Draw the molecules from the IUPAC names:
a)(2S)-2bromo-4-methylhexane
b)(R,E)-6-aminohept-2-en-4-one
c)(1R,3R)-3-methylcyclopentane-1-ol
d)(2S,3S)-2,3-dihydroxysuccinic and
Draw the molecules from the IUPAC names: a)(2S)-2bromo-4-methylhexane b)(R,E)-6-aminohept-2-en-4-one c)(1R,3R)-3-methylcyclopentane-1-ol d)(2S,3S)-2,3-dihydroxysuccinic and
(2) Hta H- CH CAH CH3 is properly named: A) (3R.4S,5R)-3,5-Dichloro-4-methylhexane B) (2S,3S,4S)-2,4-Dichloro-3-methylhexane c) (2S 3R 4R)-2,4-Dichloro-3-methylhexane D) (25.3R.45)-2,4-Dichloro-3-methylhexane E) (2S,3S,4R)-2,4-Dichloro-3-methylhexane AO BO co DO Е О MacBook Air
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
2a. Draw the dash-wedge structures and Fischer projections of the following molecules. R-1-bromoethanol (2S, 3R) - 2-chloro-3-iodobutan-1-ol (HOCH-CHCICHBCH) .. Draw a diastereomer for (2S, 3R) - 2-chloro-3-iodobutan-1-ol.
(4) Draw the 3-dimensional representation for each of the following. (2S,3S)-2-fluoro-3-methylhexane (E)-2-methylbut-2-enal
11. Draw a dash-wedge structure for the following? (1 pt each) (a) (1R)-1-bromo-1,3,3trimethylcyclohexane (b) (2S, 4S)- 2-bromo-4-methylhexane 12. Draw fisher projection formula of (2S, 3R, 4S)- 2,4-dichloro-3-methylhexane? (1 pt)
10.18 Draw structures corresponding to the following IU PAC names (a) 2,3-Dichloro-4-methylhexane (b) 4-Bromo-4-ethyl-2-methylhexane (c) 3-lodo-2,2,4,4-tetramethylpentane (d) cis-1-Bromo-2-ethylcyclopentane
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
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) Choose the correct IUPAC Name of the compound Он B.(Z)-5-methylhex-2-en-4-ol A. (E)-5-methylhex-2-en-4-ol D. (Z)-2-methylhex-4-en-3-ol C. (E)-2-methylhex-4-en-3-ol (2) Choose the correct order according to the activity of carbonyl OO RCOR' RCOCR' RČNR'2 RCCI 4 3 2 B. 1>4>3>2 C. 2>1>4>3 D. 4>1>3>2 1>2>4>3 A. (3) Choose the correct structure of 2-chloroethylbenzoate В. A. CH, CH,CОСH, CH, CОСH,СH, II C. D. -соснCH, -сосH,CH, CI Cl (4) The name of the following structure is A. 5-heptanal B. 5-hexanal D.4-hexenal C. 5-hexenal (5)...
(a) Draw the saw-horse (or wedge-dash) projection of (2S,3R)-3-methylpentan-2-ol. [Marks: 1] (b) Draw the Newman projections of the 2-3 bond in (2S,3R)-3-methylpentan-2-ol. [Marks: 2] (c) Based on the Newman projections from part b. - draw a rotation vs. energy diagram (you do NOT need to give specific energy values in this diagram) that will allow you to identify the most stable confirmation around the 2-3 bond. Assume the greatest steric and torsional strain occurs when the hydroxyl and ethyl groups...