What are the absolute configurations of the indicated
stereoisomer of 2-bromo-3-methylpentane?
What are the absolute configurations of the indicated
stereoisomer of 2-bromo-3-methylpentane?
(2S,3R) |
(2S,3S) |
(2R,3S) |
(2R,3R) |
Answer option : 4) (2R, 3R)
====================XXXXXXXXXXXXXXXXXXXXX===========================
What are the absolute configurations of the indicated stereoisomer of 2-bromo-3-methylpentane? What are the absolu...
18. Assign the absolute configuration of the two stereocenters in stereoisomer of 2-bromo-3-pentanol shown below. Br ОН a) 2R, 3R b) 2R, 3S c) 2S, 3R d) 2S, 3S 19. The following are 5 stereorepresentations of 1,5-dimercaptopentane-1,5-diol. Taking (1) as a reference structure. Determine if each of the other stereorepresentations are conformers to (1), enantiomers to (1) and diastereomers of (1). OH OH Enantiomer Diastereomer Conformer HS SH (2) он SH Enantiomer Diastereomer Conformer OH OH HS "ОН (3) ON...
What are the configurations of the indicated stereoisomer of dihydroxypentane? Chapter 5 Reading Quiz Question 7 What are the configurations of the indicated stereoisomer of dihydroxypentane? CH 3 OH HO CH3 Hints O 2S,4R O 2S,4S O 2R,4S O 2R,4R Submit My Answers Give Up
please help for part A, B, and C (a) Make models of the four 2-bromo-3-hydroxybutanal isomers. Accurately sketch them in the boxes. Use solid and dashed wedges where necessary. (2 pts) (b) For each isomer, draw a Newman projection for the most stable conformation of the C(2)-C(3) bond. (2 pts) (c) Use the RIS system to assign the absolute configuration of each chiral (stereogenic) center. (1 pt) Configuration? (2R, 3S) (2s, 3R (2S, 3S) (2R 3R) Configuration? (2R, 3S) (2S,...
Name the following compound below with correct stereochemistry. CH Br r -H H-CH, CH,CH, (25,3S)-2-bromo-3-methylpentane (20,35)-2-bromo-3-methylpentane (25,3R)-2-bromo-3-methylpentane (2R 3R)-2-bromo-3-methylpentane
what major E2 product would form on the reaction of (2S,3R) 2-bromo-3-methylpentane with base? QuesLIUI What major E2 product would form on reaction of (2S,3R) 2-bromo-3-methylpentane with ba CH3 O (Z) 3-methylpent-2-ene (E) 3-methylpent-2-ene (3R) 3-methylpent-1-ene (Z) 3-methylpenta-1,3-diene
Which is the correct name for the compound shown below? H. O (2R,35)-2-Bromo-3-chlorobutane (25,3R)-2-Bromo-3-chlorobutane (2R, 3R)-2-Bromo-3-chlorobutane (2S,3S)-2-Bromo-3-chlorobutane Which compound is achiral? O meso-2,5-Difluorohexane O trans-1,2-Dimethylcyclohexane O (S)-3-lodohexane (2R, 3R)-2,3-Dibromoheptane 1
What is the correct IUPAC name for the enantiomer of the following molecule?(2S, 3R) -2-bromo-3-chlorobutane2R, 3S) -3-bromo-2-chlorobutane2S, 3S) -2-bromo-3-chlorobutane(2R, 3R) -2-bromo-3-chlorobutane(2R, 3S) -2-bromo-3-chlorobutane
What is the product when (2R,3R)-2-bromo-3-methylpentane is reacted with NaOH? So what I'm curious about is if this reaction will go sn1 or sn2. Please explain which one and why.
9. Treatment of (2R,3S)-2-chloro-3-methylpentane with potassium t-butoxide in t-butanol gives a single stereoisomer of 3-phenyl-2-butene. (15 pts) CI CH, | (CH, CƠ K, CH,CH=C-CH-CH, CHE (CH3),COH Draw the three possible Newman projections of the staggered conformations of (2R,3S)-2- chloro-3-methylpentane. Circle the one Newman projection with the conformation most suited for the elimination reaction. Conformation 2 Conformation 3 Conformation 1 Show the stereoisomer of the product expected from this elimination path.
QUESTION 2 What major E2 product would form on reaction of (2S,3R) 2-bromo-3-methylpentane with base? |||11111 CH3 A. (Z) 3-methylpent-2-ene B. (E) 3-methylpent-2-ene C. (3R) 3-methylpent-1-ene D. (Z) 3-methylpenta-1,3-diene