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An alkene contains a double bond. Why is the C=C of an alkene rigid and unable to freely rotate? The C-C bond is very strong, and it is impossible to break it. The s bond becomes blocked by the hydrogen atoms. The sp2 hybrid orbitals of carbon take up too much room The p electrons are delocalized through the s bonds The 2p orbitals of the p bond overlap above and below the C-C plane to restrict rotation.

An alkene contains a double bond. Why is the C=C of an alkene rigid and unable to freely rotate? The C-C bond is very strong, and it is impossible to break it. The s bond becomes blocked by the hydrogen atoms. The sp2 hybrid orbitals of carbon take up too much room The p electrons are delocalized through the s bonds The 2p orbitals of the p bond overlap above and below the C-C plane to restrict rotation.

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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An alkene contains a double bond. Why is the C=C of an alkene rigid and unable to freely rotate? The C-C bond is very strong, and it is impossible to break it. The s bond becomes blocked by the hydrogen atoms. The sp2 hybrid orbitals of carbon take up too much room The p electrons are delocalized through the s bonds The 2p orbitals of the p bond overlap above and below the C-C plane to restrict rotation.
Transcribed Image Text:An alkene contains a double bond. Why is the C=C of an alkene rigid and unable to freely rotate? The C-C bond is very strong, and it is impossible to break it. The s bond becomes blocked by the hydrogen atoms. The sp2 hybrid orbitals of carbon take up too much room The p electrons are delocalized through the s bonds The 2p orbitals of the p bond overlap above and below the C-C plane to restrict rotation.
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