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If cyclobutane were flat, it would have exactly 90 degree bond angles and could theoretically use only p orbitals to form its C-C bonds.

- Propose a hybridization scheme for the carbon atoms in this hypothetical flat butane that would allow all the C-H bonds to be equivalent.

- Exactly where would the hydrogens on each carbon be located?

- What features of the real cyclobutane contradict this hypothesis?

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