Show how could you prepare the following cyclohexenone by combining a Stork enamine reaction with an intramolecular aldol condensation by drawing theappropriate pyrrolidine enamine and enone precursors.CH3-You do not have to consider stereochemistry.Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.Separate multiple reactants using the + sign from the drop-down menu.

Step 1: Remember the stork-enamine reaction taking a ketone 1 and pyrrolidine 2 to produce the…

Answered: Show how could you prepare the…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter26: Aldol And Claisen Reactions

Section: Chapter Questions

Problem 5E

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Similar questions

Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol below. ОН You do not have to consider stereochemistry. • Draw the enolate nucleophile in its carbanion form. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate multiple reactants using the + sign from the drop-down menu.
Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol below. You do not have to consider stereochemistry. Draw the enolate nucleophile in its carbanion form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu.
3) Provide example reactions for Aldol and Claisen condensations. [self-study not grade: For each of your example reactions, use the product as a starting material for another reaction.]
I need help determining the starting materials for these three aldol reactions.
Help me
Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol below. OH f O • You do not have to consider stereochemistry. • Draw the enolate nucleophile in its carbanion form. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu. ● + ChemDoodle O. #[ ] در ↑
Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol below. OH H You do not have to consider stereochemistry. • Draw the enolate nucleophile in its carbanion form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the sign from the drop-down menu. ? ChemDoodle Sn [F
Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol below. OH ● ● You do not have to consider stereochemistry. Draw the enolate nucleophile in its carbanion form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu. VI ? ChemDoodleⓇ n [ ]#
Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone below. H • You do not have to consider stereochemistry. • Draw the enolate ion in its carbanion form. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop- down menu.
Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol below. OH нео ● ● ● ● You do not have to consider stereochemistry. Draw the enolate nucleophile in its carbanion form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu. ? ChemDoodle n[1
Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol below. OH H усо You do not have to consider stereochemistry. Draw the enolate nucleophile in its carbanion form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate multiple reactants using the + sign from the drop-down menu. ? ChemDoodle t OO. Sn [F Q
In a mixed aldol condensation with unknown aldehydes and ketones experiment, some aldol condensation reactions need to be heated for the dehydration step to occur. Explain why that was not necessary for the reactions carried out in this experiment? [Hint: what makes the product especially stable?]. This experiment used ethanol, acetic acid, sodium hydroxide, cyclohexanone and 4- methoxybenzaldehyde.

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