Add the reagents and conditions above and below the arrow that complete this proposed acetoacetic ester synthesis.If that's not possible, because an acetoacetic ester synthesis will not achieve this transformation efficiently, then check the box below the drawingarea instead.Note: if you need to use alkyl halide reagents, please use only alkyl bromides.If you need to write reagents above and below the arrow that have complex hydrocarbon groups in them, there is a set of standard abbreviationsyou can use.+ More...The complex hydrocarbon group abbreviations listed below each structure are recognized by ALEKS.CH3-BrBrMeBrPrBrBrBriBuBrCyBrCyCH₂BrBrBrBrBrEtBrBriPrBrBrTsBuBrPhBrBnBruAdd rxn conditionsAdd rxn conditions

Answered: Image /qna-images/answer/8f511d2c-a413-446e-904a-9aabefb22df8.jpg

Answered: Add the reagents and conditions above…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter14: Elimination

Section: Chapter Questions

Problem 32CTQ

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4. Provide a synthetic route to the following molecule using benzene and cyclohexane. Reagents cannot contain more than one carbon. Provide a mechanism for the last step of your synthetic route.
need to check answers; Acetylene is an important synthetic building block that can be used to produce organic compounds with a wide variety of other functional groups. Consider the transformation of 3-phenylpropanal from acetylene shown below, which requires several steps. Part 1; image part 2 : The first step in this synthetic sequence involves an alkyne coupling reaction. Acetylene is deprotonated, and the acetylide anion is reacted with an organic halide. Draw the structure of the halide required in this step. Part 3: image
Add the necessary reagents and reaction conditions above and below the arrow in this organic reaction.
A student claims the right-hand side of the reaction in the drawing area below shows the product of a Claisen condensation. • If the student is correct, complete the reaction by adding the necessary organic reactants to the left-hand side, and by adding any necessary reagents and reaction conditions above and below the arrow. • If the student is incorrect, because it's not possible to obtain this product from a Claisen condensation, check the box under the drawing area instead. • Note for advanced students: If you have a choice, use the most efficient reactants and reagents - those that will minimize any byproducts or competing reactions. 0 0 Click and drag to start drawing a structure. siren rondensation 0: + I X &
Draw the reagents and solvent necessary to conduct the following reactions. ( You may need to use more than one step to accomplish the transformations). DRAW ALL REAGENTS, SUBSTRATE, AS WELL AS THE PRODUCT OF EACH STEP.
Background: In an experiment, dibenzalacetone is prepared using a Claisen-Schmidt reaction between aceton and two equivalents of benzaldehyde. [Image 1] Draw out the complete mechanism (curved arrow formalism) for the preparation of benzalacetophenone.
Show how you would synthesize the target compound ne right from the starting compound on the left. Show reagents and conditions, and the structures of important intermediate compounds. Do not show any (arrow pushing) mechanism. Ignore stereochemistry in this question.
Redact the major new product resulting from each of the following reaction. I provide an example how i look like it set it please following direction. Step by step. I want to know where the arrow goes too.
Complete the synthesis of the following compound from the starting material given (2- oxocyclohexane-1-carbaldehyde). Over/next to the reaction arrows, list out all reagents/solvents used. Draw intermediate structures in the boxes. You may use as many steps as you think necessary. You do NOT have to draw the mechanisms.
t please don't provide handwritten solution
Above each arrow, supply the reagent(s)/reaction conditions that is(are) needed for each of the following (Only one reaction is necessary for each transformation.) transformations. Br SH

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