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organic chemistry - Does a tertiary carbocation rearrange to another tertiary carbocation? - Chemistry Stack Exchange
![The following transformation involves a carbocation rearrangement. The carbocation is generated by protonation of the hydroxyl group, followed by the loss of water. Which bond has to migrate in the carbocation to The following transformation involves a carbocation rearrangement. The carbocation is generated by protonation of the hydroxyl group, followed by the loss of water. Which bond has to migrate in the carbocation to](https://www.vedantu.com/question-sets/97d2b2a0-4558-4034-875a-fd3f78c832d06735196971758023596.png)
The following transformation involves a carbocation rearrangement. The carbocation is generated by protonation of the hydroxyl group, followed by the loss of water. Which bond has to migrate in the carbocation to
![Carbocation Rearrangements in Ring Expansion Reactions - Practice Problem | Reactions, Chemistry, How to become Carbocation Rearrangements in Ring Expansion Reactions - Practice Problem | Reactions, Chemistry, How to become](https://i.pinimg.com/736x/24/75/41/247541177d19d0e05ead3a18a7f13206.jpg)
Carbocation Rearrangements in Ring Expansion Reactions - Practice Problem | Reactions, Chemistry, How to become
A photochemical ring expansion of 6- to 8-membered nitrogen heterocycles by [1,3]-sigmatropic rearrangement - Chemical Communications (RSC Publishing)
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