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Draw both resonance structures of the most stable carbocation intermediate in the reaction shown.
- You do not have to consider stereochemistry.
- Do not include anionic counter-ions, e.g, I‾ , in your answer.
- Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
- Separate resonance structures using the ↔ symbol from the drop-down menu.
Depending on their chemical structure, we can divide carbocations into one of two types: classical or unorthodox. The main difference between unclassified and classical carbocations is that unclassified carbocations are composed of a single carbon atom, six electrons in three chemical bond structures, while classical carbocations contain a single carbon with six electrons in one. Unclassified carbocations however have a two-centred, two-electron structure. A methenium ion is an example of a classic carbocation, while a 2-norboryl is an example of unclassified carbocation.
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