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  2. Carbon–nitrogen bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–nitrogen_bond

    Similar to carbon–carbon bonds, these bonds can form stable double bonds, as in imines; and triple bonds, such as nitriles. Bond lengths range from 147.9 pm for simple amines to 147.5 pm for C-N= compounds such as nitromethane to 135.2 pm for partial double bonds in pyridine to 115.8 pm for triple bonds as in nitriles. [2]

  3. Triple bond - Wikipedia

    en.wikipedia.org/wiki/Triple_bond

    Triple bonds are stronger than the equivalent single bonds or double bonds, with a bond order of three. The most common triple bond is in a nitrogen N 2 molecule; the second most common is that between two carbon atoms, which can be found in alkynes. Other functional groups containing a triple bond are cyanides and isocyanides.

  4. 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.

  5. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    A 3D model of ethylene, the simplest alkene. In organic chemistry, an alkene, or olefin, is a hydrocarbon containing a carbon–carbon double bond. [1] The double bond may be internal or in the terminal position.

  6. Linnett double-quartet theory - Wikipedia

    en.wikipedia.org/wiki/Linnett_Double-Quartet_Theory

    [1] [25] Most strikingly, the molecule changes its geometry upon excitation, going from a simple linear symmetry to a trans-bent structure. This is in excellent agreement with both the landmark results of Ingold and King, [ 26 ] which were the first demonstration of an excited state having a qualitatively different geometry than the ground ...

  7. Bond length - Wikipedia

    en.wikipedia.org/wiki/Bond_length

    A table with experimental single bonds for carbon to other elements is given below. Bond lengths are given in picometers.By approximation the bond distance between two different atoms is the sum of the individual covalent radii (these are given in the chemical element articles for each element).

  8. Simple Lie group - Wikipedia

    en.wikipedia.org/wiki/Simple_Lie_group

    Once these are known, the ones with non-trivial center are easy to list as follows. Any simple Lie group with trivial center has a universal cover whose center is the fundamental group of the simple Lie group. The corresponding simple Lie groups with non-trivial center can be obtained as quotients of this universal cover by a subgroup of the ...

  9. Peptide bond - Wikipedia

    en.wikipedia.org/wiki/Peptide_bond

    Peptide bond formation via dehydration reaction. When two amino acids form a dipeptide through a peptide bond, [1] it is a type of condensation reaction. [2] In this kind of condensation, two amino acids approach each other, with the non-side chain (C1) carboxylic acid moiety of one coming near the non-side chain (N2) amino moiety of the other.