Home > Community > Why is cis-bicyclo [4.1.0]-heptane more stable than its trans isomer?
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Manoj Bhai

Why is cis-bicyclo [4.1.0]-heptane more stable than its trans isomer?

Chief Thunder  Follow

Because of the bridge without any carbons…. [0] bridge. You can picture this molecule as a “pinched” cyclohexane, where the carbons in the nor-adjacent (1,3) positions are pinched together with a 1-carbon bridge.

bicyclo [4.1.0]=heptane or norcarane is stable in the “boat” (cis-) configuration, because of the bridge. The chair conformation induces too much torsional strain on the C-C bonds involved.

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Allan Ashworth  Follow

You cannot have a trans (E) alkene in any ring smaller than 7.

Rings 8 carbons or larger can accommodate that geometry.

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