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1. (12 points) Consider each of the neutral CBH2 carbocyclic molecules in the following table. Assume that the ring strain (if any) of

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1. (12 points) Consider each of the neutral " CBH2 " carbocyclic molecules in the following table. Assume that the ring strain (if any) of being planar is not sufficient to override the stability gained by aromaticity. [Note: Radical species are indicated by the single electron dot] [Hint: The Hackel rule for aromaticity is 4n+2 electrons.] a. Specify the number of electrons in the system for the neutral species. b. State whether the neutral species is aromatic, non-aromatic, or antlaromatic. c. If the neutral species can gain or lose up to two electrons to become a( n ) (di)cation or (di)anion to become aromatic, list the molecular formula with its associated charge for the charged aromatic species. d. Pick one of the charged aromatic species and sketch the energy MO diagram for its system

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