Consider the following reaction sequence: Part: 0/3 Part 1 of 3 OH pyridine [1] -SO,CI NaSCH₂ [2] Draw the structure of the tosylate formed in Step [1] of the reaction sequence shown, including appropriate stereochemistry. Do not use abbreviations for any portion of the tosylate structure. Click and drag to start drawing a structure.

Predict the organic product for the reaction and complete the arrow pushing mechanism. Complete the mechanism for the reaction by adding the missing curved arrows, atoms, bonds, charges, and nonbonding electron pairs

Compound A reacts with B in the presence of sodium hydride to give C as the majority product.1. Give the detailed mechanism of the formation of C and draw the product C in the box above.2. Draw the energy diagram of the reaction. Indicate with an arrow the rate-determining step of the reaction then draw its transition state3.The rate of the reaction observed is 5 x 10-2 M.s-1 when the concentrations of A and B are 0.2 M and 0.1 M respectively.Determine the rate of the reaction if the concentrations of A and B are now 0.3 M and 0.2 M respectively. Show your calculation

Show the mechanism of the reaction of drawing 1 mole of water from the 2,2,5-trimethyl-3-hexanol compound, indicating the reaction conditions, step by step. Indicate the main product and by-product. b) Does the main product show the geometric isomer? If it does not show the isomers, please indicate why it does not. c) Write the products formed when the. main product ozonlamp is reduced.

Complete the generic mechanism for an electrophilic aromatic substitution (EAS) reaction using E as the electrophile, and show how the sigma complex is resonance stabilized. Use curved arrows to show the mechanism and the conversion between resonance structures. Make sure to add any missing charges. Note the use of a generic base (B) in the last step. Then, label the reaction coordinate diagram for a typical EAS reaction by correctly placing the structures on the diagram. Step 1: add a curved arrow. Select / |||||| Draw CH Rings Groups More Erase slow WE

Give detailed mechanism Solution with explanation needed..don't give Handwritten answer

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!

Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C NH₂ HCI/H₂O reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na+, I, in your answer. • In cases where there is more than one answer, just draw one.

ivatives: Nucleophilic Acyl Substitution Reactions - EOC [References] From the table of available reagents select the one(s) you would use to convert butanoic acid to each of the following products: (Use the minimum number of steps; from one to six are required. List reagents by letter in the order that they are used; example: fa. NOTE: Assume that a normal aqueous (or mild acid) workup follows each reaction; you do not need to add reagents for the workup.) Reagents Available a. benzene/AlCl3 d. H2O, H2SO4 g. LiAlH4 j. PBг3 b. (CH3)2CuLi e. H₂, Pd/C h. NaCN C. CH3NH2 f. K* -OC(CH3)3 i. NH3 k. Dess-Martin periodinane I. SOCI₂ 1-butanol butanenitrile

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