What product is formed when ethanethiol is treated with KOH? A CH3CH2SCH3 B) CH3CH2SCH2CH3 CH3CH2SK D) CH3CH2OK

Q: What product is formed when ethanethiol is treated with KOH?     CH3CH2OK   CH3CH2SCH3…

A: Etanethiol can be represented as CH3CH2SH  -SH functional group is known as thiol or thioalcohol…

Q: What reagents are needed to convert each compound to acetophenone (C6H5COCH3)?

A: Reagent use to convert acetophenone (C6H5COCH3) to Benzene (C6H6) is CH3COCl in presence of AlCl3.

Q: Draw a stepwise mechanism for the following reaction, one step in the synthesis of the…

A: A stepwise mechanism for the following reaction, one step in the synthesis of the…

Q: Give the IUPAC name (including any E,Z designation) for each unsaturated aldehyde. Neral is obtained…

A: The numbering and conformation is mentioned heer.

Q: Draw the products formed when phenol (C6H5OH) is treated with following set of reagents. [1]…

A:

Q: The compound shown below is the cyclic hemiacetal of НаС ОН O. CH2CH3 O 6-hydroxyheptanal.…

A:

Q: Lovastatin is a statin drug or an HMG-COA reductase inhibitor used for the management of high…

A:

Q: Etoposide, sold as a phosphate derivative with the trade name ofEtopophos, is used for the treatment…

A: In this question, we want to write all the products when all of the acetals are Hydrolyzed by acid…

Q: What products are formed when X, which contains both a lactone and an acetal, is treated with each…

A: Lactone: These are organic compound having O atoms as main heteroatom and theses compound are called…

Q: What hemiacetal is formed when hydroxy aldehyde D is cyclized?

A: Addition of alcohol with aldehyde results in a chemical species which is called hemiacetal.…

Q: What unsaturated carbonyl compound is formed by dehydration of each β-hydroxy carbonyl compound?

A: The dehydration of β-hydroxy carbonyl compound involves two steps: 1. Base removes a proton from the…

Q: [ 16 ] which of following compound(s) is/are neither acetal nor hemiacetal ? он Но Он осH-CHз CHз ОН…

A: option c Compound I and V

Q: Draw the structure (including stereochemistry) of the cyclic hemiacetal(s) formed when each hydroxy…

A: Concept introduction: Hemiacetal are formed for the compound having both hydroxyl group and aldehyde…

Q: What product is formed when each compound is treated with Tollens reagent (Ag 2O, NH 4OH)?

A: There are several tests available to identify the presence of certain functional groups in organic…

Q: Draw the product when each compound is treated with either (CH3)2CuLi, followed by H2O, or HC≡CLi,…

A: a. figure 3

Q: What product is formed when each compound is treated with either LiAlH4 (followed by H2O), or NaBH4…

A:

Q: Give the IUPAC name (including any E,Z designation) for each unsaturated aldehyde. Neral is obtained…

A: E,Z designation :  If two prior groups present at the same side of the double bond then the…

Q: What enolate is formed when each ketone is treated with LDA in THF solution? What enolate is formed…

A: When a ketone is treated with LDA in presence of THF solution to form an enolate ion. The strong…

Q: What lactol (cyclic hemiacetal) is formed from intramolecular cyclization of each hydroxy aldehyde?…

A: What lactol is formed from the intramolecular cyclization of each hydroxy aldehyde? (a) (b)

Q: What lactol (cyclic hemiacetal) is formed from intramolecular cyclization of each hydroxy aldehyde?

A: (a) The lactol (cyclic hemiacetal) is formed from intramolecular cyclization of the given hydroxy…

Q: What are the products of ozonolysis of 3-Methylpent-2-ene? A Ethanal and Butanal B Ethanal and…

A: Ozonolysis: It is the organic chemical reaction where ozone is employed to cleave the unsaturated…

Q: Draw the structure of each molecule. (a) 2,2-dimethylpropyl hex-3-ynoate; (b) cyanoethanoic…

A: (a) The structure for IUPAC name 2, 2-Dimethylpropyl hex-3-ynoate is:

Q: What product is formed when each carbonyl compound is treated with K2Cr207?

A: a.  The given carbonyl compound contains a -CHO group. On the oxidation of aldehydes in the presence…

Q: What products are formed when each compound is subjected to a Kiliani–Fischer synthesis?

A: The steps involved in Kiliani—Fischer synthesis of D-lyxose follows:Step-I Reaction of given aldose…

Q: Draw the product formed when CH3CH2CH2CH2NH2 reacts with each carbonyl compound in the presence of…

A: a. Given compound: Reaction:

Q: Draw the unsaturated carbonyl compound formed by dehydration of the following B-hydroxy carbonyl…

A:

Q: What product is formed when each pair of compounds is treated with NaOEt in ethanol?

