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  2. Element–reactant–product table - Wikipedia

    en.wikipedia.org/wiki/Element–reactant...

    An elementreaction–product table is used to find coefficients while balancing an equation representing a chemical reaction. Coefficients represent moles of a substance so that the number of atoms produced is equal to the number of atoms being reacted with. [1] This is the common setup: Element: all the elements that are in the reaction ...

  3. Kolbe electrolysis - Wikipedia

    en.wikipedia.org/wiki/Kolbe_electrolysis

    The Kolbe reaction is formally a decarboxylative dimerisation of two carboxylic acids (or carboxylate ions). The overall reaction is: The overall reaction is: If a mixture of two different carboxylates are used, all combinations of them are generally seen as the organic product structures:

  4. Sodium hydroxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_hydroxide

    Sodium hydroxide can form several hydrates NaOH·nH 2 O, which result in a complex solubility diagram that was described in detail by Spencer Umfreville Pickering in 1893. [18] The known hydrates and the approximate ranges of temperature and concentration (mass percent of NaOH) of their saturated water solutions are: [13]

  5. 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.

  6. Energy profile (chemistry) - Wikipedia

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

    Figure 6:Reaction Coordinate Diagrams showing reactions with 0, 1 and 2 intermediates: The double-headed arrow shows the first, second and third step in each reaction coordinate diagram. In all three of these reactions the first step is the slow step because the activation energy from the reactants to the transition state is the highest.

  7. Ketone halogenation - Wikipedia

    en.wikipedia.org/wiki/Ketone_halogenation

    Reaction mechanism for the bromination of acetone while in the presence of acetic acid. Basic (in aqueous NaOH): Reaction mechanism for the bromination of acetone while in the presence of aqueous NaOH. In acidic solution, usually only one alpha hydrogen is replaced by a halogen, as each successive halogenation is slower than the first.

  8. Sodium acetate - Wikipedia

    en.wikipedia.org/wiki/Sodium_acetate

    This is the reaction taking place in the well-known "volcano" that occurs when the household products, baking soda and vinegar, are combined. CH 3 COOH + NaHCO 3 → CH 3 COONa + H 2 CO 3 H 2 CO 3 → CO 2 + H 2 O. Industrially, sodium acetate trihydrate is prepared by reacting acetic acid with sodium hydroxide using water as the solvent. CH 3 ...

  9. Castner process - Wikipedia

    en.wikipedia.org/wiki/Castner_process

    The cathode reaction is 2 Na + + 2 e − → 2Na. The anode reaction is 4 OH − → O 2 + 2 H 2 O + 4 e −. Despite the elevated temperature, some of the water produced remains dissolved in the electrolyte. [4] This water diffuses throughout the electrolyte and results in the reverse reaction taking place on the electrolyzed sodium metal: