15. Which of the compounds shown are possible products of the following reaction? 1) Hg(OAc)2, CH,OH 2) NABH, ÓCH3 OCH; OCH3 II II III only I, II and III II only I and III only А. В. С. D.

Q: What are the structures of the products in each step of the reaction sequence shown? H3O* РСС A B…

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Q: ILe H;CCO H;CO H2O I II III IV

A: Nucleophilicity  is the tendency of Nucleophile to donate electrons. Nucleophilicity is directly…

Q: Predict product: SO H A fuming H₂SO4, HgSO4 230 °C B SO₂H SO₂H D SO₂H

A: This Reaction of Pyridine is Electrophilic Substitution Reaction. In this Reaction we have to see…

Q: Describe the hazards of (i) trioxygen: () hydroxide ion; (ii) hydrogen sulfide. Explain why an…

A: Reducing agent reduced the various functional groups like alkene to alkane, aldehyde to alcohol,…

Q: What is the expected product of the reaction below? O NH₂ O NH₂ O None of these O H₂N. O NH₂ O NH3…

A: Correct Answer is -None of these. Mechanism can be shown below -

Q: Rank the reactivity towards SN1 reactions for the following compounds: 12) 1= fastest; 5 = slowest…

A: SN1 reactions are a type of nucleophilic substitution reaction mechanism. In a SN1 ( Substitution…

Q: 17. Provide all four products for steps i-iv. i. NaH, DMF ii. CH3CH₂Br iii. NaOH, H₂O iv. H₂O*, heat…

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Q: 2) Predict the major products A- K for each of the following reactions NaBH4 PBr3 Mg 1). H. Na,Cr207…

A: Major products are given below

Q: Predict the product of the following reaction. 1. CH3I(x's)/Ag20,heat 2.KMN04, cold, neutral NH2 HO…

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Q: ) Propose a mechanism for the substitution reaction in Step 2.

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Q: OH NazCr207 H2SO4, H20 H. OH II II HO. IV V

A: Here we are required to predict the product of the reaction

Q: 1)Predict reaction products for the reaction:[Cp2W(n3-C3H5)](2BF4) + 2 Meli → 2)Write the reactions…

A: Hello. Since your question has multiple parts, we will solve first question for you. If you want…

Q: What is the predicted product of the reaction shown? NH3 O,N- O2N- -NH2 II O2N- CI O2N NH2 IV O2N-…

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Q: Arrange the following compounds in increasing reactivity towards E*. CI Select one: O a. O b. O c.…

A: Benzene under go aromatic electrophilic substitution reactions. Positively charged species is called…

Q: 6. Predict the products of the following reactions and in each case determine which product will…

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Q: MC02 How many of the compounds shown are not expected to be converted into Grignard reagent on…

A: How many of the compounds shown are not expected to be converted into Grignard reagent on reaction…

Q: (b) Predict the product(s) of the following reaction with plausible mechanisms : SiMe3 H2SO4 (i) →?…

A:

Q: the product expected for the reaction wn. 1) N₂OEt 2) 4CH₂Br H₂ C EtO₂C CO₂Et EtO₂C. CO₂Et CH₂ H₂…

A: Organic reactions are those in which organic reactant react to form organic products.

Q: Predict the major products of each of the following reactions. (a) (b) CI CI Br. (CH),COK NaBr ?…

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Q: . Provide the major organic product of the reaction below: Brz hv Br Br Br None A. 36. What is the…

A: I sloved first three. Remaining repost

Q: An organic chemist reacts (S)-2-butanol with PBr3 in pyridine, removes the major organic product,…

A: The above reaction is proceed by SN2 mechanism in which attack of -OCH3  is done in back side of OH.…

Q: Given the nature of electrocyclic reactions, which of the pi MOs shown below is involved in the…

A: During the electrocyclic reaction HOMOis involved in the reaction

Q: What would be the MAJOR product(s) of the following reaction? ... ELOH RT OEt Eto I. II. III. IV.…

A: Substitution nucleophilic unimolecular (SN1) is favoured by the formation of a tertiary carbocation.…

Q: SO II OI CONV O III 3 OV For the reaction shown, select the expected major organic product. Na/NH3…

A: Which one of the following is correct

Q: IV %3D a. d. II b. e. II c. IV

A: ->CH3SH is hard nucleophile hence it give addition at the hard center. -> I think there is…

Q: What would be the MAJOR product(s) of the following reaction? Br ELOH RT EtO II. III. IV. A Il only…

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Q: Identify the final product for the following reaction. H2O, H2SO, ? H9SO, OH II IV V.

