Step 1 CI Benzoic Acid Thionyl Chloride Benzoyl Chloride Step 2 "y" NH2 HNH Benzoyl Chloride Nitrogen Trihydride Benzamide Step 3 NH2 NH2 Br-Br Na-OH Benzamide Bromine Sodium Hydroxide Aniline

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Draw a reasonable arrow-pushing mechanism for the transformation shown. Make sure you identify nucleophiles and electrophiles/acids and bases. Name any type of reactions taking place. Either Ingold-mechanistic designator or if this isn't appropriate, a description of the process. Account for and regio or stereoselectivity. HO B12 Br DCM

Question in Image. Synthesis.

Please provide detailed curved arrow mechanism for this scheme.?

D 1. a)Please show the mechanism for the below (b) indicate the parts that can be labeled products. as E and electrophilic addition. () Show the potential energy diagrams for the last two steps of the meintinism assuming the kinetic and thermodynamic products are the Saume. GM H₂J Oy> #₂0 для низои хат ха Product A bp 104°C Product B bp 101-102°t

Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the curved arrows to draw the structure of the missing intermediates and products in the following mechanism. Include all lone pairs and charges as appropriate. Ignore stereochemistry. Ignore inorganic byproducts. (The structures there are incorrect and I do not know why. Please help. Thank you.)

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