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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. Rotamer - Wikipedia

    en.wikipedia.org/wiki/Rotamer

    The short timescale of interconversion precludes the separation of conformer in most cases. Atropisomers are conformational isomers which can be separated due to restricted rotation. [ 18 ] The equilibrium between conformational isomers can be observed using a variety of spectroscopic techniques .

  4. Aldol reaction - Wikipedia

    en.wikipedia.org/wiki/Aldol_reaction

    The disposition of the formed stereocenters is deemed syn or anti, depending if they are on the same or opposite sides of the main chain: Syn and anti products from an aldol (addition) reaction. The principal factor determining an aldol reaction's stereoselectivity is the enolizing metal counterion.

  5. endo–exo isomerism - Wikipedia

    en.wikipedia.org/wiki/Endo–exo_isomerism

    The prefix endo is reserved for the isomer with the substituent located closest, or "syn", to the longest bridge. The prefix exo is reserved for the isomer with the substituent located farthest, or "anti", to the longest bridge. Here "longest" and "shortest" refer to the number of atoms that comprise the bridge.

  6. 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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  8. Retrosynthetic analysis - Wikipedia

    en.wikipedia.org/wiki/Retrosynthetic_analysis

    Retrosynthetic analysis is a technique for solving problems in the planning of organic syntheses.This is achieved by transforming a target molecule into simpler precursor structures regardless of any potential reactivity/interaction with reagents.

  9. Syngas to gasoline plus - Wikipedia

    en.wikipedia.org/wiki/Syngas_to_gasoline_plus

    The STG+ process eliminates multiple condensation and evaporation, and the process converts syngas to liquid transportation fuels directly without producing intermediate liquids. [7] This eliminates the need for storage of two products, including pressure storage for liquefied petroleum gas and storage of liquid methanol.

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