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A: The Detailed steps attached belowExplanation:
write down the mechanism for the reduction of cyclohex-2-en-1-one with sodium borohydride and then H3O+
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- When 2-Methylcyclohexane-1,3-dione was treated with 3-buten-2-one in the presence of EtONa (base), the corresponding bicyclic compound was obtained. Draw the product of this reaction and explain the reaction mechanism of this reaction with figures and sentences. CH3 de EtONa EtOH ?What is the mechanism for the reaction of 2,5-cyclohexadiene-1,4-dione with sodium borohydride with EtOH as the solvent?The reaction of 2-ethyl-1-pentene with Br2, with H2 + Pd/C, or with R2BH/THF followed by aqueous HO- + H2O2 leads to a racemic mixture. Explain why a racemic mixture is obtained in each case.
- Addition of hydrochloride acid to 1-isopropenyl-1-methylcyclopentane generates 1-chloro-1,2,2 trimethylcyclohexane. Draw the complete mechanism, including intermediates, to illustrate electron flow in the reaction.Reaction Mechanism for the Synthesis of 1,1’-(buta-1,3-diyne-1,4-diyl)di(cyclohexan-1-ol) from 1-ethynylcyclohexan-1-olwhat series of synthetic steps could be used to prepare 1-methylcyclohexanol from cyclohexane?
- Draw the major organic product for the reaction of 1-phenylpropan-1-one with sodium hydride followed by ethyl iodide. Ignore stereochemistry.Electrophilic addition of hydroiodic acid to (3S)-3-tert- butoxypent-1-ene gives an unequal mixture of two products [Reaction 1, 99:1 ratio]. The same reaction carried out on (3S)-3-methoxy-pent-1-ene also gave two stereoisomers albeit in a much lower ratio [Reaction 2, 55:45 ratio]. What is the major product for reaction 1? 0 HỌC LỊCH CH₂ OtBu = o OCH₂=CH₂ Product 2 Product 1 H₂C H₂C Y CH₂ OtBu CH₂H₂C CH₂ OCH, HI ECO Ⓒ1Bu Product 1 H₂C CH₁₂ H₂C H + OCH₂ Product 3 CH₂ CH₂ OtBu Product 2 H₂C T CH₂ OCH, Product 4 Reaction 1 99:1 Reaction 2 50:45Draw and explain the mechanism of substitution of 3-bromopentane in the presence of ammonia. explain clearly.
- Draw the products (including stereoisomers) formed when (S)-2,4-dimethylhex-2-ene is treated with HBr and peroxides under similarconditions.What would the major organic reaction product be from the reaction of 1-bromo-1-methylcyclopentane withsodium hydroxide? Would the elimination reaction outcome be affected if a student accidentally adds sodium tertbutoxide instead of sodium hydroxide?Write a mechanism that explains how acid-catalyzed dehydration of2,2-dimethylcyclohexanol forms 1,2-dimethylcyclohexene.
