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- What alkene with the molecular formula C6H12, when treated with ozone and then dimethyl sulfide, gives the following product(s)?How many allylic substituted bromoalkenes are formed from the reaction of 2-pentene with NBS? Disregard stereoisomers.Identify two alkenes that react with HBr to form 1-bromo-1-methylcyclohexane without undergoing a carbocation rearrangement.
- One compound that contributes to the “seashore smell” at beaches in Hawai‘i is dictyopterene D', a component of a brown edible seaweed called limu lipoa. Hydrogenation of dictyopterene D' with excess H2 in the presence of a Pd catalyst forms butylcycloheptane. Ozonolysis with O3 followed by (CH3)2S forms CH2(CHO)2, HCOCH2CH(CHO)2, and CH3CH2CHO. What are possible structures of dictyopterene D'?An alkene having the molecular formula C5H10 is treated sequentially with ozone (O3) and zinc/acetic acid to give the product/s shown. H3C O CH3CHCH + H. Draw a structural formula for the alkene. You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. In cases where there is more than one answer, just draw one. P opy aste [* Previous NextHow many alkenes or cycloalkenes with the general formula C9H16 can you treat with HCl to obtain 1-chloro-1-ethyl-3,4-dimethylcyclopentane as a major product?
- Draw the alkene structure that produced the following compounds in a ozonolysis reaction as specified. 8.4 H C7H12 1.03 2. (CH3)2S H4. Draw structural formulas for all possible monohalogenation products that might be formed in the following reactions, then assign them IUPAC names. (a) + Cl₂ lightWhat is the major product formed when 3-methyl-1-butene is treated with Hg(C2H3O2)2 in a THF/ethanol mixture followed by NaBH4 in base?