e) What primary amine and carbonyl compound are needed to prepare this imine?

Q: Which N in DBU compound acts to accept a proton in an E2 reaction and why?

A: DBU is  Diazabicycloundecene. It is a Nucleophilic, bulky base. It is Stable, water-soluble, and…

Q: Draw the product for the following reaction.

A:

Q: Please help me solve this synthesis. It takes 5 steps

A: OKAY, I will give complete synthesis by using 5 steps.  You can see step by step solution. How to…

Q: Using retrosynthetic analysis, design a synthesis of the following target. HO Br Target

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: Write detailed mechanism for pathway from pinacol to pinacolone. You need to use curved arrows to…

A: Pinacol Pinacolone Rearrangement: A 1,2-rearrangement is used in the pinacol pinacolone…

Q: Complete the mechanism of the given enamine to imine tautomerization by adding any missing atoms,…

A:

Q: In a lab, we synthesized guaifenesin using Williamson synthesis mechanism. We used NaOH as the…

A: The Williamson ether synthesis is the most widely used method to produce ethers. It occurs by an SN2…

Q: explanation

A:

Q: Complete the mechanism of the given acid-catalyzed imine to enamine tautomerization by adding any…

A: The acid-catalyzed imine to enamine tautomerization is similar to keto-enol tautomerization.

Q: k of the electrophile on the aromatic ring. neration of the stable aromatic system by loss of a p…

A: We need to draw the detailed mechanism for the chemical reaction.

Q: Draw the product for the following reaction

A: Solution

Q: Highlight which site is most basi

A: The base is the species of a compound that can attack the proton and easily abstract the proton. It…

Q: Ph Ph ZI

A: Ans

Q: Show how you would synthesize this reaction.

A: When any arene is treated with halogen like chlorine in the occurrence of Lewis acid (like FeCl3…

Q: Show how you would synthesize this reaction.

A: Benzene is mainly utilized as an essential compound for the preparation of organic compounds. It is…

Q: Please draw the missing product(s) and please answer A through E

A: When an -OH and an -OR group is attached to a carbon atom in a molecule it is called a hemiacetal…

Q: (SYN) Show how you would synthesize this compound using propanal as your only carbon source. OH OH

A: In order to synthesize the desired product, two intermediate compounds 1 and 2 are required.…

Q: Encircle the most nuclleophilic site

A: We have to circle the most nucleophilic site. Nucleophilic center is one where the electron density…

Q: (SYN) Show how propoxybenzene can be synthesized using phenol and alcohols as your only source of…

A:

Q: Propose a reasonable multi-step synthetic route that would accomplish the following Ph

A:

Q: Reductive amination is one of the best methods to prepare amines. However, direct alkylation with…

A: Introduction: Amines: Amines are the functional group with nitrogen atom having alone pair. It is…

Q: What is the azo dye produced from the given coupling (left) and amine components (right)

A: At first, the amine group of the second compound converts into diazonium salt. Then, the diazonuim…

Q: (SYN) Show how to synthesize each of the following amines from an alkyl halide via a Gabriel…

A: Potassium phthalimide is a -NH2-synthon which allows the preparation of primary amines by reaction…

Q: Please help me how to get this answer form this reaction. Can you show step by step and explain.…

A:

Q: Synthesize the following targets.

A: The synthesis of first compound with reaction scheme and mechanism are shown in image.

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

A: The following steps are involved in the attack of acetylide as a nucleophile over acetone: The…

Q: Does the reductive amination only make secondry and tertiary amine? Bc i draw the mechanism and…

A: Reductive amination is the process of formation of amines with the help of carbonyl compounds which…

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: Which of the following compounds will react with methylo to form the imine shown below? N.

A: Since you have asked multiple question, we will solve the first question for you. If you want any…

Q: an you select the answers in each bracket? The imine functionality is similar to [ carbonyl /…

A: Imine and enamine both are formed from reaction of aldehyde and ketone with amine

Q: Determine what reagents are needed to perform the Stork enamine synthesis and then draw the…

A: The given reaction is,

Q: a) Draw the mechanism for the reaction of a secondary amine with an acid chloride to make an…

A:

Q: Which ketone you think has the most stable nsystem? Explain your answer clearly based on the…

A: Aromatic compounds are stabilized very much by resonance . They follow (4n+2)π Huckel rule which…

Q: The compound below exists in two tautomeric forms. Circle the most acidic proton in the keto form…

A: Keto and enol are form of tautomerism.

Q: What kinds of halides cannot be used to alkylate an amine? Why not? a.Tertiary halides form alkenes…

A: Correct Option :  d.  all of the above

Q: Draw the synthetic pathway including reagants + products

A: The question is based on the concept of organic reactions.   we have to convert given reactant into…

Q: An NH2 group_the ring toward electrophilic aromatic substitution by. a. activates, the inductive…

A: An NH2 group activates the ring toward electrophillic aromatic substitution by resonance. Option "c"…

Q: Which of the following compounds will react with methylamine to form the imine shown below?

A: Given as,

Q: sentence.] КОН, ТHF (Name reaction?) N. ww QUESTION 13 Which reaction sequence will successfully…

A: Ans

Q: Draw out complete mechanism of an acid hydrolysis of N,N-Dimethylbutanamide

A:

Q: Draw out the mechanism of synthesis of lopinavir by using a curved arrows |

A: Synthesis of lopinavir?

Q: OH + + b) What direction would you expect the equilibrium to lie and by how much? c) If an amine was…

A: A question based on equilibrium concept that is to be accomplished.

Q: tage yield ðf the product.

A: limiting reactant  It is a reagent that is completely used in a chemical reaction and when they…

Q: Propose a synthesis of the following target compound starting from benzonitrile. Remember to start…

A: Benzonitrile is first fluorinated then reduced to give benzyl amine which was then alkylated.

Q: In the window below, draw both the starting acid derivative and the ultimate carboxylic acid…

A: Benzoyl chloride when reacted with methane amine forms a tetrahedral alkoxide ion. The negative…

Q: Draw the hyperconjugation interaction that lessens the electrophilicity of the carbonyl on the…

A: The answer is as follows:

Q: True/False: This transition state will result in a syn-aldol product: O True False

A:

Q: Using what you have learned in the amines chapter; give the reagents that will perform the following…

A: