Show the product(s) with the correct stereochemistry, if applicable. а. -CH3 OsO4 Pyridine CH3

Q: ng Teactiolls, give tile maj Show relevant stereochemistry. a) CH3OH 25°C b) HBr c) (E) – 3,4 –…

A: Since you have posted question with multiple subparts as per guidelines we can solve only three per…

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Q: Give the Major product(s) and name the starting compound with stereochemistry: H,0 H,O H,SO, H,SO,…

A: To give major product and name of the starting compound with stereochemistry.

Q: H H. H2SO4 C=C H2O CH;CH, CH2CH3

A: The reaction would proceed through the addition of proton to double bond. Then carbocation is…

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A: It is a type of Reduction reaction in which alkene is reduced to alkane. Here palladium (pd) acts as…

Q: Br2 1. m-CPBA H*, H20 m-CPBA + HCI H2, Pt 5. + 2. 3. 4.

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Q: 1. N3 Br NaOEt, ELOH EtO OEt 2. КОН, Н,О 3. H30*, heat 4. NaOH, H2O NHAC

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Q: 1. BH3, THF C=C-H 7. 2. Н.О, NaOH, Н,0

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Q: 1-ВНСу2, ТHF 2 HаО2, NaOН ОН HO ÓCH3 E LOH

A: We have to carry out the given synthesis. We also give the structures of the reactants, products and…

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A: Solution : In Diels-Alder reaction the stereochemistry of both diene and dienophile is retained.…

Q: 1) Mg 2) CO2 Br 3) H30*

A: Aryl halide on reaction with Mg and CO2 gives carboxylic acid.

Q: An inexperienced student adds a solution of catalytic H2SO4 and water to the alkene shown below,…

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Q: [Review Topics] [References] Draw the predominant product(s) of the following reactions including…

A: Alkynes react with 1 equivalent of HBr to form an bromo substituted alkene.

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A: For the above given reactions. The combination of particular reagent and reactant leads to the…

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Q: Predict the products of each reaction below. Indicate regiochemistry and stereochemistry when…

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Q: 1. Predict the products of the following reactions, showing stereochemistry and regiochemistry where…

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A: Given

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A: Addition of halogen to akyne or alkene is trans addition

Q: (a) NaOEt heat (b) Br heat Br NaCN DMF (d) dil HCI

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Q: CH3 CH3ONA 8. H D. H20 Br 9.

A: The product that form in 8 is shown below.

Q: 3. Predict the major products of each reaction below, with their respective stereochemistry where…

A: All the reactions are shown below.

Q: а. LİAIH4 NaBH CH3CH2OH CH;CH,OH b. NABH4 CH;OH с. H. NaBH4 CH3 CH;OH H;C OCH3

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Q: HgCOAc)z, water O con. Hq SO4 O NBS, 120OR OH NGOH, A 3 cat. Osu, NMO

A: The reactions given are,

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A: Given reaction is cis dihydroxylation reaction.

Q: uu. 3,3-dimethylbutan-2-ol + H:PO4 in water Reaction Type(s) Mechanism(s) CH3 CHy- CH-ċ-CH3 OH CH3…

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Q: i. 3-methyl-1-butene with HBr CH3 H,C=CH-ĆH-CH3 Major Product(s) of i. j. 2-methylbut-1-ene + Br2 in…

A: The major products obtained in each case have been described below.

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A: Kmno4 is strong oxidising agent. Over oxidation takes place.

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Q: Predict the Product of the reaction and indicate regiochemistry and stereochemistry when relevant

A: Cis–trans isomerism (or) geometric isomerism or configurational isomerism: The two similar groups…

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A: Given reactions:

Q: S H3C-CH-CH2-CH3 + NaOH Reaction Type(s) nn. Mechanism(s)

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Q: Br

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Q: Considering both stereochemistry and regiochemistry, which of the following methods is the best way…

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Q: Cl2, FeCla HNO3 H2SO4

A: “Since there are multiple questions and it is not mentioned that which one has to be solved so I am…

Q: КCN Br NaOCH2CH3 Br Br H2O Br NaOCH,CH3 l1!|llווא

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Q: 4. Predict the products of the following reactions, showing both regiochemistry and stereochemistry…

A: When alkenes reacts with Ozone in presences of Zn/ H+ gives carbonyl compounds. alkenes reacts with…

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A: Alkene react with H+, the π bond will be break such as a stable carbonation is formed. The order of…

Q: 1) H3O* 2) NaOEt

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Q: 3) Complete the following chemical equations. Make sure to clearly indicate the stereochemistry in…

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Q: Draw the structure(s) of the product(s) of the reactions below. Be sure to indicate any relevant…

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Q: Predict the major products of the following reactions. Include stereochemistry whereapplicable.(a)…

A: (a) 1-methyl cycloheptene + BH3, THF, then H2O2, OH-(b) trans-4,4-dimethylpent-2-ene + BH3, THF,…

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A: Welcome to bartleby ! As per company norms we cannot answer more than one question per session .So,…

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.