Chemical Forums
Chemistry Forums for Students => Organic Chemistry Forum => Topic started by: the_negro_puppy on July 06, 2006, 06:31:44 AM
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Hi guys, its 12 hours to my final exam and i really need help with this question. I have posted this in a previous thread but forgot to add the Br!
I need to complete this synthesis using any reagents in 3 steps or less
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Thanks very much for your help.
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:)
1.) 1-bromo-2-cyclohexylethane -----------> vinylcyclohexane
Dehydrohalogenation using bulky base in DMSO solvent . Using NaOEt in EtOH as solvent will
give substitution product rather than elimination one.
2.) vinylcyclohexane ---------------> 1-cyclohexylethane-1,2-diol
Hydroxylation using following reagents
(i) Cold aqueous alkaline KMnO4
OR
(ii) OsO4 followed by hydrolysis
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Thanks you are a degree saver-literally lol.