Adding 1 mole of hydrogen chloride (HCI) to 1,3-octadiene gives two products. Give their structures, and write all of the steps in a reaction mechanism that explains how each product is formed.
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Q: Addition of HBr to 3,3-dimethyl-1-butene gives a mixture of two isomeric alkyl bromide products.…
A: The addition of HBr to alkene follows a carbocation intermediate formation mechanism. hence first…
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A: Ozonolysis is oxidative cleavage of alkene to corresponding carbonyl compounds.
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A: Hydration of given alkene to alcohol via hydroboration is first shown below,
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A: This can be accomplished by duethlation followed by reduction with Lindlar catalyst.
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A: The halogenation reaction is the reaction which gives product with one or more halogens attached.…
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Q: Alkenes can be hydrated to form alcohols by (1) hydroboration followed by oxidation with alkaline…
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Q: Alkenes can be hydrated to form alcohols by (1) hydroboration followed by oxidation with alkaline…
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Q: Draw a structural formula for the alkene with the molecular formula C5H10 that reacts with Br2 to…
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Q: Identify the reagents necessary to convert cyclohexane into 1, 3 cyclohexadiene.
A: CYCLO HEXANE ON CHLORINATION INPRESENCE OF LIGHT TO FOR CHLORO CYCLOHEXANE CHLORO CYCLOHEXANE IN…
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A: Applying concept of organic synthesis and reagent.
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A: The given compound is 3-Nitrocyclohexene.
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A: The structural formula of the alkene that reacts with ozone followed by dimethyl sulfide to give the…
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- You are required to synthesize 2-bromopentane from the reaction between an alkene with HBr. Which alkene, 1-pentene or 2-pentene, should you react with HBr in order to get 2-bromopentane? Give an explanation.Acrolein and 1,3-cyclohexadiene react in a one-step concerted manner to yield a single product. Give the structure of the product. What kind of reaction is this an example of? In terms of this reaction, how would you classify acrolein? How would you classify 1,3-cyclohexadiene? Hint: acrolein is not a systematic name so you may need to look up its structure if you are not already familiar with it.Define the Mechanism of the Radical Addition of HBr to an Alkene ?
- What are the respective products of the: hydroboration reaction, and ozonolysis of 1-propylcyclohexene?An unknown hydrocarbon A with the formula C6H12 reacts with 1 molar equivalent of H2 over a palladium catalyst. Hydrocarbon A also reacts with OsO4 to give diol B. When oxidized with KMnO4 in acidic solution, A gives two fragments. One fragment is propanoic acid, CH3CH2CO2H, and the other fragment is ketone C. What are the structures of A, B, and C? Write all reactions, and show your reasoning.The rate law for addition of Br2 to an alkene is first orderin Br2 and first order in the alkene. Does this informationsuggest that the mechanism of addition of Br2 to analkene proceeds in the same manner as for addition of HBr?Explain.
- Which will be more stable, cis or trans-1,4-tert-butylcyclohexane? Explain by drawing their structures?Give the skeletal structure of the reacting alkene and the reagents the must eb used to produce BrCH2CHOHCH2ClWould both alkenes form the same alkyl halide if DBr were used instead of HBr? (D is an isotope of H, so D+ reacts like H+.)
- Bicyclo-2,5-heptadiene can be prepared in two steps from cyclopentadiene and vinyl chloride. Provide a mechanism for each step.A hydrocarbon of molecular mass 72 g mol–1 gives a single monochloro derivative and two dichloro derivatives on photo chlorination. Give the structure of the hydrocarbonReaction of HBr with 3-methylcyclohexene yields a mixture of four products: cis-and trans-1-bromo-3-methylcyclohexane and cis-and trans-1-bromo-2-methylcyclohexane. The analogous reaction of HBr with 3-bromocyclohexene yields trans-1, 2-dibromocyclohexane as the soleproduct. Draw structures of the possible intermediates, and then explain why only a single product is formed in this reaction.