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  2. 1-Bromohexane - Wikipedia

    en.wikipedia.org/wiki/1-Bromohexane

    Most 1-bromoalkanes are prepared by free-radical addition of hydrogen bromide to the 1-alkene. These conditions lead to anti-Markovnikov addition, giving the 1-bromo derivative. [2] 1-Bromohexane undergoes reactions expected of simple alkyl bromides. It can form Grignard reagents. [3]

  3. Bromocyclohexane - Wikipedia

    en.wikipedia.org/wiki/Bromocyclohexane

    A mixture of cis-decalin and CXB can simultaneously match optical index and density of PMMA. [1] Due to the moderate dielectric constant of CXB (ε = 7.9 [ 2 ] ), PMMA acquires charges that can be screened by the addition of salt (e.g. tetrabutyl ammonium bromide ), leading to a very good approximation of colloidal hard sphere . [ 3 ]

  4. C6H13Br - Wikipedia

    en.wikipedia.org/wiki/C6H13Br

    Download as PDF; Printable version; In other projects Wikidata item; ... 1-Bromohexane; 2-Bromohexane This page was last edited on 12 November 2022, at 16: ...

  5. 1-Iodohexane - Wikipedia

    en.wikipedia.org/wiki/1-Iodohexane

    1-Iodohexane is a chemical compound from the group of aliphatic saturated halogenated hydrocarbons. The chemical formula is CH 3 (CH 2 ) 5 I . [ 2 ] [ 3 ] It is a colorless liquid.

  6. Retrosynthetic analysis - Wikipedia

    en.wikipedia.org/wiki/Retrosynthetic_analysis

    These simpler/commercially available compounds can be used to form a synthesis of the target molecule. E.J. Corey formalized this concept in his book The Logic of Chemical Synthesis. [1] [2] [3] The power of retrosynthetic analysis becomes evident in the design of a synthesis. The goal of retrosynthetic analysis is a structural simplification.

  7. Category:Bromoalkanes - Wikipedia

    en.wikipedia.org/wiki/Category:Bromoalkanes

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  8. Ring-opening metathesis polymerisation - Wikipedia

    en.wikipedia.org/wiki/Ring-opening_metathesis...

    In polymer chemistry, ring-opening metathesis polymerization (ROMP) is a type of chain-growth polymerization involving olefin metathesis. [1] The reaction is driven by relieving ring strain in cyclic olefins. [2] A variety of heterogeneous and homogeneous catalysts have been developed for different polymers and mechanisms. [3]

  9. Dehydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Dehydrohalogenation

    Likewise, 1-chloropropane and 2-chloropropane give propene. Zaitsev's rule helps to predict regioselectivity for this reaction type. In general, the reaction of a haloalkane with potassium hydroxide can compete with an S N 2 nucleophilic substitution reaction by OH − a strong, unhindered nucleophile .