In the reaction shown below draw curly arrows to show how the acetylide can act as a nucleophile.

Q: Identify the cyclohexyl substrate which would undergo the fastest E2 with base.

A: E2 elimination is a one step concerted mechanism reaction in which dehydrohalogenation (or any other…

Q: B. In each of the following pairs, circle the species that is more reactive toward nucleophilic…

A: We know that greater electrophilicity of  the carbonyl, then faster will be the nucleophilic attack

Q: Following Curved Arrows to Draw a Reaction Product Follow the curved arrows and draw the products of…

A: This reaction is an elimination reaction  In which alkyl halide is converted into an alkene with the…

Q: Step 1. Protonation of carboxylic acid. Draw curved arrows. Select Draw Rings More Erase H HH H :0 :…

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Q: please explain how aldol condensation reaction work please

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Q: Draw the major product for the following reaction, Then draw the mechanism for the following…

A: Arrangement of carbonation is for stability as we know that 3degree carbonation is more stable than…

Q: Use the curved arrow formalism to draw the complete mechanism for the aldol addition reaction. (It…

A: Initially one Molecule of butyraldehyde reacts with potassium Hydroxide base, where OH- ions acts as…

Q: Draw the complete, detailed E1 mechanism for each of the following reactions. (a) (b) I -Br CH3OH…

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Q: 2. Circle all the compounds below that will racemize when treated with a weak acid or base. Explain…

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Q: Complete the following base-catalyzed Self-Aldol Condensation reaction mechanism. Draw the structure…

A: Reactant is cyclohexanone. It has alpha hydrogens which in the presence of a base can be extracted…

Q: What are the errors in the following answer?  Note: If the product has ortho or para substitution,…

A: In a substitution reaction, one substituent in a chemical compound is replaced by another.  When a…

Q: What starting materials are needed to synthesize each compound using an aldol or similar reaction?

A: Given compound,

Q: Draw the mechanism that shows how α-D-allopyranose converts to β-D-allopyranose under acidic…

A: From the given, β-D-allopyranose is more stable than α-D-allopyranose because of less steric…

Q: Make one reaction scheme using proper compounds in the box below for Williamson ether synthesis.…

A: The reaction given is Williamson ether synthesis.

Q: Step 3: Add curved arrows. Select Draw Rings More Erase Select Draw Rings More Erase " CHO H. HCI…

A: Alphahydrogen containing etone enolizes to enol form which attacks on the aldehyde to produce aldol.…

Q: CI

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Q: n micxed aldol condensation of acetone with excess benzaldehyde in the presence of NaOH. Draw the…

A: Aldol condensation takes place in those carbonyl compounds that have alpha hydrogen.  In the case of…

Q: Identify the cyclohexyl substrate which would undergo the slowest E2 with base.

A: To identify the cyclohexyl substrate which would undergo the slowest E2 with base.

Q: Circle every active position and indicate at each whether it is electrophilic or nucleophilic.

A: An electrophile is an atom or group of atoms that is deficient of electrons and hence attracted…

Q: Draw the mechanism for the aldol addition reaction OH shown here, which is catalyzed by acid. Hint:…

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Q: Propionaldehyde undergoes an aldol condensation to form the aldol dehydration product. HCI = Product…

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Q: Circle the better nucleophile in polar protic solvent. Below each answer, BRIEFLY explain your…

A: Polar protic solvents are capable of forming hydrogen bonding because they have atleast one hydrogen…

Q: Br КОН

A: At first the base attacked to the most acidic H and generate a negative charge then the carbanion…

Q: HO HO Draw the mechanism for the following reaction.

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Q: Draw a mechanism to show how the following molecule forms a racemate when exposed to base. Think…

A: We have to give the mechanism of the given racemate reaction. Now, we know that sodium ethoxide…

Q: Draw the structures of the TWO Reactants that will be needed to synthesized the desired product from…

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Q: please place the reagent in the proper order as to complete the below synthesis in a way that…

A: Ans

Q: For the following reaction, draw a complete reaction mechanism using curvy arrows being sure to show…

A: Solution Two sensible sources of binary compound-like reactivity ar the complicated metal hydrides…

Q: сн NaOCH,CH3 н CнCH2он heat

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Q: Draw the mechanism for each of the following reaction. Show all steps in the reaction, the…

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Q: NaOH +

A: Acetophenone and benzaldehyde in presence of base NaOH undergoes Claisen-Schmidt condensation…

Q: The transform below undoes a nucleophilic substitution reaction. How would you carry out the…

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Q: НО Draw a full mechanism that illustrates the hydrolysis of the compound above

A: The imine functional group is identified by the presence of a carbon-nitrogen double bond. It is…

Q: Please provide mechanism (arrows, fish hook, leaving group, nuc attack,  etc.)  steps to get to the…

A: It is a problem based on radical rearrangement. Radical is formed when light falls on reactant. NBS…

Q: Draw a complete, detailed mechanism for the reaction shown here.

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Q: Identify whether the hydroxide ion is functioning as a base or as a nucleophile (see first pic)…

A: Two questions based on organic reactions, which are to be accomplished.

Q: Find one Aldol condensation reaction in acidic conditions and draw a step-by-step mechanism

A: Aldol condensation reaction is a reaction in which a ketone or aldehyde with alpha H present in them…

Q: Draw

A: Missing reagent should be nucleophile which attack on carbonyl carbon.

Q: Rank the nucleophiles in following group in order of increasing nucleophilicity. −OH, Br−, F− (polar…

A: The given groups are -OH, Br-, F- To find: The increasing order of nucleophilicity

Q: Carefully draw the mechanism of the following reaction using arrows to show the movement of…

A: The given reaction is an example of Electrophilic Bromination of Benzene.   This reaction occurs in…

Q: Illustrate detailed mechanisms for below attempted aldol reaction.

A: The given reaction is an aldol reaction in which one substrate is a ketone and the other is an…

Q: Draw the major product of this SN1 reaction. Ignore any inorganic byproducts.

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Q: Complete the following multi-step synthesis.

A: First nitrobenzene reduce to aniline by Sn-HCl, then it converted to benzene diazonium chloride by…

Q: For the following reaction step, indicate which pattern of arrow pushing it represents. A…

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Q: Question attached

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Q: For each compound shown below, draw the carbonyl compound and the nucleophile that were reacted to…

A: Given compounds are made-up from carbonyl compounds.

Q: then

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Q: If you react acetaldehyde and acetone in the precensce of NaOH in H2O, how many aldol condensation…

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Q: Draw a complete stepwise mechanism for the aldol self-condensation reaction shown below. You must…

A: Two moles of Cyclohexanone undergoes self aldol condensation when treated with ethanol in basic…