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1,2-Wittig rearrangement; 2,3-Wittig rearrangement; Wittig–Horner reaction; Wohl degradation; Wohl–Aue reaction; Wohler synthesis; Wohl–Ziegler reaction; Wolffenstein–Böters reaction; Wolff rearrangement; Wolff–Kishner reduction; Woodward cis-hydroxylation; Woodward–Hoffmann rule; Wulff–Dötz reaction; Wurtz coupling, Wurtz ...
strong base used in organic chemistry for the deprotonation of weakly acidic compounds Manganese dioxide: used as a pigment and as a precursor to other manganese compounds; used as a reagent in organic synthesis for the oxidation of allylic alcohols Meta-Chloroperoxybenzoic acid: used as an oxidant in organic synthesis Methyl tert-butyl ether
A mnemonic is a memory aid used to improve long-term memory and make the process of consolidation easier. Many chemistry aspects, rules, names of compounds, sequences of elements, their reactivity, etc., can be easily and efficiently memorized with the help of mnemonics.
The following outline is provided as an overview of and topical guide to organic chemistry: Organic chemistry is the scientific study of the structure, properties, composition, reactions, and preparation (by synthesis or by other means) of carbon-based compounds, hydrocarbons, and their derivatives.
This is a list of common chemical compounds with chemical formulae and CAS numbers, indexed by formula.This complements alternative listing at list of inorganic compounds. ...
In organic chemistry, a type of chemical reaction in which two or more molecules combine to make a larger one. adduct A distinct chemical species that is the sole product of an addition reaction between two other distinct reactant species, in which all of the atoms comprising the reactants are retained in the single product. Changes in ...
As of 2017 there are 100 titles in the series, written by a wide range of authors. The editors are Steve G. Davies (Organic Chemistry), [2] Richard G. Compton (Physical Chemistry), John Evans (Inorganic Chemistry) and Lynn Gladden (Chemical Engineering).
It can also be named by replacing the "-oic acid" of their corresponding carboxylic acids with "-carbonitrile." The prefix form is "cyano-." Functional class IUPAC nomenclature may also be used in the form of alkyl cyanides. For example, CH 3 CH 2 CH 2 CH 2 C≡N is called pentanenitrile or butyl cyanide.