
For the stereoisomers below, use the R/S configuration given in the compound name to finish drawing the structure by connecting the appropriate groups. Be sure to specify the stereochemistry via wedge-and-dash bonds. If needed, you may restore a module to its orignal state by clicking on the module and then clicking on the red over-under arrows.
(s)-1-bromo-1-chloroethane - H gets the wedge and Cl gets the dash, (s) - 1- chloro - 2- propanol - CH3 gets dash and CH2 gets wedge, (3R)-5-bromo-2-chloro-3-fluoro-3-methylhexane - F gets dash and CH3 ges wedge
For the stereoisomers below, use the R/S configuration given in the compound name to finish drawing the structure by...
Draw one product structure for the following Diels–Alder
reaction. For ONLY the chirality centers with D and C(=O)H groups,
specify the stereochemistry via wedge-and-dash bonds. (D is
deuterium, an isotope of hydrogen. Include it in your drawing by
either double clicking on an atom and typing \"d\" or by choosing D
in the bottom row of the atoms menu.)
Draw one product structure for the following Diels-Alder reaction. For ONLY the chirality centers with D and C(=0)H groups, specify the stereochemistry via wedge-and-dash bonds. (D is deuterium, an isotope of hydrogen. Include it in your drawing by either double clicking on an atom and typing "d" or by choosing D in the bottom row of the atoms menu.)
[References] - ? In the box below draw the organic product(s) expected when this compound undergoes the Simmons-Smith reaction. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If the reaction produces a racemic mixture, draw both stereoisomers. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate multiple products using the + sign from the drop-down menu. [References) Draw the products of the following reactions,...