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  2. Pentadiene - Wikipedia

    en.wikipedia.org/wiki/Pentadiene

    In organic chemistry, pentadiene is any hydrocarbon with an open chain of five carbons, connected by two single bonds and two double bonds. All those compounds have the same molecular formula C 5 H 8. The inventory of pentadienes include: 1,2-pentadiene, or ethyl allene, H 2 C=C=CH−CH 2 −CH 3. [1] 1,3-pentadiene, H 2 C=CH−CH=CH−CH 3 ...

  3. 1,4-Pentadiyne - Wikipedia

    en.wikipedia.org/wiki/1,4-Pentadiyne

    While for 1,4-pentadiene the sp 2-hybridization leads to a bond angle of 120° between the single and double bond, in 1,4-pentadiyne it is a 180° angle due to the sp-hybrid orbital. Both triple bonds in 1,4-position destabilize each other according to another study by 3.9 kcal · mol −1 , a repulsion between the p orbital lobes close to the ...

  4. Butadiene - Wikipedia

    en.wikipedia.org/wiki/Butadiene

    That implies a stabilization energy of 3.5 kcal/mol. [25] Similarly, the hydrogenation of the terminal double bond of 1,4-pentadiene releases 30.1 kcal/mol of heat, while hydrogenation of the terminal double bond of conjugated (E)-1,3-pentadiene releases only 26.5 kcal/mol, implying a very similar value of 3.6 kcal/mol for the stabilization ...

  5. Allyl group - Wikipedia

    en.wikipedia.org/wiki/Allyl_group

    The weakened C−H bonds is reflected in the easy oxidation of compounds containing 1,4-pentadiene (C=C−CH 2 −C=C) linkages. Some polyunsaturated fatty acids feature this pentadiene group: linoleic acid, α-linolenic acid, and arachidonic acid. They are susceptible to a range of reactions with oxygen (O 2), starting with lipid peroxidation.

  6. Allenes - Wikipedia

    en.wikipedia.org/wiki/Allenes

    At 298 K, the ΔG° of this reaction is –1.9 kcal/mol, corresponding to K eq = 24.7. [25] The first allene to be synthesized was penta-2,3-dienedioic acid, which was prepared by Burton and Pechmann in 1887. However, the structure was only correctly identified in 1954. [26] Laboratory methods for the formation of allenes include:

  7. Conjugated system - Wikipedia

    en.wikipedia.org/wiki/Conjugated_system

    Cinnamaldehyde is a naturally-occurring compound that has a conjugated system penta-1,3-diene is a molecule with a conjugated system Diazomethane conjugated pi-system. In theoretical chemistry, a conjugated system is a system of connected p-orbitals with delocalized electrons in a molecule, which in general lowers the overall energy of the molecule and increases stability.

  8. Lipoxygenase - Wikipedia

    en.wikipedia.org/wiki/Lipoxygenase

    Lipoxygenases (EC 1.13.11.-) (LOX) are a family of (non-heme) iron-containing enzymes, more specifically oxidative enzymes, most of which catalyze the dioxygenation of polyunsaturated fatty acids in lipids containing a cis,cis-1,4-pentadiene into cell signaling agents that serve diverse roles as autocrine signals that regulate the function of their parent cells, paracrine signals that regulate ...

  9. Chemical bonding of water - Wikipedia

    en.wikipedia.org/wiki/Chemical_bonding_of_water

    Lewis Structure of H 2 O indicating bond angle and bond length. Water (H 2 O) is a simple triatomic bent molecule with C 2v molecular symmetry and bond angle of 104.5° between the central oxygen atom and the hydrogen atoms.