Но. NaOH HO Br

Q: Show how to carry out the synthesis below. Br HO

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Q: Provide a multi-step synthesis to create the intended product for the listed original reactant. The…

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Q: H*, H20, heat NH,* + NH2 HO,

A: Applying concept of organic synthesis and reagent.

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

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

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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: NO2 Br

A: The conversion is given below in pic.

Q: Draw the major organic product of the reaction shown below.

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Q: and II, propose a sequenced reaction, identifying the two (or more if you are bold) individual…

A: In Mannich reaction nucleophilic addition of an amine to a carbonyl group occurs. If the product…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. H. NaCN, HCI Type here to…

A: Organic reactions are those in which organic reactant react to form organic products.

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

A: When a ketone is reduced with sodium borohydride and acidic hydrolysis, then ketone is changed into…

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 mechanism for the given base-catalyzed formation of a hemiacetal from…

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Q: Please give the reagents that will perform the following reaction.

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Q: Draw the curved mechanism arrows that show the SN2 reaction of phenoxide with chloroethane and draw…

A: SN2 is bimolecular substitution reaction , which occurs in a single step and in this case no…

Q: CH;OH Br (solvolysis) Sn1 Sn2 E1 E2 Sn1 & E1 Sn2 & E2

A: The correct answer about above reaction mechanism is given below

Q: Show the organic product formed when methyl propanoate is reacted with lithium diisopropyl amide,…

A: ester in presence of base form enolate and carry out cross clasisen condensation with other ester.

Q: I need a detailed reaction mechanism of this synthesis

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Q: NaOH NH, + NH3 H20

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Q: NaOEt ELOH, heat

A: -> NaOEt is base which can abstract most acidic hydrogen and generate nucleophile. ->Then…

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: Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…

A: In the given reaction benzaldehyde react with methyl amine.

Q: OMe cm Clz mCP BA MeO `OH

A: Given reaction is example of Baeyer-Villiger oxidation. The Baeyer–Villiger oxidation is an organic…

Q: Predict the product of the following substitution reaction?

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: Draw the major product of the substitution reaction shown below. Ignore any inorganic byproducts.

A: We have given the organic reaction and we have to find the major product of the reaction.

Q: Fill in the box with the major organic product of the following reaction mechanism. NaOH Draw the…

A: -> Base can abstract most acidic proton from the compound . -> In case of alcohol proton…

Q: TM H Show the synthetic sequence that converts acetylene to the target molecule (TM) shown below.

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Q: OH Ph PhMgBr OEt Ph

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Q: エース z-z L H H + CH Anything you need け。

A: Detail mechanistic pathway is given below

Q: OCH3 OCH, CH,N2 NH,, in aqueous CH;0 COCI CH;O СОCHN2 AGNO3 OCH3 OCH3 diazoketone OCH; OCH3 LIAIH4.…

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

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Q: 1. BH3 THF 2. H₂O2/NaOH/H₂O ●

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Q: Please provide a complete reaction mechanism (This includes arrow pushing mechanism, resonance…

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Q: What is a multi-step synthesis for the following:

A: The final product can be prepared in the following steps:Step 1 : Preparation of alkene from alkyl…

Q: `MgBr

A: In the above Reaction RMgX React with the epoxide . When the epoxide React with the grignard reagent…

Q: Draw curved arrows to illustrate the mechanism for the reaction of cyclohexanol and HI. The starting…

A: Given reaction

Q: e major product of

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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: CH3OH, H*

A: Aldehyde react with alcohol to give hemiacetal when react with 1 equivalent.

Q: Can someone help me with these and explain how they did it? The question is to predict the major…

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Q: HONH, CI- , NaOH

A: This is an example of condensation reaction in which hydroxylamine condensed with 1,3-dikketone to…

Q: Which of the following reagents, in which order, produce this multiple step synthesis reaction?

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Q: Can you please help show how to use the given reactant in order to synthesize this molecule?

A: Alcohols react with alkyl halides to give an ether. Alkene undergo epoxidation followed by…

Q: Ph Na Oet Eto OEt

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Q: Show the retrosynthesis mechanism of this equation with curved arrows representing electron transfer…

A: Note : 1-Butene on hydroboration and oxidation produces the 1-butanol. Benzoic acid and 1-butanol…

Q: Draw a reasonable mechanism for this reaction. Interactive 3D display mode Ph Ph-P=CH, CH2 Ph

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Q: Construct a three-step synthesis of trans-2-pentene from acetylene by dragging the appropriate…

A: Given scheme,

Q: Draw the product of the reaction. 2 equiv. HO, H*

A: A question based on organic reaction, which is to be accomplished.

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Show your work.

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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.