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  2. Acetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetic_acid

    Dimers also occur in the liquid phase in dilute solutions with non-hydrogen-bonding solvents, and to a certain extent in pure acetic acid, [23] but are disrupted by hydrogen-bonding solvents. The dissociation enthalpy of the dimer is estimated at 65.0–66.0 kJ/mol, and the dissociation entropy at 154–157 J mol −1 K −1 . [ 24 ]

  3. Dimerization - Wikipedia

    en.wikipedia.org/wiki/Dimerization

    Dimers of carboxylic acids are often found in the vapour phase.. Anhydrous carboxylic acids form dimers by hydrogen bonding of the acidic hydrogen and the carbonyl oxygen. For example, acetic acid forms a dimer in the gas phase, where the monomer units are held together by hydrogen bonds. [3]

  4. Insertion reaction - Wikipedia

    en.wikipedia.org/wiki/Insertion_reaction

    The former converts alkenes, hydrogen, and carbon monoxide into aldehydes. The production of acetic acid by carbonylation proceeds via two similar industrial processes. More traditional is the rhodium-based Monsanto acetic acid process, but this process has been superseded by the iridium-based Cativa process. [23] [24] By 2002, worldwide annual ...

  5. Aldol condensation - Wikipedia

    en.wikipedia.org/wiki/Aldol_condensation

    A mechanism for aldol condensation in basic conditions, which occurs via enolate intermediates and E1CB elimination. The process begins when a free hydroxide (strong base) strips the highly acidic proton at the alpha carbon of the aldehyde. This deprotonation causes the electrons from the C–H bond to shift and create a new C–C pi bond.

  6. Ester - Wikipedia

    en.wikipedia.org/wiki/Ester

    An ester of a carboxylic acid.R stands for any group (typically hydrogen or organyl) and R ′ stands for any organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (R ′). [1]

  7. Deprotonation - Wikipedia

    en.wikipedia.org/wiki/Deprotonation

    Deprotonation of acetic acid by a hydroxide ion. Deprotonation (or dehydronation) is the removal (transfer) of a proton (or hydron, or hydrogen cation), (H +) from a Brønsted–Lowry acid in an acid–base reaction. [1] [2] The species formed is the conjugate base of that acid.

  8. Cyanohydrin reaction - Wikipedia

    en.wikipedia.org/wiki/Cyanohydrin_reaction

    The chemist Urech in 1872 was the first to synthesize cyanohydrins from ketones with alkali cyanides and acetic acid [2] and therefore this reaction also goes by the name of Urech cyanohydrin method. References

  9. Hydroxy group - Wikipedia

    en.wikipedia.org/wiki/Hydroxy_group

    Representation of an organic compound hydroxy group, where R represents a hydrocarbon or other organic moiety, the red and grey spheres represent oxygen and hydrogen atoms respectively, and the rod-like connections between these, covalent chemical bonds. In chemistry, a hydroxy or hydroxyl group is a functional group with the chemical formula ...