Please don't provide handritten solution...    Mechanism of the reaction below

Q: Amines A. Predict the major product: CH3 Sn, HCI 1. O2N КОН `NO2 + H. 2. 0 °C phenol .NH, + HONO 3.…

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Q: Give a clear handwritten answer with explanation...give the mechanism of all sub parts  reactions…

A: 1) SN2 mechanism: Concerted mechanism with inversion of configuration 2) E2 mechanism: Concerted…

Q: 16.69 Use the reactions in this chapter along with those learned in Chapters 11 and 12 to synthesize…

A: Answer: The question is based on the concept of organic reactions.   We have to convert the reactant…

Q: a) propose an outline of a possible mechanism for the conversion of a to b. provide illustrations as…

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Q: a. b. CH3CH2 OCH3 + H₂O or Cl + H₂O HCI d. CH3CH₂ HCI `NHCH,CH3 + H,O A CH3 + H₂O

A: Note: As per our guidelines, we are supposed to answer only three subparts when multiple subparts…

Q: For the reaction below, provide a mechanism for the formation of intermediate A and product B. Show…

A: Reaction 1 : 6 pi electrocyclization and dis rotation is favored under thermal conditions. Reaction…

Q: Give the appropriate reagents for each of the following synthetic conversions......?

A: Reaction 1 , 2,

Q: 10 mol% Til (NMe2)2(dpma) PhNH, + n-Bu- + t-Bu-NC Ph Bu' tol. 100 °C, 48 h, 77% n-Bu

A: In the given reaction Ti(NMe2)2(dpma) acts as catalyst.

Q: Identify first if it is SN1/SN2 or E,/E, Predict the major substitution product. Identify first…

A: Let us try to understand SN1 vs SN2 and E1 vs E2. Then we can solve the reactions.

Q: Select the major product of the following reactions. 1. equ. NBS/heat/ CCI 2. tert-butoxide -Br గగన…

A: NBS/CCl4/heat performs the allylic bromination of a compound. We can see that only one place is…

Q: O2N Br

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Q: Diels-Alder reaction A E

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Q: CI ***** A Et Et Et B Et C Et Et D

A: ->In E2 elimination reaction antiperiplanar beta hydrogen eliminated and alkene formed.

Q: .give the mechanism of given bleow reaction with explanation

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Q: Give a clear explanation handwritten answer with textual explanation...give the mechanism of given…

A: The given reactant is a tertiary alkyl bromide which is an alkyl halide.  The reagent is KCN and the…

Q: Consider 300 mL of 0.100 M sodium formate (HCOONa, Ka =1.80x10-4 for formic acid, HCOOH) that is…

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Q: Draw the major product of this reaction. Ignore inorganic byproducts. OCH 3 TSOH, H₂O Drawing + OH Q

A: The given reversible reaction is the acid catalysed hydrolysis of ketal. The formation of ketal to…

Q: Predict the major product for the following reaction.

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Q: Br (3)+(3 Br t-BuOK (2 equiv.) t-BuOH, heat

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Q: -NH2 N CI CI A B C Aniline Imine Aminal Stan and Kyle have observed a reaction between the aniline…

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Q: a. H. Br OH Ph Ph "P HO

A: a. (i) Acid catalyzed amide hydrolysis. (ii) Acid FG to alcohol FG using LAH. (iii) Alcohol FG to…

Q: CH3CH₂OH + CH3CH₂ + HO → CH2CHBr + CN- > CH2CHCN + Br CH3CH₂CN + CH3S → CH3CH₂SCH3 + CN™

A: Nucleophilic substitution is faster when the nucleophile is strong and leaving group is good.

Q: H₂O H₂SO HgSO4 What is the structure of compound C? H3C CH A- B H₂C HO CN H₂O - CH3 H₂PO4 с 1. LIAIH…

A: Hydration of terminal alkynes catalysed by Hg2+ leads to ketone formation

Q: 200

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Q: 14. What reagents are needed to synthesize the following alcohols? но, OH (B) (C) (A)

A: Hydration of alkene in presence of acid (H2SO4) produce markovnikov product with possible…

Q: Draw the structure(s) of the major organic product(s) of the following reaction. NH₂ NaNO₂ aqueous…

A: Reactions are given below

Q: 14. 15. 16. 17. 18. 19. 20 21. 1. 2. 3. 4. Br 사 Br + + OH Br + Br Br + peroxyacid HBr NaOEt EtOH…

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Q: One frequently used method for preparing methyl esters is by reaction of carboxylic acids with…

A: Interpretation -  According to given reaction we have to basically explain the mechanism here -  To…

Q: b) Suggest the major product of the following reactions and predict the mechanism of each reaction.…

A: Protonation of alkene/alkyne to produce carbocationAddition of Br- to produce product

Q: a. b. HBr, A Peroxide NBR, A Peroxide

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Q: We have seen that the alpha carbon atom of an enamine can function as a nucleophile in a Michael…

A: The question is based on organic reactions.     we need to identify the product formed and explain…

Q: HO НВг

A: As the alcohol is 3° so for substitution of -OH with -Br, first -OH should be expelled. But as -OH…

Q: HO 1. NaH 2. CH,CH,Br 1. CH,CH,OH/ (CF,CO,),Hg 2. NaBH,

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Q: Draw a mechanism for the following reaction: Br t-Buo

A: The mechanism for the following question is- The tert-butoxide was used to form alkene by the…

Q: CHO CH,CCH, NaOH CH CHCCH=CH• MW 40.01 Dibenzalacetone Acetone Benzaldehyde MW 106.13, bp 178°C den.…

A: This reaction is an example of aldol condensation. Here base abstracts alpha hydrogen from carbonyl…

Q: HN KON HC Her. H0

A: The mechanism of the following is:

Q: Which of the following is the MAJOR product of the following reaction? NaOEt ELOH Br ... (A

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Q: Predict the maior organic product formed when the compound shown below undergoes a reaction with…

A: Alkyl halide gives an elimination reaction by reacting with a strong base. E2 reaction involves 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.