Let's analyze each reaction:
n-Hexane with Mo2O3 at 773K and 10-20 atm: This is catalytic reforming or aromatization. n-Hexane can be converted to benzene under these conditions.
Acetylene (Ethyne) with Red Hot Iron Tube at 873 K: This is a classic method for synthesizing benzene. Three molecules of acetylene undergo cyclic polymerization to form benzene.
Benzenediazonium Ion with Warm Water: Benzenediazonium ion (C6H5N2+) reacts with warm water to form phenol (C6H5OH), not benzene. The diazonium group is replaced by a hydroxyl group.
Benzoate with Sodalime and Heat: This is decarboxylation. The benzoate loses CO2 to form benzene.
Therefore, the reaction that does not produce benzene as a major product is the reaction of benzenediazonium ion with warm water.
Total number of possible isomers (both structural as well as stereoisomers) of cyclic ethers of molecular formula $C_{4}H_{8}O$ is:
A full wave rectifier circuit with diodes (\(D_1\)) and (\(D_2\)) is shown in the figure. If input supply voltage \(V_{in} = 220 \sin(100 \pi t)\) volt, then at \(t = 15\) msec: