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+
Match List-I with List-II for the following reaction pattern: \[ \text{Glucose} \quad \text{Reagent} \quad \rightarrow \quad \text{Product} \quad \rightarrow \quad \text{Structural prediction} \]
Which of the following is not an aromatic compound?
Among the following, identify the compound that is not an isomer of hexane:
Chlorobenzene reacts with bromine gas in the presence of Anhydrous AlBr_3 to yield p-Bromochlorobenzene. This reaction is classified as
The organic compound can be classified as