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Other common double bonds are found in azo compounds (N=N), imines (C=N), and sulfoxides (S=O). In a skeletal formula, a double bond is drawn as two parallel lines (=) between the two connected atoms; typographically, the equals sign is used for this. [1] [2] Double bonds were introduced in chemical notation by Russian chemist Alexander Butlerov.
A chemical bond is the association of atoms or ions to form molecules, crystals, and other structures. The bond may result from the electrostatic force between oppositely charged ions as in ionic bonds or through the sharing of electrons as in covalent bonds, or some combination of these effects.
The nitrate ion is one such example with three equivalent structures. The bond between the nitrogen and each oxygen is a double bond in one structure and a single bond in the other two, so that the average bond order for each N–O interaction is 2 + 1 + 1 / 3 = 4 / 3 . [8]
Wavy single bonds represent unknown or unspecified stereochemistry or a mixture of isomers. For example, the adjacent diagram shows the fructose molecule with a wavy bond to the HOCH 2 - group at the left. In this case the two possible ring structures are in chemical equilibrium with each other and also with the open-chain structure.
The nitrogen atom has only 6 electrons assigned to it. One of the lone pairs on an oxygen atom must form a double bond, but either atom will work equally well. Therefore, there is a resonance structure. Tie up loose ends. Two Lewis structures must be drawn: Each structure has one of the two oxygen atoms double-bonded to the nitrogen atom.
A carbon–carbon bond is a covalent bond between two carbon atoms. [1] The most common form is the single bond : a bond composed of two electrons , one from each of the two atoms. The carbon–carbon single bond is a sigma bond and is formed between one hybridized orbital from each of the carbon atoms.
Hydrogen has only one valence electron, but it can form bonds with more than one atom. In the bifluoride ion ([HF 2] −), for example, it forms a three-center four-electron bond with two fluoride atoms: [F−H F − ↔ F − H−F] Another example is the three-center two-electron bond in diborane (B 2 H 6).
Double bonds are shorter than single bonds with an average bond length of 1.33 Å (133 pm) vs 1.53 Å for a typical C-C single bond. [7] Each carbon atom of the double bond uses its three sp 2 hybrid orbitals to form sigma bonds to three atoms (the other carbon atom and two