O O acetophenone O benzoyl chloride 2-methylcyclohexanone benzyl acetate O butyrolactone cyclopentanone methyl benzoate O methyl propionate

Q: Name the following amine: N O diethylmethylamine O diethylamine O trimethylamine O…

A: Namenclature of amine: Amines are organic derivatives of ammonia, NH3, in which one or more of the…

Q: Draw the products formed when each ester is treated with lithium hydroxide and water

A:

Q: draw and name the product of hydrolysis of 3-bromo,2 methyl hexyl amide

A: Mechanism of acid catalyzed hydrolysis of corresponding amide is given below by which we get acid…

Q: Draw the strcture of the following compounds. vinyl formate tert-butyl acetate…

A:

Q: What are the products of the neutralization of benzoic acid with sodium hydroxide? Select one or…

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Q: A: aromatic compound B: A C:

A: In the given question we have to discuss the functional group or types of molecules present in the…

Q: chyl-4-dimethylamine chyl-N,N-dimethylpentyl-2-amine chyl-N,N-dimethylpentyl-2-amine…

A:

Q: O 3,5,6-trimethyl-3-heptanamine O 2,3,5-trimethyl-5-heptanamine O 5,6,N-trimethylheptanamine O…

A:

Q: What are your final product when 2-nitrobenzaldehyde is mixed with each of these:…

A: The details solution for this reaction is provided below in attach image.

Q: draw butylamine

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Q: CI ol oor CN H 0

A: We know acid derivatives can undergo hydrolysis to give acid .

Q: What is the IUPAC name for the following molecule? Br O N-ethyl-N-methyl-5-bromohexan-2-amine…

A: IUPAC name should be written by following some IUPAC rules.

Q: What are the products of the following hydrolysis? a primary amine and an aldehyde O a primary amine…

A: The objective of the question is to identify the products of hydrolysis when different types of…

Q: Name the carbonyl compound that would be formed by the complete acidic hydrolysis of the following…

A: This question belong to reaction mechanism of organic compounds. Hydrolysis: addition of water

Q: Phenol can only be made starting with benzene by using an/the

A: As per guidelines first question is allowed to answer, please post seperately to answer remaining…

Q: Which of the following functional groups are present in decanedioic acid? Group of answer choices

A: Functional groups are the substituents which are directly attached to the alkyl chains of…

Q: Draw the major organic product for the acid hydrolysis of cyclohexanimine. NH H3o+ HO

A: major product of acid hydrolysis of cyclohexanimine :

Q: How many of the compounds A-E possess a hydroxyl group which is NOT part of a carboxylic acid group?…

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Q: Identify the most acidic carboxylic acid. O ICH2COOH O BrCH2COOH O FCH2COOH O CICH2COOH

A: Electron withdrawing groups increase the stability of the conjugate base.

Q: Draw the reactants and products formed in the following acid-base neutralization reaction (carboylic…

A: The solution is as follows :

Q: H, SO4 H,O

A: during the ester hydrolysis the acid and the alcohol is formed .

Q: How many ester groups does Taxol contain? ofle O O five one Otwo four three HO OH H

A: EsterCompound contains COO group is called as ester

Q: Why is methyl salicylate so easily absorbed through the skin?

A: When applied topically, adequate methyl salicylate is assimilated to give relief from discomfort to…

Q: Rank the compounds in order of electrophilicity. (X > Y means X is more electrophilic than Y). O…

A: An electrophile is a chemical species that forms bonds with nucleophiles by accepting an electron…

Q: What is the name of the product formed as a result of the reaction between benzylamine and…

A: Ethyl acrylate reacts with amines in a Michael addition. The reaction is catalyzed by Lewis acids.…

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.