Synthesis Using Alkenes 8-50 How would you carry out the following transformations? Tell what reagents you would use in each case. 2 ( (c) (e) 8. A = ∞ CH3 CHỊCH CH₂CH=CHCHCH₂ CH₂ CH₂C=CH₂ OH CH₂CH + CH₂ CH CHCH OH cyclohexane (b) H₂C CH₂CHCH OH -OH CH3
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- Vinylcyclopropane reacts with HBr to yield a rearranged alkyl bromide. Follow the flow of electrons as represented by the curved arrows, show the structure of the carbocation intermediate in brackets, and show the structure of the final product.Provide the mechanism and products for the acid-catalyzed epoxide opening reactions below, including appropriate stereochemistry.Draw the structures of the organoboranes formed when borane reacts with each alkene below, including the regiochemistry and stereochemistry as appropriate. Propose a mechanism for each reaction.
- 13). What is the major product of the following two reactions? H₂ H3C H3C NH (A) H3C ОН H3C NH₂ OH-, then H2O (D) H3C H₂ (В) CH3 ? H3C H3C (E) ОН NH (C) CH3 -CH₂What is the major Organic product of the reaction Shown below? H CA CH3CH₂CH=H OH # CD CHECHC NH + t NH3 (B) CH3CH₂ CEN OH CD) CH ₂ CH ₂ CHN H₂ CC) CH 3 CH ₂ CH = NOHNaming Alkenes 7-37 Name the following alkenes: (а) CH3 (b) CH3 CH2CH3 (с) CH2CH3 CH3CHCH,CH,CH C=C H3C H CHCH2CH3 CH3 H2C=CCH2CH3 H H. (d) H CH3 (e) H. (f) H2C=C=CHCH3 H3C C=C c=c H3C =c CH,CH,CH2 H2C=CHCHCH H. CH3 CH3 CH3
- Which one(s) is(are) possible product(s) for the shown reaction? OH H₂C-C-H U 0 A B 0 C D E Na₂Cr₂O7 H₂SO4 A OH H₂C-C-CH3 B O H₂C-C-H с D E H₂C-C-CH₂ H₂C-C-OH No reaction8) Select the structure of the major product in the following reaction. H OH m-CPBA ? H OH I II III 0 IV V10:06 AM Tue Nov 28 Attach File Provide the reagents needed (A-HO to accomplish the transformations presented below: OH G C D H H B E A 85% Ⓒ 0
- Complete the following reactions by identifying the major product(s) or the missing reaction conditions. No mechanism is needed. a) PCC OH HO CH₂Cl2 no necessary reagents for this equilibrium b) c) Hg(OAc)2 H₂SO4, H₂OThe following sequence of reactions gives cyclooctanone. Propose a structural formula for compound A and a mechanism for its conversion to cyclooctanone. OH H, Pt HNO, A (C,H1;NO) C=N46. Which alkene below would result in the most regioselective reaction with HCl? Which would result in the least regioselective? oor of ook oor o + 10 20 30 A |3ა B C D E