In a given iupac name we write the structure based on connectivity of atoms and groups
What is the structure of (1R, 2R, 5S, 3Z)-5-bromo-2-propylcyclohex-3-en-1-ol?
Draw the structures for the following compounds. a) (3Z,5S)-4-bromo-5-chloro-2-methylhexa-1,3-diene b) (5S,7S)-5-(bromomethyl)-7-chloro-oct-2-yne c) (1S,5S,6S)-6-bromo-5-[(1R)-1-chloroethyl]cyclohex-3-enol d) 2-bromo-4-[(1R)-1-hydroxyethyl]benzoic acid e) (3S,4S,5S)-5-amino-3-hydroxy-4-methylhexanal f) (Z,2R,4R)-6-bromo-4-chloro-N-ethyl-N-methylhept-5-en-2-amine g) [(1S)-1-chloroethyl] (Z,3R)-5-chloro-3-methoxyhex-4-enoate h) (Z,3R)-3-bromo-4-chloro-7-methyloct-4-enoic acid i) (3S)-6-bromo-N-ethyl-N,3-dimethylhex-4-ynamide j) (Z,3R,4S)-6-bromo-3-[(1S)-1-chloroethyl]-4-hydroxyhept-5-en-2-one
1. Draw a structure for: (Z)-3-Bromo-2-hexene (Z)-1-methylcyclononene (3Z,6E)-1,3,6-Octatriene (E)-2-methoxy-2-pentene (3S,4S)-4-methyl-3-hexanol (1R, 3S)-3-methylcyclohexanol
2. Give the structure of each of the following molecules. 1,2,3-propanetrith iol (1R, 2R)-2-methylcyclohexanol 1,2,3-propanetriol 2-propen-1-ol
how to draw wedge dash structure for (1R,2R,3R,5S)5-bromo-2-chloro-3-ethyl-5-methylcyclohexanolhow to draw wedge dash structure for (1R,2R,3R,5S)5-bromo-2-chloro-3-ethyl-5-methylcyclohexanol
2. Name or draw (as appropriate for the following compounds: OH 1701111 B. (1R)-1-(1-methylethyl)-4-propoxycyclohex-3-en-ol D. (1R, 32, 55, 6E, 95)-5-ethyl-9(N,N-diethylamino)cyclodec-3,6-dien-1-ol ol بما
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
Draw and name the SN2 major product formed when (2R,5S)-2-bromo-5-chlorohexane is treated with sodium iodide in acetone. (Use only one equivalent of NaI.)
Select the most stable chair conformation for (1R,3S,5S)-1-chloro-3-isopropyl-5-methylcyclohexane. Select the most stable chair conformation for (1R,3S,5S)-1-chloro-3-isopropyl-5-methylcyclohexane Select the most stable chair conformation. CH(CH3)2 (1R,3S,5S)-1-chloro-3-isopropyl-5-methylcyclohexane Chair choices: CI CH CH3 CH3 (H3C)2HC CH(CH3)2 (H3C)2HC CH3 CH3 CH3 Cl CH(CH3)2 (H3C2HC (H3C)2HC
Part A Which compound is the major product of the treatment of (1R 2R)-1-bromo-1,2-dimethylcyclohexane with NaOCH, in CH, OH solvent? & NOCH, CHOH 2 Soon & А B С D B ОООО
Draw and name the major SN2 product when (2R,5S)-2-bromo-5-chlorohexane is treated with sodium iodine in acetone. * Use only one equivalent of NaI and use wedge and dash bonds