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  2. Iodosobenzene - Wikipedia

    en.wikipedia.org/wiki/Iodosobenzene

    Iodosobenzene is prepared from iodobenzene. [3] It is prepared by first oxidizing iodobenzene by peracetic acid.Hydrolysis of resulting diacetate affords "PhIO": [4] C 6 H 5 I + CH 3 CO 3 H + CH 3 CO 2 H → C 6 H 5 I(O 2 CCH 3) 2 + H 2 O

  3. Jemmis mno rules - Wikipedia

    en.wikipedia.org/wiki/Jemmis_mno_rules

    In chemistry, the Jemmis mno rules represent a unified rule for predicting and systematizing structures of compounds, usually clusters.The rules involve electron counting. They were formulated by E. D. Jemmis to explain the structures of condensed polyhedral boranes such as B 20 H 16, which are obtained by condensing polyhedral boranes by sharing a triangular face, an edge, a single vertex, or ...

  4. Polyhedral skeletal electron pair theory - Wikipedia

    en.wikipedia.org/wiki/Polyhedral_skeletal...

    In chemistry the polyhedral skeletal electron pair theory (PSEPT) provides electron counting rules useful for predicting the structures of clusters such as borane and carborane clusters. The electron counting rules were originally formulated by Kenneth Wade , [ 1 ] and were further developed by others including Michael Mingos ; [ 2 ] they are ...

  5. Tosyl group - Wikipedia

    en.wikipedia.org/wiki/Tosyl_group

    Tosyl group (blue) with a generic "R" group attached Tosylate group with a generic "R" group attached. Note the extra oxygen, compared to plain tosyl. In organic chemistry, a toluenesulfonyl group (tosyl group, abbreviated Ts or Tos [nb 1]) is a univalent functional group with the chemical formula −SO 2 −C 6 H 4 −CH 3.

  6. Outline of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/Outline_of_organic_chemistry

    The following outline is provided as an overview of and topical guide to organic chemistry: . Organic chemistry is the scientific study of the structure, properties, composition, reactions, and preparation (by synthesis or by other means) of carbon-based compounds, hydrocarbons, and their derivatives.

  7. Brosyl group - Wikipedia

    en.wikipedia.org/wiki/Brosyl_group

    In organic chemistry, brosyl (or para-bromophenylsulfonyl) group is a functional group with the chemical formula BrC 6 H 4 SO 2 and structure Br−C 6 H 4 −SO 2 −R. This group is usually introduced using the compound brosyl chloride , BrC 6 H 4 SO 2 Cl , which forms sulfonyl esters and amides of p -bromophenylsulfonic acid .