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  2. Intramolecular reaction - Wikipedia

    en.wikipedia.org/wiki/Intramolecular_reaction

    For the 'small rings' (3- and 4- membered), the slow rates is a consequence of angle strain experienced at the transition state. Although three-membered rings are more strained, formation of aziridine is faster than formation of azetidine due to the proximity of the leaving group and nucleophile in the former, which increases the probability that they would meet in a reactive conformation.

  3. Sigmatropic reaction - Wikipedia

    en.wikipedia.org/wiki/Sigmatropic_reaction

    As a general approach, one can simply draw the transition state of the reaction. For a sigmatropic reaction, the transition state will consist of two fragments, joined by the forming and breaking σ-bonds. The sigmatropic reaction is named as a [i,j]-sigmatropic rearrangement (i ≤ j) if these two fragments consist of i and j atoms. This is ...

  4. Curtin–Hammett principle - Wikipedia

    en.wikipedia.org/wiki/Curtin–Hammett_principle

    The Curtin–Hammett principle is a principle in chemical kinetics proposed by David Yarrow Curtin and Louis Plack Hammett.It states that, for a reaction that has a pair of reactive intermediates or reactants that interconvert rapidly (as is usually the case for conformational isomers), each going irreversibly to a different product, the product ratio will depend both on the difference in ...

  5. Ternary complex - Wikipedia

    en.wikipedia.org/wiki/Ternary_complex

    A ternary complex is a protein complex containing three different molecules that are bound together. In structural biology, ternary complex can also be used to describe a crystal containing a protein with two small molecules bound, such as a cofactor and a substrate; or a complex formed between two proteins and a single substrate. [1]

  6. Crossover experiment (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Crossover_experiment...

    Crossover experiments allow for experimental study of a reaction mechanism. Mechanistic studies are of interest to theoretical and experimental chemists for a variety of reasons including prediction of stereochemical outcomes, optimization of reaction conditions for rate and selectivity, and design of improved catalysts for better turnover number, robustness, etc. [6] [7] Since a mechanism ...

  7. Ramberg–Bäcklund reaction - Wikipedia

    en.wikipedia.org/wiki/Ramberg–Bäcklund_reaction

    Small-ring application of the Ramberg–Bäcklund reaction. This reaction type gives access to 1,2-dimethylenecyclohexane. Scheme 5. Ramberg–Bäcklund synthesis of dimethylene-cyclohexane. and the epoxide variation access to allyl alcohols. A recently developed application of the Ramberg–Bäcklund reaction is the synthesis of C-glycosides.

  8. Free-radical addition - Wikipedia

    en.wikipedia.org/wiki/Free-radical_addition

    Chain termination: Two radicals react with each other to create a non-radical species; In a free-radical addition, there are two chain propagation steps. In one, the adding radical attaches to a multiply-bonded precursor to give a radical with lesser bond order. In the other, the newly-formed radical product abstracts another substituent from ...

  9. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    The σ from the 2p is more non-bonding due to mixing, and same with the 2s σ. This also causes a large jump in energy in the 2p σ* orbital. The bond order of diatomic nitrogen is three, and it is a diamagnetic molecule. [12] The bond order for dinitrogen (1σ g 2 1σ u 2 2σ g 2 2σ u 2 1π u 4 3σ g 2) is three because two electrons are now ...