- can act as
nucleophiles.
Because nucleophiles donate electrons, they are
Lewis bases.
Nucleophilic describes the
affinity of a
nucleophile to bond with...
-
addition is a
reaction between a
Michael donor (an
enolate or
other nucleophile) and a
Michael acceptor (usually an α,β-unsaturated carbonyl) to produce...
-
mechanism that is
common in
organic chemistry. In the SN2 reaction, a
strong nucleophile forms a new bond to an sp3-hybridised
carbon atom via a
backside attack...
- and zero-order
dependence on the
nucleophile. This
relationship holds for
situations where the
amount of
nucleophile is much
greater than that of the...
-
chemical reactions in
which an electron-rich
chemical species (known as a
nucleophile)
replaces a
functional group within another electron-deficient molecule...
- chemistry, an
electrophile is a
chemical species that
forms bonds with
nucleophiles by
accepting an
electron pair.
Because electrophiles accept electrons...
-
chemical compound with an
electrophilic double or
triple bond
reacts with a
nucleophile, such that the
double or
triple bond is broken.
Nucleophilic additions...
-
second carbon atom.
Enamines are both good
nucleophiles and good bases.
Their behavior as carbon-based
nucleophiles is
explained with
reference to the following...
-
usually minor constituent of water. It
functions as a base, a ligand, a
nucleophile, and a catalyst. The
hydroxide ion
forms salts, some of
which dissociate...
- substitution, elimination, and
solvation reactions in
which water is the
nucleophile.
Biological hydrolysis is the
cleavage of
biomolecules where a water...
