Complete the mechanism for this acid-catalyzed transesterification by drawing out allthe individual steps. Draw the important resonance contributors for each resonancestabilized intermediate.

Q: Draw the detailed mechanism and the product for the following reaction. Be sure to include…

A:

Q: Draw a complete, detailed mechanism for the following 1. R'—ОН, Н reaction. R-C=N 2. H20, НО R OR'

A: The above reaction is an acid catalyzed reaction of nitrile with an alcohol which results in the…

Q: Provide the mechanism for the 1st reaction in this synthesis: ВНЗ/ТHF

A:

Q: Draw the complete, detailed mechanism for the addition of hexan-3-ol to dihydropyran and predict the…

A: The given reaction is,

Q: Provide the mechanism for the 1st reaction in this synthesis: КОН

A: We have to draw the mechanism of given reaction

Q: Give a complete mechanism for the following substitution reaction. at Br ethanol

A: it is nucleophilic substitution, solvolysis reaction in which ether formation takes place.

Q: Draw the complete mechanism for the reaction below, including stereochemistry.

A: H2SO4 and H2O act as dehydrating agent on double bond.  Mechanism steps  In first step, alkene…

Q: Draw a complete mechanism for the following reaction. Be sure to start with the formation of the…

A:

Q: Draw a detailed mechanism for the following reaction, clearly showing all electron movement NH H*,…

A: Treatment of imine with water leads to formation of ketone/aldehyde . This reaction is called…

Q: H2C (SYN) (a) Draw the alcohol that would be required to form the alkyl chloride shown here using…

A: The reaction between alcohol and phosphorous chloride (PCl3) results in chloroalkanes.

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

A: Concept introduction: Ozonolysis: It is the process in which ozone is added to alkene and form…

Q: Show the complete mechanism using Curved Arrow Formalism for the reaction of the compound shown…

A: INTRODUCTION: p-chlorobenzaldehyde reacts with EtOH and HCl to give an acetal.

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

A:

Q: Draw mechanism for the following reaction and fully explain Ph Ph Ph Ph CF,SO,H Ph- -Ph но он…

A: The above reaction is an example of the formation of an new aromatic unit by elimination of two H2O…

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: 3) Give a complete, detailed mechanism for the following transformation. C, HCI HCI

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Q: Draw the mechanism for the following reaction. H2O, HCI H2N

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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: (a) Draw the mechanism for the following transformation including reagents and any isolable species…

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Q: Ticls, k H2, Pdle CH3 Pooduch

A: In presence of TiCl3, McMurray coupling is occurred.  Followed by reduction of alkene .

Q: Draw

A: Water molecule react with H2O

Q: Draw the complete, detailed E1 mechanism for each of the following reactions, and show all resonance…

A: E1 mechanism follows through two steps 1) In the first step by eliminating leaving group (halide…

Q: An enamine, R2C=C-NR2, behaves as a nucleophile in much the same way that an enolate anion does.…

A: Enolate ions have two or more reactive sites so they are called, ambident reactive species. The…

Q: When phenyl-5-bromopentanone is treated with triphenylphosphine, followed by base, a compound is…

A: The structure of triphenyl phosphine is

Q: For each sequence of reactions, draw the complete, detailed mechanism and predict the major organic…

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

Q: H3C-NH2 но. „CH3 H3C-NH2 но. CH3

A: Ans

Q: The reaction shown here is an example of the Favorskii reaction, which involves an R¯ leaving group…

A: The Favroskii reaction involves the rearrangement of a ketone with the alpha halogen substituent to…

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: Give a complete mechanism for the following Reaction: CI NH2 NH2 NANH2 / NH3 ČH3 ČH3 CH3

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Q: Which of the listed conditions and nucleophile/s will open the epoxide at carbon A? Which will open…

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Q: Draw the complete mechanism for this reaction. p-CH3- CgH4– SO;H + H3C-OH

A: The organic conversion helps in the conversion of one organic compound into other compounds. This is…

Q: сн NaOCH,CH3 н CнCH2он heat

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Q: Explain mechanism-  Tautomerization in Acid ?

A: Tautomerization of a compound is a phenomenon in which the compound tends to exist in two structures…

Q: The following transformation is an example of a Darzens reaction. Draw its complete, detailed…

A: The Darzens reaction is an organic reaction that takes place between an aldehyde or ketone and an…

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

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

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Q: hv D. C.

A: This is an example of 1,3-sigmatropic carbon shift followed by electrocyclic ring opening.

Q: Draw the mechanism of how you can make cyclohexyl ethanoate from ethane

A: The details solution for this reaction is provided below in attach image.

Q: Which out of the given nucleophiles will open the following epoxide at the A carbon? Which will…

A:

Q: Predict the major organic product of this reaction and draw the complete mechanism to form it: H2SO4…

A: See product in red box.

Q: please explain the mechanism of ring opening of an epoxide by reaction with nucleophile under acidic…

A: The reactions of Epoxides with strong nucleophiles requires a strong driving force that helps in the…

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

A:

Q: Draw the complete, detailed mechanism for each of the following reactions, including the major…

A: All the reactions given above are Markovnikov addition reaction

Q: a) Draw a complete, detailed mechanism for the following reaction and label the rate- determining…

A:

Q: Predict the major organic product of this reaction and draw the complete mechanism to form it: Br…

A: Given: Reactant = Bromo benzene.                           Reagent = NaOMe To find : major product…

Q: Which rearrangement product will form preferentially during the [1,2]-rearrangement of an R-group?…

A: The rearrangement product is stable if the intermediate carbocation formed is stable. We have to see…

Q: An alternative solvent to alkylate saccharin nucleophile could have been another OA. protic; ethanol…

A: Given statement is :  An alternative solvent to alkylated saccharin nucleophile could have been…

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.