The typical reaction of an aldehyde is

  • A
    Electrophilic addition
  • B
    Nucleophilic substitution
  • C
    Nucleophilic addition
  • D
    Nucleophilic elimination

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Similar Questions

In which of the following reactions is a carbon$-$carbon bond $NOT$ formed during the formation of the product?

Which of the following on reaction with $NH_3$ gives a urinary antiseptic compound?

In the Cannizzaro reaction given below,the slowest step is $:-$
$2Ph-CHO \xrightarrow{\stackrel{\ominus}{O}H} PhCH_2OH + PhCO_2^{\ominus}$

The option$(s)$ with the correct sequence of reagents for the conversion of $P$ to $Q$ is(are):
$(A)$ $i$) Lindlar's catalyst,$H_2$; $ii$) $SnCl_2 / HCl$; $iii$) $NaBH_4$; $iv$) $H_3O^{+}$
$(B)$ $i$) Lindlar's catalyst,$H_2$; $ii$) $H_3O^{+}$; $iii$) $SnCl_2 / HCl$; $iv$) $NaBH_4$
$(C)$ $i$) $NaBH_4$; $ii$) $SnCl_2 / HCl$; $iii$) $H_3O^{+}$; $iv$) Lindlar's catalyst,$H_2$
$(D)$ $i$) Lindlar's catalyst,$H_2$; $ii$) $NaBH_4$; $iii$) $SnCl_2 / HCl$; $iv$) $H_3O^{+}$

Assertion : Isobutanal does not give iodoform test.
Reason : It does not have $\alpha - $ hydrogen.

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