describe the product formed as a result of the reaction between benzylamine and ethylacrylate by writing the mechanism of the reaction?

Q: H3O* H2O H

A: The epoxide ring-opened when it reacts with aqueous acid. The reaction proceeds via a.nucleophilic…

Q: Enamines can serve as enolate surrogates in reactions at the a-carbon. In the following reaction…

A: An enamine is an unsaturated compound derived by the condensation of an aldehyde or ketone

Q: lease explain the mechanism for the ring opening of epoxide by reaction with nucleophile in base

A: Epoxides are called the cyclic ethers. The epoxide rings are very stable. When a nucleophile attacks…

Q: a. What reagent must be used in the preparation of an acid chloride from a carboxylic acid? b.…

A: Reagents are the species that are needed to react with reactants in order to yield the desired…

Q: eChkrapars

A:

Q: Here in Chapter 19, we learned that converting a ketone or aldehyde to an acetal is a good way to…

A: Protecting groups are the groups which selectively mask a particular functional group so that it…

Q: how can you prepare diethyl ether from an alkyl halide and any other organic or inorganic compound?

A: Diethyl ether is prepared from an alkyl halide by Williamson's synthesis . Williamson's synthesis is…

Q: CO₂E1 CH3CHCO₂E1 1. Na+ "QEt 2. PhBr 3. H30¹, heat prevented. CH3 I CHCO₂H The intended reaction is…

A:

Q: Explain why a methoxy group (CH3O) increases the rate of electrophilic aromatic substitution, but…

A: Methoxy group (CH3O) increases the rate of the rate of electrophilic aromatic substitution reaction,…

Q: What site on the alkyl halide is likely to get attacked by the cyanide (in other words, which atom…

A: Electrophilic sites are those sites which are electron deficient.

Q: Acetal formation must be catalyzed by an acid. Explain why it cannot be catalyzed by CH3O-.

A: Since in the reaction, CH3O- can not replace the OH- group. This is because CH3O- is a better…

Q: Draw the product of cyclohexanone, bromine and base catalysis. thank you for your explanation in…

A: The major product of the given reaction is illustrate here: Let the base is NaOH. We know that Br is…

Q: Use a mechanism to give a explanation of the following reaction.

A:

Q: Which sequence of reactions will convert benzene to 3-chloroaniline in a reasonable yield? (Hint: a…

A:

Q: Which ketone cannot be made by the acid catalyzed hydration of an alkyne? A B C D E

A:

Q: What is the major product of bromination of p-methylbenzoic acid reactions?

A: p-methylbenzoic acid is an aromatic compound in which benzene ring is substituted with a carboxylic…

Q: Although two products (A and B) are possible when naphthalene undergoes electrophilic aromatic…

A:

Q: Show how the benzaldehyde can be prepared from benzene:

A: Preparation of compound from reacting species with the help of various reagents is achieved.…

Q: Explain Reaction of Organometallic Reagents with Aldehydes and Ketones ?

A:

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: CO₂E1 i CH3CHCO₂E 1. Na* "Ot 2. PhBr 3. H30, heat The intended reaction is the because the alkyl…

A:

Q: How does propane synthesized from propanone? Show its mechanism

A: To solve this problem we will use the Clemmensen reduction.

Q: Shown below is the tetrahedral intermediate in a nucleophilic acyl substitution reaction. Draw the…

A: In this equation, we want to draw starting material ( carbonyl reactant ) on left side box and also…

Q: CH3O- CH;OH

A: Michael addition is the nucleophilic addition of a carbanion or another nucleophile to an alpha-bita…

Q: a) Predict the products of the following reaction: NaOE/ELOH A Catalytic amount b) Draw the…

A:

Q: NH2 (Benzyl amine) (a) H.

A:

Q: Why does bromination give exclusively anti products while chlorination gives a mixture of syn and…

A: Halogenation is the addition of halogens to alkenes. Halogenation usually gives anti products. If…

Q: Draw the product of the reaction and explain the reason OMe

A: Pericyclic reactions are proceeds by a cyclic shift of electrons by a single-step reaction…

Q: Draw the organic products of the reactions

A: The answer for first question is given below. Kindly repost the other question as separate one

Q: ONLY SOLVE BOLDED QUESTIONS PLEASE. Synthesis of Diphenylacetylene This synthesis requires two…

A: Hello. Since your question has multiple sub-parts, we will solve the first three sub-parts for you.…

Q: Give the minor elimination product(s) of the following compound. ? NaOH heat Br

A:

Q: Draw the structure of unsaturated carbonyl compound(s) formed when…

A: Hydroxy aldehyde when heated in either (ii) acid or (i) base, it will undergo aldol condensation in…

Q: earn the term “oxime” and then look up a reaction called the “Beckmann rearrangement.” Why is this…

A:

Q: Draw the major product formed in the reaction of an epoxide with acidic methanol.

A:

Q: Why aldehydes and ketones do not undergo nucleophilic substitution reaction?

A: The reaction in which an electron donor pair called the nucleophile is replaced by an electron…

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

A:

Q: `CI Ме

A: Here the starting material given is 2-chloropyridine

Q: Benzalacetone is a side product formed in the aldol condensation of dibenzalacetone. Show the…

A: Concept is based on aldolcondensation reaction.

Q: Draw the organic product(s) of the reaction of phenylacetaldehyde with CH3MgBr, then H3O*.

A: GRIGNARD REAGENT ACTS AS THE NUCLEOPHILE AND ATTACKS THE ALDEHYDE GROUP AND FORMS THE ALCOHOL

Q: Rank the derivatives of phenol in order of increasing acidity (Please explain) 

A: The compounds given are,

Q: Although two products (A and B) are possible when naphthalene undergoes electrophilic aromatic…

A: Concept introduction: Resonance structures differ only in the position of the lone pair of electrons…

Q: Which of the following is an intermediate when 1,2- dibromo-4-nitrobenzene is heated with NaOH in a…

A:

Q: Aniline on oxidation by chromic acid produces ans All the above p-benzophenone Nitrosobenzene…

A: In this question, we will see that which Compound is formed after oxidation of Aniline. You can see…

Q: Draw the mechanism for the formation of diphenylacetylene

A: It is a 2- step process in which we generate triple bond of an alkyne by brominating the double bond…

Q: ic ring protonation b.loss of the electrophilic aromatic ring c. deprotonation of the aromatic…

A: An electrophile is the electron loving species there is a deficit of electron and want to attach…

Q: HO HO

A: 3-Hydroxypropionic acid in presence of base Sodium hydroxide undergoes dehydration reaction and…

Q: I would like some help finding the detailed arrow reaction mechanism for the ethylidene cyclopentane…

A: Alcohols undergo dehydration reactions in the presence of sulfuric acid followed by heat. The…

Aldehydes and Ketones

Aldehydes and ketones are organic compounds that have a carbonyl group, C = O, as their functional group. They both differ in the placement of this carbonyl group in their structures.