Use a dash and/or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. Ignore acid byproducts. mCPBA
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- app.101edu.co oudy @ 2 X V * UL Week 7: Panopto ||| 3 D E PII $ 4 R Rank these alkyl halides in order of increasing reactivity in an SN2 reaction. F 4x X UL LTU 7-1A F4 HHH % 5 T G 4, CI F5 A 6 4) Y X Question 16 of 24 F6 C|Chegg.com & 7 U F7 ★ A) III < | < || 8 B) || < | < ||| C) ||| < || < | D) || < ||| < | E) | < ||| < || PrtScn 1 FB X + Home ( 9 F9 O ) End 0 D 67 ENG F10 P PgUp Tp S ( D [ * O 6:15 PM 10/18/2022 PgDn + F12 0 SL 3" ΟΝ Ο CON|OU|G fic | G b C COU app.101edu.co Tube Maps > > 2 W X |2|GD|QC| GA W |G1|CS|UO N Question 15 of 31 Provide the correct IUPAC name for the skeletal (line-bond) structure shown here. Stereochemistry is ignored. 4- 5,5- 3- 3,3- 2- 5- di sec- ISO tri cyclo tert- oct meth hex 99 MacBook Air F6 F2 3 E 80 F3 > $ 4 R Aav D₂ % 5 0 모 F5 T 6 Y & v lo 7 F7 U 00 * 8 DII F8 - 9 F9 0 EE 0 G B F10 ☆ Done G PN|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 + (
- H H ČH3 Br р. + CH;C=C: in acetone Reaction Type(s) Mechanism(s) Product(s). Stereochemistry (if applicable) q. p-chloronitrobenzene + sodium ethoxide Reaction Type(s) Mechanism(s) Product(s). Stereochemistry (if applicable)Treatment of 1,2-dimethylcyclopentene with OsO4 with NMO produces which of the following? 1 OH CH3 CH3 OH OI O II ||| OIV OV OH CH3 A || OH CH3 OH CH3 H CH3 CH3 ..H for OH CH3 IV CH3 ..H H CH34:31 PM Mon May 8 ← Problem 22 of 30 1) PhMgCl (C6H5MgCl) 2) HCI/H₂O Draw the products resulting from addition of a Grignard reagent to an aldehyde. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore any inorganic byproducts. CI @ 90% H Submit
- Esc Content 54°F Clear ! Draw the major products of the SN1 reaction shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. Ignore any inorganic byproducts. 1 * app.101edu.co F1 Aktiv Chemistry. @ 2 Select to Draw SN1 Product * H₂O F2 X QSN2/SN1 Reactions Fl # 3 DIL F3 $ 4 ▬▬ F4 X % 5 4₁ G Which alkyl bromide i X F5 Question 3 of 22 A 6 OI F6 G whats a stronger nue 1 Please select a dra & 7 F7 PrtSQ. 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 10tab ← Chrome File Edit View ● C esc h Hulu | Watch app.aktiv.com ! 1 Draw the product of an SN2 reaction shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts. Q CỘN History Bookmarks Profiles Tab F1 X NaCN acetonitrile 2 F2 Aktiv Chemistry W • # 3 -35 -- -- 80 F3 E Window Help $ 4 a F4 X R + NOV 2 % 5 @ Problem 8 of 20 Atoms, Bonds and Rings Draw or tap a new bond to see suggest A T 6 FG Charges 8 7 O FT
- Chemistry C с dy app.101edu.co 44 # 3 E X | C UL Week 7: Panopto pll III CI $ R F Rank these alkyl halides in order of increasing reactivity in an SN2 reaction. % 5 UL LTU 7-1A T Q CI ^ 6 J Y H X Question 5 of 24 & 7 C|Chegg.com N U A) ||| < | < || B) || < | < ||| C) ||| < || < | D) || < ||| < | E) | < ||| < || PrtScn 8 1 M X + K Home O End A O 2 ENG O 12 ☆ L F10 Tp P PgUp - ¡ * п ( 0 Submin + 6:10 P 10/18/202 ( PgOnPlease help with 4c, 4d, and 4e. We havent learned kaw of equivalents so please do 4c a different way. thank youPart A || CH2=CH' CH3 Draw the molecules on the canvas by choosing buttons from the Tools (for bonds), Atoms, and Advanced Template toolbars. The single bond is active by default. Show the appropriate stereochemistry by choosing the dashed or wedged buttons and then clicking a bond on the canvas. EXP. CONT. H +) C CI Br Marvin JS [1] by O ChemAxon F P.