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Acid catalysed hydration of alkene gives...

Acid catalysed hydration of alkene gives alcohol. In this reaction addition of water takes place according to Markownikoff's rule. Since intermediate carbocation is formed in this reaction, rearrangement of carbocation takes place. In oxymercuration-demercuration reaction hydration of alkene takes place according to Markownikoff's rule. Oxymercuration demercuration is a better process than the catalytic hydration of alkene because in oxymercuration-demercuration, no rearrangement is possible. In hydroboration oxidation, hydration of alkene takes place as if it is according to anti-Markownikoff's addition. In hydroboration oxidation reaction rearrangement is not possible. Both in oxymercuration-demercuration and hydroboration oxidation intermediate carbocation are not formed.
The product formed in the following reaction is

A

B

C

D

Text Solution

Verified by Experts

The correct Answer is:
B

Hydroboration oxidation, anti-Markownikoff.s addition of water gives product.
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Knowledge Check

  • Acid catalysed hydration of alkene gives alcohol. In this reaction addition of water takes place according to Markownikoff's rule. Since intermediate carbocation is formed in this reaction, rearrangement of carbocation takes place. In oxymercuration-demercuration reaction hydration of alkene takes place according to Markownikoff's rule. Oxymercuration demercuration is a better process than the catalytic hydration of alkene because in oxymercuration-demercuration, no rearrangement is possible. In hydroboration oxidation, hydration of alkene takes place as if it is according to anti-Markownikoff's addition. In hydroboration oxidation reaction rearrangement is not possible. Both in oxymercuration-demercuration and hydroboration oxidation intermediate carbocation are not formed. 2-phenyl propene on acidic hydration gives

    A
    2-phenyl-2-propanol
    B
    2-phenyl-1-propanol
    C
    3-phenyl-1-propanol
    D
    1-phenyl-2-propanol
  • Acid catalysed hydration of alkene gives alcohol. In this reaction addition of water takes place according to Markownikoff's rule. Since intermediate carbocation is formed in this reaction, rearrangement of carbocation takes place. In oxymercuration-demercuration reaction hydration of alkene takes place according to Markownikoff's rule. Oxymercuration demercuration is a better process than the catalytic hydration of alkene because in oxymercuration-demercuration, no rearrangement is possible. In hydroboration oxidation, hydration of alkene takes place as if it is according to anti-Markownikoff's addition. In hydroboration oxidation reaction rearrangement is not possible. Both in oxymercuration-demercuration and hydroboration oxidation intermediate carbocation are not formed. CH_(3)-C=C-Hunderset((ii)H_(2)O_(2)//OH^(-))overset((i)B_(2)H_(6))toA . A is

    A
    `CH_(3)-CH_(2)-CHO`
    B
    `H_(3)C-underset(O)underset(||)(C)-CH_(3)`
    C
    `CH_(3)-CHO`
    D
    `CH_(3)-CH_(2)-CH_(2)-OH`
  • Acid-catalysed hydration of alkenes except ethene leads to the formation of

    A
    primary alcohol
    B
    secondary and teritary alcohol
    C
    mixture of primary and secondary alcohols
    D
    mixture of secondary and teritary alcohols
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