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  2. Inductive effect - Wikipedia

    en.wikipedia.org/wiki/Inductive_effect

    The inductive effect can be used to determine the stability of a molecule depending on the charge present on the atom and the groups bonded to the atom. For example, if an atom has a positive charge and is attached to a - I group its charge becomes 'amplified' and the molecule becomes more unstable.

  3. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    The inductive effect is the transmission of charge through covalent bonds and Bent's rule provides a mechanism for such results via differences in hybridisation. In the table below, [ 26 ] as the groups bonded to the central carbon become more electronegative, the central carbon becomes more electron-withdrawing as measured by the polar ...

  4. Electronic effect - Wikipedia

    en.wikipedia.org/wiki/Electronic_effect

    An electric effect influences the structure, reactivity, or properties of a molecule but is neither a traditional bond nor a steric effect. [1] In organic chemistry , the term stereoelectronic effect is also used to emphasize the relation between the electronic structure and the geometry ( stereochemistry ) of a molecule.

  5. Electron-withdrawing group - Wikipedia

    en.wikipedia.org/wiki/Electron-withdrawing_group

    Electron-withdrawing groups exert an "inductive" or "electron-pulling" effect on covalent bonds. The strength of the electron-withdrawing group is inversely proportional to the pKa of the carboxylic acid. [2] The inductive effect is cumulative: trichloroacetic acid is 1000x stronger than chloroacetic acid.

  6. Electrophilic aromatic directing groups - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_aromatic...

    Due to the electronegativity difference between carbon and oxygen / nitrogen, there will be a slight electron withdrawing effect through inductive effect (known as the –I effect). However, the other effect called resonance add electron density back to the ring (known as the +M effect) and dominate over that of inductive effect.

  7. Taft equation - Wikipedia

    en.wikipedia.org/wiki/Taft_equation

    It was developed by Robert W. Taft in 1952 [2] [3] [4] as a modification to the Hammett equation. [5] While the Hammett equation accounts for how field, inductive, and resonance effects influence reaction rates, the Taft equation also describes the steric effects of a substituent. The Taft equation is written as:

  8. 24 Discontinued '70s and '80s Foods That We'll Never ... - AOL

    www.aol.com/finance/24-discontinued-70s-80s...

    3. Keebler Fudge Magic Middles. Neither the chocolate fudge cream inside a shortbread cookie nor versions with peanut butter or chocolate chip crusts survived.

  9. Fragmentation (mass spectrometry) - Wikipedia

    en.wikipedia.org/wiki/Fragmentation_(mass...

    Fragmentation is a type of chemical dissociation, in which the removal of the electron from the molecule results in ionization. Removal of electrons from either sigma bond, pi bond or nonbonding orbitals causes the ionization. [2] This can take place by a process of homolytic cleavage or homolysis or heterolytic cleavage or heterolysis of the ...