Can you explain the mechanism Lewis acid produce cyclooligomerization+ BF3-O-BF3 +2

The objective of the question is to understand the mechanism of how a Lewis acid, in this case, BF3…

Answered: Lewis acid produce cyclooligomerization…

Science

Chemistry

Lewis acid produce cyclooligomerization + BF3 -O-BF3 +2

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

Chapter8: Haloalkanes, Halogenation, And Radical Reactions

Section: Chapter Questions

Problem 8.24P

See similar textbooks

Related questions

Q: Predict the major organic product of this reaction and draw the complete mechanism to form it: 1)…

A: LiAlH4 acts as reducing agent.

Q: - Reaction of methyl 4-fluoro-3-nitrobenzoate with morpholine LOCH3 NH ? F NO₂ MeOH

Q: Please show me the mechanism on paper that way it's easy for me to understand

A: To give the mechanism of the two step given reaction.

Q: HBr ROOR

Q: 23. The major product of the following reaction is (CH,CO),0 BF; Et,0, 0°C

Q: Can you explain it ? And the mechanism

Q: CF3 NH₂ N ม. ผ Br

A: The given reaction is simple nucleophilic substitution reaction.

Q: 1. LAH 2. Hyo® f. Et Me

A: LAH is Lithium aluminum hydride. it can give hydride ion which acts as a nucleophile. Reduction of…

Q: HBr peroxide

A: To draw the product of the given organic reaction mechanism.

Q: (a) Discuss the synthesis of 1,3-thiazole derivative from thioamide and an a-haloketone.

Q: Draw the product of this nydrogenation reaction. Use wedge and dash bonds to indicate…

A: Interpretation: We have to determine the product for the following given reaction.

Q: Predict the major organic product of this reaction and draw the complete mechanism to form it: 1)…

Q: 1. CH3M9BR 2. H30+

A: Grignard reagents are commonly written as RMgX where R is the alkyl group and the X is the halogen.…

Q: Me i) H2SO4, heat ii) NaOH N. Br

Q: Br HBr HO

Q: Is the given mechanism is correct or not,please confirm?

A: Yes, the above reaction to acid catalyzed ring opening of epoxide. So, the first step is attack of…

Q: Predict the major organic product of this reaction and draw the complete mechanism to form it: HO-…

A: This reaction generates cyclic anhydride from Dicarboxylic acid by heating.

Q: 미 ㅇ >06-H - -> yfoot '애 옙 2 →>> 0 -OR 0 0 0 -OR - OR -OH (A) (B)

A: what is the correct mechanism given?

Q: correct

Q: Can you explain whats happenning here due the mechanism?

A: Generally, in a Swern-type reaction stronger base is used like triethylamine (Et3N). As the sodium…

Q: Ph Ph g心ールH Ho 41 Ph Ph ~ーNH Ho ~がメ

A: The reaction mechanism given is,

Q: K,co, 3. но Br CO,H 4. 1 ME 2 co: CS Scanned with CamScanner

Q: How is this incorrect and what is the correct mechanism?

A: Given : We have to tell what will be the correct mechanism.

Q: H HNO3 H2Sou 여 N Но

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

Q: tautomerization HO-

A: Given : We have to draw the keto-enol tatutomerization product.

Q: Write the mechanism TSOH (d)

A: Answer: TsOH is acidic in nature. In presence of TsOH will be hydrolysed and converted into alcohol.

Q: Is this mechanism correct

A: The mechanism is in a simple manner that is to attack on carbonyl carbon to the departure of…

Q: 2 Select the major product(s) of the following reaction. OH 1) Ts-C1 pyridine 2) NaCN, DMSO

A: TsCl, Pyridine converts OH to OTs which is better leaving group NaCN is a good nucleophile which in…

Q: Indicate the major organic product from the reaction shown. Grubb's catalyst 2.

A: Grubbs catalyst is,

Q: ......

Q: ration toutomenizalion| -0어

Q: Explain how you would synthesize the following organic molecule. Be sure to list the name of the…

Q: please explain mechanism

A: A question based on reaction mechanisms. A reactant is given whose product and mechanism are to be…

Q: Can you explain the rules and the mechanism and provide examples

Q: What is the systematic name of the product P of this chemical reaction? 0 O OH + KOH P + H₂O

A: This question belongs to organic reaction mechanism.

Question

Can you explain the mechanism

Lewis acid produce cyclooligomerization
+ BF3
-O-BF3 +2

AI-Generated Solution

AI-generated content may present inaccurate or offensive content that does not represent bartleby’s views.

Unlock instant AI solutions

Tap the button
to generate a solution

Click the button to generate
a solution

SEE SOLUTION

Similar questions

What type of cycloaddition reaction is shown below? Diels-Alder + CH=CH reaction Norbornadiene (A) Select one: O [2+4] o [8+2] o [2+2] O [4+2]
Draw the structure of (Z)-1-bromo-1-chloro-1-butene. • Consider E/Z stereochemistry of alkenes. • You do not have to explicitly draw H atoms. AAVII ? ChemDoodle [F Ⓡ
Based on the structure below, what form of EDTA is represented? -0OCCH, +H N CH, CH,-N-H+ "ООСCH, CH,COO- CH,COO-
d) H3PO4 + 5 HBr PBrs + 4 H20 e) 3 Fe(OH)2 + 2 H3PO4 Fe(PO4)2 + 6 H2O f) 2K + Br2 2 KBr Teve Closed - enerqy ISolu
Use the Woodward Hoffmann rule {Σ(4q+2) + (4r)a} to determine if the following 1,3-dipolar cycloaddition is thermally or photochemically allowed.
2. Show the mechanism with arrow formalism to show the formation of the most stable product. Which of the following terms apply to the mechanism(s) i) Regioselectivity (ii)stereoselectivity (iii)stereospecificity. Explain H+ (aq) from sulfuric acid NaCN most stable product
Organic chemistry
Propose a series of chain initiation, propagation, and termination steps for this reaction and estimate its heat of reaction. light + Br2 Br + HBr (racemic)
[Li],[Cd,Se,(SPh)16 + H,NC16H33 → [CdSe]„(H,NC16H3)m + Other Products Can Someone help me balance this and predict the extra products!
which one be the stereochemical outcome of the Sn1 reaction?
Explain why cyclopentadiene (pKa = 15) is more acidic than pyrrole (pKa ∼17), even though nitrogen ismore electronegative than carbon.
The following reaction is electrophilic substitution: 3- [Pt(CH₂)(CI)(PMePh₂)₂] + N° + CI Select one: True O False [Pt(CH₂)(N) (PMePh₂)₂]