In which of the following reaction is the rate of reaction not affected by increasing concentration of nucleophile?
Correct answer: C. SN1
- A. SN2
- B. E2
- C. SN1
- D. None of these
Explanation
Option A: SN2 (substitution nucleophilic bimolecular) reaction: The rate of an SN2 reaction is influenced by the concentration of the nucleophile. As the concentration of the nucleophile increases, the rate of the reaction also increases.Option B: E2 (elimination bimolecular) reaction: Similar to the SN2 reaction, the rate of an E2 reaction is affected by the concentration of the nucleophile. As the concentration of the nucleophile increases, the rate of the reaction also increases.Option C: SN1 (substitution nucleophilic unimolecular) reaction: The rate of an SN1 reaction is not affected by the concentration of the nucleophile. The rate-determining step in an SN1 reaction involves the formation of a carbocation intermediate, which is independent of the concentration of the nucleophile. The rate of the reaction is primarily determined by the stability of the carbocation intermediate. Option D: This option suggests that none of the given reactions have a rate that is unaffected by increasing the concentration of the nucleophile. However, the correct answer is C).
Last updated
About Alkyl Halides
Alkyl halides are named and related to their carbon-halogen structure, polarity and reactivity. The key reactions are nucleophilic substitution by SN1 and SN2 mechanisms and elimination by E1 and E2 mechanisms, including how substrate structure, nucleophile, base, solvent and temperature influence substitution versus elimination.
Practise Alkyl Halides
458 free Alkyl Halides MCQs from Chemistry, each with the correct answer and an explanation. Unlimited attempts, no account needed.
Exams that ask Chemistry questions like this
Chemistry is on 12 papers prepared for on TestUstad, and all of them draw the same bank, so this question is worth knowing for every one of them.
Related questions
1-Chloropropane and 2-Chloropropane are _.
𝑂𝐻− + 𝐶2𝐻5 − 𝐼 ⟶ 𝐶2𝐻5 − 𝑂𝐻 + 𝐼− One of the species in the above reaction is a substrate. It is:
2-Chloro-2-methylpropane is an example of:
2-Chlorobutane belongs to:
A compound X (C4H9Br) undergoes the following reactions: C4H9Br NaOH(aq)/heat > C4H10O Cr2O7(2-), H+(aq)/ heat> C4H8O. What is X?