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A Newman projection is a drawing that helps visualize the 3-dimensional structure of a molecule. [1] This projection most commonly sights down a carbon-carbon bond, making it a very useful way to visualize the stereochemistry of alkanes.
Figure 5 shows 2-chloro-2,3-dimethylbutane in a sawhorse projection with chlorine and a hydrogen anti-periplanar to each other. Syn-periplanar or synperiplanar is similar to anti-periplanar. In the syn-periplanar conformer, the A and D are on the same side of the plane of the bond, with the dihedral angle of A−B and C−D between +30° and ...
Melvin Spencer Newman (March 10, 1908 – May 30, 1993) was an American chemist, Ohio State University professor, best known for inventing the Newman projection. Newman was born in New York City in a Jewish family, the youngest of Mae (née Polack) and Jacob K. Newman's four children. [ 1 ]
Newman projections of two of many conformations of ethane: eclipsed on the left, staggered on the right. Ball-and-stick models of the two rotamers of ethane. The spatial arrangement of the C-C and C-H bonds are described by the torsion angles of the molecule is known as its conformation.
Free energy diagram of n-butane as a function of dihedral angle. In stereochemistry, a torsion angle is defined as a particular example of a dihedral angle, describing the geometric relation of two parts of a molecule joined by a chemical bond. [4] [5] Every set of three non-colinear atoms of a molecule defines a half-plane. As explained above ...
Eclipsed conformation (image right in Newman projection) Staggered conformation. In chemistry an eclipsed conformation is a conformation in which two substituents X and Y on adjacent atoms A, B are in closest proximity, implying that the torsion angle X–A–B–Y is 0°. [1]
Tomographic reconstruction: Projection, Back projection and Filtered back projection. Tomographic reconstruction is a type of multidimensional inverse problem where the challenge is to yield an estimate of a specific system from a finite number of projections. The mathematical basis for tomographic imaging was laid down by Johann Radon.
In chemistry, the Natta projection (named for Italian chemist Giulio Natta) is a way to depict molecules with complete stereochemistry in two dimensions in a skeletal formula.