Answered: What products would result after…

What products would result after hydrolysis from reaction of the enamine prepared from cyclopentanone and pyrrolidine with the following x,ß-unsaturated acceptors? H₂C=CHCO₂Et iv B I US X₂ x²

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter23: Carbonyl Condensation Reactions

Section23.11: Carbonyl Condensations With Enamines: The Stork Reaction

Problem 19P

See similar textbooks

Related questions

Q: If benzamide (PhCONH₂) undergoes a Hofmann rearrangement, what is the major product? O acetophenone…

Q: Predict the products formed when cyclohexanone reacts with the following reagents.PhMgBr and then…

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: Reaction of p-nitroaniline with sodium nitrite and hydrochloric acid at 0°C, followed by treatment…

A: The objective of teh question is to predict the product formed in the following reaction given.

Q: What is the major product when cyclohexanone is reacted with ammonia and trace acid? NNH, NCH, NH2…

Q: CH3 CO₂Et Hagemann's ester The compound known as Hagemann's ester is prepared by treatment of a…

Q: Indicate how the following compounds can be synthesized from cyclohexanone and any other necessary…

A: a.

Q: Procaine (its hydrochloride salt is marketed as Novocaine) was one of the first local anesthetics…

A: Esterification occurs when a carboxylic acid reacts with an alcohol. This reaction can only occur in…

Q: What is the name of this compound? CH3 H3C N' NH2 CH3

A: Generally, the IUPAC system gives nomenclature to the different compounds. This nomenclature system…

Q: Starting from benzylamine, draw the structure of the major products upon reaction with the following…

A: Given:

Q: Identify the reagents necessary for the reaction:

A: Epoxides on reaction with nucleophile(OH-) in the presence of acid/base catalyst produces trans…

Q: 10) Which of the following is (2R, 3S)-2,3-pentanediol?

Q: In each reaction box, place the best reagent and conditions from the available reagent list. 1.…

A: “Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: Predict the products formed when cyclohexanone reacts with the following reagents. h) sodium…

A: SOLUTION: Step 1: The reaction of sodium acetylide with the cyclohexanone (ketone) is an example of…

Q: What product is obtained when the following compound undergoes two successive elimination reactions?

A: The reactant with two halogens when undergoes two successive elimination reactions, it forms a…

Q: The following diol is prepared from propanal (CH3CH2CHO) and 3-bromopropanol. Which derivatives will…

A: Grignard reaction - is the reaction that uses on organometallic compound to create carbon- carbon…

Q: 2) When 4-hydroxybutanal is treated with methanol in the presence of an acid catalyst, 2-…

Q: The following compound forms a six-membered cyclic hemiacetal. Select the -OH group (A, B, C, D)…

Q: 1. Which pair of aldehydes can lead to the following product? 10% NaOH(aq) ОН Н 2 moles of propanal…

A: Here the product formed is from aldol condensation reaction .

Q: Draw the products formed when each carbonyl compound reacts with the following amines: [1]…

A: Primary and secondary amines reacts with different carbonyl compounds to give different products.…

Q: 1) How might you convert geraniol into either ethyl geranylacetate or geranylacetone? Geraniol CH₂OH…

Q: Which one of the following carboxylic acid derivatives can undergo nucleophilic acyl substitution…

A: Nucleophilic acyl substitution (acyl transfer reaction) occurs by a two-step mechanism. First,…

Q: Treatment of r-butyrolactone with two equivalents of methylmagnesium bromide, followed by hydrolysis…

Q: The reaction of meta-Bromoaniline with NaNO, and HCl yields a diazonium salt. Draw the structure of…

Q: Which of the following compounds CAN'T be formed starting from malonic ester?

Q: propanoyl bromide No reaction 3-bromopropanal 1-bromopropan-1-ol 2-bromopropanal Br₂ H₂SO4

Q: Propose a synthesis of the topical anesthetic cyclomethycaine from 4-hydroxybenzoic acid,…

Q: The Stork reaction is a condensation reaction between an enamine donor and an α,β-unsaturated…

A: The structure of enamine formed is drawn as,

Q: Which of the following compounds will not undergo keto-enol tautomerism'

A: Condition for keto enol tautomerism Double bond and OH group must be on the same group .

Q: (c) Reaction of acetanilide with bromine Br: CH3 (d) Hydrolysis of 4-bromo-2-chloroacetanilide with…

Q: What products are formed by acidie hydrolysis of the following compound? benzaldehyde and butan-1-d…

A: Acidic hydrolysis of the following compounds (Ester hydrolysis ) gives

Q: Start with NH3 and show step by step how the compound N-sec - butyl - N - propyl-2 - pentanamine can…

A: The given reaction is a simple alkylation reaction of ammonia and ammonia derivatives.

Question

What products would result after hydrolysis from reaction of the enamine prepared from
cyclopentanone and pyrrolidine with the following x,ß-unsaturated acceptors?
H₂C=CHCO₂Et
1
BI
III
S
ab
X₂
x²

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

SEE SOLUTION Check out a sample Q&A here

Step 1: Introduce question

VIEW

Step 2: Explain reaction pathway

VIEW

Solution

VIEW

Step by step

Solved in 3 steps with 1 images

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

Predict the products formed when cyclohexanone reacts with the following reagents. h) sodium acetylide, then mild H3O+
What carboxylic acid and amine are needed to synthesize the pain reliever phenacetin? Phenacetin was once a component of the over-the-counter pain reliever APC (aspirin, phenacetin, caffeine), but it is no longer used because of its kidney toxicity.
The reaction of meta-Bromoaniline with NaNO2 and HCI yields a diazonium salt. Draw the structure of the products formed when the following reagents are added: Reagent H20 Products HBF4 CUCN НЗРО CuBr
Predict the products formed when cyclohexanone reacts with the following reagents.PhMgBr and then mild H3O+
Rimantadine is an antiviral drug used to treat people infected with life-threatening influenza viruses. Identify the starting ketone that would be necessary in order to prepare rimantadine via a reductive amination. NH2 Rimantadine
What is the name of this compound? CH3 H3C NH2 CH3 O ethylmethylbutylammonium O cthylmethyl-sec-butyl-ammoium ON-ethyl-N-methyl-3-butamine ON-ethyl-N-methyl-2-butanamine Z-
Treatment of r-butyrolactone with two equivalents of methylmagnesium bromide, followed by hydrolysis in aqueous acid, gives a compound with the following molecular formula: 1. 2 CH;MgBr C,H1402 2. Н,0, НCI Which of the following is the structural formula for this product? HO OH HO -O- O O O
What products are obtained when the following tertiary amines react with hydrogen peroxide followed by heat?
Treatment of 1-aminoadamantane, C10H17N, with methyl 2,4-dibromobutanoate in the presence of a nonnucleophilic base, R3N, involves two successive SN2 reactions and gives compound A. Propose a structural formula for compound A.
Which carbonyl groups in the anticancer drug Taxol will undergo nucleophilic addition, and which will undergo nucleophilic substitution?
If benzamide (PhCONH₂) undergoes a Hofmann rearrangement, what is the major product? O acetophenone O aniline O benzyl azide O cyclohexylamine benzylamine
Identify A, B, and C, intermediates in the synthesis of the five-membered ring called an α-methylene-γ-butyrolactone. This heterocyclic ring system is present in some antitumor agents.