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Sarett Oxidation
The Sarett oxidation is an organic reaction that oxidizes primary and secondary alcohols to aldehydes and ketones, respectively, using chromium trioxide and pyridine. Unlike the similar Jones oxidation, the Sarett oxidation will not further oxidize primary alcohols to their carboxylic acid form, neither will it affect carbon-carbon double bonds. Use of the original Sarett oxidation has become largely antiquated however, in favor of other modified oxidation techniques. The unadulterated reaction is still occasionally used in teaching settings and in small scale laboratory research. History First appearance The reaction is named after the American chemist Lewis Hastings Sarett (1917–1999). The first description of its use appears in a 1953 article co-authored by Sarett that relates to the synthesis of adrenal steroids. The paper proposes the use of the pyridine chromium complex CrO3-2C5H5N to oxidize primary and secondary alcohols. The complex would later become known as the ...
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Lewis Hastings Sarett
Lewis Hastings Sarett (December 22, 1917 – November 29, 1999) was an American organic chemist. While serving as a research scientist at Merck & Co., Inc., synthesized cortisone. Biography He was born in Champaign, Illinois. His father was Lew Sarett, a renowned Jewish poet and professor and an uncle of former Secretary of Defense Donald Rumsfeld. He lived in Laona, Wisconsin for a time and then attended high school in Highland Park, Illinois . He received a Bachelor of Science from Northwestern University in 1939 (Phi Beta Kappa) and his doctorate from Princeton University. He worked for Merck & Co. for 38 years retiring in 1982. He invented a Process of Treating Pregnene Compounds Cortisone, Patent Number 2,462,133. Named after him is the Sarett Oxidation which is the oxidation of an alcohol to a ketone or an aldehyde using chromic oxide and pyridine. Primary alcohols will be oxidised to aldehydes and not carboxylic acids. Writing career He is also famous for writing the ...
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Collins Reagent
Collins reagent is the complex of chromium(VI) oxide with pyridine in dichloromethane. This metal-pyridine complex, a red solid, is used to oxidize primary alcohols to the corresponding aldehydes and secondary alcohols to the corresponding ketones. This complex is a hygroscopic orange solid. Synthesis and structure The complex is produced by treating chromium trioxide with pyridine. The complex is diamagnetic. According to X-ray crystallography, the complex is 5-coordinate with mutually trans pyridine ligands. The Cr-O and Cr-N distances are respectively 163 and 215 picometers. In terms of history, the complex was first produced by Sisler et al. Reactions Collins reagent is especially useful for oxidations of acid sensitive compounds. Primary and secondary alcohols are oxidized respectively to aldehydes and ketones in yields of 87-98%. Like other oxidations by Cr(VI), the stoichiometry of the oxidations is complex because the metal undergoes 3e reduction and the substrate ...
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Pyridinium Chlorochromate
Pyridinium chlorochromate (PCC) is a yellow-orange salt (chemistry), salt with the chemical formula, formula [C5H5NH]+[CrO3Cl]−. It is a reagent in organic synthesis used primarily for organic redox reaction, oxidation of Alcohol (chemistry), alcohols to form carbonyls. A variety of related compounds are known with similar reactivity. PCC offers the advantage of the selective oxidation of alcohols to aldehydes or ketones, whereas many other reagents are less selective. Structure and preparation PCC consists of a pyridinium cation, [C5H5NH]+, and a tetrahedral chlorochromate anion, [CrO3Cl]−. Related salts are also known, such as 1-butylpyridinium chlorochromate, [C5H5N(C4H9)][CrO3Cl] and potassium chlorochromate. PCC is commercially available. Discovered by accident, the reagent was originally prepared via addition of pyridine into a cold solution of chromium trioxide in concentrated hydrochloric acid: :C5H5N + HCl + CrO3 → [C5H5NH][CrO3Cl] In one alternative method, form ...
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Thioether
In organic chemistry, an organic sulfide (British English sulphide) or thioether is an organosulfur functional group with the connectivity as shown on right. Like many other sulfur-containing compounds, volatile sulfides have foul odors. A sulfide is similar to an ether except that it contains a sulfur atom in place of the oxygen. The grouping of oxygen and sulfur in the periodic table suggests that the chemical properties of ethers and sulfides are somewhat similar, though the extent to which this is true in practice varies depending on the application. Nomenclature Sulfides are sometimes called thioethers, especially in the old literature. The two organic substituents are indicated by the prefixes. (CH3)2S is called dimethylsulfide. Some sulfides are named by modifying the common name for the corresponding ether. For example, C6H5SCH3 is methyl phenyl sulfide, but is more commonly called thioanisole, since its structure is related to that for anisole, C6H5OCH3. The modern sy ...
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Double Bond
In chemistry, a double bond is a covalent bond between two atoms involving four bonding electrons as opposed to two in a single bond. Double bonds occur most commonly between two carbon atoms, for example in alkenes. Many double bonds exist between two different elements: for example, in a carbonyl group between a carbon atom and an oxygen atom. Other common double bonds are found in azo compounds (N=N), imines (C=N), and sulfoxides (S=O). In a skeletal formula, a double bond is drawn as two parallel lines (=) between the two connected atoms; typographically, the equals sign is used for this. Double bonds were first introduced in chemical notation by Russian chemist Alexander Butlerov. Double bonds involving carbon are stronger and shorter than single bonds. The bond order is two. Double bonds are also electron-rich, which makes them potentially more reactive in the presence of a strong electron acceptor (as in addition reactions of the halogens). File:Ethene structural.svg ...
