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  2. Cyclopropyl group - Wikipedia

    en.wikipedia.org/wiki/Cyclopropyl_group

    A cyclopropyl group is a chemical structure derived from cyclopropane; it is typically produced in a cyclopropanation reaction. The group has an empirical formula of C 3 H 5 and chemical bonds from each of the three carbons to both of the other two.

  3. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    Alkyl groups that contain one ring have the formula −C n H 2n−1, e.g. cyclopropyl and cyclohexyl. The formula of alkyl radicals are the same as alkyl groups, except the free valence "−" is replaced by the dot "•" and adding "radical" to the name of the alkyl group (e.g. methyl radical •CH 3).

  4. Propyl group - Wikipedia

    en.wikipedia.org/wiki/Propyl_group

    From left to right: the two isomeric groups propyl and 1-methylethyl (iPr or isopropyl), and the non-isomeric cyclopropyl group. In organic chemistry, a propyl group is a three-carbon alkyl substituent with chemical formula −CH 2 CH 2 CH 3 for the linear form.

  5. Alkyl cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Alkyl_cycloalkane

    Alkyl cycloalkanes are chemical compounds with an alkyl group with a single ring of carbons to which hydrogens are attached according to the formula C n H 2n . They are named analogously to their normal alkane counterpart of the same carbon count: methylcyclopropane , methylcyclobutane , methylcyclopentane , methylcyclohexane , etc. [ 1 ]

  6. Cyclopropanes - Wikipedia

    en.wikipedia.org/wiki/Cyclopropanes

    Most cyclopropanes are not prepared from the parent cyclopropane, which is somewhat inert. Cyclopropyl groups are often prepared by cyclization of 1,3-difunctional alkanes. An example of the former, cyclopropyl cyanide is prepared by the reaction of 4-chlorobutyronitrile with a strong base. [1]

  7. Vinylcyclopropane rearrangement - Wikipedia

    en.wikipedia.org/wiki/Vinylcyclopropane...

    In the 1960s, shortly after the rearrangement was discovered, it was established that the activation energy for the vinylcyclopropane rearrangement is around 50 kcal/mol. [21] The kinetic data obtained for this rearrangement were consistent with a concerted mechanism where cleavage of the cyclopropyl carbon-carbon bond was rate-limiting.

  8. Alicyclic compound - Wikipedia

    en.wikipedia.org/wiki/Alicyclic_compound

    An exocyclic group is always shown outside the ring structure, take for instance the exocyclic double bond of the former molecule. Isotoluenes are a prominent class of compounds with exocyclic double bonds. The placement of double bonds in many alicyclic compounds can be predicted with Bredt's rule.

  9. Cyclopropanol - Wikipedia

    en.wikipedia.org/wiki/Cyclopropanol

    Cyclopropanol is an organic compound with the chemical formula C 3 H 6 O. It contains a cyclopropyl group with a hydroxyl group attached to it. The compound is highly unstable due to the three-membered ring, and is susceptible to reactions that open the ring.