Predict the major product when treated with H2/ Pd/c

Q: Draw a stepwise mechanism for the following reaction.

A: This reaction is the hydrolysis of Amide in basic medium. Here, one tetrahedral intermediate is…

Q: Which compound is the major product of the reaction sequence shown? (1) NANH,NH3, -35°C (2) CH3 CH2-…

A: 1) first reaction is acid base reaction.  2) second reaction is SN2 reaction  3) third reaction is…

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

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Q: Draw a stepwise, detailed mechanism for each reaction.

A: Please find below the reaction mechanism for the reaction 1.

Q: What is the curved arrow mechanism of the reaction of p-t-butyl phenol treated with acetic anhydride…

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Q: HNO3 H₂SO4 er nitration reaction, the nitro substituent in the product will be located on carbon…

A: In nitration reaction, the -NO2 substituent is attached to a carbon atom depending upon the ortho,…

Q: Show a reaction scheme on how to prepare the following ether using Williamsonether synthesis. Draw…

A: Answer:- This question is answered by using the simple concept of preparation of ether using the…

Q: Predict the major product in the following reaction. Be sure to draw it with well-defined…

A: Welcome to bartleby ! Introduction :  We have to tell reaction of alkene with mCPBA

Q: What two carbonyl compounds are needed to synthesize of the following compound, using a Robinson…

A: Interpretation: The two carbonyl compounds are needed to synthesize of the following compound, using…

Q: NaOH NaOCH3 Choose. H3CO OCH3 heat

A: The primary carbanion is more reactive then the secondary and tertiary one .

Q: major

A: When the given compound is treated with chlorine, the double bond is broken and the chlorine atoms…

Q: Draw a stepwise, detailed mechanism for the following reaction.

A:

Q: Draw a stepwise mechanism for the following reaction. (Hint: Conjugate addition can occur with…

A: Given reaction is,

Q: Draw a stepwise mechanism showing how two alkylation products are formed in the following reaction.

A: LDA- It is Lithium DiisopropylAmide. It is used to generate enolate anions in alkylation reaction.…

Q: G. Н. I.

A: "Since you have posted a question with multiple sub-parts, we will solve the first thee subparts for…

Q: MCPBA

A: The given reaction is the Baeyer-Villiger reaction where the mCPBA (meta-chloroperoxybenzoic acid)…

Q: Draw a stepwise, detailed mechanism for the following reaction.

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Q: AICI3 CI

A: This is intramolecular F. C. Acylation reaction. They undergoes cyclisation to form cyclic ketone

Q: Draw a stepwise, detailed mechanism for the following reaction.

A: The following reaction proceeds by the formation of the carbocation. The detailed mechanism is as…

Q: A) Propose an efficient synthesis for the following transformation: + en B) Propose an efficient…

A: To propose an efficient synthesis for the following transformation:

Q: CN

A:

Q: Draw a stepwise mechanism for the attached reaction that illustrateshow two substitution products…

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Q: Devise a synthetic strategy to complete the following transformation. H2N

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Q: Draw the product and stepwise mechanism for the following reaction. HCI Low Temperature

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Q: Complete the following multistep synthesis using appropriate reagents. Indicate the major product…

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Q: III IV

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Q: R OR1 -R2 R R-CEN

A:

Q: Draw a stepwise, detailed mechanism for the following reaction.

A: In intramolecular reactions, the reactive sites are present in the same molecule. The simplest…

Q: CH3 -CI OH

A: The given structure is; The name of the above structure is 1-Chloro-1-methyl cyclohexane. Here, -OH…

Q: Devise a stepwise mechanism for the following reaction.

A: Please find below the reaction mechanism

Q: Draw a stepwise mechanism for the following reaction.

A: LiAlH4 ( Lithium Aluminum Hydride) is a powerful reducing agent. This can be used for reducing…

Q: Complete the following synthesis with the missing reagent(s) or major product(s). OH MCPBA OH CN…

A: Here we have to write the reactant, reagent and products-

Q: NaOH N2OCH3 H3CO OCH heat

A: "Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: b) CH,CH,MgBr, ether

A: Given : Reaction of  Acetophenone with ethyl magnesium bromide Product = ?

Q: Draw stepwise mechanisms illustrating how each product is formed.

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Q: Draw a stepwise mechanism for the following reaction.

A: Ketones can be protected with the help of diols or thiols in acidic medium. In the given…

Q: Draw a stepwise mechanism for the following reaction. The four-membered ring in the starting…

A: The four membraned ring in the starting material and product is called as beta-lactum ring. DBN is a…

Q: Draw a stepwise mechanism showing how two alkylation products areformed in the following reaction.

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Q: Draw a stepwise mechanism for the following reaction.

A: The the gien reaction is called Haloform reaction.  presence of a methyl ketone is essential for the…

Q: Draw the products formed when attached compound is treated with HNO3 and H2SO4. State whether the…

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Q: e) + PPh,

A: A question based on alkene formation, which is to be accomplished.

Q: S O NaBH4 OLIAIH4 OBH3, THF OLIAIH(O'Bu) 3 OH

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

Q: What reagents (A-D) are needed to carry out each reaction in the following sequence? A в O2N `SO3H…

A: Reagent is a  compound which is added to a system to cause a chemical reaction, or added to test if…

Q: CI CI HCI (xs)

A:

Q: Predict the major product for each reaction:

A: At first alkene being nucleophilic undergo protonation to give most stable tertiary carbocation.…

Q: Draw the expected major product and the complete reaction mechanism for the following reaction. i.…

A: Ketones are the organic compounds that contain carbonyl group in a compound.

Q: Draw a stepwise, detailed mechanism for the following intramolecular reaction that forms a cyclic…

A: The given reaction is  To find: The stepwise mechanism for the given intramolecular reaction

Q: Draw the major product and explain: Br LDA

A: Elimination reaction with LDA.

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.