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  2. Ether - Wikipedia

    en.wikipedia.org/wiki/Ether

    They are far less acidic than alpha hydrogens of carbonyl groups (such as in ketones or aldehydes), however. Ethers can be symmetrical of the type ROR or unsymmetrical of the type ROR'. Examples of the former are dimethyl ether, diethyl ether, dipropyl ether etc. Illustrative unsymmetrical ethers are anisole (methoxybenzene) and dimethoxyethane.

  3. Self-condensation - Wikipedia

    en.wikipedia.org/wiki/Self-condensation

    In organic chemistry, self-condensation is an organic reaction in which a chemical compound containing a carbonyl group (C=O) acts both as the electrophile and the nucleophile in an aldol condensation. It is also called a symmetrical aldol condensation as opposed to a mixed aldol condensation in which the electrophile and nucleophile are ...

  4. Carbonyl group - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_group

    For organic chemistry, a carbonyl group is a functional group with the formula C=O, composed of a carbon atom double-bonded to an oxygen atom, and it is divalent at the C atom. It is common to several classes of organic compounds (such as aldehydes , ketones and carboxylic acids ), as part of many larger functional groups.

  5. Dicarbonyl - Wikipedia

    en.wikipedia.org/wiki/Dicarbonyl

    General structure of 1,2-, 1,3-, and 1,4-dicarbonyls. In organic chemistry, a dicarbonyl is a molecule containing two carbonyl (C=O) groups.Although this term could refer to any organic compound containing two carbonyl groups, it is used more specifically to describe molecules in which both carbonyls are in close enough proximity that their reactivity is changed, such as 1,2-, 1,3-, and 1,4 ...

  6. Tetrahedral molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Tetrahedral_molecular_geometry

    In a tetrahedral molecular geometry, a central atom is located at the center with four substituents that are located at the corners of a tetrahedron.The bond angles are arccos(− ⁠ 1 / 3 ⁠) = 109.4712206...° ≈ 109.5° when all four substituents are the same, as in methane (CH 4) [1] [2] as well as its heavier analogues.

  7. Ketone - Wikipedia

    en.wikipedia.org/wiki/Ketone

    The carbonyl group is polar because the electronegativity of the oxygen is greater than that for carbon. Thus, ketones are nucleophilic at oxygen and electrophilic at carbon. Because the carbonyl group interacts with water by hydrogen bonding, ketones are typically more soluble in water than the related methylene compounds. Ketones are hydrogen ...

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  9. Carbonate ester - Wikipedia

    en.wikipedia.org/wiki/Carbonate_ester

    This functional group consists of a carbonyl group flanked by two alkoxy groups. The general structure of these carbonates is R−O−C(=O)−O−R' and they are related to esters (R−O−C(=O)−R'), ethers (R−O−R') and also to the inorganic carbonates. Monomers of polycarbonate (e.g. Makrolon or Lexan) are linked by carbonate groups ...