Match each synthesis of racemic leucine to what R has to be to complete it. Answers may be repeated. 'N'Na v Choose. 2-methylpropyl 1-methylbutyl 3-methylbutyl PBry Bn H2NNH, leucine none of the other answers OH

Q: Draw the major and minor product(s) that are expected for the following reaction. If only one…

A: As there are two alpha H to leaving present in the given substrate, thus there are possibility of…

Q: Glucose and galactose Energy of activation with lactase Energy Lactose and water Energy of…

A: Answer: In this question we have to mark the energy profile of the hydrolysis reaction of Lactose,…

Q: Lake Baikal in Siberia is the largest freshwater body on Earth by volume, at 5666 mi What is this…

A: Given: The volume of Lake Baikal in Siberia = 5666 mi3 We have to convert this volume to L.

Q: 3. Starting with 2-bromo-2-methylbutane make the TM. Show the retrosynthesis (no synthons required)…

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Q: Draw the major product of this SN1 reaction. Ignore any inorganic byproducts.

A: The given reaction is an example to SN1 reaction where a secondary carbocation is formed initially…

Q: Draw the major product of this SN1 reaction. Ignore any inorganic byproducts

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Q: Draw the organic product of the nucleophilic substitution reaction. Include all hydrogens atoms.…

A: In the given nucleophile substitution reaction ether compound is formed.Explanation:Approach to…

Q: if something is inductively favorable, is it an Electron withdrawing group?

A: Electron withdrawing groups :- The groups or atoms which pulls electron density towards itself…

Q: Draw the mechanism that shows how α-D-allopyranose converts to α-D-allofuranose under acidic…

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Q: Draw the complete, detailed mechanism (curved arrows) for the reaction between alanine and DCC and…

A: Step 1:Step 2: Step 3: Step 4:

Q: Active Site 2 3 HN- NH2 2-OPO 4 Но Но- HO OHa 1

A: In the given question, the active side contains many functional moieties.

Q: Complete the mechanism of the following step by adding the missing curved arrow(s). Edit Drawing…

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

Q: Draw the major product of this SN1 reaction. Ignore any inorganic byproducts. Br Drag To Pan Pinch…

A: SN1 reactions are unimolecular nucleophilic substitution reactions. They are first order reactions.…

Q: NH, HCN H,O leucine Choose... 2-methylpropyl 1-methylbutyl 3-methylbutyl RBr NAOH/H*heat none of the…

A: The first reaction is known as strecker amino acid synthesis.

Q: meta-directing group will place the electrophile into a 1,2- or 1,4-relationship with the dirscting…

A: A meta-directing group will place the electrophile into a 1,2- or 1,4-relationship with the…

Q: Curved arrows are used to illustrate e flow of electrons. Follow the curved arrows a draw the…

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Q: Dehydration via an E1cb mechanism Michael Reaction Intramolecular Aldol Reaction А C KOH / ETOH /…

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Q: Match each synthesis of racemic leucine to what R has to be to complete it. Answers may be repeated.…

A:

Q: Draw the mechanism that shows how α-D-allopyranose converts to β-D-allopyranose under acidic…

A: From the given, β-D-allopyranose is more stable than α-D-allopyranose because of less steric…

Q: Draw the complete electron pushing mechanism that is enzyme catalyzed.

A: In this question, we will draw the complete stepwise electron pushing mechanism by using enzyme…

Q: H NaOH, H₂O

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Q: Draw the mechanism for Fmoc deprotection. Hint: start with the most acidic proton on the Fmoc…

A: It is one of the efficient protection group for -NH2 functionality and can undergo deprotection in…

Q: In witting synthesis experiment what compounds describes the oxaphosphetane intermediate? Draw

A: The reaction given is witting synthesis.

Q: Draw an appropriate reactant on the left-hand side of this organic reaction. Also, if any additional…

A: The detailed solution is uploaded in explanation section.Explanation:

Q: Encircle the most nuclleophilic site

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

Q: Design an aldol synthesis to form the target.

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Q: CH3 CI A) C) CH3 NaNH, NH3 NH₂ CH,NH2 B) D) CH3 NH₂ NHCH3 CH3 NH₂ ?

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Q: Supply the missing curved arrows in this intermediate to show how it is converted to the product…

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Q: CH₂(CH₂), C=C_H 4 1 equiv. C

A: Alkyne are unsaturated hydrocarbon which have triple bond so they are reactive in nature.  Here we…

Q: НО ОН

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

Q: The ring with C=N i weakly activating directing and it is strongly deactivating

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Q: I believe that this rxn will proceed via Eliminatin but I can't draw the mechanism.

A: Elimination reaction: An elimination reaction is removal of two substituents in a molecule and forms…

Q: From first picture what will the product be with an interaction with H2CrO4

A: H2CrO4 under acidic condition oxidized a primary alcohol into aldehyde which again oxidized to…

Q: H ОН Pt + H2 CH2CH3

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Q: Consider the hypothetical reaction: ADP + ATP NH2 a) Identify the molecule in box above marked "?"…

A: Reference: Self “Since you have asked multiple questions, we will solve the first question for you.…

Q: Use the reaction bank as directed and devise a synthetic route

A: To carry out the given synthesis, the following types of reactions are usedAmine protection by BOC…

Q: H,O/H;O* H2O OH H b. a. OH с. d.

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Q: What would be the product, D, of the following reaction sequence? OH PB13 A I Li IV ether B Cul C…

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Q: Draw the major product of this SN1 reaction. Ignore any inorganic byproducts.

A: To  draw the product of the given organic reaction mechanism.  we are asked to draw the product…

Q: онон CHI H* но OH Et;N EIOH Meo OMe Meo OMe Meo OMe Meo- Meo OMe A Meo- OMe mOEt OMe Eto OEt EIo OEt…

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Q: 3. Starting with cyclopentylmethanol and any inorganic reagents required make the target molecule.…

A: Retrosynthesis is the reverse synthetic process in which a target molecule is broken down into…

Q: Draw the products of the following proton transfer reaction. Show all unshared valence electron…

A: Concept introduction: Elimination reaction are those reaction in which small amount of molecule are…

Q: 8) Consider the below desired transformation. Develop a retrosynthesis and forward synthesis that…

A: We have to convert methyl butyrate to 2-methylpent-2-ene

Q: Complete the following reaction by providing missing reactants or products as appropriate. (See…

A: Terminal alkyne gives a hydration reaction in the presence of mercuric sulfate and sulfuric acid to…

Q: GHy OH

A: These reaction are the three step reaction, first step is the halogenation and second step is the…

Q: Major + + Minor OH Minor

A: The question is based on organic reactions.     we need to identify the product formed and explain…

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.