Show the mechanisms for the following reactions. Show all movement of the electrons. Do not skip or combine any steps. Show all relevant bonds, charges, and intermediates. (Note: D = deuterium)

Q: 85. a. Propose a mechanism for the following reaction: CH30 Br + Br

A: Organic reaction mechanisms.

Q: Complete the following retrosynthetic analysis. Supply all reagents and precursors. Parts A and B…

A: Here we have to synthesize the following compounds by retro synthesis reaction.

Q: Propose a mechanism for the following reaction. (Hint: Number the carbons to help you see where they…

A: The mechanism is as given below:

Q: The following reactions give two different products. Shows the mechanism leading to their formation.…

A: For the ring opening of epoxide there is a rule ,  1) When the reaction is performed in the…

Q: Devise a detailed mechanism for formation of the major product of the substitution reaction below.…

A: The reaction given is,

Q: 2. Propose a synthetic strategy for the following reactions. Make sure to include the structures of…

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Q: NABH4 МеОн of (CH3CH2)2NH, mild acid NaBH3CN H3CSH

A: The product of the reaction is given as follows

Q: Complete the reaction and provide a mechanism for the formation of the product Na OCH2CH3…

A: Organic reaction mechanisms:

Q: Identify the final product of the sequence of reactions shown below: 1) NaOMe, MeOH 2) `Br 3) NaOMe,…

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Q: OR `NH2 ОН R Z-I ZIR

A: Since you have posted multiple questions with multiple sub-parts, we are entitled to answer the…

Q: (CH3),COCH3 HI (CH3)½CI CH3I + + H20

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: a) но н sock pyridine h)

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

Q: Br O,N O,N AIBR3

A:

Q: 5,0<o H20 + NHtz

A:

Q: How do you complete the following syntheses? Show all reagents and important conditions, and all…

A: The complete synthetic route with reagent are provided below in attach image.

Q: Using curved arrows to illustrate the flow of electrons, propose a mechanism to account for the…

A: Here we have to write the mechanism of the following given reaction. The given reaction is E1…

Q: Propose a mechanism for the following reaction:

A: A Grignard reagent is an organomagnesium compound which can be described by the chemical formula…

Q: (10 points) Complete the reaction scheme below. Show all reagents and intermediates. No reaction is…

A: Ans

Q: Complete the following retrosynthetic analysis (the final product is shown first, and the initial…

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Q: 1. NaOH, A 2. H3O⁺ OH + OH

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Q: Show the deprotonation with curved arrows and the resulting product. Include the resonance structure…

A: The H which is most acidic is reacting in the reaction with base. And since the H present on O where…

Q: light Br2, k ROOR HBr но н soch pyridine

A: as per the honor code we are bounded to solve only first three sub parts. for other sub parts please…

Q: 3) write a detailed mechanism for the following reaction: Br hv light + HBr + Br2

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Q: 3. Propose a mechanism for the following reaction sequence. Et 1. BuLi, 2 moles 2. CH3CH,Br Ph

A: Organic reaction:

Q: Show the complete mechanism for the formation of the major product(s) for the following reaction?…

A: The reaction follows free radical mechanism:

Q: a) Brz, light b) ROOR HBr

A:

Q: Show a detailed mechanism for the following reaction. 1. Cl2, NaOH 2. Hзо*

A: Applying concept of haloform reaction followed by acidic hydrolysis.

Q: CH3 CH3 NO2 H2SO4 + HNO3 + H20 ČH3 ČH3

A: mechanism of p-Xylene follows some steps which are given as below

Q: Perform a retrosynthetic analysis of the target molecule shown below, from starting materials…

A: Please find the attachment.

Q: 7. + CH₂ I ₂ Zn (Cu) Ether

A: This is an example of Simmon Smith reaction of alkene using organozinc carbenoid forming to…

Q: Show your reaction mechanisms for the formation of: a. RCNOH, from the reaction of RCOOR' with NH₂…

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Q: Using curved arrows to illustrate the flow of electrons, propose a mechanism to account for the…

A: In this question, we will draw the reaction mechanism by using curved arrows and showing all the…

Q: 1. Show a detailed mechanism for the following reaction and give the structure of the major product.…

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Q: Draw detailed mechanisms for the following transformations Мео. Br2, NaOH Meo, NH2 `NH2 H20

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

Q: pentanal + 2 equivalents of methanol d. valeric acid + xs NaBH4 followed by acid

A:

Q: Consider the reaction shown below. Provide a complete arrow-pushing mechanism that accounts for the…

A: Alkynes undergo hydrolysis reaction in the presence of acid catalyst produces carbonyl compounds.

Q: H;O*

A: In the given reaction the alkene is hydrated to form an alcohol.

Q: Propose reagents that can be used to accomplish the following reactions. CN Br Br ОН Br

A: Interpretation- Reagent to accomplish the given reactions are to be proposed.

Q: NGOH/H,O 4

A: Since you have asked multiple question, we will solve the first question for you as per our…

Q: _MgBr i) BrMg ii) H,0

A: Reaction of gridnard reagent to carbonyl

Q: The following reaction can be carried out in two steps. Choose the correct reagents i) and ii) to…

A:

Q: Show the mechanism and products for the reaction of 2-methyl-2-hydroxypropane + methanol.

A: In first step, methanol has acidic proton hydrogen bonded to oxygen, so H of -OH in…

Q: CH3 CH3 from OH and isopropyl alcohol

A:

Q: Show your reaction mechanisms for the formation of: a. RCNOH, from the reaction of RCOOR' with NH₂…

A: These are the Nucleophilic substitution reactions.  Nucleophile will substitute the leaving groups…

Q: 3. Provide the major product of the following reactions. Show the complete mechanism for products A,…

A: Above reactions are the nucleophilic substitution and elimination reactionsl of the alkene.

Q: The following reaction can be carried out in two steps. Choose the correct reagents i) and ii) to…

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Q: Show the product formed in each step of this multi-step synthesis.

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Q: HCI CH3-CH2-CEN CH3-CH2-C-OH + NH,CI H2O

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Q: Propose a mechanism for the following reaction (remember to use curved arrows to show the movement…

A: Please go through the below pic for the mechanism.

Q: benzaldehyde 9 H ethyl formate -OCH₂CH3 1. pyrolidine O 2. 3. H₂O* 8 10 ya ii + excess benzaldehyde…

A: Since you have posted a question with multiple sub-parts, we will solve the first three subparts for…