enow.com Web Search

Search results

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

    en.wikipedia.org/wiki/Cyclohexane

    The chair and twist-boat are energy minima and are therefore conformers, while the half-chair and the boat are transition states and represent energy maxima. The idea that the chair conformation is the most stable structure for cyclohexane was first proposed as early as 1890 by Hermann Sachse, but only gained widespread acceptance much later.

  3. Cyclohexyl chloride - Wikipedia

    en.wikipedia.org/wiki/Cyclohexyl_chloride

    Cyclohexyl chloride (or chlorocyclohexane) is a chlorinated hydrocarbon with the formula (CH 2) 5 CHCl. It is a colorless liquid. It is a colorless liquid. Cyclohexyl chloride can be prepared from cyclohexanol by treatment with hydrogen chloride .

  4. Cyclohexane conformation - Wikipedia

    en.wikipedia.org/wiki/Cyclohexane_conformation

    If we hold carbon atoms 1, 2, and 3 stationary, with the correct bond lengths and the tetrahedral angle between the two bonds, and then continue by adding carbon atoms 4, 5, and 6 with the correct bond length and the tetrahedral angle, we can vary the three dihedral angles for the sequences (2,3,4), (3,4,5), and (4,5,6).

  5. Chloroethane - Wikipedia

    en.wikipedia.org/wiki/Chloroethane

    Chloroethane has a low boiling point, so when applied topically, the heat absorbed by the boiling liquid produces a deep and rapid chill. When sprayed on the skin, this chill has a mild anesthetic effect, which can be useful when removing splinters or incising abscesses in a clinical setting. Chloroethane was standard equipment in casualty wards.

  6. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    Norbornane (also called bicyclo[2.2.1]heptane). Unsubstituted cycloalkanes that contain a single ring in their molecular structure are typically named by adding the prefix "cyclo" to the name of the corresponding linear alkane with the same number of carbon atoms in its chain as the cycloalkane has in its ring.

  7. Williamson ether synthesis - Wikipedia

    en.wikipedia.org/wiki/Williamson_ether_synthesis

    In order for the S N 2 reaction to take place there must be a good leaving group which is strongly electronegative, commonly a halide. [ 4 ] In the Williamson ether reaction there is an alkoxide ion (RO − ) which acts as the nucleophile, attacking the electrophilic carbon with the leaving group, which in most cases is an alkyl tosylate or an ...

  8. AOL Mail

    mail.aol.com

    Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!

  9. Cyclohexylmethanol - Wikipedia

    en.wikipedia.org/wiki/Cyclohexylmethanol

    Cyclohexylmethanol is an organic compound with the formula C 6 H 11 −CH 2 −OH. It is a cyclohexane ring functionalized with an alcohol , specifically a hydroxymethyl group. The compound is a colorless liquid, although commercial samples can appear yellow.