Search results
Results from the WOW.Com Content Network
1,3-Cyclohexanedione is an organic compound with the formula (CH 2) 4 (CO) 2. It is one of three isomeric cyclohexanediones. It is a colorless compound that occurs ...
[1] [2] [3] Introduced by Gilbert N. Lewis in his 1916 article The Atom and the Molecule, a Lewis structure can be drawn for any covalently bonded molecule, as well as coordination compounds. [4] Lewis structures extend the concept of the electron dot diagram by adding lines between atoms to represent shared pairs in a chemical bond.
Dimedone is an organic compound with the formula (CH 3) 2 C(CH 2) 2 (CO) 2 (CH 2). Classified as a cyclic diketone, it is a derivative of 1,3-cyclohexanedione. It is a white solid that is soluble in water, as well as ethanol and methanol. It once was used as a reagent to test for the aldehyde functional group.
1,2-Cyclohexanedione; 1,3-Cyclohexanedione; 1,4-Cyclohexanedione This page was last edited on 23 June 2017, at 01:22 (UTC). Text is available under the Creative ...
In enzymology, a cyclohexane-1,3-dione hydrolase (EC 3.7.1.10) is an enzyme that catalyzes the chemical reaction. cyclohexane-1,3-dione + H 2 O 5-oxohexanoate. Thus, the two substrates of this enzyme are cyclohexane-1,3-dione and H 2 O, whereas its product is 5-oxohexanoate.
Hyperconjugation affects several properties. [6] [10]Bond length: Hyperconjugation is suggested as a key factor in shortening of sigma bonds (σ bonds). For example, the single C–C bonds in 1,3-butadiene and propyne are approximately 1.46 Å in length, much less than the value of around 1.54 Å found in saturated hydrocarbons.
Cyclohexa-1,3-diene is an organic compound with the formula (C 2 H 4)(CH) 4. It is a colorless, flammable liquid. It is a colorless, flammable liquid. Its refractive index is 1.475 (20 °C, D).
1,3-CHD.png (298 × 356 pixels, file size: 9 KB, MIME type: image/png) This is a file from the Wikimedia Commons . Information from its description page there is shown below.