An alkene having the molecular formula CH20 is treated sequentially with ozone (O3) and zinc/acetic acid to give the product/s shown. + 0= CH,CH,CCHCH,
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Q: How many alkenes yield 2,3−dimethylbutane on catalytic hydrogenation?
A: Two alkenes on catalytical hydrogenation yields 2,3-dimethyl butane.
Q: What would be the expected major product or products when 1-ethylcyclohexene is treated with ozone…
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- How many alkenes yield 2,3−dimethylbutane on catalytic hydrogenation?Q2: Give the structure of the possible Claisen condensation product from the following reaction .Tell which , If any you would expect to predominate in each case .(a) CH3CO2Et + CH3CH2CO2Et (b) C6H6CO2Et + C6H5CH2CO2Et(c) EtOCO2Et + Cyclohexanones (d) C6H5CHO + CH3CO2EtA certain hydrocarbon, C5H6, yields the two products shown below upon ozonolysis with 1. O3/CH2Cl2 2. Zn/H3O . Deduce the structure of the hydrocarbon.
- A chemist requires a large amount of 1-bromo-5-methyl-2-hexene as starting material for a synthesis and decides to carry out the following NBS allylic bromination reaction in the presence of UV light. Draw the structures of all of the observed products.The following questions ask you to choose which of the pair reactions shown has been correctly identified as faster. Choose all correct answers with explanation In the SN2 displacement by iodide of CH3Cl or of CH3OTs, CH3OTs reacts faster. In the SN2 displacement by acetate of bromoethane or bromocyclohexane, bromocyclohexane reacts faster. In the SN2 displacement by CH3CH2O- or by CN- on 2-bromopropane, CN- reacts faster. n the SN2 displacement by HC≡C- on bromomethane in benzene or in acetonitrile, reaction in benzene goes faster.When buta-1,3-diene (CH2 = CH – CH = CH2) is treated with HBr, two constitutional isomers are formed, CH3CHBrCH = CH2 and BrCH2CH = CHCH3. Draw a stepwise mechanism that accounts for the formation of both products.
- When 3-bromo-1-methylcyclohexene undergoes solvolysis in hot ethanol, two productsare formed. Propose a mechanism that accounts for both of these productsWhen 2-bromo-3-phenylbutane is treated with sodium methoxide, two alkenes result (by E2 elimination). The Zaitsevproduct predominates.(a) Draw the reaction, showing the major and minor productsWhat 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?
- The spirocyclic pentadiene derivative F shown below is converted stereospecificallyinto compound G on heating. The transformation involves two consecutive pericyclicreactions of the same type, and proceeds via compound H which is not isolated. Identify the type of pericyclic reaction occurring, and determine the structure ofcompound H.A certain hydrocarbon, C7H10, yields the two products shown below upon oxidative cleavage with KMnO4/H3O+ . Deduce the structure of the hydrocarbon.cis-3,4-Dimethylcyclobutene undergoes thermal ring opening to form the two products shown. One of the products is formed in 99% yield, the other in 1% yield. Which is which?