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  2. SNi - Wikipedia

    en.wikipedia.org/wiki/SNi

    When the solvent is also a nucleophile such as dioxane two successive S N 2 reactions take place and the stereochemistry is again retention. With standard S N 1 reaction conditions the reaction outcome is retention via a competing S N i mechanism and not racemization and with pyridine added the result is again inversion. [5] [3]

  3. Antarafacial and suprafacial - Wikipedia

    en.wikipedia.org/wiki/Antarafacial_and_suprafacial

    In particular, antarafacial topology corresponds to inversion of configuration for the carbon atom of a [1, n]-sigmatropic rearrangement, and conrotation for electrocyclic ring closure, while suprafacial corresponds to retention and disrotation.

  4. Walden inversion - Wikipedia

    en.wikipedia.org/wiki/Walden_inversion

    In the Walden inversion, the backside attack by the nucleophile in an S N 2 reaction gives rise to a product whose configuration is opposite to the reactant. Therefore, during S N 2 reaction, 100% inversion of product takes place. This is known as Walden inversion. It was first observed by chemist Paul Walden in 1896.

  5. Inversion (music) - Wikipedia

    en.wikipedia.org/wiki/Inversion_(music)

    An interval is inverted by raising or lowering either of the notes by one or more octaves so that the higher note becomes the lower note and vice versa. For example, the inversion of an interval consisting of a C with an E above it (the third measure below) is an E with a C above it – to work this out, the C may be moved up, the E may be lowered, or both may be moved.

  6. Sigmatropic reaction - Wikipedia

    en.wikipedia.org/wiki/Sigmatropic_reaction

    Sigmatropic rearrangements are concisely described by an order term [i,j], which is defined as the migration of a σ-bond adjacent to one or more π systems to a new position (i−1) and (j−1) atoms removed from the original location of the σ-bond. [3]

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  8. Mitsunobu reaction - Wikipedia

    en.wikipedia.org/wiki/Mitsunobu_reaction

    The reaction mechanism of the Mitsunobu reaction is fairly complex. The identity of intermediates and the roles they play has been the subject of debate. Initially, the triphenyl phosphine (2) makes a nucleophilic attack upon diethyl azodicarboxylate (1) producing a betaine intermediate 3, which deprotonates the carboxylic acid (4) to form the ion pair 5.

  9. Spread between 2- and 10-year Treasuries at deepest inversion ...

    www.aol.com/news/us-2yr-10yr-yield-curve...

    The closely-watched spread between the 2-year and 10-year U.S. Treasury note yields hit the widest since 1981 at -109.50 in early trade, a deeper inversion than in March during the U.S. regional ...