enow.com Web Search

Search results

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

    en.wikipedia.org/wiki/Alkyne

    In acetylene, the H–C≡C bond angles are 180°. By virtue of this bond angle, alkynes are rod-like. Correspondingly, cyclic alkynes are rare. Benzyne cannot be isolated. . The C≡C bond distance of 118 picometers (for C 2 H 2) is much shorter than the C=C distance in alkenes (132 pm, for C 2 H 4) or the C–C bond in alkanes (153 p

  3. Saturated and unsaturated compounds - Wikipedia

    en.wikipedia.org/wiki/Saturated_and_unsaturated...

    alkene (unsaturated) vs alkane (saturated) alkyne (unsaturated) vs alkane (saturated) arene (unsaturated) vs cycloalkane (saturated) For organic compounds containing heteroatoms (other than C and H), the list of unsaturated groups is long but some common types are: carbonyl, e.g. ketones, aldehydes, esters, carboxylic acids (unsaturated) vs ...

  4. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    A 3D model of ethylene, the simplest alkene. In organic chemistry, an alkene, or olefin, is a hydrocarbon containing a carbon–carbon double bond. [1] The double bond may be internal or in the terminal position. Terminal alkenes are also known as α-olefins.

  5. Syn and anti addition - Wikipedia

    en.wikipedia.org/wiki/Syn_and_anti_addition

    In organic chemistry, syn-and anti-addition are different ways in which substituent molecules can be added to an alkene (R 2 C=CR 2) or alkyne (RC≡CR).The concepts of syn and anti addition are used to characterize the different reactions of organic chemistry by reflecting the stereochemistry of the products in a reaction.

  6. Ozonolysis - Wikipedia

    en.wikipedia.org/wiki/Ozonolysis

    The reaction is predominantly applied to alkenes, but alkynes and azo compounds are also susceptible to cleavage. The outcome of the reaction depends on the type of multiple bond being oxidized and the work-up conditions. [1] Detailed procedures have been reported. [2] [3] [4]

  7. Hydroamination - Wikipedia

    en.wikipedia.org/wiki/Hydroamination

    As a result, there are now numerous catalysts that can be utilised in the hydroamination of alkene, allene and alkyne substrates, including various metal based heterogeneous catalysts, early-transition metal complexes (e.g. titanium and zirconium), late-transition metal complexes (e.g. ruthenium and palladium), lanthanide and actinide complexes ...

  8. Hydrosilylation - Wikipedia

    en.wikipedia.org/wiki/Hydrosilylation

    Alkenes and alkynes give alkyl and vinyl silanes; aldehydes and ketones give silyl ethers. Hydrosilylation has been called the "most important application of platinum in homogeneous catalysis." Hydrosilylation has been called the "most important application of platinum in homogeneous catalysis."

  9. Migratory insertion - Wikipedia

    en.wikipedia.org/wiki/Migratory_insertion

    The neutral ligand can be CO, alkene, alkyne, or in some cases, even carbene. Diverse reactions apply to the migratory insertion. One mechanism involves the attack of the anionic ligand on the electrophilic part of the neutral ligand (the anionic ligand migrates to the neutral ligand). The other mechanism involves the neutral ligand inserts ...