Draw the structure(s) of the major organic product(s) of the following reaction after aqueous workup.NH₂+CH3CH3. You do not have to consider stereochemistry.•Include counter-ions, e.g., Na+, I, in your submission, but draw them in their own separate sketcher.•If no reaction occurs, draw the organic starting material.••Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.Separate multiple products using the + sign from the drop-down menu.+H3CNH?ChemDoodle√n [An error has been detected in your answer. Check for typos,miscalculations etc. before submitting your answer.<>

After reaction of aniline and acetic anhydride, the main product will be N_acetylaniline.However,…

Answered: Draw the structure(s) of the major…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter16: Synthesis Workshop 1

Section: Chapter Questions

Problem 10CTQ

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Several reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used.
Construct a multistep synthetic route from ethylbenzene to (2-bromoethyl)benzene by dragging the appropriate items into the bins. Note that each bin will hold only one item, and not all reagents and structures will be used.
Assume that 2-chloropropane reacts with CN− in an SN2 reaction. Use the JSME editor () to draw the structure of the substitution product of the reaction. The guide on how to draw your structure can be found here Important Note: When drawing the structures in the JME editor please adhere to the following formats: 1. If the nucleophile is OH−, DO NOT manually add the "H" to the final product 2. If the nucleophile is CN−, be sure to include the appropriate bonding between the C and N in the final product
draw the product of the reaction shown below. Use wedge and dash bonds to indicate stereochemistry where appropriate. Ignore inorganic byproducts.
Complete the reactions below using the required reagents or products. If there is no reaction, indicate so. If a product is in the majority, specify which one.
Chemistry Show retro-synthetic analysis leading from the target molecule to the precursor molecule showing all intermediate molecules.Using organic chemistry from your textbook show an efficient synthesis of your target molecule starting from its parent molecule and showing the structure of each isolable intermediate.Assume you have access to usual reagents like Br2, AlCl3, Fe, HBr, HNO3, H2SO4, etc.Assume that each intermediate can be purified from other products at each step of the synthesis.
In the following reaction Series, write down the appropriate reagents that can be used where there are question marks
Construct an efficient three-step synthesis of 1,2-epoxycyclopentane from bromocyclopentane by dragging the appropriate formulas into the bins. Note that each bin will hold only one item, and not all of the given reagents or structures will be used.
Please help with the attached OChem reaction. Fill in the correct reagents, provide the stepwise mechanism for both step 1 and 2, and include the correct use of arrows showing the flow of electrons. Thanks!
Using the wittig reaction, synthesise aldehyde 4 to form cis alkene 2, and trans alkene 3. In your answer, with your choice of R group, describe synthetic routes to each alkene and include reagents and conditions
a. Can you predict an undesirable side reaction that might occur using ethanol as a solvent that would not occur if we used THF as a solvent?b. Based on your knowledge of SN2 reactions, what would happen if we used 1-ethyl-2- naphthoxide instead of 2-naphthoxide? Explain.
1, part A) In the reaction below, draw all of the possible products. 1, part B) For all the products you have drawn, draw their corresponding carbocations while also identifying if each is 1o/2o/3o carbocation. In addition, starting from alkene - provide complete accurate arrow-pushing mechanisms of each carbocation formation. 1, part C) In part B, circle the carbocation which is *most* stable, indicate why.

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