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  2. 2-Bromohexane - Wikipedia

    en.wikipedia.org/wiki/2-Bromohexane

    Most 2-bromoalkanes are prepared by addition of hydrogen bromide to the 1-alkene. Markovnikov addition proceeds in the absence of free-radicals, i.e. give the 2-bromo derivatives. [ 2 ]

  3. 1-Bromopentane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopentane

    Most 1-bromoalkanes are prepared by free-radical addition of hydrogen bromide to the 1-alkene, which is 1-pentene in the case of 1-bromopentane. These conditions lead to anti-Markovnikov addition, giving the 1-bromo derivative. [2] It is also formed by the reaction of 1-pentanol with hydrogen bromide.

  4. Organobromine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organobromine_chemistry

    Carbon–halogen bond strengths, or bond dissociation energies are of 115, 83.7, 72.1, and 57.6 kcal/mol for bonded to fluorine, chlorine, bromine, or iodine, respectively. [3] The reactivity of organobromine compounds resembles but is intermediate between the reactivity of organochlorine and organoiodine compounds. For many applications ...

  5. Carbonyl olefin metathesis - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_olefin_metathesis

    The metal-mediated processes include a carbonyl-olefination and an olefin–olefin metathesis event. There are two general mechanistic schemes to perform this overall transformation: one, reaction of a [M=CHR 1] reagent with an alkene to generate a new metal alkylidene, which then couples with a carbonyl group to form the desired substituted alkene and an inactive [M=O] species (type A); two ...

  6. Takai olefination - Wikipedia

    en.wikipedia.org/wiki/Takai_olefination

    Prior to the introduction of this chromium-based protocol, olefination reactions generally gave Z alkenes or mixtures of isomers. [1] Similar olefination reactions had been performed using a variety of reagents such as zinc and lead chloride; [5] however, these olefination reactions often lead to the formation of diols—the McMurry reaction—rather than the methylenation or alkylidenation of ...

  7. Wittig reaction - Wikipedia

    en.wikipedia.org/wiki/Wittig_reaction

    The main limitation of the traditional Wittig reaction is that the reaction proceeds mainly via the erythro betaine intermediate, which leads to the Z-alkene. The erythro betaine can be converted to the threo betaine using phenyllithium at low temperature. [18] This modification affords the E-alkene. The Schlosser variant of the Wittig reaction

  8. NYT ‘Connections’ Hints and Answers Today, Wednesday, December 11

    www.aol.com/nyt-connections-hints-answers-today...

    today's connections game answers for wednesday, december 11, 2024: 1. utopia: paradise, seventh heaven, shangri-la, xanadu 2. things you shake: hairspray, magic 8 ...

  9. Alkylidene group - Wikipedia

    en.wikipedia.org/wiki/Alkylidene_group

    In organic chemistry, alkylidene is a general term for divalent functional groups of the form R 2 C=, where each R is an alkane or hydrogen. [1] They can be considered the functional group corresponding to mono- or disubstituted divalent carbenes (known as alkylidenes), [2] or as the result of removing two hydrogen atoms from the same carbon atom in an alkane.