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  2. Pi bond - Wikipedia

    en.wikipedia.org/wiki/Pi_bond

    Two p-orbitals forming a π-bond. Pi bonds are usually weaker than sigma bonds.The C-C double bond, composed of one sigma and one pi bond, [1] has a bond energy less than twice that of a C-C single bond, indicating that the stability added by the pi bond is less than the stability of a sigma bond.

  3. Double bond - Wikipedia

    en.wikipedia.org/wiki/Double_bond

    In chemistry, a double bond is a covalent bond between two atoms involving four bonding electrons as opposed to two in a single bond. Double bonds occur most commonly between two carbon atoms, for example in alkenes. Many double bonds exist between two different elements: for example, in a carbonyl group

  4. Carbon–carbon bond - Wikipedia

    en.wikipedia.org/wiki/Carboncarbon_bond

    In fact, the carbon atoms in the single bond need not be of the same hybridization. Carbon atoms can also form double bonds in compounds called alkenes or triple bonds in compounds called alkynes. A double bond is formed with an sp 2-hybridized orbital and a p-orbital that is not involved in the hybridization. A triple bond is formed with an sp ...

  5. Double bond rule - Wikipedia

    en.wikipedia.org/wiki/Double_bond_rule

    Moreover, the multiple bonds of the elements with n=2 are much stronger than usual, because lone pair repulsion weakens their sigma bonding but not their pi bonding. [2] An example is the rapid polymerization that occurs upon condensation of disulfur , the heavy analogue of O 2 .

  6. Degree of unsaturation - Wikipedia

    en.wikipedia.org/wiki/Degree_of_unsaturation

    For hydrocarbons, the DBE (or IHD) tells us the number of rings and/or extra bonds in a non-saturated structure, which equals the number of hydrogen pairs that are required to make the structure saturated, simply because joining two elements to form a ring or adding one extra bond (e.g., a single bond changed to a double bond) in a structure reduces the need for two H's.

  7. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    In 1 H NMR spectroscopy, the hydrogen bonded to the carbon adjacent to double bonds will give a δ H of 4.5–6.5 ppm. The double bond will also deshield the hydrogen attached to the carbons adjacent to sp 2 carbons, and this generates δ H =1.6–2. ppm peaks. [14] Cis/trans isomers are distinguishable due to different J-coupling effect.

  8. Aromaticity - Wikipedia

    en.wikipedia.org/wiki/Aromaticity

    The single bonds are formed with electrons in line between the carbon nuclei — these are called σ-bonds. Double bonds consist of a σ-bond and a π-bond. The π-bonds are formed from overlap of atomic p-orbitals above and below the plane of the ring. The following diagram shows the positions of these p-orbitals:

  9. Allenes - Wikipedia

    en.wikipedia.org/wiki/Allenes

    The central carbon atom of allenes forms two sigma bonds and two pi bonds. The central carbon atom is sp-hybridized, and the two terminal carbon atoms are sp 2-hybridized. The bond angle formed by the three carbon atoms is 180°, indicating linear geometry for the central carbon atom.