10. (5pts) Provide the complete arrow pushing mechanism for the chemical transformation →depicted belowUse proper curved arrow notation that explicitly illustrates all bonds being broken, andall bonds formed in the transformation.Also, be sure to include all lone pairs and formal charges on all atoms involved in theflow of electrons.CH3OIIHAHCH3O-HH①

Answered: Image /qna-images/answer/a8f441ff-18d8-4255-8d95-43c2cfe5d561.jpg

Answered: 10. (5pts) Provide the complete arrow…

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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OChem help with the following reaction schemes (see attached image) Please provide the bond line structures for the products obtained in the following reaction schemes... Notice in question #1 that A, B, and C are actually shown as C, B, and finally A in the actual reaction scheme so C correlates with PCC, and so on Question #2 is in order.
Use bond-dissociation enthalpies (Table 4-2, p. 167) to calculate values of ∆H° for the following reactions. (a) CH3¬CH3 + I2 ¡ CH3CH2I + HI(b) CH3CH2Cl + HI ¡ CH3CH2I + HCl(c) (CH3)3C¬OH + HCl ¡ (CH3)3C¬Cl + H2O (d) CH3CH2CH3 + H2 ¡ CH3CH3 + CH4 (e) CH3CH2OH + HBr ¡ CH3CH2¬Br + H2O
The compound below is treated with chlorine in the presence of light
Determine the major organic products for the reactions in addition to whether they are racemic or not?
(3) HI does not undergo free radical addition with 1-butene, even in the presence of a peroxide. Please provide an explanation by analyzing the propagation steps if the same radical reaction occurred with HI. Besides the bond dissociation enthalpies in the appendix, the following approximate bond dissociate enthalpies might be useful to you: ~310 kJ/mol The component of C=C CH3CH₂CH₂CH₂-Br CH3CH₂CH₂CH2-I -290 kJ/mol (C-Br bond) ~235 kJ/mol (C-I bond)
Predict the major organic product formed when the compund shown below undergoes a reaction with H2O2 and then is heated in H2O. The 2nd photo is what I thought was the answer, but when I put it into Mastering Chemistry, it was counted as wrong and my feedback was, "What configuration is the C=C bond expected to haev?" I'm confused as to what this is referring to, so I appreciate any help given.
Please don't provide handwritten solution ...
7.) Carbocations are high energy intermediates in organic synthesis that are open-shelled carbon atoms. In the reaction below (a) we see that carbocations are also excellent Lewis acids, readily accepting a water molecule to form the product isopropanol. Given this, explain why when reaction (b) was set up, there were two regioisomeric products formed? Please draw a Lewis acid base reaction mechanism with arrows to justify your answer. H20 H OH H3CO CH3 H3C CH3 a.) carbocation Product open-shell H H20 Н. ОН b.) H3C H3C H3C and HO, ČH3 ČH3 ČH3
3. An alkene can be converted into an ether in the three mechanistic steps shown below. Complete this mechanism by: Draw curved arrows to indicate the flow of electrons for each step. Lone pairs are omitted for clarity but be sure to include lone pairs on atoms that are involved in bond formation/breaking. Draw the reaction intermediates in the appropriate boxes. Include all nonzero formal charges. Classify each step of the mechanism using the boxes below each arrow as one of the following: acid- base proton transfer (AB), nucleophilic attack (NA), elimination (E), or rearrangement (R). + H-OMe H-OO + MeOH + MeOH + H-OMe H-OO 48
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2. meo. Using Woodward - Hoofman rules predict the outcome of the following reactions. heat me and heat
91. Subject :-Chemistry

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