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Amine. In chemistry, amines (/ ə ˈ m iː n, ˈ æ m iː n /, [1] [2] UK also / ˈ eɪ m iː n / [3]) are compounds and functional groups that contain a basic nitrogen atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3), wherein one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group [4] (these may respectively be called alkylamines ...
phosphines of the formula PR 3−x Ar x. compounds of O, S, Se and Te in oxidation state −2, including water, ethers, ketones; The most common Lewis bases are anions. The strength of Lewis basicity correlates with the pK a of the parent acid: acids with high pK a 's give good Lewis bases.
Base (chemistry) Soaps are weak bases formed by the reaction of fatty acids with sodium hydroxide or potassium hydroxide. In chemistry, there are three definitions in common use of the word " base ": Arrhenius bases, Brønsted bases, and Lewis bases. All definitions agree that bases are substances that react with acids, as originally proposed ...
In organic chemistry, an amide, [1][2][3] also known as an organic amide or a carboxamide, is a compound with the general formula R−C (=O)−NR′R″, where R, R', and R″ represent any group, typically organyl groups or hydrogen atoms. [4][5] The amide group is called a peptide bond when it is part of the main chain of a protein, and an ...
Weak. v. t. e. As the name suggests, a non-nucleophilic base is a sterically hindered organic base that is a poor nucleophile. Normal bases are also nucleophiles, but often chemists seek the proton-removing ability of a base without any other functions. Typical non-nucleophilic bases are bulky, such that protons can attach to the basic center ...
Carbon–nitrogen bond. A carbon–nitrogen bond is a covalent bond between carbon and nitrogen and is one of the most abundant bonds in organic chemistry and biochemistry. [ 1 ] Nitrogen has five valence electrons and in simple amines it is trivalent, with the two remaining electrons forming a lone pair. Through that pair, nitrogen can form an ...
Aromatic amine. In organic chemistry, an aromatic amine is an organic compound consisting of an aromatic ring attached to an amine. It is a broad class of compounds that encompasses anilines, but also many more complex aromatic rings and many amine substituents beyond NH2. Such compounds occur widely. [1] Representative aromatic amines.
Amidine. The skeletal formula of acetamidine (acetimidamide). Amidines are organic compounds with the functional group RC (NR)NR 2, where the R groups can be the same or different. They are the imine derivatives of amides (RC (O)NR 2). The simplest amidine is formamidine, HC (=NH)NH 2. Examples of amidines include: