Draw the product formed by the reaction of t-butoxide with (1R, 2S)-1-bromo-2-methyl-1-phenylbutane (shown below). (Draw the...
Draw the product formed by the reaction of t-butoxide with (1R,2S) 1-bromo-2-methyl-1-phenylbutane (shown below). Draw the correct ste of the product. Draw the product as a skeletal structure Br (CH, Co K CH, COH H3C CH2 H3C
Draw the product formed by the reaction of t-butoxide with (1R,2S)-1-bromo-2-methyl-1-phenylbutane (shown below). Draw the correct stereoisomer of the product. Draw the product as a skeletal structure. H, Br (CH3),coºk* (CH3),COH Hzclllll CH2 H3C/ Previous Check Answer Next Exit
Draw the product formed by the reaction of t-butoxide with (1R,2S)-1-bromo-2-methyl-1-phenylbutane (shown below). (Draw the correct stereoisomer of the product.)
Draw the product formed by the reaction of t-butoxide with (1R,2S)-1-bromo-2-methyl-1-phenylbutane (shown below). (Draw the correct stereoisomer of the product.)
Draw the product formed by the reaction of t-butoxide with (1R,2S)-1-bromo-2-methyl-1-phenylbutane (shown below). (Draw the correct stereoisomer of the product.)
Draw the product formed by the reaction of potassium t-butoxide with (1S,2S)-1-bromo-2-methyl-1-phenylbutane (shown below). (Draw the correct stereoisomer of the product.) Draw the product formed by the reaction of potassium t-butoxide with (1S,2S)-1-bromo-2-methyl-1-phenylbutane (shown below). (Draw the correct stereoisomer of the product.)
Draw the (1R,2S,4S)-1-bromo-2-ethyl-4-methyl cyclopentane in the line angle representation
Draw a dash-wedge structure for the following? (a) (1R)-1-bromo-1,3,3trimethylcyclohexane (b) (2S, 4S)- 2-bromo-4-methylhexane provide r and s please
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.
1. (1R, 2R)-1-bromo-1,2-dimethylcyclohexane is heated in the presence of potassium tert-butoxide (KO-tert-Bu). Name minor product/s only 2. 2-iodo-1,1,2,3,3-pentamethylcyclohexane is heated in the presence of sodium ethoxide in ethanol, don’t name the product/s of the reaction 3. ,2,2-trimethylcyclohexan-1-ol is heated in aqueous sulfuric acid 4. (3S)-2-methyl-3-pentanol is heated in aqueous sulfuric acid