H,CO OCH3 Compound ZEREF Compound MAVIS END Predict the structures of the starting material given the following information: Test reagent Compounds Tollens Reagent 1/KI then NaOH ZEREF (+) (-) MAVIS (-) (-) END (-) (-)
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- INTRODU Achemcal anmlysis of compound Catlan Or upot 12.56 alyeny showshi made the mais 12.5 100 m CGn than)= 32 %3D O:125A ALEKS - Alec Nema - Learn G Arrange the compounds below ir x A www-awu.aleks.com/alekscgi/x/Isl.exe/1o_u-lgNslkr7j8P3jH-IvUrTNdLZh5A8CnG03PBGuXr8iCPa7ZMmym9pTWPGPMQBZuhqGO-ia6eFgZ0OQdKyhK7Uw7cw-OpH... ☆ : Apps Sprouts Academy. 9 Online Tutoring C 400 Request Heade... Q Weather & Soil CH.. O CHEMICAL BONDING Predicting the relative ionic character of chemical bonds Alec V Arrange the compounds below in decreasing order of the jonic character of the bonds in them. That is, pick 1 for the compound with the most ionic bonds, pick 2 for the compound with the next most ionic bonds, and so on. jonic character compound of bonds dla CaCl, (Choose one) ▼ Cl, (Choose one) ▼ SiCl, (Choose one) AICI, (Choose one) ▼ Explanation Check O 2020 McGraw-Hill Education. All Rights Reserved. Terms of Use | Privacy I Accessibi 3:5 12/ P Type here to search (15 IIPredit ds produc 1. Br ght 2.1-BuOK 38 Which represet soy depis 2mthyleyclohexeol where the wo ubatitum are S.BH, in THE 4 HO, NaOH (A) (m) CH (A) 1014 (B) BH CH OH (C) (D) (9 O он (D) 25. What radical interediate is fonmed in CHa this reaction? CH HC 2 HOOH H,C 30 Which molecules sre chiral? H. hv HO (m) COH Br (C) HO (D) HO V 26. Predict the product OH SOci II IV (A) 1,II, II, & IV (C) H& II pyridine (B) II, II, A IV (D) I1& IV (A) (B) CI 31. Explain why this synthetic route will not produce this product. şoCi 1) CHMgr 2) HHP (C) (D) SOCI H,HO heal Which reagents produce this transformation? 27. (A) The Grigrard reagent will not add to the ketone. OH HO. (B) The Grignard reagent will not add to the alcohol. (A) 1) LIAIH 2) H, H;0 (C) The Markovnikov rule will lead to a different product. (B) NABH,, HO (D) Acid catalyzed dehydration will lead to the formation of the more (C) PCC, CH,Cl; (D) KMNO, NaOH, H;O, heat thermodynamically stable alkene. What is the formal charge of oxygen in…
- F1 2) Which term best describes the relationship between the two molecules depicted in the box (below): .:0: 2 O (A) O (B) HO₂C O (C) O (D) O (E) F2 OH #3 CO₂H OH 80 F3 $ 4 HO₂C F4 OH % 5 CO₂H OH F5 6 F6 A) Constitutional Isomers B) Enantiomers C) Diastereomers D) Meso E) Newman Projections & 7 & F7 * DII 8 F8 F9 7 F10 0 T F11What is the name of the following compound +1 Br Brill.. |||| OH₂ OH₂ Co Br H₂O OH₂ trans-teraaquadibromocobalt(1) bromide trans-teraaquadibromocobaltate(1) bromide Ocis-teraaquadibromocobalt(1) bromide cis-teraaquadibromocobaltate(1) bromide14. Protons H, and H, in the following compound are Br HD А. homotopic enantiotopic diastereotopic mesotopic none of thes В. C. D. Е. I
- Erling Appoint... Opportunity Queue WHY? RC RRL EGoogle Docs m Elms College Genetics 1,3-Cyclopentadiene (pKa = 16) is a much stronger acid than cyclopentane (pka = 44). WS02 9 Blackboard Uhart Select one: O A. The pi electrons of 1,3-cyclopentadiene repel a hydrogen ion away from the molecule O B. The conjugate base of 1,3-cyclopentadiene is a stable, aromatic species, while the conjugate base of cyclopentane is not aromatic and is much less stable. O C. The shorter C-C bonds of 1,3-cyclopentadiene greatly augment its acid strength. Steric effects render 1,3-cyclopentadiene a stronger acid. COD. O E. 1,3-cyclopentadiene (the acid) has resonance stability; cyclopentane does not. US g Mar 16 6:26 8mapter 4 Problem 54 Part A Identify all meso compounds. CI H3C H A H3C оо 00 Check all that apply. 64°F A В C D Submit CI CA Provide Feedback CI M H3C Н CI В H3C Request Answer CI н FIA Н. CI с H3C H3C Н CI C "!!!! H CI H3C .... D H3C H 0 H CI ГBr LiCu(CH3)2 6 (1) LiAlH4 2 3 Ahol follow (2) H₂O 0 Aci HBr (xs) H (2) H₂O+ -Li