Draw a structural formula for each compound:
(a) 1-Isopropyl-4-methylcyclohexene
(b) (6E)-2,6-Dimethyl-2,6-octadiene
(c) trans-1,2-Diisopropylcyclopropane
Note: use wedged and dashed bonds to show
stereochemistry.
(d) 2-Methyl-3-hexyne
(e) 2-Chloropropene
(f) Tetrachloroethylene
Draw a structural formula for each compound: (a) 1-Isopropyl-4-methylcyclohexene (b) (6E)-2,6-Dimethyl-2,6-octadiene (c) trans-1,2-Diisopropylcyclopropane Note: use wedged...
4. Draw structures corresponding to the following systematic names; a) 1-isopropyl-4-methylcyclohexene b) 3-butyl-2-heptene c) 4-methyl-1,2- hexadiene d) trans-3,3-dimethyl-4-propyl-1,5-octadiene e) (42)-2,4-diethyl-1,4-hexadiene f) 1.2-propadiene g) (32,5E) -2,6-dimethyl-1,3,5,7-octatetraene h) cis-2,2,5,5-tetramethyl-3-hexene i) Methylenecyclohexane, j) trans- 1,2 divinylcyclohexane
Draw a structural formula for 3,4-dimethyl 2-pentanol. You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. . Do not include lone pairs in your answer. They will not be considered in the grading aato opy ChemDoodle Draw a structural formula for 2-cyclopenten-1-ol. Show stereochemistry only if given in the name If a group is achiral, do not use wedged or hashed bonds on it .In cases where there is more than one answer,...
(References] Draw a structural formula for trans-1-bromo-3-isopropylcyclobutane. • Show stereochemistry only if given in the name. • Include H atoms at chiral centers only. • If a group is achiral, do not use wedged or hashed bonds on it. • In cases where there is more than one answer, just draw one. - - -O0O-O" ChemDoodle
Draw the structure of each compound 1. Draw the structure of each compound: (a) cis-1,2-Cyclohexanediol (b) Isobutanol (c) 2,4,6-Trinitrophenol (d) (R)-2,2-Dimethyl-3-heptanol (e) Ethylene glycol (0) (s)-2-Methyl-1-butanol 2. Acid-catalyzed hydration of 3,3-dimethyl-1-butene produces 2,3-dimethyl-2-butanol. Show a mechanism for this reaction 3. Acid-catalyzed hydration of 1-methylcyclohexene yields two alcohols. The major product does not undergo oxidation, while the minor product will undergo oxidation. Explain. 4. Using 2-propanol as your only source of carbon, show how you would prepare 2-methyl- 2-pentanol. 5. Identify...
1) 2) Draw a structural formula of the S configuration of the compound shown below. CO2H Use the wedge/hash bond tools to indicate stereochemistry where it exists. Include H atoms at chiral centers only . If a group is achiral, do not use wedged or hashed bonds on it
1. Draw the structure of each compound: (a) cis-1,2-Cyclohexanediol (b) Isobutanol (c) 2,4,6-Trinitrophenol (d) (R)-2,2-Dimethyl-3-heptanol (e) Ethylene glycol (f) (S)-2-Methyl-1-butanol
1. Draw the structure of each compound: (a) cis-1,2-Cyclohexanediol (b) Isobutanol (c) 2,4,6-Trinitrophenol (d) (R)-2,2-Dimethyl-3-heptanol (e) Ethylene glycol (f) (S)-2-Methyl-1-butanol
1. Draw the structure of each compound: (a) cis-1,2-Cyclohexanediol (b) Isobutanol (c) 2,4,6-Trinitrophenol (d) (R)-2,2-Dimethyl-3-heptanol (e) Ethylene glycol (f) (S)-2-Methyl-1-butanol
Draw a structural formula of the RS configuration of the compound shown below. Use the wedge/hash bond tools to indicate stereochemistry where it exists. Include H atoms at chiral centers only. If a group is achiral, do not use wedged or hashed bonds on it 1. 2. OH CH NH2 RS CN NH2 NH2
1. Draw the structure of each compound: (a) cis-1,2-Cyclohexanediol (b) Isobutanol (c) 2,4,6-Trinitrophenol (d) (R)-2,2-Dimethyl-3-heptanol (e) Ethylene glycol (1) (S)-2-Methyl-1-butanol