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- Show how to convert alkenes, alkyl halides, and carbonyl compounds to alcohStart with a cyclohexane. Add double bonds at the 1st, 3rd and 5th carbons. Add an OH group somewhere on the ring. Fill the empty carbons with iodines so that they are in positions 2 and 4 on the ring.Create a hydrohalogenation reaction using a 5 carbon alkene illustrating Markovnikov's rule. Draw and name all reagents
- How could 2,6-dimethylheptane be prepared from an alkyne and an alkyl halide?Using alkanes and/or cycloalkanes of six carbons or fewer (as your source of carbon) synthesize the following compound. Show each step with starting material, reagents, and product.Draw the products expected from the addition of bromine to an alkene and to an alkyne.
- 2. Show a reaction sequence to convert oil of wintergreen (methyl salicylate) into Aspirin (acetyl salicylic acid). This is a two-step sequence. You must show the structures for the intermediate product and the final product, along with the reagents/reaction conditions. OHStarting with cyclohexane and using any other carbon compounds containing 3 carbons or less, synthesize two of the following compounds. These will be multi-step processes. CH a) H,C b) CH, HO c) HO.How to synthesize 2-methylhexane from acetylene?