CO5T0306483 What is the correct IUPAC name of the following compound? (15,2R)-1-ethyl-2-methylcyclohexane (1R, 2S)-1-ethyl-2-methylcyclohexane (1R 2R)-1-ethyl-2-methylcyclohexane (15,2S)-1-ethyl-2-methylcyclohexane
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
What is the correct IUPAC name of the following compound? (1S,2R)-1-iodo-2-methylcyclohexane (1S,2S)-1-iodo-2-methylcyclohexane (1R,2R)-1-iodo-2-methylcyclohexane (1R,2S)-1-iodo-2-methylcyclohexane Which group has the highest priority in the Cahn-Ingold-Prelog priority system? Give the highest ranking group a priority of 1 and the lowest ranking group a priority of 4. --CO2H-CONH2 Rank the following groups in terms of their priority according to the Cahn-Ingold-Prelog system of prioritles. Give the highest ranking group a priority of 1 and the lowest ranking group a priority of 4
Draw the most stable conformation for; a. trans-1-chloro-3-methylcyclohexane b. cis-1-ethyl-2-isopropylcyclohexane c. trans-1-bromo-4-ethylcyclohexane d. cis-2-bromo-1-methylcycclohexane Sppecifically, show the ring flipping and calculate the strain using the table given in the power point slides.
12. What is the correct IUPAC name of the following compound? CH2CH3 CH3 B. cis-1-ethyl-2-methylcyclohexane trans-1-ethyl-2-methylcyclohexane cis-1-ethyl-6-methylcyclohexane trans-1-ethyl-6-methylcyclohexane
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
How would you draw the most stable conformation of trans-1-ethyl-3-methylcyclohexane? Axial ethyl group on C-1, Axial methyl group on C-3 Axial ethyl group on C-1, Equatorial methyl group on C-3 Equatorial ethyl group on C-1, Axial methyl group on C-3 Equatorial ethyl group on C-1, Equatorial methyl group on C-3 Choices b and c are both correct Choices a and d are both correct How would you draw the most stable conformation of trans-1-chloro-2-fluorocyclohexane? Axial chlorine on C-1, Axial fluorine...
Draw the substitution product of the reaction of (1 S,3R)-1-chloro-3-methylcyclohexane with hydroxide.
1. Draw the compounds named below. (3R)-3-chloro-2-methylpentane (1R, 3S)-1-bromo-3-ethylcyclohexane 2. Draw the mechanisms for the reactions shown. Br XX- Br ~ SH - SH 1
2. Draw structures of the compound based on the given IUPAC name 1) (2E,5E-N-ethyl-N-methylhepta-2,5-dienamide 2) (1R,2R,3R,5R)-1-ethyl-5-isopropyl-3-methyl-2-(3-methylpentyl)cyclohexane Identify aromatic ring system 3. 2. Draw structures of the compound based on the given IUPAC name 1) (2E,5E-N-ethyl-N-methylhepta-2,5-dienamide 2) (1R,2R,3R,5R)-1-ethyl-5-isopropyl-3-methyl-2-(3-methylpentyl)cyclohexane Identify aromatic ring system 3.