Aldehydes are more reactive than ketones towards nucleophilic attack because of?

  • A
    less steric hindrance in ketones
  • B
    presence of two alkyl groups on ketones decreases their electrophilicity
  • C
    presence of one alkyl group on aldehydes decreases their electrophilicity
  • D
    alkyl groups have electron-withdrawing effect

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Similar Questions

Which one of the following is used for the purification of aldehydes?

Propyne was subjected to a reaction with $HgSO_4/dil. H_2SO_4$,which resulted in a product $P$. The product $P$ was heated with $Ba(OH)_2$ to give the product $Q$. The molecular formula of the product $Q$ is

The reagent$(s)$ which can be used to bring about the following transformation is(are):
$(A)$ $LiAlH_4$ in $(C_2H_5)_2O$
$(B)$ $BH_3$ in $THF$
$(C)$ $NaBH_4$ in $C_2H_5OH$
$(D)$ Raney $Ni / H_2$ in $THF$

The products $(A)$ and $(B)$ are formed by the following reaction sequence:
$1$. $\text{NH}_2\text{OH}$
$2$. $\text{H}^+, \Delta$
$3$. $\text{LiAlH}_4$
Identify the products $(A)$ and $(B)$.

If formaldehyde and potassium hydroxide are heated,then we get

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