A: The reaction will be as :-

Q: Explain, please 3.) Predict the products of the following. (17.41) (a) 1. LIAIH, 2. D20 ct (b) 1.…

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Q: What is the expected major product for the reaction below? EGMU 2020737654 t-BUOK Br ? t-BUOH 4.…

A: This reaction is an elimination reaction . H and Br should be anti to each other. As it is a anti…

Q: Predict the product of reaction shown. fuming H,SO, SO,H so, он IV O II

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Q: What is the most likely product of the following reaction? он H;PO, H2PO3 II II IV O a. I O b. II O…

A: Correct answer is (c) III.

Q: Predict the major product of the reaction shown. Hg2*, H2SO4, H2O а. O b. OH Ос. O d.

A: Hydration of alkyne: Alkyne gives hydration reactions in presence of an H2SO4 and HgSO4 catalyst. In…

Q: Account for the following relative rates of solvolysis under experimental conditions favoring S,1…

A: Concept introduction: SN1 reaction: The displacement of atom or group by nucleophilic is known as…

Q: 6. Given the reactions below, provide the missing products and explain the differences among the…

A: LiAlH4 (Lithium aluminium hydride) is a strong reducing agent.  It reduces almost all functional…

Q: The structures of alkenes can affect their reactivity in the reaction with H-Br. H;C H H;C H H H `H…

A: Given : We have tell the ease of alkene to accept a proton from HBr.

Q: Which of the following reagent/s will efficiently convert isopropylbenzene to 2- and…

A: Benzene is an aromatic compound and gives the different type of substitution reaction. These…

Q: 31. Predict the major product for the following reaction. 1. NaOHBr, 2, H,0 Bro IV II A) I B) II…

A: In any carbonyl carbon, carbon is electron deficient because it is directly bonded to oxygen atom…

Q: Match the reactions with their products below. Кон (аq) 1. a.) OCH3 b.) Ph3P: MnO2 c.) OH OCH3 3. 2.

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Q: 9) Predict the reactants for the ff products: SH (a) CH3OCH2CH2CH3 (b) „OCH3 (c) (d) CH3…

A: the reactants are as follows:

Q: HzS 04 + 2 NH4 Br >2 Br t INH4)2 S04 + 2 HzO 2 AOH +

A: Here , side reaction is E1- Elimination this reaction occurs in two steps . But-2-ene is the side…

Q: Consider the reaction below of isoquinoline. Which is the expected product? HNO3/H2SO4 NO2 NO2 O2N.…

A: Nitration is a process in which a nitro group is attached to an organic compound.

Q: 1. BH3 2. H2O2, OH H20 1. Hg(OAc)2, H2O 2. NaBH4 1. OsO4 2. NaHSO3, H20 HD d) HO CI DMF CH OH e)…

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Q: 1. What organic product would you expect from the reaction of compounds with excess ethylmagnesium…

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Q: 9. H3C-C -CI + NaBr

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Q: For the reaction given below, predict which product will be the major one and by what mechanism it…

A: In given reaction -  Sovlent used is DMF which is aprotic and non polar.  In reactant —OTs is very…

Q: Give the product of following reaction from the image 1. H2 Pt 2. Br2, H2O 3. a. O3 b. DMS 4. a.…

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Q: Provide the expected major organic product of the reaction sequence shown. 03 - IV and V O V only II…

A: This reaction is known as reductive ozonolysis. Let us discuss its mechanism to find out the answer.…

Q: Give the molecular structures of reagent or products for the following chemical reactions: (i)…

A: We have to predict the molecular structures of reagent or products for the the following given…

Q: Identify the most Hkely: 1 HCI 1. Kinetic Product. 2. Thermodynarnic Product. 3. Remembering the…

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Q: Predict the (major) product(s) of the reactions given below: (i) HSCH;CH,SH (1) TiCl, Mg-Hg (i)…

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Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.