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4. Draw structures for the following compounds (12 points): a. 6,6-dimethylhept-2-yne b. 5-amino-4-methoxyhept-6-yn-2-o...
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...
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
9. (10 pts) Draw structures for the following compounds: (a) (2S,4S)-2-Bromo-4,5-diethylheptane (b)(R)-3-hexyn-2-ol
9. (10 pts) Draw structures for the following compounds: (a) (2S,4S)-2-Bromo-4,5-diethylheptane (b)(R)-3-hexyn-2-ol
1) 2-amino-3-hydroxybutanoic acid 2) 2,3-dinitrobutane A. Draw the skeletal structure (line-bond) for the following compounds. B....
1) 2-amino-3-hydroxybutanoic acid
2) 2,3-dinitrobutane
A. Draw the skeletal structure (line-bond) for the following compounds. B. Convert the structures to the Most Stable and the Least Stable Newmann projections around (looking down) C2-C3 bond. (The numbering is based on the nomenclature locator numbers) C. On your skeletal structures, label the stereogenic centers (chiral carbons) if there are any. D. Draw all the possible stereoisomers for the compounds. Indicate which are enantiomer pairs. which are diastereomers to each other, and if...
Draw the structures of the following organic compounds a) 2,4-dicholoroheptane b) 2,2-dicholorohexane c) 2-methyl-4-ethylnoname d) 2,2,4-trimethyldecane...
Draw the structures of the following organic compounds a) 2,4-dicholoroheptane b) 2,2-dicholorohexane c) 2-methyl-4-ethylnoname d) 2,2,4-trimethyldecane e) 2-methyl-3-isoprophylheptane f) 1-methylcyclohexane g) 1,1-diethylcyclopentane h) 1-bromo-2-methylcycloheptane i) 1,2-dichlorocyclobutane
9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne ...
Draw structures corresponding to the following names:
9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
1.) 2-amino-3-hydroxybutanoic acid 2.) 2,3-dinitrobutane A. Draw the skeletal structure (line-bond) for the following compounds. B....
1.) 2-amino-3-hydroxybutanoic acid
2.) 2,3-dinitrobutane
A. Draw the skeletal structure (line-bond) for the following compounds. B. Convert the structures to the Most Stable and the Least Stable Newmann projections around (looking down) C2-C3 bond. (The numbering is based on the nomenclature locator numbers) C. On your skeletal structures, label the stereogenic centers (chiral carbons) if there are any. D. Draw all the possible stereoisomers for the compounds. Indicate which are enantiomer pairs. which are diastereomers to each other, and if...
(3) L1150 2. Draw the Fischer projections of the following compounds and assign (R) or (S) for chiral carbon atom....
(3) L1150 2. Draw the Fischer projections of the following compounds and assign (R) or (S) for chiral carbon atom. (30') СН3 (2) PH (1) (R)-2-pentanol (4) (S)-(1-bromoethyl)benzene (3) (S)-CH2OH-CHOH—CH NH (5) 2-methyl-3-chloropentane 9) (2R,3R,4S)-2,3-dibromo-4-chlorohexane
