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!

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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[References) Rank the set of substituents below in order of priority according to the Cahn-Ingold-Prelog sequence rules. (a) -CH=CH2 e (b) -CH(CH3)2 8 (c) -C(CHa)s e (d) -CH,CH, Submit Answer Try Another Vernion 10 item attempts remaining Visitod
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2. What is the IUPAC name of the following alkene? (A) (3E,5Z)-3-bromoocta-3,5-diene (B) (3Z,5E)-6-bromoocta-3,5-diene C (3E,5Z)-3-bromoocta-4,6-diene (D) (32,5E)-3-bromoocta-3,5-diene (E) (3E,5Z)-3-bromohepta-3,5-dienc Br 3,5 8
-A on 2. Which class of pericyclic reactions is the Diels-Alder reaction? What is a (4+ 2) n cycloaddition reaction? Explain •a cycloaddikon where ore reactant moleculee cortriautes 41 ele ctrons & the other a electrans 3. 4. (a) Give the systematic name of the diene in this reaction 15-cis)1,4-diphenyl-1,3-betadiene (b) Calculate the difference in the standard Yree energy, AG° (kJ/mol) between the two major conformations of this diene? (Write the formula and show your work.) = (-617.920458au- AGO Product- reactants k017.9259320 = 0.00S 47444K/ml.005474qu 14.37 KJ/ mol 1au= alas.KLcis) (trans) 5. Give the systematic name of the dienophile in this reaction. Maleie nhydride 6. Give the systematic name of the adduct in this reaction. 7. What is the melting point of your synthesized Diels-Alder adduct 8. Calculate the standard free energy of activation AG # for this reaction (Write the formula and show your work). AG = G75- G°R = (-994.1304ay au)-(-997.194182 au) - 0.039898au= .639898ay•…
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Draw one enantiomer of the major product of the following Diels- Alder reaction. (Use wedge/dash bonds to indicate the orientation of substituents in the product. Hydrogen atoms on chirality centers must be shown explicitly.) H.
Bromine in methylene chloride is added in stoichiometric proportions to cyclopentane, What color is the final solution? Bromine in methylene chloride is added in stoichiometric proportion to cyclohexa-1,3-diene. What color is the final solution?
Use the inscribed polygon method to show the pattern of molecularorbitals in cyclooctatetraene. Indicate the arrangement of electrons in these orbitals forcyclooctatetraene, and explain why cyclooctatetraene is not aromatic.
12.2. Predict the products of the following reactions. Be careful to consider all stereochemical aspects. CH3 CH3 m-chloroperoxy- benzoic acid (b) H2C (g) H CH2 OsO4 H. (k) OH t-BUOOH VO(acac)2 CH3
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