Synthesize using an epoxide.

Q: Arrange following halides towards nucleophilic substitution reaction

A: Nucleophilic substitution reaction where one nucleophile replaces another nucleophile. The…

Q: What is the major neutral organic product for the following transformation? ONa ? Major Organic…

A: A base abstracts a proton from the alpha-position of a Carbonyl compound to form an enolate ion.…

Q: Draw a reasonable synthesis for this reaction

A:

Q: مشهد

A: Given is organic synthesis reaction.In given reaction epoxide is converted into ketone and alpha…

Q: J

A: Aldol condensation is a specific type of reaction the condensation (joining together) of two…

Q: The mechanism for this reaction is the reverse of the one in Eg. 18-13. H3CO OCH3 Hао (ехсess) + 2…

A:

Q: Dehydration via an E1cb mechanism Michael Reaction Intramolecular Aldol Reaction В KOH / ELOH / heat…

A: We know, Micheal reaction is basically the nucleuphilic addition reaction which is basically 1-4…

Q: h) Draw a stepwise mechanism for the following reaction. OH N° NH,OH MEOH

A: The reaction in which intramolecular transfer of proton is known as tautomerism.

Q: In the mechanism for acetal hydrolysis shown, the ring oxygen atom was protonated first, the ring…

A:

Q: Give typed full explanation   draw the reaction of alcohol alkoxylation using soudim methoxide…

A: Alcohol alkoxylation is a reaction in which epoxide is added to alcohol resulting in the formation…

Q: Provide the retrosynthesis and a forward synthesis for the transformation from the starting material…

A: Synthesis: Step 1: Dehydrobromination using NaOEt. Step 2: Epoxidation using mCPBA. Step 3: Acid…

Q: An imino chloride can be prepared from an amide according to the reaction shown here. Propose a…

A: A mechanism for this reaction can be proposed as

Q: Provide a synthesis for the attached problem

A: Needed compound is an alkene, in general elimination reactions give alkenes, like dehydration of…

Q: Draw a stepwise, detailed mechanism for the following reaction. + CH,NH2 N-CH3 CH,NH, Cr- (excess)

A: Organic reaction mechanism.

Q: OH H₂SO,

A:

Q: What alkene yields attached set of oxidative cleavage products ?

A: What alkene yields an attached set of oxidative cleavage products has to be determined.

Q: Provide the reagents to carry out the following reaction: A. )-

A: Here we have to establish the pathway of benzene to  1-cyclohexyl-1-phenylmethaneLet us work…

Q: 1) Draw the mechanism for the following reaction. Но H2SO4

A: Usually, the hydration of a double bond occurs in the presence of an acid catalyst, and a…

Q: Synthesize the following molecule using any reagents you desire. Ph HO,

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: CHON CHOH CH,OH HA OCH semes somes

A:

Q: How can the following compound be made via and Aldol Condensation? NaOH H3C Ethanol H3C CH3

A: It is an aldol condensation product of propanone. Steps of the reaction is given belowStep…

Q: BuLi

A: Organolithium is a reagent that acts as a base or nucleophile in the reaction as per the given…

Q: Draw a complete, detailed mechanism for this reaction.

A: The product consists of a two phenyl groups that are joined via a carbon atoms. The structure is…

Q: Devise a synthesis of attached alkene using a Wittig reaction to form the double bond. You may use…

A: 1). Oxidation of 2-propanol with PCCpyridine chlorochromate to give 2-propanone2).…

Q: Propose a synthesis of the following product from the starting material shown and any other required…

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

Q: Draw the mechanism for the following reaction. Provide all resonance structures for the arenium ion…

A: This reaction is known as Electrophilic  aromatic substitution  and Electrophile is Nitronium ion.

Q: Provide an IUPAC name for the following compound: XX OH

A: IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds as…

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.