ОН О Он О Me2SO4 K2CO3 HO `OH 2 MeO OMe 3 он о benzaldehyde 3 КОН, МЕОН MeO OMe 1

Q: 2. Draw the complete mechanism, using arrow-pushing, for the reaction of tert-butanol with bromide…

A: Given is organic reaction.This is reaction between tert-butanol and bromide ion.This is substitution…

Q: During electrophilic aromatic substitution, a resonance-stabilized cation intermediate is formed,…

A:

Q: 1) Which of the following sequences this? ОН ? of reagents -OH will accomplish

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: What is the slow (rate-determining) step in any electrophilic aromatic substitution reaction? Please…

A: Please find below a example of the reaction mechanism

Q: 7. Amide Formation Mechanism: Draw the proper FULL electron-pushing mechanism for the reaction below…

A:

Q: HBr "SN1-like" H :0. :Br: H 2° alcohol 3° alkyl bromide

A: Given reaction follows Sn1 mechanism.

Q: She

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Q: Predict the Major Product and draw the Curved Arrow Mechanism for the following elimination…

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Q: 1) Provide a synthesis for the product shown below given the starting material. ? ob OMe

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: After the formation of the enolate anion, the intramolecular nucleophilic addition takes place.

A: Answer shown in attachment provide in explanation box Explanation:

Q: For each reaction, draw the complete, detailed mechanism and the major organic product. (a) (b)…

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Q: Q1. Draw a detailed curved arrow mechanism for the following Friedel-Crafts acylation. 1. OH MeO OMe…

A: This is an example of Friedel-Crafts acylation reaction

Q: Which of the following is a stronger nucleophile in a polar, aprotic solvent? Br

A: A polar aprotic solvent does not have a hydrogen atom that can participate in hydrogen bonding.

Q: DHG (OACameay

A: The above-given reaction is an example of Oxymercuration demarcation reaction:

Q: Draw the product of the reaction where methoxide behaves as a nucleophile. Br H H H H + OCH3

A:

Q: In an unsymmetrical epoxide, the nucleophile attacks at the lesssubstituted carbon atom. Explain…

A: In an unsymmetrical epoxide, the nucleophile attacks at the less substituted carbon atom because of…

Q: draw the mechanism (assuming an SN1pathway) for the reaction of cyclopentyl bromide with the cyanide…

A: We have reaction of the cyclopentyl bromide with the cyanide ion , to give the cyclopentyl cyanide .…

Q: Draw the product(s) of the following reactions. H2 CEC-CH3 Pd/C • Consider E/Z stereochemistry of…

A: When 1-phenylpropyne treated with Lindlar catalyst (Pd/C/H2) then initially 1-phenyl-cis-propene is…

Q: Draw the major product of the aldol addition reaction between two of equivalents of this aldehyde…

A: Given is organic reaction. Given reaction is Aldol reaction. In Aldol reaction aldehyde reacts in…

Q: Show the full curved arrow mechanism for the following reaction, clearly showing how the indicated…

A: Chemical reaction- It consists of reactant (starting material) and products (substances formed in…

Q: Draw a detailed mechanism using curved arrow notation that leads to the formation of the major…

A: Pinacole-pinacolone rearrangement.

Q: 8. For the following reaction draw the flipped chair and draw the elimination product of the…

A: The most stable form of cyclohexane is chair form. This is because in cyclohexane, all carbons are…

Q: From malonic acid synthesize this molecule shown

A:

Q: Sort in increasing order of reaction rate against electrophilic aromatic substitution:…

A: Step 1: Step 2: Step 3: Step 4:

Q: Draw the major product of the following reaction. Use wedged and dashed bonds where appropriate.…

A: Given,The reaction:

Q: 9. Draw mechanism for all the substitution and elimination products for the following reaction.…

A:

Q: он о он trace of acid or base оно 13c atom он

A: We need to draw mechanism using enolization.Enolization is a chemical process where a compound like…

Q: Draw the major product of the alkene reaction shown below. Stereochemistry can be ignored. NBS ROOR…

A: In the above question isopropyl benzene is treated with NBS, RO-OR (peroxide) which lead to the…

Q: In EAS bromination reaction directly on aniline, there will be multiple products including ones in…

A: "Bromination reaction directly on aniline, there will be multiple products including ones in which…

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.