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  2. Lewis acids and bases - Wikipedia

    en.wikipedia.org/wiki/Lewis_acids_and_bases

    The E and C parameters refer, respectively, to the electrostatic and covalent contributions to the strength of the bonds that the acid and base will form. The equation is −ΔH = E A E B + C A C B + W. The W term represents a constant energy contribution for acid–base reaction such as the cleavage of a dimeric acid or base.

  3. Ethylene - Wikipedia

    en.wikipedia.org/wiki/Ethylene

    Ethylene (IUPAC name: ethene) is a hydrocarbon which has the formula C 2 H 4 or H 2 C=CH 2. It is a colourless, flammable gas with a faint "sweet and musky " odour when pure. [ 7 ] It is the simplest alkene (a hydrocarbon with carbon–carbon double bonds ).

  4. Pi bond - Wikipedia

    en.wikipedia.org/wiki/Pi_bond

    Ethylene (ethene), a small organic molecule containing a pi bond, shown in green.. In chemistry, pi bondsbonds) are covalent chemical bonds, in each of which two lobes of an orbital on one atom overlap with two lobes of an orbital on another atom, and in which this overlap occurs laterally.

  5. Covalent bond - Wikipedia

    en.wikipedia.org/wiki/Covalent_bond

    In organic chemistry, covalent bonding is much more common than ionic bonding. Covalent bonding also includes many kinds of interactions, including σ-bonding, π-bonding, metal-to-metal bonding, agostic interactions, bent bonds, three-center two-electron bonds and three-center four-electron bonds. [2] [3] The term covalent bond dates from 1939 ...

  6. Electrophilic addition - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_addition

    In organic chemistry, an electrophilic addition (A E) reaction is an addition reaction where a chemical compound containing a double or triple bond has a π bond broken, with the formation of two new σ bonds. [1] The driving force for this reaction is the formation of an electrophile X + that forms a covalent bond with an electron-rich ...

  7. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    The π bonds of alkenes hydrocarbons are also susceptible to hydration. The reaction usually involves strong acid as catalyst. [19] The first step in hydration often involves formation of a carbocation. The net result of the reaction will be an alcohol. The reaction equation for hydration of ethylene is: H 2 C=CH 2 + H 2 O→ H 3 C-CH 2 OH

  8. Hydration reaction - Wikipedia

    en.wikipedia.org/wiki/Hydration_reaction

    In chemistry, a hydration reaction is a chemical reaction in which a substance combines with water. In organic chemistry, water is added to an unsaturated substrate, which is usually an alkene or an alkyne. This type of reaction is employed industrially to produce ethanol, isopropanol, and butan-2-ol. [1]

  9. 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