QUESTION 8 CH3 HBr CH3C-0-CH2CH2CH3 ČH3 Cleavage of this ether involves OI. E1 mechanism O II. E2 mechanism O II. SN1 mechnism OIV.SN2 mechanism

Q: ch of the following reactions is classified as a Williamson ether synthesis? A) B) C) D) E) OA OC OD…

A: Introduction Williamson The SN2 reaction between an alkoxide ion and a primary alkyl halide is…

Q: Rank the relative rates of the alkyl halides in an SN1 reaction. H3C-1 CH3 CH3 CH₂ H₂C Fastest SN 1…

A: SN1 reaction means unimolecular nucleophilic substitution reaction.  The reaction proceeds in two…

Q: 1. Draw the mechanism for the following reactions. -CH3 Br₂, Nal a. b. c. H3C H3C CH3 CH3 CH₂ H. H_O…

A: Alkenes undergo addition reaction when treated with bromine , H+/H2O and HcL reagents.  “Since you…

Q: fallowing What are theproducts reactions. Draw mechanis.m. and specify their stereachemistry- fthe…

A: since you have posted multiple questions in a single session, we are entitiled to answer only first…

Q: Which compound shows the highest rate of reaction when shaken vigorously with ethanolic silver…

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Q: 50. Which illustration accurately shows the curved arrow mechanism for the initial step in the…

A: The electron pushing arrows are to represent or indicate the electron flow from one atom to another…

Q: d. КОН (аq) heat cis-jasmor (a perfum

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Q: CH3 HBr CH3C-0-CH2CH2CH3 ČH3 Cleavage of this ether involves O I. E1 mechanism II. E2 mechanism III.…

A: Cleavage of C-O bond in ether is predicted by the stability of carbocation. Using this we will…

Q: Draw a stepwise mechanism for the following reaction: HO H,SO,

A: protonation of alcoholic group loss of leaving group carbocation rearrangement  deprotonation…

Q: a, HC- b. H3C в CH3 ОН CH₂CH₂OH Н+ CH₂CH₂OH Н+

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Q: Select two reagents that will synthesize the following ether using Williamson ether synthe O a. None…

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Q: 8. Identify the reagents needed to carry out the following conversion. 0 ? HC=CCH₂CH₂CH3 A.…

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Q: Draw the major product formed when the compound shown below is mononitrated. CH3CH2 0 OCH₂CH3 Fill…

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Q: Which is the major product of the following multistep synthesis? A. X 1.NaBH4 2. H₂O НО SOCI₂…

A: This is multistep synthesis. Find out final product of the reaction

Q: Which sequence of reagents would give the NO2 HO 1. Propene/O2 2. AICI3/CH3CI . 3. HNO3/H2SO4 1.…

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Q: Rank the following molecules in order of increasing relative rate of SN1 Solvolysis with methanol…

A: The concept of the question is taken from general Organic chemistry.  According to question. 1) Rate…

Q: O SN2 mechanism

A: Cl nucleophile is substituted with OH nucleophile.  So, it is substitution reaction.  And reaction…

Q: 8. Draw a plausible mechanism for each of the following transformations: -OH for conc. H₂SO4 heat a.…

A: Short explanation : Conc. sulfuric acid is donate its proton to alcohol and formation of…

Q: 1. 1 eq NANH2. 1. BH3/THF 2. HOT, H20, H2Oz H2C= CH2 + Brz 2 eaNaNH2 CH2Clz 2. CH3 Br 2-3

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Q: i need to predict the product wothout ghe mechanism for the following 2 reactions OCH 3 0001. 3 2.…

A: There are two reactions: 1. Reductive amination 2. Amide formation

Q: HOCH3 a b A NaSCH3 Br DMSO КОН d. ELOH CI H2SO4 e ELOH HCI f Br2 g КОН h EEOH CH3

A: These are Organic chemistry reactions.

