
More substituted free radicals are more stable: 3° > 2° > 1°.
More substituted free radicals are more stable: 3° > 2° > 1°.
Q10. Which reaction involves formation of a Meisenheimer complex?
✅ Correct Answer: B
SNAr (nucleophilic aromatic substitution) forms a Meisenheimer intermediate.
SNAr (nucleophilic aromatic substitution) forms a Meisenheimer intermediate.

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