In the following reaction,the reason why the meta-nitro product is also formed is:

  • A
    low temperature
  • B
    $-NH_2$ group is highly meta-directive
  • C
    Formation of anilinium ion
  • D
    $-NO_2$ substitution always takes place at meta-position

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Similar Questions

What is the product formed when acetamide is reacted with $Br_2$ and caustic soda $(NaOH)$?

How will you carry out the following conversion?
$Aniline \rightarrow m-Bromonitrobenzene$

$Ph-C \equiv CH$ $\xrightarrow[Excess]{HCl} X$ $\xrightarrow{KOH (aq.)} Y$ $\xrightarrow{CH_3-CH_2-NH_2} Z,$
$Z$ is known as

The relation between $(A)$ and $(B)$ is:
$CH_3-CONH_2 \xrightarrow{KOBr} (A)$
$CH_3-CONH_2 \xrightarrow{LiAlH_4} (B)$

Assertion : Boiling and melting points of amides are higher than corresponding acids.
Reason : It is due to strong intermolecular hydrogen bonding in their molecules.

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