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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. Trifluoromethylation - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethylation

    In the CF 3 radical the fluorine atom is an electron-withdrawing group via the inductive effect but also a weak pi donor through interaction of the fluorine lone pair with the radical center's SOMO. Compared to the methyl radical the CF 3 radical is pyramidal (angle 107.8 °C ) with a large inversion barrier , electrophilic and also more reactive.

  5. Field effect (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Field_effect_(chemistry)

    The polarization of a molecule through its bonds is a separate phenomenon known as induction. [3] Field effects are relatively weak, and diminish rapidly with distance, but have still been found to alter molecular properties such as acidity. [1] Field effect on a carbonyl arising from the dipole in a C-F bond.

  6. Markovnikov's rule - Wikipedia

    en.wikipedia.org/wiki/Markovnikov's_rule

    In a titanium(IV) chloride-catalyzed formal nucleophilic substitution at enantiopure 1 in the scheme below, two products are formed – 2a and 2b Due to the two chiral centers in the target molecule, the carbon carrying chlorine and the carbon carrying the methyl and acetoxyethyl group, four different compounds are to be formed: 1R,2R- (drawn ...

  7. Hammett equation - Wikipedia

    en.wikipedia.org/wiki/Hammett_equation

    This effect is depicted in scheme 3, where, in a para substituted arene 1a, one resonance structure 1b is a quinoid with positive charge on the X substituent, releasing electrons and thus destabilizing the Y substituent. This destabilizing effect is not possible when X has a meta orientation. Scheme 3. Hammett Inductive Mesomeric Effects

  8. Manhattan drivers face $9 fee in first such US effort to ...

    www.aol.com/news/manhattan-drivers-face-9-fee...

    New York City drivers on Monday had to pay $9 to enter Manhattan under the first such congestion fee in the U.S., which seeks to raise billions for mass transit and reduce traffic jams. The fee ...

  9. Vinyl cation - Wikipedia

    en.wikipedia.org/wiki/Vinyl_cation

    Usually, the inductive effect brought upon by multiple bonds to a heteroatom can be counterbalanced by p donation from the same heteroatom. For instance, based on absolute b-inductive power, -CN is more inductive than CF 3, but since there can be p donation from the nitrogen of CN, its inductive capability is reduced. In common heteroatomic ...