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Name the
Use ONLY E/Z designators to indicate stereochemistry.
H2C=C=CHCH3
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- Draw (3R,5S)-3,5-dimethylheptane. Use wedges and dashes to show stereochemistry.a. What alkane, with molecular formula C5H12, forms only one monochlorinated product when it is heated with Cl2? b. What alkane, with molecular formula C7H16, forms seven monochlorinated products (disregarding stereoisomers) when heated with Cl2?Name the alkene. Be sure to indicate stereochemistry and use hyphens (-) not endashes (–). The alkene is named:
- draw the two possible carbocations that can form when this alkene reacts with a strong acid (such as HBr or H3O+). of the two structures you drew, circle the more stable carbocationWhich choice best describes the alkene below?Predict the relative stabilities of alkenes and cycloalkenes based on their structure and stereochemistry.
- Please draw the line structures of all of the C8H17+ carbocations that have the carbon-skeleton below. And circle the most stable carbocation of those drawn.Illustrate the differences between stereoisomers and conformations in a 1,3-diene: ?Write equations for the reaction of cyclohexane with:a. Br2/H2O indoorsb. Br2/H2O in the presence of sunlight.