In cach case below select the synthetic procedure/s that could be used to carry out the transformation, giving the alcohol shown as the single major product.

Q: First, draw the structure of the alkyl bromide that will ONLY give the alkene shown in an…

A: Elimination reaction are those reaction where functional group is lost to form unsaturated compound…

Q: HO,

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Q: Draw the arrow pushing mechanism for the following reaction

A: The reaction of an alkene with HBr is complete in 2 steps – Formation of carbocation Nucleophilic…

Q: Draw the reactant of the following reaction sequence that would give the product shown as the major…

A: reaction is given below

Q: Show the mechanism for this reaction using arrow pushing

A: Friedel craft alkylation  Catalyst AlCl3 Carbocation stability…

Q: how will this methyl shift be drawn?

A:

Q: Is it possible to synthesize from these two when cutting in this way? Also, please explain the…

A: The provided retrosynthesis will not work for the synthesis of given target molecule. This…

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: Predict the major product for the folowing reaction

A: Any molecule or ion which are electron-rich species is called nucleophile, and electron-deficient…

Q: williamson

A: In Williamson etherification Synthesis reagent is used NaOH or NaH ( base ) and solvent is THF .…

Q: lowing transformation e

A:

Q: For the reaction shown, draw the product of one mole of reagent adding across the triple bond, and…

A: In the given reaction Product A and Product B are to be determined. This is an addition reaction and…

Q: Mechanism of this reaction please!

A: Given enzymatic reaction is:

Q: which of these has tautorimzation occur during the mech of the final product

A: Tautomers are isomers of a compound which differ only in the position of the protons and electrons.…

Q: What are the compounds X,Y and Z in the given reaction sequence ?

A: When potassium dichromate react with the Silver nitrate it gives the silver chromate as a insoluble…

Q: Synthetic

A:

Q: Complete the following multi-step synthesis.

A: Nito benzene upon nitration agin it give meta-dinitrobenzene , it  reduced selectively with NH4HS…

Q: I need a detailed reaction mechanism of this synthesis

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Q: In each case below select the synthetic procedure/s that could be used to carry out the giving the…

A: Given : structure of reactant and products.  Both the reaction are addition of water.

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: Given the reaction at the photo, what is the major product?

A: In an aromatic nucleophilic substitution reaction, a nucleophile attacks on the carbon atom of the…

Q: Show the complete synthesis for the following reaction that forms the following product(s) PLEASE…

A: The question is based on the concept of organic reactions. it involves carrying out a series of…

Q: Perform the Synthesis of this.

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Q: Draw the arrow pushing mechanism of the following reaction

A: Given substrate is 3°alkylhalide hence in presence of polar solvent and heating conditions favours…

Q: Please show the complete steps as well as arrowing pushing mechanisms for the following reaction.

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Q: For the reaction shown, choose the most likely reaction pathway and draw the organic product.

A: This reaction can happen by Nucleophilic substitution reaction .  Here azide ion as the nucleophile…

Q: Provide the missing

A: In the given question, a reagent [36] and a transition state [37] needs to be determined.

Q: draw a complete synthesis from starting material. List out all solvents and reagents used and draw…

A: Here we have to write the major products formed in the following sequence of reactions.

Q: ) Complete the following Oxymercuration-demercuration reaction. (Pay attention to the…

A: In oxymercuration and demercuration (OMDM) an alkene is treated with Hg(OAc)2 and the product is…

Q: Which can ot be used in the second step of the reaction sequence

A: Azide ion is a strong nucleophile (far better than amines) and will readily participate in…

Q: Using

A: We will give mechanism of the reaction.

Q: Brz. FeBr NaOMe

A: Organic Transformation and Mechanism

Q: This reaction can be completed with which reagents?

A:

Q: For the following reaction, draw a complete reaction mechanism using curvy arrows being sure to show…

A: Solution Two sensible sources of binary compound-like reactivity ar the complicated metal hydrides…

Q: out the stepwise mechanism (include intermediates or transition state) for: CH3CH2OH CHCH2)3CBr…

A: Close observation of reactant will confirm the reaction mechanistic pathway which is SN1 for the…

Q: Above each arrow, supply the reagent(s)/reaction conditions that is(are) needed for each of the…

A: Alkanes in presence of sun light conditions Free radical substitution reactions takes place , If…

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: Fill in the appropriate reagent or starting material in each of the attached reaction.

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Q: Br

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Q: This is a retro synthetic analysis problem, shown here is the final product (initial material is…

A:

Q: Show all the arrow mechanism including the RIGHT reagents.

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Q: Show all the arrow-push mechanism including the RIGHT reagents.

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Q: complete

A: We will write the reaction conversion

Q: complete the following synthesis produces using a proper reagent and products

A: Organic synthesis is a special branch of chemical synthesis and is concerned with the intentional…

Q: Question attached

A: Given reactions:

Q: Give major product part a,b,c properly

A: Solution- major product of given below with there reaction;

Q: b) T.

A: The question is based on the concept of organic reactions. We have to identify the reagents used in…

Q: for this reaction scheme suggest a reagent that could be used to accomplish the first step and draw…

A: Alcohols on reaction with sodium metal forms sodium alkoxide . R-OH + Na ------> R-O-Na+ Sodium…

Q: 11. heat -N+-CH3 CH3 12. 1) NaOCH3 H3CO OCH3 2) H*

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.