EF Effects on Halogenated Groups of Aniline

I have given you Rachel Davis and Ejorh’s paper. Their research paper is exactly like mine but with a couple of differences. I want you to follow the same format and the same explanations in the introduction, discussions, and conclusion as well as the abstract. All of the materials you will need for this paper are given in the helpful directions word doc please refer to that. And if you have any questions Rachels Davis and Ejorh are the best papers to look at but in addition to that, I have also given you other credible resources that you should also look at to write this paper. Attached is also my last semester ‘s report which talks about the same topic. The main focus of this paper is to focus on which of the halogenated groups is the most enhance and why is it the most and hands. Electronegativity plays a big role and you should explain why.

The purpose of this paper is to study the effects of halogenated groups of aniline. For example, does Fluoro-aniline, Chloro-aniline, Bromo-aniline, Iodo-aniline have the highest enhancement factor. By looking at table 1, you will see the different enhancement factors and vibrational modes the correspond to each peak. The highest exponential power is the most and enhanced isomer. Which position of these different isomers is the most enhanced and why. Ortho Meta or Para? What role do chemisorption and plasmonic enhancement affect play? What role does charge transfer play? Compare the vibration mode throughout each I isomers. For example, NH2 wags in the Fluoroaniline compared to Chloroaniline. CH2 stretch in the Chloro aniline compared to the Bromoaniline.