The right-hand side of this reaction shows the product of an aldol condensation. What are the reactants missing from theleft-hand side? Draw them below.NaOHH?AIf there aren't any reactants that would lead to these products under the reaction conditions given, just check the box underthe drawing area.Note for advanced students: don't worry if the reactants you propose might also make some other products under thesereaction conditions. Just make sure the product above is one of the major products.

Step 1:Write about an aldol condensation reactionIn an aldol condensation reaction, two carbonyl…

Answered: The right-hand side of this reaction…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter24: Carboxylic Acids & Derivatives

Section: Chapter Questions

Problem 16CTQ

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In this chapter, we will study three types of Condensation reactions: Michael, Aldol and Claisen. Match the right reaction with the statements below. ● This condensation reaction takes place between two esters. The electrophile in this reaction must be an a,B-unsaturated carbonyl compound. The B-hydroxy carbonyl products of this reaction are often dehydrated to form a,B- unsaturated carbonyl products.
The right-hand side of this reaction shows the product of an aldol condensation. What are the reactants missing from the left-hand side? Draw them below. 2 NaOH ? A If there aren't any reactants that would lead to these products under the reaction conditions given, just check the box under the drawing area. Note for advanced students: don't worry if the reactants you propose might also make some other products under these reaction conditions. Just make sure the product above is one of the major products. No answer. Click and drag to start drawing a structure. X G O: A P olo Ar
Can you please draw out this reaction mechanism and explain what is happening in detailed steps? How are the reacgents acting? Please use curve arrows to show this reaction.
ed [Review Topics] [References] Write structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol below. ОН O ● ● ● ● 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 ↑
how do i go about this mechanism? is it a cross aldol reaction?
For each acetal below, show hydrolysis product
This reaction is an example of conjugate addition of a nucleophile to an a,ẞ-unsaturated carbonyl. H3C LOCH3 H₂O H3C OCH3 OCH3 Draw the two resonance structures of the enolate anion intermediate for this reaction. • Draw an R1 group in place of CoA. The R group tool is located in the charges and lone pairs drop-down menu. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate resonance structures using the symbol from the drop-down menu. • O H CH3 ? [F
Draw the aldol product that will form when the two reactants shown here are reacted in the presence of an amine base. Do not draw the conjugate acid of the triethylamine base that results. Be sure to include all lone pairs of electrons and formal charges in your product.
A student proposes the following reaction mechanism for the reaction in Model 6. Which step inthis mechanism is least favorable? Explain your reasoning.
This reaction is an example of conjugate addition of a nucleophile to an a,ẞ-unsaturated carbonyl. O CH3CH2CH2CH=CHCSCOA H₂O OH CH3CH2CH2CHCH2CSCOA Draw the two resonance structures of the enolate anion intermediate for this reaction. • Draw an R1 group in place of COA. The R group tool is located in the charges and lone pairs drop-down menu. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate resonance structures using the symbol from the drop-down menu. ->> 90-87 O + ? ChemDoodle >

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