How would we know using aromatic vicinal coupling that the c-c bond was formed between compound B and C to for the product A? (HO)₂B. Br compound A compound B compound C
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- O (1) H20, H*; (2) Jones reagent (1) H20, H*; (2) PCC, CH2CI2 (1) conc. H2SO4: (2) Jones reagent O (1) H20, H*; (2) Tollens reagent (1) conc. H2SO4: (2) PCC, CH2CI2 O (1) conc. H2SO4: (2) Tollens reagentA.) B.) ? H₂4 C.) NH₂ NO₂ By & -f -N CH3 -CH3 OH ŢSaquinavir (trade name Incirase) belongs to a class of drugs called protease inhibitors, which are used to treat HIV. Locate all the stereogenic centers in the drug saquinavir. H. H. N. N. H. NH2 OH O: saquinavir Trade name: Invirase NH O:
- 9) Which compound is NOT aromatic 09?? B B DA. B. C. Me CH3 ClC H ¿ OH NH₂ H Br-C-C H3C H Br CH3 Comparing structure pair in B OH Comparing structure pair in C [Select] Me HC CI Comparing structure pair in A [Select] [Select] Same structure drawn differently Enantiomers Diastereomers NH₂ Br H3C CH3 Br HC-CCH3 H For the following two structures compared in parts A and B, determine whether they are enantiomers OR diastereomers OR the same structure drawn differently (non-bonding electrons not included for clarity).Click the "draw structure" button to launch the drawing utility. Under certain reaction conditions, 2,3-dibromobutane reacts with two equivalents of base to give three products, each of which contains two new 7 bonds. Product A has two sp hybridized carbon atoms, product B has one sp hybridized carbon atom, and product C has none. What is the structure of C? H 3HC C C=CH₂ edit structure ...
- Compound A has the formula C5H10O that is produced by oxidation of a conpound that has the formula C5H12O. Compound A has an IT spectrum the has an absorbance at 1700 cm^-1 and no broad absorbance from 2500-3500 cm^-1. The 1H and 13C spectrums of Compound A both have 4 peaks. What is tbe structure of Compound A? Thank you for the help!1) 1544565- NH₂ 2) CI of & 7) 8) reagents used: FeCl3/Cl₂ HNO3/H₂SO4 MeCI/AICI3 ACCI/Et₂N SO3/H₂SO4 Pd/C, H₂ NaOH H₂SO4/heat ACCI= CI [Choose ]4. For each of the following substituted benzenes below, answer the following questions: ( h) [1] C6H5Br [2] C6H5CN [3] C6H5OCOCH 3 a.) Does the substituent donate or withdraw electron density by an inductive effect? b.) Does the substituent donate or withdraw electron density by a resonance effect? c.) On balance, does the substituent make a benzene ring more or less electron rich than benzene itself? d.) Does the substituent activate or deactivate the benzene ring in electrophilic aromatic substitution?
- Draw the major product(s) of each of the following reactions. (c) (b) (a) CI HO,S C2, ? HNO, AICI, FeCla H2SO4 H,CO (e) (d) Br2, ? conc HNO, FeBr3Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Long and detailed explanations are not needed. Keep it short, brief, and direct because I only need the answers as soon as possible. Calculate the % ee of a mixture containing 80% of one enantiomer and 20% of the other? A. 80B. 120C. 60D. 90Draw all stereoisomers formed in each reaction. to [1] CH3LI а. [2] H2O 1m( Culi b. [1] [2] H2O [1] LIAIH4 С. с. [2] H2O [1] mCРBA d. [2] MgBr [3] H2O ..||