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  2. Phosphoryl chloride - Wikipedia

    en.wikipedia.org/wiki/Phosphoryl_chloride

    The reaction of phosphorus pentachloride (PCl 5) with phosphorus pentoxide (P 4 O 10). 6 PCl 5 + P 4 O 10 → 10 POCl 3. The reaction can be simplified by chlorinating a mixture of PCl 3 and P 4 O 10, generating the PCl 5 in situ. The reaction of phosphorus pentachloride with boric acid or oxalic acid: [12] 3 PCl 5 + 2 B(OH) 3 → 3 POCl 3 + B ...

  3. Vilsmeier–Haack reaction - Wikipedia

    en.wikipedia.org/wiki/Vilsmeier–Haack_reaction

    The reaction of a substituted amide with phosphorus oxychloride gives a substituted chloroiminium ion (2), also called the Vilsmeier reagent. The initial product is an iminium ion (4b), which is hydrolyzed to the corresponding ketone or aldehyde during workup. [7] The Vilsmeier–Haack reaction

  4. Phosphorus pentachloride - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_pentachloride

    This reaction is used to produce around 10,000 tonnes of PCl 5 per year (as of 2000). [6] PCl 3 + Cl 2 ⇌ PCl 5 (ΔH = −124 kJ/mol) PCl 5 exists in equilibrium with PCl 3 and chlorine, and at 180 °C the degree of dissociation is about 40%. [6] Because of this equilibrium, samples of PCl 5 often contain chlorine, which imparts a greenish ...

  5. Pyridinium chlorochromate - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_chlorochromate

    Pyridinium chlorochromate in a vial. Pyridinium chlorochromate (PCC) is a yellow-orange salt with the formula [C 5 H 5 NH] + [CrO 3 Cl] −.It is a reagent in organic synthesis used primarily for oxidation of alcohols to form carbonyls.

  6. 2-Chloropyridine - Wikipedia

    en.wikipedia.org/wiki/2-Chloropyridine

    2-Chloropyridine reacts with nucleophiles to generate pyridine derivatives substituted at the second and fourth carbons on the heterocycle. Therefore, many reactions using 2-chloropyridine generate mixtures of products which require further workup to isolate the desired isomer.

  7. Nucleophilic aromatic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_aromatic...

    This reaction differs from a common S N 2 reaction, because it happens at a trigonal carbon atom (sp 2 hybridization). The mechanism of S N 2 reaction does not occur due to steric hindrance of the benzene ring. In order to attack the C atom, the nucleophile must approach in line with the C-LG (leaving group) bond from the back, where the ...

  8. I Trained Myself to Feel Good About Saving Money—Here’s How ...

    www.aol.com/trained-myself-feel-good-saving...

    This chemical reaction is thanks to the part of our brains associated with pleasure and reward. Even when we’re spending our money to buy something, the reward center says, “Yay, for you!”

  9. List of psychological effects - Wikipedia

    en.wikipedia.org/wiki/List_of_psychological_effects

    Ambiguity effect; Assembly bonus effect; Audience effect; Baader–Meinhof effect; Barnum effect; Bezold effect; Birthday-number effect; Boomerang effect; Bouba/kiki effect