- an
alkoxy (-OR) group.
Usually phenol ethers are
synthesized through the
condensation of
phenol and an
organic alcohol; however,
other known reactions...
- by
plants and microorganisms.
Phenols are more
acidic than
typical alcohols. The
acidity of the
hydroxyl group in
phenols is
commonly intermediate between...
-
Phenol (also
known as
carbolic acid,
phenolic acid, or benzenol) is an
aromatic organic compound with the
molecular formula C6H5OH. It is a
white crystalline...
- as an
antifoaming agent in the
chloroform isoamyl alcohol reagent.
Isoamyl alcohol is used in a
phenol–chloroform
extraction mixed with the
chloroform to...
- group, in
contrast to the
phenols,
where the
hydroxyl group is
bonded directly to an
aromatic carbon atom.
Aromatic alcohols are
produced by the yeast...
-
separately as a
phenol and is
named using the
IUPAC rules for
naming phenols.
Phenols have
distinct properties and are not
classified as
alcohols. In other...
-
Isopropyl alcohol (IUPAC name propan-2-ol and also
called isopropanol or 2-propanol) is a colorless, flammable,
organic compound with a
pungent alcoholic...
-
family of
naturally occurring phenols. They are
abundant in
plants and
structurally diverse.
Polyphenols include phenolic acids, flavonoids,
tannic acid...
- The ****ene
process (****ene-
phenol process, Hock process) is an
industrial process for
synthesizing phenol and
acetone from
benzene and propylene. The term...
- co-reactants
including polyfunctional amines,
acids (and acid anhydrides),
phenols,
alcohols and
thiols (sometimes
called mercaptans).
These co-reactants are often...
