please give reaction and Mechanism for the preparation of given molecule. PLEASE MECHANISM Please show the synthesis of the following molecule. Show each step, reagents, andproduct.Allowed Starting Reagents:Any reagent containing 4 carbon atoms or less, and any of the following compounds:Ph3P=Molecule:

You can see how to make this molecule step by step with mechanism also.

Answered: please give reaction and Mechanism for…

Science

Chemistry

please give reaction and Mechanism for the preparation of given molecule. PLEASE MECHANISM

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter9: Nucleophilic Substitution And Β-elimination

Section: Chapter Questions

Problem 9.60P: Another important pattern in organic synthesis is the construction of CC bonds. Using your reaction...

See similar textbooks

Related questions

Q: 1. CH₂CO3H 2.NaOCH3, CH3OH

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: synthesis question . . . what mechanisms should i use to get to the product?

A: Step 1: This illustrates the conversion of an alkyne into a cyclic molecule with an imine group…

Q: please explain the reaction with mechanism

A: in the given question, it is secondary alkyl halide which reacts with a very good nucleophile. This…

Q: Q2: Write the mechanism for the following polymerization? toº Anionic polymerisation

A: A polymer is a large molecule that is formed by the repetition of small units called a monomer, and…

Q: NH₂

Q: Provide a complete mechanism (including all arrows, lone pairs and formal charges) for the formation…

A: This is an example of Claisen condensation reaction

Q: Draw the molecular ion (M) for this molecule formed in the mass spectrometer.

A: Mass spectrometry is an important tool for the determination of the molecular mass of the compound…

Q: mechanism, please explain each step because I need understand

A: Ans. Isomerization and hydroisomerization of normal paraffins to conversion in monobranched and…

Q: Propese the below epoxide Starting with cycloheptanone a mechanism for HC CH3 SCH3 CH3 CHs

A: Detail mechanistic pathway is given below

Q: NaOEt EtOH Į Br. H30Ⓡ A Reactive Intermediate

A: NaOEt abstracts a proton from the alpha-carbon of beta-keto esters and forms an anion, which…

Q: T6DPSO OTIPS Zncl2 Tich TIPSO -> MOTEDPS CHzel, TIPso SPy TMS

A: The first step involved the coordination of the aldehyde with lewis acid ZnCl2, which makes it…

Q: Provide the major organic product of the reaction shown below. 1) Н2О, Н.О. А 2) CH CH OH, H.Oº, А…

A: -> In presence of H2O /heat and acidic medium Acetal can break and form carbonyl compound. ->…

Q: OCH3 OCH3 OCH3 PC5. H,-Pd CH;NO, co,H- > CH;O CH;0 OCOC- > CH3O CO,H BaSO4 СНО NAOH (Rosenmund…

Q: NaOH, H20 Cl CH2OH ÇO,H ÇO,H ÇO.H C) D) B) A) Cl HO, Cl CH2ONA ČH2OH CH,OH ČO,H

A: ->NaOH is base hence, it can abstract most acidic hydrogen present in the given compound.

Q: Why does one react but not the other? Please show mechanism

A: The trans-2-chlorocyclohexanol has the —OH and Cl in trans arrangement. The abstraction of a proton…

Q: 107. In the following reaction, the structure of the major product is COOEt THE

A: Rearrangement reactions are those reaction in which a molecule in the presence of some reagent…

Q: this synthesis have flaw. ellaborate why this synthesis is wrong and do the ncessary corrections

A: We have to predict the flaw and propose the correct synthesis.

Q: Organic Chemistry Problem Please help. Find product of reaction. Thank you

A: Approach to solving the question: Detailed explanation: Examples: Key references:

Q: 7. Provide the major organic product of the following reaction.

A: The reaction of potassium permanganate (KMnO4) with a secondary alcohol would result in an oxidation…

Q: write down adetaled mechanism fer the fllowing? otH H*

Q: (a) PHOOC-CH,-C-CH,-COOP. (1) KCN, A (2) H,0® (o) СООН Onl

Q: Answer with mechanism ASAP

A: see below

Q: Me. Me Me Br Br KNH2, NH3 1. KNH2, NH3 2. NaN3 3. H₂O

A: The above given reactions will follow benzyne mechanism and there will be possibility to produce one…

Q: draw all mechanisms and resonance structures for this given organic structure

A: To solve this problem we have to write the mechanism of this reaction .

Q: Predict the product for the following reaction. Na, CH3OH NH3

A: The given reacting species is methylbenzene also known as toluene. It is a non-polar organic…

Q: The solubility product constant for MX2 is 7.48E-3. What is the molar solubility of MX2? (the answer…

Q: Draw the molecular ion (M) for this molecule formed in the mass spectrometer. - e- Drawing :0:

A: A useful analytical technique for determining the mass-to-charge ratio (m/z) of one or more…

Q: Please show arrows for mech. thank you f. он Cu(CH;CN);OTf, TEMPO, air, NMI, bpy Ph OH Ph он РОС,…

Q: ph ph (CH3)3 CONa (CH2)3 COH ㅋ ?

