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  2. Conjugate (acid-base theory) - Wikipedia

    en.wikipedia.org/wiki/Conjugate_(acid-base_theory)

    A conjugate acid, within the Brønsted–Lowry acid–base theory, is a chemical compound formed when an acid gives a proton (H +) to a base—in other words, it is a base with a hydrogen ion added to it, as it loses a hydrogen ion in the reverse reaction.

  3. Brønsted–Lowry acid–base theory - Wikipedia

    en.wikipedia.org/wiki/Brønsted–Lowry_acid...

    H 2 O is a base because it accepts a proton from CH 3 COOH and becomes its conjugate acid, the hydronium ion, (H 3 O +). [9] The reverse of an acid–base reaction is also an acid–base reaction, between the conjugate acid of the base in the first reaction and the conjugate base of the acid.

  4. Resonance (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Resonance_(chemistry)

    Contributing structures of the carbonate ion. In chemistry, resonance, also called mesomerism, is a way of describing bonding in certain molecules or polyatomic ions by the combination of several contributing structures (or forms, [1] also variously known as resonance structures or canonical structures) into a resonance hybrid (or hybrid structure) in valence bond theory.

  5. Hydrogen ion - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_ion

    By definition, an acid is an ion or molecule that can donate a proton, and when introduced to a solution it will react with water molecules (H 2 O) to form a hydronium ion (H 3 O +), a conjugate acid of water. [4] For simplistic reasoning, the hydrogen ion (H +) is often used to abbreviate the hydronium ion.

  6. Deprotonation - Wikipedia

    en.wikipedia.org/wiki/Deprotonation

    Acid–base reactions typically occur faster than any other step which may determine the product of a reaction. The conjugate base is more electron-rich than the molecule which can alter the reactivity of the molecule. For example, deprotonation of an alcohol forms the negatively charged alkoxide, which is a much stronger nucleophile.

  7. Carbonyl α-substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_α-substitution...

    As a result, enolate ions are more common than enols in both laboratory and biological chemistry. Because they are resonance hybrids of two nonequivalent forms, enolate ions can be looked at either as vinylic alkoxides (C=C- O −) or as α-ketocarbanions (− C-C= O). Thus, enolate ions can react with electrophiles either on oxygen or on carbon.

  8. Acid–base reaction - Wikipedia

    en.wikipedia.org/wiki/Acid–base_reaction

    An acid–base reaction is, thus, the removal of a hydrogen ion from the acid and its addition to the base. [21] The removal of a hydrogen ion from an acid produces its conjugate base, which is the acid with a hydrogen ion removed. The reception of a proton by a base produces its conjugate acid, which is the base with a hydrogen ion added.

  9. Azide - Wikipedia

    en.wikipedia.org/wiki/Azide

    In chemistry, azide (/ ˈ eɪ z aɪ d /, AY-zyd) is a linear, polyatomic anion with the formula N − 3 and structure − N=N + =N −.It is the conjugate base of hydrazoic acid HN 3. Organic azides are organic compounds with the formula RN 3, containing the azide functional group. [1]