c) Draw a mechanism for the formation of EtCH2COOH from the reaction of MeCOCH(Et)COOEt with NaOH in EtOH.

Q: given acetyl chloride, how form you is the + a 요. benzene and AlCl3 can anniline? What Synthesis + 2…

A: We have to carry out the below given synthesis. Introduction: Hofmann rearrangement.

Q: CI CH3OH

A:

Q: Draw the organic product formed in the following reaction. OEt OEt [1] NaOEt [2] CI [3] H₂O+, A NHAC…

A: The given reaction is a multi-step multi-reagent reaction. The first reagent in the reaction is a…

Q: a,B-Unsaturated aldehydes and ketones can undergo reaction with nucleophiles at the B carbon, as…

A:

Q: 0 CHOCH2OH H+ -OCHSCHR OH

A: Answer is given below

Q: Draw an electron pushing mechanism for the following reaction: Hama H₂CO (i) NaOCH, (ii) H₂O OCHS

A: Given that, the reaction is:

Q: 3) Draw the mechanism for the nitration of benzene using nitric acid. 4) Care has to be taken when…

A: The nitration of benzene using nitric acid involves the substitution of a hydrogen atom on the…

Q: Draw the mechanism for the following reaction. wwwwwwwww AICI3

A:

Q: 14) Devise a synthesis of the following compound using 1-bromobutane as the only organic starting…

A: The given compound is synthesized by using the 1-bromobutane. One molecule of 1-bromobutane…

Q: provide a synthetic route

A: Step 1: Step 2: Step 3: Step 4:

Q: 1) NaBH4/ether 2) H2O КОСН3 in CH,OН TH. H;O+

A: The reaction mechanism is given below

Q: which compound is most activated toward electrophilic aromatic substitution. a) ģ رما Br Br Br ³ or…

A: The electrophilic aromatic substitution reaction involves carbocation intermediate this is called…

Q: Draw the major organic product of the reaction. Indicate the stereochemistry via wedge-and-dash…

A: • Nucleophillic substitution SN2 reaction has the           following charactershics :-i if follow…

Q: Synthesize the m form of benzocaine from benzene

A: Given: benzene To synthesize: benzocaine from benzene.

Q: Notice in Problem 25.63 that the hydroperoxide forms at the C atom that is α to the O atom and not…

A: A free radical chain reaction involves free radicals in a cyclic sequence of steps, called…

Q: H2SO4, H2O DMSO, (COCI)2 EtgN OH

A: The reactions given are,

Q: Explain the Two Mechanisms for Nucleophilic Substitution ?

A:

Q: Draw the structures of all possible products formed in the reaction involving an acid anhydride…

A: Anhydride react with alcohol give ester and carboxylic acid

Q: Draw the major product formed in attached reaction

A: Amine being a nucleophile can react with the alkyl halide. When an excess of CH3I is added to a…

Q: How to synthesize cyclohexylbenze from cyclohexanone?

A: Cyclohexylbenzene can be synthesized from cyclohexanone

Q: Draw the organic products formed in attached reactions?

A: The first reaction scheme involves two reactions. One is esterification and the other one is…

Q: H2SO4 (aq.) heat HO

A: In organic reaction, a acid attacks epoxide, and the lone pair of O, attacks to open the epoxide.

Q: AICI,

A: Using concept of fredalcraft acylation ,this can be determined.

Q: Draw the reaction mechanism of the elimination reaction of 2 bromobutane with a hydroxide ion acting…

A: Elimination reaction : An elimination reaction is a type of chemical reaction in which several atoms…

Q: We saw that it is necessary to use excess amine in the reaction of an acyl chloride with an amine.…

A: It is not necessary to use excess alcohol in the reaction of an acyl chloride with an alcohol…

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.