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  2. 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 ...

  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. Carbon group - Wikipedia

    en.wikipedia.org/wiki/Carbon_group

    Carbon is most commonly used in its amorphous form. In this form, carbon is used for steelmaking, as carbon black, as a filling in tires, in respirators, and as activated charcoal. Carbon is also used in the form of graphite, for example as the lead in pencils. Diamond, another form of carbon, is commonly used in jewelry. [18]

  5. Carbon - Wikipedia

    en.wikipedia.org/wiki/Carbon

    Carbon (from Latin carbo 'coal') is a chemical element; it has symbol C and atomic number 6. It is nonmetallic and tetravalent—meaning that its atoms are able to form up to four covalent bonds due to its valence shell exhibiting 4 electrons. It belongs to group 14 of the periodic table. [13]

  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. Orbital hybridisation - Wikipedia

    en.wikipedia.org/wiki/Orbital_hybridisation

    Chemist Linus Pauling first developed the hybridisation theory in 1931 to explain the structure of simple molecules such as methane (CH 4) using atomic orbitals. [2] Pauling pointed out that a carbon atom forms four bonds by using one s and three p orbitals, so that "it might be inferred" that a carbon atom would form three bonds at right angles (using p orbitals) and a fourth weaker bond ...

  8. Fullerene - Wikipedia

    en.wikipedia.org/wiki/Fullerene

    Since each carbon atom is connected to only three neighbors, instead of the usual four, it is customary to describe those bonds as being a mixture of single and double covalent bonds. The hybridization of carbon in C 60 has been reported to be sp 2.01. [58]

  9. 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.