please help answer / explain these questions

Question 11. Based on the electrostatic potential surface (EPS) maps below of benzene 1 and related derivatives 2-6, predict which arene A-system is more electron rich. (scale of electron density: high in red, relatively high in orange, medium in yellow, low in green, and extremely low in blue) 2 Question 12. Based on the electrostatic potential surface (EPS) maps above, rank the arenes 1 through 6 from least to most electron rich 2-systems. Question 13. Based on the electrostatic potential surface (EPS) maps above, explain the trend of electron density between compounds 1, 3 (phenol) and 4 (aniline). Question 14. -systems of arenes can bind to cations. This phenomenon is called cation- interaction. Based on the electrostatic potential surface (EPS) maps above, explain the ranking of -cation binding strength: 4 >> 3-1 > 2-6>5 Benzene Question 8. Draw the resonance forms of the phenol to the ketone shown below. How many electrons are in conjugation? . Question 9. From the resonance forms drawn above, determine which carbons are 8 and 8 around the benzene ring. Question 10. Based on the electrostatic potential surface (EPS) maps of indole, benzene and pyridine shown below (left to right), predict which arene is more electron rich. Also use this depiction to propose a range of chemical shift in 'H NMR for the hydrogens that are flanking those arene rings