Alkaline Hydrolysis
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Alkaline Hydrolysis
Alkaline hydrolysis, in organic chemistry, usually refers to types of nucleophilic substitution reactions in which the attacking nucleophile is a hydroxide ion. Example In the alkaline hydrolysis of esters and amides the hydroxide ion nucleophile attacks the carbonyl carbon in a nucleophilic acyl substitution reaction. This mechanism is supported by isotope labeling experiments. For example, when ethyl propionate with an oxygen-18 labeled ethoxy group is treated with sodium hydroxide (NaOH), the oxygen-18 is completely absent from the sodium propionate product and is found exclusively in the ethanol formed. Uses The reaction is often used to turn solid organic matter into a liquid form for easier disposal. Drain cleaners take advantage of this method to dissolve hair and fat in pipes. The reaction is also used to dispose of human and other animal remains as an alternative to traditional burial or cremation. See also * Acid hydrolysis * Enzymatic hydrolysis * Saponificati ...
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Organic Chemistry
Organic chemistry is a subdiscipline within chemistry involving the scientific study of the structure, properties, and reactions of organic compounds and organic materials, i.e., matter in its various forms that contain carbon atoms.Clayden, J.; Greeves, N. and Warren, S. (2012) ''Organic Chemistry''. Oxford University Press. pp. 1–15. . Study of structure determines their structural formula. Study of properties includes physical and chemical properties, and evaluation of chemical reactivity to understand their behavior. The study of organic reactions includes the chemical synthesis of natural products, drugs, and polymers, and study of individual organic molecules in the laboratory and via theoretical ( in silico) study. The range of chemicals studied in organic chemistry includes hydrocarbons (compounds containing only carbon and hydrogen) as well as compounds based on carbon, but also containing other elements, especially oxygen, nitrogen, sulfur, phosphorus (included in ...
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Sodium Hydroxide
Sodium hydroxide, also known as lye and caustic soda, is an inorganic compound with the formula NaOH. It is a white solid ionic compound consisting of sodium cations and hydroxide anions . Sodium hydroxide is a highly caustic base and alkali that decomposes proteins at ordinary ambient temperatures and may cause severe chemical burns. It is highly soluble in water, and readily absorbs moisture and carbon dioxide from the air. It forms a series of hydrates . The monohydrate crystallizes from water solutions between 12.3 and 61.8 °C. The commercially available "sodium hydroxide" is often this monohydrate, and published data may refer to it instead of the anhydrous compound. As one of the simplest hydroxides, sodium hydroxide is frequently used alongside neutral water and acidic hydrochloric acid to demonstrate the pH scale to chemistry students. Sodium hydroxide is used in many industries: in the manufacture of pulp and paper, textiles, drinking water, soaps and deterge ...
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Saponification
Saponification is a process of converting esters into soaps and alcohols by the action of aqueous alkali (for example, aqueous sodium hydroxide solutions). Soaps are salts of fatty acids, which in turn are carboxylic acids with long carbon chains. Sodium stearate is a typical soap. Saponification of fats Vegetable oils and animal fats are the traditional materials that are saponified. These greasy materials, triesters called triglycerides, are mixtures derived from diverse fatty acids. Triglycerides can be converted to soap in either a one- or a two-step process. In the traditional one-step process, the triglyceride is treated with a strong base (e.g. lye), which cleaves the ester bond, releasing fatty acid salts (soaps) and glycerol. This process is also the main industrial method for producing glycerol. In some soap-making, the glycerol is left in the soap. If necessary, soaps may be precipitated by salting it out with sodium chloride. Fat in a corpse converts into adipoce ...
