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A Carbene in the Singlet State Is Typically Portrayed as

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A carbene in the singlet state is typically portrayed as sp2 hybridized, with a vacant p -orbital and a pair of nonbonding electrons residing in one sp2 hybrid orbital. Using molecular orbital theory, describe how a neighboring A carbene in the singlet state is typically portrayed as  sp<sup>2 </sup>hybridized, with a vacant  p -orbital and a pair of nonbonding electrons residing in one   sp<sup>2</sup> hybrid orbital. Using molecular orbital theory, describe how a neighboring  -bond can act as a nucleophile with the carbene in the formation of a cyclopropyl ring.  -bond can act as a nucleophile with the carbene in the formation of a cyclopropyl ring.
A carbene in the singlet state is typically portrayed as  sp<sup>2 </sup>hybridized, with a vacant  p -orbital and a pair of nonbonding electrons residing in one   sp<sup>2</sup> hybrid orbital. Using molecular orbital theory, describe how a neighboring  -bond can act as a nucleophile with the carbene in the formation of a cyclopropyl ring.


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