24. Draw the structures for 4 of the following 5 compounds. a. 4-(1,1-dimethylethyl)heptane b. 2,...
PLEASE PROVIDE EXPLANATION
24. Draw the structures for 4 of the following 5 compounds. a. 4-(1,1-dimethylethyl)heptane b. 2,6-dimethyl-4-(2-methylpropyl)decane c. 1-bromo-4-(3,3,3-trifluoro-2-methylpropyl)-7-fluorooctane d. 6-ethyl-2,6,7-trimethyl-5-propylnonane e. 4-sec-butyl-1,2-dimethylcyclohexane
24. Draw the structures for 4 of the following 5 compounds. a. 4-(1,1-dimethylethyl)heptane b. 2,6-dimethyl-4-(2-methylpropyl)decane c. 1-bromo-4-(3,3,3-trifluoro-2-methylpropyl)-7-fluorooctane d. 6-ethyl-2,6,7-trimethyl-5-propylnonane e. 4-sec-butyl-1,2-dimethylcyclohexane
4) Draw the following compounds a. (2S,5R)-5-chloro-2-ethylhexanoic acid b. (1R,2R,4R)-4-ethylcyclohexane-1,2-diol c. (2S
4) Draw the following compounds a. (2S,5R)-5-chloro-2-ethylhexanoic acid b. (1R,2R,4R)-4-ethylcyclohexane-1,2-diol c. (2S,3R)-3-amino-2-phenylbutanal d. (1S,2S,3R)-2-fluoro-3-propylcyclobutanol e. (2E, 7Z)-5-bromo-2,7-nonadiene
Help please Draw the following alkynes: 4-bromo-3, 3-diethylhex-i-en-5-yne 3, 10-dimethy-6-secbutylcyclodecyne) 1, 3-hexadien-5-yne s-ethyl-s-methyl-1.6.8-decatriyne Z-5, 7-dimethyl-4-octen-1-yne
Help please
Draw the following alkynes: 4-bromo-3, 3-diethylhex-i-en-5-yne 3, 10-dimethy-6-secbutylcyclodecyne) 1, 3-hexadien-5-yne s-ethyl-s-methyl-1.6.8-decatriyne Z-5, 7-dimethyl-4-octen-1-yne
9. (10 pts) Draw structures for the following compounds: (a) (2S,4S)-2-Bromo-4,5-diethylheptane (b)(R)-3-hexyn-2-ol
1) 2-amino-3-hydroxybutanoic acid
2) 2,3-dinitrobutane
A. Draw the skeletal structure (line-bond) for the following compounds. B. Convert the structures to the Most Stable and the Least Stable Newmann projections around (looking down) C2-C3 bond. (The numbering is based on the nomenclature locator numbers) C. On your skeletal structures, label the stereogenic centers (chiral carbons) if there are any. D. Draw all the possible stereoisomers for the compounds. Indicate which are enantiomer pairs. which are diastereomers to each other, and if...
Draw structures corresponding to the following names:
9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
9.19 Draw structures corresponding to the following names: (b) 3-Ethyl-5-methyl-1,6,8-decatriyne (a) 3,3-Dimethyl-4-octyne (c) 2,2,5,5-Tetramethyl-3-hexyne (d) 3,4-Dimethylcyclodecyne (e) 3,5-Heptadien-1-yne (g) 3-sec-Butyl-1-heptyne (f) 3-Chloro-4,4-dimethyl-1-nonen-6-yne (h) S-tert-Butyl-2-methyl-3-octyne
1.) 2-amino-3-hydroxybutanoic acid
2.) 2,3-dinitrobutane
A. Draw the skeletal structure (line-bond) for the following compounds. B. Convert the structures to the Most Stable and the Least Stable Newmann projections around (looking down) C2-C3 bond. (The numbering is based on the nomenclature locator numbers) C. On your skeletal structures, label the stereogenic centers (chiral carbons) if there are any. D. Draw all the possible stereoisomers for the compounds. Indicate which are enantiomer pairs. which are diastereomers to each other, and if...
(3) L1150 2. Draw the Fischer projections of the following compounds and assign (R) or (S) for chiral carbon atom. (30') СН3 (2) PH (1) (R)-2-pentanol (4) (S)-(1-bromoethyl)benzene (3) (S)-CH2OH-CHOH—CH NH (5) 2-methyl-3-chloropentane 9) (2R,3R,4S)-2,3-dibromo-4-chlorohexane
PLEASE PROVIDE EXPLANATION
24. Draw the structures for 4 of the following 5 compounds. a. 4-(1,1-dimethylethyl)heptane b. 2,6-dimethyl-4-(2-methylpropyl)decane c. 1-bromo-4-(3,3,3-trifluoro-2-methylpropyl)-7-fluorooctane d. 6-ethyl-2,6,7-trimethyl-5-propylnonane e. 4-sec-butyl-1,2-dimethylcyclohexane
24. Draw the structures for 4 of the following 5 compounds. a. 4-(1,1-dimethylethyl)heptane b. 2,6-dimethyl-4-(2-methylpropyl)decane c. 1-bromo-4-(3,3,3-trifluoro-2-methylpropyl)-7-fluorooctane d. 6-ethyl-2,6,7-trimethyl-5-propylnonane e. 4-sec-butyl-1,2-dimethylcyclohexane
Help please
Draw the following alkynes: 4-bromo-3, 3-diethylhex-i-en-5-yne 3, 10-dimethy-6-secbutylcyclodecyne) 1, 3-hexadien-5-yne s-ethyl-s-methyl-1.6.8-decatriyne Z-5, 7-dimethyl-4-octen-1-yne
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