a. For the following indicated bonds, rank them in order of decreasing AH° for homolyticcleavage. Based on your answer, which bond would be most likely to break homolytically?(a)(c)H3CCH3.CH3CH3CH3(b)Page 1 of 5Chem 0310 Organic Chemistry 1 Recitationsb. Draw all the possible radical products for 2-methylbutane, and determine which bond is mostlikely to be broken.

Answered: Image /qna-images/answer/351d570d-d9d1-4e1e-a436-1d5438e70c27.jpg

Answered: a. For the following indicated bonds,…

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 8.21P

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Identify the major product of the reaction of an alkene shown below. ||| 1. Hg(OAc)2, H2O 2. NaBH4, NaOH ....... ОН || IV ОН о, ОН
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44a) Draw the bond-line structure of 1,4-dimethyl-cyclohexa-1,3-diene here: STRUCTURE: b) Circle all the sp²-hybridized carbons in your drawing of the structure. c) In the spaces below, draw two potential products from a chlorination reaction (addition of Cl2) with your first structure Product 1: Product 2:
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Please draw the structures of (E)-1-chloropropene, 1,1-dichloro-2-methylpropene, and (E)-2,3-dichloro-2-butene and please rank them in terms of increasing dipole moment Arrange the following alkenes in order of increasing stability: 1-pentene; (E)-2-pentene; (Z)-2-pentene; 2-methyl-2-butene, thank you
N(CH2CH3)3 + HNO3 --------> a.) rewrite the reaction using bond-line structure of reagents and products of the reaction b.) supply the curved arrows explaining the mechanism of the reaction
3. (i) Classify the following carbocations (methyl, primary, secondary, tertiary, benzylic, allyl, or vinyl). (ii) Which of the following carbocations is more stable? (iii) What kind of rearrangement (methyl shift, alkyl shift, hydride shift, anion shift, other) can be used to interconvert these carbocations? + +
[References] The two alkenes below react with HI at different rates. CH3 CH3CH=CHCH3 and CH;ċ=CHCH3 Draw the structural formula of the MAJOR product formed by the alkene having the HIGHER reaction rate. You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. In cases where there is more than one answer, just draw one. C P opy aste Previous Next ChemDoodle®
1) RCO H 2) [H₂SOJ. ? Modify the given structure to draw the major product(s). Use the single bond tool to interconvert between double and single bonds. If a racemic mixture of enantiomers is expected, draw both enantiomers. Note: you can select a structure and use Copy and Paste to save drawing time. H₂C. OH th CH, CH₂ OH H₂C OH aff CH₂ CH₂ Edit Drawing
2. Label the following reactions as most likely occuring by an SN1 or SN2 mechanism. Explain your answer. (4 marks) HBr A) HO, CH;CH2OH 'Br B) Na* SCH; CH;CN ‚Br „SCH3

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