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  2. Hughes–Ingold symbol - Wikipedia

    en.wikipedia.org/wiki/Hughes–Ingold_symbol

    A Hughes–Ingold symbol describes various details of the reaction mechanism and overall result of a chemical reaction. [1] For example, an S N 2 reaction is a substitution reaction ("S") by a nucleophilic process ("N") that is bimolecular ("2" molecular entities involved) in its rate-determining step .

  3. Transition state - Wikipedia

    en.wikipedia.org/wiki/Transition_state

    The concept of a transition state has been important in many theories of the rates at which chemical reactions occur. This started with the transition state theory (also referred to as the activated complex theory), which was first developed around 1935 by Eyring, Evans and Polanyi, and introduced basic concepts in chemical kinetics that are still used today.

  4. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    The bimolecular nucleophilic substitution (S N 2) is a type of reaction mechanism that is common in organic chemistry. In the S N 2 reaction, a strong nucleophile forms a new bond to an sp 3 -hybridised carbon atom via a backside attack, all while the leaving group detaches from the reaction center in a concerted (i.e. simultaneous) fashion.

  5. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    [1] [2] [3] Introduced by Gilbert N. Lewis in his 1916 article The Atom and the Molecule, a Lewis structure can be drawn for any covalently bonded molecule, as well as coordination compounds. [4] Lewis structures extend the concept of the electron dot diagram by adding lines between atoms to represent shared pairs in a chemical bond.

  6. Hammond's postulate - Wikipedia

    en.wikipedia.org/wiki/Hammond's_postulate

    Therefore, by definition, the transition state for tertiary reactions will be at a lower energy than for secondary reactions. However, the BEP principle cannot justify why the energy is lower. Using Hammond's postulate, the lower energy of the tertiary transition state means that its structure is relatively closer to its reactants R(tertiary)-X ...

  7. Lewis number - Wikipedia

    en.wikipedia.org/wiki/Lewis_number

    It is named after Warren K. Lewis (1882–1975), [6] [7] who was the first head of the Chemical Engineering Department at MIT. Some workers in the field of combustion assume (incorrectly) that the Lewis number was named for Bernard Lewis (1899–1993), who for many years was a major figure in the field of combustion research. [citation needed]

  8. Sialyl-Lewis X - Wikipedia

    en.wikipedia.org/wiki/Sialyl-Lewis_X

    Sialyl Lewis X (sLeX), also known as cluster of differentiation 15s (CD15s) or stage-specific embryonic antigen 1 (SSEA-1), is a tetrasaccharide carbohydrate which is usually attached to O-glycans on the surface of cells.

  9. Electron pair - Wikipedia

    en.wikipedia.org/wiki/Electron_pair

    In chemistry, an electron pair or Lewis pair consists of two electrons that occupy the same molecular orbital but have opposite spins. Gilbert N. Lewis introduced the concepts of both the electron pair and the covalent bond in a landmark paper he published in 1916. [1] [2]