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  2. Double bond - Wikipedia

    en.wikipedia.org/wiki/Double_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. 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 ...

  3. 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 ...

  4. Wikipedia:Molecular structure diagram - Wikipedia

    en.wikipedia.org/wiki/Wikipedia:Molecular...

    Three dimensionality is best highlighted by the depictions of bonds, using wedges, bolding, and hashed formats. Some artists highlight three-dimensionality by varying fonts sizes, e.g. slightly larger fonts for the "front" atoms. In organic chemistry, double bonds and C-H bonds are shorter than most single bonds.

  5. Carbonyl group - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_group

    The polarity of C=O bond also enhances the acidity of any adjacent C-H bonds. Due to the positive charge on carbon and the negative charge on oxygen, carbonyl groups are subject to additions and/or nucleophilic attacks. A variety of nucleophiles attack, breaking the carbon-oxygen double bond, and leading to addition-elimination reactions.

  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. Methylene group - Wikipedia

    en.wikipedia.org/wiki/Methylene_group

    The group may be represented as −CH 2 − or >CH 2, where the '>' denotes the two bonds. This stands in contrast to a situation where the carbon atom is bound to the rest of the molecule by a double bond, which is preferably called a methylidene group, represented =CH 2. [2] Formerly the methylene name was used for both isomers.

  8. Structural formula - Wikipedia

    en.wikipedia.org/wiki/Structural_formula

    Skeletal structural formula of Vitamin B 12.Many organic molecules are too complicated to be specified by a molecular formula.. The structural formula of a chemical compound is a graphic representation of the molecular structure (determined by structural chemistry methods), showing how the atoms are possibly arranged in the real three-dimensional space.

  9. Allenes - Wikipedia

    en.wikipedia.org/wiki/Allenes

    In organic chemistry, allenes are organic compounds in which one carbon atom has double bonds with each of its two adjacent carbon atoms (R 2 C=C=CR 2, where R is H or some organyl group). [1] Allenes are classified as cumulated dienes. The parent compound of this class is propadiene (H 2 C=C=CH 2), which is itself also called allene.