Home
Class 11
CHEMISTRY
Explain the following reaction . Wh...

Explain the following reaction .

Why `(A)` mainy give `(B)(1^(@)` alcohol `)`, while `(C)` mainly gives `(D)^(2^(@)` alcohol `)` ?

Text Solution

Verified by Experts

Electron `-` withdrawing effect of `CH_(2)Br` makes `2^(@) C^(o+)` less stable , hence, the attack of `H_(2) ddot(O):` takes place on the carbon `(C^(a))`

In propene `(C)`, the electron`-` donating effect of the `(Me)` group stabilises the `2^(@)C^(o+)` and the attack of `H_(2)ddot(O):`takes place on `C^(a)`, so `Br` attaches itself to the terminal position.
Promotional Banner

Topper's Solved these Questions

  • ALKENES AND ALKADIENES

    CENGAGE CHEMISTRY ENGLISH|Exercise linked Comprehension Type|38 Videos
  • ALKENES AND ALKADIENES

    CENGAGE CHEMISTRY ENGLISH|Exercise Multiple Correct Answer Type|41 Videos
  • ALKENES AND ALKADIENES

    CENGAGE CHEMISTRY ENGLISH|Exercise SOLVED Example|62 Videos
  • ALKANES AND CYCLOALKANES

    CENGAGE CHEMISTRY ENGLISH|Exercise Archives|13 Videos
  • ALKYNES

    CENGAGE CHEMISTRY ENGLISH|Exercise Exercises (Archives - Analytical and Desriptive Type)|4 Videos

Similar Questions

Explore conceptually related problems

Which of the following on reduction with LiAlH_(4) will give ethyl alcohol ?

Which of the following on reaction with conc. NaOH gives an alcohol ?

Answer the following questions : Why is methyl alcohol known as wood alcohol ?

Explain the mechanism of the following reactions : Acid catalysed dehydration of an alcohol forming an alkene.

Which of the following compounds reacts with NaNO_2 and HCl at 0- 4^(@)C to give alcohol/phenol?

Give balanced equations for the following conversions. An alkane to an alcohol.

Which of the following alcohols on dehydration gives most stable carbocation?