Table of Contents
212 relations: Acid, Acid dissociation constant, Aether (classical element), Akkadian language, Al-Farabi, Al-Kindi, Al-Zahrawi, Alcohol (drug), Alcohol dehydrogenase, Alcoholic beverage, Aldehyde, Alicyclic compound, Aliphatic compound, Alkane, Alkene, Alkoxide, Alkyl group, Allyl alcohol, Aluminium isopropoxide, Amine, Amino acid, Amyl alcohol, Andreas Libavius, Antimony, Antimony trisulfide, Antiseptic, Aqua vitae, Arabic definite article, Aristotle, Arnaldus de Villa Nova, Aromatic compound, Article (grammar), Asymmetric hydrogenation, Barbier reaction, Bartholomew Traheron, Barton–McCombie deoxygenation, Base (chemistry), Beer chemistry, Biomass, Blend word, Carbonyl group, Carboxylic acid, Catalysis, Cellulose, Cetyl alcohol, Chemical nomenclature, Chemical polarity, Chemistry, Cholesterol, Clostridium acetobutylicum, ... Expand index (162 more) »
- Alcohol
Acid
An acid is a molecule or ion capable of either donating a proton (i.e. hydrogen ion, H+), known as a Brønsted–Lowry acid, or forming a covalent bond with an electron pair, known as a Lewis acid.
See Alcohol (chemistry) and Acid
Acid dissociation constant
In chemistry, an acid dissociation constant (also known as acidity constant, or acid-ionization constant; denoted) is a quantitative measure of the strength of an acid in solution.
See Alcohol (chemistry) and Acid dissociation constant
Aether (classical element)
According to ancient and medieval science, aether (alternative spellings include æther, aither, and ether), also known as the fifth element or quintessence, is the material that fills the region of the universe beyond the terrestrial sphere.
See Alcohol (chemistry) and Aether (classical element)
Akkadian language
Akkadian (translit)John Huehnergard & Christopher Woods, "Akkadian and Eblaite", The Cambridge Encyclopedia of the World's Ancient Languages.
See Alcohol (chemistry) and Akkadian language
Al-Farabi
Postage stamp of the USSR, issued on the 1100th anniversary of the birth of Al-Farabi (1975) Abu Nasr Muhammad al-Farabi (Abū Naṣr Muḥammad al-Fārābī; — 14 December 950–12 January 951), known in the Latin West as Alpharabius, was an early Islamic philosopher and music theorist.
See Alcohol (chemistry) and Al-Farabi
Al-Kindi
Abū Yūsuf Yaʻqūb ibn ʼIsḥāq aṣ-Ṣabbāḥ al-Kindī (أبو يوسف يعقوب بن إسحاق الصبّاح الكندي; Alkindus) was an Arab Muslim polymath active as a philosopher, mathematician, physician, and music theorist.
See Alcohol (chemistry) and Al-Kindi
Al-Zahrawi
Abū al-Qāsim Khalaf ibn al-'Abbās al-Zahrāwī al-Ansari (أبو القاسمخلف بن العباس الزهراوي;‎ 936–1013), popularly known as al-Zahrawi (الزهراوي), Latinised as Albucasis or Abulcasis (from Arabic Abū al-Qāsim), was a physician, surgeon and chemist from al-Andalus.
See Alcohol (chemistry) and Al-Zahrawi
Alcohol (drug)
Alcohol, sometimes referred to by the chemical name ethanol, is one of the most widely used and abused psychoactive drugs in the world and falls under the depressant category. Alcohol (chemistry) and Alcohol (drug) are alcohol and alcohols.
See Alcohol (chemistry) and Alcohol (drug)
Alcohol dehydrogenase
Alcohol dehydrogenases (ADH) are a group of dehydrogenase enzymes that occur in many organisms and facilitate the interconversion between alcohols and aldehydes or ketones with the reduction of nicotinamide adenine dinucleotide (NAD+) to NADH.
See Alcohol (chemistry) and Alcohol dehydrogenase
Alcoholic beverage
An alcoholic beverage (also called an adult beverage, alcoholic drink, strong drink, or simply a drink) is a beverage containing alcohol.
See Alcohol (chemistry) and Alcoholic beverage
Aldehyde
In organic chemistry, an aldehyde is an organic compound containing a functional group with the structure. Alcohol (chemistry) and aldehyde are functional groups.
See Alcohol (chemistry) and Aldehyde
Alicyclic compound
In organic chemistry, an alicyclic compound contains one or more all-carbon rings which may be either saturated or unsaturated, but do not have aromatic character.
See Alcohol (chemistry) and Alicyclic compound
Aliphatic compound
In organic chemistry, hydrocarbons (compounds composed solely of carbon and hydrogen) are divided into two classes: aromatic compounds and aliphatic compounds (G. aleiphar, fat, oil).
See Alcohol (chemistry) and Aliphatic compound
Alkane
In organic chemistry, an alkane, or paraffin (a historical trivial name that also has other meanings), is an acyclic saturated hydrocarbon.
See Alcohol (chemistry) and Alkane
Alkene
In organic chemistry, an alkene, or olefin, is a hydrocarbon containing a carbon–carbon double bond.
See Alcohol (chemistry) and Alkene
Alkoxide
In chemistry, an alkoxide is the conjugate base of an alcohol and therefore consists of an organic group bonded to a negatively charged oxygen atom. Alcohol (chemistry) and alkoxide are functional groups.
See Alcohol (chemistry) and Alkoxide
Alkyl group
In organic chemistry, an alkyl group is an alkane missing one hydrogen.
See Alcohol (chemistry) and Alkyl group
Allyl alcohol
Allyl alcohol (IUPAC name: prop-2-en-1-ol) is an organic compound with the structural formula.
See Alcohol (chemistry) and Allyl alcohol
Aluminium isopropoxide
Aluminium isopropoxide is the chemical compound usually described with the formula Al(O-i-Pr)3, where i-Pr is the isopropyl group (–CH(CH3)2).
See Alcohol (chemistry) and Aluminium isopropoxide
Amine
In chemistry, amines are compounds and functional groups that contain a basic nitrogen atom with a lone pair. Alcohol (chemistry) and amine are functional groups.
See Alcohol (chemistry) and Amine
Amino acid
Amino acids are organic compounds that contain both amino and carboxylic acid functional groups.
See Alcohol (chemistry) and Amino acid
Amyl alcohol
Amyl alcohols are alcohols with the formula C5H11OH.
See Alcohol (chemistry) and Amyl alcohol
Andreas Libavius
Andreas Libavius or Andrew Libavius was born in Halle, Germany and died in July 1616.
