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Devise an in depth mechanism for formation of the primary made of the elimination response underneath. C(CH3)3...

Devise an in depth mechanism for formation of the main fabricated from the removal response underneath. C(CH3)3 (CH3)3COK (CH3)3COH HZCCI Draw curved arrows to display electron reorganization for the mechanism step below. Make the ends of your arrows specify the starting place and destination of reorganizing electrons. Arrow-pushing Instructions ON XIN C(CH3)Three CH3 СН: -¢-CH3 Hoy H2C :C: okay*:0—C—CH CH3 CH3 Devise a detailed mechanism for formation of the primary product of the elimination response under. CH3 H2SO4 Draw curved arrows to...

b Use curved arrows to show the mechanism of the step beneath. Make the ends of...

b Use curved arrows to show the mechanism of the step beneath. Make the ends of your arrows specify the foundation and destination of reorganizing electrons. Arrow-pushing Instructions no XT +MgBr CH3 Submit b Use curved arrows to show the mechanism of the step beneath. If a couple of resonance type of the product is possible, display the most solid form. Arrow-pushing Instructions nn-XT Submit

Devise an in depth mechanism for formation of the major product of the removal reaction under. H2SO4...

Devise a detailed mechanism for formation of the main fabricated from the removal reaction underneath. H2SO4 Draw curved arrows to show electron reorganization for the mechanism step beneath. Make the ends of your arrows specify the origin and vacation spot of reorganizing electrons. Arrow-pushing Instructions unex you *** - H -ö-s-on

bankruptcy 7 EOC the electrophilic addition response proven below involves a carbocation rearrangement. for the mechanism...

bankruptcy 7 EOC the electrophilic addition response proven underneath involves a carbocation rearrangement. for the mechanism step under, draw curved arrows to display electron reprganization. use the arrow tool to specify the starting place and the vacation spot of the reorganizing electrons. The electrophilic addition reaction shown below involves a carbocation rearrangement HBr For the mechanism step beneath, draw curved arrows to display electron reorganization. Use the arrow instrument to specify the origin and the destination of the reorganizing electrons. Consult the...

Use curved arrows to display the mechanism of the step beneath. Make the ends of your...

Use curved arrows to show the mechanism of the step below. Make the ends of your arrows specify the starting place and vacation spot of reorganizing electrons. Base : H--0: :OH HO +1ニ11110.

[References) Shown underneath is the reaction of an alkene with an electrophile 1pt 1 pt 1pt...

[References) Shown underneath is the response of an alkene with an electrophile 1pt 1 pt 1pt ΚΙ Н3РО4 For the mechanism step below, draw curved arrows to display electron reorganization. Use the arrow software to specify the starting place and the destination of the reorganizing electrons. Consult the arrow-pushing instructions for the conference on regiospecific electrophilic assault on a double bond Arrow pushing Instructions + CH3 . 1 pt 1 pt no ② ipt eleven 1 pt 12 pt Thirteen ①...

This question has multiple parts. Work all the parts to get the most points. Table of...

This question has multiple parts. Work all the parts to get the most points. Table of Bond Dissociation Enthalpies C-H bond BDE (kJ/mol) C-X bond BDE (kJ/mol) X, and HX bonds BDE (kJ/mol) CH3-H 439 CH3-F 481 F2 157 C2H3-H 422 HF 568 (CH3)2 CH-H 414 (CH3)3C-H 405 C2H5-F 472 (CH3)2 CH-F 464 (CH3)Three C-F 455 CH3 CH3 CH3CHCHCH3 digne a CH3CHCH2CH3 + F2 F + HF Using the desk of bond dissociation energies in the first part of this...

HBT CH3 CH3 Hoc Electrophilic addition of HBr to alkenes yields a bromoalkane. The reaction begins...

HBT CH3 CH3 Hoc Electrophilic addition of HBr to alkenes yields a bromoalkane. The response begins with an attack on the hydrogen of the elect HBr by the electrons of the double bond to give a carbocation. This step follows Markovnikov's rule with the electrophilic H adding to the sp- carbon containing the most hydrogens, leading to the formation of the most stable carbocation (1° 2°<3). If conceivable, a 1,2-shift of both a neighboring hydride or methyl crew can occur...

This question has multiple parts. Work all the parts to get the most points. 242 Table...

This question has multiple parts. Work all the parts to get the most points. 242 Table of Bond Dissociation Enthalpies C-H bond BDE (kJ/mol) C-X bond BDE (kJ/mol) X2 and EX bonds BDE (kJ/mol) CH3-H 439 CH3-I IL 151 CH3-H 422 C,HS-I 238 HI 297 (CH3), CH-H 414 (CH3)2CH-I 238 (CH3),C-H 405 (CH3),CI 234 CH3 CH3CHCH2CH2 CH3 + HI CH3CHCH2CH3 1 Using the table of bond dissociation energies in the first a part of this question: Calculate AH for this reaction...

This question has multiple parts. Work all the parts to get the most points. 1 pt...

This question has multiple parts. Work all the parts to get the most issues. 1 pt 1 pt Table of Bond Dissociation Enthalpies C-H bond BDE (kJ/mol) C-X bond BDE (kJ/mol) X, and HX bonds BDE (kJ/mol) CH3-H 439 CH3-I 242 1 151 CH-H 422 CH3-1 238 HI 297 (CH3)2 CH-H 414 (CH), CH-I 238 (CH3),C-H 405 (CH),C-I 234 CH3 CH3CCH2CH3 CH3 CH3CHCH2CH3 HI Using the desk of bond dissociation energies in the first part of this question: Calculate AH...