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  2. Acetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetic_acid

    acetyl chloride SOCl 2 acetic acid (i) Li[AlH 4], ether (ii) H 3 O + ethanol Two typical organic reactions of acetic acid Acetic acid undergoes the typical chemical reactions of a carboxylic acid. Upon treatment with a standard base, it converts to metal acetate and water. With strong bases (e.g., organolithium reagents), it can be doubly deprotonated to give LiCH 2 COOLi. Reduction of acetic ...

  3. Autoprotolysis - Wikipedia

    en.wikipedia.org/wiki/Autoprotolysis

    For example, water undergoes autoprotolysis in the self-ionization of water reaction. 2 H 2 O ⇌ OH − + H 3 O + For example, ammonia in its purest form may undergo autoprotolysis: 2 NH 3 ⇌ NH − 2 + NH + 4. Another example is acetic acid: 2 CH 3 COOH ⇌ CH 3 COO − + CH 3 COOH + 2

  4. Acid strength - Wikipedia

    en.wikipedia.org/wiki/Acid_strength

    Acetic acid is said to be a differentiating solvent for the three acids, while water is not. [6]: (p. 217) An important example of a solvent which is more basic than water is dimethyl sulfoxide, DMSO, (). A compound which is a weak acid in water may become a strong acid in DMSO.

  5. Carboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Carboxylic_acid

    In the Koch reaction, the addition of water and carbon monoxide to alkenes or alkynes is catalyzed by strong acids. Hydrocarboxylations involve the simultaneous addition of water and CO. Such reactions are sometimes called "Reppe chemistry." HC≡CH + CO + H 2 O → CH 2 =CH−CO 2 H. Hydrolysis of triglycerides obtained from plant or animal oils.

  6. Sodium acetate - Wikipedia

    en.wikipedia.org/wiki/Sodium_acetate

    It is sometimes produced in a laboratory experiment by the reaction of acetic acid, commonly in the 5–18% solution known as vinegar, with sodium carbonate ("washing soda"), sodium bicarbonate ("baking soda"), or sodium hydroxide ("lye", or "caustic soda"). Any of these reactions produce sodium acetate and water.

  7. Acetic anhydride - Wikipedia

    en.wikipedia.org/wiki/Acetic_anhydride

    Acetic anhydride, or ethanoic anhydride, is the chemical compound with the formula (CH 3 CO) 2 O. Commonly abbreviated Ac 2 O, it is the simplest isolable anhydride of a carboxylic acid and is widely used as a reagent in organic synthesis. It is a colorless liquid that smells strongly of acetic acid, which is formed by its reaction with ...

  8. Magnesium acetate - Wikipedia

    en.wikipedia.org/wiki/Magnesium_acetate

    Synthesis of magnesium acetate from the reaction of magnesium hydroxide with acetic acid. [7] 2 CH 3 COOH + Mg(OH) 2 → (CH 3 COO) 2 Mg + 2 H 2 O. Magnesium carbonate suspended in distilled water with 20% acetic acid solution. [8] 2 CH 3 COOH + MgCO 3 → Mg(CH 3 COO) 2 + CO 2 + H 2 O

  9. Chemical equilibrium - Wikipedia

    en.wikipedia.org/wiki/Chemical_equilibrium

    The catalyst will speed up both reactions thereby increasing the speed at which equilibrium is reached. [2] [6] Although the macroscopic equilibrium concentrations are constant in time, reactions do occur at the molecular level. For example, in the case of acetic acid dissolved in water and forming acetate and hydronium ions,