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The oxidation products derived from methyl are hydroxymethyl group −CH 2 OH, formyl group −CHO, and carboxyl group −COOH. For example, permanganate often converts a methyl group to a carboxyl (−COOH) group, e.g. the conversion of toluene to benzoic acid. Ultimately oxidation of methyl groups gives protons and carbon dioxide, as seen in ...
Methylation, in the chemical sciences, is the addition of a methyl group on a substrate, or the substitution of an atom (or group) by a methyl group. Methylation is a form of alkylation, with a methyl group replacing a hydrogen atom. These terms are commonly used in chemistry, biochemistry, soil science, and biology.
The methylene bridge (methanediyl group) In organic chemistry, a methylene bridge, methylene spacer, or methanediyl group is any part of a molecule with formula −CH 2 −; namely, a carbon atom bound to two hydrogen atoms and connected by single bonds to two other distinct atoms in the rest of the molecule.
For example, alkyl lithium reagents have the empirical formula Li(alkyl), where alkyl = methyl, ethyl, etc. A dialkyl ether is an ether with two alkyl groups, e.g., diethyl ether O(CH 2 CH 3 ) 2 . In medicinal chemistry
The group may be represented as −CH 2 − or >CH 2, where the '>' denotes the two bonds. This stands in contrast to a situation where the carbon atom is bound to the rest of the molecule by a double bond, which is preferably called a methylidene group, represented =CH 2. [2] Formerly the methylene name was used for both isomers.
For example, the tert-butyl group (A-value=4.9) has a larger A-value than the trimethylsilyl group (A-value=2.5), yet the tert-butyl group actually occupies less space. This difference can be attributed to the longer length of the carbon–silicon bond as compared to the carbon–carbon bond of the tert-butyl group.
SAM is the classical methyl donor for methyltransferases, however, examples of other methyl donors are seen in nature. The general mechanism for methyl transfer is a S N 2 -like nucleophilic attack where the methionine sulfur serves as the leaving group and the methyl group attached to it acts as the electrophile that transfers the methyl group ...
This functional group is composed of a methyl group bonded to an atom of mercury. Its chemical formula is CH 3 Hg + (sometimes written as MeHg +). The Methylmercury compound has an overall charge of +1, with Hg in the +2 oxidation state. Methylmercury exists as a substituent in many complexes of the type [MeHgL] + (L = Lewis base) and MeHgX (X ...