



To determine which of the given compounds are aromatic, we need to verify the following aromaticity criteria:
Now, let's examine each option to identify which compounds are aromatic:
Compound 1: This compound is not aromatic because it does not satisfy all the aromaticity criteria. It might be cyclic and planar, but it doesn't meet the (4n + 2) π-electron rule for aromaticity.
Compound 2: This compound is aromatic. It is cyclic, planar, and has complete delocalization of π-electrons. Additionally, it satisfies Hückel's rule with (4n + 2) π-electrons, for example, with n = 1.
Compound 3: This compound is not aromatic. While it may be cyclic, it fails to meet the necessary criteria for π-electron delocalization or the (4n + 2) rule.
Compound 4: This compound is aromatic. It is cyclic, allows for π-electron delocalization, is planar, and also satisfies Hückel's rule, having (4n + 2) π-electrons with n=1 or another valid integer.
Conclusion: Based on the analysis, the aromatic compounds are:
Compound 2 and Compound 4.
Which of the following are aromatic?

Give plausible explanation for:
(a) Diazonium salts of aromatic amines are stable.
(b) Aniline does not undergo Friedel-Crafts reaction.
(c) Aniline on nitration gives substantial meta product.
Identify the taxa that constitute a paraphyletic group in the given phylogenetic tree.
The vector, shown in the figure, has promoter and RBS sequences in the 300 bp region between the restriction sites for enzymes X and Y. There are no other sites for X and Y in the vector. The promoter is directed towards the Y site. The insert containing only an ORF provides 3 fragments after digestion with both enzymes X and Y. The ORF is cloned in the correct orientation in the vector using the single restriction enzyme Y. The size of the largest fragment of the recombinant plasmid expressing the ORF upon digestion with enzyme X is ........... bp. (answer in integer) 