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 products of attached elimination reaction.

A: Given,

Q: OH Ketone + Grignard reagent b. Different ketone and different Grignard reagent.

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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…

Q: please explain how aldol condensation reaction work please

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Q: Draw the major product of this reaction. Ignore inorganic byproducts. 1. NaBH4 2. H3O+ Drawing Q 4

A: From given question there is need to determine product when ketone react with NaBH4

Q: Draw the product of the reaction of cyclohexanecarboxylic acid with first thionyl chloride and then…

A: This question based on find out products will formed by using different reagent

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

A: The carbonyl group consists of a carbon atom double-bonded to an oxygen atom, with the oxygen atom…

Q: raw a complete mechanism using curved arrows for the Br HBr

A: In this reaction carbocation form as a intermediate.

Q: Draw the major product of this reaction. Ignore inorganic byproducts and the alcohol side product.…

A: This is an example of basic hydrolysis of ester

Q: 1. NaOEt 2. CH3CH2CH;CO,Et 3. NaOEt 4. CgH5CH2Br

A: A base in an organic reaction is involved in abstracting a proton. An acid in an organic reaction is…

Q: 2. Draw a stepwise mechanism for the following reaction. Use curved arrows to show electron flow.…

A: Deprotonation of Acetals:

Q: 1. Brz, hy 2. 1 equivalent of NaOEt 3. Br2 / CH,Cl,

A: The first step of the reaction is the free-radical bromination of the given alkane. The bromination…

Q: Br D KOCH3 DMF (solvent)

A: In the given reaction a polar aprotic solvent DMF is used, hence this reaction proceeds through SN2…

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

A: The reaction of unsaturated primary alcohol gives a carboxylic acid product and the alkene group…

Q: Draw the product of the following reaction sequence. 1. HBr 2. NaOMe ?

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

A: The mechanism  is given below

Q: Circle all molecules that contain acetals.

A:

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: An aldehyde commonly exhibits a nucleophilic addition type of reaction. When a nucleophile attacks a…

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

A: Information about the question

Q: Classify each solvent as protic or aprotic. a. HOCH,CH2OH b. CH3CH,OCH,CH3 c. CH,COOCH,CH3

A: A solvent plays the role of a medium in which the reaction will take place to give the products. The…

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.

Q: raw the major product of the Claisen condensation reaction between two molecules of this ester.…

A: Claisen condensation: The reaction between two esters or one ester and another carbonyl compound…

Q: Ignore any inorganic byproducts. CI NaOH heat €

A: The rate of E2 elimination reaction depends upon the concentration of both alkyl halide and base. E2…

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…

Q: 2. Which compound would work out to form a Grignard reagent. Circle the portion of the molecule that…

A: The question is based on the concept of organic reactions.   we have to identify the compound in…

Q: .N.

A:

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

A: In organic chemistry, inter conversion of organic molecule takes place from one form to another form…

Q: An activator molecule like DCC is important to create a good leaving group from a -COOH functional…

A: DCC is named as dicyclohexylcarbodiimide. It is used as a coupling agent in most of the organic…

Q: Finish the synthesis by listing out the reagents/solvents used and draw intermediate structures. You…

A: Here we have to synthesize 4-ethylcyclohexanone from given starting material.

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

A: Approach to solving the question: Detailed explanation: Examples: Key references:

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.