After a carbocation rearrangement (hydride-shift) to a tertiary position, methylene cyclohexane is formed. Methylene becomes cyclohexane when the proton and hydrogen are removed.
What is carbocation rearrangements?
- The migration of a carbocation from an unstable form to a more stable one using different structural reorganizational "shifts" inside the molecule is known as a carbocation rearrangement, which is a common process in organic chemistry.
- A rearrangement is feasible because the SN1 mechanism involves the creation of a carbocation. Let's examine this SN1 reaction now. Our alkyl halide is on the left, ethanol is our solvent, and our product is on the right.
- Methylene cyclohexane is created by a carbocation rearrangement (hydride-shift) to a tertiary position. When the proton and hydrogen are taken out of methylene, cyclohexane results.
To learn more about carbocation rearrangements refer to:
https://brainly.com/question/20388467
#SPJ4