A: Given that, a reaction is We have to give the major product of the reaction with the mechanism.…

Q: H MgBr Ci Br P F

A: Given : We have to draw the product for given reaction.

Q: HO OH OH OH H,SO4 но HO H. HO OH OH OH

Q: TSOH HO. Q

A: In this question, we will draw the reaction mechanism for the formation of the product ( hemiacetal…

Q: Provide mechanism

A: The required answer is given below Explanation:Step 1: Step 2: Step 3: Step 4:

Q: 1) NaH HOʻ 2) Br

Q: R-O-O-R

A: This is Free radical decarbonylation. 1st product is without radical rearrangement via less stable…

Q: ОН H да стан ОН

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: Can you show me how the mechanism is done? 1.3 BH₂ THF 2. 3 H₂O₂, 3 NaOH, 3 H₂O

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: ca) CI (CH2=CH)2CuLi ether, -78° C (9) 1. 2 CH3CH2CH2MgBr, ether CI 2. H;0* (C) who 1. 2 H3C- -MgBr…

A: In acyl substitution reaction, nucleophile can always attack on electrophilic carbonyl centre and…

Question

please give reaction and Mechanism for the preparation of given molecule. PLEASE MECHANISM

Please show the synthesis of the following molecule. Show each step, reagents, and
product.
Allowed Starting Reagents:
Any reagent containing 4 carbon atoms or less, and any of the following compounds:
Ph3P=
Molecule:

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

VIEW

Step 2

VIEW

Step 3

VIEW

Step by step

Solved in 3 steps with 2 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

Alcohols are important for organic synthesis, especially in situations involving alkenes. The alcohol might be the desired product, or the OH group might be transformed into another functional group via halogenation, oxidation, or perhaps conversion to a sulfonic ester derivative. Formation of an alcohol from an alkene is particularly powerful because conditions can be chosen to produce either the Markovnikov or non-Markovnikov product from an unsymmetrical alkene. Using your reaction roadmap as a guide, show how to convert 4-methyl-1-pentene into 5-methylhexanenitrile. You must use 4-methyl-1-pentene and sodium cyanide as the source of all carbon atoms in the target molecule. Show all reagents needed and all molecules synthesized along the way.
How would you synthesize the followingcompounds from benzene using thereagents from the table? Each requires 3-4steps.
Hello please help with this organic chemistry question attached below.
• Same reagents as acid-catalyzed dehydration, except starting with a instead of an alcohol. • Same as the general mechanism hydrohalogenation, except with . Remember that EVERY acid-cat. mechanism begins with General Reaction: EXAMPLE: Provide H₂O H₂SO4 EXAMPLE: Provide the mechanism for the following addition reaction. H₂O H₂SO4 OH WH H₂O H₂SO4 as the nucleophile and ends with do PRACTICE: Provide the mechanism and predict the product of the following reaction. MAXO
Need help with question.
3) Draw the structures of the major organic product(s) for the following reactions. HI in CH₂Cl₂ 3 excess Cl₂ in H₂O H₂SO4 in H₂O (Two products) Br-Cl in THF 1) BH3 2) alkaline H₂O₂ OSO4 + HOOH
Ethers/Aldehydes/Ketones SynthesisDraw and Prepare the following compounds from any simple alkyl halide having four carbons or less,cyclohexane, and/or benzene. You may also use ethylene oxide (oxacyclopropane). SHOW ALLSTEPS AND REAGENTS with arrows.
Complete the following reactions
Three reactions between a Grignard reagent and a carbonyl compound are given. Draw the main organic product for each reaction and indicate if H+ or H¯ is needed to complete each reaction. The starting material structures are provided in the answer fields as a starting point for your drawings. The first reaction involves a ketone. 1. CH₂MgBr 2. H+ or H™? Select Draw / |||||| C Rings O More Erase
What alkene is needed to synthesize the following 1,2-diol using the given reagents? Be sure to answer all parts. CH3CH₂CH2 [1] OsO4 followed by NaHSO3 in H₂O: [2] CH3CO3H followed by "OH in H₂O: H OH OH CH₂CH₂CH3 draw structure... draw structure ...
The reagents below (A-E) are used for the following questions. A H D Br PPh3 :0: H. e B :0: PPh3 (+) E H Which reagents are Wittig reagents? [Select] H Br. :0: Which Wittig reagent would yield a Z alkene when reacted when an aldehyde/ketone? [Select] C Recall the definition/structure of a Wittig reagent. Which reagents could be used to make a Wittig reagent? [Select] H
Provide the major organic product in the reaction shown below.