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  2. Orbital hybridisation - Wikipedia

    en.wikipedia.org/wiki/Orbital_hybridisation

    For this molecule, carbon sp 2 hybridises, because one π (pi) bond is required for the double bond between the carbons and only three σ bonds are formed per carbon atom. In sp 2 hybridisation the 2s orbital is mixed with only two of the three available 2p orbitals, usually denoted 2p x and 2p y. The third 2p orbital (2p z) remains unhybridised.

  3. Isovalent hybridization - Wikipedia

    en.wikipedia.org/wiki/Isovalent_hybridization

    The value of 1 J 13 C-1 H for cyclopropane, cyclobutane and cyclopentane are 161, 134, and 128 Hz, respectively. This is a consequence of the fact that the C-C bonds in small, strained rings (cyclopropane and cyclobutane) employ excess p character to accommodate their molecular geometries (these bonds are famously known as ' banana bonds ').

  4. List of chemical classifications - Wikipedia

    en.wikipedia.org/wiki/List_of_chemical...

    Chemical classification systems attempt to classify elements or compounds according to certain chemical functional or structural properties. Whereas the structural properties are largely intrinsic, functional properties and the derived classifications depend to a certain degree on the type of chemical interaction partners on which the function is exerted.

  5. Carbon–carbon bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–carbon_bond

    Carbon is one of the few elements that can form long chains of its own atoms, a property called catenation.This coupled with the strength of the carbon–carbon bond gives rise to an enormous number of molecular forms, many of which are important structural elements of life, so carbon compounds have their own field of study: organic chemistry.

  6. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    In the case of water, with its 104.5° HOH angle, the OH bonding orbitals are constructed from O(~sp 4.0) orbitals (~20% s, ~80% p), while the lone pairs consist of O(~sp 2.3) orbitals (~30% s, ~70% p). As discussed in the justification above, the lone pairs behave as very electropositive substituents and have excess s character.

  7. Carbon–hydrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–hydrogen_bond

    A bond between a hydrogen atom and an sp 2 hybridised carbon atom is about 0.6% shorter than between hydrogen and sp 3 hybridised carbon. A bond between hydrogen and sp hybridised carbon is shorter still, about 3% shorter than sp 3 C-H. This trend is illustrated by the geometry of ethane, ethylene and acetylene. [citation needed]

  8. Brie Larson on Why the ‘Lessons in Chemistry ... - AOL

    www.aol.com/brie-larson-why-lessons-chemistry...

    SPOILER ALERT: This story contains spoilers from “Introduction to Chemistry,” the series finale of “Lessons in Chemistry,” now streaming on Apple TV+. Elizabeth Zott, hero of the people.

  9. Conjugated system - Wikipedia

    en.wikipedia.org/wiki/Conjugated_system

    Cinnamaldehyde is a naturally-occurring compound that has a conjugated system penta-1,3-diene is a molecule with a conjugated system Diazomethane conjugated pi-system. In theoretical chemistry, a conjugated system is a system of connected p-orbitals with delocalized electrons in a molecule, which in general lowers the overall energy of the molecule and increases stability.