See Alcohol (chemistry) and Andreas Libavius
Antimony
Antimony is a chemical element; it has symbol Sb and atomic number 51.
See Alcohol (chemistry) and Antimony
Antimony trisulfide
Antimony trisulfide is found in nature as the crystalline mineral stibnite and the amorphous red mineral (actually a mineraloid) metastibnite.
See Alcohol (chemistry) and Antimony trisulfide
Antiseptic
An antiseptic (lit and label) is an antimicrobial substance or compound that is applied to living tissue to reduce the possibility of sepsis, infection or putrefaction. Alcohol (chemistry) and antiseptic are antiseptics.
See Alcohol (chemistry) and Antiseptic
Aqua vitae
Aqua vitae (Latin for "water of life") or aqua vita is an archaic name for a concentrated aqueous solution of ethanol.
See Alcohol (chemistry) and Aqua vitae
Arabic definite article
(ٱلْـ, also romanized as el-, il-, and l- as pronounced in some varieties of Arabic), is the definite article in the Arabic language: a particle (ḥarf) whose function is to render the noun on which it is prefixed definite.
See Alcohol (chemistry) and Arabic definite article
Aristotle
Aristotle (Ἀριστοτέλης Aristotélēs; 384–322 BC) was an Ancient Greek philosopher and polymath.
See Alcohol (chemistry) and Aristotle
Arnaldus de Villa Nova
Arnaldus de Villa Nova (also called Arnau de Vilanova in Catalan, his language, Arnaldus Villanovanus, Arnaud de Ville-Neuve or Arnaldo de Villanueva, c. 1240–1311) was a physician and a religious reformer.
See Alcohol (chemistry) and Arnaldus de Villa Nova
Aromatic compound
Aromatic compounds or arenes usually refers to organic compounds "with a chemistry typified by benzene" and "cyclically conjugated." The word "aromatic" originates from the past grouping of molecules based on odor, before their general chemical properties were understood.
See Alcohol (chemistry) and Aromatic compound
Article (grammar)
In grammar, an article is any member of a class of dedicated words that are used with noun phrases to mark the identifiability of the referents of the noun phrases.
See Alcohol (chemistry) and Article (grammar)
Asymmetric hydrogenation
Asymmetric hydrogenation is a chemical reaction that adds two atoms of hydrogen to a target (substrate) molecule with three-dimensional spatial selectivity.
See Alcohol (chemistry) and Asymmetric hydrogenation
Barbier reaction
The Barbier reaction is an organometallic reaction between an alkyl halide (chloride, bromide, iodide), a carbonyl group and a metal.
See Alcohol (chemistry) and Barbier reaction
Bartholomew Traheron
Bartholomew Traheron (1510?–1558?) was an English Protestant writer and Marian exile.
See Alcohol (chemistry) and Bartholomew Traheron
Barton–McCombie deoxygenation
The Barton–McCombie deoxygenation is an organic reaction in which a hydroxy functional group in an organic compound is replaced by a hydrogen to give an alkyl group.
See Alcohol (chemistry) and Barton–McCombie deoxygenation
Base (chemistry)
In chemistry, there are three definitions in common use of the word "base": Arrhenius bases, Brønsted bases, and Lewis bases.
See Alcohol (chemistry) and Base (chemistry)
Beer chemistry
The chemical compounds in beer give it a distinctive taste, smell and appearance.
See Alcohol (chemistry) and Beer chemistry
Biomass
Biomass is a term used in several contexts: in the context of ecology it means living organisms, and in the context of bioenergy it means matter from recently living (but now dead) organisms.
See Alcohol (chemistry) and Biomass
Blend word
In linguistics, a blend—also known as a blend word, lexical blend, or portmanteau—is a word formed, usually intentionally, by combining the sounds and meanings of two or more words.
See Alcohol (chemistry) and Blend word
Carbonyl group
For organic chemistry, a carbonyl group is a functional group with the formula, composed of a carbon atom double-bonded to an oxygen atom, and it is divalent at the C atom. Alcohol (chemistry) and carbonyl group are functional groups.
See Alcohol (chemistry) and Carbonyl group
Carboxylic acid
In organic chemistry, a carboxylic acid is an organic acid that contains a carboxyl group attached to an R-group. Alcohol (chemistry) and carboxylic acid are functional groups.
See Alcohol (chemistry) and Carboxylic acid
Catalysis
Catalysis is the increase in rate of a chemical reaction due to an added substance known as a catalyst.
See Alcohol (chemistry) and Catalysis
Cellulose
Cellulose is an organic compound with the formula, a polysaccharide consisting of a linear chain of several hundred to many thousands of β(1→4) linked D-glucose units.
See Alcohol (chemistry) and Cellulose
Cetyl alcohol
Cetyl alcohol, also known as hexadecan-1-ol and palmityl alcohol, is a C-16 fatty alcohol with the formula CH3(CH2)15OH.
See Alcohol (chemistry) and Cetyl alcohol
Chemical nomenclature
Chemical nomenclature is a set of rules to generate systematic names for chemical compounds.
See Alcohol (chemistry) and Chemical nomenclature
Chemical polarity
In chemistry, polarity is a separation of electric charge leading to a molecule or its chemical groups having an electric dipole moment, with a negatively charged end and a positively charged end.
See Alcohol (chemistry) and Chemical polarity
Chemistry
Chemistry is the scientific study of the properties and behavior of matter.
See Alcohol (chemistry) and Chemistry
Cholesterol
Cholesterol is the principal sterol of all higher animals, distributed in body tissues, especially the brain and spinal cord, and in animal fats and oils.
See Alcohol (chemistry) and Cholesterol
Clostridium acetobutylicum
Clostridium acetobutylicum, ATCC 824, is a commercially valuable bacterium sometimes called the "Weizmann Organism", after Jewish Russian-born biochemist Chaim Weizmann.
See Alcohol (chemistry) and Clostridium acetobutylicum
Collins reagent
Collins reagent is the complex of chromium(VI) oxide with pyridine in dichloromethane.
See Alcohol (chemistry) and Collins reagent
Cracking (chemistry)
In petrochemistry, petroleum geology and organic chemistry, cracking is the process whereby complex organic molecules such as kerogens or long-chain hydrocarbons are broken down into simpler molecules such as light hydrocarbons, by the breaking of carbon–carbon bonds in the precursors.
See Alcohol (chemistry) and Cracking (chemistry)
Cyclohexanol
Cyclohexanol is the organic compound with the formula HOCH(CH2)5.
