enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. 2,2,4,4-Tetramethyl-3-t-butyl-pentane-3-ol - Wikipedia

    en.wikipedia.org/wiki/2,2,4,4-Tetramethyl-3-t...

    2,2,4,4-Tetramethyl-3-t-butyl-pentane-3-ol or tri-tert-butylcarbinol is an organic compound with formula C 13 H 28 O, ((H 3 C) 3 C) 3 COH, or t Bu 3 COH. [1] It is an alcohol that can be viewed as a structural analog of a tridecane isomer ( 2,2,4,4-tetramethyl-3- t -butylpentane ) where the central hydrogen has been replaced by a hydroxyl group ...

  3. Aldol reaction - Wikipedia

    en.wikipedia.org/wiki/Aldol_reaction

    [2] [3] [4] The aldol reaction is paradigmatic in organic chemistry and one of the most common means of forming carbon–carbon bonds in organic chemistry . [ 5 ] [ 6 ] [ 7 ] It lends its name to the family of aldol reactions and similar techniques analyze a whole family of carbonyl α-substitution reactions , as well as the diketone ...

  4. Triphenylmethane - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethane

    The Ph 3 C-H bond is relatively weak, with a bond dissociation energy (BDE) of 81 kcal/mol, or about 24 kcal/mol less than methane. [4] Correspondingly, triphenylmethane is mildly acidic, with a pK a of 33.297.

  5. Reaction mechanism - Wikipedia

    en.wikipedia.org/wiki/Reaction_mechanism

    The experimental reaction order is 3/2, [4] which can be explained by a Rice-Herzfeld mechanism. [5] This reaction mechanism for acetaldehyde has 4 steps with rate equations for each step : Initiation : CH 3 CHO → •CH 3 + •CHO (Rate=k 1 [CH 3 CHO]) Propagation: CH 3 CHO + •CH 3 → CH 4 + CH 3 CO• (Rate=k 2 [CH 3 CHO][•CH 3])

  6. One-pot synthesis - Wikipedia

    en.wikipedia.org/wiki/One-pot_synthesis

    A sequential one-pot synthesis with reagents added to a reactor one at a time and without work-up is also called a telescoping synthesis. In one such procedure [ 2 ] the reaction of 3-N-tosylaminophenol I with acrolein II affords a hydroxyl substituted quinoline III through 4 sequential steps without workup of the intermediate products (see image).

  7. Solvated electron - Wikipedia

    en.wikipedia.org/wiki/Solvated_electron

    Solvated electrons are involved in the reaction of alkali metals with water, even though the solvated electron has only a fleeting existence. [10] Below pH = 9.6 the hydrated electron reacts with the hydronium ion giving atomic hydrogen, which in turn can react with the hydrated electron giving hydroxide ion and usual molecular hydrogen H 2 .

  8. Heterogeneous water oxidation - Wikipedia

    en.wikipedia.org/wiki/Heterogeneous_Water_Oxidation

    Water oxidation is one of the half reactions of water splitting: 2H 2 O → O 2 + 4H + + 4e − Oxidation (generation of dioxygen) 4H + + 4e − → 2H 2 Reduction (generation of dihydrogen) 2H 2 O → 2H 2 + O 2 Total Reaction Of the two half reactions, the oxidation step is the most demanding because it requires the coupling of 4 electron and ...

  9. Click chemistry - Wikipedia

    en.wikipedia.org/wiki/Click_chemistry

    Cu 2 O in water at room temperature was found also to catalyze the same reaction in 15 minutes with 91% yield. [18] The first reaction mechanism proposed included one catalytic copper atom; but isotope, kinetic, and other studies have suggested a dicopper mechanism may be more relevant.