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  2. Captodative effect - Wikipedia

    en.wikipedia.org/wiki/Captodative_effect

    The ethoxy and cyano groups are able to delocalize the radical ion in the transition state, thus stabilizing the radical center. The rate enhancement is due to the captodative effect. When R = H, the reaction has the largest energy of activation because the radical center is not stabilized by the captodative effect.

  3. Radical (chemistry) - Wikipedia

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

    In chemistry, a radical, also known as a free radical, is an atom, molecule, or ion that has at least one unpaired valence electron. [1] [2] With some exceptions, these unpaired electrons make radicals highly chemically reactive. Many radicals spontaneously dimerize. Most organic radicals have short lifetimes.

  4. List of weight training exercises - Wikipedia

    en.wikipedia.org/wiki/List_of_weight_training...

    This exercise targets the hamstrings, glutes, and quadriceps, making it a great full-body movement. This movement also requires good balance and stability, so core strength is also an important aspect. Equipment required Bench, dumbbell or body weight. Variations

  5. 10 Best Stability Exercises To Build Strength - AOL

    www.aol.com/lifestyle/10-best-stability...

    We chatted with Nadia Murdock, CPT, a certified fitness instructor at Garage Gym Reviews, who shares her top 10 stability exercises to build strength that you can seamlessly work into your

  6. List of elements by stability of isotopes - Wikipedia

    en.wikipedia.org/wiki/List_of_elements_by...

    An even number of protons or neutrons is more stable (higher binding energy) because of pairing effects, so even–even nuclides are much more stable than odd–odd. One effect is that there are few stable odd–odd nuclides: in fact only five are stable, with another four having half-lives longer than a billion years.

  7. Stable phosphorus radicals - Wikipedia

    en.wikipedia.org/wiki/Stable_phosphorus_radicals

    The phosphinyl radicals synthesised by Lappert and co-workers were found to be stable at room temperature for periods of over 15 days with no effect from short-term heating at 360 K. [4] This stability was assigned to the steric bulk of the substituents and the absence of beta-hydrogen atoms.

  8. Conservative watchdog unveils list of ‘radical leftist ...

    www.aol.com/conservative-watchdog-unveils-list...

    A conservative watchdog has unveiled a list of “radical leftist” officials working in or with the Department of Homeland Security — as immigration and the crisis at the southern border ...

  9. Thiyl radical - Wikipedia

    en.wikipedia.org/wiki/Thiyl_radical

    The formation of thiyl radicals in vivo primarily occurs through the action of various radicals on the amino acid cysteine incorporated into proteins. The rate of radical formation is highest with the OH · radical (k = 6.8 x 10 9 M −1 s −1) [3] and decreases through the H · radical (k = 6.8 x 10 9 M −1 s −1) [3] down to peroxyl radicals R-CHOO · (k = 4.2 x 10 3 M −1 s −1).