See Alcohol (chemistry) and Cyclohexanol
Dess–Martin periodinane
Dess–Martin periodinane (DMP) is a chemical reagent used in the Dess–Martin oxidation, oxidizing primary alcohols to aldehydes and secondary alcohols to ketones.
See Alcohol (chemistry) and Dess–Martin periodinane
Detergent
A detergent is a surfactant or a mixture of surfactants with cleansing properties when in dilute solutions.
See Alcohol (chemistry) and Detergent
Diazonium compound
Diazonium compounds or diazonium salts are a group of organic compounds sharing a common functional group where R can be any organic group, such as an alkyl or an aryl, and X is an inorganic or organic anion, such as a halide. Alcohol (chemistry) and diazonium compound are functional groups.
See Alcohol (chemistry) and Diazonium compound
Diethyl ether
Diethyl ether, or simply ether, is an organic compound with the chemical formula, sometimes abbreviated as.
See Alcohol (chemistry) and Diethyl ether
Dimethyl sulfoxide
Dimethyl sulfoxide (DMSO) is an organosulfur compound with the formula (CH3)2.
See Alcohol (chemistry) and Dimethyl sulfoxide
Distillation
Distillation, also classical distillation, is the process of separating the component substances of a liquid mixture of two or more chemically discrete substances; the separation process is realized by way of the selective boiling of the mixture and the condensation of the vapors in a still.
See Alcohol (chemistry) and Distillation
Elimination reaction
An elimination reaction is a type of organic reaction in which two substituents are removed from a molecule in either a one- or two-step mechanism.
See Alcohol (chemistry) and Elimination reaction
Enol
In organic chemistry, alkenols (shortened to enols) are a type of reactive structure or intermediate in organic chemistry that is represented as an alkene (olefin) with a hydroxyl group attached to one end of the alkene double bond. Alcohol (chemistry) and enol are alcohols and functional groups.
See Alcohol (chemistry) and Enol
Erythritol
Erythritol is an organic compound, the naturally occurring achiral meso four-carbon sugar alcohol (or polyol).
See Alcohol (chemistry) and Erythritol
Ethane
Ethane is a naturally occurring organic chemical compound with chemical formula.
See Alcohol (chemistry) and Ethane
Ethanol
Ethanol (also called ethyl alcohol, grain alcohol, drinking alcohol, or simply alcohol) is an organic compound with the chemical formula.
See Alcohol (chemistry) and Ethanol
Ethanol fuel
Ethanol fuel is fuel containing ethyl alcohol, the same type of alcohol as found in alcoholic beverages.
See Alcohol (chemistry) and Ethanol fuel
Ether
In organic chemistry, ethers are a class of compounds that contain an ether group—an oxygen atom bonded to two organyl groups (e.g., alkyl or aryl). Alcohol (chemistry) and ether are functional groups.
See Alcohol (chemistry) and Ether
Ethyl group
In organic chemistry, an ethyl group (abbr. Et) is an alkyl substituent with the formula, derived from ethane.
See Alcohol (chemistry) and Ethyl group
Ethylene
Ethylene (IUPAC name: ethene) is a hydrocarbon which has the formula or.
See Alcohol (chemistry) and Ethylene
Ethylene glycol
Ethylene glycol (IUPAC name: ethane-1,2-diol) is an organic compound (a vicinal diol) with the formula.
See Alcohol (chemistry) and Ethylene glycol
Ethylene oxide
Ethylene oxide is an organic compound with the formula. It is a cyclic ether and the simplest epoxide: a three-membered ring consisting of one oxygen atom and two carbon atoms. Ethylene oxide is a colorless and flammable gas with a faintly sweet odor. Because it is a strained ring, ethylene oxide easily participates in a number of addition reactions that result in ring-opening.
See Alcohol (chemistry) and Ethylene oxide
Fatty alcohol
Fatty alcohols (or long-chain alcohols) are usually high-molecular-weight, straight-chain primary alcohols, but can also range from as few as 4–6 carbons to as many as 22–26, derived from natural fats and oils.
See Alcohol (chemistry) and Fatty alcohol
Favorskii reaction
The Favorskii reaction is an organic chemistry reaction between an alkyne and a carbonyl group, under basic conditions.
See Alcohol (chemistry) and Favorskii reaction
Fermentation
Fermentation is a metabolic process that produces chemical changes in organic substances through the action of enzymes.
See Alcohol (chemistry) and Fermentation
Fischer–Speier esterification
Fischer esterification or Fischer–Speier esterification is a special type of esterification by refluxing a carboxylic acid and an alcohol in the presence of an acid catalyst.
See Alcohol (chemistry) and Fischer–Speier esterification
Formaldehyde
Formaldehyde (systematic name methanal) is an organic compound with the chemical formula and structure, more precisely.
See Alcohol (chemistry) and Formaldehyde
Fractional distillation
Fractional distillation is the separation of a mixture into its component parts, or fractions.
See Alcohol (chemistry) and Fractional distillation
Fructose
Fructose, or fruit sugar, is a ketonic simple sugar found in many plants, where it is often bonded to glucose to form the disaccharide sucrose.
See Alcohol (chemistry) and Fructose
Functional group
In organic chemistry, a functional group is a substituent or moiety in a molecule that causes the molecule's characteristic chemical reactions. Alcohol (chemistry) and functional group are functional groups and organic chemistry.
See Alcohol (chemistry) and Functional group
Geraniol
Geraniol is a monoterpenoid and an alcohol.
See Alcohol (chemistry) and Geraniol
Giovanni da Vigo
Giovanni da Vigo (1450–1525) was an Italian surgeon.
See Alcohol (chemistry) and Giovanni da Vigo
Glucose
Glucose is a sugar with the molecular formula.
See Alcohol (chemistry) and Glucose
Glycerol
Glycerol, also called glycerine or glycerin, is a simple triol compound.
See Alcohol (chemistry) and Glycerol
Grignard reagent
Grignard reagents or Grignard compounds are chemical compounds with the general formula, where X is a halogen and R is an organic group, normally an alkyl or aryl.
See Alcohol (chemistry) and Grignard reagent
Haloalkane
The haloalkanes (also known as halogenoalkanes or alkyl halides) are alkanes containing one or more halogen substituents. Alcohol (chemistry) and haloalkane are functional groups.
See Alcohol (chemistry) and Haloalkane
Halohydrin
In organic chemistry a halohydrin (also a haloalcohol or β-halo alcohol) is a functional group in which a halogen and a hydroxyl are bonded to adjacent carbon atoms, which otherwise bear only hydrogen or hydrocarbyl groups (e.g. 2-chloroethanol, 3-chloropropane-1,2-diol). Alcohol (chemistry) and halohydrin are functional groups.
