Williamson's Ether Synthesis - Practice Questions & MCQ

Nucleophilic addition

Electrophilic addition   
 

Electrophilic substitution

Nucleophilic substitution

$\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{Br}+\mathrm{CH}_3 \mathrm{ONa} \xrightarrow{\mathrm{CH}_3 \mathrm{OH}}$

$\mathrm{CH}_2=\mathrm{CH}-\mathrm{CH}_2 \mathrm{Br}+\mathrm{PhONa} \xrightarrow{\mathrm{PhOH}}$

$\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{Br}+\mathrm{CH}_3 \mathrm{ONa} \xrightarrow{\mathrm{CH}_3 \mathrm{OH}}$

$\mathrm{CH}_2=\mathrm{CH}-\mathrm{CH}_2 \mathrm{Br}+\mathrm{PhONa} \xrightarrow{\mathrm{PhOH}}$

CH₃CHO;RMgX

C₆H₅OH; NaOH; CH₃I

C₆H₅OH; neutral FeCl₃

C₆H₅ - CH₃; CH₃COCl; AlCl₃

Williamson's Synthesis

Fries Rearrangement

Friedel Crafts Reaction

Corey House Synthesis

 Benzene, MeBr

$\mathrm{PhO}^{\ominus} \mathrm{Na}^{\oplus}, \mathrm{MeOH}$

$\mathrm{Ph}-\mathrm{Br}, \mathrm{MeO}^{\ominus} \mathrm{Na}^{\oplus}$

$\mathrm{PhO}^{\ominus} \mathrm{Na}^{\oplus}, \mathrm{MeBr}$

hydrolysis of an easter

hydrolysis of an amide

hydrolysis of an ether

hydrolysis of an acid chloride

Passing ethanol over heated aluminium

Reacting sodium ethoxide with ethyl bromide

Reacting ethyl alcohol with sulphuric acid

Reacting ethyl idodide and dry sliver oxide

It is formed by E₂ mechanism.

It can't show geometrical isomerism.

It is formed by E₁ mechanism.

Loss of H⁺ occur from 3rd carbon.