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

  • A
    Cyclopentanecarboxylic acid methyl ester
  • B
    $2$-methoxycyclohexanone
  • C
    Cyclohexane-$1,2$-dione
  • D
    Cyclopentanecarboxylic acid

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Similar Questions

The products $(A)$ and $(B)$ of the above reaction are:

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The major product in the following reaction is

The arenium ion which is not involved in the bromination of aniline is:

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:

State True or False for the following statements:
$(i)$ Positive and negative ions are formed by homolytic cleavage of a covalent bond.
$(ii)$ Positive and negative ions are formed by heterolytic cleavage of a covalent bond.
$(iii)$ Only homolytic cleavage is possible in the $C-Cl$ bond of $CH_3-Cl$.
$(iv)$ If heterolytic cleavage of a bond occurs,then ionic or polar type reactions take place.

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