Can you please draw me the synthetic route (not mechanisms) for this reaction by using reagents/conditions from the list? Order of the step matters and please help.

Q: Sort the following nucleophiles as adding reversibly or irreversibly to the ketone substrate.…

A: Reversible reactions: The reactions which can take place in both forward direction as well as…

Q: an alke

A: Alkanes, alkenes and alkynes are simple hydrocarbon chains with no functional groups. The simplest…

Q: "hat reaction step is between structures I and II in the following reaction mechanism?

A: The compounds of alcohol contains -OH group. The oxygen atom carries two non-bonded e-ns (lone…

Q: Complete the mechanism for the reaction of butanone with NABH, followed by the addition of aqueous…

A:

Q: As some of you have seen while reading/watching outside sources, most textbooks say that SMI and El…

A:

Q: Draw the major product of this elimination. Consider regiochemistry and stereochemistry. Ignore…

A: An E1 elimination reaction shows the deprotonation by a base and the removal of a leaving group from…

Q: Draw the major product of this elimination. Consider regiochemistry and stereochemistry. Ignore…

A: Alcohols undergo a dehydration reaction in acidic medium to eliminate water molecules. The product…

Q: NO2 Hint: you will need an alpha bromination and a Robinson annulation reaction. Do not forget your…

A: Note : Michael addition between EAA and eneone followed by ester hydrolysis and decarboxylation…

Q: Please show me the retrosynthesis and synthesis with detail steps.

A: To get the starting material we have to do the retrosynthetic analysis by doing this we get, 2-…

Q: help please answer in text form with proper workings and explanation for each and every part and…

A: Step 1: Reactants:2,5-dimethyl-3-bromohexane: This is a secondary alkyl…

Q: 2. Show how you would synthesize the target compound on the right from the starting compound on the…

A: Here is the answer First we will make grignard reagentThen it will attack to the respective carbonyl…

Q: by the number of the third intermediate, etc., until you have selected the correct intermediates and…

A:

Q: PBr3

A: ***Since you have posted multiple independent questions in the same request, we will solve the first…

Q: Classify the following products as either aldol products, Claisen products, or neither. سے شعر می A…

A: We have to classify the given structures as aldol product, Claisen product or neither

Q: b. Hint: take "inventory" first of the process and think about whether you have a nucleophile or…

A: DMF or Dimethyl formamide is a polar aprotic solvent. Its chemical formula is HCON(CH3)2 . The term…

Q: [Review Topics] [References] Draw structures for the carbonyl electrophile and enolate nucleophile…

A: Enone formation involves reaction of an enolate (formed from a carbonyl compound treated with a…

Q: THF, HMPA HWE -> Diene] Kide+Aldehyde] OH PPh₂ У OH

A: The given reaction involves the reaction of the carbonyl compound with the phosphine oxide salt. The…

Q: Chem, please answer with detail.

A:

Q: 7. Draw the major 1,2-addition product and the major 1,4-addition product of the following reaction…

A: The 1,2-addition is the reaction where only one of the two double bonds reacts via a stable tertiary…

Q: H2N. Br N° H2N

A:

Q: 10. For each set of reactions, 1) identify the reaction mechanism as SN1, Sn2, E1, and/or E2 (write…

A:

Q: Show how you would synthesize the target compound on the right from the starting compound on the…

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: o O tt. AILLS Ⓒ 2n (Hg) HCl * актион Naor ⒸH3 HOH

A: The above reaction is based on organic reaction mechanism. In the first step of the reaction, first…

Q: 10. For each set of reactions, 1) identify the reaction mechanism as SN1, SN2, E1, and/or E2 (write…

A:

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Incorrect, 1 attempt remaining…

A: LiAlH4 (Lithium aluminium hydride)is nucleophilic reagent. It reduces mostly all functional group.

Q: Draw the major product of the aldol addition reaction between two of equivalents of this aldehyde…

A: An aldol condensation occurs in aldehydes which contain 𝛼-hydrogen with a dilute base to give…

Q: Choose one (and only one) of the reactions below and draw the complete mechanism for the major…

A: All the given reactions are electrophilic aromatic substitution reactions. This particular reaction…

Q: 3. Name other two reagents which are used for acetylation. Give mechanism for each reagent.

A: Acetic anhydride and acetyl chloride are two reagents for acetylation of aniline.Mechanism for…

Q: Draw the complete, detailed mechanism (curved arrows) for the following reaction. Br 2. H₂O OK

A: This is nucleophilic substitution reaction.We need to explain the formation of given product based…

Q: Can the target compound at right be efficiently synthesized from the starting material at left? Br…

A:

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.