Describe two ways the following reaction can be carried out

Q: Which of these would be the fastest to react via Sy1? .CI A) B) CI CI C) D)

A: SN1 is also called unimolecular nucleophilic substitution reaction.

Q: Explain why the following reaction sequence will not occur:

A: -NH2 is an electron donating group. Hence, it increases electron density more on ortho and para…

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

A: Applying concept of organic synthesis and reagent.

Q: H2SO4 но H20

A: Hydrolysis of ester into acid and alcohol.

Q: What is the target product formed after the following sequential reactions?

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Q: Select the correct product of the reaction mechanism step shown below.

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Q: The rate of bromination of the following three alkenes is very different: 2-methyl-1-pentene,…

A: Bromination of alkene or alkene halogenation reaction means addition of dihalide on the…

Q: NaOH `NH, NH3 + H2O

A:

Q: 3. Propose a possible synthetic pathway for the following reaction. multiple steps

A: Bromination is electrophilic aromatic substitution reaction where benzene ring acts as nucleophile.…

Q: Show the full mechanism for the following reaction.

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Q: Complete the following reaction scheme , Complete the following reaction scheme

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Q: In the following reaction, propose a mechanism that explains its formation:

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Q: Describe three ways the following reaction can be carried out:

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Q: 3. Write a detailed reaction mechanism for the following transformation. Upload your answer as an…

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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: Provide the mechanism for the 2nd reaction in this synthesis: H2O CI

A: Step 1: Acid chloride reaction with Grignard will give the ketone. Step 2: keto compound react with…

Q: Predict the main mechanism that occur for the following reaction

A: Nucleophilic substitution reactions the electron-rich nucleophile attacks on a positively charged…

Q: NaOH но. Н-О, Неat

A: When an acid and base react they form a salt and water.    Here benzoic acid react with NaOH to form…

Q: Complete the following reaction below:

A: We have to Complete the given reaction

Q: Explain why this reaction is not possible

A: In elimination reaction the olefins are formed. Elimination reaction are two types E1 and E2.  If…

Q: provide the mechanism and reagents to perform the reaction. Br Но

A: To provide the mechanism and reagents for the given reaction

Q: I. Complete the reaction map below A.

A: alkyne upon catalytic reduction (H2/Pt) to give alkane alkyne with ozonolysis triple bond…

Q: 4. Provide the reagent(s) needed to complete the following reaction scheme. Provide the complete…

A:

Q: Give two possible [1,2]-rearrangement products where an alkyl group migrates in the following…

A: Organic reaction mechanisms:

Q: What is the final product (D) of the following reaction sequence?

A: In the first step, p-chloronitrobenzene reacts with Fe/HCl followed by NaOH to form p-chloroaniline

Q: Select the best set of reagents for carrying out the following synthesis

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Q: Come up with a reasonable mechanism for the following reaction

A: In this question we want to draw reasonable mechanism for this reaction.  This reaction is Aldol…

Q: Please write the mechanism for the following reaction.

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Q: CI

A: The detailed solution of your question given below_ Since, we know that the nucleophile attack in…

Q: Draw a detailed, step-wise mechanism for the reaction shown below. SHOW ALL BOND-FORMING AND…

A: In the above reaction, the OH- present in the base NaOH will attack on the carbon making ester bond…

Q: The correct sequence of reactions to carry out the following transformation is:

A: B is the correct option. The Wittig reaction is a chemical reaction of an aldehyde or ketone with a…

Q: NAOH NH2 + NH, H2O

A: See mechanism below.

Q: а. b. HO,

A:

Q: HONH, CI- , NaOH

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

Q: product

A: Reaction of an aldehyde or a ketone with excess alcohol in the presence of an acid gives acetal as a…

Q: Choose the two major products of the following reaction.

A: The given reactant i.e. 2-bromopentane is a secondary alkyl halide and the reaction is carried out…

Q: H3CO, NaOH H,CO H3CO OCH3

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Q: Ph Na Oet Eto OEt

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Q: Identify the four products in this sequence of reactions:

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Q: HO OH H+ to

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Q: Question attached

A: Given reactions:

Q: a) Show a detailed mechanism for the reaction to produce nitrogen gas and the two carbon radicals…

A: "Since there are multiple sub-parts in this question and it is not mentioned that which one has to…

Q: Please complete the reactions given below.

A: Given reactions: g)                               h)                                i)…

Q: break down of this reaction in sequence and a complete reaction scheme

A: In the given reaction ferrocene is reacting with acetic anhydride in the presence of H3PO4 to…

Q: Following the two-step reaction sequence depicted , write out the steps needed to convert A to B.

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.