ÇN N-Ts N-Ts -2HCI CN ci 2-Phenylacetonitrile p-Toulenesulphonyl Nitrogen mustard (IN2OH (ii) ELOH/HCI NH, 4 amino phenyl ethyl chloride 'N-H CI(CH,), -NH, C,H,000 C,H,00C Anileridine

help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all working

Show ALL your steps and details in your calculations, by using GRASPS: Given, Required, Analysis, Solution, and Paraphrase. Answer in complete sentences and therefore statements. Show All of your work, in full solutions

Curved arrows are used to illustrate the flow of electrons. Using the provided starting structure, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. Then draw any missing organic intermediates or products for this reaction. Include all lone pairs in the structures. Ignore inorganic byproducts and counterions. H 0:0- HsC H Select to Add Arrows H HaC Select to Add Arrows CH₂OH, H CH3OH, H* CH3OH, H* HaC H Select to Add Arrows 1 CH3OH, H+ HaC H H Select to Add Arrows I