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  2. Kinetic isotope effect - Wikipedia

    en.wikipedia.org/wiki/Kinetic_isotope_effect

    A primary kinetic isotope effect (PKIE) may be found when a bond to the isotopically labeled atom is being formed or broken. [3] [4]: 427 Depending on the way a KIE is probed (parallel measurement of rates vs. intermolecular competition vs. intramolecular competition), the observation of a PKIE is indicative of breaking/forming a bond to the isotope at the rate-limiting step, or subsequent ...

  3. Hyperconjugation - Wikipedia

    en.wikipedia.org/wiki/Hyperconjugation

    Hyperconjugation can be used to rationalize a variety of chemical phenomena, including the anomeric effect, the gauche effect, the rotational barrier of ethane, the beta-silicon effect, the vibrational frequency of exocyclic carbonyl groups, and the relative stability of substituted carbocations and substituted carbon centred radicals, and the thermodynamic Zaitsev's rule for alkene stability.

  4. Hydrogen–deuterium exchange - Wikipedia

    en.wikipedia.org/wiki/Hydrogen–deuterium_exchange

    The exchange reaction can be followed using a variety of methods (see Detection). Since this exchange is an equilibrium reaction, the molar amount of deuterium should be high compared to the exchangeable protons of the substrate. For instance, deuterium is added to a protein in H 2 O by diluting the H 2 O solution with D 2 O (e.g. tenfold ...

  5. Baker–Nathan effect - Wikipedia

    en.wikipedia.org/wiki/Baker–Nathan_effect

    Other researchers have found similar results or very different results. An alternative explanation for the effect is differential solvation as orders invert on going from the solution phase to the gas phase. [5] Today, the conjugation of neighbouring pi orbitals and polarised sigma bonds is known as hyperconjugation.

  6. Alpha effect - Wikipedia

    en.wikipedia.org/wiki/Alpha_effect

    The alpha effect is also dependent on solvent but not in a predictable way: it can increase or decrease with solvent mix composition or even go through a maximum. [12] At least in some cases, the alpha effect has been observed to vanish if the reaction is conducted in the gas phase, leading some to conclude that it is primarily a solvation ...

  7. Markovnikov's rule - Wikipedia

    en.wikipedia.org/wiki/Markovnikov's_rule

    Adding the hydrogen ion to one carbon atom in the alkene creates a positive charge on the other carbon, forming a carbocation intermediate. The more substituted the carbocation, the more stable it is, due to induction and hyperconjugation. The major product of the addition reaction will be the one formed from the more stable intermediate.

  8. Cannizzaro reaction - Wikipedia

    en.wikipedia.org/wiki/Cannizzaro_reaction

    Due to the strongly alkaline reaction conditions, aldehydes that have alpha hydrogen atom(s) instead undergo deprotonation there, leading to enolates and possible aldol reactions. Under ideal conditions the reaction produces 50% of both the alcohol and the carboxylic acid (it takes two aldehydes to produce one acid and one alcohol). [5]

  9. Nuclear transmutation - Wikipedia

    en.wikipedia.org/wiki/Nuclear_transmutation

    Hydrogen and helium together account for 98% of the mass of ordinary matter in the universe, while the other 2% makes up everything else. The Big Bang also produced small amounts of lithium, beryllium and perhaps boron. More lithium, beryllium and boron were produced later, in a natural nuclear reaction, cosmic ray spallation.