See Alcohol (chemistry) and Halohydrin
Hemicellulose
A hemicellulose (also known as polyose) is one of a number of heteropolymers (matrix polysaccharides), such as arabinoxylans, present along with cellulose in almost all terrestrial plant cell walls.
See Alcohol (chemistry) and Hemicellulose
Hexane
Hexane or n-hexane is an organic compound, a straight-chain alkane with six carbon atoms and the molecular formula C6H14.
See Alcohol (chemistry) and Hexane
Hexanol
Hexanol may refer to any of the following isomeric organic compounds with the formula C6H13OH: |- ! Structure !! Type !! IUPAC name !! Boiling point (°C) |- | | Primary | Hexan-1-ol | 158 |- | | Secondary | Hexan-2-ol | 140 |- | | Secondary | Hexan-3-ol | 135 |- | | Primary | 2-Methylpentan-1-ol | 147 |- | | Primary | 3-Methylpentan-1-ol | 152 |- | | Primary | 4-Methylpentan-1-ol | 151 |- | | Tertiary | 2-Methylpentan-2-ol | 121 |- | | Secondary | 3-Methylpentan-2-ol | 134 |- | | Secondary | 4-Methylpentan-2-ol | 131 |- | | Secondary | 2-Methylpentan-3-ol | 126 |- | | Tertiary | 3-Methylpentan-3-ol | 122 |- | | Primary | 2,2-Dimethylbutan-1-ol | 137 |- | | Primary | 2,3-Dimethylbutan-1-ol | 145 |- | | Primary | 3,3-Dimethylbutan-1-ol | 143 |- | | Tertiary | 2,3-Dimethylbutan-2-ol | 119 |- | | Secondary | 3,3-Dimethylbutan-2-ol | 120 |- | | Primary | 2-Ethylbutan-1-ol | 146 |- |.
See Alcohol (chemistry) and Hexanol
Hydration reaction
In chemistry, a hydration reaction is a chemical reaction in which a substance combines with water.
See Alcohol (chemistry) and Hydration reaction
Hydroboration–oxidation reaction
Hydroboration–oxidation reaction is a two-step hydration reaction that converts an alkene into an alcohol.
See Alcohol (chemistry) and Hydroboration–oxidation reaction
Hydrocarbon
In organic chemistry, a hydrocarbon is an organic compound consisting entirely of hydrogen and carbon.
See Alcohol (chemistry) and Hydrocarbon
Hydrochloric acid
Hydrochloric acid, also known as muriatic acid or spirits of salt, is an aqueous solution of hydrogen chloride (HCl).
See Alcohol (chemistry) and Hydrochloric acid
Hydroformylation
In organic chemistry, hydroformylation, also known as oxo synthesis or oxo process, is an industrial process for the production of aldehydes from alkenes.
See Alcohol (chemistry) and Hydroformylation
Hydrogen bond
In chemistry, a hydrogen bond (or H-bond) is primarily an electrostatic force of attraction between a hydrogen (H) atom which is covalently bonded to a more electronegative "donor" atom or group (Dn), and another electronegative atom bearing a lone pair of electrons—the hydrogen bond acceptor (Ac).
See Alcohol (chemistry) and Hydrogen bond
Hydroxy group
In chemistry, a hydroxy or hydroxyl group is a functional group with the chemical formula and composed of one oxygen atom covalently bonded to one hydrogen atom. Alcohol (chemistry) and hydroxy group are alcohols and functional groups.
See Alcohol (chemistry) and Hydroxy group
Hydroxyacetone
Hydroxyacetone, also known as acetol, is the organic chemical with the formula CH3C(O)CH2OH.
See Alcohol (chemistry) and Hydroxyacetone
Hydroxylation
In chemistry, hydroxylation can refer to.
See Alcohol (chemistry) and Hydroxylation
Index of alcohol-related articles
Alcohol is any organic compound in which a hydroxyl functional group (-OH) is bound to a carbon atom, usually connected to other carbon or hydrogen atoms. Alcohol (chemistry) and Index of alcohol-related articles are alcohol.
See Alcohol (chemistry) and Index of alcohol-related articles
Inositol
In biochemistry, medicine, and related sciences, inositol generally refers to myo-inositol (formerly meso-inositol), the most important stereoisomer of the chemical compound cyclohexane-1,2,3,4,5,6-hexol.
See Alcohol (chemistry) and Inositol
International Union of Pure and Applied Chemistry
The International Union of Pure and Applied Chemistry (IUPAC) is an international federation of National Adhering Organizations working for the advancement of the chemical sciences, especially by developing nomenclature and terminology.
See Alcohol (chemistry) and International Union of Pure and Applied Chemistry
Isobutanol
Isobutanol (IUPAC nomenclature: 2-methylpropan-1-ol) is an organic compound with the formula (CH3)2CHCH2OH (sometimes represented as i-BuOH).
See Alcohol (chemistry) and Isobutanol
Isobutylene
Isobutylene (or 2-methylpropene) is a hydrocarbon with the chemical formula.
See Alcohol (chemistry) and Isobutylene
Isopropyl alcohol
Isopropyl alcohol (IUPAC name propan-2-ol and also called isopropanol or 2-propanol) is a colorless, flammable organic compound with a pungent alcoholic odor. Alcohol (chemistry) and Isopropyl alcohol are antiseptics.
See Alcohol (chemistry) and Isopropyl alcohol
IUPAC nomenclature of organic chemistry
In chemical nomenclature, the IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds as recommended by the International Union of Pure and Applied Chemistry (IUPAC). Alcohol (chemistry) and IUPAC nomenclature of organic chemistry are organic chemistry.
See Alcohol (chemistry) and IUPAC nomenclature of organic chemistry
Jabir ibn Hayyan
Abū Mūsā Jābir ibn Ḥayyān (Arabic: أَبو موسى جابِر بِن حَيّان, variously called al-Ṣūfī, al-Azdī, al-Kūfī, or al-Ṭūsī), died 806−816, is the purported author of a large number of works in Arabic, often called the Jabirian corpus.
See Alcohol (chemistry) and Jabir ibn Hayyan
Jean de Roquetaillade
Jean de Roquetaillade, also known as John of Rupescissa, (ca. 1310 – between 1366 and 1370) was a French Franciscan alchemist and eschatologist.
See Alcohol (chemistry) and Jean de Roquetaillade
Jones oxidation
The Jones oxidation is an organic reaction for the oxidation of primary and secondary alcohols to carboxylic acids and ketones, respectively.
