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In organic chemistry, syn-and anti-addition are different ways in which substituent molecules can be added to an alkene (R 2 C=CR 2) or alkyne (RC≡CR). The concepts of syn and anti addition are used to characterize the different reactions of organic chemistry by reflecting the stereochemistry of the products in a reaction.
Anti-periplanar geometry will put a bonding orbital and an anti-bonding orbital approximately parallel to each other, or syn-periplanar. Figure 6 is another representation of 2-chloro-2,3-dimethylbutane (Figure 5), showing the C–H bonding orbital, σ C–H, and the C–Cl anti-bonding orbital, σ* C–Cl, syn-periplanar.
syn/anti peri/clinal. a torsion angle between 0° and ±90° is called syn (s) a torsion angle between ±90° and 180° is called anti (a) a torsion angle between 30° and 150° or between −30° and −150° is called clinal (c) a torsion angle between 0° and ±30° or ±150° and 180° is called periplanar (p)
2006-11-30T05:51:12Z E kwan 1295x258 (9602 Bytes) syn vs anti convention; Uploaded with derivativeFX. ... Date/Time Thumbnail Dimensions User Comment; current: 14:27 ...
Click on a date/time to view the file as it appeared at that time. ... 1,360 × 435 (31 KB) Innerstream {{Information |description={{en|Chemical diagram of ...
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The following reaction gives a syn:anti ratio of 80:20 using a lithium enolate compared to 97:3 using a bibutylboron enolate. Where the counterion determines stereoinduction strength, the enolate isomer determines its direction. E isomers give anti products and Z give syn: [21] Anti-aldol formation through E-enolate Syn-aldol formation through ...
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