Organic Chemistry
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Provide the reaction scheme that shows the inorganic reagents necessary to convert acetylene and 1-bromo-3-ethylpentane into meso-3,10-diethyldodecane-6,7-diol.
Draw the structure of the predicted product between the phenylethyn-1-ide ion and each of the compounds listed below.
a) 1-chloropropane
b) 1-chloro-3-methylbutane
c) propionaldehyde followed by water workup
Provide the synthetic step(s) required to complete the following conversion. (Ignore stereochemistry)
1-methylcyclohexanol → 2-bromo-1-methylcyclohexanol
Using 1-methylcyclohex-1-ene as the starting material, outline the step-by-step process for synthesizing the compound shown below. If a step forms a chiral center, assume the reaction results in a racemic mixture.
Draw the expected products from the following metathesis reaction:
Provide the expected products from the following metathesis reaction:
Draw the smaller molecules used to assemble the following alkenes through olefin metathesis. (Use the smallest alkenes needed)
Starting with but-1-yne, outline the steps required to synthesize (3S,4R)-4-chlorohexan-3-ol and (3R,4S)-4-chlorohexan-3-ol.