Propan - 1 - ol cannot be prepared by acid catalysed hydration of propene, then how is propene converted into propan - I - ol?
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Hello dear,
Acid catalyzed hydration of alkenes takes place by Markonicov's rule. Thus propene gives propan-2-ol on acid catalysed hydration.
CH3-CH=CH2 + H2O --> CH3-CH(OH)-CH3
◆ Propene to propan-1-ol -
Propene is first treated with HBr/peroxide to give bromopropane which on hydroxylation by aq.KOH gives propanol.
CH3-CH=CH2 + HBr --> CH3-CH2-CH2-Br
CH3-CH2-CH2-Br + KOH --> CH3-CH2-CH2-OH + KBr
Hope this helped you. Thanks for asking..
Acid catalyzed hydration of alkenes takes place by Markonicov's rule. Thus propene gives propan-2-ol on acid catalysed hydration.
CH3-CH=CH2 + H2O --> CH3-CH(OH)-CH3
◆ Propene to propan-1-ol -
Propene is first treated with HBr/peroxide to give bromopropane which on hydroxylation by aq.KOH gives propanol.
CH3-CH=CH2 + HBr --> CH3-CH2-CH2-Br
CH3-CH2-CH2-Br + KOH --> CH3-CH2-CH2-OH + KBr
Hope this helped you. Thanks for asking..
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