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The reaction most often occurs at an aliphatic sp 3 carbon center with an electronegative, stable leaving group attached to it, which is frequently a halogen (often denoted X). The formation of the C–Nu bond, due to attack by the nucleophile (denoted Nu), occurs together with the breakage of the C–X bond.
Aprotic solvents do not add protons (H + ions) into solution; if protons were present in S N 2 reactions, they would react with the nucleophile and severely limit the reaction rate. Since this reaction occurs in one step, steric effects drive the reaction speed. In the intermediate step, the nucleophile is 185 degrees from the leaving group and ...
Two enantiomers of a generic amino acid at the stereocenter. In stereochemistry, a stereocenter of a molecule is an atom (center), axis or plane that is the focus of stereoisomerism; that is, when having at least three different groups bound to the stereocenter, interchanging any two different groups creates a new stereoisomer.
Aromatic rings are usually nucleophilic, but some aromatic compounds do undergo nucleophilic substitution. Just as normally nucleophilic alkenes can be made to undergo conjugate substitution if they carry electron-withdrawing substituents, so normally nucleophilic aromatic rings also become electrophilic if they have the right substituents.
In quantum mechanics, a sum rule is a formula for transitions between energy levels, in which the sum of the transition strengths is expressed in a simple form. Sum rules are used to describe the properties of many physical systems, including solids, atoms, atomic nuclei, and nuclear constituents such as protons and neutrons.
The D- and L- prefixes describe the molecule as a whole, as do the (+) and (−) prefixes for optical rotation. In contrast, the ( R )- and ( S )- prefixes from the Cahn–Ingold–Prelog priority rules characterize the absolute configuration of each specific chiral stereocenter with the molecule, rather than a property of the molecule as a whole.
The space of bounded linear operators B(X) on a Banach space X is an example of a unital Banach algebra. Since the definition of the spectrum does not mention any properties of B(X) except those that any such algebra has, the notion of a spectrum may be generalised to this context by using the same definition verbatim.
The leaving group is denoted "X", and the nucleophile is denoted "Nu–H". The unimolecular nucleophilic substitution ( S N 1 ) reaction is a substitution reaction in organic chemistry . The Hughes-Ingold symbol of the mechanism expresses two properties—"S N " stands for " nucleophilic substitution ", and the "1" says that the rate ...