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  2. Dibenzylideneacetone - Wikipedia

    en.wikipedia.org/wiki/Dibenzylideneacetone

    Dibenzylideneacetone or dibenzalacetone, often abbreviated dba, is an organic compound with the formula C 17 H 14 O. It is a pale-yellow solid insoluble in water, but soluble in ethanol. It is a pale-yellow solid insoluble in water, but soluble in ethanol.

  3. Water cluster - Wikipedia

    en.wikipedia.org/wiki/Water_cluster

    Water clusters have been proposed as an explanation for some anomalous properties of liquid water, such as its unusual variation of density with temperature. Water clusters are also implicated in the stabilization of certain supramolecular structures. [3] They are expected to play a role also in the hydration of molecules and ions dissolved in ...

  4. Tris(dibenzylideneacetone)dipalladium(0) - Wikipedia

    en.wikipedia.org/wiki/Tris(dibenzylideneacetone...

    Tris(dibenzylideneacetone)dipalladium(0) or [Pd 2 (dba) 3] is an organopalladium compound.The compound is a complex of palladium(0) with dibenzylideneacetone (dba). It is a dark-purple/brown solid, which is modestly soluble in organic solvents.

  5. Cis–trans isomerism - Wikipedia

    en.wikipedia.org/wiki/Cis–trans_isomerism

    Very often, cis–trans stereoisomers contain double bonds or ring structures. In both cases the rotation of bonds is restricted or prevented. [4] When the substituent groups are oriented in the same direction, the diastereomer is referred to as cis, whereas when the substituents are oriented in opposing directions, the diastereomer is referred to as trans.

  6. Claisen–Schmidt condensation - Wikipedia

    en.wikipedia.org/wiki/Claisen–Schmidt_condensation

    In organic chemistry, the Claisen–Schmidt condensation is the reaction between an aldehyde or ketone having an α-hydrogen with an aromatic carbonyl compound lacking an α-hydrogen.

  7. Benzylideneacetone - Wikipedia

    en.wikipedia.org/wiki/Benzylideneacetone

    As with most methyl ketones, benzylideneacetone is moderately acidic at the alpha position, and it can be readily deprotonated to form the corresponding enolate [6]. The compound undergoes the reactions expected for its collection of functional groups: e.g., the double bond adds bromine, the heterodiene adds electron-rich alkenes in Diels-Alder reactions to give dihydropyrans, the methyl group ...

  8. Benzil - Wikipedia

    en.wikipedia.org/wiki/Benzil

    The compound's most noteworthy structural feature is the long carbon-carbon bond of 1.54 Å, which indicates the absence of pi-bonding between the two carbonyl centers.The PhCO centers are planar, but the pair of benzoyl groups are twisted with respect to the other with a dihedral angle of 117°. [5]

  9. Benzoylacetone - Wikipedia

    en.wikipedia.org/wiki/Benzoylacetone

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