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  2. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    In organic chemistry, an alkene, or olefin, is a hydrocarbon containing a carbon –carbon double bond. [ 1 ] The double bond may be internal or in the terminal position. Terminal alkenes are also known as α-olefins. The International Union of Pure and Applied Chemistry (IUPAC) recommends using the name "alkene" only for acyclic hydrocarbons ...

  3. Glycosidic bond - Wikipedia

    en.wikipedia.org/wiki/Glycosidic_bond

    A glycosidic bond or glycosidic linkage is a type of ether bond that joins a carbohydrate (sugar) molecule to another group, which may or may not be another carbohydrate. Formation of ethyl glucoside: Glucose and ethanol combine to form ethyl glucoside and water. The reaction often favors formation of the α-glycosidic bond as shown due to the ...

  4. Open-chain compound - Wikipedia

    en.wikipedia.org/wiki/Open-chain_compound

    An open-chain compound having no side groups is called a straight-chain compound (also spelled as straight chain compound). [2][3] Many of the simple molecules of organic chemistry, such as the alkanes and alkenes, have both linear and ring isomers, that is, both acyclic and cyclic. For those with 4 or more carbons, the linear forms can have ...

  5. Fischer projection - Wikipedia

    en.wikipedia.org/wiki/Fischer_projection

    Fischer projections were originally proposed for the depiction of carbohydrates and used by chemists, particularly in organic chemistry and biochemistry. The use of Fischer projections in non-carbohydrates is discouraged, as such drawings are ambiguous and easily confused with other types of drawing. The main purpose of Fischer projections is ...

  6. Straight-chain terminal alkene - Wikipedia

    en.wikipedia.org/wiki/Straight-chain_terminal_alkene

    Straight-chain terminal alkenes, also called linear alpha olefins (LAO) or normal alpha olefins (NAO), are alkenes (olefins) having a chemical formula C n H 2n, distinguished from other alkenes with a similar molecular formula by being terminal alkenes, in which the double bond occurs at the alpha (α-, 1-or primary) position, and by having a linear (unbranched) hydrocarbon chain.

  7. Stereoisomerism - Wikipedia

    en.wikipedia.org/wiki/Stereoisomerism

    Le Bel-van't Hoff rule states that for a structure with n asymmetric carbon atoms, there is a maximum of 2 n different stereoisomers possible. As an example, D-glucose is an aldohexose and has the formula C 6 H 12 O 6. Four of its six carbon atoms are stereogenic, which means D-glucose is one of 2 4 =16 possible stereoisomers. [25] [26]

  8. Monosaccharide - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide

    Monosaccharide. Monosaccharides (from Greek monos: single, sacchar: sugar), also called simple sugars, are the simplest forms of sugar and the most basic units (monomers) from which all carbohydrates are built. Chemically, monosaccharides are polyhydroxy aldehydes with the formula H- [CHOH] n-H with three or more carbon atoms.

  9. Dimerization - Wikipedia

    en.wikipedia.org/wiki/Dimerization

    Chemical process of joining two molecular entities by bonds of any kind. In chemistry, dimerization is the process of joining two identical or similar molecular entities by bonds. The resulting bonds can be either strong or weak. Many symmetrical chemical species are described as dimers, even when the monomer is unknown or highly unstable.