The mechanism for the dehydration of ethanol (CH3CH2OH) to ethene (CH2=CH2) under acidic conditions involves the following steps:
Step 1: Formation of protonated alcohol (Fast step)
Ethanol (CH3CH2OH) reacts with the proton (H+) to form the protonated alcohol (ethyl oxonium ion).
CH3CH2OH + H+ → CH3CH2OH+
Step 2: Formation of carbocation (Slow step)
The protonated alcohol undergoes the loss of water to form a carbocation, which is the rate-determining step.
CH3CH2OH+ → CH3C+ + H2O
Step 3: Formation of ethene by elimination of a proton (Fast step)
The carbocation formed in Step 2 loses a proton to form ethene.
Thus, the overall reaction is:
CH3C+CH2 → C2H4 (Ethene) + H+
For the thermal decomposition of \( N_2O_5(g) \) at constant volume, the following table can be formed, for the reaction mentioned below: \[ 2 N_2O_5(g) \rightarrow 2 N_2O_4(g) + O_2(g) \] Given: Rate constant for the reaction is \( 4.606 \times 10^{-2} \text{ s}^{-1} \).
“One of these days you’re going to talk yourself into a load of trouble,” her father said aggressively. What do you learn about Sophie’s father from these lines? (Going Places)