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  2. 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 ...

  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 between a carbon atom and an oxygen atom ...

  4. 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.

  5. Isovalent hybridization - Wikipedia

    en.wikipedia.org/wiki/Isovalent_hybridization

    Only bonding with 4 equivalent substituents results in exactly sp 3 hybridization. For molecules with different substituents, we can use isovalent hybridization to rationalize the differences in bond angles between different atoms. In the molecule methyl fluoride for example, the HCF bond angle (108.73°) is less than the HCH bond angle (110.2 ...

  6. 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.

  7. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    For a tetrahedral molecule such as difluoromethane with two types of atom bonded to the central atom, the C-F bond to the more electronegative substituent (F) will involve a carbon orbital with less s character than the C-H bond, so that the angle between the C-F bonds is less than the tetrahedral bond angle of 109.5°.

  8. Bond order - Wikipedia

    en.wikipedia.org/wiki/Bond_order

    In carbon monoxide, − C≡O +, the bond order between carbon and oxygen is 3. In thiazyl trifluoride N≡SF 3, the bond order between sulfur and nitrogen is 3, and between sulfur and fluorine is 1. In diatomic oxygen O=O the bond order is 2 (double bond). In ethylene H 2 C=CH 2 the bond order between the two carbon atoms is also 2. The bond ...

  9. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehyde molecules have a central carbon atom that is connected by a double bond to oxygen, a single bond to hydrogen and another single bond to a third substituent, which is carbon or, in the case of formaldehyde, hydrogen. The central carbon is often described as being sp 2-hybridized. The aldehyde group is somewhat polar.