2. Draw a detailed mechanism for the following reaction and give the structure of the product. NH2 CAH&N20

Q: H3C CI -*NEN ? H3C A H2O в H3PO2 C H3PO4 D H₂SO4

A: The reaction of hypophosphorous acid is treated with diazonium salts is a type of reaction in which…

Q: 1. Provide a detailed mechanism for the following reaction and show the structure of the final…

A: Thank you.

Q: H2Cro4 FHO- H2 / Pd

A:

Q: Answers to Question: How would you prepare the target product from benzene? It takes more than two…

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

Q: Fill in the missing intermediates and reagents in the scheme below 1) BH3 THF 2) NaOH/H2O2 OH H2CrO4

A: The given reagents and conditions suggest two main reactions. The first reaction is a…

Q: What is the major product of electrophilic addition of HBr to the following alkene? Explain your…

A: The given reactant is shown below. The addition of HBr to the given reactant will take place via…

Q: Propose a mechanism that accounts for the formation of the product.

A: The given compound undergoes cycloaddition reaction in presence of HCl with elimination of H2O.

Q: Fill in the missing intermediates and reagents in the scheme below 1) BH3 THF 2) NaOH/H2O2 OH H2CrO4

A:

Q: b) CH3 H₂C NBS Δ -CH₂ AICI3 HO™ Br₂ FeBr 3 H3C AICI 3 CrO. H₂SO

A: NBS is a source of Br radical . OH- acts as a nucleophile then Friedalcraft acylation .…

Q: Complete the following reactions by providing the proper substitution AND the proper elimination…

A:

Q: 8 e (xs.) NaOCH, CH₂OH

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

Q: 1. Provide the MAJOR product only for the following reactions. Make sure to show the correct…

A:

Q: Tertiary alkyl halides will react by E2     under neutral conditions     under acidic conditions…

A: We are to find conditions under which tertiary alkyl halides undergo E2.

Q: What phosphorus ylide and carbonyl compound required to make the following alkene? are

A: Carbonyl compound and phosphorus ylide are required to give alkene and this reaction is known as…

Q: O₂N. Br

A:

Q: 2. Draw the structure of A and B and show the mechanism for the following reaction. Write all the…

A: This is an example of Aldol condensation

Q: 1) Complete the following reactions by drawing in the starting materials, reagents, or products.…

A:

Q: Drawing H3O+ -OH Atoms, Bonds and Rings Charges Draw or tap a new bond to see suggestions. ← Undo Ⓒ…

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Q: What is the major product of this E2 reaction? CH3 он CH:-ÇH-CH-CH-CH; F CH

A: The given Reaction is the elimination Reaction . In this reaction we get the Alkene as the product…

Q: 2. Propose a mechanism to account for the formation of this product. HO, H2SO4,Heat

A: When cyclopentylmethanol undergoes dehydration Reaction in presence of heat and sulfuric acid then…

Q: etanol ОН ácido

A:

Q: Br NH2 NANH2 NaBr

A: The reaction of bromobenzene with sodium amide results in the generation of aniline and sodium…

Q: Please show reaekson and don't use hend raiting

A: The alkyne 2,2-dimethylhex-3-yne undergoes protonation by sulfuric acid.Water adds to the protonated…

Q: Treatment of 1,2-dibromoethane with the dithiolate dianion shown in the reaction below leads to two…

A: 1st product C4H8S2

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: 3. Provide the products or the necessary reagents for the two following transformations. 1. NaNH2 2.…

A: 1) Please find below the reaction

Q: 7. Propose a mechanism for the following transformation. H* `NH2

A: In the mechanism of the above reaction ; 1st step involves the protonation  2nd step : attack on…

Q: Predict the structure of the final product. Draw the structure of each reaction step of the…

A: We have to predict the product of the reaction.

Q: Please provide the major product of the following reaction via an E2 mechanism. ..... Br KO'Bu (one…

A: Alkyl halides give an E2 elimination reaction with a strong base. In the E2 elimination reaction,…

Q: 4. Supply the missing reagents/conditions to make the following transformations. но OTf CN

A: In the first step the OH is basically replaced by OTf. OTf is basically the triflate functional…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Br2 (1 equiv) CH3CO₂H Q

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

Q: Provide the reagents and mechanism for each step of the synthesis.

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Q: Frovide the mechanism fer the following reaction. OH H2 SO4 HeAt CH2 CH3 CH3

A: ->In presence of acid there occur protonation and after removal of H2O carbocation formed then…

Q: H- -CO₂ Intermediate? Final Product?

A:

Q: 5. Provide the products or the necessary reagents for the two following transformations. Br 1. xs…

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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.