A: The product formed by the reaction of the given pair of compounds with NaOEt is shown as, In this…

Q: What enolate is formed when each ketone is treated with LDA in THF solution? What enolate is formed…

A: LDA is a strong non nucleophilic base and it abstracts proton from alpha position of less hindered…

Q: Which of the following reactions represents the synthesis of dibenzalacetone? Ph = phenyl

A: All the reactions given are same and we only need to check which one is the balanced chemical…

Q: What is the major enolate (or carbanion) formed when each compound is treated with LDA?

A: The major product of enolate (carbanion) formed when the compound is treated with LDA is given…

Q: Which of the following is a hemiacetal? ОН ОН A) H;C-C-OH В) Н,С-С—ОСH Н н ОН нс- OCH3 D) H,C-С—ОСН,…

A: Hemiacetals are having two oxygen atoms directly attached to the same carbon atom and in the two…

Q: Draw a stepwise mechanism for the following reaction, one step in thesynthesis of the…

A: A stepwise mechanism for the following reaction, one step in the synthesis of the…

Q: Draw the product that is formed when the carbonyl compound is treated with K2Cr2O7? CH3CH2CHO

A: K2Cr2O7 is an oxidising agent which oxidises alcohol and carbonyl compounds

Q: .C. + CH,ОН CH;CH, CH2CH3

A:

Q: Draw the products formed when attached ether is treated with twoequivalents of HBr.

A: The most common reaction of ethers is the cleavage of the C–O bond by strong acids.

Q: what product is formed after recrystallizing a mixture of 4-phenylcyclohexanone and…

A: Recrystallization of 4-phenylcyclohexanone and 4-phenylcyclohexanol forms a ketal .i.e.…

Q: What product is formed when each pair of compounds is treated with NaOEt in ethanol ?

A: (a)

Q: What product is formed when Ethyl phenyl Ketone is treated with NABH4?

A: NaBH4 is a reducing agent for the reduction of aldehydes and ketones. Aldehydes are reduced to…

Q: What products are formed when each ester is treated with H,O and H,SO,? b.tooi CH;CHCH, C.…

A: This is an example of acid catalysed hydrolysis of ester which result in the formation of carboxylic…

Q: Answer the following questions about 2-acetylcyclopentanone.a. What starting materials are needed to…

A: Since you have posted a question with multiple subparts, we will solve the first three subparts for…

Q: What carbonyl compound and what phosphonium ylide are needed to synthesize the Attached compound?

A: The carbonyl compound and phosphonium ylide needed to synthesize the given compound has to be given.

Q: What Grignard reagent and carbonyl compound can be used to prepare the antidepressant venlafaxine…

A: The reaction of Grignard reagent and carbonyl compound joins the 2 compounds and alcohol is formed.

Q: Two naturally occurring compounds that contain stable cyclic hemiacetals and acetals are monensin…

A: Carbonyl compounds and imide generally undergo a process called tautomerization. Tautomerization is…

Q: What product is formed when 2-acetylcyclopentanone is treated withNaOCH2CH3, followed by CH3I?

A: The product formed on treatment of 2-acetylcyclopentanone with NaOCH2CH3 followed by CH3I is drawn…

Q: Draw the products formed when phenol (C6H5OH) is treated with following set of reagents. [1] HNO3 ,…

A: In a mono-substituted benzene ring, the position of substitution of the incoming electrophile is…

Q: What products are formed when each acetal is hydrolyzed with aqueous acid?

A: The reaction of an alcohol with aldehyde and ketone in the presence of acid produces acetal or…

Q: K2Cr2O7

A: K2Cr2O7 is an oxidizing agent.  Aldehydes are more reactive than Ketones. So, Aldehydes oxidizes to…

Q: What product is formed when 2,2-dimethyloxirane is treated with each set ofreagents: −OCH3 followed…

A: The required products are

Q: What reagents are needed to convert each compound to butanal (CH3CH2CH2CHO)?

A: Simple organic compounds with simple functional groups such as ester, alcohol,c C-C triple bond, or…

Reactions at the Alpha Carbon Atom

The position next to the ketone or aldehyde functional group is termed as alpha position and the reaction which occurs at alpha position is called alpha substitution reaction. In an alpha substitution reaction, the alpha proton atom is substituted by an electrophile by the formation of an enol intermediate or enolate ion intermediate. Most of the carbonyl compounds go through an alpha substitution reaction.