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How to go from 3-oxocyclohexane-1-carbaldehyde to 3-hydroxycyclohexane-1-carbaldehyde.
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- How to go from 3-oxocyclohexane-1-carbaldehyde to 3-hydroxycyclohexane-1-carbaldehyde, using a protection reagent for the aldehyde group.What are the reaction products of (R)-3-methylcyclohexene in the reaction sequence of hydroboration-oxidation: I- (1S,2R)-2-methylcyclohexanol + (1R,2R)-2-methylcyclohexanol, barely II- (1S,2R)-2-methylcyclohexanol + (1R,2S)-2-methylcyclohexanol, barely III- (1S,3R)-3-methylcyclohexanol + (1R,3R)-3-methylcyclohexanol, barely IV- (1S,3R)-3-methylcyclohexanol + (1S,3S)-3-methylcyclohexanol, barely V- Alternatives I and III contain the reaction products VI- ndaObtain 4-hydroxy-4-methylpentan-2-one from methyl 3-oxobutanoate.
- What reagents in what order would you use to convert 3,3-dimethyl-1-butene to 4,4-dimethylpentanal?Match the two starting reagents with the corresponding specta 3-Nitrobenzaldehyde and AcetophenoneFor each reaction, show the generation of the electrophile and predict the products.(a) benzene + cyclohexene + HF (b) tert@butyl alcohol + benzene + BF3
