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

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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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Please help me with this i am very confused, if I have a current answer it is incorrect and I am just using this to study and I am very confused
please help me with all parts of this question, it is a single question with multiple subparts
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 &
Please step by step answer and don't use ASI Answer please
When naphthalene undergoes an irreversible electrophilic aromatic substitution, the major product is the kinetic product, which proceeds through the most stable arenium ion intermediate. With this in mind, draw the curved arrow mechanism for the first step of the electrophilic aromatic substitution of naphthalene with CH3+. Then draw the curved arrows and a resonance structure in step 2 with an unbroken benzenoid ring. Draw all atoms, electrons, and charges, if necessary, on all structures; draw all curved arrows on all structures except the last one. Do not draw any inorganic byproducts or counterions. 2nd attempt Br Heat See Periodic Table i Draw all curved arrows for the electrophilic aromatic substitution mechanism.
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.
Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. You do not have to consider stereochemistry. Include all valence lone pairs in your answer. Do not include counter-ions, e.g., Na+, I-, in your answer. In cases where there is more than one answer, just draw one.
Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. You do not have to consider stereochemistry. Include all valence lone pairs in your answer. Do not include counter-ions, e.g., Na+, I-, in your answer. In cases where there is more than one answer, just draw one.
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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