See Figure 8-1. Match the reaction to its category. 1 2 3 4 5 [Choose ] [Choose ] [Choose ] [Choose ] ✓ [Choose ] elimination substitution addition rearrangement
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- H3C₂ Br H₂O a. Enantiopure (1R, 3R)-3-Methylcyclohexanol b. Achiral 1-Methylcyclohexanol C. Racemic mixture (1R, 3R)- and (1S, 3S)-3-Methylcyclohexanol d. Diastereomeric mixture of (1R, 3R)- and (1S, 3R)-3-Methycyclohexanolca/Fecb major product CH + CH;CI. AlCl3 7. 8. LIAIHY pcls ---> Alcis 2) t20 LiD H20 10. Br 11. 2) NH4 CI DB2/Fech 2) Mg /Ether acetone ------> 12. 6. 9.enantiomers, or identical H₂CC. H Br Br HC. CN b. Label the following as structural isomers, conformational isomers, diastereomers, CN HO CH₂ Br H H H hundreds of H H H H-Br Bri OH HH OH Br OH O OH ÕH Br -CH₂ HO H HO- H OH HOH₂C H H HO H 5. Provide arrows for the reaction mechanism shown below. The arrows should show 'electron flow' as we've done in class and should be consistent with the formal charges that show up on the intermediates in this multistep process All the structures with relevant atoms are provided below H H Br H O RO-OR heat or hvi H HOH H HO H O O Br H H H OH OH H LOH H Br Br Br Br HO Br CO₂H H₂N-H CH₂SH H CH₂ Supply mechanisms for the following reactions showing all intermediates, all formal charges and using arrows to show 'electron flow'. The first two mechanisms represent an 'easy' and a 'hard' exam mechanism. HS. e Br HNH₂ OH CH₂ HOH N A you only need to show initiation and propagatin steps where n hundreds
- Determine the product(s) formed when 2-methylprop-1-ene is treated with the following reagents. CH3 CH3 HO-C-CHa H-C-CH3 CHa CH2OH NBS DMSO, H20 CH3 CH3 HO-C-CHa H3C-C-CH3 CH3 CH;Br ÓCH,CH, HBr Br2 H2C=c CH3 |[1) 9-ВBN (2) H2O2, HO CH3 CH3 Br-C-CH3 Br-C-CHa ČH3 ČH;Br CHa CH Br-C-CH3 H,C-C-CH3 ČH;OH ÓCH, ResetQ. Identify the products (from 1 to 10) in the following scheme: CI HNO3 1 2 AICI3 H,SO4 Zn(Hg) HCI KMNO4 (hot, concd.) 4 3 Br2 |hv (CH3),CO¯ K* Mg, ether Br2 5 C„H14B12 CH;COCH3 NaOCH3 PHCO3H Fused KOH, 200°C 10 8 Alcohol (3º) An Ether Epoxide derivative 2 5 6 8 9 10Figine 9-2 A. B. CI 1- butene Nao H NaOH c. D. CI ∙CI KT- OC(CH₂) ₂ K+ - 0 C(CH3)3
- Draw the mechanism for the following reaction: Et - OH x+a CH3 CH₂ Et Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron-flow arrows should start on the electron(s) of an atom or a bond and should end on an atom, bond, or location where a new bond should be created.Rank the compounds by DECREASING reactivity towards nitration with HNO3/ H2SO4 (most reactive on the left). NO2 CH3 II III IV O A. V>V>I> || > || O B. V>I> III > || > IV oCV> || >1> V> I| O D. I > V> > || > IV O E. II > V >1> [IV >| Moving to another question will save this response. Co searchN|ON|OU|G fic|Gb| app.101edu.co Maps YouTube 0³ A ℗ 2 F2 W S CO X G d B 2|GD|QC|GA Question 13 of 31 Provide the correct IUPAC name for the skeletal (line-bond) structure shown here. Stereochemistry is ignored. 1- 3- 2- 6- 4- 5- iso tert- di tri sec- cyclo pent hept non 99 MacBook Air # 3 > 0 80 F3 E D $ S4 Aav F4 R F 0, % 5 F F5 T G 6 Y & 7 H F7 U * 00 8 J DII F8 W G 1 CS UONEE 9 K F9 ) O O F10 L Done P Gri J F11 + (