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  2. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    If the acyl groups are different, then they are named in alphabetical order in the same way, with anhydride replacing acid and IUPAC name consists of three words. For example, CH 3 CO−O−OCCH 3 is called ethanoic anhydride and CH 3 CO−O−OCCH 2 CH 3 is called ethanoic propanoic anhydride.

  3. Neophyl chloride - Wikipedia

    en.wikipedia.org/wiki/Neophyl_chloride

    Neophyl chloride is of interest to organic chemists due to its substitution properties. Neophyl chloride is a neopentyl halide which means it is subject to the neopentyl effect. This effect makes SN 2 nucleophilic substitution highly unlikely because of steric interactions due to the branching of the β-carbon.

  4. Pentyl group - Wikipedia

    en.wikipedia.org/wiki/Pentyl_group

    Pentyl is a five-carbon alkyl group or substituent with chemical formula-C 5 H 11.It is the substituent form of the alkane pentane.. In older literature, the common non-systematic name amyl was often used for the pentyl group.

  5. IUPAC nomenclature of chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    IUPAC nomenclature is used for the naming of chemical compounds, based on their chemical composition and their structure. [1] For example, one can deduce that 1-chloropropane has a Chlorine atom on the first carbon in the 3-carbon propane chain.

  6. Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Amyl_alcohol

    Common name Structure Type IUPAC name Boiling point (°C) [3] 1-pentanol or normal amyl alcohol primary Pentan-1-ol: 138.5 2-methyl-1-butanol or active amyl alcohol primary 2-Methylbutan-1-ol: 128.7 3-methyl-1-butanol or isoamyl alcohol or isopentyl alcohol primary 3-Methylbutan-1-ol: 131.2 2,2-dimethyl-1-propanol or neopentyl alcohol primary

  7. List of inorganic compounds - Wikipedia

    en.wikipedia.org/wiki/List_of_inorganic_compounds

    Although most compounds are referred to by their IUPAC systematic names (following IUPAC ... chloride diamine) – [PtCl 2 (NH 3) 2] Cobalt(II) chloride – CoCl 2;

  8. Neopentane - Wikipedia

    en.wikipedia.org/wiki/Neopentane

    The preferred IUPAC name is the systematic name 2,2-dimethylpropane, but the substituent numbers are superfluous because it is the only possible “dimethylpropane”. A neopentyl group attached to a generic group R. A neopentyl substituent, often symbolized by "Np", has the structure Me 3 C–CH 2 – for instance neopentyl alcohol (Me 3 CCH 2 OH

  9. IUPAC nomenclature of inorganic chemistry 2005 - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    Ligands may bridge two or more centres. The prefix μ is used to specify a bridging ligand in both the formula and the name. For example the dimeric form of aluminium trichloride: Al 2 Cl 4 (μ-Cl) 2 di-μ-chlorido-tetrachlorido-1κ 2 Cl,2κ 2 Cl-dialuminium. This example illustrates the ordering of bridging and non bridging ligands of the same ...