Which of the following reaction schemes would make the alcohol hown below? Select any that apply. OH 0 0 & H + CH3MgBr CH3MgBr MgBr HMgBr 2) H₂0¹ 2) H30¹ 2) H30* 2) H30*

Q: Draw the product of attached reaction ?

A: When R-SH reacts with bromine, it gets oxidized to disulfide. The hydrogen atoms from both the thiol…

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Q: explain why carbonyl compounds are so attractive to both nucleophiles and electrophiles

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A: Deprotonation of Acetals:

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Q: 8) What reagent can be used to do the following reaction? a) KMnO/NaOH/H₂O b) Na2Cr₂O/H₂SO//H₂O c)…

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Q: Step 2 Step 3 OH NO2 NO2 NH2 2 3 4

A: The mechanism  is given below

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Q: Draw a stepwise, detailed mechanism for the following reaction. Use curved arrows to show the…

A: Br acts as leaving group and CH3CH2OH as nucleophile, which results into formation of nucleophilic…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. O 1. NaOEt, room temperature…

A: Information about the question

Q: Choose all correct statements. 1. Gilman reagents react with alkyl halides, including vinyl and aryl…

A: Gilman reagents take part in  coupling reactions with organochlorides. where alkyl halides,…

Q: Please complete the following synthesis. 1. Li Gilman Ragent ? 2. Cul

A: Given is reaction of alkyl bromide with Gilman reagent.

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Q: Ignore any inorganic byproducts. CI NaOH heat €

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Q: Draw the major product of this reaction. Ignore inorganic byproducts. 1. Hg(OAc)2, H20 2. NaBH4,…

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Q: Circle the compound(s) that can be prepared from the reaction of a Grignard reagent and an ester? #

A: Grignared reagent is the source of carbanion used to produce a new C-C bond.

Q: Drag and drop the reagents into the right places. CI Cl2 CI- hv HNO3 H2SO4 FeCl3

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Q: Please correct answer and don't use hand rating

A: Hell-Volhard-Zelinsky Reaction :This reaction is employed for the bromination of the alpha position…

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Q: .N.

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Q: Hello can someone tell me if this will work for this reagent please help

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Q: Draw the Michael adduct and the final product of the Robinson annulation reaction. Ignore inorganic…

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Q: Draw both combinations of alkoxide and alkyl iodide that are commonly used to try and form the…

A: Given reaction conditions are of Williamson ether synthesis where alkyl halide reacts with alkoxide…

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.