The question states... "Draw structures for the following names. Show stereochemistry explicitly." a.) R-3-ethyl-4-methylhexane b.) 2R,4S-4-chloro-2-fluoroheptane
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
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
Draw the structures that correspond to the following names. Correct any names that are not in accord with the rules of systematic nomenclature. 4-Chloro-5-methylhexane 3-methyl-3-propylpentane 1,1,1-trifluoro-2-methylpropane 4-(3-bromobutyl)nonane
Alkyl Halides: Elimination reaction with (2R,3R)-2-chloro-3-methylpentane Draw the product formed when (2R,3R)-2-chloro-3-methylpentane under-goes an elimination reaction with NaOCH3. Alkyl Halides: Elimination reaction with 3-chloro-3-ethyl-2,2-dimethylpentane. Draw the structure of the product that is formed when 3-chloro-3-ethyl-2,2-dimethylpentane undergoes an elimination reaction with NaOCH3. Indicate the stereochemistry of the product. Identify the three products formed when 2-bromo-2-methylpropane is dissolved in a mixture of 80% ethanol and 20% water.
Draw bond line structures for the following: 1,1,3-triethylcyclooctane 4,5-diethylnonane 1-butyl-3-fluorocyclobutane 4-ethyl-3-isopropyl-2-methylhexane
Draw the following molecules: 1. (Z)-3-heptene 2. (R)-3-fluorocycloheptene 3. (R)-2-ethyl-2-hexanol 4. trans-1,2-dimethylcyclohexane 5. 1,1-dipentylcyclopropane 6. (R)-1-chloro-2-methylpropane 7. (2R,3S)-2,3-dibromobutane
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
Draw the unique stereoisomers for 2-chloro-2,3-dimethylpentane. Show stereochemistry clearly. To ensure proper grading, explicitly draw all four groups, including wedge/dash bonds, around a chirality center. Indicate whether the compounds could exist in an optically active form.
Give the structures for the following: A. (2R)-2-heptanol B. (4S)-bromopentanal
1. Draw the MOST stable and the LEAST stable isomer of 3- chloro -4- methylhexane by drawing Newman Projections looking down the bond between Carbon -3 and Carbon-4 2. Circle the most acidic Hydrogen and then explain its acidity as needed with structures and sentençes NH2 OH