Predict the product of the first and third steps and propose a mechanism for all three steps. Br2 NaH ..... CH;OH H20 + EN H*

Q: For the reaction sequence below, select the expected major product. 1) Br2 2) 3 eq. NaNH2/NH3 3) H.O

A: The solution is as follows:

Q: Give a clear handwritten answer..... give the mechanism of given bleow reactions ....

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Q: OH BrCH2 COCH, CHCHN Co,CH heat The synthesis of this morpholino derivative occurs in several steps.…

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

Q: Give a reasonable mechanism for each indicated reaction above. Use auditional sheets, make sure you…

A: On treating the given alkene with Hg(OAc)2, intermediates (I & II) and product (III) are formed.

Q: NaOEt CH3CH2 Br NaOH H+ ? ?

A:

Q: Write a detailed mechanism. OH りNaoH 2)Brz in CH2C 2

A: First step of the the reaction is Favorskii rearrangement. This reaction is followed as follows:

Q: 5. Provide the mechanism for the Wittig reaction below. H3C H3C- FPPH3 CH3

A: The  Wittig reaction is the chemical reaction of aldehyde or ketone with a triphenyl phosphonium…

Q: Write a detailed mechanism for the following reaction. OEt H -OEt 2 ELOH

A:

Q: Provide a detailed step by step mechanism for the formation of the product in the reaction Brm Na H>…

A: NaH is a strong base and will extract hydrogen from a compound. In this compound, Na will be…

Q: H+ SOCI2 NH3 CH3 ?

A:

Q: Which of these reactions are likely to produce both elimination and substitutionproducts?(a)…

A: In order to predict elimination and substitution reaction products we will use saytzeff rules. Since…

Q: Provide the mechanism for the 4th and final reaction in this synthesis: КОН/D20 D FHN- OH

A: Answer

Q: Provide the mechanism for the 4th and final reaction in this synthesis: KMNO4/H+ НО OH

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Q: 5,0<o H20 + NHtz

A:

Q: a) CH;CH,0 CH3CH2CH, b) Br NH2 c) Br d) + CH3

A: Note: Ether functional group is produced for parts a and parts b.

Q: Which of these reactions are likely to produce both elimination and substitutionproducts?…

A: Given reaction,         3-bromo-3-methylpentane + NaOMe (Me = methyl, CH3)

Q: Propose a mechanism for the following observed reaction. Be sure to intermediates. H20 HOCH,CH;OH, +

A: We have to predict the mechanism for given reaction.

Q: Provide a detailed step-by-step mechanisms for the reaction shown. CH;CH2SH + Br, + NaOH

A:

Q: Provide a reasonable mechanism for the following reaction. + NH xs. MeBr 样 Br

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Q: HO-CH3 Br + Na :0-CH3 al. O.. + Na 0-CH3 CH;OH + CH;OH + NaCI + a2. CI + Na :CEN bl. :CEN + HCN +…

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Q: HCIO4 Br2 MECO2H Br

A:

Q: Complete the multi-step synthesis below by filling in the missing reagents in boxes below. Write…

A: In this multistep synthesis, there is one step where , there is inversion in stereochemistry.  This…

Q: 6. Complete the following reactions: 1. NaNH3 (CH,),CHCH,CH,C#CH 2. D,0 a. Lindlar's Catalyst H2 1.…

A: The answer is given as follows

Q: Complete the following syntheses by providing the reagents and conditions at the reaction arrows.…

A: 1.  Friedl craft's alkylation : alkylation of benzene, -Br group is ortho/para directing group…

Q: 2 Propose a mechanism to account for the formation of this product. он H2SO4,Heat

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Q: Write a detailed mechanism for this transformation. OH HCI НО НО H2O -OH

A:

Q: HO NH2 H3O+ HO NH HO Но

A: 4-(2-aminoethyl)bnzene-1,2 diol reacts with acetaldehyde in the presence of acid, it results in the…

Q: HO. CH2-NEN: + N2 (CH, =R=R)

A:

Q: Provide the mechanism for the 5th and final reaction in this synthesis: OH KMAO4

A: This is an oxidation reaction.  Here secondary alcohol is converyed into ketone using potassium…

Q: Br (1 eq.) Br 1. NaOEt, E1OH 2. NaOH, H20 3. H*, heat

A: Given is multistage synthesis reaction.

Q: NaOH (аc) Ph NaOH (ac) Ph O Na CHI3 1. Ph 12 H20

A: The reaction taking place is given as,

Q: 2. Propose a mechanism to account for the formation of this product. HO, H2SO4,Heat

A: When cyclopentylmethanol undergoes dehydration Reaction in presence of heat and sulfuric acid then…

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: 2. Provide a detailed mechanism for the following reaction: NaOH + NH3 `NH, H20

A: When NH2 group react with H form a good leaving group NH3

Q: Supply the missing reagents, intermediates, and final product in the following synthesis. OH A 1. B…

A: The above given series of the reactions includes various type of reagents which reacts with the…

Q: NEN N. +] の☆

A:

Q: OEt 1. NaOEt 2. H3O*

A: The given reaction is,

Q: Select an alkyl halide and a nucleophile that will give each of the following products: b.…

A: Alkyl halide and nuclophiles are given below for the given products.

Q: sayura OH H + CH ₂ OH ? ?

A: Esterification - it is the process in which carboxylic acid react with alcohol in the presence of…

Q: H;O*

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

Q: CH3 H3C ´CH3 H H Mechanism:

A: The reaction given is,

Q: 6) Which of the following steps would successfully complete the following reaction? OCH3 но. Br2, 2)…

A:

Q: Which structure is a reasonable intermediate for this reaction? (HA = generic acid) 1) CH3MGB…

A: The above reaction is the addition of grignard group to the ester. In the Reaction RMgX is used as…

Q: NGOH/H,O 4

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

Q: 5. Complete the multi-step synthesis below by filling in the missing reagents in boxes (a) through…

A:

Q: Propose a mechanism that accounts for the formation of the product.

A: The required mechanism for the formation of product is

Q: Which solvent will allow this reaction to occur the most rapidly? NaCN "Br CN DMSO acetone/water…

A: The perfect solven for this subsitution reaction would be DMSO  * DMSO is polar aprotic solvent(THAT…

Q: 3. Show a plausible mechanism for the reaction below. , CH NH2 EIOH, cat. HCI H,C- -CH, CH "NH2

A: The plausible mechanism for a given reaction has to be drawn.

Q: 5. Please write out the mechanism for the following reaction (Note: SN1) CH3OH CH3 Br OCH3

A: Here in this reaction we can see that the nucleophile is not naked nucleophile , so the reaction…

Q: 1. Excess LIAIH4 MeO НО 2. H2о

A: Given reaction: We have to write the mechanism of the reaction.