Please answer only if you know the exactcorrect answer for the question, if not pleasedo not answer. I need helping in drawing thearrow-pushing mechanism for the reaction ofthe following diene with HBr.(4) A Conjugated dieneH H Hf=と-と-と-と-(CsHe)IUPAC Name of this Compound2 3 4Hュ=CH-CH=CHEH,Penta -1,3-dienePenta –1,3-diene present in two isomer (heometoicalFirstIsomers)Cis-1,3-PentadieneIf more than one product is formed, makesure the mechanism accounts for theformation of all of the products. Include alllone-pairs and non-zero formal charges in tehmechanism. If there are multiple products,label the MAJOR product and explain how itwas determined which product would bemajor.Thank you so much for your help. I appreciateit!

Given: Reaction of conjugated diene with hydrogen bromide. To find: Products of the above Reaction…

Please answer only if you know the exact correct answer for the question, if not please do not answer. I need helping in drawing the arrow-pushing mechanism for the reaction of the following diene with HBr. (1) A Conjugated diene HHHH (CsHe) IUPAC Name of this Compound 23. 4 Penta -1,3-diene Penta -1,3-diene present in two isomer (beometoical First CHs Isomers) Cis-1,3-Pentadiene If more than one product is formed, make sure the mechanism accounts for the formation of all of the products. Include all lone-pairs and non-zero formal charges in teh mechanism. If there are multiple products, label the MAJOR product and explain how it was determined which product would be major. Thank you so much for your help. I appreciate it!

Please answer only if you know the exact correct answer for the question, if not please do not answer. I need helping in drawing the arrow-pushing mechanism for the reaction of the following diene with HBr. (1) A Conjugated diene HHHH (CsHe) IUPAC Name of this Compound 23. 4 Penta -1,3-diene Penta -1,3-diene present in two isomer (beometoical First CHs Isomers) Cis-1,3-Pentadiene If more than one product is formed, make sure the mechanism accounts for the formation of all of the products. Include all lone-pairs and non-zero formal charges in teh mechanism. If there are multiple products, label the MAJOR product and explain how it was determined which product would be major. Thank you so much for your help. I appreciate it!

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

Section9.7: Experimental Evidence For E1 And E2 Mechanisms

Problem 9.7P

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When Br2 is added to buta-1,3-diene at -15 °C, the product mixture contains 60% ofproduct A and 40% of product B. When the same reaction takes place at 60 °C, theproduct ratio is 10% A and 90% B.Show why A predominates at -15 °C and B predominates at 60 °C.
When Br2 is added to buta-1,3-diene at -15 °C, the product mixture contains 60% ofproduct A and 40% of product B. When the same reaction takes place at 60 °C, theproduct ratio is 10% A and 90% B.(a) Propose structures for products A and B. (Hint: In many cases, an allylic carbocationis more stable than a bromonium ion.)(b) Propose a mechanism to account for formation of both A and B.(c) Show why A predominates at -15 °C and B predominates at 60 °C.(d) If you had a solution of pure A, and its temperature were raised to 60 °C, what wouldyou expect to happen? Propose a mechanism to support your prediction
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When Br2 is added to buta-1,3-diene at -15 °C, the product mixture contains 60% ofproduct A and 40% of product B. When the same reaction takes place at 60 °C, theproduct ratio is 10% A and 90% B.) Propose a mechanism to account for formation of both A and B
a) What product is formed from the [1,7] sigmatropic rearrangement of a deuterium in the following triene? (b) Does this reaction proceed in a suprafacial or antarafacial manner under thermal conditions? (c) Does this reaction proceed in a suprafacial or antarafacial manner under photochemical conditions?
When Br2 is added to buta-1,3-diene at -15 °C, the product mixture contains 60% ofproduct A and 40% of product B. When the same reaction takes place at 60 °C, theproduct ratio is 10% A and 90% B.(a) Propose structures for products A and B. (Hint: In many cases, an allylic carbocationis more stable than a bromonium ion.)
Name the 2 cumulated dienes with formula C6H10 that contain an unbranched chain. please answer fast i give upvote