A student proposes the following mechanism for a nucleophilic substitution reaction::CN?Notice that the products are missing. In the drawing space below, draw the major organic products the student would expect from their mechanism. Be sure touse wedge and dash bonds where appropriate, for example to distinguish between different products.

Answered: Image /qna-images/answer/c798da83-81db-49c8-a073-a69f4c911c34.jpg

Answered: A student proposes the following…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter5: Resonance

Section: Chapter Questions

Problem 8E

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draw the major organic products the student would expect from their mechanism. Be sure to use wedge and dash bonds where appropriate, for example, to distinguish between different products
Substitution and elimination: predict the product Maximum allowed tries per question: Unlimited (7) Draw the major organic product of the reaction. Follow this procedure: determine whether the reaction conditions are acidic or basic; identify the most nucleophilic/basic atom, the electrophilic atom, and the leaving group; predict whether elimination or substitution will occur; and then draw the product. Indicate the stereochemistry at every stereocenter with a single wedged (up), hashed (down), or wavy (a mixture of up and down; either) bond. Launch MarvinJSTM viewer or click image to copy source CH3 H3C EtONa EtOH Br
Substitution and elimination: predict the product Maximum allowed tries per question: Unlimited (5) Draw the major organic product of the reaction. Follow this procedure: determine whether the reaction conditions are acidic or basic; identify the most nucleophilic/basic atom, the electrophilic atom, and the leaving group; predict whether elimination or substitution will occur; and then draw the product. Indicate the stereochemistry at every stereocenter with a single wedged (up), hashed (down), or wavy (a mixture of up and down; either) bond. Launch MarvinJSTM viewer or click image to copy source CI benzene A
Substitution and elimination: predict the product Maximum allowed tries per question: Unlimited (3) Draw the major organic product of the reaction. Follow this procedure: determine whether the reaction conditions are acidic or basic; identify the most nucleophilic/basic atom, the electrophilic atom, and the leaving group; predict whether elimination or substitution will occur; and then draw the product. Indicate the stereochemistry at every stereocenter with a single wedged (up), hashed (down), or wavy (a mixture of up and down; either) bond. Launch MarvinJSTM viewer or click image to copy source H₁₂C CH3 EtOH Br
For the reaction can someone please synthesize the given products from the given reactants. Multiple reactions/steps will be needed (the arrows designate the minimum number of steps). Also, for the 1st step (reaction) in each synthesis, can you please draw an energy diagram showing the correct number of hills and valleys for that step’s mechanism?
Q2. What are elimination reactions? Illustrate and describe the E2 reaction mechanism. Compare and contract elimination and substitution reactions with relevant examples.
Bha Please don't provide the handwriting solution
Ll.116.
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
The reaction between propionyl chloride and acetate ion is outlined below. a) Complete the mechanism of the forward reaction by placing curved arrows to show the electron movements in the reactants and intermediate product. i: :0: b) Draw the structures of the final product and leaving group, including any charges. (Electrons may be omitted.) 1L
2) Provide a detailed mechanism for the addition reaction shown below. State the regiochemistry and explain why it's unusual. SCH3 HBr Br SCH3 EN Please be sure to include all structures (use line angle notation or perspective diagrams as appropriate to illustrate the stereochemistry of the process), resonance forms, intermediates, transition states, curved arrows, formal charges, or lone pairs as necessary. Please redraw the substrate
Electron pairs CH3 .. Erase H3C - С — СІ: H3C – S- CH3 CH3 CH, CH3 THF/H,0 + H,C--CH, CH C- CH CHs CH, Use curved arrows to write the first step of this nucleophilic substitution mechanism. :ö: | :ö:

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