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  2. Bradsher cycloaddition - Wikipedia

    en.wikipedia.org/wiki/Bradsher_cycloaddition

    Download as PDF; Printable version; In other projects ... The Bradsher cycloaddition was first reported by C. K. Bradsher and T. W. G. Solomons in 1958. [1] [2] [3 ...

  3. Aromatic sulfonation - Wikipedia

    en.wikipedia.org/wiki/Aromatic_sulfonation

    In organic chemistry, aromatic sulfonation is an reaction in which a hydrogen atom on an arene is replaced by a sulfonic acid (−SO 2 OH) group. Together with nitration and chlorination, aromatic sulfonation is a widely used electrophilic aromatic substitutions. [1] Aryl sulfonic acids are used as detergents, dye, and drugs.

  4. Wurtz reaction - Wikipedia

    en.wikipedia.org/wiki/Wurtz_reaction

    In organic chemistry, the Wurtz reaction, named after Charles Adolphe Wurtz, is a coupling reaction in which two alkyl halides are treated with sodium metal to form a higher alkane. 2 R−X + 2 Na → R−R + 2 NaX. The reaction is of little value except for intramolecular versions, such as 1,6-dibromohexane + 2 Na → cyclohexane + 2 NaBr.

  5. File:Organic Chemistry.pdf - Wikipedia

    en.wikipedia.org/wiki/File:Organic_Chemistry.pdf

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Donate

  6. Allan–Robinson reaction - Wikipedia

    en.wikipedia.org/wiki/Allan–Robinson_reaction

    The o-hydroxyaryl ketone first undergoes tautomerization to form the respective enol.The pi electrons of the double bond then attack the electrophilic carbon of the anhydride; a carboxylate anion is subsequently lost as a leaving group.

  7. Hemiacetal - Wikipedia

    en.wikipedia.org/wiki/Hemiacetal

    In organic chemistry, a hemiacetal is a functional group the general formula R 1 R 2 C(OH)OR, where R 1, R 2 is a hydrogen atom or an organic substituent. They generally result from the nucleophilic addition of an alcohol (a compound with at least one hydroxy group) to an aldehyde (R−CH=O) or a ketone (R 2 C=O) under acidic conditions.

  8. Absolute configuration - Wikipedia

    en.wikipedia.org/wiki/Absolute_configuration

    In chemistry, absolute configuration refers to the spatial arrangement of atoms within a molecular entity (or group) that is chiral, and its resultant stereochemical description. [1] Absolute configuration is typically relevant in organic molecules where carbon is bonded to four different substituents .

  9. Bredt's rule - Wikipedia

    en.wikipedia.org/wiki/Bredt's_rule

    In organic chemistry, an anti-Bredt molecule is a bridged molecule with a double bond at the bridgehead. Bredt's rule is the empirical observation that such molecules only form in large ring systems. For example, two of the following norbornene isomers violate Bredt's rule, and are too unstable to prepare: Bridgehead atoms violating Bredt's ...