Which of the following statements about an S_N1 reaction mechanism is true? the

Question

Which of the following statements about an S_N1 reaction mechanism is true? the reaction is fastest with primary alkyl halide. the reaction exhibits a one - step mechanism. the reaction rate increases as the leaving group ability increases. the reaction rate increases as the strength of the nucleophile increases. Which of the following alkyl halides will react fastest with CH_3OH in an S_Nl mechanism? What it the rate-determining step of an S_N 1 reaction mechanism? Reaction of the nucleophile with the carbocation lo form the product Breaking the bond between the carbon and the leaving group lo generate a carbonation. Attack of the nucleophile on the substrate lo generate a pentavalent carbon. None of the above. Which of the following carbocation is the most stable? which of the following statement about carbocation stability is true? carbocation are stabilized by electron-withdrawing inductive effects only carbocation are stabilized by electron-withdrawing inductiv

Explanation / Answer

30) The correct answer is Option C

31) In SN1, the reaction will be fastest in the case of tertiary carbocation formation

The compound IV will form the tertiary carbocation which is the most stable

Hence the correct answer is Option D

32) The correct answer is Option B i,e, the loss of leaving group to form an intermediate carbocation

33) The most stable carbocation will be the Option B, since it is the only 2nd degree carbocation whereas remaining all the carbocation are first degree carbocation

34) The correct answer is Option D

Related Questions

Navigate

• Browse (All)
• Browse W
• Subjects

---

---

Integrity-first tutoring: explanations and feedback only — we do not complete graded work. Learn more.