This is newman projection of the molecule. In gauche conformation, bulky groups are present at diahedral angle of 600. So, from given structures, strucutre A that is option D is correct. Please find attached file for complete guide and answer .
Rotating around the selected bond select the gauche conformation. Br OH Br Br Br HBr OH...
Which represents a gauche conformation? A B C D E CI Н. CI CI CI H H CBr Br H H Н. H I H H Br H HY H H H Br Br H H HH B?
What is the major product of the reaction? HBr Select one: Br a. Br Br. O b. Br a C. Which polymer is formed from the following conditions? ||||| ROOR heat n a b Select one: 白。自 b.b C.C Which Fischer projection represents R-2-chloropentane? Select one: CH3 a. ci-to -CH2CH2CH3 H CH3 b. H+CH2CH2CH3 CI H C. H3C-CH2CH2CH3 CI CI d. Hgc +H CH2CH2CH3 What is the major product of the reaction below? ОН 1) LIAIHA 2) H20 Select one:...
6. Conformational Analysis: Newman Projections (25 points) Consider the rotation around the C3-C4 bond of (3R 4R)-3,4-dibromohexane. C3-C4 bond. B Draw all three eclipsed Newman projections. In no particular order. Calculate the total strain associated with each conformation using the table below, enter on the provided line, and identify the least stable conformation (Circle it) Briefly explain your assignment of the least stable conformation - including which specific types of steric strain are involved. Short phrases are great complete sentences...
Select the correct product from the following
reactions:
16. + HBr Br 0 c - rowns - polo con for the 17. + HBr/peroxide 1. OsO4 2. NaHSO3 OH + do - 19. + NBS - Br | A t-BuOK 1. BH3 OH 20. OH t-BuOH, 750c 2. HO, OH NaOEt/EtOH | 1. BH3 2. H₂O, OH OH 2. 550c | B.
Use bond energies to estimate the enthalpy of formation of HBr(g). BE(H–H) = 436 kJ/mol BE(Br–Br) = 192 kJ/mol BE(H–Br) = 366 kJ/mol A –52 kJ/mol B +262 kJ/mol C +104 kJ/mol D +52 kJ/mol E –104 kJ/mol
Q7.1 6 Points Br OH OH CI Br F А D E OH ОН. H2N- F G H J Which of these rings is OPTICALLY ACTIVE? (select all that apply) Compound A Compound B Compound C Compound D Compound E Compound F Compound G Compound H Compound Compound J None of these Q7.2 3 Points Br OH OH CI Br F А B с D E OH OH xazk HN F G H Which of these rings is MESO? (select...
Question 7 Select the stronger acid. 0 Bir OH OH Br Selected Coordinates Clear
H3PO4 1. НО. 165° OH 2. Aqueous acetone + H2O Br + ОН + HBr a = Proton transfer d = Electrophilic addition e=E1 Elimination f=E2 Elimination g=Snl Nucleophilic substitution h=Sn2 Nucleophilic substitution b = Lewis acid/base c= Radical chain substitution Identify the mechanism by which each of the reactions above proceeds from among the mechanisms listed. Use the letters a - i for your answers. 1. 2.g
CO2H CO2H HNO3/H2SO4 H20 2. +conc. HBr H20 Br OH a Electrophilic addition b E2 Elimination c-SNI Nucleophilic substitution d S2 Nucleophilic substitution e-Electrophilic aromatic substitution f-carbonyl nucleophilic addn g = Nucleophilic subs at carbonyl(acyl Xfer) h = Conjugate (nucleophilic) addn for your answers 1. 2.
What is Major product of the following reaction? NHOCH.CH CH,CH, OH Br & de a А B C D m OB kod OD DA