Question:

Which of the following is not correct regarding the elecolytic preparation of $H_{2}O_{2}$ ?

Updated On: Jul 12, 2022
  • Lead is used as cathode
  • $50\% H_{2}SO_{4}$ is used
  • Hydrogen is liberated at anode
  • Sulphuric acid undergoes oxidation
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The Correct Option is C

Solution and Explanation

$H _{2} O _{2}$ can be prepared by electrolysis of $50 \%$ $H _{2} SO _{4}$. In this method, hydrogen is liberated at cathode. $H _{2} SO _{4} \rightleftharpoons 2 H ^{+}+2 HSO _{4}^{-}$ At anode : $2 HSO _{4}^{-} \longrightarrow H _{2} S _{2} O _{8}+2 e^{-}$ $H _{2} S _{2} O _{8}+2 H _{2} O \longrightarrow 2 H _{2} SO _{4}+ H _{2} O _{2}$ At cathode $: 2 H ^{+}+2 e^{-} \longrightarrow H _{2} \uparrow$
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Top Questions on Organic Chemistry- Some Basic Principles and Techniques

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Concepts Used:

Organic Chemistry – Some Basic Principles and Techniques - Reaction Mechanism

SN1 Reaction Mechanism:

SN1 reaction mechanism takes place by following three steps –

  • Formation of carbocation 
  • Attack of nucleophile 
  • Deprotonation 

SN2 Reaction Mechanism:

The SN2 reaction mechanism involves the nucleophilic substitution reaction of the leaving group (which generally consists of halide groups or other electron-withdrawing groups) with a nucleophile in a given organic compound.

Electrophilic Aromatic Substitution Reaction Mechanism:

The mechanism of an electrophilic aromatic substitution reaction contains three main components which are:

  1. A new sigma bond from C=C is formed during the reaction in the arene nucleophile.
  2. Due to the breaking of the C-H sigma bond, a proton is removed.
  3. The C=C bond is reformed and it restores the aromaticity of the compound.

Electrophilic Substitution Reaction Mechanism:

The electrophilic substitution reaction mechanism is composed of three steps, which will be discussed more below.

  • Electrophile Generation
  • Carbocation Formation
  • Proton Removal