Predict the location where a new substituent will be added when this aromatic compound undergoes an electrophilic aromatic substitution reaction. A) I B) II IV C) II D) IV HO

Q: What is the major product generally formed when a tertiary alkyl bromide  (R3Br) reacts with sodium…

A: the solution are as follows:

Q: 2) Draw the structure of the major product that results when the diene shown is treated with HBr at…

A: The question is based on organic reactions. We need to identify the product and explain its…

Q: The lone pairs of which heteroatoms(s) contribute to the aromaticity of the following molecule? N $

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Q: Name each of the following compounds according to IUPAC rules. NO₂ MeO امن OH OH

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Q: The following molecule can be synthesized from an epoxide and alkyllithium reagent, followed by…

A: Alcohols can be prepared from an epoxide by reacting it with an alkyl lithium reagent, followed by…

Q: Write out the complete reactions below showing the structure of all reactants and products. Provide…

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Q: Where does the indicated aromatic system undergo electrophilic substitution? NO2 iv i ii CO2M. ii

A: Aromatic electrophilic substitution occurs at the site where the electron density is maximum.…

Q: Но -OH

A: Ketone react with HCN to give cyanohydrin then further hydrolysis to give alpha hydroxy acid

Q: он OH OH OH п он III OH IV OH

A: H2CrO4 oxidizes: Primary alcohol   ----->  Carboxylic acid Secondary alcohol  ----> Ketone…

Q: aromatic

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Q: i) Give the IUPAC name of this molecule. ii) Outline the mechanism of this reaction. Your mechanism…

A: IUPAC nomenclature of alkenes : Select the longest chain of alkene containing both the carbons of…

Q: Which of the following is aromatic? www www.

A: Aromatic compound which obey 4n+2 rule and it should be cyclic, conjugated and planar.

Q: The isomeric phenols shown below have drastically different boiling points. Explain why. ОН ОН NO,…

A: The boiling point of p-nitrophenol is greater than o-nitrophenol. This is because of strong…

Q: Question 11 What synthetic goal is achieved by subjecting an alkene to treatment with hydrogen…

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Q: Structure of compound A: H CH3

A: To find : several small molecules from the compound and to give the reason for the breakage of bond.…

Q: 1) Provide the IUPAC name of the following molecule. god H 2) Predict the major product. 1. HOC…

A: The question is based on the concept of IUPAC naming of the compounds.We have to write the correct…

Q: Rank the nitrogen-containing aromatic molecules in order of increasing basicity. Least basic HIZ: Br…

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Q: Which of the following conversions is essentially irreversible? A) The reaction of an aldehyde with…

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Q: Which of the following is anti aromatic?

A: The anti aromatic compound has to be identified.

Q: H-

A: IUPAC means International Union of Pure and Applied Chemistry. The nomenclature of compounds is…

Q: Name your compound according to the IUPAC system. Include stereochemistry (E/Z/R/S). H₂C H₂C

A: For IUPAC naming following steps are required->First of all select the largest carbon chain…

Q: 8) Show how the following conversions might be accomplished, including all reagents and…

A: The chemical reaction in which an alkyl magnesium halide reacts with carbonyl compound followed by…

Q: Please don't provide handwritten solution ....

A: The reaction between ethanal (acetaldehyde, (CH3​CHO)) and ethanol ((CH3​CH2​OH)) forms a…

Q: & S 요 OH OCH 3 연 H

A: IUPAC nomiculture depends upon the orientation, functional group as well as carbon skeleton. So…

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Q: O sp² to sp² (the hybridization remains the same) sp to sp² sp² to sp³ O sp³ to sp²

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Q: which of the structures is aromatic, according to Huckle? list the 3 features that make them…

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Q: which is an aromatic ring and why?

A: Highly stable and highly conjugated cyclic compounds that do not give addition reactions and follow…

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.