1. Predict the major product 2. Use curved arrow to show the mechanism step by step for the follow catalyzed hydrolysis of ester. 0 18-CH3 H D₂O +

Q: EX→DUU Step 1: Nucleophilic addition of hydroxide ion to the ester carbonyl group A INFRARR H3C.…

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Q: НО, Me N OH NH2 НО, Me `N ОН ОН

A: To propose a synthetic route for the given target molecule from the given starting material

Q: A common ketone starting material is shown below. Predict the major product for each reaction based…

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Q: mark mechnism of catalysis

A: Solution: The given figures is the active sites of the metal-amino acids catalysis.

Q: Draw the structure of the product that would result from successful nucleophilic attack of methyl…

A: It is given that an alkyl halide is present which is undergoing a nucleophilic attack, a nucleophile…

Q: Which reaction will not give the indicated product? 1. CH, CHO 2. H₂O OH O CH₂CH₂OH, H* N H OH…

A: Check the options by the mechanism process.

Q: In the presence of an acid catalyst, acetaldehyde forms a trimer known as paraldehyde. Because it…

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Q: Draw and identify the corresponding product for the following base-acid reaction. H2SO4 + H20 H…

A: When we add water to sulphuric acid, it breaks up into it's cations and anions, resulting in H+ ion…

Q: Identify one substrate and one reagent that could be combined to make the completed produc

A: Imines are produced from the condensation between amines and carbonyl compounds and reduction of…

Q: raw the major product of this reaction. Ignore inorganic byproducts and the carboxylic acid side…

A: Given is organic reaction. The reactant is acid anhydride. Reagent Gilman reagent.

Q: Draw a mechanism for the following acid catalysed hydrolysis reaction. Explain verbally within your…

A: In the first step, acid-base reaction between water and substrate to give protonated ether, which…

Q: Which set of reagents will turn acetic acid into 2-bromoacetic acid? O Br2/NAOH/ETOH O…

A: The given conversion can take place with the help of HVZ Reaction to form a alpha-halo carboxylic…

Q: Reaction of phenol with acetone in the presence of an acid catalyst gives a compound known as…

A: Acetone has a carbonyl group in it, which can act both as a nucleophile as well as an electrophile.…

Q: Ketones are converted to enolates on treatment with base. Draw the structures of the enolates formed…

A: Enolate: This organic compound are formed by action of base on carbonyl group, in which base remove…

Q: The carboxylic acid G can be converted into the lactone H. Give a reagent for the above reaction.

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Q: Ph OH OH OH Ph OH OH

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

Q: 4.Consider the following reaction. Draw arrow pushing mechanisms for each of the following steps in…

A: GIVEN

Q: An unsaturated ketone is converted to the 3-cyano derivative shown below. Which reagent could be…

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Q: Which sequence of steps will give the highest yield of a carboxylic ester product? Mix 0.1 mole of…

A: Esterification is based on nucleophilic addition followed by substitution.

Q: 15. Show the mechanism for the acid catalyzed hydration of acetophenone. ( H. 0-H ОН HO. CH3 CH3

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Q: The product in this reaction is basic enough to be protonated by a dilute HCl solution. Draw the…

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Q: Draw the expected product from the following reaction.

A: Final answer is given in explanation please see from there.Explanation:Approach to solving the…

Q: 5. Propose a mechanism to explain the given byproduct. H,(OSI/AI), андан OH CH₂ CH3

A: The given reaction scheme is shown below.We have to give the mechanism of the above reaction.

Q: H,0 H,CrO, CH,NH. H+ NABH,CN он но -H- NABH но -OH HO, CH,OH H,C. HO, Br Br H,CO NaBH, H+ agua CH,OH…

A: H2CrO4 oxidizes secondary alcohol to ketone Ketone undergoes reductive amination with amine in the…

Q: 9. Complete the following acetal hydrolysis reactions. Draw the structures of the products. Name the…

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Q: Нас- H₂ 1) МСРВА 2) HC1 CH₂ H3C H2 HU С. C

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

Q: 14. Indicate an alkyl halide with an appropriate choice of leaving group and the nucleophile that…

A: Given that, the reaction is:

Q: 3A Complete the reactions below. H₂SO4/H₂O HgSO4 A NaBH4 EtOH B лH₂SO4 A C

A: Kucherov's reaction involves the addition of water to alkyne to form carbonyl compound.

Q: Show reaekson and don't use hend raiting and step by step solutions please

A: Step 1:Nucleophilic Substitution (S(_N)2 Reaction):Identify the electrophilic carbon (the one…

Q: Ph cat. H,SO4 H2O heat Ill.

A: Hydrolysis of acetals is a reverse reaction of acetal formation. In the presence of aqueous acid…

Q: Provide the reagents necessary to complete the following reactions. More than one step may be…

A: In this question, we have to synthesized the product from given reactant by using necessary…

Q: 8. Draw the structures of the conjugate acid and base for the following reaction. Provide the…

A: pKa is inversely proportional to acidity.  So lesser pka, stringer the acid is.

Q: a) Using your knowledge of organic reaction mechanisms, explain the formation of EACH product (A,B)…

A: a). The two products A and B result from the different mechanisms.

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…

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Q: Which is the major product from the acid catalyzed hydrolysis of cyclohexene oxide? но OH но он ||…

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Q: Complete the following reaction and write the IUPAC names of the two products. H20 + NaOH HÖNHCH2CH3…

A: The answer to the following question is-

Q: Complete the following nucleophilic substitution reactions. In each reaction, show all electron…

A: In a chemical reaction; the substance which involves in conversion is said to be reactant whereas…

Q: esize this compound by the > t-butyl ethyl ether Show the steps necessary to synthesize this…

A: Alkyl halide react with mg to form grignard reagent then react methanal to form primary alcohol

Q: acetone 1. NaOH 2. enol ester Identify the reagent (2) and draw the mechanism of reaction.

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Q: H3C NH₂ H3C Amides can be hydrolyzed to yield carboxylic acids. The conditions are much more severe…

A: In an acidic medium, amide interacts with the water molecule to give a carboxylic acid and the salt…

Q: CH3OH Br-Br H3CO The mechanism proceeds through a first cationic intermediate, intermediate 1.…

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Q: HE OCH, H,C The most reactive compound(s) towards nucleophilic acyl substitution reactions? H.C OH…

A: The compounds given are,

Q: Acyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a…

A: H2NCH2CH2OH have two nucleophilic centers. One is N center and another is O center. N is less…

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.