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Protecting Groups
A protecting group or protective group is introduced into a molecule by chemical modification of a functional group to obtain chemoselectivity in a subsequent chemical reaction. It plays an important role in multistep organic synthesis. In many preparations of delicate organic compounds, some specific parts of their molecules cannot survive the required reagents or chemical environments. Then, these parts, or groups, must be protected. For example, lithium aluminium hydride is a highly reactive but useful reagent capable of reducing esters to alcohols. It will always react with carbonyl groups, and this cannot be discouraged by any means. When a reduction of an ester is required in the presence of a carbonyl, the attack of the hydride on the carbonyl has to be prevented. For example, the carbonyl is converted into an acetal, which does not react with hydrides. The acetal is then called a protecting group for the carbonyl. After the step involving the hydride is complete, the ace ...
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Basic (chemistry)
In chemistry, there are three definitions in common use of the word base, known as Arrhenius bases, Brønsted bases, and Lewis bases. All definitions agree that bases are substances that react with acids, as originally proposed by G.-F. Rouelle in the mid-18th century. In 1884, Svante Arrhenius proposed that a base is a substance which dissociates in aqueous solution to form Hydroxide ions OH−. These ions can react with hydrogen ions (H+ according to Arrhenius) from the dissociation of acids to form water in an acid–base reaction. A base was therefore a metal hydroxide such as NaOH or Ca(OH)2. Such aqueous hydroxide solutions were also described by certain characteristic properties. They are slippery to the touch, can taste bitter and change the color of pH indicators (e.g., turn red litmus paper blue). In water, by altering the autoionization equilibrium, bases yield solutions in which the hydrogen ion activity is lower than it is in pure water, i.e., the water has ...
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Redox COOH And CrO3 2
Redox (reduction–oxidation, , ) is a type of chemical reaction in which the oxidation states of substrate change. Oxidation is the loss of electrons or an increase in the oxidation state, while reduction is the gain of electrons or a decrease in the oxidation state. There are two classes of redox reactions: * ''Electron-transfer'' – Only one (usually) electron flows from the reducing agent to the oxidant. This type of redox reaction is often discussed in terms of redox couples and electrode potentials. * ''Atom transfer'' – An atom transfers from one substrate to another. For example, in the rusting of iron, the oxidation state of iron atoms increases as the iron converts to an oxide, and simultaneously the oxidation state of oxygen decreases as it accepts electrons released by the iron. Although oxidation reactions are commonly associated with the formation of oxides, other chemical species can serve the same function. In hydrogenation, C=C (and other) bonds ar ...
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Chrom(VI)-oxid
Chrom is a fictional character in the video game ''Fire Emblem Awakening'' and its related ''Fire Emblem'' franchise. Chrom is the prince of the Kingdom of Ylisse, and a descendant of Marth. He is the brother of Lissa and Emmeryn, and the father of Lucina. He is in charge of the state-sponsored militia force known as The Shepherds investigating the actions of an enemy state. He is the wielder of the legendary Falchion. Chrom has also appeared in other games in the ''Fire Emblem'' series, as well as appearances in crossover video games like ''Project X Zone 2'', ''Tokyo Mirage Sessions ♯FE'' and ''Super Smash Bros. Ultimate''. He is voiced by Tomokazu Sugita in Japanese, and by Matthew Mercer in English. One of the most popular characters in the ''Fire Emblem'' franchise, Chrom has received a mostly positive reception from reviewers for his appearances in ''Awakening'' and related spin-off games, with praise focusing on his appearance and personality. His subsequent inclusion ...
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Pyrophoric
A substance is pyrophoric (from grc-gre, πυροφόρος, , 'fire-bearing') if it ignites spontaneously in air at or below (for gases) or within 5 minutes after coming into contact with air (for liquids and solids). Examples are organolithium compounds and triethylborane. Pyrophoric materials are often water-reactive as well and will ignite when they contact water or humid air. They can be handled safely in atmospheres of argon or (with a few exceptions) nitrogen. Fire Classes#Metal, Class D fire extinguisher#Class D dry powder and other agents for metal fires, fire extinguishers are designated for use in fires involving pyrophoric materials. A related concept is hypergolic propellant, hypergolicity, in which two compounds spontaneously ignite when mixed. Uses The creation of spark (fire), sparks from metals is based on the pyrophoricity of small metal particles, and pyrophoric alloys are made for this purpose. The sparking mechanisms in lighters and various toys, using fe ...
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Hygroscopic
Hygroscopy is the phenomenon of attracting and holding water molecules via either absorption or adsorption from the surrounding environment, which is usually at normal or room temperature. If water molecules become suspended among the substance's molecules, adsorbing substances can become physically changed, e.g., changing in volume, boiling point, viscosity or some other physical characteristic or property of the substance. For example, a finely dispersed hygroscopic powder, such as a salt, may become clumpy over time due to collection of moisture from the surrounding environment. ''Deliquescent'' materials are sufficiently hygroscopic that they absorb so much water that they become liquid and form an aqueous solution. Etymology and pronunciation The word ''hygroscopy'' () uses combining forms of '' hygro-'' and '' -scopy''. Unlike any other ''-scopy'' word, it no longer refers to a viewing or imaging mode. It did begin that way, with the word ''hygroscope'' referring in th ...
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