Draw skeletal structure corresponding to each IUPAC name 1,2-dimethylcyclopentene 6-ethyl-2-octyne 3,3-dimethyl-1,4-pentadiene trans-5-methyl-2-hexene 5,6-dimethyl-2-heptyne 3,4,5,6-tetramethyl-1-decyne 4-methyl-1-hexene methylcyclohexene
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- Draw the following organic compounds: a) 2-Methylhexa-1,5-diene b) 3-Ethyl-2,2-dimethylhept-3-ene c) (4E)-2,4-Dimethylhexa-1,4-diene d) cis-3,3-Dimethyl-4propylocta-1,5-diene e) trans-1-Bromo-3-chloracyclopentane f) isopropyl bromide g) 3,3-Dimethyloct-4-yne h) 3-Ethyl-5-methyl-1,6,8-decatriyne i) 2,2,5,5-Tetramethylhex-3-yne j) 3,4-DimethylcyclodecyneDraw the structure of each molecule. (a) (S)-1-chloro-2,2-dimethyl-1-phenylcyclopentane; (b) (1R,2S)-1-methyl-1,2-dinitrocyclopropane; (c) (R)-4-ethoxycyclohexene; (d) (3S,4S)-3-chloro-4-fluoro-2-methylhepta-1,6-dieneDraw both the condensed and line-bond structure of these 4 compounds: * 4-ethylcycloheptene * 4,4-dimethylpent-2-ene * 3-chloro-2,7-dimethylnon-4-yne (Cl- Chloro branch) * 1-cyclohexylbut-2-yne
- Draw the structure for these molecules. (a) 3-phenylmethylhex-4-en-1-yne; (b) 7-phenylcyclohepta-1,3,5-triene;(c) 3,5,6-trinitro-4-phenylmethylhepta-1,3,5-triene; (d) 5,5-dichloro-6-ethenyl-7-phenylcyclooct-3-en-1-yneDraw the compunds below. (2e,4z)-1-bromo-4-methylhexa-2,4-diene (2e,4z)-5-bromo-3-methylhexa-2,4-diene (2z,4e)-1-bromo-4-methylhexa-2,4-diene (2z,4e)-1-bromo-3-methylhexa-2,4-dieneWhich of the following functional isomers should NOT correctly linked together? Choose one: 1,2-dimethylcyclopent-1-ene: 5-methylhex-1-yne 4-methylcyclohept-1-ene: 1-octyne penta-1,4-diene: 3-methylbut-1-yne 3-methylbut-1-ene: pent-2-yne
- Name the molecule given below its open structure according to the IUPAC system.A. (E) -6-chloro-5-methyl-4-decene-2,8-dioneB. trans-6-chloro-5-methyldec-4-ene-2,8-dioneC. trans-5-methyl-6-chloro-4-decene-2,8-dioneD. (Z) -6-chloro-5-methyldec-4-en-2,8-dioneE. (E) -5-methyl-6-chloro-4-decene-2,8-dioneDraw the following organic compounds cis-3,3-Dimethyl-4propylocta-1,5-diene trans-1-Bromo-3-chloracyclopentane isopropyl bromide 3,3-Dimethyloct-4-yne 3-Ethyl-5-methyl-1,6,8-decatriyne 2,2,5,5-Tetramethylhex-3-yne 3,4-DimethylcyclodecyneIDENTIFY IF IOCANT, CHAIN LENGTH, PREFIX, SUBSTITUENT 1. 2,2-diethylheptane 2. 3-methyl-3-butene 3. cis-3-pentene 4. trans-4-hexene 5. 2-chlorocyclopentene 6. trans-4-ethyl-3-pentene 7. cis-2-methyl-2-pentene
- A.) Draw both the condensed and line-bond structure of the following compounds: 1) 3-ethylhexane 2) 1,3-dimethylcyclopentane 3) 1,3-dichloro-3-methylheptane ( Cl- , Chloro branch) 4) bromocyclobutane (Br-, Bromo branch) 5) 5-sec-butylnonane 6) 4-t-butylheptane 7) 4-ethylcycloheptene 8) 4,4-dimethylpent-2-ene 9) 3-chloro-2,7-dimethylnon-4-yne (Cl- Chloro branch) 10) 1-cyclohexylbut-2-yneDraw the following compounds: a) 6-[1-chloropropyl]-5-methyl-1-decyne b) 2-bromo-3-methyl-3,5-octadiene c) 4,6,6-trimethylcyclooctene d) 2-Bromobicyclo[3.3.1]nonaneA.) On any clean sheet of paper, draw both the condensed and line-bond structure of the following compounds: 4) bromocyclobutane (Br-, Bromo branch) 5) 5-sec-butylnonane 6) 4-t-butylheptane 7) 4-ethylcycloheptene 8) 4,4-dimethylpent-2-ene 9) 3-chloro-2,7-dimethylnon-4-yne (Cl- Chloro branch) 10) 1-cyclohexylbut-2-yne