enow.com Web Search

Search results

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

    en.wikipedia.org/wiki/Ring_strain

    In some molecules, torsional strain can contribute to ring strain in addition to angle strain. One example of such a molecule is cyclopropane. Cyclopropane's carbon-carbon bonds form angles of 60°, far from the preferred angle of 109.5° angle in alkanes, so angle strain contributes most to cyclopropane's ring strain. [10]

  3. Phosphiranes - Wikipedia

    en.wikipedia.org/wiki/Phosphiranes

    Phosphirane functional group is a very strained structure - the C-P-C bond angle in phosphirane ring structure is 49°, [1] even lower than the C-N-C angle in aziridine and the C-C-C angle in cyclopropane (60°). This high angle strain causes a higher inversion barrier as well as the increased s-character of the lone pair on the phosphorus atom ...

  4. Strain (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Strain_(chemistry)

    The simplest examples of angle strain are small cycloalkanes such as cyclopropane and cyclobutane, which are discussed below. ... 11 11.3 5 6.2 12 4.1 6 0.1 13 ...

  5. Cyclopropane - Wikipedia

    en.wikipedia.org/wiki/Cyclopropane

    One theory invokes σ-aromaticity: the stabilization afforded by delocalization of the six electrons of cyclopropane's three C-C σ bonds to explain why the strain of cyclopropane is "only" 27.6 kcal/mol as compared to cyclobutane (26.2 kcal/mol) with cyclohexane as reference with E str =0 kcal/mol, [18] [19] [20] in contrast to the usual π ...

  6. Cycloalkane - Wikipedia

    en.wikipedia.org/wiki/Cycloalkane

    The prefix consists of three numbers that are arranged in descending order, separated by dots: [2.2.1]. Before the numerical prefix is another prefix indicating the number of rings (e.g., "bicyclo+"). Thus, the name is bicyclo[2.2.1]heptane. Cycloalkanes as a group are also known as naphthenes, a term mainly used in the petroleum industry. [4]

  7. Cyclopropanation - Wikipedia

    en.wikipedia.org/wiki/Cyclopropanation

    In organic chemistry, cyclopropanation refers to any chemical process which generates cyclopropane ((CH 2) 3) rings.It is an important process in modern chemistry as many useful compounds bear this motif; for example pyrethroid insecticides and a number of quinolone antibiotics (ciprofloxacin, sparfloxacin, etc.).

  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. Bicyclobutane - Wikipedia

    en.wikipedia.org/wiki/Bicyclobutane

    Bicyclo[1.1.0]butane is an organic compound with the formula C 4 H 6. It is a bicyclic molecule consisting of two cis-fused cyclopropane rings, and is a colorless and easily condensed gas. [1] Bicyclobutane is noted for being one of the most strained compounds that is isolatable on a large scale — its strain energy is estimated at 63.9 kcal ...