See Alcohol (chemistry) and Jones oxidation
Ketone
In organic chemistry, a ketone is an organic compound with the structure, where R and R' can be a variety of carbon-containing substituents. Alcohol (chemistry) and ketone are functional groups.
See Alcohol (chemistry) and Ketone
Kohl (cosmetics)
Kohl is an eye cosmetic, traditionally made by grinding stibnite for use similar to that of charcoal in mascara.
See Alcohol (chemistry) and Kohl (cosmetics)
Libfix
In linguistics, a libfix is a productive bound morpheme affix created by rebracketing and back-formation, often a generalization of a component of a blended or portmanteau word.
See Alcohol (chemistry) and Libfix
Lignin
Lignin is a class of complex organic polymers that form key structural materials in the support tissues of most plants.
See Alcohol (chemistry) and Lignin
Liquor
Liquor or distilled beverage is an alcoholic drink produced by the distillation of grains, fruits, vegetables, or sugar that have already gone through alcoholic fermentation.
See Alcohol (chemistry) and Liquor
List of alkanols
This list is ordered by the number of carbon atoms in an alcohol.
See Alcohol (chemistry) and List of alkanols
List of gasoline additives
Petrol additives may increase petrol's octane rating, thus allowing the use of higher compression ratios for greater efficiency and power, or act as corrosion inhibitors or lubricants.
See Alcohol (chemistry) and List of gasoline additives
Lithium aluminium hydride
Lithium aluminium hydride, commonly abbreviated to LAH, is an inorganic compound with the chemical formula or.
See Alcohol (chemistry) and Lithium aluminium hydride
Lone pair
In chemistry, a lone pair refers to a pair of valence electrons that are not shared with another atom in a covalent bondIUPAC Gold Book definition: and is sometimes called an unshared pair or non-bonding pair.
See Alcohol (chemistry) and Lone pair
Lucas' reagent
"Lucas' reagent" is a solution of anhydrous zinc chloride in concentrated hydrochloric acid.
See Alcohol (chemistry) and Lucas' reagent
Mannitol
Mannitol is a type of sugar alcohol used as a sweetener and medication.
See Alcohol (chemistry) and Mannitol
Median lethal dose
In toxicology, the median lethal dose, LD50 (abbreviation for "lethal dose, 50%"), LC50 (lethal concentration, 50%) or LCt50 is a toxic unit that measures the lethal dose of a given substance.
See Alcohol (chemistry) and Median lethal dose
Meerwein–Ponndorf–Verley reduction
The Meerwein–Ponndorf–Verley (MPV) reduction in organic chemistry is the reduction of ketones and aldehydes to their corresponding alcohols utilizing aluminium alkoxide catalysis in the presence of a sacrificial alcohol.
See Alcohol (chemistry) and Meerwein–Ponndorf–Verley reduction
Menthol
Menthol is an organic compound, more specifically a monoterpenoid, made synthetically or obtained from the oils of corn mint, peppermint, or other mints.
See Alcohol (chemistry) and Menthol
Metal
A metal is a material that, when polished or fractured, shows a lustrous appearance, and conducts electricity and heat relatively well.
See Alcohol (chemistry) and Metal
Methanol
Methanol (also called methyl alcohol and wood spirit, amongst other names) is an organic chemical compound and the simplest aliphatic alcohol, with the chemical formula (a methyl group linked to a hydroxyl group, often abbreviated as MeOH).
See Alcohol (chemistry) and Methanol
Methyl group
In organic chemistry, a methyl group is an alkyl derived from methane, containing one carbon atom bonded to three hydrogen atoms, having chemical formula (whereas normal methane has the formula). In formulas, the group is often abbreviated as Me. Alcohol (chemistry) and methyl group are functional groups.
See Alcohol (chemistry) and Methyl group
Miscibility
Miscibility is the property of two substances to mix in all proportions (that is, to fully dissolve in each other at any concentration), forming a homogeneous mixture (a solution).
See Alcohol (chemistry) and Miscibility
N-Bromosuccinimide
N-Bromosuccinimide or NBS is a chemical reagent used in radical substitution, electrophilic addition, and electrophilic substitution reactions in organic chemistry.
See Alcohol (chemistry) and N-Bromosuccinimide
Nozaki–Hiyama–Kishi reaction
The Nozaki–Hiyama–Kishi reaction is a nickel/chromium coupling reaction forming an alcohol from the reaction of an aldehyde with an allyl or vinyl halide.
See Alcohol (chemistry) and Nozaki–Hiyama–Kishi reaction
Nucleophilic substitution
In chemistry, a nucleophilic substitution (SN) 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).
See Alcohol (chemistry) and Nucleophilic substitution
Nylon
Nylon is a family of synthetic polymers with amide backbones, usually linking aliphatic or semi-aromatic groups.
See Alcohol (chemistry) and Nylon
Octanol
Octanols are alcohols with the formula C8H17OH.
See Alcohol (chemistry) and Octanol
Online Etymology Dictionary
The Online Etymology Dictionary or Etymonline, sometimes abbreviated as OED (not to be confused with the Oxford English Dictionary, which the site often cites), is a free online dictionary that describes the origins of English words, written and compiled by Douglas R. Harper.
See Alcohol (chemistry) and Online Etymology Dictionary
Organic compound
Some chemical authorities define an organic compound as a chemical compound that contains a carbon–hydrogen or carbon–carbon bond; others consider an organic compound to be any chemical compound that contains carbon. Alcohol (chemistry) and organic compound are organic chemistry.
See Alcohol (chemistry) and Organic compound
Organic reaction
Organic reactions are chemical reactions involving organic compounds. Alcohol (chemistry) and organic reaction are organic chemistry.
See Alcohol (chemistry) and Organic reaction
Organoboron chemistry
Organoboron chemistry or organoborane chemistry studies organoboron compounds, also called organoboranes.
See Alcohol (chemistry) and Organoboron chemistry
Organobromine chemistry
Organobromine chemistry is the study of the synthesis and properties of organobromine compounds, also called organobromides, which are organic compounds that contain carbon bonded to bromine.
See Alcohol (chemistry) and Organobromine chemistry
Organochlorine chemistry
Organochlorine chemistry is concerned with the properties of organochlorine compounds, or organochlorides, organic compounds containing at least one covalently bonded atom of chlorine.
See Alcohol (chemistry) and Organochlorine chemistry
Organosulfate
In organosulfur chemistry, organosulfates are a class of organic compounds sharing a common functional group with the structure.
