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  2. Syn and anti addition - Wikipedia

    en.wikipedia.org/wiki/Syn_and_anti_addition

    The concepts of syn and anti addition are used to characterize the different reactions of organic chemistry by reflecting the stereochemistry of the products in a reaction. The type of addition that occurs depends on multiple different factors of a reaction, and is defined by the final orientation of the substituents on the parent molecule .

  3. Anti-periplanar - Wikipedia

    en.wikipedia.org/wiki/Anti-periplanar

    Anti-periplanar geometry will put a bonding orbital and an anti-bonding orbital approximately parallel to each other, or syn-periplanar. Figure 6 is another representation of 2-chloro-2,3-dimethylbutane (Figure 5), showing the C–H bonding orbital, σ C–H, and the C–Cl anti-bonding orbital, σ* C–Cl, syn-periplanar.

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  5. File:Zincophorin showing syn and anti 1,3-diols.svg - Wikipedia

    en.wikipedia.org/wiki/File:Zincophorin_showing...

    English: Chemical diagram of zincophorin showing syn and anti 1,3-diols. Date: 20 October 2024: Source: Own work: Author: User:Innerstream: Permission (Reusing this file)

  6. File:Aldol syn-anti.svg - Wikipedia

    en.wikipedia.org/wiki/File:Aldol_syn-anti.svg

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  7. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    syn/anti peri/clinal. a torsion angle between 0° and ±90° is called syn (s) a torsion angle between ±90° and 180° is called anti (a) a torsion angle between 30° and 150° or between −30° and −150° is called clinal (c) a torsion angle between 0° and ±30° or ±150° and 180° is called periplanar (p)

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  9. Peterson olefination - Wikipedia

    en.wikipedia.org/wiki/Peterson_olefination

    The Peterson olefination (also called the Peterson reaction) is the chemical reaction of α-silyl carbanions (1 in diagram below) with ketones (or aldehydes) to form a β-hydroxysilane (2) which eliminates to form alkenes (3).

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