A student proposes the following mechanism for a nucleophilic substitution reaction:HHO:0:ноNotice that the products are missing. In the drawing space below, draw the major organic products the student would expect fromtheir mechanism. Be sure to use wedge and dash bonds where appropriate, for example to distinguish between different products.Click and drag to start drawing astructure.XGटेoloArB?

Step 1: ReactionSN1 : It is two step reaction and having carbocation intermediate. Products are…

Answered: A student proposes the following…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter8: Addition Via Carbocation

Section: Chapter Questions

Problem 18CTQ: The reactants, intermediates, final products, and all curved arrows showing bonds forming...

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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
don 13. (1) Draw the (E)- and (Z)- isomers of 1,3-dichloro-2-methylbut-2-ene. Using curved arrows, draw (a) an SN2 mechanism and (b) and SN1 mechanism for the substitution reaction shown below. Br ) Draw the organic product(s) formed in the following reactions: 1)0, by 2) Zn. H,0 MShow a sequence of reactions that could be used to synthesize the following compound. You must start from 3-pentanol. No mechanisms needed (HINT: You wil need to bring together more than one of the reactions you have seen in Modules 3 and 4]
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1,3-Butadiene undergoes an electrophilic addition with HBr. Complete the steps in the mechanism to produce the product shown. 2) Draw both the organic and inorganic intermediate species. Include all nonbonding electrons and charges. Draw a curved arrow to convert the intermediate into the product shown. 1) Add curved arrows for the first step. -Br: H, :Br: Нзс -сн—CH2 н
The reactants, intermediates, final products, and all curved arrows showing bonds forming andbreaking are collectively referred to as the mechanism of a reaction. For the following reactants: a. Explain why the original statement of Markovnikov’s rule does not help in this case, but themodern restatement of Markovnikov’s rule tells you which carbon will get the X (Cl). b. Show the mechanism of the most likely addition reaction between the reactants.
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