Advertisements
Advertisements
Question
Give the mechanism of the following reaction:
\[\ce{CH3CH2OH ->[H2SO4][413 K] CH3CH2-O-CH2CH3 + H2O}\]
Advertisements
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) \[\begin{array}{cc}
\ce{CH3CH2-\overset{+}{O}-CH2CH3 -> CH3CH2-O-CH2CH3 + H^+}\\
|\phantom{..................................}\\
\ce{H}\phantom{..................................}
\end{array}\]
\[\ce{H^+ + HSO^Θ_4 -> H2SO4}\]
APPEARS IN
RELATED QUESTIONS
What happens when chlorobenzene is subjected to hydrolysis?
What happens when ethyl chloride is treated with aqueous KOH?
C–Cl bond length in chlorobenzene is shorter than C–Cl bond length in CH3–Cl.
Which of the following is an optically active compound?
Racemic compound has ____________.
Identify the end product (C) in the following sequence:
\[\ce{C2H5OH ->[SOCl2][Pyridine] A ->[KCN {(alc.)}] B ->[2H2O/H^+] C}\]
The increasing order of nucleophilicity would be:

Which of the statements are correct about above reaction?
(i) (a) and (e) both are nucleophiles.
(ii) In (c) carbon atom is sp3 hybridised.
(iii) In (c) carbon atom is sp2 hybridised.
(iv) (a) and (e) both are electrophiles.
How do polar solvents help in the first step in SN1 mechanism?
Which alkyl halide from the following pair would you expect to react more rapidly by an SN2 mechanism? Explain your answer.
\[\begin{array}{cc}\ce{CH3CHCH2CH2Br}\\|\phantom{.........}\\\ce{CH3}\phantom{......}\end{array}\] or \[\begin{array}{cc}\ce{CH3CH2CHCH2Br}\\\phantom{}|\\\phantom{...}\ce{CH3}\end{array}\]