See Alcohol (chemistry) and Organosulfate
Oxford English Dictionary
The Oxford English Dictionary (OED) is the principal historical dictionary of the English language, published by Oxford University Press (OUP), a University of Oxford publishing house.
See Alcohol (chemistry) and Oxford English Dictionary
Oxford University Press
Oxford University Press (OUP) is the publishing house of the University of Oxford.
See Alcohol (chemistry) and Oxford University Press
Oxidase
In biochemistry, an oxidase is an oxidoreductase (any enzyme that catalyzes a redox reaction) that uses dioxygen (O2) as the electron acceptor.
See Alcohol (chemistry) and Oxidase
Oxymercuration reaction
In organic chemistry, the oxymercuration reaction is an electrophilic addition reaction that transforms an alkene into a neutral alcohol.
See Alcohol (chemistry) and Oxymercuration reaction
Paracelsus
Paracelsus (1493 – 24 September 1541), born Theophrastus von Hohenheim (full name Philippus Aureolus Theophrastus Bombastus von Hohenheim), was a Swiss physician, alchemist, lay theologian, and philosopher of the German Renaissance.
See Alcohol (chemistry) and Paracelsus
Paracetamol
Paracetamol (acetaminophen) is a non-opioid analgesic and antipyretic agent used to treat fever and mild to moderate pain.
See Alcohol (chemistry) and Paracetamol
Petroleum
Petroleum or crude oil, also referred to as simply oil, is a naturally occurring yellowish-black liquid mixture of mainly hydrocarbons, and is found in geological formations.
See Alcohol (chemistry) and Petroleum
Phenols
In organic chemistry, phenols, sometimes called phenolics, are a class of chemical compounds consisting of one or more hydroxyl groups (−O H) bonded directly to an aromatic hydrocarbon group. Alcohol (chemistry) and phenols are functional groups.
See Alcohol (chemistry) and Phenols
Phosphorus tribromide
Phosphorus tribromide is a colourless liquid with the formula PBr3.
See Alcohol (chemistry) and Phosphorus tribromide
Plasticizer
A plasticizer (UK: plasticiser) is a substance that is added to a material to make it softer and more flexible, to increase its plasticity, to decrease its viscosity, and/or to decrease friction during its handling in manufacture.
See Alcohol (chemistry) and Plasticizer
Pliny the Elder
Gaius Plinius Secundus (AD 23/24 AD 79), called Pliny the Elder, was a Roman author, naturalist, natural philosopher, naval and army commander of the early Roman Empire, and a friend of the emperor Vespasian.
See Alcohol (chemistry) and Pliny the Elder
Polyol
In organic chemistry, a polyol is an organic compound containing multiple hydroxyl groups.
See Alcohol (chemistry) and Polyol
Polyvinyl chloride
Polyvinyl chloride (alternatively: poly(vinyl chloride), colloquial: vinyl or polyvinyl; abbreviated: PVC) is the world's third-most widely produced synthetic polymer of plastic (after polyethylene and polypropylene).
See Alcohol (chemistry) and Polyvinyl chloride
Potassium hydroxide
Potassium hydroxide is an inorganic compound with the formula KOH, and is commonly called caustic potash.
See Alcohol (chemistry) and Potassium hydroxide
Potassium permanganate
Potassium permanganate is an inorganic compound with the chemical formula KMnO4.
See Alcohol (chemistry) and Potassium permanganate
Preferred IUPAC name
In chemical nomenclature, a preferred IUPAC name (PIN) is a unique name, assigned to a chemical substance and preferred among all possible names generated by IUPAC nomenclature.
See Alcohol (chemistry) and Preferred IUPAC name
Proceedings of the Chemical Society
The Proceedings of the Chemical Society was a scientific journal published at various times in the life of the Chemical Society, a scientific society in the United Kingdom that combined with other societies to form the Royal Society of Chemistry in 1980.
See Alcohol (chemistry) and Proceedings of the Chemical Society
Propane
Propane is a three-carbon alkane with the molecular formula.
See Alcohol (chemistry) and Propane
Propanol
There are two isomers of propanol.
See Alcohol (chemistry) and Propanol
Propargyl alcohol
Propargyl alcohol, or 2-propyn-1-ol, is an organic compound with the formula C3H4O.
See Alcohol (chemistry) and Propargyl alcohol
Propyl group
In organic chemistry, a propyl group is a three-carbon alkyl substituent with chemical formula for the linear form.
See Alcohol (chemistry) and Propyl group
Propylene glycol
Propylene glycol (IUPAC name: propane-1,2-diol) is a viscous, colorless liquid.
See Alcohol (chemistry) and Propylene glycol
Pyridine
Pyridine is a basic heterocyclic organic compound with the chemical formula. Alcohol (chemistry) and Pyridine are functional groups.
See Alcohol (chemistry) and Pyridine
Radical substitution
In organic chemistry, a radical-substitution reaction is a substitution reaction involving free radicals as a reactive intermediate.
See Alcohol (chemistry) and Radical substitution
Redox
Redox (reduction–oxidation or oxidation–reduction) is a type of chemical reaction in which the oxidation states of the reactants change.
See Alcohol (chemistry) and Redox
Relative volatility
Relative volatility is a measure comparing the vapor pressures of the components in a liquid mixture of chemicals.
See Alcohol (chemistry) and Relative volatility
Roman Egypt
Roman Egypt; was an imperial province of the Roman Empire from 30 BC to AD 641.
See Alcohol (chemistry) and Roman Egypt
Rubbing alcohol
Rubbing alcohol (in America, surgical spirit elsewhere) is either an isopropyl alcohol or an ethanol-based liquid, with isopropyl alcohol products being the most widely available. Alcohol (chemistry) and Rubbing alcohol are antiseptics.
See Alcohol (chemistry) and Rubbing alcohol
Salt (chemistry)
In chemistry, a salt or ionic compound is a chemical compound consisting of an assembly of positively charged ions (cations) and negatively charged ions (anions), which results in a compound with no net electric charge (electrically neutral).
See Alcohol (chemistry) and Salt (chemistry)
Salt-effect distillation
Salt-effect distillation is a method of extractive distillation in which a salt is dissolved in the mixture of liquids to be distilled.
See Alcohol (chemistry) and Salt-effect distillation
Semitic languages
The Semitic languages are a branch of the Afroasiatic language family.
See Alcohol (chemistry) and Semitic languages
Serine
Serine (symbol Ser or S) is an α-amino acid that is used in the biosynthesis of proteins.
See Alcohol (chemistry) and Serine
Skeletal formula
The skeletal formula, line-angle formula, bond-line formula or shorthand formula of an organic compound is a type of molecular structural formula that serves as a shorthand representation of a molecule's bonding and some details of its molecular geometry. Alcohol (chemistry) and skeletal formula are organic chemistry.
See Alcohol (chemistry) and Skeletal formula
Sodium
Sodium is a chemical element; it has symbol Na (from Neo-Latin natrium) and atomic number 11.
See Alcohol (chemistry) and Sodium
Sodium borohydride
Sodium borohydride, also known as sodium tetrahydridoborate and sodium tetrahydroborate, is an inorganic compound with the formula (sometimes written as). It is a white crystalline solid, usually encountered as an aqueous basic solution.
See Alcohol (chemistry) and Sodium borohydride
Sodium hydride
Sodium hydride is the chemical compound with the empirical formula NaH.
See Alcohol (chemistry) and Sodium hydride
Sodium hydroxide
Sodium hydroxide, also known as lye and caustic soda, is an inorganic compound with the formula.
See Alcohol (chemistry) and Sodium hydroxide
Solvation
Solvation describes the interaction of a solvent with dissolved molecules.
See Alcohol (chemistry) and Solvation
Sorbitol
Sorbitol, less commonly known as glucitol, is a sugar alcohol with a sweet taste which the human body metabolizes slowly.
See Alcohol (chemistry) and Sorbitol
Starch
Starch or amylum is a polymeric carbohydrate consisting of numerous glucose units joined by glycosidic bonds.
See Alcohol (chemistry) and Starch
Stibnite
Stibnite, sometimes called antimonite, is a sulfide mineral with the formula Sb2S3.
See Alcohol (chemistry) and Stibnite
Structural formula
The structural formula of a chemical compound is a graphic representation of the molecular structure (determined by structural chemistry methods), showing how the atoms are possibly arranged in the real three-dimensional space.
See Alcohol (chemistry) and Structural formula
Sublimation (phase transition)
Sublimation is the transition of a substance directly from the solid to the gas state, without passing through the liquid state.
See Alcohol (chemistry) and Sublimation (phase transition)
Substituent
In organic chemistry, a substituent is one or a group of atoms that replaces (one or more) atoms, thereby becoming a moiety in the resultant (new) molecule. Alcohol (chemistry) and substituent are organic chemistry.
See Alcohol (chemistry) and Substituent
Sucrose
Sucrose, a disaccharide, is a sugar composed of glucose and fructose subunits.
See Alcohol (chemistry) and Sucrose
Sugar
Sugar is the generic name for sweet-tasting, soluble carbohydrates, many of which are used in food.
See Alcohol (chemistry) and Sugar
Sugar alcohol
Sugar alcohols (also called polyhydric alcohols, polyalcohols, alditols or glycitols) are organic compounds, typically derived from sugars, containing one hydroxyl group attached to each carbon atom.
See Alcohol (chemistry) and Sugar alcohol
Sulfuric acid
Sulfuric acid (American spelling and the preferred IUPAC name) or sulphuric acid (Commonwealth spelling), known in antiquity as oil of vitriol, is a mineral acid composed of the elements sulfur, oxygen, and hydrogen, with the molecular formula.
See Alcohol (chemistry) and Sulfuric acid
Taddeo Alderotti
Taddeo Alderotti (Latin: Thaddaeus Alderottus, French: Thaddée de Florence), born in Florence between 1206 and 1215, died in 1295, was an Italian doctor and professor of medicine at the University of Bologna, who made important contributions to the renaissance of learned medicine in Europe during the High Middle Ages.
See Alcohol (chemistry) and Taddeo Alderotti
Terminal alkene
In organic chemistry, terminal alkenes (alpha-olefins, α-olefins, or 1-alkenes) are a family of organic compounds which are alkenes (also known as olefins) with a chemical formula, distinguished by having a double bond at the primary, alpha (α), or 1- position.
See Alcohol (chemistry) and Terminal alkene
Tert-Amyl alcohol
tert-Amyl alcohol (TAA) or 2-methylbutan-2-ol (2M2B), is a branched pentanol.
See Alcohol (chemistry) and Tert-Amyl alcohol
Tert-Butyl alcohol
tert-Butyl alcohol is the simplest tertiary alcohol, with a formula of (CH3)3COH (sometimes represented as t-BuOH).
See Alcohol (chemistry) and Tert-Butyl alcohol
The BMJ
The BMJ is a weekly peer-reviewed medical journal, published by BMJ Group, which in turn is wholly-owned by the British Medical Association (BMA).
See Alcohol (chemistry) and The BMJ
Theophrastus
Theophrastus (Θεόφραστος||godly phrased) was a Greek philosopher and the successor to Aristotle in the Peripatetic school.
See Alcohol (chemistry) and Theophrastus
Thionyl chloride
Thionyl chloride is an inorganic compound with the chemical formula.
See Alcohol (chemistry) and Thionyl chloride
Threitol
Threitol is the chiral four-carbon sugar alcohol with the molecular formula C4H10O4.
See Alcohol (chemistry) and Threitol
Tosyl group
In organic chemistry, a toluenesulfonyl group (tosyl group, abbreviated Ts or TosIn this article, "Ts", unless otherwise stated, means tosyl, not tennessine.) is a univalent functional group with the chemical formula.
See Alcohol (chemistry) and Tosyl group
Toxicity
Toxicity is the degree to which a chemical substance or a particular mixture of substances can damage an organism.
See Alcohol (chemistry) and Toxicity
Transesterification
Transesterification is the process of exchanging the organic functional group R″ of an ester with the organic group R' of an alcohol.
See Alcohol (chemistry) and Transesterification
Tributyltin hydride
Tributyltin hydride is an organotin compound with the formula (C4H9)3SnH.
See Alcohol (chemistry) and Tributyltin hydride
Triethylaluminium
Triethylaluminium is one of the simplest examples of an organoaluminium compound.
See Alcohol (chemistry) and Triethylaluminium
Triphenylmethanol
Triphenylmethanol (also known as triphenylcarbinol and TrOH) is an organic compound.
See Alcohol (chemistry) and Triphenylmethanol
Volemitol
Volemitol is a naturally occurring seven-carbon sugar alcohol.
See Alcohol (chemistry) and Volemitol
Water
Water is an inorganic compound with the chemical formula.
See Alcohol (chemistry) and Water
Williamson ether synthesis
The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol (alkoxide).
See Alcohol (chemistry) and Williamson ether synthesis
Wine chemistry
Wine is a complex mixture of chemical compounds in a hydro-alcoholic solution with a pH around 4.
