An aldehyde/ˈældᵻhaɪd/ or alkanal is an organic compound containing a formyl group. The formyl group is a functional group, with the structure R-CHO, consisting of a carbonyl center (a carbon double bonded to oxygen) bonded to hydrogen and an R group, which is any generic alkyl or side chain. The group without R is called the aldehyde group or formyl group. Aldehydes differ from ketones in that the carbonyl is placed at the end of a carbon skeleton rather than between two carbon atoms. Aldehydes are common in organic chemistry. Many fragrances are aldehydes.
Structure and bonding
Aldehydes feature an sp2-hybridized, planar carbon center that is connected by a double bond to oxygen and a single bond to hydrogen. The C-H bond is not acidic. Because of resonance stabilization of the conjugate base, an α-hydrogen in an aldehyde (not shown in the picture above) is far more acidic, with a pKa near 17, than a C-H bond in a typical alkane (pKa about 50). This acidification is attributed to (i) the electron-withdrawing quality of the formyl center and (ii) the fact that the conjugate base, an enolate anion, delocalizes its negative charge. Related to (i), the aldehyde group is somewhat polar.
It is given Wythoff symbol4/3 4 | 3, although that is a double-covering of this figure.
A nonconvex polyhedron has intersecting faces which do not represent new edges or faces. In the picture vertices are marked by golden spheres, and edges by silver cylinders.
It is a hemipolyhedron with 4 hexagonal faces passing through the model center. The hexagons intersect each other and so only triangle portions of each are visible.
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