enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. N-Bromosuccinimide - Wikipedia

    en.wikipedia.org/wiki/N-Bromosuccinimide

    N-Bromosuccinimide or NBS is a chemical reagent used in radical substitution, electrophilic addition, and electrophilic substitution reactions in organic chemistry. NBS can be a convenient source of Br • , the bromine radical.

  3. Bouveault aldehyde synthesis - Wikipedia

    en.wikipedia.org/wiki/Bouveault_aldehyde_synthesis

    The Bouveault aldehyde synthesis (also known as the Bouveault reaction) is a one-pot substitution reaction that replaces an alkyl or aryl halide with a formyl group using a N,N-disubstituted formamide. [1] [2] For primary alkyl halides this produces the homologous aldehyde one carbon longer. For aryl halides this produces the corresponding ...

  4. Kharasch addition - Wikipedia

    en.wikipedia.org/wiki/Kharasch_addition

    chemical reactions for the Kharasch addition reaction of chloroform to a terminal alkene. The Kharasch addition is an organic reaction and a metal-catalysed free radical addition of CXCl 3 compounds (X = Cl, Br, H) to alkenes. [1] The reaction is used to append trichloromethyl or dichloromethyl groups to terminal alkenes.

  5. Hofmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Hofmann_rearrangement

    Several reagents can be substituted for bromine. Sodium hypochlorite, [4] lead tetraacetate, [5] N-bromosuccinimide, and (bis(trifluoroacetoxy)iodo)benzene [6] can effect a Hofmann rearrangement. The intermediate isocyanate can be trapped with various nucleophiles to form stable carbamates or other products rather than undergoing decarboxylation.

  6. Free-radical addition - Wikipedia

    en.wikipedia.org/wiki/Free-radical_addition

    Free-radical reactions depend on one or more relatively weak bonds in a reagent. Under reaction conditions (typically heat or light), some weak bonds homolyse into radicals, which then induce further decomposition in their compatriots before recombination. Different mechanisms typically apply to reagents without such a weak bond.

  7. AOL Mail is free and helps keep you safe.

    mail.aol.com/?offerId=netscapeconnect-en-us

    Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!

  8. Bartoli indole synthesis - Wikipedia

    en.wikipedia.org/wiki/Bartoli_indole_synthesis

    (Upon reaction workup, the magnesium salt will liberate a carbonyl compound (6).) Reaction of the nitrosoarene (4) with a second equivalent of the Grignard reagent (2) forms intermediate 7. The steric bulk of the ortho group causes a [3,3]-sigmatropic rearrangement forming the intermediate 8.

  9. Mortgage and refinance rates for Jan. 6, 2025: Average rates ...

    www.aol.com/finance/mortgage-and-refinance-rates...

    Average mortgage rates are edging down moderately week over week of Monday, January 6, 2024, though remain at elevated levels for benchmark 30-year and 15-year fixed terms, this despite three back ...