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Question
Give the mechanism of the following reaction:
\[\ce{CH3CH2OH ->[H2SO4][413 K] CH3CH2-O-CH2CH3 + H2O}\]
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Solution
\[\ce{CH3CH2OH ->[H2SO4][413 K] \underset{Diethylether}{CH3CH2-O-CH2CH3} + H2O}\]
Mechanism: The formation of ether is a nucleophilic bimolecular reaction SN2 involving the attack of alcohol molecules on protonated alcohol as below:
(1) \[\ce{CH3CH2 - \underset{\bullet\bullet}{\overset{\bullet\bullet}{O}} - H + H+ -> CH3CH2 -^+ \underset{\bullet\bullet}{\overset{\ce{H}}{\overset{\bullet\bullet}{O}}} - H}\]
(2)

(3) \[\begin{array}{cc}
\ce{CH3CH2-\overset{+}{O}-CH2CH3 -> CH3CH2-O-CH2CH3 + H^+}\\
|\phantom{..................................}\\
\ce{H}\phantom{..................................}
\end{array}\]
\[\ce{H^+ + HSO^Θ_4 -> H2SO4}\]
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RELATED QUESTIONS
Arrange the compounds of the following set in order of reactivity towards SN2 displacement:
1-Bromo-3-methylbutane, 2-Bromo-2-methylbutane, 2-Bromo-3-methylbutane
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Tertiary alkyl halides are practically inert to substitution by SN2 mechanism because of ____________.
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Which of the following statements are correct about this reaction?

(i) The given reaction follows SN2 mechanism.
(ii) (b) and (d) have opposite configuration.
(iii) (b) and (d) have same configuration.
(iv) The given reaction follows SN1 mechanism.
Which one is the correct order of nucleophilic strength (pKa) of following nucleophiles?
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undergoes SN2 reactions faster than
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Reason (R): Iodine is a better leaving group because of its large size.
In the light of the above statements, choose the correct answer from the options given below:
