Draw the structure(s) of the major organic product(s) of the following reaction.••1. in acetonitrile / refluxOCH32. aqueous HCI•You do not have to consider stereochemistry.•You do not have to explicitly draw H atoms.•Do not include lone pairs in your answer. They will not be considered in the grading.•Do not include the amine from which the enamine was derived.•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.Θ?ChemDoodleⓇ<>

First one is the product. But due to the presence of acid, the ester undergoes hydrolysis to give…

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

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter25: Enolate & Enol Nucleophiles

Section: Chapter Questions

Problem 11CTQ

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Similar questions

Draw the structure(s) of the major organic product(s) obtained after workup of the following reaction. Use the wedge/hash bond tools to indicate stereochemistry where it exists. If no reaction occurs, draw the organic starting material. Draw structure(s) of product(s) after aqueous workup. Include counter-ions, e.g., Na+, I-, in your submission, but draw them in their own separate sketcher. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
- The reaction that will be carried out in the lab will convert 9-fluorenol to 9-methoxy fluorene usinga nucleophilic substitution reaction. Question: Why is concentrated sulfuric acid used in this reaction and not aqueous acid? Draw the reaction and show the equilibrium that is dependent on the acid.
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 organic product(s) of the following reaction. You do not have to consider stereochemistry. Include cationic counter-ions, e.g., Na+ in your answer, but draw them in their own sketcher. If no reaction occurs, draw the organic starting material. Separate multiple products using the + sign from the drop-down menu.
What are the characteristics of the a good nucleophile for SN2? How does a chemist tell a strong versus weak or bulky versus not bulky nucleophile? What is the best type of solvent for this reaction? Please define the terms. Thank you.
For SN2 Explain if 3o ( tertiary) alkyl halides reacted (fastest or slowest) explain why. Be sure to explain if alkyl halides did not react or did react and why. 3o (tertiary) compounds listed are: 2-chloro-2-methylpropane (see picture) Base your explanations on the following considerations: the nature of leaving group, the effect of structure, steric hindrance and any other feature.
Chemistry Please answer the following two questions. 1.) Why are functional group interconversions controversial? (double bonds into epoxide) 2.) Explain the clincal trials that happen for epoxide containing molecules
Bulky, nonnucleophilic bases favor elimination over substitution. Define this ?
Why is the reaction of the type shown below usually done? a.To make an aldehyde or ketone less water soluble b.To make the molecule more reactive c.To protect a ketone or aldehyde carbonyl d.To increase the oxygen content e.To make the alpha hydrogens more acidic
a. Write the complete mechanism, step by step, for the reaction shown in the image A, in such a way that it explains the formation of the products (Please do not forget the correct use of arrows!). b. Write the complete mechanism (suppose an E2), step by step of the reaction shown in the figure B, in such a way that it explains the formation of a single product (DO NOT FORGET THE CORRECT USE OF THE ARROWS!). Using structures, justify the formation of the chosen product and not others. c. Write the complete mechanism (suppose a bimolecular reaction), step by step of the reaction shown in the figure C, in such a way that it explains the formation of all possible products (there are three). (DON'T FORGET TO USE THE ARROWS CORRECTLY!). Watch out for stereochemistry!
When the hypochlorite oxidation is performed on secondary alcohols such as 1-phenolethanol, the product of the reaction is benzoate ion and trichloromethane if an excess of hypochlorite is used in the absence of a buffer to keep the pH below 10. Explain the formation of these products (Hint: what reaction do the products remind you of?) Provide a complete mechanism?
Based on your answer to the above question and the structures you draw in question 1, what group/bond in the structure that causes the increased reactivity towards bromine addition?

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