Which of the following choices describes the most likely product and mechanism of the following reaction conditions? + NaOH Ether OF.22 E2 OH E1 - 52 Tries 0/1 Which of the following choices describes the most likely product and mechanism of the following reaction conditions? H₂O for. o tom. *Kº O E2 Tries 0/1 Which of the following choices describes the most likely product and mechanism of the following reaction conditions? NaOCH, à CH₂OH OCHS, SN² E1 SN1 Tries 0/1

Q: c. Draw the product and reaction mechanism of the following reaction لام HO OH B: E1cB

A: E1CB-: It is called elimination unimolecular conjugate base mechanism. E1CB elimination mostly…

Q: C. CH;OH Is this reaction E1 or E2? elimination product(s) d. NaOH Is this reaction SN1 or SN2?…

A:

Q: OH 87. What product do you expect to obtain from each of the following reactions? OH HCI b. CH₂…

A: The objective of this question is to give the products for the given reactions.

Q: OSO₂CF To NUO CH₂CH₂OH Pamer b) Clº Nu "Triflate" is a good leaving group "Triflate"-oso,CF> Fo…

A: In SN1 reaction polar protic solvent is used.in this reaction polar protic solvent is used so…

Q: What is the expected product for the following reaction sequence? il НО. OH NC ΝΗ H₂N. OH 1) xs…

A: In first step of reaction sequence when amine reacts with anhydride it will produce an amide as a…

Q: 17. picecti O₂N. NH₂ and the expected final product of the following reactions: t. AICI,

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Q: 43. Which mechanistic step does NOT occur in the accepted mechanism of the following reaction? OH…

A: Answer is  C) nucleophilic attack.

Q: H DCC „N. Вос + HO. H2N, OCH3 MECHANISM (Structure of DCC below) N=C=N'

A: When DCC is treated with carboxylic acid and amine it gives amide as final product.

Q: Identify the reagent(s) you could use to accomplish the following transformation. Select all that…

A: We have given the organic reaction and we have to identify the reagents needed to carry out the…

Q: 21

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: erfi C. the tiva Consider the reaction below. OH HCI methanol H3CO 12. Propose the mechanism using…

A: Here we have to write the mechanism of the following given reaction.

Q: Which of the following alkyl bromides reacts the slowest with NaSCH3 in DMF (dimethylformamide)? „Br…

A: ANS. Option a. 1

Q: с. НО, d. НО НО. НО ОН ОН CH₂OH ОН CH₂OH ОН HCI CH3CH₂OH HCI ОН

A: Glucoside formation involves the attachment of a glucose molecule to another compound, resulting in…

Q: What type of electrophile is 1-iodo-2,4-dimethylpentane? O A. Tertiary B. Secondary O C. Methyl O D.…

A: 1. the 1iodo 2,4-dimethylpentane is primary branched electrophile. 2.  the reaction between 1iodo…

Q: What is the mechanism of the following reaction? EN : Nu Nu №₂ A two-step mechanism involving the…

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Q: Select a correct product for E2 elimination reaction of a compound provided below. Ph H Ph H Br Br ?

A:

Q: Please predict the product for each of the following reactions. Make sure to clearly indicate the…

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A:

Q: Draw the major organic product generated in the reaction below. Pay particular attention to regio-…

A: Addition of HCl to unsymmetrical alkene take place according to Markovnikove's rule.  That is attach…

Q: Only typed solution

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Q: What is the product of the following reaction? он он I н. ОН н I ОН ОН I H3COH HCI ???

A: A question based on introduction to organic chemistry that is to be accomplished.

Q: Br CI НО О ОН ОН SCH3 ОН

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Q: 1. Draw the mechanism and predict the major product for each of the following reactions to NH₂ OH…

A:

Q: hat is the likely mechanism of the following action ? CH3CH₂CH₂Br lect one: ) Α. Ε1 OB. SN1 O C. E2…

A: LDA (lithium di isopropyl amide ) work as non nucleophilic base    hence it work as only base

Q: Propose an appropriate intermediate for the following reaction

A: Given that, a reaction scheme is  The mechanism of the above reaction is We have to give an…

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.