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  2. Sodium bicarbonate - Wikipedia

    en.wikipedia.org/wiki/Sodium_bicarbonate

    Sodium bicarbonate reacts spontaneously with acids, releasing CO 2 gas as a reaction product. It is commonly used to neutralize unwanted acid solutions or acid spills in chemical laboratories. [32] It is not appropriate to use sodium bicarbonate to neutralize base [33] even though it is amphoteric, reacting with both acids and bases. [34]

  3. Gluconic acid - Wikipedia

    en.wikipedia.org/wiki/Gluconic_acid

    Gluconic acid is typically produced by the aerobic oxidation of glucose in the presence of the enzyme glucose oxidase. The conversion produces gluconolactone and hydrogen peroxide. The lactone spontaneously hydrolyzes to gluconic acid in water. [3] C 6 H 12 O 6 + O 2 → C 6 H 10 O 6 + H 2 O 2 C 6 H 10 O 6 + H 2 O → C 6 H 12 O 7

  4. Saponification - Wikipedia

    en.wikipedia.org/wiki/Saponification

    Typically aqueous sodium hydroxide solutions are used. [1] [2] It is an important type of alkaline hydrolysis. When the carboxylate is long chain, its salt is called a soap. The saponification of ethyl acetate gives sodium acetate and ethanol: C 2 H 5 O 2 CCH 3 + NaOH → C 2 H 5 OH + NaO 2 CCH 3

  5. Tyrode's solution - Wikipedia

    en.wikipedia.org/wiki/Tyrode's_solution

    Tyrode's solution is a solution that is roughly isotonic with interstitial fluid and used in physiological experiments and tissue culture. It resembles lactated Ringer's solution , but contains magnesium , a sugar (usually glucose ) as an energy source and uses bicarbonate and phosphate as a buffer instead of lactate .

  6. Blue bottle experiment - Wikipedia

    en.wikipedia.org/wiki/Blue_bottle_experiment

    The aqueous solution in the classical reaction contains glucose, sodium hydroxide and methylene blue. [14] In the first step an acyloin of glucose is formed. The next step is a redox reaction of the acyloin with methylene blue in which the glucose is oxidized to diketone in alkaline solution [6] and methylene blue is reduced to colorless leucomethylene blue.

  7. Transesterification - Wikipedia

    en.wikipedia.org/wiki/Transesterification

    Transesterification is the process of exchanging the organic functional group R″ of an ester with the organic group R' of an alcohol. These reactions are often catalyzed by the addition of an acid or base catalyst. [1] Strong acids catalyze the reaction by donating a proton to the carbonyl group, thus making it a more potent electrophile.

  8. 5 Tips to Make the Best Alcohol-Free Cocktails, According to ...

    www.aol.com/5-tips-best-alcohol-free-182900197.html

    But when omitting alcohol from a drink you need to consider a range of factors: alcohol adds body and richness to drinks, it balances sweet flavors, and its astringency adds texture.

  9. Acid salt - Wikipedia

    en.wikipedia.org/wiki/Acid_salt

    The solution is expected to be neutral only when K a = K b. [12] Other possible factors that could vary pH level of a solution are the relevant equilibrium constants and the additional amounts of any base or acid. For example, in ammonium chloride solution, NH + 4 is the main influence for acidic solution.