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The linear molecular geometry describes the geometry around a central atom bonded to two other atoms (or ligands) placed at a bond angle of 180°. Linear organic molecules , such as acetylene ( HC≡CH ), are often described by invoking sp orbital hybridization for their carbon centers.
Linear pathways follow a step-by-step sequence, where each enzymatic reaction results in the transformation of a substrate into an intermediate product. This intermediate is processed by subsequent enzymes until the final product is synthesized. A linear chain of four enzyme-catalyzed steps. A linear pathway can be studied in various ways.
The names for the degrees may be applied to the polynomial or to its terms. For example, the term 2x in x 2 + 2x + 1 is a linear term in a quadratic polynomial. The polynomial 0, which may be considered to have no terms at all, is called the zero polynomial. Unlike other constant polynomials, its degree is not zero.
The Taft equation is a linear free energy relationship (LFER) used in physical organic chemistry in the study of reaction mechanisms and in the development of quantitative structure–activity relationships for organic compounds. It was developed by Robert W. Taft in 1952 [2] [3] [4] as a modification to the Hammett equation. [5]
In chemistry, an open-chain compound (or open chain compound) or acyclic compound (Greek prefix α 'without' and κύκλος 'cycle') is a compound with a linear structure, rather than a cyclic one. [1] An open-chain compound having no side groups is called a straight-chain compound (also spelled as straight chain compound).
Example cheletropic reactions: Case 1: the single atom is the carbonyl carbon ( C=O ) that ends up in carbon monoxide ( C≡O ). Case 2: the single atom is the nitrogen atom in the diazenyl group ( N=N ), which ends up as dinitrogen ( N≡N ).
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.
IUPAC has suggested that this name should be replaced by linear Gibbs energy relation, but at present there is little sign of acceptance of this change. [1] The area of physical organic chemistry which deals with such relations is commonly referred to as 'linear free-energy relationships'.
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