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Enzymatic Hydrolysis
In biochemistry, enzymatic hydrolysis is a process in which enzymes facilitate the cleavage of bonds in molecules with the addition of the elements of water (i.e. hydrolysis). It plays an important role in the digestion of food. It may be used to help provide renewable energy, as with cellulosic ethanol.Ethanol from biomass by enzymatic hydrolysis - JD Wright - Chemical Engineering Progress, 1988 osti.gov/ref> See also *Acid hydrolysis *Alkaline hydrolysis *Digestion enzyme Digestive enzymes are a group of enzymes that break down polymeric macromolecules into their smaller building blocks, in order to facilitate their absorption into the cells of the body. Digestive enzymes are found in the digestive tracts of anim ... References Digestive system {{enzyme-stub ...
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Acid Hydrolysis
In organic chemistry, acid hydrolysis is a hydrolysis process in which a protic acid is used to catalyze the cleavage of a chemical bond via a nucleophilic substitution reaction, with the addition of the elements of water (H2O). For example, in the conversion of cellulose or starch to glucose. For the case of esters and amides, it can be defined as an acid catalyzed nucleophilic acyl substitution reaction. The term is also applied to certain nucleophilic addition reactions, such as in the acid catalyzed hydrolysis of nitriles to amides. Acid hydrolysis ''does not'' usually refer to the acid catalyzed addition of the elements of water to double or triple bonds by electrophilic addition as may originate from a hydration reaction. Acid hydrolysis is used to prepare monosaccharide with the help of acids, such as: * Hydrochloric acid * Sulfuric acid * Trifluoroacetic acid * Formic acid * Nitric acid Acid hydrolysis can be utilized in the pretreatment of cellulosic material, so as to ...
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Alkaline Hydrolysis (body Disposal)
Alkaline hydrolysis (also called biocremation, resomation, flameless cremation, aquamation or water cremation) is a process for the disposal of human and pet remains using lye and heat, and is an alternative to burial or cremation. Process The process is based on alkaline hydrolysis: the body is placed in a pressure vessel that is then filled with a mixture of water and potassium hydroxide, and heated to a temperature around , but at an elevated pressure, which prevents boiling. Instead, the body is effectively broken down into its chemical components, which takes approximately four to six hours. A lower temperature and pressure may be used, but at a longer duration (, 14 to 16 hours). At the beginning of the process, the mixture is fairly basic, with a pH level of approximately 14; pH drops to 11 by the end, but the final pH level depends on the total operation time and the amount of fat in the body. The result is a quantity of green-brown tinted liquid (containing amino acids ...
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Drain Cleaner
A drain cleaner is method for unblocking sewer pipes or clogged wastewater drains. The term may also refer to a mechanical device such as a plumber's snake, drain auger, toilet plunger, or similar device. Occasionally, the term is applied to a plumber or other individual who performs the drain cleaning and hygiene. Chemical drain cleaners can also be used. * Chemical drain cleaners, plungers, handheld drain augers, and air burst drain cleaners are typically applied to the problem of a clogged single drain, such as a sink, toilet, tub, or shower drain. An effective drain cleaner can remove soft obstructions (such as hair and grease) accumulating near the fixture's drain inlet. *If more than one plumbing fixture is clogged then electric drain cleaners, battery powered drain cleaners, sewer jetters or such mechanical devices are usually required to clear obstructions along the entire length of the drain piping system, that is, from fixture drain inlets through the main building drai ...
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Nucleophilic Acyl Substitution With A Labeled Oxygen
In chemistry, a nucleophile is a chemical species that forms bonds by donating an electron pair. All molecules and ions with a free pair of electrons or at least one pi bond can act as nucleophiles. Because nucleophiles donate electrons, they are Lewis bases. ''Nucleophilic'' describes the affinity of a nucleophile to bond with positively charged atomic nuclei. Nucleophilicity, sometimes referred to as nucleophile strength, refers to a substance's nucleophilic character and is often used to compare the affinity of atoms. Neutral nucleophilic reactions with solvents such as alcohols and water are named solvolysis. Nucleophiles may take part in nucleophilic substitution, whereby a nucleophile becomes attracted to a full or partial positive charge, and nucleophilic addition. Nucleophilicity is closely related to basicity. History The terms ''nucleophile'' and ''electrophile'' were introduced by Christopher Kelk Ingold in 1933, replacing the terms ''anionoid'' and ''cationoid'' p ...
