Assign E or Z stereochemistry to the following compound (red = 0): SH3 3-omon-1-(3) enelb-E,t-s A ne od vndeimerlopenade duob odt of vijeimeroo919 40 ngiza/
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- siacell 1%IV lI. B7:21 PM A docs.google.com 47% V:E1 نور Four auswer Determine the double bond 1 point stereochemistry (E or Z) for the following molecules: * F F Br A В O A: Z; B: Z А: E;B B: Z А: E; B: E А: Z;B B: E Bromination of alkanes is a much 1 point slower reaction than chlorination. Which of the following is expected to | be the major organic product whenName the following compound including stereochemistry i CI Br,Alkenes are one of the organic compounds that are commonly used in the pharmaceutical industries. Recentiy. Ms R Maluleka, one of the Hon student at Sefako Makgatho Health Sciences University slated two compounds, Band Cfrom avocado leaves. OH OH A B These two compounds were shown to exhbit nteresting biological acivitie against SARS-COV-2, a new type of coronavirus that causes COVID-19. These two Compounds can also be synthesized in the laboratories using suitable reagents. Ms
- chem 534 cha Hư OAC H please show stereochemistry H₂ COCH ? H CO₂CH3 O Ac 2. + ? hv 9 40°C 3. H₂ C 4. 0°C Catq Q-0 + [6+4] NGC ?. لك 5. [ V-CO₂CH3 + II NCCN [4+2] C6H5 6. 2 C6H5Arrange the following groups in increasing CIP priority order: * -C-OCH3 С-ОН C–CH3 -C-NH2 I II III IV III, IV, II, I O II, I, IV, II O II, III, I, IV O I, I, IV, IPredit 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…
- Describe the E/Z stereochemistry for the molecules shown below: A: Z; B: Z A: Z; B: E A: E; B: E A: E; B: ZDraw 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.What is the appropriate systematic name for the compound below? HO., SH ) (15,45)-4-hydroxycyclohex-2-enethiol O (35,65)-6-mercaptocyclohexen-3-ol )(1S,4S)-4-mercaptocyclohex-2-enol (3S,65)-6-hydroxycyclohexene-3-thiol
- What is the E/Z stereochemistry for the molecules shown: Choose from the choices below. a. A: Z; B: Z b. A: E; B: E c. A: Z; B: E d. A: E; B: ZWhat is the stereochemical configuration of the enantiomer of (2S, 4R)-2, 4-octanediol? (A diol is a compound with two —OH groups.)structures for c and d with stereochemistry MeO OMe O OH CH3C(OME)3 heat C p-TSA