The major product $A$ obtained in the above reaction is:

  • A
    Option A
  • B
    Option B
  • C
    Racemic mixture
  • D
    Diastereomers

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Similar Questions

What is the fission of covalent bonds?

Show the heterolytic and homolytic cleavage of $H_3C-Br$.

Ionic reactions with organic compounds proceed through:
$(A)$ Homolytic bond cleavage
$(B)$ Heterolytic bond cleavage
$(C)$ Free radical formation
$(D)$ Primary free radical
$(E)$ Secondary free radical
Choose the correct answer from the options given below:

$A$ rather interesting example of the Wolff rearrangement with $2$-diazocyclohexanone in methanol is given below. Identify the major product.

In the above reaction,the electrophile is substituted at the meta position only,due to:
$I$. Electron density is more at ortho $\&$ para positions
$II$. Electron density is relatively less at ortho $\&$ para positions
$III$. Electron density is less at meta position
$IV$. Electron density is relatively more at meta position
The correct answer is:

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