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 reagent9) Which compound is NOT aromatic 09?? B B DSaquinavir (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:
- 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!A.) B.) ? H₂4 C.) NH₂ NO₂ By & -f -N CH3 -CH3 OH Ţ1) 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 ]
- A. 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).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?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 ...
- 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, FeBr3a) Which molecule has a higher electron density in the aromatic ring? Explain. H₂C O CO₂H CO₂H H₂C-N CH3 CH3 b) which is more acidic?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-Methycyclohexanol