See Alcohol (chemistry) and Wine chemistry
Xenobiotic
A xenobiotic is a chemical substance found within an organism that is not naturally produced or expected to be present within the organism.
See Alcohol (chemistry) and Xenobiotic
Xylitol
Xylitol is a chemical compound with the formula, or HO(CH2)(CHOH)3(CH2)OH; specifically, one particular stereoisomer with that structural formula.
See Alcohol (chemistry) and Xylitol
Zaytsev's rule
In organic chemistry, Zaytsev's rule (or Zaitsev's rule, Saytzeff's rule, Saytzev's rule) is an empirical rule for predicting the favored alkene product(s) in elimination reactions.
See Alcohol (chemistry) and Zaytsev's rule
Ziegler process
In organic chemistry, the Ziegler process (also called the Ziegler-Alfol synthesis) is a method for producing fatty alcohols from ethylene using an organoaluminium compound.
See Alcohol (chemistry) and Ziegler process
1-Butanol
1-Butanol, also known as butan-1-ol or n-butanol, is a primary alcohol with the chemical formula C4H9OH and a linear structure.
See Alcohol (chemistry) and 1-Butanol
1-Octanol
1-Octanol, also known as octan-1-ol, is the organic compound with the molecular formula CH3(CH2)7OH.
See Alcohol (chemistry) and 1-Octanol
1-Pentanol
1-Pentanol, (or n-pentanol, pentan-1-ol), is an organic compound with the formula and is classified as a primary alcohol.
See Alcohol (chemistry) and 1-Pentanol
1-Propanol
1-Propanol (also propan-1-ol, propanol, n-propyl alcohol) is a primary alcohol with the formula and sometimes represented as PrOH or n-PrOH.
See Alcohol (chemistry) and 1-Propanol
4-Toluenesulfonyl chloride
4-Toluenesulfonyl chloride (p-toluenesulfonyl chloride, toluene-p-sulfonyl chloride) is an organic compound with the formula CH3C6H4SO2Cl.
See Alcohol (chemistry) and 4-Toluenesulfonyl chloride
See also
Alcohol
- Acetaldehyde dehydrogenase inhibitors
- Alcohol (chemistry)
- Alcohol (drug)
- Alcohol and Drugs History Society
- Alcohol and health
- Alcohol and sex
- Alcohol and spaceflight
- Alcohol education
- Alcohol in association football
- Alcohol industry
- Alcohol inhalation
- Alcohol law
- Alcohol powder
- Alcohol tolerance
- Alcohol-infused whipped cream
- Alcoholate
- Alcoholic drinks
- Alcoholic spirits measure
- Alcoholism in adolescence
- Breathometer
- Cocoroco
- Comparison of psychoactive alcohols in alcoholic drinks
- Disulfiram-like drug
- Disulfiram-like drugs
- Drinking culture
- Drunk driving
- Dutch courage
- Ethyl glucuronide
- Ethylphenidate
- Index of alcohol-related articles
- Pharmacology of ethanol
- Religion and alcohol
References
Also known as Alcohols, Alcohols (chemistry), Alkanol, Higher alcohols, Non-beverage alcohol, Secondary alcohol, Secondary alcohols, Substituted alcohol, Substituted alcohols, Tertiary Alcohols, Tertiary alcohol, Tertiary hydroxyl groups, Toxic alcohol, Toxic alcohols.
, Collins reagent, Cracking (chemistry), Cyclohexanol, Dess–Martin periodinane, Detergent, Diazonium compound, Diethyl ether, Dimethyl sulfoxide, Distillation, Elimination reaction, Enol, Erythritol, Ethane, Ethanol, Ethanol fuel, Ether, Ethyl group, Ethylene, Ethylene glycol, Ethylene oxide, Fatty alcohol, Favorskii reaction, Fermentation, Fischer–Speier esterification, Formaldehyde, Fractional distillation, Fructose, Functional group, Geraniol, Giovanni da Vigo, Glucose, Glycerol, Grignard reagent, Haloalkane, Halohydrin, Hemicellulose, Hexane, Hexanol, Hydration reaction, Hydroboration–oxidation reaction, Hydrocarbon, Hydrochloric acid, Hydroformylation, Hydrogen bond, Hydroxy group, Hydroxyacetone, Hydroxylation, Index of alcohol-related articles, Inositol, International Union of Pure and Applied Chemistry, Isobutanol, Isobutylene, Isopropyl alcohol, IUPAC nomenclature of organic chemistry, Jabir ibn Hayyan, Jean de Roquetaillade, Jones oxidation, Ketone, Kohl (cosmetics), Libfix, Lignin, Liquor, List of alkanols, List of gasoline additives, Lithium aluminium hydride, Lone pair, Lucas' reagent, Mannitol, Median lethal dose, Meerwein–Ponndorf–Verley reduction, Menthol, Metal, Methanol, Methyl group, Miscibility, N-Bromosuccinimide, Nozaki–Hiyama–Kishi reaction, Nucleophilic substitution, Nylon, Octanol, Online Etymology Dictionary, Organic compound, Organic reaction, Organoboron chemistry, Organobromine chemistry, Organochlorine chemistry, Organosulfate, Oxford English Dictionary, Oxford University Press, Oxidase, Oxymercuration reaction, Paracelsus, Paracetamol, Petroleum, Phenols, Phosphorus tribromide, Plasticizer, Pliny the Elder, Polyol, Polyvinyl chloride, Potassium hydroxide, Potassium permanganate, Preferred IUPAC name, Proceedings of the Chemical Society, Propane, Propanol, Propargyl alcohol, Propyl group, Propylene glycol, Pyridine, Radical substitution, Redox, Relative volatility, Roman Egypt, Rubbing alcohol, Salt (chemistry), Salt-effect distillation, Semitic languages, Serine, Skeletal formula, Sodium, Sodium borohydride, Sodium hydride, Sodium hydroxide, Solvation, Sorbitol, Starch, Stibnite, Structural formula, Sublimation (phase transition), Substituent, Sucrose, Sugar, Sugar alcohol, Sulfuric acid, Taddeo Alderotti, Terminal alkene, Tert-Amyl alcohol, Tert-Butyl alcohol, The BMJ, Theophrastus, Thionyl chloride, Threitol, Tosyl group, Toxicity, Transesterification, Tributyltin hydride, Triethylaluminium, Triphenylmethanol, Volemitol, Water, Williamson ether synthesis, Wine chemistry, Xenobiotic, Xylitol, Zaytsev's rule, Ziegler process, 1-Butanol, 1-Octanol, 1-Pentanol, 1-Propanol, 4-Toluenesulfonyl chloride.