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Can someone show the movement of atoms when finding the product?
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- Name the alkene below.Use only E/Z designators to indicate stereochemistry.Draw a structural formula for the product formed upon hydroboration/oxidation of the alkene below. Use wedge and hash bonds ONLY for rings. Do not show stereochemistry in other cases. If the reaction produces a racemic mixture, just draw one stereoisomer.Consider a reaction where cis-but-2-ene is treated with OsO4 followed by NaHSO3/H2O. Draw the structure of one product that is formed in the reaction, including correct stereochemistry.
- Assign E or Z configuration to the following alkenes:Draw every stereoisomer for 1‑bromo‑2‑chloro‑1,2‑difluorocyclopentane. Use wedge‑and‑dash bonds for the substituent groups, and be sure that they are drawn on the outside of the ring, adjacent to each other. Clearly show stereochemistry by drawing the wedge‑and‑dashed bonds like the example. You should replace the X with the appropriate halide.Ignoring stereochemistry, draw the alkylborane formed from the addition of one equivalent of BH3 to the alkene. The alkylborane formed in Part 1 is further treated with H2O2 and HO−. Draw the two stereoisomers of the final product of the reaction. Include stereochemistry where relevant. How many stereocenters are formed from the reaction? What is the relationship between the stereoisomers?
- 4-Chloro-2-pentene has a double bond that can have either the E or the Z configuration and a stereogenic center that can have either the R or the S configuration. How many stereoisomers arepossible altogether? Draw the structure of each, and group the pairs of enantiomers.Name (including E/Z stereochemistry) the five alkenes that can produce 3-bromo-3-methylhexane on reaction with HBr. Draw the skeletal structure of each molecule.A hydrocarbon of unknown structure has the formula C8H10. On catalytichydrogenation over the Lindlar catalyst, 1 equivalent of H2 is absorbed. Onhydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed.(a) How rnany degrees of unsaturation are present in the unknown?(b) How many triple bonds are present?(c) How many double bonds are present?(d) How many rings ar e present?(e) Draw a structure that fits the data.
- Assign E or Z configuration and name the following alkenes:Consider a reaction where cis-but-2-ene is treated with a peroxy acid followed by OH- /H20. Draw the structure of one product that is formed in the reaction, including correct stereochemistry.Draw the possible products of this epoxied ring opening reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore any inorganic byproducts.