Q: Which of the following reactions is classified as a Williamson ether synthesis? O Nat 1. MCPBA 2.…

A: Product of following reaction can be made by applying appropriate reaction mechanism.

Q: Devise a 5-step synthesis of the racemic mixture shown using the reagents available. 1. reagent 1 2.…

A: Given that : We have to predict the best reagents for the following synthesis :

Q: Propose a mechanism for the following reactions. There may be more than one produc dentify whether…

A: following reaction can be Substituion elemination addition as per reaction mechanism.

Q: What reagents would be needed to produce the product shown as the major product? ОН Br A) 1. H2SO4 /…

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Q: What is the correct mechanism and product for the following reaction? HBr A. H Br C. OA COB. O C.…

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Q: Draw the major product of this reaction. Ignore stereochemistry. Ignore inorganic byproducts. 1. Li…

A: Lithium organocuprates, R2CuLi is known as Gilman reagent.  Gilman reagent is very selective for…

Q: 1. Draw a reasonable mechanism for each of the following reactions. H.g-H 1) H 2) H;O, OH "NH, Na*…

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

Q: 8. To draw the structure of major product and relevant arrow-pushed stepwise mechanism: CH3 O | ||…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Br NaSH DMF

A: In SN2 reaction, we get the inversion form as a product because reaction completes in one step.

Q: Explain the reaction mechanism in the picture attached

A: A question based on ether that is to be accomplished.

Q: H3C. H3C A CH3 4-0: H H3C. H3C на о HỌC ĐH B CH3 CH3 H3C. H₂C CH3 H3C. H3C :0: 0: I Н

A: Given is a mechanism of a reaction.To find the product of the reaction.

Q: What is the predominant mechanism by which this reaction occurs?

A: In an E1 reaction, the first step is formation of a less stable carbocation, followed by…

Q: O A. No reaction O B. SN2 O C. E2 O D. SN1/E1

A: When NaNHCH2CH3 and 1-iodo-2,4-dimethylpentane are combined in a flask, the following mechanism…

Q: Determine whether each of these reactions occur through an SN 1, SN2, E1, or E2 mechanism. A. B. Br…

A: SN1 Reaction: It is a nucleophilic substitution reaction in which the rate determining step depends…

Q: Which compound will undergo solvolysis most rapidly?     A. t-hexyl-I   B. t-hexyl-OSO2CH3…

A: Given   Which compound will undergo solvolysis most rapidly?     A. t-hexyl-I   B.…

Q: 13-25 Draw the structures for A and B. 1) Hg(OAC)₂, H₂0 A 2) NaBH₂ B

A: Alkene reacts with mercuric acetate to form cyclic mercurium ion intermediate which on reduction…

Q: The resonance stabilized carbocation formed in step one has two electrophilic centers draw. The…

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Q: What is the major product of this reaction sequence? CH3-C=C-H Select one: O A. OB. O C. NaNH, -I…

A: Terminal alkyne react with strong base (NaNH2) formed Acetylide.   Acetylide is conjugate base of…

Q: 6. Determine whether the following reactions are SN1 or SN2. Draw the mechanism and the products…

A: As you have asked submultiple type questions more than three. Therefore according to the bartleby Q…

Q: Which nucllophile to favor conjugate addi an alpha, bela-unsat 3. 2. O CH3 CHz)3 mg Br CH,Li LIATHY…

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Q: a) 1. PhCH₂Li 2. H₂O Ⓒ

A: In this question we have to tell the product of the reaction and also mechanism.

Q: 8. Which option would work better to synthesize the given ether using a Williamson ether synthesis?…

A: In Williamson ether synthesis, the alcohol first reacts with the NaH to produce alkoxide. And in the…

Q: d. ... x Br KOt-Bu 50°C CH3NH₂ undergoing E2 undergoing SN2

A: Note: It is specifically mentioned to solve c and d only. Tertiary alkyl halides undergo SN1 and E1…