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Ethanol
Ethanol (abbr. EtOH; also called ethyl alcohol, grain alcohol, drinking alcohol, or simply alcohol) is an organic compound. It is an Alcohol (chemistry), alcohol with the chemical formula . Its formula can be also written as or (an ethyl group linked to a hydroxyl group). Ethanol is a Volatility (chemistry), volatile, Combustibility and flammability, flammable, colorless liquid with a characteristic wine-like odor and pungent taste. It is a psychoactive recreational drug, the active ingredient in alcoholic drinks. Ethanol is naturally produced by the fermentation process of Carbohydrate, sugars by yeasts or via Petrochemistry, petrochemical processes such as ethylene hydration. It has medical applications as an antiseptic and disinfectant. It is used as a chemical solvent and in the Chemical synthesis, synthesis of organic compounds, and as a Alcohol fuel, fuel source. Ethanol also can be dehydrated to make ethylene, an important chemical feedstock. As of 2006, world produ ...
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Sodium Propionate
Sodium propanoate or sodium propionate is the sodium salt of propionic acid which has the chemical formula Na( C2 H5 C O O). This white crystalline solid is deliquescent in moist air. Reactions It is produced by the reaction of propionic acid and sodium carbonate or sodium hydroxide. Uses It is used as a food preservative and is represented by the food labeling E number E281 in Europe; it is used primarily as a mold inhibitor in bakery products. It is approved for use as a food additive in the EU, USA and Australia and New ZealandAustralia New Zealand Food Standards Code (where it is listed by its INS number 281). See also * Propionic acid, E 280 * Calcium propionate, E 282 * Potassium propionate Potassium propanoate or potassium propionate has formula K(C2H5COO). Its melting point is 410 °C. It is the potassium salt of propanoic acid. Use It is used as a food preservative and is represented by the food labeling E number E283 in Europe ..., E 283 References External li ...
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Oxygen-18
Oxygen-18 (, Ω) is a natural, stable isotope of oxygen and one of the environmental isotopes. is an important precursor for the production of fluorodeoxyglucose (FDG) used in positron emission tomography (PET). Generally, in the radiopharmaceutical industry, enriched water () is bombarded with hydrogen ions in either a cyclotron or linear accelerator, creating fluorine-18. This is then synthesized into FDG and injected into a patient. It can also be used to make an extremely heavy version of water when combined with tritium (hydrogen-3): or . This compound has a density almost 30% greater than that of natural water. The accurate measurements of rely on proper procedures of analysis, sample preparation and storage. Paleoclimatology In ice cores, mainly Arctic and Antarctic, the ratio of to (known as δ) can be used to determine the temperature of precipitation through time. Assuming that atmospheric circulation and elevation has not changed significantly over the poles, ...
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Nucleophilic Substitution
In chemistry, a nucleophilic substitution is a class of chemical reactions in which an electron-rich chemical species (known as a nucleophile) replaces a functional group within another electron-deficient molecule (known as the electrophile). The molecule that contains the electrophile and the leaving functional group is called the substrate. The most general form of the reaction may be given as the following: :\text\mathbf + \ce + \text\mathbf The electron pair (:) from the nucleophile (Nuc) attacks the substrate () and bonds with it. Simultaneously, the leaving group (LG) departs with an electron pair. The principal product in this case is . The nucleophile may be electrically neutral or negatively charged, whereas the substrate is typically neutral or positively charged. An example of nucleophilic substitution is the hydrolysis of an alkyl bromide, R-Br under basic conditions, where the attacking nucleophile is hydroxyl () and the leaving group is bromide (). :R-Br + OH- ...
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